Extractability of water-soluble soil organic matter as monitored by spectroscopic and chromatographic analyses.

Science.gov (United States)

Nkhili, Ezzhora; Guyot, Ghislain; Vassal, Nathalie; Richard, Claire

2012-07-01

Cold and hot water processes have been intensively used to recover soil organic matter, but the effect of extraction conditions on the composition of the extracts were not well investigated. Our objective was to optimize the extraction conditions (time and temperature) to increase the extracted carbon efficiency while minimizing the possible alteration of water extractable organic matter of soil (WEOM). WEOM were extracted at 20°C, 60°C, or 80°C for 24 h, 10-60 min, and 20 min, respectively. The different processes were compared in terms of pH of suspensions, yield of organic carbon, spectroscopic properties (ultraviolet-visible absorption and fluorescence), and by chromatographic analyses. For extraction at 60°C, the time 30 min was optimal in terms of yield of organic carbon extracted and concentration of absorbing and fluorescent species. The comparison of WEOM 20°C, 24 h; 60°C, 30 min; and 80°C, 20 min highlighted significant differences. The content of total organic carbon, the value of specific ultraviolet absorbance (SUVA(254)), the absorbance ratio at 254 and 365 nm (E (2)/E (3)), and the humification index varied in the order: WEOM (20°C, 24 h) < WEOM (80°C, 20 min) < WEOM (60°C, 30 min). The three WEOM contained common fluorophores associated with simple aromatic structures and/or fulvic-like and common peaks of distinct polarity as detected by ultra performance liquid chromatography. For the soil chosen, extraction at 60°C for 30 min is the best procedure for enrichment in organic chemicals and minimal alteration of the organic matter.

Soil tension mediates isotope fractionation during soil water evaporation

Science.gov (United States)

Gaj, Marcel; McDonnell, Jeffrey

2017-04-01

Isotope tracing of the water cycle is increasing in its use and usefulness. Many new studies are extracting soil waters and relating these to streamflow, groundwater recharge and plant transpiration. Nevertheless, unlike isotope fractionation factors from open water bodies, soil water fractionation factors are poorly understood and until now, only empirically derived. In contrast to open water evaporation where temperature, humidity and vapor pressure gradient define fractionation (as codified in the well-known Craig and Gordon model), soil water evaporation includes additionally, fractionation by matrix effects. There is yet no physical explanation of kinetic and equilibrium fraction from soil water within the soil profile. Here we present a simple laboratory experiment with four admixtures of soil grain size (from sand to silt to clay). Oven-dried samples were spiked with water of known isotopic composition at different soil water contents. Soils were then stored in sealed bags and the headspace filled with dry air and allowed to equilibrate for 24hours. Isotopic analysis of the headspace vapor was done with a Los Gatos Inc. water vapor isotope analyzer. Soil water potential of subsamples were measured with a water potential meter. We show for the first time that soil tension controls isotope fractionation in the resident soil water. Below a Pf 3.5 the δ-values of 18O and 2H of the headspace vapor is more positive and increases with increasing soil water potential. Surprisingly, we find that the relationship between soil tension and equilibrium fractionation is independent of soil type. However, δ-values of each soil type plot along a distinct evaporation line. These results indicate that equilibrium fractionation is affected by soil tension in addition to temperature. Therefore, at high soil water tension (under dry conditions) equilibrium fractionation is not consistent with current empirical formulations that ignore these effects. These findings may have

In situ remediation of Jet A in soil and ground water by high vacuum, dual phase extraction

International Nuclear Information System (INIS)

Kirshner, M.; Pressly, N.C.; Roth, R.J.

1996-01-01

This report summarizes the initial results of subsurface remediation at Terminal 1, Kennedy International Airport, to remediate soil and ground water contaminated with Jet A fuel. The project was driven and constrained by the construction schedule of a major new terminal at the facility. The remediation system used a combination of ground water pumping, air injection, and soil vapor extraction. In the first five months of operation, the combined processes of dewatering, volatilization, and biodegradation removed a total of 36,689 pounds of total volatile and semivolatile organic jet fuel hydrocarbons from subsurface soil and ground water. The results of this case study have shown that 62% of the removal resulted from biodegradation, 27% occurred as a result of liquid removal, and 11% resulted from the extraction of volatile organic compounds (VOCs)

[Effect of Water Extracts from Rhizosphere Soil of Cultivated Astragalus membranaceus var. mongholicus on It's Seed Germination and Physiological Characteristics].

Science.gov (United States)

Lang, Duo-yong; Fu, Xue-yan; Rong, Jia-wang; Zhang, Xin-hui

2015-01-01

To explore the relationship between continuous cropping obstacle and autotoxicity of Astragalus membranaceus var. mongholicus. Distilled water(CK), water extracts of rhizosphere soil(50, 100, 200 and 400 mg/mL) were applied to test their effect on early growth and physiological characteristics of Astragalus membranaceus var. mongholicus. The water extracts from rhizospher soil of cultivated Astragalus membranaceus var. mongholicus significantly increased seedling emergence rate, root length and vigor index of Astragalus membranaceus var. mongholicus seedling when at the concentration of 100 mg/mL or below, however,there was no significant effect at 200 mg/mL or higher. The water extracts from rhizosphere soil of cultivated Astragalus membranaceus var. mongholicus significantly reduced the SOD activity in Astragalus membranaceus var. mongholicus seedling at 400 mg/mL and POD activity at 200 mg/mL and 400 mg/mL,while significantly increased the MDA content. Water extracts from Astragalus membranaceus var. mongholicus rhizosphere soil significantly affected Astragalus membranaceus var. mongholicus germination and seedling growth in a concentration-dependent manner, generally, low concentrations increased the SOD and POD activity which improved seed germination and seedling growth, while high concentrations caused cell membrane damage of the seedling.

Mixed functional monomers-based monolithic adsorbent for the effective extraction of sulfonylurea herbicides in water and soil samples.

Science.gov (United States)

Pei, Miao; Zhu, Xiangyu; Huang, Xiaojia

2018-01-05

Effective extraction is a key step in the determination of sulfonylurea herbicides (SUHs) in complicated samples. According to the chemical properties of SUHs, a new monolithic adsorbent utilizing acrylamidophenylboronic acid and vinylimidazole as mixed functional monomers was synthesized. The new adsorbent was employed as the extraction phase of multiple monolithic fiber solid-phase microextraction (MMF-SPME) of SUHs, and the extracted SUHs were determined by high-performance liquid chromatography with diode array detection (HPLC-DAD). Results well evidence that the prepared adsorbent could extract SUHs in environmental waters and soil effectively through multiply interactions such as boronate affinity, dipole-dipole and π-π interactions. Under the optimized extraction conditions, the limits of detection for target SUHs in environmental water and soil samples were 0.018-0.17μg/L and 0.14-1.23μg/kg, respectively. At the same time, the developed method also displayed some analytical merits including wide linear dynamic ranges, good method reproducibility, satisfactory sensitivity and low consume of organic solvent. Finally, the developed were successfully applied to monitor trace SUHs in environmental water and soil samples. The recoveries at three fortified concentrations were in the range of 70.6-119% with RSD below 11% in all cases. The obtained results well demonstrate the excellent practical applicability of the developed MMF-SPME-HPLC-DAD method for the monitoring of SUHs in water and soil samples. Copyright © 2017 Elsevier B.V. All rights reserved.

Assimilable organic carbon (AOC) in soil water extracts using Vibrio harveyi BB721 and its implication for microbial biomass.

Science.gov (United States)

Ma, Jincai; Ibekwe, A Mark; Wang, Haizhen; Xu, Jianming; Leddy, Menu; Yang, Ching-Hong; Crowley, David E

2012-01-01

Assimilable organic carbon (AOC) is commonly used to measure the growth potential of microorganisms in water, but has not yet been investigated for measuring microbial growth potential in soils. In this study, a simple, rapid, and non-growth based assay to determine AOC in soil was developed using a naturally occurring luminous strain Vibrio harveyi BB721 to determine the fraction of low molecular weight organic carbon in soil water extract. Calibration of the assay was achieved by measuring the luminescence intensity of starved V. harveyi BB721 cells in the late exponential phase with a concentration range from 0 to 800 µg l(-1) glucose (equivalent to 0-16.0 mg glucose C kg(-1) soil) with the detection limit of 10 µg l(-1) equivalent to 0.20 mg glucose C kg(-1) soil. Results showed that bioluminescence was proportional to the concentration of glucose added to soil. The luminescence intensity of the cells was highly pH dependent and the optimal pH was about 7.0. The average AOC concentration in 32 soils tested was 2.9±2.2 mg glucose C kg(-1). Our data showed that AOC levels in soil water extracts were significantly correlated (Pgrowth bioluminescence based assay. Understanding the levels of AOC in soil water extract provides new insights into our ability to estimate the most available carbon pool to bacteria in soil that may be easily assimilated into cells for many metabolic processes and suggest possible the links between AOC, microbial regrowth potential, and microbial biomass in soils.

Some plant extracts retarde nitrification in soil

Directory of Open Access Journals (Sweden)

Abdul–Mehdi S. AL-ANSARI

2015-12-01

Full Text Available An incubation experiment was conducted to evaluate the effect of aqueous extracts of 17 plant materials on nitrification inhibition of urea- N in soil as compared with chemical inhibitor Dicyandiamide (DCD. Plant materials used in study were collected from different areas of Basrah province, south of Iraq. Aqueous extracts were prepared at ratio of 1:10 (plant material: water and added at conc. of 0.05, 0.10 and 0.20 ml g– 1 soil to loamy sand soil. DCD was added to soil at rate of 50 µg g-1 soil . Soil received urea at rate of 1000 µg N g-1 soil. Treated soils were incubated at 30 OC for 40 days. Results showed that application of all plant extracts, except those of casuarina, date palm and eucalyptus to soil retarded nitrification in soil. Caper, Sowthistle ,bladygrass and pomegranate extracts showed highest inhibition percentage (51, 42, 40 and 40 %, respectively and were found to be more effective than DCD (33 %. Highest inhibition was achieved by using those extracts at conc. of 0.1 ml g-1 soil after 10 days of incubation . Data also revealed that treated soil with these plant extracts significantly increased amount of NH4+–N and decreased amount of NO3-–N accumulation in soil compared with DCD and control treatments. Results of the study suggested a possibility of using aqueous extracts of some studied plants as potent nitrification inhibitor in soil.

Organic compounds in hot-water-soluble fractions from water repellent soils

Science.gov (United States)

Atanassova, Irena; Doerr, Stefan

2014-05-01

Water repellency (WR) is a soil property providing hydrophobic protection and preventing rapid microbial decomposition of organic matter entering the soil with litter or plant residues. Global warming can cause changes in WR, thus influencing water storage and plant productivity. Here we assess two different approaches for analysis of organic compounds composition in hot water extracts from accelerated solvent extraction (ASE) of water repellent soils. Extracts were lyophilized, fractionated on SiO2 (sand) and SPE cartridge, and measured by GC/MS. Dominant compounds were aromatic acids, short chain dicarboxylic acids (C4-C9), sugars, short chain fatty acids (C8-C18), and esters of stearic and palmitic acids. Polar compounds (mainly sugars) were adsorbed on applying SPE clean-up procedure, while esters were highly abundant. In addition to the removal of polar compounds, hydrophobic esters and hydrocarbons (alkanes and alkenes particle wettability and C dynamics in soils. Key words: soil water repellency, hot water soluble carbon (HWSC), GC/MS, hydrophobic compounds

Mobility of arsenic and its compounds in soil and soil solution: the effect of soil pretreatment and extraction methods.

Science.gov (United States)

Száková, J; Tlustos, P; Goessler, W; Frková, Z; Najmanová, J

2009-12-30

The effect of soil extraction procedures and/or sample pretreatment (drying, freezing of the soil sample) on the extractability of arsenic and its compounds was tested. In the first part, five extraction procedures were compared with following order of extractable arsenic portions: 2M HNO(3)>0.43 M CH(3)COOH>or=0.05 M EDTA>or=Mehlich III (0.2M CH(3)COOH+0.25 M NH(4)NO(3)+0.013 M HNO(3)+0.015 M NH(4)F+0.001 M EDTA) extraction>water). Additionally, two methods of soil solution sampling were compared, centrifugation of saturated soil and the use of suction cups. The results showed that different sample pretreatments including soil solution sampling could lead to different absolute values of mobile arsenic content in soils. However, the interpretation of the data can lead to similar conclusions as apparent from the comparison of the soil solution sampling methods (r=0.79). For determination of arsenic compounds mild extraction procedures (0.05 M (NH(4))(2)SO(4), 0.01 M CaCl(2), and water) and soil solution sampling using suction cups were compared. Regarding the real soil conditions the extraction of fresh samples and/or in situ collection of soil solution are preferred among the sample pretreatments and/or soil extraction procedures. However, chemical stabilization of the solutions should be allowed and included in the analytical procedures for determination of individual arsenic compounds.

Decontamination of PCBs-containing soil using subcritical water extraction process.

Science.gov (United States)

Islam, Mohammad Nazrul; Park, Jeong-Hun; Shin, Moon-Su; Park, Ha-Seung

2014-08-01

Polychlorinated biphenyls (PCBs) are one of the excision compounds listed at the Stockholm convention in 2001. Although their use has been heavily restricted, PCBs can be found in some specific site-contaminated soils. Either removal or destruction is required prior to disposal. The subcritical water extraction (SCWE) of organic hazardous compounds from contaminated soils is a promising technique for hazardous waste contaminated-site cleanup. In this study, the removal of PCBs by the SCWE process was investigated. The effects of temperature and treatment time on removal efficiency have been determined. In the SCWE experiments, a removal percentage of 99.7% was obtained after 1h of treatment at 250°C. The mass removal efficiency of low-chlorinated species was higher than high-chlorinated congeners at lower temperatures, but it was oppositely observed at higher temperatures because the lower chlorinated congeners are formed by dechlorination of higher chlorinated congeners. Gas chromatography/mass spectrometry analysis confirmed that the PCBs underwent partial degradation. Several degradation products including mono- and di-chlorinated biphenyls, oxygen-containing aromatic compounds, and small-size hydrocarbons were identified in the effluent water, which were not initially present in the contaminated soil. Copyright © 2014 Elsevier Ltd. All rights reserved.

Assimilable organic carbon (AOC in soil water extracts using Vibrio harveyi BB721 and its implication for microbial biomass.

Directory of Open Access Journals (Sweden)

Jincai Ma

Full Text Available Assimilable organic carbon (AOC is commonly used to measure the growth potential of microorganisms in water, but has not yet been investigated for measuring microbial growth potential in soils. In this study, a simple, rapid, and non-growth based assay to determine AOC in soil was developed using a naturally occurring luminous strain Vibrio harveyi BB721 to determine the fraction of low molecular weight organic carbon in soil water extract. Calibration of the assay was achieved by measuring the luminescence intensity of starved V. harveyi BB721 cells in the late exponential phase with a concentration range from 0 to 800 µg l(-1 glucose (equivalent to 0-16.0 mg glucose C kg(-1 soil with the detection limit of 10 µg l(-1 equivalent to 0.20 mg glucose C kg(-1 soil. Results showed that bioluminescence was proportional to the concentration of glucose added to soil. The luminescence intensity of the cells was highly pH dependent and the optimal pH was about 7.0. The average AOC concentration in 32 soils tested was 2.9±2.2 mg glucose C kg(-1. Our data showed that AOC levels in soil water extracts were significantly correlated (P<0.05 with microbial biomass determined as microbial biomass carbon, indicating that the AOC concentrations determined by the method developed might be a good indicator of soil microbial biomass. Our findings provide a new approach that may be used to determine AOC in environmental samples using a non-growth bioluminescence based assay. Understanding the levels of AOC in soil water extract provides new insights into our ability to estimate the most available carbon pool to bacteria in soil that may be easily assimilated into cells for many metabolic processes and suggest possible the links between AOC, microbial regrowth potential, and microbial biomass in soils.

Phosphate fertilizers with varying water-solubility applied to Amazonian soils: II. Soil P extraction methods

International Nuclear Information System (INIS)

Muraoka, T.; Brasil, E.C.; Scivittaro, W.B.

2002-01-01

A pot experiment was carried out under greenhouse conditions at the Centro de Energia Nuclear na Agricultura, Piracicaba (SP, Brazil), to evaluate the phosphorus availability of different phosphate sources in five Amazonian soils. The soils utilized were: medium texture Yellow Latosol, clayey Yellow Latosol, very clayey Yellow Latosol, clayey Red-Yellow Podzolic and very clayey Red-Yellow Podzolic. Four phosphate sources were applied: triple superphosphate, ordinary Yoorin thermophosphate, coarse Yoorin termo-phosphate and North Carolina phosphate rock at P rates of 0, 40, 80 and 120 mg kg -1 soil. The dry matter yield and the amount of P taken up by cowpea and rice were correlated with the extractable P by anionic exchangeable resin, Mehlich-1, Mehlich-3 and Bray-I. The results showed that the extractable P by Mehlich-1 was higher in the soils amended with North Carolina rock phosphate. Irrespective of the phosphorus sources used, the Mehlich-3 extractant showed close correlation with plant response. The Mehlich-3 and Bray-I extractants were more sensitive to soil variations. The Mehlich-3 extractant was more suitable in predicting the P availability to plants in the different soils and phosphorus sources studied. (author)

Emerging organic pollutants in the vadose zone of a soil aquifer treatment system: Pore water extraction using positive displacement.

Science.gov (United States)

Sopilniak, Alexander; Elkayam, Roy; Rossin, Anna Voloshenko; Lev, Ovadia

2018-01-01

Trace organic compounds in effluents, water streams and aquifers are amply reported. However, the mobile pool of Emerging Organic Contaminants (EOCs) in the deep parts of the vadose zone is hard to estimate, due to difficulties in extraction of sufficient quantity of pore water. Here, we present a new methodology for depth profiling of EOCs in pore water by Positive Displacement Extraction (PDE): Pore water extraction from unsaturated soil samples is carried out by withdrawal of soil cores by direct-push drilling and infiltrating the core by organics free water. We show that EOC concentrations in the water eluted in the plateau region of the inverse breakthrough curve is equal to their pore water concentrations. The method was previously validated for DOC extraction, and here the scope of the methodology is extended to pore water extraction for organic pollutants analysis. Method characteristics and validation were carried out with atrazine, simazine, carbamazepine, venlafaxine, O-desmethylvenlafaxine and caffeine in the concentration range of several ng to several μg/liter. Validation was carried out by laboratory experiments on three different soils (sandy, sandy-clayey and clayey). Field studies in the vadose zone of a SAT system provided 27 m deep EOC profiles with less than 1.5 m spatial resolution. During the percolation treatment, carbamazepine remained persistent, while the other studied EOCs were attenuated to the extent of 50-99%.The highest degradation rate of all studied EOCs was in the aerobic zone. EOC levels based on PDE and extraction by centrifugation were compared, showing a positive bias for centrifugation. Copyright © 2017 Elsevier Ltd. All rights reserved.

Similarity index between irrigation water and soil saturation extract in the experimental field of Yachay University, Ecuador

Science.gov (United States)

Carrera-Villacrés, D. V.; Sánchez-Gómez, V. P.; Portilla-Bravo, O. A.; Bolaños-Guerrón, D. R.

2017-08-01

Soil monitoring is a job that demands a lot of time and money. therefore, measuring the same parameters in the water becomes simple because it can be done in situ. The objective of this work was to find a similarity index for the validation of mathematical correlation models based on physicochemical parameters to verify if there is a balance between irrigation water and soil saturation extract in the experimental field Yachay that is known as the city of knowledge that is located in Imbabura province, Ecuador, for which, the sampling of water was carried out in two representative periods (dry and rainy). Sampling of 10 soil profiles was also performed, covering the total area; these samples were obtained results of Electrical Conductivity (EC), pH and total dissolved salts (TDS). With correlation models between soils and water, it is possible to predict concentrations of elements in the irrigation water. It was concluded that there is a balance between soil and water, so that the salts present in the soil are highly soluble, in addition, there is a high probability that the elements in the irrigation water are in the soil. In sample water, the same concentrations were found in the soil, at their saturation point, and very close to the field capacity.

Retention and loss of water extractable carbon in soils: effect of clay properties.

Science.gov (United States)

Nguyen, Trung-Ta; Marschner, Petra

2014-02-01

Clay sorption is important for organic carbon (C) sequestration in soils, but little is known about the effect of different clay properties on organic C sorption and release. To investigate the effect of clay content and properties on sorption, desorption and loss of water extractable organic C (WEOC), two experiments were conducted. In experiment 1, a loamy sand alone (native) or mixed with clay isolated from a surface or subsoil (78 and 96% clay) resulting in 90, 158 and 175 g clay kg(-1) soil. These soil treatments were leached with different WEOC concentrations, and then CO2 release was measured for 28 days followed by leaching with reverse osmosis water at the end of experiment. The second experiment was conducted to determine WEOC sorption and desorption of clays isolated from the loamy sand (native), surface soil and subsoil. Addition of clays isolated from surface and subsoil to sandy loam increased WEOC sorption and reduced C leaching and cumulative respiration in percentage of total organic C and WEOC added when expressed per g soil and per g clay. Compared to clays isolated from the surface and subsoil, the native clay had higher concentrations of illite and exchangeable Ca(2+), total organic C and a higher CEC but a lower extractable Fe/Al concentration. This indicates that compared to the clay isolated from the surface and the subsoil, the native clay had fewer potential WEOC binding sites because it had lower Fe/Al content thus lower number of binding sites and the existing binding sites are already occupied native organic matter. The results of this study suggest that in the soils used here, the impact of clay on WEOC sorption and loss is dependent on its indigenous organic carbon and Fe and/or Al concentrations whereas clay mineralogy, CEC, exchangeable Ca(2+) and surface area are less important. © 2013.

Comparison of different soil water extraction systems for the prognoses of solute transport at the field scale using numerical simulations, field and lysimeter experiments

Energy Technology Data Exchange (ETDEWEB)

Weihermueller, L

2005-07-01

To date, the understanding of processes, factors, and interactions that influence the amount of extracted water and the solute composition sampled with suction cups is limited. But this information is required for process description of solute transport in natural soils. Improved system understanding can lead to a low cost and easy to install water sampling system which can help to predict solute transport in natural soils for the benefit of environmental protection. The main objectives of this work were to perform numerical simulations with different boundary conditions and to implement the findings in the interpretation of the lysimeter and field experiments. In a first part of this thesis, theoretical considerations on the processes affecting the spatial influence of a suction cup in soil and changes in solute transport initiated by the suction cups are presented, including testing and validation of available model and experimental approaches. In the second part, a detailed experimental study was conducted to obtain data for the comparison of the different soil water sampling systems. Finally, the numerical experiments of the suction cup influence were used for the interpretation of the experimental data. The main goals are summarized as follows: - Characterization of the suction cup activity domain (SCAD), suction cup extraction domain (SCED) and suction cup sampling area (SCSA) of active suction cups (definitions are given in Chapter 6). - Determination of the boundary conditions and soil properties [e.g. infiltration, applied suction, duration of water extraction, soil hydraulic properties and soil heterogeneity] affecting the activity domain, extraction domain and sampling area of a suction cup. - Identification of processes that change the travel time and travel time variance of solutes extracted by suction cups. - Validation of the numerically derived data with analytical and experimental data from literature. - Comparison of the experimental data obtained

Water isotope partitioning and ecohydrologic separation in mixed conifer forest explored with a centrifugation water extraction method

Science.gov (United States)

Bowers, W.; Mercer, J.; Pleasants, M.; Williams, D. G.

2017-12-01

Isotopic partitioning of water within soil into tightly and loosely bound fractions has been proposed to explain differences between isotopic water sources used by plants and those that contribute to streams and ground water, the basis for the "two water worlds" hypothesis. We examined the isotope ratio values of water in trees, bulk soil, mobile water collected from soil lysimeters, stream water, and GW at three different hillslopes in a mixed conifer forest in southeastern Wyoming, USA. Hillslopes differed in aspect and topographic position with corresponding differences in surface energy balance, snowmelt timing, and duration of soil moisture during the dry summer. The isotopic results support the partitioning of water within the soil; trees apparently used a different pool of water for transpiration than that recovered from soil lysimeters and the source was not resolved with the isotopic signature of the water that was extracted from bulk soil via cryogenic vacuum distillation. Separating and measuring the isotope ratios values in these pools would test the assumption that the tightly bound water within the soil has the same isotopic signature as the water transpired by the trees. We employed a centrifugation approach to separate water within the soil held at different tensions by applying stepwise increases in rotational velocity and pressures to the bulk soil samples. Effluent and the remaining water (cryogenically extracted) at each step were compared. We first applied the centrifugation method in a simple lab experiment using sandy loam soil and separate introductions of two isotopically distinct waters. We then applied the method to soil collected from the montane hillslopes. For the lab experiment, we predicted that effluents would have distinct isotopic signatures, with the last effluent and extracted water more closely representing the isotopic signature of the first water applied. For our field samples, we predicted that the isotopic signature of the

SIMPLE METHOD FOR ESTIMATING POLYCHLORINATED BIPHENYL CONCENTRATIONS ON SOILS AND SEDIMENTS USING SUBCRITICAL WATER EXTRACTION COUPLED WITH SOLID-PHASE MICROEXTRACTION. (R825368)

Science.gov (United States)

A rapid method for estimating polychlorinated biphenyl (PCB) concentrations in contaminated soils and sediments has been developed by coupling static subcritical water extraction with solid-phase microextraction (SPME). Soil, water, and internal standards are placed in a seale...

A multistratum approach to soil vapor extraction

International Nuclear Information System (INIS)

Fuhr, J.M.; Giesler, R.S.

1993-01-01

An innovative soil remediation design was implemented to address petroleum hydrocarbon contamination in a gradationally stratified subsurface environment containing alternating layers of clay, sand and clayey sand, and perched water tables in north Florida. The soil vapor extraction (SVE) design enables remediation to focus on distinct subsurface intervals depending on changing site conditions such as constituent concentration levels and periodic water-table fluctuations. Contaminated soils were assessed from the land surface to the top of a two foot thick perched water table located at 13 feet below land surface (bls), and also were encountered below the perched water table downward to another perched water table at 45 feet bls. Use of an organic vapor analyzer equipped with a flame ionization detector revealed hydrocarbon vapor concentrations in soil samples ranging to greater than 1,000 parts per million (ppm). Nonaqueous phase liquids were encountered on both perched water tables. Based on the site assessment, a multistratum soil and ground-water remediation system was designed and constructed. A pilot test was conducted to aid in the design of an effective SVE system

Rare earth elements in soil extracts by ICP-MS

Energy Technology Data Exchange (ETDEWEB)

Tobler, L.; Furrer, V.; Wyttenbach, A. [Paul Scherrer Inst. (PSI), Villigen (Switzerland); Burger, M.; Jakob, A. [AC-Laboratorium Spiez (Switzerland)

1997-09-01

Three different horizons of a soil profile were extracted with water and with a complexing solution. 14 REEs were determined in the extracts. The distribution patterns obtained from the different horizons were rather similar and did not show the large fractionations observed between different plant species growing on this soil. (author) 2 figs., 1 ref.

Solubility of Benzo[a]pyrene and Organic Matter of Soil in Subcritical Water

Directory of Open Access Journals (Sweden)

Svetlana Sushkova

2015-12-01

Full Text Available A dynamic subcritical water extraction method of benzo[a]pyrene from soils is under consideration. The optimum conditions for benzo[a]pyrene extraction from soil are described including the soil treatment by subcritical water at 250 °C and 100 atm for 30 min. The effectiveness of developed method was determined using the matrix spiking recovery technique. A comparative analysis was made to evaluate the results of benzo[a]pyrene extraction from soils using the subcritical water and organic solvents. The advantages of the subcritical water extraction involve the use of ecologically friendly solvent, a shorter time for the analysis and a higher amount of benzo[a]pyrene extracted from soil (96 %. The influence of subcritical water extraction on soil properties was measured the investigation of the processes occurring within soil under the influence the high temperature and pressure. Under appropriate conditions of the experiment there is the destruction of the soil organic matter while the composition of the soil mineral fraction remains practically unchanged.

CHARACTERIZING SOIL/WATER SORPTION AND DESORPTION BEHAVIOR OF BTEX AND PAHS USING SELECTIVE SUPERCRITICAL FLUID EXTRACTION (SFE); TOPICAL

International Nuclear Information System (INIS)

Steve Hawthorne

1998-01-01

The first goal of the proposed study was to generate initial data to determine the ability of selective SFE behavior to mimic the soil/water sorption and desorption behavior of BTEX (benzene, toluene, and xylenes) and PAHs (polycyclic aromatic hydrocarbons).Samples generated by Professor Bill Rixey's column sorption studies (aged for 2 weeks to 8 months) and desorption studies (six weeks desorption of the aged soil columns with pure water) were extracted using sequentially-stronger SFE conditions to selectively remove different fractions of each BTEX and PAH component which range from loosely to tightly bound in the soil matrices. The selective SFE results parallel the sorption/desorption leaching behavior and mechanisms determined by Professor Rixey's investigations (under separate funding) using water desorption of soil columns previously aged with BTEX and PAHs. These results justify more intensive investigations of the use of selective SFE to mimic soil/water sorption and desorption of organic pollutants related to fossil fuels which will be performed under separate funding. The second goal of the study was to determine if selective SFE extraction behavior parallels the remediation behavior displayed by PAHs currently undergoing in-situ bioremediation at a manufactured gas plant (MGP) site. Based on soil analyses of several individual PAHs (as well as total PAHs) before remediation began, and after 147 days of remediation, selective SFE successfully mimicked remediation behavior. These results strongly support the use of selective SFE to predict remediation behavior of soils contaminated with PAHs, and are expected to provide a powerful and rapid analytical tool which will be useful for determining the remediation endpoints which are necessary for environmental protection. Based on the initial success found in the present study, additional investigations into the use of SFE for predicting and monitoring the remediation behavior of PAH-contaminated soils will be

Comparison of extraction fluids used with contaminated soils

International Nuclear Information System (INIS)

Erickson, D.C.; White, E.; Loehr, R.C.

1991-01-01

Five separate solutions were evaluated for use as leaching fluids with soils containing petroleum refining waste residues. The extraction fluids were: (a) water, (b) dilute hydrochloric acid, (c) 0.05 molar EDTA, (d) acetate buffer and (e) a dilute sulfuric/nitric acid mixture. The soils were collected from former refinery land treatment sites which had been used to treat petroleum refining wastes. The extractions were performed using a rotary tumbler (30 RPM, 18 hours) and the resulting solutions were analyzed for polynuclear aromatic hydrocarbons (PAHs) and metals. Concentrations of the PAHs in each of the five solutions were near or below the analytical quantitation limits. Metal concentrations were highest in the HCL and EDTA extracts, although only a small fraction of the total available metal present in the soils was extracted by the solutions evaluated

Six-phase soil heating accelerates VOC extraction from clay soil

International Nuclear Information System (INIS)

Gauglitz, P.A.; Roberts, J.S.; Bergsman, T.M.; Caley, S.M.; Heath, W.O.; Miller, M.C.; Moss, R.W.; Schalla, R.; Jarosch, T.R.; Eddy-Dilek, C.A.

1994-08-01

Six-Phase Soil Heating (SPSH) was demonstrated as a viable technology for heating low permeability soils containing volatile organic contaminants. Testing was performed as part of the Volatile Organic Compounds in Non-Arid Soils Integrated Demonstration (VOC Non-Arid ID) at the Savannah River Site. The soil at the integrated demonstration site is contaminated with perchloroethylene (PCE) and trichloroethylene (TCE); the highest soil contamination occurs in clay-rich zones that are ineffectively treated by conventional soil vapor extraction due to the very low permeability of the clay. The SPSH demonstration sought to heat the clay zone and enhance the performance of conventional soil vapor extraction. Thermocouples at thirty locations quantified the areal and vertical heating within the treated zone. Soil samples were collected before and after heating to quantify the efficacy of heat-enhanced vapor extraction of PCE and TCE from the clay soil. Samples were taken (essentially every foot) from six wells prior to heating and adjacent to these wells after heating. Results show that contaminant removal from the clay zone was 99.7% (median) within the electrode array. Outside the array where the soil was heated, but to only 50 degrees C, the removal efficiency was 93%, showing that heating accelerated the removal of VOCs from the clay soil. The accelerated remediation resulted from effective heating of the contaminated clay zone by SPSH. The temperature of the clay zone increased to 100 degrees C after 8 days of heating and was maintained near 100 degrees C for 17 days. Electrical heating removed 19,000 gal of water from the soil as steam, with peak removal rate of 1,500 gpd of condensed steam

Analysis of perfluorinated carboxylic acids in soils II: optimization of chromatography and extraction.

Science.gov (United States)

Washington, John W; Henderson, W Matthew; Ellington, J Jackson; Jenkins, Thomas M; Evans, John J

2008-02-15

With the objective of detecting and quantitating low concentrations of perfluorinated carboxylic acids (PFCAs), including perfluorooctanoic acid (PFOA), in soils, we compared the analytical suitability of liquid chromatography columns containing three different stationary phases, two different liquid chromatography-tandem mass spectrometry (LC/MS/MS) systems, and eight combinations of sample-extract pretreatments, extractions and cleanups on three test soils. For the columns and systems we tested, we achieved the greatest analytical sensitivity for PFCAs using a column with a C(18) stationary phase in a Waters LC/MS/MS. In this system we achieved an instrument detection limit for PFOA of 270 ag/microL, equating to about 14 fg of PFOA on-column. While an elementary acetonitrile/water extraction of soils recovers PFCAs effectively, natural soil organic matter also dissolved in the extracts commonly imparts significant noise that appears as broad, multi-nodal, asymmetric peaks that coelute with several PFCAs. The intensity and elution profile of this noise is highly variable among soils and it challenges detection of low concentrations of PFCAs by decreasing the signal-to-noise contrast. In an effort to decrease this background noise, we investigated several methods of pretreatment, extraction and cleanup, in a variety of combinations, that used alkaline and unbuffered water, acetonitrile, tetrabutylammonium hydrogen sulfate, methyl-tert-butyl ether, dispersed activated carbon and solid-phase extraction. For the combined objectives of complete recovery and minimization of background noise, we have chosen: (1) alkaline pretreatment; (2) extraction with acetonitrile/water; (3) evaporation to dryness; (4) reconstitution with tetrabutylammonium-hydrogen-sulfate ion-pairing solution; (5) ion-pair extraction to methyl-tert-butyl ether; (6) evaporation to dryness; (7) reconstitution with 60/40 acetonitrile/water (v/v); and (8) analysis by LC/MS/MS. Using this method, we

Isotopic fractionation of soil water during evaporation

Energy Technology Data Exchange (ETDEWEB)

Leopoldo, P R [Faculdade de Ciencias Medicas e Biologicas de Botucatu (Brazil); Salati, E; Matsui, E [Centro de Energia Nuclear na Agricultura, Piracicaba (Brazil)

1974-07-01

The study of the variation of D/H relation in soil water during evaporation is studied. The isotopic fractionation of soil water has been observed in two soils of light and heavy texture. Soil columns were utilized. Soil water was extracted in a system operated under low pressure and the gaseous hydrogen was obtained by decomposition of the water and was analyzed in a GD-150 mass spectrometer for deuterium content. The variation of the delta sub(eta) /sup 0///sub 00/ value during evaporation showed that for water held at potentials below 15 atm, the deuterium content of soil water stays practically constant. For water held at potentials higher than 15 atm, corresponding to the third stage of evaporation, there is a strong tendency of a constant increase of delta sub(eta) /sup 0///sub 00/ of the remaining water.

Extraction agents for the removal of polycyclic aromatic hydrocarbons (PAHs) from soil in soil washing technologies

International Nuclear Information System (INIS)

Lau, Ee Von; Gan, Suyin; Ng, Hoon Kiat; Poh, Phaik Eong

2014-01-01

Polycyclic aromatic hydrocarbons (PAHs) in soil have been recognised as a serious health and environmental issue due to their carcinogenic, mutagenic and teratogenic properties. One of the commonly employed soil remediation techniques to clean up such contamination is soil washing or solvent extraction. The main factor which governs the efficiency of this process is the solubility of PAHs in the extraction agent. Past field-scale soil washing treatments for PAH-contaminated soil have mainly employed organic solvents or water which is either toxic and costly or inefficient in removing higher molecular weight PAHs. Thus, the present article aims to provide a review and discussion of the alternative extraction agents that have been studied, including surfactants, biosurfactants, microemulsions, natural surfactants, cyclodextrins, vegetable oil and solution with solid phase particles. These extraction agents have been found to remove PAHs from soil at percentages ranging from 47 to 100% for various PAHs. -- Highlights: • The alternative and advancement in extraction agents to remove PAHs from soil using soil washing technology is summarised. • The soil regulations for PAH level in various countries are summarized for reference to researchers. • The concentration levels of PAHs in soil at present and the need for soil remediation is presented. -- The efficiency of the extraction agent plays a significant role in soil washing of PAH-contaminated soil

Microbial assisted phyto extraction of metals and growth of soybean (glycine max l. merrill) on industrial waste water contaminated soil

International Nuclear Information System (INIS)

Ali, I.; Bano, A.

2012-01-01

Pots experiments were made to investigate the role of effective microorganisms (EM) in improving phyto extraction of metals (Cd/sup +2/ and Mn/sup +2/) and growth of soybean plant in industrial waste water polluted soil. Waste water applications to soil were made in four different dilutions (i.e. 25%, 50%, 75% and 100%). Effective microorganisms were added into waste water prior to application. Effect of treatments on growth parameters was studied. The Cd/sup +2/ and Mn/sup +2/ concentrations in different parts of plant were measured by Atomic Absorption Spectrophotometer. Plant height significantly increased at all treatments except at 25% waste water treatment. Plant dry biomass and oil contents in seed significantly increased with all treatments compared to control but were higher at low concentration of waste water. Waste water treatments significantly increased the Cd and Mn accumulation in plant while inoculation of EM further enhanced the metals accumulation. The maximum accumulation of Cd and Mn found in plant treated with 100% waste water in combination with effective microorganisms. At harvest, the Cd/sup +2/ concentration decreased in leaves but increased in roots followed by stem > seeds, while, Mn/sup +2/ accumulation increased in leaves followed by roots > stem > seeds. Conclusively, EM enhanced the phyto extraction of Cd and Mn and also increased the oil contents in soybean on polluted soil. These findings suggest further investigation to find out a suitable concentration of industrial waste water in combination with EM for better growth of soybean and improving phyto extraction of metals. (author)

Selective extraction of hydrocarbons, phosphonates and phosphonic acids from soils by successive supercritical fluid and pressurized liquid extractions.

Science.gov (United States)

Chaudot, X; Tambuté, A; Caude, M

2000-01-14

Hydrocarbons, dialkyl alkylphosphonates and alkyl alkylphosphonic acids are selectively extracted from spiked soils by successive implementation of supercritical carbon dioxide, supercritical methanol-modified carbon dioxide and pressurized water. More than 95% of hydrocarbons are extracted during the first step (pure supercritical carbon dioxide extraction) whereas no organophosphorus compound is evidenced in this first extract. A quantitative extraction of phosphonates is achieved during the second step (methanol-modified supercritical carbon dioxide extraction). Polar phosphonic acids are extracted during a third step (pressurized water extraction) and analyzed by gas chromatography under methylated derivatives (diazomethane derivatization). Global recoveries for these compounds are close to 80%, a loss of about 20% occurring during the derivatization process (co-evaporation with solvent). The developed selective extraction method was successfully applied to a soil sample during an international collaborative exercise.

Effect of ageing on benzo[a]pyrene extractability in contrasting soils

Energy Technology Data Exchange (ETDEWEB)

Duan, Luchun [CERAR-Centre for Environmental Risk Assessment and Remediation and Cooperative Research Centre for Contamination Assessment and Remediation of the Environment (CRC CARE), Building X, University of South Australia, Mawson Lakes, SA 5095 (Australia); Naidu, Ravi, E-mail: Ravi.Naidu@newcastle.edu.au [CERAR-Centre for Environmental Risk Assessment and Remediation and Cooperative Research Centre for Contamination Assessment and Remediation of the Environment (CRC CARE), Building X, University of South Australia, Mawson Lakes, SA 5095 (Australia); Liu, Yanju; Palanisami, Thavamani; Dong, Zhaomin; Mallavarapu, Megharaj [CERAR-Centre for Environmental Risk Assessment and Remediation and Cooperative Research Centre for Contamination Assessment and Remediation of the Environment (CRC CARE), Building X, University of South Australia, Mawson Lakes, SA 5095 (Australia); Semple, Kirk T. [Lancaster Environment Centre, Lancaster University, Lancaster LA1 4YQ (United Kingdom)

2015-10-15

Highlights: • In vitro assessment of B[a]P in contaminated soils using 4 different methods. • An exponential kinetic model fits well with the extractability data. • Fitting parameter and {sup 14}C residue correlates with key soil properties. • Fractionation of B[a]P was obtained based on extractability by extractants. - Abstract: Changes in benzo[a]pyrene (B[a]P) extractability over 160 days ageing in four contrasting soils varying in organic matter content and clay mineralogy were investigated using dichloromethane: acetone 1:1 (DCM/Ace), 60 mM hydroxypropyl-β-cyclodextrin (HPCD) solution, 1-butanol (BuOH) and Milli-Q water. The B[a]P extractability by the four methods decreased with ageing and a first-order exponential model could be used to describe the kinetics of release. Correlation of the kinetic rate constant with major soil properties showed a significant effect of clay and sand contents and pore volume fraction (<6 nm) on sequestration of the desorbable fraction (by HPCD) and the water-extractable fraction. Analysis of {sup 14}C-B[a]P in soils after ageing showed a limited loss of B[a]P via degradation. Fractionation of B[a]P pools associated with the soil matrix was analysed according to extractability of B[a]P by the different extraction methods. A summary of the different fractions is proposed for the illustration of the effect of ageing on different B[a]P-bound fractions in soils. This study provides a better understanding of the B[a]P ageing process associated with different fractions and also emphasises the extraction capacity of the different methods employed.

Effect of ageing on benzo[a]pyrene extractability in contrasting soils

International Nuclear Information System (INIS)

Duan, Luchun; Naidu, Ravi; Liu, Yanju; Palanisami, Thavamani; Dong, Zhaomin; Mallavarapu, Megharaj; Semple, Kirk T.

2015-01-01

Highlights: • In vitro assessment of B[a]P in contaminated soils using 4 different methods. • An exponential kinetic model fits well with the extractability data. • Fitting parameter and 14 C residue correlates with key soil properties. • Fractionation of B[a]P was obtained based on extractability by extractants. - Abstract: Changes in benzo[a]pyrene (B[a]P) extractability over 160 days ageing in four contrasting soils varying in organic matter content and clay mineralogy were investigated using dichloromethane: acetone 1:1 (DCM/Ace), 60 mM hydroxypropyl-β-cyclodextrin (HPCD) solution, 1-butanol (BuOH) and Milli-Q water. The B[a]P extractability by the four methods decreased with ageing and a first-order exponential model could be used to describe the kinetics of release. Correlation of the kinetic rate constant with major soil properties showed a significant effect of clay and sand contents and pore volume fraction (<6 nm) on sequestration of the desorbable fraction (by HPCD) and the water-extractable fraction. Analysis of 14 C-B[a]P in soils after ageing showed a limited loss of B[a]P via degradation. Fractionation of B[a]P pools associated with the soil matrix was analysed according to extractability of B[a]P by the different extraction methods. A summary of the different fractions is proposed for the illustration of the effect of ageing on different B[a]P-bound fractions in soils. This study provides a better understanding of the B[a]P ageing process associated with different fractions and also emphasises the extraction capacity of the different methods employed

Short term spatio-temporal variability of soil water-extractable calcium and magnesium after a low severity grassland fire in Lithuania.

Science.gov (United States)

Pereira, Paulo; Martin, David

2014-05-01

Fire has important impacts on soil nutrient spatio-temporal distribution (Outeiro et al., 2008). This impact depends on fire severity, topography of the burned area, type of soil and vegetation affected, and the meteorological conditions post-fire. Fire produces a complex mosaic of impacts in soil that can be extremely variable at small plot scale in the space and time. In order to assess and map such a heterogeneous distribution, the test of interpolation methods is fundamental to identify the best estimator and to have a better understanding of soil nutrients spatial distribution. The objective of this work is to identify the short-term spatial variability of water-extractable calcium and magnesium after a low severity grassland fire. The studied area is located near Vilnius (Lithuania) at 54° 42' N, 25° 08 E, 158 masl. Four days after the fire, it was designed in a burned area a plot with 400 m2 (20 x 20 m with 5 m space between sampling points). Twenty five samples from top soil (0-5 cm) were collected immediately after the fire (IAF), 2, 5, 7 and 9 months after the fire (a total of 125 in all sampling dates). The original data of water-extractable calcium and magnesium did not respected the Gaussian distribution, thus a neperian logarithm (ln) was applied in order to normalize data. Significant differences of water-extractable calcium and magnesium among sampling dates were carried out with the Anova One-way test using the ln data. In order to assess the spatial variability of water-extractable calcium and magnesium, we tested several interpolation methods as Ordinary Kriging (OK), Inverse Distance to a Weight (IDW) with the power of 1, 2, 3 and 4, Radial Basis Functions (RBF) - Inverse Multiquadratic (IMT), Multilog (MTG), Multiquadratic (MTQ) Natural Cubic Spline (NCS) and Thin Plate Spline (TPS) - and Local Polynomial (LP) with the power of 1 and 2. Interpolation tests were carried out with Ln data. The best interpolation method was assessed using the

Easy and fast extraction methods to determine organochlorine pesticides in sewage sludge, soil, and water samples based at low temperature.

Science.gov (United States)

Mesquita, Tayane C R; Santos, Rizia R; Cacique, Ane P; De Sá, Ludimara J; Silvério, Flaviano O; Pinho, Gevany P

2018-03-04

Organochlorine pesticides present in sewage sludge can contaminate soil and water when they are used as either fertilizer or agricultural soil conditioner. In this study, the technique solid-liquid extraction with low temperature purification was optimized and validated for determination of ten organochlorine pesticides in sewage sludge and soil samples. Liquid-liquid extraction with low temperature purification was also validated for the same compounds in water. Analyses were performed by gas chromatography-mass spectrometry operating in the selective ion monitoring mode. After optimization, the methods showed recoveries between 70% and 115% with relative standard deviation lower than 13% for all target analytes in the three matrices. The linearity was demonstrated in the range of 20 to 70 µg L -1 , 0.5 to 60 µg L -1 , and 3 to 13 µg L -1 , for sludge, soil, and acetonitrile, respectively. The limit of quantification ranged between 2 and 40 µg kg -1 , 1 and 6 µg kg -1 , and 0.5 µg L -1 for sludge, soil, and water, respectively. The methods were used in the study of pesticide lixiviation carried out in a poly vinyl chlorine column filled with soil, which had its surface layer mixed with sludge. The results showed that pesticides are not leached into soil, part of them is adsorbed by the sewage sludge (4-40%), and most pesticides are lost by volatilization.

Remediation of soils combining soil vapor extraction and bioremediation: benzene.

Science.gov (United States)

Soares, António Alves; Albergaria, José Tomás; Domingues, Valentina Fernandes; Alvim-Ferraz, Maria da Conceição M; Delerue-Matos, Cristina

2010-08-01

This work reports the study of the combination of soil vapor extraction (SVE) with bioremediation (BR) to remediate soils contaminated with benzene. Soils contaminated with benzene with different water and natural organic matter contents were studied. The main goals were: (i) evaluate the performance of SVE regarding the remediation time and the process efficiency; (ii) study the combination of both technologies in order to identify the best option capable to achieve the legal clean up goals; and (iii) evaluate the influence of soil water content (SWC) and natural organic matter (NOM) on SVE and BR. The remediation experiments performed in soils contaminated with benzene allowed concluding that: (i) SVE presented (a) efficiencies above 92% for sandy soils and above 78% for humic soils; (b) and remediation times from 2 to 45 h, depending on the soil; (ii) BR showed to be an efficient technology to complement SVE; (iii) (a) SWC showed minimum impact on SVE when high airflow rates were used and led to higher remediation times for lower flow rates; (b) NOM as source of microorganisms and nutrients enhanced BR but hindered the SVE due the limitation on the mass transfer of benzene from the soil to the gas phase. (c) 2010 Elsevier Ltd. All rights reserved.

Chelant extraction of heavy metals from contaminated soils

Energy Technology Data Exchange (ETDEWEB)

Peters, R.W. [Energy Systems Division, Argonne National Laboratory, 9700 South Cass Avenue, Argonne, IL 60439 (United States)

1999-04-23

The current state of the art regarding the use of chelating agents to extract heavy metal contaminants has been addressed. Results are presented for treatability studies conducted as worst-case and representative soils from Aberdeen Proving Ground's J-Field for extraction of copper (Cu), lead (Pb), and zinc (Zn). The particle size distribution characteristics of the soils determined from hydrometer tests are approximately 60% sand, 30% silt, and 10% clay. Sequential extractions were performed on the 'as-received' soils (worst case and representative) to determine the speciation of the metal forms. The technique speciates the heavy metal distribution into an easily extractable (exchangeable) form, carbonates, reducible oxides, organically-bound, and residual forms. The results indicated that most of the metals are in forms that are amenable to soil washing (i.e. exchangeable+carbonate+reducible oxides). The metals Cu, Pb, Zn, and Cr have greater than 70% of their distribution in forms amenable to soil washing techniques, while Cd, Mn, and Fe are somewhat less amenable to soil washing using chelant extraction. However, the concentrations of Cd and Mn are low in the contaminated soil. From the batch chelant extraction studies, ethylenediaminetetraacetic acid (EDTA), citric acid, and nitrilotriacetic acid (NTA) were all effective in removing copper, lead, and zinc from the J-Field soils. Due to NTA being a Class II carcinogen, it is not recommended for use in remediating contaminated soils. EDTA and citric acid appear to offer the greatest potential as chelating agents to use in soil washing the Aberdeen Proving Ground soils. The other chelating agents studied (gluconate, oxalate, Citranox, ammonium acetate, and phosphoric acid, along with pH-adjusted water) were generally ineffective in mobilizing the heavy metals from the soils. The chelant solution removes the heavy metals (Cd, Cu, Pb, Zn, Fe, Cr, As, and Hg) simultaneously. Using a multiple

Chelant extraction of heavy metals from contaminated soils

International Nuclear Information System (INIS)

Peters, R.W.

1999-01-01

The current state of the art regarding the use of chelating agents to extract heavy metal contaminants has been addressed. Results are presented for treatability studies conducted as worst-case and representative soils from Aberdeen Proving Ground's J-Field for extraction of copper (Cu), lead (Pb), and zinc (Zn). The particle size distribution characteristics of the soils determined from hydrometer tests are approximately 60% sand, 30% silt, and 10% clay. Sequential extractions were performed on the 'as-received' soils (worst case and representative) to determine the speciation of the metal forms. The technique speciates the heavy metal distribution into an easily extractable (exchangeable) form, carbonates, reducible oxides, organically-bound, and residual forms. The results indicated that most of the metals are in forms that are amenable to soil washing (i.e. exchangeable+carbonate+reducible oxides). The metals Cu, Pb, Zn, and Cr have greater than 70% of their distribution in forms amenable to soil washing techniques, while Cd, Mn, and Fe are somewhat less amenable to soil washing using chelant extraction. However, the concentrations of Cd and Mn are low in the contaminated soil. From the batch chelant extraction studies, ethylenediaminetetraacetic acid (EDTA), citric acid, and nitrilotriacetic acid (NTA) were all effective in removing copper, lead, and zinc from the J-Field soils. Due to NTA being a Class II carcinogen, it is not recommended for use in remediating contaminated soils. EDTA and citric acid appear to offer the greatest potential as chelating agents to use in soil washing the Aberdeen Proving Ground soils. The other chelating agents studied (gluconate, oxalate, Citranox, ammonium acetate, and phosphoric acid, along with pH-adjusted water) were generally ineffective in mobilizing the heavy metals from the soils. The chelant solution removes the heavy metals (Cd, Cu, Pb, Zn, Fe, Cr, As, and Hg) simultaneously. Using a multiple-stage batch extraction

Soil solution extraction techniques for microbial ecotoxicity testing: a comparative evaluation.

Science.gov (United States)

Tiensing, T; Preston, S; Strachan, N; Paton, G I

2001-02-01

The suitability of two different techniques (centrifugation and Rhizon sampler) for obtaining the interstitial pore water of soil (soil solution), integral to the ecotoxicity assessment of metal contaminated soil, were investigated by combining chemical analyses and a luminescence-based microbial biosensor. Two different techniques, centrifugation and Rhizon sampler, were used to extract the soil solution from Insch (a loamy sand) and Boyndie (a sandy loam) soils, which had been amended with different concentrations of Zn and Cd. The concentrations of dissolved organic carbon (DOC), major anions (F- , CI-, NO3, SO4(2-)) and major cations (K+, Mg2+, Ca2+) in the soil solutions varied depending on the extraction technique used. Overall, the concentrations of Zn and Cd were significantly higher in the soil solution extracted using the centrifugation technique compared with that extracted using the Rhizon sampler technique. Furthermore, the differences observed between the two extraction techniques depended on the type of soil from which the solution was being extracted. The luminescence-based biosensor Escherichia coli HB101 pUCD607 was shown to respond to the free metal concentrations in the soil solutions and showed that different toxicities were associated with each soil, depending on the technique used to extract the soil solution. This study highlights the need to characterise the type of extraction technique used to obtain the soil solution for ecotoxicity testing in order that a representative ecotoxicity assessment can be carried out.

COMPARISON OF DIFFERENT EXTRACTION METHODS REPRESENTING AVAILABLE AND TOTAL CONCENTRATIONS OF Cd, Cu, Fe, Mn and Zn IN SOIL

Directory of Open Access Journals (Sweden)

Vladimir Ivezić

2013-06-01

Full Text Available Various extraction methods are used to predict plant uptake of trace metals. Most commonly it is total concentration that is used for risk assessment and evaluation of trace metal availability. However, recent studies showed that total concentration is a poor indicator of availability while concentrations in soil solution show good correlation with plant uptake. Present study was conducted on magricultural soils with low levels of trace metals where 45 soil samples were collected from different soil types. The main objective was to compare four different extraction methods and examine how total and reactive (EDTA trace metal concentrations correlate ,with soil solution concentration (in this study determined by water extraction. The samples were analyzed by four extraction methods: strong acid extraction (ultra-pure HNO3 extraction and aqua regia, weak acid extraction by EDTA and the most available fraction, fraction in soil solution, were represented by water extraction (weakest extractant. Five elements were investigated (Cd, Cu, Fe, Mn and Zn. Water extraction significantly correlated with EDTA extraction for Cu, Fe and Mn, while total extraction (HNO3 extraction and aqua regia correlated significantly with water extraction only for Cu. No correlation between water extraction and total extraction confirmed poor role of total concentration as an indicator of availability. EDTA extraction can be used to represent reactive pool of trace metals in soil but it should be also taken with caution when using it to describe available fraction.

Stability studies of arsenic, selenium, antimony and tellurium species in water, urine, fish and soil extracts using HPLC/ICP-MS

Energy Technology Data Exchange (ETDEWEB)

Lindemann, T.; Prange, A.; Neidhart, B. [GKSS Research Centre, Geesthacht (Germany). Inst. of Physical and Chemical Analysis; Dannecker, W. [Hamburg Univ. (Germany). Inst. fuer Anorganische und Angewandte Chemie

2000-10-01

The stability of arsenic, selenium, antimony and tellurium species in water and urine (NIST SRM 2670n) as well as in extracts of fish and soil certified reference materials (DORM-2 and NIST SRM 2710) has been investigated. Stability studies were carried out with As(III), As(V), arsenobetaine, monomethylarsonic acid (MMA), dimethylarsinic acid (DMA), phenylarsonic acid (PAA), Se(IV), Se(VI), selenomethionine, Sb(III), Sb(V) and Te(VI). Speciation analysis was performed by on-line coupling of anion exchange high-performance liquid chromatography (HPLC) with inductively coupled plasma mass spectrometry (ICP-MS). Best storage of aqueous mixtures of the examined species was achieved at 3 C whereas at -20 C species transformation especially of selenomethionine and Sb(V) took place and a new selenium species appeared within a period of 30 days. Losses and species transformations during extraction processes were investigated. Extraction of the spiked fish material with methanol/water led to partial conversion of Sb(III), Sb(V) and selenomethionine to two new antimony and one new selenium species. The other arsenic, selenium and tellurium species were almost quantitatively extracted. For soil spiked with MMA, PAA, Se(IV) and Sb(III), recoveries after extraction with water and sulfuric acid (0.01 mol/L) were below 20%. (orig.)

Non-destructive estimates of soil carbonic anhydrase activity and associated soil water oxygen isotope composition

Science.gov (United States)

Jones, Sam P.; Ogée, Jérôme; Sauze, Joana; Wohl, Steven; Saavedra, Noelia; Fernández-Prado, Noelia; Maire, Juliette; Launois, Thomas; Bosc, Alexandre; Wingate, Lisa

2017-12-01

The contribution of photosynthesis and soil respiration to net land-atmosphere carbon dioxide (CO2) exchange can be estimated based on the differential influence of leaves and soils on budgets of the oxygen isotope composition (δ18O) of atmospheric CO2. To do so, the activity of carbonic anhydrases (CAs), a group of enzymes that catalyse the hydration of CO2 in soils and plants, needs to be understood. Measurements of soil CA activity typically involve the inversion of models describing the δ18O of CO2 fluxes to solve for the apparent, potentially catalysed, rate of CO2 hydration. This requires information about the δ18O of CO2 in isotopic equilibrium with soil water, typically obtained from destructive, depth-resolved sampling and extraction of soil water. In doing so, an assumption is made about the soil water pool that CO2 interacts with, which may bias estimates of CA activity if incorrect. Furthermore, this can represent a significant challenge in data collection given the potential for spatial and temporal variability in the δ18O of soil water and limited a priori information with respect to the appropriate sampling resolution and depth. We investigated whether we could circumvent this requirement by inferring the rate of CO2 hydration and the δ18O of soil water from the relationship between the δ18O of CO2 fluxes and the δ18O of CO2 at the soil surface measured at different ambient CO2 conditions. This approach was tested through laboratory incubations of air-dried soils that were re-wetted with three waters of different δ18O. Gas exchange measurements were made on these soils to estimate the rate of hydration and the δ18O of soil water, followed by soil water extraction to allow for comparison. Estimated rates of CO2 hydration were 6.8-14.6 times greater than the theoretical uncatalysed rate of hydration, indicating that CA were active in these soils. Importantly, these estimates were not significantly different among water treatments, suggesting

Remediation of sandy soils contaminated with hydrocarbons and halogenated hydrocarbons by soil vapour extraction.

Science.gov (United States)

Albergaria, José Tomás; Alvim-Ferraz, Maria da Conceição M; Delerue-Matos, Cristina

2012-08-15

This paper presents the study of the remediation of sandy soils containing six of the most common contaminants (benzene, toluene, ethylbenzene, xylene, trichloroethylene and perchloroethylene) using soil vapour extraction (SVE). The influence of soil water content on the process efficiency was evaluated considering the soil type and the contaminant. For artificially contaminated soils with negligible clay contents and natural organic matter it was concluded that: (i) all the remediation processes presented efficiencies above 92%; (ii) an increase of the soil water content led to a more time-consuming remediation; (iii) longer remediation periods were observed for contaminants with lower vapour pressures and lower water solubilities due to mass transfer limitations. Based on these results an easy and relatively fast procedure was developed for the prediction of the remediation times of real soils; 83% of the remediation times were predicted with relative deviations below 14%. Copyright © 2012 Elsevier Ltd. All rights reserved.

In-Situ Resource Utilization: Water Extraction from Regolith

Data.gov (United States)

National Aeronautics and Space Administration — Several technologies are being evaluated to extract water from a variety of water-bearing extraterrestrial soils, including near-surface granular and hard hydrated...

Importance of soil-water relation in assessment endpoint in bioremediated soils: Plant growth and soil physical properties

International Nuclear Information System (INIS)

Li, X.; Sawatsky, N.

1995-01-01

Much effort has been focused on defining the end-point of bioremediated soils by chemical analysis (Alberta Tier 1 or CCME Guideline for Contaminated Soils) or toxicity tests. However, these tests do not completely assess the soil quality, or the capability of soil to support plant growth after bioremediation. This study compared barley (Hordeum vulgare) growth on: (i) non-contaminated, agricultural topsoil, (2) oil-contaminated soil (4% total extractable hydrocarbons, or TEH), and (3) oil-contaminated soil treated by bioremediation (< 2% TEH). Soil physical properties including water retention, water uptake, and water repellence were measured. The results indicated that the growth of barley was significantly reduced by oil-contamination of agricultural topsoil. Furthermore, bioremediation did not improve the barley yield. The lack of effects from bioremediation was attributed to development of water repellence in hydrocarbon contaminated soils. There seemed to be a critical water content around 18% to 20% in contaminated soils. Above this value the water uptake by contaminated soil was near that of the agricultural topsoil. For lower water contents, there was a strong divergence in sorptivity between contaminated and agricultural topsoil. For these soils, water availability was likely the single most important parameter controlling plant growth. This parameter should be considered in assessing endpoint of bioremediation for hydrocarbon contaminated soils

Effect of decreasing acidity on the extractability of inorganic soil phosphorus

Directory of Open Access Journals (Sweden)

Helinä Hartikainen

1981-01-01

Full Text Available The extractability of P by the water and anion exchange resin methods and reactions of soil inorganic P were investigated with seven acid mineral soil samples incubated with KOH solutions of various concentrations. The results were compared with the analytical data obtained from three soil samples incubated in a prolonged liming experiment. The resin extraction method proved more effective than the water extraction method. The amounts of P desorbed by both methods seemed to increase exponentially as the pH in the soil suspensions rose. The factors involved were discussed. On the basis of fractionation analyses P reacting to changes in the pH and participating in desorption processes was supposed to originate from secondary NH4F and NaOH soluble reserves. In general, as the acidity decreased NH4F-P increased at the expense of NaOH-P. In heavily limed gyttja soil also H2SO4-P increased. This was possibly induced by the precipitation of mobilized P as a Ca compound. The significance of pH in the extractability of soil P seemed somewhat to lessen as the amount of secondary P increased. The results were in accordance with the conception that liming improves the availability of inorganic P to plants and reduces the need for P fertilization. However, increasing of the soil pH involves the risk that P is more easily desorbed to the recipient water by the eroded soil material carried into the watercourse. Therefore, intensive liming is not recommendable close to the shoreline. Further, it should be taken into account that liming of lakes may also result in eutrophication as desorption of sedimentary inorganic P is enhanced.

Extraction and Capture of Water from Martian Regolith Experimental Proof-of-Concept

Science.gov (United States)

Linne, Diane L.; Kleinhenz, Julie E.; Bauman, Steven W.; Johnson, Kyle A.

2016-01-01

A novel concept for extraction of water from the Mars soil in a real-time, open-air process was demonstrated in a Mars environment chamber. The concept breadboard uses radiative heating to bake off water from exposed soil contained in a bin. An enclosure, intended to mimic the bottom of a rover, covers the bin. A fan continuously blows the Mars atmospheric gases through the enclosure to collect the evolved water while a tiller was used to churn up moist subsurface soil. These initial tests verified concept feasibility. The sweep gas generated by commercially available muffin fans at 7 Torr was sufficient to transfer water vapor into a condenser flow loop. The radiative heating, while non-optimized, heated the soil surface to 60 C to generate water vapor. A rototiller working through the soil bin brought sufficient amounts of new moist soil to the heated surface to show an increase in rate of water extraction.

Migration through soil of organic solutes in an oil-shale process water

Science.gov (United States)

Leenheer, J.A.; Stuber, H.A.

1981-01-01

The migration through soil of organic solutes in an oil-shale process water (retort water) was studied by using soil columns and analyzing leachates for various organic constituents. Retort water extracted significant quantities of organic anions leached from ammonium-saturated-soil organic matter, and a distilled-water rinse, which followed retort-water leaching, released additional organic acids from the soil. After being corrected for organic constitutents extracted from soil by retort water, dissolved-organic-carbon fractionation analyses of effluent fractions showed that the order of increasing affinity of six organic compound classes for the soil was as follows: hydrophilic neutrals nearly equal to hydrophilic acids, followed by the sequence of hydrophobic acids, hydrophilic bases, hydrophobic bases, and hydrophobic neutrals. Liquid-chromatographic analysis of the aromatic amines in the hydrophobic- and hydrophilic-base fractions showed that the relative order of the rates of migration through the soil column was the same as the order of migration on a reversed-phase, octadecylsilica liquid-chromatographic column.

Factors influencing the chemical extractability of 241Am from a contaminated soil

International Nuclear Information System (INIS)

Nishita, H.; Hamilton, M.

1976-01-01

Factors influencing the extractability of 241 Am from an artificially contaminated soil were investigated. This was done with an equilibrium batch technique using CH 3 COOH-NH 4 OH and HNO 3 -NaOH extracting systems. The influence of several soil components was determined indirectly by selectively removing them from the soil. The effect of water- and HCl-soluble salts and organic matter on 241 Am extractability was small. The most marked effect was due to the soil organic fraction that was not water- or HCl-soluble. This organic fraction was influential under both low and high pH conditions, but its influence was particularly marked under low pH conditions. The free iron-oxides had an appreciable effect under low pH conditions, but no observable effect in the high pH range. Though to a lesser extent, the free silica and alumina, amorphous alumino-silicate, and possibly residual organic matter also showed some influence. These results provide some implications on the conditions that influence the movement of 241 Am in soils and its availability to plants. A review of the literature on the behavior of Am in soils is included

Isotope fractionation of sandy-soil water during evaporation - an experimental study.

Science.gov (United States)

Rao, Wen-Bo; Han, Liang-Feng; Tan, Hong-Bing; Wang, Shuai

2017-06-01

Soil samples containing water with known stable isotopic compositions were prepared. The soil water was recovered by using vacuum/heat distillation. The experiments were held under different conditions to control rates of water evaporation and water recovery. Recoveries, δ 18 O and δ 2 H values of the soil water were determined. Analyses of the data using a Rayleigh distillation model indicate that under the experimental conditions only loosely bound water is extractable in cases where the recovery is smaller than 100 %. Due to isotopic exchange between vapour and remaining water in the micro channels or capillaries of the soil matrix, isotopic fractionation may take place under near-equilibrium conditions. This causes the observed relationship between δ 2 H and δ 18 O of the extracted water samples to have a slope close to 8. The results of this study may indicate that, in arid zones when soil that initially contains water dries out, the slope of the relationship between δ 2 H and δ 18 O values should be close to 8. Thus, a smaller slope, as observed by some groundwater and soil water samples in arid zones, may be caused by evaporation of water before the water has entered the unsaturated zone.

SUPERCRITICAL FLUID EXTRACTION OF POLYCYCLIC AROMATIC HYDROCARBON MIXTURES FROM CONTAMINATED SOILS

Science.gov (United States)

Highly contaminated (with PAHs) topsoils were extracted with supercritical CO2 to determine the feasibility and mechanism of supercritical fluid extraction (SFE). Effect of SCF density, temperature, cosolvent type and amount, and of slurrying the soil with water were ...

Towards a more appropriate water based extraction for the assessment of organic contaminant availability

International Nuclear Information System (INIS)

Hickman, Zachary A.; Reid, Brian J.

2005-01-01

This study correlated extractabilities of 37 d aged phenanthrene residues in four dissimilar soils with the fraction that was available for earthworm (Lumbricus rubellus) accumulation and microorganism (Pseudomonas sp.) mineralisation. Extractability was determined using two established techniques, namely (1) a water based extraction using CO 2 equilibrated water and (2) an aqueous based hydroxypropyl-β-cyclodextrin (HPCD) extraction. Results showed no relationship between earthworm accumulation and phenanthrene extractability using either HPCD (r 2 =0.07; slope=-4.76; n=5) or the water based extraction (r 2 =0.31; slope=-5.34; n=5). Earthworm accumulation was overestimated by both techniques. In contrast, the fraction of phenanthrene extractable using both the HPCD technique and the water based extraction correlated strongly with microbial mineralisation. However, the slopes of these linear relationships were 0.48 (r 2 =0.96; n=10), and 0.99 (r 2 =0.88; n=10) for the water based extraction and HPCD, respectively. Thus, the HPCD extraction provided values that were numerically close to the mineralisation values, whilst the water based extraction values were approximately half the mineralisation values. It is submitted that HPCD extraction provided an appropriate method of assessing the fraction of contaminant available for microbial mineralisation in these dissimilar soils. - No significant difference was found between microbially mineralised phenanthrene and extractability using hydroxypropyl-β-cyclodextrin in four dissimilar soils; the water-only extraction removed half of this fraction

The use of high vacuum soil vapor extraction to improve contaminant recovery from ground water zones of low transmissivity

International Nuclear Information System (INIS)

Brown, A.; Farrow, J.R.C.; Burgess, W.

1996-01-01

This study examines the potential for enhancing hydrocarbon contaminant mass recovery from ground water using high vacuum soil vapor extraction (SVE). The effectiveness of this form of remediation is compared with the effectiveness of conventional pump-and-treat. This study focuses on the performance of a high vacuum SVE system at two ground water monitoring wells (MW-17 and MW-65b) at a site in Santa Barbara, California, US. The site is a highly characterized site with vadose zone and ground water petroleum hydrocarbon contamination (gasoline). The ground water wells are located beyond a defined area of vadose zone soil contamination. Ground water hydrocarbon contamination [light non-aqueous phase liquid (LNAPL) and dissolved phase] is present at each of the wells. the ground water wells have been part of a low-flow, pump-and-treat, ground water treatment system (GWTS) since August, 1986. The low transmissivity of the aquifer sediments prevent flow rates above approximately 0.02 gpm (0.01 l/min) per well

Influence of soil and hydrocarbon properties on the solvent extraction of high-concentration weathered petroleum from contaminated soils.

Science.gov (United States)

Sui, Hong; Hua, Zhengtao; Li, Xingang; Li, Hong; Wu, Guozhong

2014-05-01

Petroleum ether was used to extract petroleum hydrocarbons from soils collected from six oil fields with different history of exploratory and contamination. It was capable of fast removing 76-94 % of the total petroleum hydrocarbons including 25 alkanes (C11-C35) and 16 US EPA priority polycyclic aromatic hydrocarbons from soils at room temperature. The partial least squares analysis indicated that the solvent extraction efficiencies were positively correlated with soil organic matter, cation exchange capacity, moisture, pH, and sand content of soils, while negative effects were observed in the properties reflecting the molecular size (e.g., molecular weight and number of carbon atoms) and hydrophobicity (e.g., water solubility, octanol-water partition coefficient, soil organic carbon partition coefficient) of hydrocarbons. The high concentration of weathered crude oil at the order of 10(5) mg kg(-1) in this study was demonstrated adverse for solvent extraction by providing an obvious nonaqueous phase liquid phase for hydrocarbon sinking and increasing the sequestration of soluble hydrocarbons in the insoluble oil fractions during weathering. A full picture of the mass distribution and transport mechanism of petroleum contaminants in soils will ultimately require a variety of studies to gain insights into the dynamic interactions between environmental indicator hydrocarbons and their host oil matrix.

Toxicity Thresholds Based on EDTA Extractable Nickel and Barley Root Elongation in Chinese Soils

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Guangyun Zhu

2018-04-01

Full Text Available The uncertainty in the risk assessment of trace metal elements in soils when total metal contents are used can be decreased by assessing their availability and/or extractability when the soils have a high background value or different sources of trace metal elements. In this study, the added water-soluble nickel (Ni toxicity to barley root elongation was studied in 17 representative Chinese soil samples with and without artificial rainwater leaching. The extractability of added Ni in soils was estimated by three sequential extractions with ethylenediaminetetraacetic acid (EDTA. The results showed that the effective concentration of EDTA extractable Ni (EC50, which caused 50% inhibition of barley root elongation, ranged from 46 to 1019 mg/kg in unleached soils and 24 to 1563 mg/kg in leached soils. Regression models for EDTA extractable Ni and total Ni added to soils against soil properties indicated that EDTA extractable Ni was significantly correlated with the total Ni added to soils and that pH was the most important control factor. Regression models for toxicity thresholds based on EDTA extractable Ni against soil properties showed that soil citrate dithionate extractable Fe was more important than soil pH in predicting Ni toxicity. These results can be used to accurately assess the risk of contaminated soils with high background values and/or different Ni sources.

Multilevel soil-vapor extraction test for heterogeneous soil

International Nuclear Information System (INIS)

Widdowson, M.A.; Haney, O.R.; Reeves, H.W.

1997-01-01

The design, performance, and analysis of a field method for quantifying contaminant mass-extraction rates and air-phase permeability at discrete vertical locations of the vadose zones are presented. The test configuration consists of a multiscreen extraction well and multilevel observation probes located in soil layers adjacent to the extraction well. For each level tested an inflatable packer system is used to pneumatically isolate a single screen in the extraction well, and a vacuum is applied to induce air flow through the screen. Test data include contaminant concentration and flow characteristics at the extraction well, and transient or steady-state pressure drawdown data at observation probes located at variable radii from the extraction well. The test method is applicable to the design of soil-vapor extraction (SVE) and bioventing remediation systems in a variety of geologic settings, particularly stratified soils. Application of the test method at a gasoline-polluted site located in the Piedmont physiographic region is described. Contaminant mass-extraction rates, expressed in terms of volatile hydrocarbons, varied from 0.16 to 14 kg/d

Determination of pyridine in soil and water samples of a polluted area

International Nuclear Information System (INIS)

Peters, R.J.B.; Renesse van Duivenbode, J.A.D. van

1994-01-01

A method for the analyses of pyridine in environmental samples is described. For soil samples a distillation procedure followed by an extraction, an acidic extraction or a Soxhlet extraction can be used. For water samples a distillation procedure followed by extraction can be employed. Deuterated pyridine is used as an internal standard and the extracts are analyzed by GC-MS. The recoveries of the methods are higher than 80%; the detection limits for pyridine are 0.01 mg/kg for soil samples and 0.2 μg/l for water samples. (orig.)

Influence of plants on the chemical extractability and biodegradability of 2,4-dichlorophenol in soil

International Nuclear Information System (INIS)

Boucard, Tatiana K.; Bardgett, Richard D.; Jones, Kevin C.; Semple, Kirk

2005-01-01

This study investigated the fate and behaviour of [UL- 14 C] 2,4-dichlorophenol (DCP) in planted (Lolium perenne L.) and unplanted soils over 57 days. Extractability of [UL- 14 C] 2,4-DCP associated activity was measured using calcium chloride (CaCl 2 ), acetonitrile-water and dichloromethane (DCM) extractions. Biodegradability of [UL- 14 C] 2,4-DCP associated activity was assessed through measurement of 14 CO 2 production by a degrader inoculum (Burkholderia sp.). Although extractability and mineralisation of [UL- 14 C] 2,4-DCP associated activity decreased significantly in both planted and unplanted soils, plants appeared to enhance the sequestration process. After 57 days, in unplanted soil, 27% of the remaining [UL- 14 C] 2,4-DCP associated activity was mineralised by Burkholderia sp., and 13%, 48%, and 38% of 14 C-activity were extracted by CaCl 2 , acetonitrile-water and DCM, respectively. However, after 57 days, in planted soils, only 10% of the [UL- 14 C] 2,4-DCP associated activity was available for mineralisation, whilst extractability was reduced to 2% by CaCl 2 , 17% by acetonitrile-water and 11% by DCM. This may be due to the effect of plants on soil moisture conditions, which leads to modification of the soil structure and trapping of the compound. However, the influence of plants on soil biological and chemical properties may also play a role in the ageing process

Comparison of pore water samplers and cryogenic distillation under laboratory and field conditions for soil water stable isotope analysis.

Science.gov (United States)

Thoma, Michael; Frentress, Jay; Tagliavini, Massimo; Scandellari, Francesca

2018-02-15

We used pore water samplers (PWS) to sample for isotope analysis (1) only water, (2) soil under laboratory conditions, and (3) soil in the field comparing the results with cryogenic extraction (CE). In (1) and (2), no significant differences between source and water extracted with PWS were detected with a mean absolute difference (MAD) always lower than 2 ‰ for δ 2 H and 1 ‰ for δ 18 O. In (2), CE water was more enriched than PWS-extracted water, with a MAD respect to source water of roughly 8 ‰ for δ 2 H and 4 ‰ for δ 18 O. In (3), PWS water was enriched relative to CE water by 3 ‰ for δ 2 H and 0.9 ‰ for δ 18 O. The latter result may be due to the distinct water portions sampled by the two methods. Large pores, easily sampled by PWS, likely retain recent, and enriched, summer precipitation while small pores, only sampled by CE, possibly retain isotopically depleted water from previous winter precipitation or irrigation inputs. Accuracy and precision were greater for PWS relative to CE. PWS is therefore suggested as viable tool to extract soil water for stable isotope analysis, particularly for soils used in this study (sandy and silty loams).

Land subsidence caused by a single water extraction well and rapid water infiltration

Directory of Open Access Journals (Sweden)

I. Martinez-Noguez

2015-11-01

Full Text Available Nowadays several parts of the world suffer from land subsidence. This setting of the earth surface occurs due to different factors such as earth quakes, mining activities, and gas, oil and water withdrawal. This research presents a numerical study of the influence of land subsidence caused by a single water extraction well and rapid water infiltration into structural soil discontinuities. The numerical simulation of the infiltration was based on a two-phase flow-model for porous media, and for the deformation a Mohr–Coulomb model was used. A two-layered system with a fault zone is presented. First a single water extraction well is simulated producing a cone-shaped (conical water level depletion, which can cause land subsidence. Land Subsidence can be further increased if a hydrological barrier as a result of a discontinuity, exists. After water extraction a water column is applied on the top boundary for one hours in order to represent a strong storm which produces rapid water infiltration through the discontinuity as well as soil deformation. Both events are analysed and compared in order to characterize deformation of both elements and to get a better understanding of the land subsidence and new fracture formations.

Extraction of Water from Lunar Permafrost

Science.gov (United States)

Ethridge, Edwin C.; Kaukler, William

2009-01-01

Remote sensing indicates the presence of hydrogen rich regions associated with the lunar poles. The logical hypothesis is that there is cryogenically trapped water ice located in craters at the lunar poles. Some of the craters have been in permanent darkness for a billion years. The presence of water at the poles as well as other scientific advantages of a polar base, have influenced NASA plans for the lunar outpost. The lunar outpost has water and oxygen requirements on the order of 1 ton per year scaling up to as much as 5 tons per year. Microwave heating of the frozen permafrost has unique advantages for water extraction. Proof of principle experiments have successfully demonstrated that microwaves will couple to the cryogenic soil in a vacuum and the sublimed water vapor can be successfully captured on a cold trap. Dielectric property measurements of lunar soil simulant have been measured. Microwave absorption and attenuation in lunar soil simulant has been correlated with measured dielectric properties. Future work will be discussed.

A microfluidic sub-critical water extraction instrument

Science.gov (United States)

Sherrit, Stewart; Noell, Aaron C.; Fisher, Anita; Lee, Mike C.; Takano, Nobuyuki; Bao, Xiaoqi; Kutzer, Thomas C.; Grunthaner, Frank

2017-11-01

This article discusses a microfluidic subcritical water extraction (SCWE) chip for autonomous extraction of amino acids from astrobiologically interesting samples. The microfluidic instrument is composed of three major components. These include a mixing chamber where the soil sample is mixed and agitated with the solvent (water), a subcritical water extraction chamber where the sample is sealed with a freeze valve at the chip inlet after a vapor bubble is injected into the inlet channels to ensure the pressure in the chip is in equilibrium with the vapor pressure and the slurry is then heated to ≤200 °C in the SCWE chamber, and a filter or settling chamber where the slurry is pumped to after extraction. The extraction yield of the microfluidic SCWE chip process ranged from 50% compared to acid hydrolysis and 80%-100% compared to a benchtop microwave SCWE for low biomass samples.

Biosynthesis of Multicomponent Nanoparticles with Extract of Mortiño (Vaccinium floribundum Kunth Berry: Application on Heavy Metals Removal from Water and Immobilization in Soils

Directory of Open Access Journals (Sweden)

Mayra Abril

2018-01-01

Full Text Available Through preparation of multicomponent nanoparticles (MCNPs using ferric chloride (FeCl3, sodium sulfate (Na2SO4, and the extract of mortiño fruit (Vaccinium floribundum Kunth, we dramatically improved the removal/immobilization of heavy metals from water and in soils. As-prepared nanoparticles were spherical measuring approximately 12 nm in diameter and contained iron oxides and iron sulfides in the crystal structure. Removal of copper and zinc from water using MCNPs showed high efficiencies (>99% at pH above 6 and a ratio of 0.5 mL of the extract:10 mL 0.5 M FeCl3·6H2O : 10 mL 0.035 M Na2SO4. The physisorption process followed by chemisorption was regarded as the removal mechanism of Cu and Zn from water. While, when MCNPs were used to treat soils contaminated with heavy metals, more than 95% of immobilization was accomplished for all metals. Nevertheless, the distribution of the metallic elements changed in the soil fractions after treatment. Results indicate that immobilization of metals after the injection of nanoparticles into soils was effective. Metals did not leach out when soils were drained with rain, drinking, and deionized water but fairly leached out under acidic water drainage.

Extraction Techniques for Polycyclic Aromatic Hydrocarbons in Soils

Science.gov (United States)

Lau, E. V.; Gan, S.; Ng, H. K.

2010-01-01

This paper aims to provide a review of the analytical extraction techniques for polycyclic aromatic hydrocarbons (PAHs) in soils. The extraction technologies described here include Soxhlet extraction, ultrasonic and mechanical agitation, accelerated solvent extraction, supercritical and subcritical fluid extraction, microwave-assisted extraction, solid phase extraction and microextraction, thermal desorption and flash pyrolysis, as well as fluidised-bed extraction. The influencing factors in the extraction of PAHs from soil such as temperature, type of solvent, soil moisture, and other soil characteristics are also discussed. The paper concludes with a review of the models used to describe the kinetics of PAH desorption from soils during solvent extraction. PMID:20396670

Extraction Techniques for Polycyclic Aromatic Hydrocarbons in Soils

Directory of Open Access Journals (Sweden)

E. V. Lau

2010-01-01

Full Text Available This paper aims to provide a review of the analytical extraction techniques for polycyclic aromatic hydrocarbons (PAHs in soils. The extraction technologies described here include Soxhlet extraction, ultrasonic and mechanical agitation, accelerated solvent extraction, supercritical and subcritical fluid extraction, microwave-assisted extraction, solid phase extraction and microextraction, thermal desorption and flash pyrolysis, as well as fluidised-bed extraction. The influencing factors in the extraction of PAHs from soil such as temperature, type of solvent, soil moisture, and other soil characteristics are also discussed. The paper concludes with a review of the models used to describe the kinetics of PAH desorption from soils during solvent extraction.

Soil and Soil Water Relationships

OpenAIRE

Easton, Zachary M.; Bock, Emily

2017-01-01

Discusses the relationships between soil, water and plants. Discusses different types of soil, and how these soils hold water. Provides information about differences in soil drainage. Discusses the concept of water balance.

Extraction of an urease-active organo-complex from soil.

Science.gov (United States)

Burns, R. G.; El-Sayed, M. H.; Mclaren, A. D.

1972-01-01

Description of an extraction from a Dublin clay loam soil of a colloidal organic matter complex that is urease active and, by X-ray analysis, free of clays. Urease activity in the clay-free precipitates, as in the soil, was not destroyed by the activity of an added proteolytic enzyme, pronase. This is attributed to the circumstance that native soil urease resides in organic colloidal particles with pores large enough for water, urea, ammonia, and carbon dioxide to pass freely, but nevertheless small enough to exclude pronase.

Aluminium, extractable from soil samples by the acid ammonium acetate soil-testing method

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Osmo Mäkitie

1968-05-01

Full Text Available The extractant, 0.5 M acetic acid –0.5 M ammonium acetate at pH 4.65, which is used in soil-testing, extracts relatively high amounts of aluminium from acid soils. The mean values of acetate-extractable aluminium at pH 4.65, 1.75 meq Al/100 g of soil, and of exchangeable aluminium (M KCI extraction, 0.41 meq Al were obtained from a material of 30 samples of acid soils (Table 2. Several other acetic acid ammonium acetate extractants, from M acetic acid to M ammonium acetate solution were also used for studying the extractability of soil aluminium. The soil-testing extractant can be used for the estimation of the soluble amounts of aluminium in acid soils, however, further studies are needed for a better interpretation of the ammonium acetate extractable (at pH 4.65 aluminium in our soils.

Remediation of heavy-metal-contaminated soil using chelant extraction: Feasibility studies

Energy Technology Data Exchange (ETDEWEB)

Peters, R.W.; Miller, G.; Taylor, J.D.; Schneider, J.F.; Zellmer, S.; Edgar, D.E.; Johnson, D.O.

1993-08-01

Results are presented of a laboratory investigation conducted to determine the efficacy of using chelating agents to extract heavy metals (Pb, Cd, Cr, Ba, Cu, and Zn) from soil, the primary focus being on the extraction of lead from the soil. Results from the batch-shaker studies and emphasizes the columnar extraction studies are described. The chelating agents studied included ethylenediaminetetraacetic acid (EDTA) and citric acid, in addition to water. Concentrations of the chelants ranged from 0.01 to 0.05 M; the suspension pH was varied between 3 and 8. Results showed that the removal of lead using citric acid and water was somewhat pH-dependent. For the batch-shaker studies, the results indicated that EDTA was more effective at removing Cd, Cu, Pb, and Zn than was citric acid (both present at 0.01 M). EDTA and citric acid were equally effective in mobilizing Cr and Ba from the soil. Heavy metals removal was slightly more effective in the more acidic region (pH {le} 5).

Combined effects of DOM extracted from site soil/compost and biosurfactant on the sorption and desorption of PAHs in a soil-water system

Energy Technology Data Exchange (ETDEWEB)

Yu Hui, E-mail: yuhui200@uregina.ca [Environmental Systems Engineering Program, Faculty of Engineering and Applied Science, University of Regina, Regina, SK S4S 0A2 (Canada); Huang Guohe, E-mail: gordon.huang@uregina.ca [Environmental Systems Engineering Program, Faculty of Engineering and Applied Science, University of Regina, Regina, SK S4S 0A2 (Canada); An Chunjiang, E-mail: an209@uregina.ca [Environmental Systems Engineering Program, Faculty of Engineering and Applied Science, University of Regina, Regina, SK S4S 0A2 (Canada); Wei Jia, E-mail: jia.wei@iseis.org [Environmental Systems Engineering Program, Faculty of Engineering and Applied Science, University of Regina, Regina, SK S4S 0A2 (Canada)

2011-06-15

Highlights: {yields} The combined DOM and biosurfactant significantly enhanced desorption of PAHs. {yields} Compost DOM exhibited higher desorption enhancement capacity than the soil DOM. {yields} Competition among PAHs, DOM and biosurfactant for sorption site determined desorption of PAHs from soil. {yields} Formation of DOM-biosurfactant complex enhance desorption extent of PAHs. - Abstract: The combined effects of DOM and biosurfactant on the sorption/desorption behavior of phenanthrene (PHE) and pyrene (PYR) in soil water systems were systematically investigated. Two origins of DOMs (extracted from soil and extracted from food waste compost) and an anionic biosurfactant (rhamnolipid) were introduced. The presence of DOM in the aqueous phase could decrease the sorption of PAHs, thus influence their mobility. Desorption enhancement for both PHE and PYR in the system with compost DOM was greater than that in the soil DOM system. This is due to the differences in specific molecular structures and functional groups of two DOMs. With the co-existence of biosurfactant and DOM, partitioning is the predominant process and the desorption extent was much higher than the system with DOM or biosurfactant individually. For PHE, the desorption enhancement of combined DOM and biosurfactant was larger than the sum of DOM or biosurfactant; however desorption enhancement for PYR in the combined system was less than the additive enhancement in two individual system under low PAH concentration. This could be explained as the competition sorption among PAHs, DOM and biosurfactant. The results of this study will help to clarify the transport of petroleum pollutants in the remediation of HOCs-contaminated soils.

Combined effects of DOM extracted from site soil/compost and biosurfactant on the sorption and desorption of PAHs in a soil-water system

International Nuclear Information System (INIS)

Yu Hui; Huang Guohe; An Chunjiang; Wei Jia

2011-01-01

Highlights: → The combined DOM and biosurfactant significantly enhanced desorption of PAHs. → Compost DOM exhibited higher desorption enhancement capacity than the soil DOM. → Competition among PAHs, DOM and biosurfactant for sorption site determined desorption of PAHs from soil. → Formation of DOM-biosurfactant complex enhance desorption extent of PAHs. - Abstract: The combined effects of DOM and biosurfactant on the sorption/desorption behavior of phenanthrene (PHE) and pyrene (PYR) in soil water systems were systematically investigated. Two origins of DOMs (extracted from soil and extracted from food waste compost) and an anionic biosurfactant (rhamnolipid) were introduced. The presence of DOM in the aqueous phase could decrease the sorption of PAHs, thus influence their mobility. Desorption enhancement for both PHE and PYR in the system with compost DOM was greater than that in the soil DOM system. This is due to the differences in specific molecular structures and functional groups of two DOMs. With the co-existence of biosurfactant and DOM, partitioning is the predominant process and the desorption extent was much higher than the system with DOM or biosurfactant individually. For PHE, the desorption enhancement of combined DOM and biosurfactant was larger than the sum of DOM or biosurfactant; however desorption enhancement for PYR in the combined system was less than the additive enhancement in two individual system under low PAH concentration. This could be explained as the competition sorption among PAHs, DOM and biosurfactant. The results of this study will help to clarify the transport of petroleum pollutants in the remediation of HOCs-contaminated soils.

Association of water spectral indices with plant and soil water relations in contrasting wheat genotypes.

Science.gov (United States)

Gutierrez, Mario; Reynolds, Matthew P; Klatt, Arthur R

2010-07-01

Spectral reflectance indices can be used to estimate the water status of plants in a rapid, non-destructive manner. Water spectral indices were measured on wheat under a range of water-deficit conditions in field-based yield trials to establish their relationship with water relations parameters as well as available volumetric soil water (AVSW) to indicate soil water extraction patterns. Three types of wheat germplasm were studied which showed a range of drought adaptation; near-isomorphic sister lines from an elite/elite cross, advanced breeding lines, and lines derived from interspecific hybridization with wild relatives (synthetic derivative lines). Five water spectral indices (one water index and four normalized water indices) based on near infrared wavelengths were determined under field conditions between the booting and grain-filling stages of crop development. Among all water spectral indices, one in particular, which was denominated as NWI-3, showed the most consistent associations with water relations parameters and demonstrated the strongest associations in all three germplasm sets. NWI-3 showed a strong linear relationship (r(2) >0.6-0.8) with leaf water potential (psi(leaf)) across a broad range of values (-2.0 to -4.0 MPa) that were determined by natural variation in the environment associated with intra- and inter-seasonal affects. Association observed between NWI-3 and canopy temperature (CT) was consistent with the idea that genotypes with a better hydration status have a larger water flux (increased stomatal conductance) during the day. NWI-3 was also related to soil water potential (psi(soil)) and AVSW, indicating that drought-adapted lines could extract more water from deeper soil profiles to maintain favourable water relations. NWI-3 was sufficiently sensitive to detect genotypic differences (indicated by phenotypic and genetic correlations) in water status at the canopy and soil levels indicating its potential application in precision

Hydroxypropyl-beta-cyclodextrin as non-exhaustive extractant for organochlorine pesticides and polychlorinated biphenyls in muck soil

Energy Technology Data Exchange (ETDEWEB)

Wong, Fiona [Centre for Atmospheric Research Experiments, Science and Technology Branch, Environment Canada, 6248 Eighth Line, Egbert, Ontario, L0L 1N0 (Canada); Department of Chemistry, University of Toronto Scarborough, 1265 Military Trail, Toronto, Ontario, M1C 1A4 (Canada); Bidleman, Terry F., E-mail: terry.bidleman@ec.gc.c [Centre for Atmospheric Research Experiments, Science and Technology Branch, Environment Canada, 6248 Eighth Line, Egbert, Ontario, L0L 1N0 (Canada)

2010-05-15

Hydroxypropyl-beta-cyclodextrin (HPCD) was used as a non-exhaustive extractant for organochlorine pesticides (OCs) and polychlorinated biphenyls (PCBs) in muck soil. An optimized extraction method was developed which involved using a HPCD to soil mass ratio of 5.8 with a single extraction period of 20 h. An aging experiment was performed by spiking a muck soil with {sup 13}C-labeled OCs and non-labeled PCBs. The soil was extracted with the optimized HPCD method and Soxhlet apparatus with dichloromethane over 550 d periodically. The HPCD extractability of the spiked OCs was greater than of the native OCs. A decreased in HPCD extractability was observed for the spiked OCs after 550 d of aging and their extractability approached those of the natives. The partition coefficient between HPCD and soil (log K{sub CD-Soil}) was negatively correlated with the octanol-water partition coefficient (log K{sub OW}) with r{sup 2} = 0.67 and p < 0.05. - The effect of aging on the extractability of organochlorine chemicals in muck soil was investigated using hydroxypropyl-beta-cyclodextrin as a mild extractant.

Relationships between stability, maturity, water-extractable organic matter of municipal sewage sludge composts and soil functionality.

Science.gov (United States)

Sciubba, Luigi; Cavani, Luciano; Grigatti, Marco; Ciavatta, Claudio; Marzadori, Claudio

2015-09-01

Compost capability of restoring or enhancing soil quality depends on several parameters, such as soil characteristics, compost carbon, nitrogen and other nutrient content, heavy metal occurrence, stability and maturity. This study investigated the possibility of relating compost stability and maturity to water-extractable organic matter (WEOM) properties and amendment effect on soil quality. Three composts from municipal sewage sludge and rice husk (AN, from anaerobic wastewater treatment plants; AE, from aerobic ones; MIX, from both anaerobic and aerobic ones) have been analysed and compared to a traditional green waste compost (GM, from green manure, solid waste and urban sewage sludge). To this aim, WEOMs were characterized through chemical analysis; furthermore, compost stability was evaluated through oxygen uptake rate calculation and maturity was estimated through germination index determination, whereas compost impact on soil fertility was studied, in a lab-scale experiment, through indicators as inorganic nitrogen release, soil microbial biomass carbon, basal respiration rate and fluorescein di-acetate hydrolysis. The obtained results indicated that WEOM characterization could be useful to investigate compost stability (which is related to protein and phenol concentrations) and maturity (related to nitrate/ammonium ratio and degree of aromaticity) and then compost impact on soil functionality. Indeed, compost stability resulted inversely related to soil microbial biomass, basal respiration rate and fluorescein di-acetate hydrolysis when the products were applied to the soil.

Soil Respiration Controls Ionic Nutrient Concentration In Percolating Water In Rice Fields

Science.gov (United States)

Kimura, M.

2004-12-01

Soil water in the plow layer in rice fields contains various kinds of cations and anions, and they are lost from the plow layer by water percolation. Some portions of CO2 produced by respirations of rice roots and soil microorganisms are also leached by water percolation to the subsoil layer as HCO3-. As the electrical neutrality of inorganic substances in percolating water is maintained when they are assumed to be in the form of simple cations and anions, soil respiration accelerates the leaching of ionic nutrients from the plow layer by water percolation. The proportion of inorganic carbon (Σ CO2) originated from photosynthates in the total Σ CO2 in soil solution in the plow layer was from 28 to 36 % in the rice straw amended soil and from 16 to 31 % in the soil without rice straw amendment in a soil pot experiment with rice plant after the maximum tillering stage. Most of Σ CO2 in percolating water from the plow layer accumulates in the subsoil layer. Periodical measurement of Σ CO2 in percolating water at 13 and 40 cm soil depths indicated that 10 % of total soil organic C in the plow layer was leached down from the plow layer (13 cm), and that about 90 % of it was retained in the subsoil layer to the depth of 40 cm. Water soluble organic materials are also leached from the plow layer by water percolation, and the leaching is accelerated by soil reduction. Soil reduction decreased the content of organic materials that were bound with ferric iron in soil (extractable by 0.1M Na4P2O7 + NaBH4) and increased the content of organic materials that were extractable by the neutral chelating solution (0.1M Na4P2O7). In addition, water percolation transformed the latter organic materials to those that were extractable by water and a neutral salt. Considerable portions of organic materials in percolating water are adsorbed in the subsoil layer, and then partially decomposed and polymerized to specific soil organic materials in the subsoil. Organic materials that were

Speciation of As(III), As(V), MMA and DMA in contaminated soil extracts by HPLC-ICP/MS

Energy Technology Data Exchange (ETDEWEB)

Bissen, M.; Frimmel, F.H. [Engler-Bunte-Institut, Univ. Karlsruhe (Germany)

2000-05-01

A method to separate and quantify two inorganic arsenic species As(III) and As(V) and two organic arsenic species, monomethylarsonic acid (MMA) and dimethylarsinic acid (DMA), by HPLC-ICP/MS has been developed. The separation of arsenic species was achieved on the anionic exchange column IonPac {sup trademark} AS11 (Dionex) with NaOH as mobile phase. The technique was successfully applied to analyze extracts of two contaminated soils, sampled at a former tannery site (soil 1) and a former paint production site (soil 2). The soils were extracted at pH values similar to the natural environment. Extractions were performed at different pH values with 0.3 M ammonium oxalate (pH = 3), milli-Q water (pH = 5.8), 0.3 M sodium carbonate (pH = 8) and 0.3 M sodium bicarbonate (pH = 11). No organically bound arsenic was found in the extracts. As(V) was the major component. Only up to 0.04% of the total arsenic contained in soil 1 were mobilized. The highest amount of extracted arsenic was found at the highest pH. In the milli-Q water extract of soil 1 As(III) and As(V) were found. High amounts of As(V) were found in the extracts of soil 2. Up to 20% of the total arsenic bound to soil 2 constituents were released. The results show that the mobilization of arsenic depended on the pH value of the extraction solution and the kind of extracted soil. Dramatic consequences have to be expected for pH changes in the environment especially in cases where soils contain high amounts of mobile arsenic. (orig.)

Subcritical-Water Extraction of Organics from Solid Matrices

Science.gov (United States)

Amashukeli, Xenia; Grunthaner, Frank; Patrick, Steven; Kirby, James; Bickler, Donald; Willis, Peter; Pelletier, Christine; Bryson, Charles

2009-01-01

An apparatus for extracting organic compounds from soils, sands, and other solid matrix materials utilizes water at subcritical temperature and pressure as a solvent. The apparatus, called subcritical water extractor (SCWE), is a prototype of subsystems of future instrumentation systems to be used in searching for organic compounds as signs of past or present life on Mars. An aqueous solution generated by an apparatus like this one can be analyzed by any of a variety of established chromatographic or spectroscopic means to detect the dissolved organic compound( s). The apparatus can be used on Earth: indeed, in proof-of-concept experiments, SCWE was used to extract amino acids from soils of the Atacama Desert (Chile), which was chosen because the dryness and other relevant soil conditions there approximate those on Mars. The design of the apparatus is based partly on the fact that the relative permittivity (also known as the dielectric constant) of liquid water varies with temperature and pressure. At a temperature of 30 C and a pressure of 0.1 MPa, the relative permittivity of water is 79.6, due to the strong dipole-dipole electrostatic interactions between individual molecular dipoles. As the temperature increases, increasing thermal energy causes increasing disorientation of molecular dipoles, with a consequent decrease in relative permittivity. For example, water at a temperature of 325 C and pressure of 20 MPa has a relative permittivity of 17.5, which is similar to the relative permittivities of such nonpolar organic solvents as 1-butanol (17.8). In the operation of this apparatus, the temperature and pressure of water are adjusted so that the water can be used in place of commonly used organic solvents to extract compounds that have dissimilar physical and chemical properties.

Measured soil water concentrations of cadmium and zinc in plant pots and estimated leaching outflows from contaminated soils

DEFF Research Database (Denmark)

Holm, P.E.; Christensen, T.H.

1998-01-01

Soil water concentrations of cadmium and zinc were measured in plant pots with 15 contaminated soils which differed in origin, texture, pH (5.1-7.8) and concentrations of cadmium (0.2-17 mg Cd kg(-1)) and zinc (36-1300 mg Zn kg(-1)). The soil waters contained total concentrations of 0.5 to 17 mu g...... to 0.1% per year of the total soil content of cadmium and zinc. The measured soil water concentrations of cadmium and zinc did not correlate linearly with the corresponding soil concentrations but correlated fairly well with concentrations measured in Ca(NO(3))(2) extracts of the soils and with soil...... water concentrations estimated from soil concentrations and pH. Such concentration estimates may be useful for estimating amounts of cadmium and zinc being leached from soils....

Model development for prediction of soil water dynamics in plant production.

Science.gov (United States)

Hu, Zhengfeng; Jin, Huixia; Zhang, Kefeng

2015-09-01

Optimizing water use in agriculture and medicinal plants is crucially important worldwide. Soil sensor-controlled irrigation systems are increasingly becoming available. However it is questionable whether irrigation scheduling based on soil measurements in the top soil could make best use of water for deep-rooted crops. In this study a mechanistic model was employed to investigate water extraction by a deep-rooted cabbage crop from the soil profile throughout crop growth. The model accounts all key processes governing water dynamics in the soil-plant-atmosphere system. Results show that the subsoil provides a significant proportion of the seasonal transpiration, about a third of water transpired over the whole growing season. This suggests that soil water in the entire root zone should be taken into consideration in irrigation scheduling, and for sensor-controlled irrigation systems sensors in the subsoil are essential for detecting soil water status for deep-rooted crops.

Roots bridge water to nutrients: a study of utilizing hydraulic redistribution through root systems to extract nutrients in the dry soils

Science.gov (United States)

Yan, J.; Ghezzehei, T. A.

2017-12-01

The rhizosphere is the region of soil that surrounds by individual plant roots. While its small volume and narrow region compared to bulk soil, the rhizosphere regulates numerous processes that determine physical structure, nutrient distribution, and biodiversity of soils. One of the most important and distinct functions of the rhizosphere is the capacity of roots to bridge and redistribute soil water from wet soil layers to drier layers. This process was identified and defined as hydraulic lift or hydraulic redistribution, a passive process driven by gradients in water potentials and it has attracted much research attention due to its important role in global water circulation and agriculture security. However, while previous studies mostly focused on the hydrological or physiological impacts of hydraulic redistribution, limited research has been conducted to elucidate its role in nutrient cycling and uptake. In this study, we aim to test the possibility of utilizing hydraulic redistribution to facilitate the nutrient movement and uptake from resource segregated zone. Our overarching hypothesis is that plants can extract nutrients from the drier but nutrient-rich regions by supplying sufficient amounts of water from the wet but nutrient-deficient regions. To test our hypothesis, we designed split-root systems of tomatoes with unequal supply of water and nutrients in different root compartments. More specifically, we transplanted tomato seedlings into sand or soil mediums, and grew them under conditions with alternate 12-h lightness and darkness. We continuously monitored the temperature, water and nutrient content of soils in these separated compartments. The above and below ground biomass were also quantified to evaluate the impacts on the plant growth. The results were compared to a control with evenly supply of water and nutrients to assess the plant growth, nutrient leaching and uptake without hydraulic redistribution.

Use of azeotropic distillation for isotopic analysis of deuterium in soil water and saturate saline solution

International Nuclear Information System (INIS)

Santos, Antonio Vieira dos.

1995-05-01

The azeotropic distillation technique was adapted to extract soil water and saturate saline solution, which is similar to the sea water for the Isotopic Determination of Deuterium (D). A soil test was used to determine the precision and the nature of the methodology to extract soil water for stable isotopic analysis, using the azeotropic distillation and comparing with traditional methodology of heating under vacuum. This methodology has been very useful for several kinds of soil or saturate saline solution. The apparatus does not have a memory effect, and the chemical reagents do not affect the isotopic composition of soil water. (author). 43 refs., 10 figs., 12 tabs

Aqueous biphasic extraction of uranium and thorium from contaminated soils. Final report

International Nuclear Information System (INIS)

Chaiko, D.J.; Gartelmann, J.; Henriksen, J.L.; Krause, T.R.; Deepak; Vojta, Y.; Thuillet, E.; Mertz, C.J.

1995-07-01

The aqueous biphasic extraction (ABE) process for soil decontamination involves the selective partitioning of solutes and fine particulates between two immiscible aqueous phases. The biphase system is generated by the appropriate combination of a water-soluble polymer (e.g., polyethlene glycol) with an inorganic salt (e.g., sodium carbonate). Selective partitioning results in 99 to 99.5% of the soil being recovered in the cleaned-soil fraction, while only 0.5 to 1% is recovered in the contaminant concentrate. The ABE process is best suited to the recovery of ultrafine, refractory material from the silt and clay fractions of soils. During continuous countercurrent extraction tests with soil samples from the Fernald Environmental Management Project site (Fernald, OH), particulate thorium was extracted and concentrated between 6- and 16-fold, while the uranium concentration was reduced from about 500 mg/kg to about 77 mg/kg. Carbonate leaching alone was able to reduce the uranium concentration only to 146 mg/kg. Preliminary estimates for treatment costs are approximately $160 per ton of dry soil. A detailed flowsheet of the ABE process is provided

Extractability of 137Cs in Response to its Input Forms into Fukushima Forest Soils.

Science.gov (United States)

Mengistu, T. T.; Carasco, L.; Orjollet, D.; Coppin, F.

2017-12-01

In case of nuclear accidents like Fukushima disaster, the influence of 137Cs depositional forms (soluble and/or solid forms) on mineral soil of forest environment on its availability have not reported yet. Soluble (137Cs tagged ultra-pure water) and solid (137Cs contaminated litter-OL and fragmented litter-OF) input forms were mixed with the mineral soils collected under Fukushima coniferous and broadleaf forests. The mixtures then incubated under controlled laboratory condition to evaluate the extractability of 137Cs in soil over time in the presence of decomposition process through two extracting reagents- water and ammonium acetate. Results show that extracted 137Cs fraction with water was less than 1% for soluble input form and below detection limit for solid input form. On the same way with acetate reagent, the extracted 137Cs fraction ranged from 46 to 56% for soluble input and 2 to 15% for solid input, implying the nature of 137Cs contamination strongly influences the extractability and hence the mobility of 137Cs in soil. Although the degradation rate of the organic materials has been calculated in the range of 0.18 ± 0.1 to 0.24 ± 0.1 y-1, its impact on 137Cs extractability appeared very weak at least within the observation period, probably due to shorter time scale. Concerning the treatments of solid 137Cs input forms through acetate extraction, relatively more 137Cs has been extracted from broadleaf organic materials mixes (BL-OL & BL-OF) than the coniferous counterparts. This probably is due to the fact that the lignified coniferous organic materials (CED-OL & CED-OF) components tend to retain more 137Cs than that of the broadleaf. Generally, by extrapolating these observations in to a field context, one can expect more available 137Cs fraction in forest soil from wet depositional pathways such as throughfall and stemflow than those attached with organic materials like litter (OL) and its eco-processed forms (OF).

Extraction of Water from Polar Lunar Permafrost with Microwaves - Dielectric Property Measurements

Science.gov (United States)

Ethridge, Edwin C.; Kaukler, William

2009-01-01

Remote sensing indicates the presence of hydrogen rich regions associated with the lunar poles. The logical hypothesis is that there is cryogenically trapped water ice located in craters at the lunar poles. Some of the craters have been in permanent darkness for a billion years. The presence of water at the poles as well as other scientific advantages of a polar base, have influenced NASA plans for the lunar outpost. The lunar outpost has water and oxygen requirements on the order of 1 ton per year scaling up to as much as 10 tons per year. Microwave heating of the frozen permafrost has unique advantages for water extraction. Proof of principle experiments have successfully demonstrated that microwaves will couple to the cryogenic soil in a vacuum and the sublimed water vapor can be successfully captured on a cold trap. The dielectric properties of lunar soil will determine the hardware requirements for extraction processes. Microwave frequency dielectric property measurements of lunar soil simulant have been measured.

Soil water management

International Nuclear Information System (INIS)

Nielsen, D.R.; Cassel, D.K.

1984-01-01

The use of radiation and tracer techniques in investigations into soil water management in agriculture, hydrology etc. is described. These techniques include 1) neutron moisture gauges to monitor soil water content and soil water properties, 2) gamma radiation attenuation for measuring the total density of soil and soil water content, 3) beta radiation attenuation for measuring changes in the water status of crop plants and 4) radioactive and stable tracers for identifying pathways, reactions and retention times of the constituents in soils and groundwater aquifers. The number and spacing of soil observations that should be taken to represent the management unit are also considered. (U.K.)

Comparison of mild extraction procedures for determination of plant-available arsenic compounds in soil

Energy Technology Data Exchange (ETDEWEB)

Szakova, Jirina; Tlustos, Pavel; Pavlikova, Daniela; Balik, Jiri [Czech University of Agriculture, Department of Agrochemistry and Plant Nutrition, Prague (Czech Republic); Goessler, Walter; Schlagenhaufen, Claudia [Karl-Franzens-University Graz, Institute of Chemistry, Analytical Chemistry, Graz (Austria)

2005-05-01

In this work three mild extraction agents for determination of plant-available fractions of elements in soil were evaluated for arsenic speciation in soil samples. Pepper (Capsicum annum, L.) var. California Wonder was cultivated in pots, and aqueous solutions of arsenite, arsenate, methylarsonic acid, and dimethylarsinic acid, at a concentration of 15 mg As kg{sup -1} soil, were added at the beginning of the experiment. Control pots (untreated) were also included. Deionized water, 0.01 mol L{sup -1} CaCl{sub 2}, and 0.05 mol L{sup -1} (NH{sub 4}){sub 2}SO{sub 4} were used to extract the plant-available fraction of the arsenic compounds in soil samples collected during the vegetation period of the plants. Whereas in control samples the extractable arsenic fraction did not exceed 1% of total arsenic content, soil amendment by arsenic compounds resulted in extraction of larger amounts, which varied between 1.4 and 8.1% of total arsenic content, depending on soil treatment and on the extracting agent applied. Among arsenic compounds determined by HPLC-ICPMS arsenate was predominant, followed by small amounts of arsenite, methylarsonic acid, and dimethylarsinic acid, depending on the individual soil treatment. In all the experiments in which methylarsonic acid was added to the soil methylarsonous acid was detected in the extracts, suggesting that the soil bacteria are capable of reducing methylarsonic acid before a further methylation occurs. No significant differences were observed between analytical data obtained by using different extraction procedures. (orig.)

The use of in-situ dual vacuum extraction for remediation of soil and groundwater

International Nuclear Information System (INIS)

Trowbridge, B.E.; Ott, D.E.

1992-01-01

Dual Extraction provides a rapid and cost-effective method of remediating soil and groundwater impacted by volatile organic compounds (VOC's). Dual Extraction is the removal of both water and vapors through the same borehole using entrainment. This technology provides for the remediation of the vadose zone, capillary fringe, smear zone, and existing water table. The effectiveness of this technology is shown in a case study. A release from an Underground Storage Tank (UST) was responsible for a hydrocarbon plume spreading over approximately 50,000 square feet. The release produced vadose zone contamination in the silty and sandy clays from 10 - 30 feet below ground surface with TPH concentrations up to 1,400 mg/kg. A layer of free floating liquid hydrocarbon was present on a shallow aquifer located at 30 feet bgs in thicknesses ranging from 0.5 feet to 3.0 feet. An in-situ dual-extraction system was installed to remediate the soils and groundwater to levels as required by the Los Angeles Regional Water Quality Control Board (RWQCB). The system operated 24 hours/day for 196 days with an operating efficiency of over 99%. After 196 days, over 17,000 pounds of hydrocarbons had been extracted from the soils. Seven confirmatory soil borings were advanced in the area of highest initial hydrocarbon concentrations and indicated that TPH and BTEX concentrations had decreased over 99% from initial soil concentrations. Three confirmatory groundwater samples were obtained from monitoring wells initially exhibiting up to 3 feet of floating product. Confirmatory samples exhibited non-detectable (ND) concentrations of TPH and BTEX. Based upon the positive confirmatory results, site closure was obtained from the RWQCB in May of 1991. In only 28 weeks of operation, the groundwater contamination was reduced from free floating product to non-detectable concentrations of TPH using Dual Vacuum Extraction

The geographic distribution of Sr isotopes from surface waters and soil extracts over the island of Bornholm (Denmark) – A base for provenance studies in archaeology and agriculture

DEFF Research Database (Denmark)

Frei, Robert; Frei, Karin Margarita

2013-01-01

In this paper we report the Sr isotope signatures, and Sr, Al and Na concentrations of 30 surface waters (lakes/ponds and rivers/creeks) and 19 soil sample extracts from the island of Bornholm (Denmark) and present a categorized 87Sr/86Sr value distribution map that may serve as a base...... for provenance studies, including archaeological migration and authenticity proof for particular food products. The Sr isotopic compositions of surface waters range from 87Sr/86Sr = 0.7097–0.7281 (average 0.7175 ± 0.0049; 1σ), whereas 0.1 M HNO3, 0.05 M HNO3, and 0.01 M CaCl2 soil extracts range from 87Sr/86Sr...... Sr isotope composition vs. Sr, Na and Al concentration relationships of soil extracts imply that lowering of the isotopic composition of leachable Sr on Bornholm results as a consequence of significant admixture to this fraction of Sr deposited as marine salts (aerosols), and that rainwater only has...

General well function for soil vapor extraction

Science.gov (United States)

Perina, Tomas

2014-04-01

This paper develops a well function applicable to extraction of groundwater or soil vapor from a well under the most common field test conditions. The general well function (Perina and Lee, 2006) [12] is adapted to soil vapor extraction and constant head boundary at the top. For groundwater flow, the general well function now applies to an extraction well of finite diameter with uniform drawdown along the screen, finite-thickness skin, and partially penetrating an unconfined, confined, and leaky aquifer, or an aquifer underneath a reservoir. With a change of arguments, the model applies to soil vapor extraction from a vadose zone with no cover or with leaky cover at the ground surface. The extraction well can operate in specified drawdown (pressure for soil vapor) or specified flowrate mode. Frictional well loss is computed as flow-only dependent component of the drawdown inside the extraction well. In general case, the calculated flow distribution is not proportional to screen length for a multiscreen well.

Assessment of soil stabilization by chemical extraction and bioaccumulation using earthworm, Eisenia fetida

Science.gov (United States)

Lee, Byung-Tae; Abd Aziz, Azilah; Han, Heop Jo; Kim, Kyoung-Woong

2014-05-01

Soil stabilization does not remove heavy metals from contaminated soil, but lowers their exposures to ecosystem. Thus, it should be evaluated by measuring the fractions of heavy metals which are mobile and/or bioavailable in soils. The study compared several chemical extractions which intended to quantify the mobile or bioaccessible fractions with uptake and bioaccumulation by earthworm, Eisenia fetida. Soil samples were taken from the abandoned mine area contaminated with As, Cd, Cu, Pb and/or Zn. To stabilize heavy metals, the soils were amended with limestone and steel slag at 5% and 2% (w/w), respectively. All chemical extractions and earthworm tests were applied to both the contaminated and the stabilized soils with triplicates. The chemical extractions consisted of six single extractions which were 0.01M CaCl2 (unbufferred), EDTA or DTPA (chelating), TCLP (acidic), Mehlich 3 (mixture), and aqua regia (peudo-total). Sequential extractions were also applied to fractionate heavy metals in soils. In earthworm tests, worms were exposed to the soils for uptake of heavy metals. After 28 days of exposure to soils, worms were transferred to clean soils for elimination. During the tests, three worms were randomly collected at proper sampling events. Worms were rinsed with DI water and placed on moist filter paper for 48 h for depuration. Filter paper was renewed at 24 h to prevent coprophagy. The worms were killed with liquid nitrogen, dried in the oven, and digested with aqua regia for ICP-MS analysis. In addition to the bioaccumulation, several toxicity endpoints were observed such as burrowing time, mortality, cocoon production, and body weight changes. Toxicokinetics was applied to determine the uptake and elimination heavy metals by the earthworms. Bioaccumulation factor (BAF) was estimated using total metal concentrations and body burdens. Pearson correlation and simple linear regression were applied to evaluate the relationship between metal fractions by single

Soil water status under perennial and annual pastures on an acid duplex soil

International Nuclear Information System (INIS)

Heng, L.K.; White, R.E.; Chen, D.

2000-01-01

A comprehensive field study of soil water balance, nitrogen (N) cycling, pasture management and animal production was carried out on an acid duplex soil at Book Book near Wagga Wagga in southern New South Wales. The experiment, carried out over a 3-year period, tested the hypothesis that sown perennial grass pastures improve the sustainability of a grazing system through better use of water and N. The treatments were: annual pastures without lime (AP-), annual pastures with lime (AP+), perennial pastures without lime (PP-) and perennial pastures with lime (PP+). Soil water measurement was made using a neutron probe on one set of the treatments comprising four adjacent paddocks. Over three winter and spring periods, the results showed that perennial grass pastures, especially PP+, consistently extracted about 40 mm more soil water each year than did the annual grass pastures. As a result, surface runoff, sub-surface flow and deep drainage (percolation below 180 cm depth) were about 40 mm less from the perennial pastures. The soil water status of the four pasture treatments was simulated reasonably well using a simple soil water model. Together with the long-term simulation of deep drainage, using past meteorological records, it is shown that proper management of perennial pastures can reduce recharge to groundwater and make pastoral systems more sustainable in the high rainfall zone. However, to completely reduce recharge, more-deeply rooted plants or trees are needed. (author)

Remediation of flare pit soils using supercritical fluid extraction

Energy Technology Data Exchange (ETDEWEB)

Nagpal, V.; Guigard, S.E. [Alberta Univ., Edmonton, AB (Canada). Dept. of Civil Engineering

2005-09-01

A laboratory study was conducted to examine the ability of supercritical fluid extraction (SFE) to remove petroleum hydrocarbons (PHCs) from two flare pit soils in Alberta. SFE is a technology for remediation of contaminated soils. In order to determine the optimal extraction conditions and to understand the effects of pressure, temperature, supercritical carbon dioxide flow rate, soil type, and extraction time on the extraction efficiency of SFE, extractions were performed on two flare pit soils at various pressures and temperatures. Chemicals in the study included diesel oil, SAE 10-30W motor oil, n-decane, hexadecane, tetratriacontane and pentacontane. The best extraction conditions were defined as conditions that result in a treated soil with a PHC concentration that meets the regulatory guidelines of the Canadian Council of Ministers of the Environment in the Canada-wide standard for PHC is soil. The study results indicate that the efficiency of the SFE process is solvent-density dependent for the conditions studied. The highest extraction efficiency for both soils was obtained at conditions of 24.1 MPa and 40 degrees C. An increase in pressure at a fixed temperature led to an increase in the extraction efficiency while an increase in temperature at a fixed pressure led to a decrease in the extraction efficiency. The treated soils were observed to be lighter in colour, drier, and grainier than the soil prior to extraction. It was concluded that SFE is an effective method for remediating flare pit soils. 63 refs., 4 tabs., 5 figs.

Absorção de água pelas plantas: água disponível versus extraível e a produtividade das culturas Water absorption by plants: available versus extractable soil water and crop production

Directory of Open Access Journals (Sweden)

Reimar Carlesso

1995-01-01

duration of water deficits despite the abundant literature available. Much attention has been given to the quantification of crop water consumption in different stages of development. However, considerations about the total amount of plant water available (extractable in the soil profile to affect plant growth and development have recieved little attention. A discussion of water extraction must first consider the problem of accurately defining the limits to soil water availability. This review presents a critical analysis of the limitations usually encountered in using the limits concept of soil water availability. The relationship between water available and extractable is analysed based on results of transpiration rates and fraction of available water, depth of water extraction and, extraction per unit soil depth.

Influence of extractable soil manganese on oxidation capacity of different soils in Korea

Science.gov (United States)

Chon, Chul-Min; Kim, Jae Gon; Lee, Gyoo Ho; Kim, Tack Hyun

2008-08-01

We examined the relationship between soil oxidation capacity and extractable soil manganese, iron oxides, and other soil properties. The Korean soils examined in this study exhibited low to medium Cr oxidation capacities, oxidizing 0.00-0.47 mmol/kg, except for TG-4 soils, which had the highest capacity for oxidizing added Cr(III) [>1.01 mmol/kg of oxidized Cr(VI)]. TG and US soils, with high Mn contents, had relatively high oxidation capacities. The Mn amounts extracted by dithionite-citrate-bicarbonate (DCB) (Mnd), NH2OH·HCl (Mnh), and hydroquinone (Mnr) were generally very similar, except for the YS1 soils, and were well correlated. Only small proportions of either total Mn or DCB-extractable Mn were extracted by NH2OH·HCl and hydroquinone in the YS1 soils, suggesting inclusion of NH2OH·HCl and hydroquinone-resistant Mn oxides, because these extractants are weaker reductants than DCB. No Cr oxidation test results were closely related to total Mn concentrations, but Mnd, Mnh, and Mnr showed a relatively high correlation with the Cr tests ( r = 0.655-0.851; P Mnh were better correlated with the Cr oxidation tests than was the Mnr concentration, suggesting that the oxidation capacity of our soil samples can be better explained by Mnd and Mnh than by Mnr. The first component in principal components analysis indicated that extractable soil Mn was a main factor controlling net Cr oxidation in the soils. Total soil Mn, Fe oxides, and the clay fraction are crucial for predicting the mobility of pollutants and heavy metals in soils. The second principal component indicated that the presence of Fe oxides in soils had a significant relationship with the clay fraction and total Mn oxide, and was also related to heavy-metal concentrations (Zn, Cd, and Cu, but not Pb).

Zinc fractionation in contaminated soils by sequential and single extractions: influence of soil properties and zinc content.

Science.gov (United States)

Voegelin, Andreas; Tokpa, Gerome; Jacquat, Olivier; Barmettler, Kurt; Kretzschmar, Ruben

2008-01-01

We studied the fractionation of zinc (Zn) in 49 contaminated soils as influenced by Zn content and soil properties using a seven-step sequential extraction procedure (F1: NH4NO3; F2: NH4-acetate, pH 6; F3: NH3OHCl, pH 6; F4: NH4-EDTA, pH 4.6; F5: NH4-oxalate, pH 3; F6: NH4-oxalate/ascorbic acid, pH 3; F7: residual). The soils had developed from different geologic materials and covered a wide range in soil pH (4.0-7.3), organic C content (9.3-102 g kg(-1)), and clay content (38-451 g kg(-1)). Input of aqueous Zn with runoff water from electricity towers during 26 to 74 yr resulted in total soil Zn contents of 3.8 to 460 mmol kg(-1). In acidic soils (n = 24; pH soils (n = 25; pH > or =6.0), most Zn was extracted in the mobilizable fraction (F2) and the intermediate fractions (F4 and F5). The extractability of Zn increased with increasing Zn contamination of the soils. The sum of mobile (F1) and mobilizable (F2) Zn was independent of soil pH, the ratio of Zn in F1 over F1+F2 plotted against soil pH, exhibited the typical shape of a pH sorption edge and markedly increased from pH 6 to pH 5, reflecting the increasing lability of mobilizable Zn with decreasing soil pH. In conclusion, the extractability of Zn from soils contaminated with aqueous Zn after decades of aging under field conditions systematically varied with soil pH and Zn content. The same trends are expected to apply to aqueous Zn released from decomposing Zn-bearing contaminants, such as sewage sludge or smelter slag. The systematic trends in Zn fractionation with varying soil pH and Zn content indicate the paramount effect of these two factors on molecular scale Zn speciation. Further research is required to characterize the link between the fractionation and speciation of Zn and to determine how Zn loading and soil physicochemical properties affect Zn speciation in soils.

Evidence for soil water control on carbon and water dynamics in European forests during the extremely dry year: 2003

DEFF Research Database (Denmark)

Granier, A.; Reichstein, M.; Breda, N.

2007-01-01

stand to estimate the water balance terms: trees and understorey transpiration, rainfall interception, throughfall, drainage in the different soil layers and soil water content. This model calculated the onset date, duration and intensity of the soil water shortage (called water stress) using measured...... measured and modelled soil water content. Our analysis showed a wide spatial distribution of drought stress over Europe, with a maximum intensity within a large band extending from Portugal to NE Germany. Vapour fluxes in all the investigated sites were reduced by drought, due to stomatal closure, when...... the relative extractable water in soil (REW) dropped below ca. 0.4. Rainfall events during the drought, however, typically induced rapid restoration of vapour fluxes. Similar to the water vapour fluxes, the net ecosystem production decreased with increasing water stress at all the sites. Both gross primary...

A fully continuous supercritical fluid extraction system for contaminated soil

International Nuclear Information System (INIS)

Ryan, M.; Stiver, W.H.

2007-01-01

Brownfield sites are contaminated sites in an urban setting. There are hundreds of thousands of such sites, where contaminants migrate to the atmosphere, seep into groundwater, runoff into surface water and enter the food chain through plant uptake and soil ingestion. The Sydney Tar Ponds alone contain more than a million tonnes of contaminated soils and sediments. Soil vapour extraction, incineration, bioremediation, solvent extraction and land filling are among the remediation techniques that have been developed for brownfield sites over the years. However, no single technology is ideally suited to all cases because of the diversity of contaminants and diversity of site characterization. This paper focused on supercritical fluid extraction (SFE) which is well suited to sites contaminated with polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs) and heavy metal. A fully continuous laboratory-scale SFE process for a slurry-based system was designed and constructed to handle the supercritical carbon dioxide (SC-CO 2 ) and the soil slurry. The system continuously pumps carbon dioxide under supercritical conditions and soil slurry into a counter-current contacting column. The testing soil was Delhi loamy sand, spiked with 10 mg/g of naphthalene. The soil slurry ranged from 0.0028 g dry soil per g slurry to 0.072 g/g. The operating temperature was 43 degrees C and the operating pressure was 7.7 MPa. Near steady state, fully continuous flow was achieved with runs lasting up to 2 hours. The quantifiable recoveries of naphthalene from the soil slurry was demonstrated and the mass transfer coefficients for the system were quantified in order to provide the foundation to advance to a full-scale system and costing analysis. 14 refs., 1 tab., 3 figs

A fully continuous supercritical fluid extraction system for contaminated soil

Energy Technology Data Exchange (ETDEWEB)

Ryan, M.; Stiver, W.H. [Guelph Univ., ON (Canada). School of Engineering

2007-04-15

Brownfield sites are contaminated sites in an urban setting. There are hundreds of thousands of such sites, where contaminants migrate to the atmosphere, seep into groundwater, runoff into surface water and enter the food chain through plant uptake and soil ingestion. The Sydney Tar Ponds alone contain more than a million tonnes of contaminated soils and sediments. Soil vapour extraction, incineration, bioremediation, solvent extraction and land filling are among the remediation techniques that have been developed for brownfield sites over the years. However, no single technology is ideally suited to all cases because of the diversity of contaminants and diversity of site characterization. This paper focused on supercritical fluid extraction (SFE) which is well suited to sites contaminated with polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs) and heavy metal. A fully continuous laboratory-scale SFE process for a slurry-based system was designed and constructed to handle the supercritical carbon dioxide (SC-CO{sub 2}) and the soil slurry. The system continuously pumps carbon dioxide under supercritical conditions and soil slurry into a counter-current contacting column. The testing soil was Delhi loamy sand, spiked with 10 mg/g of naphthalene. The soil slurry ranged from 0.0028 g dry soil per g slurry to 0.072 g/g. The operating temperature was 43 degrees C and the operating pressure was 7.7 MPa. Near steady state, fully continuous flow was achieved with runs lasting up to 2 hours. The quantifiable recoveries of naphthalene from the soil slurry was demonstrated and the mass transfer coefficients for the system were quantified in order to provide the foundation to advance to a full-scale system and costing analysis. 14 refs., 1 tab., 3 figs.

Phosphorus dynamics in soils irrigated with reclaimed waste water or fresh water - A study using oxygen isotopic composition of phosphate

Science.gov (United States)

Zohar, I.; Shaviv, A.; Young, M.; Kendall, C.; Silva, S.; Paytan, A.

2010-01-01

Transformations of phosphate (Pi) in different soil fractions were tracked using the stable isotopic composition of oxygen in phosphate (??18Op) and Pi concentrations. Clay soil from Israel was treated with either reclaimed waste water (secondary, low grade) or with fresh water amended with a chemical fertilizer of a known isotopic signature. Changes of ??18Op and Pi within different soil fractions, during a month of incubation, elucidate biogeochemical processes in the soil, revealing the biological and the chemical transformation impacting the various P pools. P in the soil solution is affected primarily by enzymatic activity that yields isotopic equilibrium with the water molecules in the soil solution. The dissolved P interacts rapidly with the loosely bound P (extracted by bicarbonate). The oxides and mineral P fractions (extracted by NaOH and HCl, respectively), which are considered as relatively stable pools of P, also exhibited isotopic alterations in the first two weeks after P application, likely related to the activity of microbial populations associated with soil surfaces. Specifically, isotopic depletion which could result from organic P mineralization was followed by isotopic enrichment which could result from preferential biological uptake of depleted P from the mineralized pool. Similar transformations were observed in both soils although transformations related to biological activity were more pronounced in the soil treated with reclaimed waste water compared to the fertilizer treated soil. ?? 2010 Elsevier B.V.

Case study of shallow soil mixing and soil vacuum extraction remediation project

International Nuclear Information System (INIS)

Carey, M.J.; Day, S.R.; Pinewski, R.; Schroder, D.

1995-01-01

Shallow Soil Mixing (SSM) and Soil Vacuum Extraction (SVE) are techniques which have been increasingly relied on for the insitu remediation of contaminated soils. The primary applications of SSM have been to mix cement, bentonite, or other reagents to modify properties and thereby remediate contaminated soils or sludges. Soil vacuum extraction has been used at numerous applications for insitu removal of contaminants from soils. At a recent project in southern Ohio, the two technologies were integrated and enhanced to extract volatile organic compounds (VOCs) from soils at a Department of Energy facility. Advantages of the integrated SSM/SVE technology over alternative technologies include a relatively rapid remediation compared to other in-situ techniques at a lower cost, less exposure of waste to the surface environment and elimination of off-site disposal. These advantages led to the selection of the use of both technologies on the project in Southern Ohio. The information presented in this paper is intended to provide Engineers and owners with the level of understanding necessary to apply soil mixing and vacuum extraction technology to a specific site. The most important steps in implementing the technology are site investigation, feasibility estimate, selection of performance criteria, selection of appropriate materials, bench scale testing and construction

Hanford soil partitioning and vapor extraction study

International Nuclear Information System (INIS)

Yonge, D.; Hossain, A.; Cameron, R.; Ford, H.; Storey, C.

1996-07-01

This report describes the testing and results of laboratory experiments conducted to assist the carbon tetrachloride soil vapor extraction project operating in the 200 West Area of the Hanford Site in Richland, Washington. Vapor-phase adsorption and desorption testing was performed using carbon tetrachloride and Hanford Site soils to estimate vapor-soil partitioning and reasonably achievable carbon tetrachloride soil concentrations during active vapor extractions efforts at the 200 West Area. (CCl 4 is used in Pu recovery from aqueous streams.)

Seasonal variations in soil water in two woodland savannas of central Brazil with different fire history.

Science.gov (United States)

Quesada, Carlos Alberto; Hodnett, Martin G; Breyer, Lacê M; Santos, Alexandre J B; Andrade, Sérgio; Miranda, Heloisa S; Miranda, Antonio Carlos; Lloyd, Jon

2008-03-01

Changes in soil water content were determined in two cerrado (sensu stricto) areas with contrasting fire history and woody vegetation density. The study was undertaken near Brasília, Brazil, from 1999 to 2001. Soil water content was measured with a neutron probe in three access tubes per site to a depth of 4.7 m. One site has been protected from fire for more than 30 years and, as a consequence, has a high density of woody plants. The other site had been frequently burned, and has a high herbaceous vegetation density and less woody vegetation. Soil water uptake patterns were strongly seasonal, and despite similarities in hydrological processes, the protected area systematically used more water than the burned area. Three temporarily contiguous patterns of water absorption were differentiated, characterized by variation in the soil depth from which water was extracted. In the early dry season, vegetation used water from throughout the soil profile but with a slight preference for water in the upper soil layers. Toward the peak of the dry season, vegetation had used most or all available water from the surface to a depth of 1.7 m, but continued to extract water from greater depths. Following the first rains, all water used was from the recently wetted upper soil layers only. Evaporation rates were a linear function of soil water availability, indicating a strong coupling of atmospheric water demand and the physiological response of the vegetation.

A Comparison of delO18 Composition of Water Extracted from Suction Lysimeters, Centrifugation, and Azeotropic Distillation

Science.gov (United States)

Figueroa, A.; Tindall, J. A.; Friedel, M. J.

2005-12-01

Concentration of delO18 in water samples extracted by suction lysimeters is compared to samples obtained by methods of centrifugation and azeotropic distillation. Intact soil cores (30 cm diameter by 40 cm height) were extracted from two different sites. Site 1 was rapid infiltration basin number 50, near Altamonte Springs in Seminole County, Florida on properties belonging to the Walt Disney World Resort Complex. Site 2 was the Missouri Management System Evaluation Area (MSEA) near Centralia in Boone County, Missouri. The delO18 water was analyzed on a mass spectrophotometer. Potassium Bromide (KBr) was also used as a tracer and analyzed by ion chromatography. A portion of the data obtained was modeled using CXTFIT. Water collected by centrifugation and azeotropic distillation data were about 2-5% more negative than that collected by suction lysimeter values from the Florida (sandy) soil and about 5-7 % more negative from the Missouri (well structured clay) soil. Results indicate that the majority of soil water in well structured soil is strongly bound to soil grain surfaces and is not easily sampled by suction lysimeters. Also, it is plausible that evaporation caused some delO18 enrichment in the suction lysimeters. Suction lysimeters preferentially sampled water held at lower matric potentials, which may not represent total soil water. In cases where a sufficient volume of water has passed through the soil profile and displaced all previous pore water, suction lysimeters will however collect a representative sample of all the water at that depth interval. It is suggested that for stable isotope studies monitoring precipitation and soil water, suction lysimeters be installed at shallow depths (10 cm). Samples should also be coordinated with precipitation events. The CXTFIT program worked well for Florida soils (a more homogeneous sand), but gave poor performance for Missouri soils (well structured clays) except for deeper depths where clay structure was less

Modelling soil-water dynamics in the rootzone of structured and water-repellent soils

Science.gov (United States)

Brown, Hamish; Carrick, Sam; Müller, Karin; Thomas, Steve; Sharp, Joanna; Cichota, Rogerio; Holzworth, Dean; Clothier, Brent

2018-04-01

In modelling the hydrology of Earth's critical zone, there are two major challenges. The first is to understand and model the processes of infiltration, runoff, redistribution and root-water uptake in structured soils that exhibit preferential flows through macropore networks. The other challenge is to parametrise and model the impact of ephemeral hydrophobicity of water-repellent soils. Here we have developed a soil-water model, which is based on physical principles, yet possesses simple functionality to enable easier parameterisation, so as to predict soil-water dynamics in structured soils displaying time-varying degrees of hydrophobicity. Our model, WEIRDO (Water Evapotranspiration Infiltration Redistribution Drainage runOff), has been developed in the APSIM Next Generation platform (Agricultural Production Systems sIMulation). The model operates on an hourly time-step. The repository for this open-source code is https://github.com/APSIMInitiative/ApsimX. We have carried out sensitivity tests to show how WEIRDO predicts infiltration, drainage, redistribution, transpiration and soil-water evaporation for three distinctly different soil textures displaying differing hydraulic properties. These three soils were drawn from the UNSODA (Unsaturated SOil hydraulic Database) soils database of the United States Department of Agriculture (USDA). We show how preferential flow process and hydrophobicity determine the spatio-temporal pattern of soil-water dynamics. Finally, we have validated WEIRDO by comparing its predictions against three years of soil-water content measurements made under an irrigated alfalfa (Medicago sativa L.) trial. The results provide validation of the model's ability to simulate soil-water dynamics in structured soils.

Field sampling of soil pore water to evaluate trace element mobility and associated environmental risk

Energy Technology Data Exchange (ETDEWEB)

Moreno-Jimenez, Eduardo, E-mail: eduardo.moreno@uam.es [Departamento de Quimica Agricola, Universidad Autonoma de Madrid, 28049 Madrid (Spain); Beesley, Luke [James Hutton Institute, Craigiebuckler, Aberdeen AB15 8QH (United Kingdom); Lepp, Nicholas W. [35, Victoria Road, Formby, Liverpool L37 7DH (United Kingdom); Dickinson, Nicholas M. [Department of Ecology, Lincoln University, Lincoln 7647, PO Box 84 (New Zealand); Hartley, William [School of Computing, Science and Engineering, University of Salford, Cockcroft Building, Salford, M5 4WT (United Kingdom); Clemente, Rafael [Dep. of Soil and Water Conservation and Organic Waste Management, CEBAS-CSIC, Campus Universitario de Espinardo, PO Box 164, 30100 Espinardo, Murcia (Spain)

2011-10-15

Monitoring soil pollution is a key aspect in sustainable management of contaminated land but there is often debate over what should be monitored to assess ecological risk. Soil pore water, containing the most labile pollutant fraction in soils, can be easily collected in situ offering a routine way to monitor this risk. We present a compilation of data on concentration of trace elements (As, Cd, Cu, Pb, and Zn) in soil pore water collected in field conditions from a range of polluted and non-polluted soils in Spain and the UK during single and repeated monitoring, and propose a simple eco-toxicity test using this media. Sufficient pore water could be extracted for analysis both under semi-arid and temperate conditions, and eco-toxicity comparisons could be effectively made between polluted and non-polluted soils. We propose that in-situ pore water extraction could enhance the realism of risk assessment at some contaminated sites. - Highlights: > In situ pore water sampling successfully evaluates trace elements mobility in soils. > Field sampling proved robust for different soils, sites and climatic regimes. > Measurements may be directly related to ecotoxicological assays. > Both short and long-term monitoring of polluted lands may be achieved. > This method complements other widely used assays for environmental risk assessment. - In situ pore water sampling from a wide variety of soils proves to be a beneficial application to monitor the stability of pollutants in soils and subsequent risk through mobility.

Complex linkage between soil, soil water, atmosphere and Eucalyptus Plantations

Science.gov (United States)

Shukla, C.; Tiwari, K. N.

2017-12-01

Eucalyptus is most widely planted genus grown in waste land of eastern region of India to meet the pulp industry requirements. Sustainability of these plantations is of concern because in spite of higher demand water and nutrients of plantations, they are mostly planted on low-fertility soils. This study has been conducted to quantify effect of 25 years old, a fully established eucalyptus plantations on i.) Alteration in physico-chemical and hydrological properties of soil of eucalyptus plantation in comparison to soil of natural grassland and ii.) Spatio-temporal variation in soil moisture under eucalyptus plantations. Soil physico-chemical properties of two adjacent plots covered with eucatuptus and natural grasses were analyzed for three consecutive depths (i.e. 0-30 cm, 30-60 cm and 60-90 cm) with five replications in each plot. Soil infiltration rate and saturated hydraulic conductivity (Ks) were measured in-situ to incorporate the influence of macro porosity caused due to roots of plantations. Daily soil moisture at an interval of 10 cm upto 160 cm depth with 3 replications and Leaf Area Index (LAI) at an interval of 15 days with 5 replications were recorded over the year. Significant variations found at level of 0.05 between soil properties of eucalyptus and natural grass land confirm the effect of plantations on soil properties. Comparative results of soil properties show significant alteration in soil texture such as percent of sand, organic matter and Ks found more by 20%, 9% and 22% respectively in eucalyptus plot as compare to natural grass land. Available soil moisture (ASM) was found constantly minimum in top soil excluding rainy season indicate upward movement of water and nutrients during dry season. Seasonal variation in temperature (T), relative humidity (RH) and leaf area index (LAI) influenced the soil moisture extraction phenomenon. This study clearly stated the impact of long term establishment of eucalyptus plantations make considerable

Integrated vacuum extraction/pneumatic soil fracturing system for remediation of low permeability soil

International Nuclear Information System (INIS)

Plaines, A.L.; Piniewski, R.J.; Yarbrough, G.D.

1994-01-01

There is wide use of vacuum extraction to remove volatile and semi-volatile organic compounds (VOCs) from unsaturated soil. At sites with soil of low permeability, VOC extraction rates may not be sufficient to meet soil clean-up objectives within the desired time frame. During vacuum extraction in low permeability soil, the diffusion rates of VOCs through the soil matrix may limit VOC removal rates. An increase in the number of subsurface paths for advective flow through the contaminated zone results in a larger mass of contaminant being removed in a shorter time frame, accelerating site remediation. One technique for increasing the number of subsurface flow paths is Terra Vac's process of pneumatic soil fracturing (PSF). In this process, pressurized air is injected into the subsurface, creating micro-fractures for the vacuum extraction system to withdraw contaminants. Similar to hydraulic fracturing techniques long used in the petroleum industry for increasing yield from oil and gas production wells, this technique has applications for soil remediation in low permeability conditions. Two case studies, one in Louisiana at a gasoline service station and one at a manufacturing plant in New York, are presented

Supercritical Fluid Extraction of Plutonium and Americium from Soil

International Nuclear Information System (INIS)

Fox, R.V.; Mincher, B.J.

2002-01-01

Supercritical fluid extraction (SFE) of plutonium and americium from soil was successfully demonstrated using supercritical fluid carbon dioxide solvent augmented with organophosphorus and beta-diketone complexants. Spiked Idaho soils were chemically and radiologically characterized, then extracted with supercritical fluid carbon dioxide at 2,900 psi and 65 C containing varying concentrations of tributyl phosphate (TBP) and thenoyltrifluoroacetone (TTA). A single 45 minute SFE with 2.7 mol% TBP and 3.2 mol% TTA provided as much as 88% ± 6.0 extraction of americium and 69% ± 5.0 extraction of plutonium. Use of 5.3 mol% TBP with 6.8 mol% of the more acidic beta-diketone hexafluoroacetylacetone (HFA) provided 95% ± 3.0 extraction of americium and 83% ± 5.0 extraction of plutonium in a single 45 minute SFE at 3,750 psi and 95 C. Sequential chemical extraction techniques were used to chemically characterize soil partitioning of plutonium and americium in pre-SFE soil samples. Sequential chemical extraction techniques demonstrated that spiked plutonium resides primarily (76.6%) in the sesquioxide fraction with minor amounts being absorbed by the oxidizable fraction (10.6%) and residual fractions (12.8%). Post-SFE soils subjected to sequential chemical extraction characterization demonstrated that 97% of the oxidizable, 78% of the sesquioxide and 80% of the residual plutonium could be removed using SFE. These preliminary results show that SFE may be an effective solvent extraction technique for removal of actinide contaminants from soil

Decontamination of Metal Ions in Soil by Supercritical CO{sub 2} Extraction with Catecholamine Ligand

Energy Technology Data Exchange (ETDEWEB)

Park, Jihye; Kim, Hakwon; Park, Kwangheon [Kyunghee University, Yongin (Korea, Republic of)

2015-10-15

The role of fuel cladding and reactor vessels is to help prevent the leakage of radioactive materials, including the fission products. However, if these shielding materials are damaged by a severe disaster such as the Fukushima Accident, radioactive materials could leak outside of a power plant site. Indeed, after the Fukushima Accident, radioactive materials have been detected in air and water samples. The air and water pollution lead to soil pollution, which is particularly difficult to decontaminate, as soil pollution has several types that vary according to the characteristics of a pollutant or its area. The existing decontamination methods generate a secondary waste owing to use of chemical toxicity solvents. It is also disadvantageous due to the additional cost of handling them. Therefore, new effective decontamination methods that reduce the use of toxicity solvents are necessary. For example, using supercritical CO{sub 2} has been studied as a new decontamination method. This study examines the method of decontaminating metallic ions inside of the soil using supercritical CO{sub 2} and a catecholamine compound. This study examined the effects of extracting metallic ions inside the soil using supercritical CO{sub 2} and catecholamine as the ligand. Based on these results, it is evident that when only the extraction agent was used, there was no extraction effect and that only when the ligand, co-ligand, and additive were used together was there an extraction effect. Following this, the optimal extraction-agent ratio was confirmed using varying amounts of extraction agents. The most effective extraction ratio of ligand to co-ligand was 1:2 in E-9 when 0.3 ml of H{sub 2}O were added.

Polycyclic aromatic hydrocarbons bioavailability in industrial and agricultural soils: Linking SPME and Tenax extraction with bioassays.

Science.gov (United States)

Guo, Meixia; Gong, Zongqiang; Li, Xiaojun; Allinson, Graeme; Rookes, James; Cahill, David

2017-06-01

The aims of this study were to evaluate the bioavailability of polycyclic aromatic hydrocarbons (PAHs) in industrial and agricultural soils using chemical methods and a bioassay, and to study the relationships between the methods. This was conducted by comparing the quantities of PAHs extracted from two manufactured gas plant (MGP) soils and an agricultural soil with low level contamination by solid-phase micro-extraction (SPME) and Tenax-TA extraction with the quantities taken up by the earthworm (Eisenia fetida). In addition, a biodegradation experiment was conducted on one MGP soil (MGP-A) to clarify the relationship between PAH removal by biodegradation and the variation in PAH concentrations in soil pore water. Results demonstrated that the earthworm bioassay could not be used to examine PAH bioavailability in the tested MGP soils; which was the case even in the diluted MGP-A soils after biodegradation. However, the bioassay was successfully applied to the agricultural soil. These results suggest that earthworms can only be used for bioassays in soils with low toxicity. In general, rapidly desorbing concentrations extracted by Tenax-TA could predict PAH concentrations accumulated in earthworms (R 2 =0.66), while SPME underestimated earthworm concentrations by a factor of 2.5. Both SPME and Tenax extraction can provide a useful tool to predict PAH bioavailability for earthworms, but Tenax-TA extraction was proven to be a more sensitive and precise method than SPME for the prediction of earthworm exposure in the agricultural soil. Copyright © 2017. Published by Elsevier Inc.

Irrigation with saline-sodic water: effects on two clay soils

Directory of Open Access Journals (Sweden)

Giovanna Cucci

2013-05-01

Full Text Available The results of a 4-year experiment aimed at evaluating the effect of irrigation with saline-sodic water on the soil are reported. The research was carried out at the Campus of the Agricultural Faculty of Bari University (Italy on 2 clay soils (Bologna – T1 and Locorotondo – T2. The soils were cropped to borlotto bean (Phaseolus vulgaris L., capsicum (Capsicum annuum L., sunflower (Helianthus annuus L., wheat (Triticum durum Desf grown in succession; the crops were irrigated with 9 saline-sodic types of water and subjected to two different leaching fractions (10% and 20% of the watering volume. The 9 solutions were obtained dissolving in de-ionised water weighted amounts of sodium chloride (NaCl and calcium chloride (CaCl2, deriving from the combination of 3 saline concentrations and 3 sodicity levels. The crops were irrigated whenever the water lost by evapotranspiration from the soil contained in the pots was equal to 30% of the soil maximum available water. The results showed that, though the soils were leached during the watering period, they showed a high salt accumulation. Consequently, the saturated soil extract electrical conductivity increased from initial values of 0.65 and 0.68 dS m-1 to 11.24 and 13.61 dS m-1 at the end of the experiment, for the soils T1 and T2, respectively. The saline concentration increase in irrigation water caused in both soils a progressive increase in exchangeable sodium, and a decrease in exchangeable calcium and non-significant variations in exchangeable potassium (K and magnesium (Mg.

Near-critical and supercritical fluid extraction of polycyclic aromatic hydrocarbons from town gas soil

International Nuclear Information System (INIS)

Kocher, B.S.; Azzam, F.O.; Cutright, T.J.; Lee, S.

1995-01-01

The contamination of soil by hazardous and toxic organic pollutants is an ever-growing problem facing the global community. One particular family of contaminants that are of major importance are polycyclic aromatic hydrocarbons (PAHs). PAHs are the result of coal gasification and high-temperature processes. Sludges from these town gas operations were generally disposed of into unlined pits and left there for eventual biodegradation. However, the high levels of PAH contained in the pits prevented the occurrence of biodegradation. PAH contaminated soil is now considered hazardous and must be cleaned to environmentally acceptable standards. One method for the remediation is extraction with supercritical water. Water in or about its critical region exhibits enhanced solvating power toward most organic compounds. Contaminated soil containing 4% by mass of hydrocarbons was ultra-cleaned in a 300-cm 3 semicontinuous system to an environmentally acceptable standard of less than 200 ppm residual hydrocarbon concentration. The effects of subcritical or supercritical extraction, solvent temperature, pressure, and density have been studied, and the discerning characteristics of this type of fluid have been identified. The efficiencies of subcritical and supercritical extraction have been discussed from a process engineering standpoint

Extraction of Plutonium From Spiked INEEL Soil Samples Using the Ligand-Assisted Supercritical Fluid Extraction (LA-SFE) Technique

International Nuclear Information System (INIS)

Fox, R.V.; Mincher, B.J.; Holmes, R.G.G.

1999-01-01

In order to investigate the effectiveness of ligand-assisted supercritical fluid extraction for the removal of transuranic contaminations from soils an Idaho National Engineering and Environmental Laboratory (INEEL) silty-clay soil sample was obtained from near the Radioactive Waste Management Complex area and subjected to three different chemical preparations before being spiked with plutonium. The spiked INEEL soil samples were subjected to a sequential aqueous extraction procedure to determine radionuclide portioning in each sample. Results from those extractions demonstrate that plutonium consistently partitioned into the residual fraction across all three INEEL soil preparations whereas americium partitioned 73% into the iron/manganese fraction for soil preparation A, with the balance partitioning into the residual fraction. Plutonium and americium were extracted from the INEEL soil samples using a ligand-assisted supercritical fluid extraction technique. Initial supercritical fluid extraction runs produced plutonium extraction technique. Initial supercritical fluid extraction runs produced plutonium extraction efficiencies ranging from 14% to 19%. After a second round wherein the initial extraction parameters were changed, the plutonium extraction efficiencies increased to 60% and as high as 80% with the americium level in the post-extracted soil samples dropping near to the detection limits. The third round of experiments are currently underway. These results demonstrate that the ligand-assisted supercritical fluid extraction technique can effectively extract plutonium from the spiked INEEL soil preparations

Arsenic mobility and speciation in contaminated kitchen garden and lawn soils: an evaluation of water for assessment of As phytoavailability.

Science.gov (United States)

Waterlot, Christophe; Douay, Francis

2015-04-01

Emissions from primary lead smelters have been recognized as one of the mainly factor which has contributed to the contamination of soils by metals. Less attention has been paid to volatile metalloids such as arsenic (As) which accompanies lead (Pb) smelting activities. One of the objectives of this study was to determine the As concentrations in various extracting solutions using a collection of urban soils located no far away from two former Pb and zinc plants in the North of France. The procedure for the determination of As, As(III), and As(V) with hydride vapor generator atomic absorption spectrometry was described in details. Pseudo-total concentrations of As in the studied soils ranged from 5.3 to 65.9 mg kg(-1). Good correlations were found between As and lead, zinc, and cadmium concentrations in soils. These depended on the soil uses and the soil distance from the source of contamination. Because the form of As may pose a health risk to human population, its speciation was determined in each urban top soils. Very good correlations were found between As(III) and As(V) versus As concentrations in soils studied, but the results did no permit to establish a relation between the location of soils and their uses. In contrast, it was shown that the highest mobility factor and lowest partitioning index values were related to the location. The mobilty of As depended on the assimilated phosphorus (P), carbonate contents, and pH. The percentages of the water-extractable As concentrations ranged from 0.3 to 3.0% of the As concentrations in soils. Very good positive correlations between water-extractable As(III) and As(V) versus water-extractable As concentrations were obtained. It was shown that the water-extractable As(III) concentrations depended on the soil uses. The results revealed that soils for which the As was the most mobile presented the highest water-extractable As concentrations. Principal component analysis indicated that mechanisms related to the release

Cadmium and zinc in soil solution extracts following the application of phosphate fertilizers.

Science.gov (United States)

Lambert, Raphaël; Grant, Cynthia; Sauvé, Sébastien

2007-06-01

This study investigated the solubility of cadmium and zinc in soils after the application of phosphate fertilizers containing those two metals. The solubility of cadmium and zinc was assessed by measuring their concentration in soil water extracts. Three monoammonium phosphate fertilizers containing various amounts of metals were applied on cultivated fields for 3 years at three different rates. In order to investigate the effects of long-term applications of fertilizers on the solubility of Cd and Zn, a similar design was used to apply contaminated fertilizers to soils in a laboratory experiment using a single fertilizer addition equivalent to 15 years of application. Phosphate fertilizers increased the concentration of Cd in soil extracts compared to control in 87% and 80% of the treatments in field and laboratory experiments respectively. Both increasing the rate of application and using fertilizer containing more Cd lead to higher Cd concentrations in extracts for the field and the laboratory experiments. The addition of the equivalent of 15 years of fertilizer application in the laboratory results in higher Cd concentration in extracts compared to the field experiment. For Zn, the fertilizer treatments enhanced the metal solution concentration in 83% of field treatments, but no significant correlations could be found between Zn inputs and its concentration in solution. In the laboratory, fertilizer additions increase the Zn concentrations in 53% of the treatments and decrease it in most of the other treatments. The decrease in Zn concentrations in the laboratory trial is attributed to the higher phosphate concentrations in the soil solution; which is presumed to have contributed to the precipitation of Zn-phosphates. For both trials, the metal concentrations in soil extracts cannot be related to the Zn concentration in the fertilizer or the rate of application. The high Zn to Cd ratio is presumably responsible for the Cd increase in the soil extracts due to

Biochar based remediation of water and soil contaminated by phenanthrene and pentachlorophenol.

Science.gov (United States)

Rao, Maria A; Di Rauso Simeone, Giuseppe; Scelza, Rosalia; Conte, Pellegrino

2017-11-01

Phenanthrene (Phe) and pentachlorophenol (PCP) are classified as persistent organic pollutants and represent serious concern for the environment as they are toxic and ubiquitous. Biochar based remediation is an emerging technology used in water and soil contamination. In this study we used poplar (BP) and conifer (BC) biochars to remediate water and soil contaminated by Phe and PCP. BP and BC were able to remove completely either Phe or PCP from contaminated water within one to three days. When biochar was confined in a porous membrane, BC and BP maintained their sorption efficiency for several remediation cycles. However, in these conditions BC allowed faster Phe removal. In soil remediation experiments, addition of two biochar rates, i.e. 2.5 and 5 mg g -1 , strongly reduced Phe extractability (up to 2.7% of the initially added Phe with the larger BC dose). This was similar to the behavior observed when compost was applied in order to verify the role of soil organic matter in the fate of both contaminants. PCP extractability was reduced only up to 75% (in average) in all samples including those with compost amendment. Only larger amount of biochar (20 and 50 mg g -1 ) allowed reduction of the extractable PCP and nullified phytotoxicity of the contaminant. Copyright © 2017 Elsevier Ltd. All rights reserved.

Assessment of chromium biostabilization in contaminated soils using standard leaching and sequential extraction techniques

International Nuclear Information System (INIS)

Papassiopi, Nymphodora; Kontoyianni, Athina; Vaxevanidou, Katerina; Xenidis, Anthimos

2009-01-01

The iron reducing microorganism Desulfuromonas palmitatis was evaluated as potential biostabilization agent for the remediation of chromate contaminated soils. D. palmitatis were used for the treatment of soil samples artificially contaminated with Cr(VI) at two levels, i.e. 200 and 500 mg kg -1 . The efficiency of the treatment was evaluated by applying several standard extraction techniques on the soil samples before and after treatment, such as the EN12457 standard leaching test, the US EPA 3060A alkaline digestion method and the BCR sequential extraction procedure. The water soluble chromium as evaluated with the EN leaching test, was found to decrease after the biostabilization treatment from 13 to less than 0.5 mg kg -1 and from 120 to 5.6 mg kg -1 for the soil samples contaminated with 200 and 500 mg Cr(VI) per kg soil respectively. The BCR sequential extraction scheme, although not providing accurate estimates about the initial chromium speciation in contaminated soils, proved to be a useful tool for monitoring the relative changes in element partitioning, as a consequence of the stabilization treatment. After bioreduction, the percentage of chromium retained in the two least soluble BCR fractions, i.e. the 'oxidizable' and 'residual' fractions, increased from 54 and 73% to more than 96% in both soils

Environmental assessment of water-salt regime of irrigated soils in the Central-Chernozem Region of Russia

Science.gov (United States)

Alaeva, Liliia; Negrobova, Elena; Jablonskikh, Lidiia; Rumyantseva, Irina

2016-04-01

A large part of Central Chernozem Region is located in the zone of risky agriculture. This led to intensive use of soil in the irrigation system. Therefore, a detailed analysis of water-salt regime of irrigated soils required for ecological state assessment of soils for irrigation. In the investigated area the fone component of the soil cover on the levelled plateau are chernozems. On the slopes formed a meadow-chernozem soils. Parent material is a cover loess-like calcareous non-saline clay. In these soils, our studies found component-quantitative composition of the aqueous extract, the chemism of salinity, which allowed us to make conclusions about the direction of the salinisation process in soils when used in the system of irrigated agriculture. By quantity water extract chernozems are non-saline, the ratio of anions and cations are chloride-sulphate magnesium-calcium salinization. In the composition of easily soluble salts dominated by Ca(HCO3)2. On sum of toxic salts in the soils are non-saline. This type and chemism of salinity deep brackish groundwater (more than 5 m) can be actively used in the system of rational irrigation. The meadow-chernozem soils formed under conditions of increased surface and soil moisture in the shallow brackish water at a depth of 3-5 m. These soils by quantity water extract are non-saline, anionic-cationic ratio - chloride-sulphate magnesium-calcium salinization. Permanent components of salt associations are Ca(HCO3)2, MgCl2, Na2SO4. On sum of toxic salts in the soil is not saline throughout the profile. The chemism of salinity and the proximity of groundwater at irregular watering can lead to the rise of groundwater level, the development of gleyed and sodium alkalinization. Thus, the introduction of intensive irrigated agriculture on chernozems and hydromorphic analogues may lead to the development in them of negative consequences. The most dynamic indicator is the water-salt regime, the systematic monitoring and control which

Soil physics and the water management of spatially variable soils

International Nuclear Information System (INIS)

Youngs, E.G.

1983-01-01

The physics of macroscopic soil-water behaviour in inert porous materials has been developed by considering water flow to take place in a continuum. This requires the flow region to consist of an assembly of representative elementary volumes, repeated throughout space and small compared with the scale of observations. Soil-water behaviour in swelling soils may also be considered as a continuum phenomenon so long as the soil is saturated and swells and shrinks in the normal range. Macroscale heterogeneity superimposed on the inherent microscale heterogeneity can take many forms and may pose difficulties in the definition and measurement of soil physical properties and also in the development and use of predictive theories of soil-water behaviour. Thus, measurement techniques appropriate for uniform soils are often inappropriate, and criteria for soil-water management, obtained from theoretical considerations of behaviour in equivalent uniform soils, are not applicable without modification when there is soil heterogeneity. The spatial variability of soil-water properties is shown in results from field experiments concerned with water flow measurements; these illustrate both stochastic and deterministic heterogeneity in soil-water properties. Problems of water management of spatially variable soils when there is stochastic heterogeneity appear to present an insuperable problem in the application of theory. However, for soils showing deterministic heterogeneity, soil-water theory has been used in the solution of soil-water management problems. Thus, scaling using similar media theory has been applied to the infiltration of water into soils that vary over a catchment area. Also, the drain spacing to control the water-table height in soils in which the hydraulic conductivity varies with depth has been calculated using groundwater seepage theory. (author)

Application of supercritical and subcritical fluids for the extraction of hazardous materials from soil

Directory of Open Access Journals (Sweden)

Skorupan Dara

2002-01-01

Full Text Available Subcritical and supercritical extractions are novel, non destructive techniques which can be applied for the removal of hazardous compounds from contaminated soil without any changes of the soil composition and structure. The aim of the presented review paper is to give information on up-to day results of this method commonly applied by several institutions worldwide. Interest in the application of SC CO2 has been more expressed in the last two decades, which may be related to its favorable characteristics (non-toxic, non-flammable, increase diffusion into small pores, low viscosity under SC conditions, low price and others. However, interest in wet oxidation (WO and especially in SCWO (the application of water under supercritical conditions with air has also increased in the last few years. Interest in H2O as a SC fluid, as well as in extraction with water under subcritical conditions may also be related to specific characteristics and the enhanced rate of extraction. Moreover, the solubility of some specific compounds present in soil can be easily changed by adjusting the pressure and temperature of extraction. The high price of the units designed to operate safely at a pressure and temperature much higher than the a critical one of the applied fluids is the main reason why, at present, there is no more broader application of such techniques for the removal hazardous materials from contaminated soil. In the present paper, among many literature citations and their overall review, some specific details related to the development of specific analytical methods under SC conditions are also considered.

Effects of different treatments of cattle slurry manure on water-extractable phosphorus

NARCIS (Netherlands)

Chapuis-Lardy, L.; Temminghoff, E.J.M.; Goede, de R.G.M.

2003-01-01

Cattle slurry manure applied to land increases the risk of phosphorus (P) movement to surface waters, which may lead to eutrophication. The water-extractable fraction of P in slurry manure is correlated with P concentration in runoff from soils amended with slurry smanure, and thus is an effective

Comparison of Chemical Extraction Methods for Determination of Soil Potassium in Different Soil Types

Science.gov (United States)

Zebec, V.; Rastija, D.; Lončarić, Z.; Bensa, A.; Popović, B.; Ivezić, V.

2017-12-01

Determining potassium supply of soil plays an important role in intensive crop production, since it is the basis for balancing nutrients and issuing fertilizer recommendations for achieving high and stable yields within economic feasibility. The aim of this study was to compare the different extraction methods of soil potassium from arable horizon of different types of soils with ammonium lactate method (KAL), which is frequently used as analytical method for determining the accessibility of nutrients and it is a common method used for issuing fertilizer recommendations in many Europe countries. In addition to the ammonium lactate method (KAL, pH 3.75), potassium was extracted with ammonium acetate (KAA, pH 7), ammonium acetate ethylenediaminetetraacetic acid (KAAEDTA, pH 4.6), Bray (KBRAY, pH 2.6) and with barium chloride (K_{BaCl_2 }, pH 8.1). The analyzed soils were extremely heterogeneous with a wide range of determined values. Soil pH reaction ( {pH_{H_2 O} } ) ranged from 4.77 to 8.75, organic matter content ranged from 1.87 to 4.94% and clay content from 8.03 to 37.07%. In relation to KAL method as the standard method, K_{BaCl_2 } method extracts 12.9% more on average of soil potassium, while in relation to standard method, on average KAA extracts 5.3%, KAAEDTA 10.3%, and KBRAY 27.5% less of potassium. Comparison of analyzed extraction methods of potassium from the soil is of high precision, and most reliable comparison was KAL method with KAAEDTA, followed by a: KAA, K_{BaCl_2 } and KBRAY method. Extremely significant statistical correlation between different extractive methods for determining potassium in the soil indicates that any of the methods can be used to accurately predict the concentration of potassium in the soil, and that carried out research can be used to create prediction model for concentration of potassium based on different methods of extraction.

Use of aqueous and solvent extraction to assess risk and bioavailability of contaminated soil

International Nuclear Information System (INIS)

Bordelon, N.; Huebner, H.; Washburn, K.; Donnelly, K.C.

1995-01-01

Contaminated media at Superfund sites typically consist of complex mixtures of organic and inorganic chemicals. These mixtures are difficult to characterize, both analytically and toxicologically, especially the complex mixtures of polycyclic aromatic hydrocarbons. The current approach to risk assessment assumes that all contaminants in the soil are available for human exposure. EPA protocol uses solvent extraction to remove chemicals from the soil as a basis for estimating risk to the human population. However, contaminants that can be recovered with a solvent extract may not represent chemicals that are available for exposure. A system using aqueous extraction provides a more realistic picture of what chemicals are bioavailable through leaching and ingestion. A study was conducted with coal tar contaminated soil spiked with benzo(a)pyrene, and trinitrotoluene. Samples were extracted with hexane:acetone and water titrated to pH 2 and pH 7. HPLC analysis demonstrated up to 35% and 29% recovery of contaminants from aqueous extracts with an estimated cancer risk one order of magnitude less than that for solvent extracts. Analysis using the Salmonella/microsome assay showed that solvent extracts were genotoxic with metabolic activation while aqueous extracts showed no genotoxicity. These results suggest that aqueous extraction may be useful in determining what contaminants are available for human exposure, as well as what compounds may pose a risk to human health

SOIL VAPOR EXTRACTION TECHNOLOGY: REFERENCE HANDBOOK

Science.gov (United States)

Soil vapor extraction (SVE) systems are being used in Increasing numbers because of the many advantages these systems hold over other soil treatment technologies. SVE systems appear to be simple in design and operation, yet the fundamentals governing subsurface vapor transport ar...

Assessment the effect of homogenized soil on soil hydraulic properties and soil water transport

Science.gov (United States)

Mohawesh, O.; Janssen, M.; Maaitah, O.; Lennartz, B.

2017-09-01

Soil hydraulic properties play a crucial role in simulating water flow and contaminant transport. Soil hydraulic properties are commonly measured using homogenized soil samples. However, soil structure has a significant effect on the soil ability to retain and to conduct water, particularly in aggregated soils. In order to determine the effect of soil homogenization on soil hydraulic properties and soil water transport, undisturbed soil samples were carefully collected. Five different soil structures were identified: Angular-blocky, Crumble, Angular-blocky (different soil texture), Granular, and subangular-blocky. The soil hydraulic properties were determined for undisturbed and homogenized soil samples for each soil structure. The soil hydraulic properties were used to model soil water transport using HYDRUS-1D.The homogenized soil samples showed a significant increase in wide pores (wCP) and a decrease in narrow pores (nCP). The wCP increased by 95.6, 141.2, 391.6, 3.9, 261.3%, and nCP decreased by 69.5, 10.5, 33.8, 72.7, and 39.3% for homogenized soil samples compared to undisturbed soil samples. The soil water retention curves exhibited a significant decrease in water holding capacity for homogenized soil samples compared with the undisturbed soil samples. The homogenized soil samples showed also a decrease in soil hydraulic conductivity. The simulated results showed that water movement and distribution were affected by soil homogenizing. Moreover, soil homogenizing affected soil hydraulic properties and soil water transport. However, field studies are being needed to find the effect of these differences on water, chemical, and pollutant transport under several scenarios.

Extraction of Volatiles from Regolith or Soil on Mars, the Moon, and Asteroids

Science.gov (United States)

Linne, Diane; Kleinhenz, Julie; Trunek, Andrew; Hoffman, Stephen; Collins, Jacob

2017-01-01

NASA's Advanced Exploration Systems ISRU Technology Project is evaluating concepts to extract water from all resource types Near-term objectives: Produce high-fidelity mass, power, and volume estimates for mining and processing systems Identify critical challenges for development focus Begin demonstration of component and subsystem technologies in relevant environment Several processor types: Closed processors either partially or completely sealed during processing Open air processors operates at Mars ambient conditions In-situ processors Extract product directly without excavation of raw resource Design features Elimination of sweep gas reduces dust particles in water condensate Pressure maintained by height of soil in hopper Model developed to evaluate key design parameters Geometry: conveyor diameter, screw diameter, shaft diameter, flight spacing and pitch Operational: screw speed vs. screw length (residence time) Thermal: Heat flux, heat transfer to soil Testing to demonstrate feasibility and performance Agglomeration, clogging Pressure rise forced flow to condenser.

The water-soluble fraction of potentially toxic elements in contaminated soils: relationships between ecotoxicity, solubility and geochemical reactivity.

Science.gov (United States)

Rocha, L; Rodrigues, S M; Lopes, I; Soares, A M V M; Duarte, A C; Pereira, E

2011-09-01

To better understand the impacts posed by soil contamination to aquatic ecosystems it is crucial to characterise the links between ecotoxicity, chemical availability and geochemical reactivity of potentially toxic elements (PTE's) in soils. We evaluated the adverse effects of water extracts obtained from soils contaminated by chemical industry and mining, using a test battery including organisms from different trophic levels (bacteria, algae and daphnids). These tests provided a quick assessment of the ecotoxicity of soils with respect to possible adverse effects on aquatic organisms although the ecotoxicological responses could be related to the solubility of PTE's only to a limited extent. The analysis of results of bioassays together with the chemical characterisation of water extracts provided additional relevant insight into the role of conductivity, pH, Al, Fe, and Mn of soil extracts on toxicity to organisms. Furthermore, an important conclusion of this study was that the toxicity of extracts to the aquatic organisms could also be related to the soil properties (pH, Org C and Fe(ox)) and to the reactivity of PTE's in soils which in fact control the soluble fraction of the contaminants. The combined assessment of ecotoxicity in water fractions, solubility and geochemical reactivity of PTE's in soils provided a more comprehensive understanding of the bioavailability of inorganic contaminants than ecotoxicological or chemical studies alone and can therefore be most useful for environmental risks assessment of contaminated soils. Copyright © 2011 Elsevier Ltd. All rights reserved.

Does wastewater from olive mills induce toxicity and water repellency in soil?

Science.gov (United States)

Peikert, B.; Bandow, N.; Schaumann, G. E.

2012-04-01

Olive oil mill wastewater is the effluent generated by the olive oil extraction process. It is the main waste product of this industry mainly being produced in the Mediterranean Basin. Because proper treatment options are rare it is often disposed into the environment, e.g. fields or wadies. Due to its high concentration of fatty acids and phytotoxic phenolic compounds and its high chemical and biological oxygen demand, olive oil mill wastewater becomes a serious environmental problem. In this screening study we investigated long-term effects of olive oil mill wastewater application on soil properties in several locations in the West Bank and Israel. We determined wettability via water drop penetration time and the contact angle as well as general soil properties including pH, EC, carbon content, and we conducted thermogravimetrical analyses in order to characterize the impact of the waste water on the quality of soil organic matter. Our results show that application of olive oil mill wastewater has various effects. We determined contact angles between 110 and 120° and water drop penetration times up to 1367 s indicating significant reduction in wettability. Furthermore, soil carbon and nitrogen content and water extractable organic matter increased as well as electric conductivity, which could be pointed out as a fertilizing effect. In contrast soil pH was significantly reduced. Conducting thermal analyses we observed an increase in the labile and refractory carbon fraction. Probably first one is responsible for induced water repellency. As a consequence the reduced wettability negatively affects soil quality. It would therefore be promising to minimize the hydrophobizing impacts without losing fertilizing effects of the olive oil mill wastewater.

Phyto extraction of 99Tc on soil cores with aged contamination

International Nuclear Information System (INIS)

Massoura, S.T.; Echevarria, G.; Morel, J.L.; Massoura, S.T.; Leclerc-Cessac, E.; Denys, D.

2004-01-01

99 Tc is an artificial radionuclide which is found in high-activity and long-lived nuclear waste. This work was designed to study the phyto-extraction of 99 Tc in soils that had received aged contamination and to monitor the resulting 99 Tc concentrations in the soil solution of undisturbed soil cores in a greenhouse. Undisturbed soil cores had been sampled previously from a Rendzic Leptosol (R), a Fluvic cambisol (F) and a Dystric cambisol (D), using 0.5-m diameter PVC tubing (3 samples/soil type) without disturbing soil structure (1). Each core was equipped with two nylon porous cups (respectively 20 and 35 cm deep) and a final leachate collector. A 99 TcNO 3 solution had been supplied at the soil surface of each core during the two previous years (4200 kBq in total) in which maize and wheat had been successively cropped. These two crops had already removed 30-65% of total contamination before the present study. After the second year no more 99 Tc was added to the cores. Thereafter, Lolium perenne was cultivated for 20 successive months. 99 Tc was determined in both plant aerial parts and water samples (from both cups and collectors), and the balance of 99 Tc in the system was established after phyto-extraction. Results showed that transfer of 99 Tc to plants vary among soils: 7% on soil R to 11% on soil D. Concentration of 99 Tc in the porous cups dramatically decreased in all soils. The plants maintained low and stable concentration levels of 99 Tc in the soil solution which decreased the potential migration of the radionuclide through the cores: The leaching of 99 Tc in the final collectors of the R soil cores decreased from 18 to 1.7 Bq mL -1 . (author)

Water repellent soils: the case for unsaturated soil mechanics

Directory of Open Access Journals (Sweden)

Beckett Christopher

2016-01-01

Full Text Available Water repellent (or “hydrophobic” or “non-wetting” soils have been studied by soil scientists for well over a century. These soils are typified by poor water infiltration, which leads to increased soil erosion and poor crop growth. However, the importance of water repellence on determining soil properties is now becoming recognised by geotechnical engineers. Water repellent soils may, for example, offer novel solutions for the design of cover systems overlying municipal or mine waste storage facilities. However, investigations into factors affecting their mechanical properties have only recently been initiated. This purpose of this paper is to introduce geotechnical engineers to the concept of water repellent soils and to discuss how their properties can be evaluated under an unsaturated soils framework. Scenarios in which water repellent properties might be relevant in geotechnical applications are presented and methods to quantify these properties in the laboratory and in the field examined.

Amendment of arsenic and chromium polluted soil from wood preservation by iron residues from water treatment

DEFF Research Database (Denmark)

Nielsen, Sanne Skov; Petersen, L. R.; Kjeldsen, Peter

2011-01-01

An iron-rich water treatment residue (WTR) consisting mainly of ferrihydrite was used for immobilization of arsenic and chromium in a soil contaminated by wood preservatives. A leaching batch experiment was conducted using two soils, a highly contaminated soil (1033mgkg−1 As and 371mgkg−1 Cr....... Pore water was extracted during 3years from the amended soil and a control site. Pore water arsenic concentrations in the amended soil were more than two orders of magnitude lower than in the control for the upper samplers. An increased release of arsenic was observed during winter in both fields...

Peroxidase-catalyzed stabilization of 2,4-dichlorophenol in alkali-extracted soils.

Science.gov (United States)

Palomo, Mónica; Bhandari, Alok

2011-01-01

Horseradish peroxidase- (HRP) mediated stabilization of phenolic contaminants is a topic of interest due to its potential for remediation of contaminated soils. This study evaluated the sorption of 2,4-dichlorophenol (DCP) and its HRP-mediated stabilization in two alkali-extracted soils. Alkali extraction reduced the soil organic matter (SOM) contents of the geomaterials and enriched the residual SOM with humin C. Sorption of DCP on these sorbents was complete within 1 d. However, most of the sorbed DCP was removed from the geomaterials by water and methanol, suggesting weak solute-sorbent interactions. The addition of HRP resulted in the generation of DCP polymerization products (DPP), which partitioned between the aqueous and solid phases. The DPP phase distribution was rapid and complete within 24 h. Between 70 and 90% of the added DCP was converted to DPP and up to 43% of the initial aqueous phase contaminant was transformed into a residue that was resistant to extraction with methanol. Bound residues of DPP increased with initial aqueous phase solute concentration and remained fairly constant after 7 d of contact. Contaminant stabilization was noted to be high in the humin-mineral geomaterial. Results illustrate that HRP may be effective in stabilizing phenolic contaminants in subsoils that are likely to contain SOM enriched in humin C.

Direct Cellular Lysis/Protein Extraction Protocol for Soil Metaproteomics

Energy Technology Data Exchange (ETDEWEB)

Chourey, Karuna [ORNL; Jansson, Janet [Lawrence Berkeley National Laboratory (LBNL); Verberkmoes, Nathan C [ORNL; Shah, Manesh B [ORNL; Chavarria, Krystle L. [Lawrence Berkeley National Laboratory (LBNL); Tom, Lauren M [Lawrence Berkeley National Laboratory (LBNL); Brodie, Eoin L. [Lawrence Berkeley National Laboratory (LBNL); Hettich, Robert {Bob} L [ORNL

2010-01-01

We present a novel direct protocol for deep proteome characterization of microorganisms in soil. The method employs thermally assisted detergent-based cellular lysis (SDS) of soil samples, followed by TCA precipitation for proteome extraction/cleanup prior to liquid chromatography-mass spectrometric characterization. This approach was developed and optimized using different soils inoculated with genome-sequenced bacteria (Gram-negative Pseudomonas putida or Gram-positive Arthrobacter chlorophenolicus). Direct soil protein extraction was compared to protein extraction from cells isolated from the soil matrix prior to lysis (indirect method). Each approach resulted in identification of greater than 500 unique proteins, with a wide range in molecular mass and functional categories. To our knowledge, this SDS-TCA approach enables the deepest proteome characterizations of microbes in soil to date, without significant biases in protein size, localization, or functional category compared to pure cultures. This protocol should provide a powerful tool for ecological studies of soil microbial communities.

The effect of soil extracts from a monoculture of spring wheat (Triticum aestivum L. grown under different tillage systems on the germination of its seeds

Directory of Open Access Journals (Sweden)

Piotr Kraska

2012-12-01

Full Text Available The present experiment was carried out in the period 2006-2008. The aim of this study was to determine the effect of aqueous soil extracts from the soil of a spring wheat monoculture on seed germination energy and capacity, the length of the first leaf and of the longest radicle as well as the number of radicles. Moreover, the content of 0-dihydroxyphenols in the soil was compared in the last year of the study. The soil used to prepare the solutions came from a field experiment established on medium heavy mixed rendzina soil. Spring wheat, cv. Zebra, was grown using plough tillage and two conservation tillage methods in the presence of undersown crops (red clover, Westerwolds ryegrass and stubble crops (lacy phacelia, white mustard. Germination energy of the seeds watered with the soil extracts from the ploughed plots was significantly higher than this trait in the seeds watered with the extracts from the conservation tillage treatments with spring disking of the catch crops. Germination energy and capacity of spring wheat in the control treatment watered with distilled water were significantly higher compared to the other treatments under evaluation. Spring wheat watered with the aqueous extract prepared from the soil obtained from the plough tillage treatment produced a significantly longer first leaf compared to the treatments in which both conservation tillage methods had been used. The shortest leaf and the lowest number of radicles were produced by the seedlings watered with the soil extract from the treatment with the white clover stubble crop. Radicle length was not significantly differentiated by the soil extracts under consideration. The content of 0-dihydroxyphenols in the rendzina soil determined during the spring period was higher than that determined in the autumn. The content of 0-dihydroxyphenols in the soil was lower in the conservation tillage treatments with autumn incorporation of the catch crops than in the plots in which

Influence of the soil/solution ratio, interaction time, and extractant on the evaluation of iron chelate sorption/desorption by soils.

Science.gov (United States)

Hernández-Apaolaza, Lourdes; Lucena, Juan J

2011-03-23

Synthetic Fe chelates are the most efficient agricultural practice to control Fe deficiency in crops, EDTA/Fe3+ and o,o-EDDHA/Fe3+ being the most commonly used. Their efficacy as Fe sources and carriers in soils can be severely limited by their retention on it. The aim of this work is to evaluate the possible bias introduced in the studies of the iron chelate retention by soils. For that purpose, results obtained for EDTA and EDDHA iron chelates from two batch studies with different soil/solution ratios were compared with data obtained for a leaching column experiment. Moreover, different extractants were tested to study the o,o-EDDHA/Fe3+ and o,p-EDDHA/Fe3+ desorption from a calcareous soil, and also the effect of the interaction time in their retention process has been evaluated. In summary, the mobility through a calcareous soil of the studied iron chelates differs greatly depending on the type of iron chelate and also on the procedure used to evaluate the retention and the soil/solution ratio used. In general, the leaching column method is preferred because the achieved conclusions are more representative of the natural conditions, but batch methods are very useful as a preliminary experiment, especially one with a high soil/solution ratio. The iron chelate desorption could be quantified by using a sequential extraction with water, sodium sulfate, and DTPA as extractants. Under the experimental conditions used in this study, o,o-EDDHA/Fe3+ retention increased with interaction time.

The Influence of Soil Particle on Soil Condensation Water

OpenAIRE

Hou Xinwei; Chen Hao; Li Xiangquan; Cui Xiaomei; Liu Lingxia; Wang Zhenxing

2013-01-01

The experiment results showed that the indoor experiment formed from the volume of soil hygroscopic water increased gradually with decreasing size of soil particles. In the outdoor experiments, the results showed that the formed condensation water in medium sand was greater than it was in fine sand; the soil hot condensation water was mainly formed in the top layer of soil between 0-5 cm. We also found that covering the soil surface with stones can increase the volume of formed soil condensat...

Effects of lead mineralogy on soil washing enhanced by ferric salts as extracting and oxidizing agents.

Science.gov (United States)

Yoo, Jong-Chan; Park, Sang-Min; Yoon, Geun-Seok; Tsang, Daniel C W; Baek, Kitae

2017-10-01

In this study, we evaluated the feasibility of using ferric salts including FeCl 3 and Fe(NO 3 ) 3 as extracting and oxidizing agents for a soil washing process to remediate Pb-contaminated soils. We treated various Pb minerals including PbO, PbCO 3 , Pb 3 (CO 3 ) 2 (OH) 2 , PbSO 4 , PbS, and Pb 5 (PO 4 ) 3 (OH) using ferric salts, and compared our results with those obtained using common washing agents of HCl, HNO 3 , disodium-ethylenediaminetetra-acetic acid (Na 2 -EDTA), and citric acid. The use of 50 mM Fe(NO 3 ) 3 extracted significantly more Pb (above 96% extraction) from Pb minerals except PbSO 4 (below 55% extraction) compared to the other washing agents. In contrast, washing processes using FeCl 3 and HCl were not effective for extraction from Pb minerals because of PbCl 2 precipitation. Yet, the newly formed PbCl 2 could be dissolved by subsequent wash with distilled water under acidic conditions. When applying our washing method to remediate field-contaminated soil from a shooting range that had high concentrations of Pb 3 (CO 3 ) 2 (OH) 2 and PbCO 3 , we extracted more Pb (approximately 99% extraction) from the soil using 100 mM Fe(NO 3 ) 3 than other washing agents at the same process conditions. Our results show that ferric salts can be alternative washing agents for Pb-contaminated soils in view of their extracting and oxidizing abilities. Copyright © 2017 Elsevier Ltd. All rights reserved.

Zinc species distribution in EDTA-extract residues of zinc-contaminated soil

International Nuclear Information System (INIS)

Chang, S.-H.; Wei, Y.-L.; Wang, H. Paul

2007-01-01

Soil sample from a site heavily contaminated with >10 wt.% zinc is sampled and extracted with aqueous solutions of ethylene diamine tetra-acetic acid (EDTA) that is a reagent frequently used to extract heavy metals in soil remediation. Three liquid/soil ratios (5/1, 20/1, and 100/1) were used in the extracting experiment. The molecular environment of the residual Zn in the EDTA-extract residues of zinc-contaminated soil is investigated with XANES technique. The results indicate that EDTA does not show considerable preference of chelating for any particular Zn species during the extraction. Zn species distribution in the sampled soil is found to resemble that in all EDTA-extract residues; Zn(OH) 2 is determined as the major zinc species (60-70%), seconded by organic zinc (21-26%) and zinc oxide (9-14%)

Methods for microbial DNA extraction from soil for PCR amplification

Directory of Open Access Journals (Sweden)

Yeates C

1998-01-01

Full Text Available Amplification of DNA from soil is often inhibited by co-purified contaminants. A rapid, inexpensive, large-scale DNA extraction method involving minimal purification has been developed that is applicable to various soil types (1. DNA is also suitable for PCR amplification using various DNA targets. DNA was extracted from 100g of soil using direct lysis with glass beads and SDS followed by potassium acetate precipitation, polyethylene glycol precipitation, phenol extraction and isopropanol precipitation. This method was compared to other DNA extraction methods with regard to DNA purity and size.

Performance evaluation of TDT soil water content and watermark soil water potential sensors

Science.gov (United States)

This study evaluated the performance of digitized Time Domain Transmissometry (TDT) soil water content sensors (Acclima, Inc., Meridian, ID) and resistance-based soil water potential sensors (Watermark 200, Irrometer Company, Inc., Riverside, CA) in two soils. The evaluation was performed by compar...

Uranium in agricultural soils and drinking water wells on the Swiss Plateau.

Science.gov (United States)

Bigalke, Moritz; Schwab, Lorenz; Rehmus, Agnes; Tondo, Patrick; Flisch, Markus

2018-02-01

Mineral phosphorus fertilizers are regularly applied to agricultural sites, but their uranium (U) content is potentially hazardous to humans and the environment. Fertilizer-derived U can accumulate in the soil, but might also leach to ground-, spring and surface waters. We sampled 19 mineral fertilizers from the canton of Bern and soils of three arable and one forest reference sites at each of four locations with elevated U concentrations (7-28 μg L -1 ) in nearby drinking water wells. The total U concentrations of the fertilizers were measured. The soils were analysed at three depth intervals down to 1 m for general soil parameters, total Cd, P, U and NaHCO 3 -extractable U concentrations, and 234/238 U activity ratios (AR). The U concentrations and AR values of the drinking water samples were also measured. A theoretical assessment showed that fertilizer-derived U may cause high U concentrations in leaching waters (up to approx. 25 μg L -1 ), but normally contributes only a small amount (approx. 0-3 μg L -1 ). The arable soils investigated showed no significant U accumulation compared to the forest sites. The close positive correlation of AR with NaHCO 3 -extractable U (R = 0.7, p water samples were close to 1, possibly suggesting an influence of fertilizer-derived U. However, based on findings from the literature and considering the heterogeneity of the catchment area, the agricultural practices, and the comparatively long distance to the groundwater, we conclude that fertilizer-derived U makes only a minor contribution to the elevated U concentrations in the water samples. Copyright © 2017 Elsevier Ltd. All rights reserved.

Sustainable Soil Water Management Systems

OpenAIRE

Basch, G.; Kassam, A.; Friedrich, T.; Santos, F.L.; Gubiani, P.I.; Calegari, A.; Reichert, J.M.; dos Santos, D.R.

2012-01-01

Soil quality and its management must be considered as key elements for an effective management of water resources, given that the hydrological cycle and land management are intimately linked (Bossio et al. 2007). Soil degradation has been described by Bossio et al. (2010) as the starting point of a negative cycle of soil-water relationships, creating a positive, self-accelerating feedback loop with important negative impacts on water cycling and water productivity. Therefore, sustainable soil...

Effect of soil contaminant extraction method in determining toxicity using the Microtox(reg.) assay

International Nuclear Information System (INIS)

Harkey, G.A.; Young, T.M.

2000-01-01

This project examined the influence of different extraction methods on the measured toxicity of contaminated soils collected from manufactured gas plant (MGP) sites differing in soil composition and contaminant concentration. Aged soils from a number of MGP sites were extracted using a saline solution, supercritical fluid extraction (SFE), and Soxhlet extraction. Toxicity was assessed using two forms of Microtox tests: acute aqueous tests on saline and SFE soil extracts and solid-phase tests (SPTs) on soil particles. Microtox SPTs were performed on soils before and after SFE to determine resulting toxicity reduction. Three hypotheses were tested: (1) Toxicity of soil extracts is related to contaminant concentrations of the extracts, (2) measured toxicity significantly decreases with less vigorous methods of extraction, and (3) supercritical fluid extractability correlates with measured toxicity. The EC50s for SPTs performed before and after SFE were not different for some soils but were significantly greater after extraction for other soils tested. The most significant toxicity reductions were observed for soils exhibiting the highest toxicity in both preextraction SPTs and acute aqueous tests. Acute Microtox tests performed on SFE extracts showed significantly lower EC50s than those reported from saline-based extraction procedures. Toxicity of the soils measured by Microtox SPTs was strongly correlated with both SFE efficiency and measures of contaminant aging. Data from this project provide evidence of sequestration and reduced availability of polycyclic aromatic hydrocarbons (PAHs) from soils extracted via physiologically based procedures compared to vigorous physical extraction protocols

Soil and groundwater remediation using dual-phase extraction technology

International Nuclear Information System (INIS)

Miller, A.W.; Gan, D.R.

1995-01-01

A gasoline underground storage tank (UST) was formerly used to fuel vehicles for a hospital in Madison, Wisconsin. Elevated concentrations of gasoline range organics (GRO) were observed in soils and groundwater at the site during the tank removal and a subsequent site investigation. Based on the extent of soil and groundwater contamination, a dual-phase extraction technology was selected as the most cost effective alternative to remediate the site. The dual-phase extraction system includes one extraction well functioning both as a soil vapor extraction (SVE) and groundwater recovery well. After six months of operation, samples collected from the groundwater monitoring wells indicated that the groundwater has been cleaned up to levels below the Wisconsin preventative action limits. The dual-phase extraction system effectively remediated the site in a short period of time, saving both operation and maintenance costs and overall project cost

[Removal of volatile organic compounds in soils by soil vapor extraction (SVE)].

Science.gov (United States)

Yin, Fu-xiang; Zhang, Sheng-tian; Zhao, Xin; Feng, Ke; Lin, Yu-suo

2011-05-01

An experiment study has been carried out to investigate effects of the diameter of soil columns, the size of soil particulate and different contaminants on efficiency of simulated soil vapor extraction (SVE). Experiments with benzene, toluene, ethylbenzene and n-propylbenzene contaminated soils showed that larger bottom area/soil height (S/H) of the columns led to higher efficiency on removal of contaminants. Experiments with contaminated soils of different particulate size showed that the efficiency of SVE decreased with increases in soil particulate size, from 10 mesh to between 20 mesh and 40 mesh and removal of contaminants in soils became more difficult. Experiments with contaminated soils under different ventilation rates suggested that soil vapor extraction at a ventilation rate of 0.10 L x min(-1) can roughly remove most contaminants from the soils. Decreasing of contaminants in soils entered tailing stages after 12 h, 18 h and 48 h for benzene, toluene and ethylbenzene, respectively. Removal rate of TVOCs (Total VOCs) reached a level as high as 99.52%. The results of the experiment have indicated that molecule structure and properties of the VOCs are also important factors which have effects on removal rates of the contaminants. Increases in carbon number on the benzene ring, decreases in vapor pressure and volatile capability resulted in higher difficulties in soil decontamination. n-propylbenzene has a lower vapor pressure than toluene and ethylbenzene which led to a significant retard effect on desorption and volatilization of benzene and ethylbenzene.

Factors responsible for the patchy distribution of natural soil water repellency in Mediterranean semiarid forest

Science.gov (United States)

Lozano, E.; Jiménez-Pinilla, P.; Mataix-Solera, J.; González-Pérez, J. A.; García-Orenes, F.; Torres, M. P.; Arcenegui, V.; Mataix-Beneyto, J.

2012-04-01

Soil water repellency (WR) is commonly observed in forest areas showing wettable and water repellent patches with high spatial variability. This has important hydrological implications; in semiarid areas where water supply is limited, even slight WR may play an important role in infiltration patterns and distribution of water into the soil (Mataix-Solera et al., 2007). It has been proposed that the origin of WR is the release of organic compounds from different plants species and sources (due to waxes and other organic substances in their tissues; Doerr et al., 1998). However, the relationship between WR and plants may not always be a direct one: a group of fungi (mainly mycorrhizal fungi) and microorganisms could be also responsible for WR. The aim of this research is to study the relationships between WR in soils under different plant cover with selected soil properties and the quantity of fungi and their exudates. The study area is located in Southeast Spain, "Sierra de la Taja" near Pinoso (Alicante)), with a semiarid Mediterranean climate (Pm=260mm). Samples were taken in September 2011, when WR is normally strongest after summer drought. Soil samples were collected from the first 2.5cm of the mineral A horizon at microsites beneath each of the four most representative species (Pinus halepensis, Rosmarinus officinalis, Quercus. rotundifolia and Cistus albidus; n=15 per specie) and 5 samples from bare soil with no influence of any species. Different soil parameters were analyzed; water content, soil organic mater content (SOM), pH, WR, easily extractable glomalin (EEG), total mycelium and extractable lipids. The occurrence of WR was higher under P. halepensis (87% of samples) and Q. rotundifolia (60% of samples). Positive significant correlations were found between WR and SOM content for all species, with the best correlations for Pinus and Quercus (r=0.855**, r= 0.934** respectively). In addition, negative significant correlations were found between WR and p

An approach using centrifugation for the extraction of the soil solution and its usefulness in studies of radionuclide speciation in soils - Approach using centrifugation for extraction of soil solution and its study for uranium speciation

Energy Technology Data Exchange (ETDEWEB)

Medeiros, Adriana S. [CAPES Foundation, Ministry of Education of Brazil, 70040-020, Brasilia, Brazil, Proc.BEX 1958/13-5 (Brazil); Lozano, J.C.; Prieto, C. [Universidad de Salamanca, 37008, Salamanca (Spain); Blanco Rodriguez, P.; Vera Tome, F. [Universidad de Extremadura, 06006, Badajoz (Spain)

2014-07-01

The centrifugation technique is tested as a methodology for extraction of soil solution, for further characterization, in order to elucidate its contribution to the speciation of radionuclides, particularly uranium, in radioactively contaminated soils, as well as the determination of its availability for vegetation. Centrifugation of a previously saturated soil core provides the soil solution with a specific origin inside the soil sample. In such way that the different soil solution origin, associate to the effective pressure applied to the soil core, will reflect different distribution coefficients which affect the radionuclide availability definition. Speciation of radionuclides in the soil solution can be also conditioned by this water origin. The development of this methodology relating to technical challenges faces materials suitable for the centrifugation process, both in terms of mechanical properties and chemical inertness. This paper reports the preparation of ceramic pellets of perlite produced with the intention of replacing glass pellets, used inserts in support to soils coupled with centrifuges. The characterization of porosity and the test of its chemical inertness and mechanical strength to the centrifugation process have been performed. Porosity characterization is required to control the saturation gradient, which conditions the flow of water from the soil. Its mechanical adequacy was tested by subjecting the pellets to the centrifugation process and assessing its integrity end. Chemical inertia was measured by placing the tablets in aqueous solutions of known composition and then evaluating the presence or absence of elements in this solution, after on time of contact between them. (authors)

Dependence of the concentrations of "1"3"7Cs and potassium in extracted soil solutions on soil humidity before centrifugation

International Nuclear Information System (INIS)

Prorok, V.V.; Datsenko, O.Yi.; Bulavyin, L.A.; Zlens'kij, S.Je.; Melnichenko, L.Yu.; Rozuvan, S.G.; Poperenko, L.V.; White, P.J.

2017-01-01

Concentrations of 137Cs and potassium in solutions extracted by centrifugation from soils selected at some experimental sites in the 10-km Exclusion Zone of Chornobyl Nuclear Plant were determined. The results showed that for the majority of investigated soils, the concentration of 137Cs in soil solution depends on the humidity of the soil before centrifugation. It is possible to explain the dependence of the concentration of 137Cs in the soil solution on soil humidity from the dependence of the concentrations of molecules of different molecular-gravimetric fractions in soil solution on soil humidity. Considerable amount of 137Cs in soil solution is associated with these molecules, that is why the concentration of 137Cs in the extracted soil solution changes with the humidity of soil. These dependences differ between soils. For the majority of investigated soils the concentration of 137Cs in the extracted soil solution increases with increasing humidity of the soil. By contrast, soil humidity had no effect on the potassium concentration in the extracted soil solution for any soil investigated. It is concluded, that potassium is practically not associated with molecules of different molecular-gravimetric fractions in the extracted soil solutions

Phyto extraction Of Cadmium And Zinc From Contaminated Soils

International Nuclear Information System (INIS)

Lotfy, S.M.; Mostafa, A.Z.; Abdel Sabour, M. F.

2012-01-01

A trial was made to study the use of different plant species to extract heavy metals out of contaminated soils. Four Kg of each air-dried surface soil sample (0-20 cm) were packed in plastic containers in three replicates. Five plant species tested in this study namely, Panikum (Panicum antidotal) and napier grass (Bennisetum purpureum), squash (Cucurbita pepo), cotton (Gossypium hirsutum), sunflower (Helianthus annuus); were grown on two different polluted soil types (Mostorud Clayey soil, irrigated with contaminated water for more than 30 years and El-Gabal EL-Asfar sandyloam soil, subjected to sewage effluent irrigation for more than 50 years) in a complete randomized block experimental design to study the mobility and fate of selected heavy metals and evaluate the efficiency of the tested plant species to extract Cadmium and Zinc out of polluted soils. Data indicated that sunflower and cotton shoots accumulated the highest Cd content among the five tested plant species, Shoot concentrations of Cd were as high as 9.6 mg/kg dry matter of sunflower, followed by panikum and napier grass, cotton then squash with a range of Cd between 9.6 to 1.6 mg/kg dry matter in case of the alluvium soil. However in the sandy soil, sunflower Cd -shoots were > penakium> napier grass > cotton> Squash with a lower order of magnitude which could be explained by the lower Cd -content in sandy soil compared to the alluvial soil .Calculation of recovery percentage based on Cd and Zn removed from the soil after cultivation ranged between 5.9 to 27.4 % and 16.1 to 49.1% of total initial Cd and Zn, Respectively. However, The percentage of Cd and Zn -removed by plant shoots from the initial total varied between 27.6 to 37.5% and 25.3 and 36.8 % of the removed Cd and Zn, Respectively, whereas the lowest values were observed in case of squash for Cd and Zn. As expected plant roots exhibited higher Cd and Zn accumulation than in shoots by 2-3 folds. Sunflower roots showed the highest Cd

Water Use Efficiency in Saline Soils under Cotton Cultivation in the Tarim River Basin

Directory of Open Access Journals (Sweden)

Xiaoning Zhao

2015-06-01

Full Text Available The Tarim River Basin, the largest area of Chinese cotton production, is receiving increased attention because of serious environmental problems. At two experimental stations (Korla and Aksu, we studied the influence of salinity on cotton yield. Soil chemical and physical properties, soil water content, soil total suction and matric suction, cotton yield and water use efficiency under plastic mulched drip irrigation in different saline soils was measured during cotton growth season. The salinity (mS·cm−1 were 17–25 (low at Aksu and Korla, 29–50 (middle at Aksu and 52–62 (high at Aksu for ECe (Electrical conductivity measured in saturation-paste extract of soil over the 100 cm soil profile. The soil water characteristic curves in different saline soils showed that the soil water content (15%–23% at top 40 cm soil, lower total suction power (below 3500 kPa and lower matric suction (below 30 kPa in low saline soil at Korla had the highest water use efficiency (10 kg·ha−1·mm−1 and highest irrigation water use efficiency (12 kg·ha−1·mm−1 and highest yield (6.64 t·ha−1. Higher water content below 30 cm in high saline soil increased the salinity risk and led to lower yield (2.39 t·ha−1. Compared to low saline soils at Aksu, the low saline soil at Korla saved 110 mm irrigation and 103 mm total water to reach 1 t·ha−1 yield and increased water use efficiency by 5 kg·ha−1·mm−1 and 7 kg·ha−1·mm−1 for water use efficiency (WUE and irrigation water use efficiency (IWUE respectively.

Bioventing - a new twist on soil vapor remediation of the vadose zone and shallow ground water

International Nuclear Information System (INIS)

Yancheski, T.B.; McFarland, M.A.

1992-01-01

Bioventing, which is a combination of soil vapor remediation and bioremediation techniques, may be an innovative, cost-effective, and efficient remedial technology for addressing petroleum contamination in the vadose zone and shallow ground water. The objective of bioventing is to mobilize petroleum compounds from the soil and ground water into soil vapor using soil vapor extraction and injection technology, and to promote the migration of the soil vapor upward to the turf root zone for degradation by active near-surface microbiological activity. Promoting and maintaining optimum microbiological activity in the turf root rhizosphere is a key component to the bioventing technique. Preliminary ongoing USEPA bioventing pilot studies (Kampbell, 1991) have indicated that this technique is a promising remediation technology, although feasibility studies are not yet complete. However, based on the preliminary data, it appears that proper bioventing design and implementation will result in substantial reductions of petroleum compounds in the capillary zone and shallow ground water, complete degradation of petroleum compounds in the turf root zone, and no surface emissions. A bioventing system was installed at a site in southern Delaware with multiple leaking underground storage tanks in early 1992 to remediate vadose zone and shallow ground-water contaminated by petroleum compounds. The system consists of a series of soil vapor extraction and soil vapor/atmospheric air injection points placed in various contamination areas and a central core remediation area (a large grassy plot). This system was chosen for this site because it was least costly to implement and operate as compared to other remedial alternatives (soil vapor extraction with carbon or catalytic oxidation of off-gas treatment, insitu bioremediation, etc.), and results in the generation of no additional wastes

Atrazine determination and some of their degradation products in soils and water by means of liquid chromatography of high resolution

International Nuclear Information System (INIS)

Olarte, Israel; Guerrero, Jairo Arturo; Fuentes, Cilia

1999-01-01

This study describes the validation of the analytical method for the simultaneous determination of atrazine (AT) and its metabolites deisopropylatrazine (DIA) and deetylatrazine (DEA) in irrigation water and agricultural soil. Field samples were collected in a cornfield located in Saldana, (Tolima, Colombia) and treated with 2.9 kg. a.i/ha of atrazine. Samples were collected for three months starting after herbicide treatment. The quantitative determination of the compounds of interest was carried out by HPLC with UV detection in a lichrospher RP-18 column of 125 x 4 mm, 5 , using a gradient of acetonitrile-water as mobile phase. The compounds were extracted from the water matrix and concentrated using solid phase extraction (SPE). From the soil matrix the compounds were extracted with methanol followed by a clean up with dichloromethane and buffer phosphate 0.01 M, pH 10.0. Calibration curves were linear over a concentration range of 6 /L- 30 /L in water and 30 /kg - 200 /kg in soil. The method is specific and sensitive with a detection limit of 0.6 /L for DIA, 0.7 /L for DIA and AT in water, 2.0 /kg for DIA, 2.3 /kg for DIA and AT in soil. Recovery experiments were performed with irrigation water samples yielding average recoveries between 80-100% and performed on soil samples yielding average recoveries between 45-65%. DIA and DEA were not detected in neither water nor soil field samples, but atrazine was found in water after the first month following herbicide application at a concentration level of 5,8 /L, and in soil AT a concentration level of 97 /kg - at the second month, no atrazine was found in water but 42 /kg were detected in soil

Effects of aluminium water treatment residuals, used as a soil amendment to control phosphorus mobility in agricultural soils.

Science.gov (United States)

Ulén, Barbro; Etana, Ararso; Lindström, Bodil

2012-01-01

Phosphorus (P) leaching from agricultural soils is a serious environmental concern. Application of aluminium water treatment residuals (Al-WTRs) at a rate of 20 Mg ha(-1) to clay soils from central Sweden significantly increased mean topsoil P sorption index (PSI) from 4.6 to 5.5 μmol kg(-1) soil. Mean degree of P saturation in ammonium lactate extract (DPS-AL) significantly decreased from 17 to 13%, as did plant-available P (P-AL). Concentrations of dissolved reactive P (DRP) decreased by 10-85% in leaching water with Al-WTR treatments after exposure of topsoil lysimeters to simulated rain. Soil aggregate stability (AgS) for 15 test soils rarely improved. Three soils (clay loam, silty loam and loam sand) were tested in greenhouse pot experiments. Aluminium-WTR application of 15 or 30 ton ha(-1) to loam sand and a clay loam with P-AL values of 80-100 mg kg(-1) soil significantly increased growth of Italian ryegrass when fertilised with P but did not significantly affect growth of spring barley on any soil. Al-WTR should only be applied to soils with high P fertility where improved crop production is not required.

In-situ measurements of soil-water conductivity

International Nuclear Information System (INIS)

Murphy, C.E.

1978-01-01

Radionuclides and other environmentally important materials often move in association with water. In terrestrial ecosystems, the storage and movement of water in the soil is of prime importance to the hydrologic cycle of the ecosystem. The soil-water conductivity (the rate at which water moves through the soil) is a necessary input to models of soil-water movement. In situ techniques for measurement of soil-water conductivity have the advantage of averaging soil-water properties over larger areas than most laboratory methods. The in situ techniques also cause minimum disturbance of the soil under investigation. Results of measurements using a period of soil-water drainage after initial wetting indicate that soil-water conductivity and its variation with soil-water content can be determined with reasonable accuracy for the plot where the measurements were made. Further investigations are being carried out to look at variability between plots within a soil type

Water-soluble organo-building blocks of aminoclay as a soil-flushing agent for heavy metal contaminated soil

International Nuclear Information System (INIS)

Lee, Young-Chul; Kim, Eun Jung; Ko, Dong Ah; Yang, Ji-Won

2011-01-01

Highlights: ► Aminoclays have synthesized using centered metals with aminopropyl silane. ► Developed aminoclay has unique nano-sized and water-soluble properties. ► Aminoclay showed high heavy metal capacity with metal ions and its less toxicity. ► Aminoclay could be used to remediate heavy metals from soils an alternative soil-flushing agent. - Abstract: We demonstrated that water-soluble aminopropyl magnesium functionalized phyllosilicate could be used as a soil-flushing agent for heavy metal contaminated soils. Soil flushing has been an attractive means to remediate heavy metal contamination because it is less disruptive to the soil environment after the treatment was performed. However, development of efficient and non-toxic soil-flushing agents is still required. We have synthesized aminoclays with three different central metal ions such as magnesium, aluminum, and ferric ions and investigated applicability of aminoclays as soil flushing agents. Among them, magnesium (Mg)-centered aminoclay showed the smallest size distribution and superior water solubility, up to 100 mg/mL. Mg aminoclay exhibited cadmium and lead binding capacity of 26.50 and 91.31 mg/g of Mg clay, respectively, at near neutral pH, but it showed negligible binding affinity to metals in acidic conditions. For soil flushing with Mg clay at neutral pH showed cadmium and lead were efficiently extracted from soils by Mg clay, suggesting strong binding ability of Mg clay with cadmium and lead. As the organic matter and clay compositions increased in the soil, the removal efficiency by Mg clay decreased and the operation time increased.

Results of chemical analyses of soil, shale, and soil/shale extract from the Mancos Shale formation in the Gunnison Gorge National Conservation Area, southwestern Colorado, and at Hanksville, Utah

Science.gov (United States)

Tuttle, Michele L.W.; Fahy, Juli; Grauch, Richard I.; Ball, Bridget A.; Chong, Geneva W.; Elliott, John G.; Kosovich, John J.; Livo, Keith E.; Stillings, Lisa L.

2007-01-01

Results of chemical and some isotopic analyses of soil, shale, and water extracts collected from the surface, trenches, and pits in the Mancos Shale are presented in this report. Most data are for sites on the Gunnison Gorge National Conservation Area (GGNCA) in southwestern Colorado. For comparison, data from a few sites from the Mancos landscape near Hanksville, Utah, are included. Twelve trenches were dug on the GGNCA from which 258 samples for whole-rock (total) analyses and 187 samples for saturation paste extracts were collected. Sixteen of the extract samples were duplicated and subjected to a 1:5 water extraction for comparison. A regional soil survey across the Mancos landscape on the GGNCA generated 253 samples for whole-rock analyses and saturation paste extractions. Seventeen gypsum samples were collected on the GGNCA for sulfur and oxygen isotopic analysis. Sixteen samples were collected from shallow pits in the Mancos Shale near Hanksville, Utah.

Extraction of Pentachlorophenol from Soils using Environmentally Benign Lactic Acid Solutions

Science.gov (United States)

Soil contamination with pentachlorophenol (PCP) is widespread across the globe. Soil washing/extraction is a common technique to remove this compound. Several soil washing/extraction solutions have been used but a majority of them have the problem of persistence in the environmen...

Pore Water Extraction Test Near 241-SX Tank Farm at the Hanford Site, Washington, USA

International Nuclear Information System (INIS)

Eberlein, Susan J.; Parker, Danny L.; Tabor, Cynthia L.; Holm, Melissa J.

2013-01-01

A proof-of-principle test is underway near the Hanford Site 241-SX Tank Farm. The test will evaluate a potential remediation technology that will use tank farm-deployable equipment to remove contaminated pore water from vadose zone soils. The test system was designed and built to address the constraints of working within a tank farm. Due to radioactive soil contamination and limitations in drilling near tanks, small-diameter direct push drilling techniques applicable to tank farms are being utilized for well placement. To address space and weight limitations in working around tanks and obstacles within tank farms, the above ground portions of the test system have been constructed to allow deployment flexibility. The test system utilizes low vacuum over a sealed well screen to establish flow into an extraction well. Extracted pore water is collected in a well sump,and then pumped to the surface using a small-diameter bladder pump.If pore water extraction using this system can be successfully demonstrated, it may be possible to target local contamination in the vadose zone around underground storage tanks. It is anticipated that the results of this proof-of-principle test will support future decision making regarding interim and final actions for soil contamination within the tank farms

Determination of phosphate in soil extracts in the field: A green chemistry enzymatic method

Directory of Open Access Journals (Sweden)

Ellen R. Campbell

2015-01-01

First, the soil sample is extracted with deionized water and filtered. Next, an aliquot of the soil extract (0.5 mL is transferred to a disposable cuvette, containing 0.5 mL of reaction mixture [200 mM HEPES, pH 7.6, 20 mM MgCl2, with 80 nmol 2-amino-6-mercapto-7-methylpurine ribonucleoside (MESG and 1 unit of recombinant purine nucleoside phosphorylase (PNP; EC 2.4.2.1], mixed, and incubated for 10 min at field temperature. Absorbance of the completed reaction is measured at 360 nm in open-source, portable photometer linked by bluetooth to a smartphone. The phosphate and phosphorus content of the soil is determined by comparison of its absorbance at 360 nm to a previously prepared standard phosphate curve, which is stored in the smartphone app.

Acute toxicity assessment of explosive-contaminated soil extracting solution by luminescent bacteria assays.

Science.gov (United States)

Xu, Wenjie; Jiang, Zhenming; Zhao, Quanlin; Zhang, Zhenzhong; Su, Hongping; Gao, Xuewen; Ye, Zhengfang

2016-11-01

Explosive-contaminated soil is harmful to people's health and the local ecosystem. The acute toxicity of its extracting solution was tested by bacterial luminescence assay using three kinds of luminescent bacteria to characterize the toxicity of the soil. An orthogonal test L 16 (4 5 ) was designed to optimize the soil extracting conditions. The optimum extracting conditions were obtained when the ultrasonic extraction time, ultrasonic extraction temperature, and the extraction repeat times were 6 h, 40 °C, and three, respectively. Fourier transform infrared spectroscopy (FTIR) results showed that the main components of the contaminated soil's extracting solution were 2,4-dinitrotoluene-3-sulfonate (2,4-DNT-3-SO 3 - ); 2,4-dinitrotoluene-5-sulfonate (2,4-DNT-5-SO 3 - ); and 2,6-dinitrotoluene (2,6-DNT). Compared with Photobacterium phosphoreum and Vibrio fischeri, Vibrio qinghaiensis sp. Nov. is more suitable for assessing the soil extracting solution's acute toxicity. Soil washing can remove most of the contaminants toxic to luminescent bacterium Vibrio qinghaiensis sp. Nov., suggesting that it may be a potential effective remediation method for explosive-contaminated soil.

Evaluation of Soxhlet extraction, accelerated solvent extraction and microwave-assisted extraction for the determination of polychlorinated biphenyls and polybrominated diphenyl ethers in soil and fish samples

International Nuclear Information System (INIS)

Wang Pu; Zhang Qinghua; Wang Yawei; Wang Thanh; Li Xiaomin; Ding Lei; Jiang Guibin

2010-01-01

Three commonly applied extraction techniques for persistent organic chemicals, Soxhlet extraction (SE), accelerated solvent extraction (ASE) and microwave-assisted extraction (MAE), were applied on soil and fish samples in order to evaluate their performances. For both PCBs and PBDEs, the two more recent developed techniques (ASE and MAE) were in general capable of producing comparable extraction results as the classical SE, and even higher extraction recoveries were obtained for some PCB congeners with large octanol-water partitioning coefficients (K ow ). This relatively uniform extraction results from ASE and MAE indicated that elevated temperature and pressure are favorable to the efficient extraction of PCBs from the solid matrices. For PBDEs, difference between the results from MAE and ASE (or SE) suggests that the MAE extraction condition needs to be carefully optimized according to the characteristics of the matrix and analyte to avoid degradation of higher brominated BDE congeners and improve the extraction yields.

Evaluation of Soxhlet extraction, accelerated solvent extraction and microwave-assisted extraction for the determination of polychlorinated biphenyls and polybrominated diphenyl ethers in soil and fish samples

Energy Technology Data Exchange (ETDEWEB)

Wang Pu [State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, 18 Shuangqing Road, Beijing 100085 (China); Zhang Qinghua, E-mail: qhzhang@rcees.ac.cn [State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, 18 Shuangqing Road, Beijing 100085 (China); Wang Yawei; Wang Thanh; Li Xiaomin; Ding Lei; Jiang Guibin [State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, 18 Shuangqing Road, Beijing 100085 (China)

2010-03-17

Three commonly applied extraction techniques for persistent organic chemicals, Soxhlet extraction (SE), accelerated solvent extraction (ASE) and microwave-assisted extraction (MAE), were applied on soil and fish samples in order to evaluate their performances. For both PCBs and PBDEs, the two more recent developed techniques (ASE and MAE) were in general capable of producing comparable extraction results as the classical SE, and even higher extraction recoveries were obtained for some PCB congeners with large octanol-water partitioning coefficients (K{sub ow}). This relatively uniform extraction results from ASE and MAE indicated that elevated temperature and pressure are favorable to the efficient extraction of PCBs from the solid matrices. For PBDEs, difference between the results from MAE and ASE (or SE) suggests that the MAE extraction condition needs to be carefully optimized according to the characteristics of the matrix and analyte to avoid degradation of higher brominated BDE congeners and improve the extraction yields.

Zinc oxide/polypyrrole nanocomposite as a novel solid phase microextraction coating for extraction of aliphatic hydrocarbons from water and soil samples

International Nuclear Information System (INIS)

Amanzadeh, Hatam; Yamini, Yadollah; Moradi, Morteza

2015-01-01

Highlights: • ZnO/polypyrrole (ZNO/PPY) nanocomposite coating was fabricated on stainless steel. • Nanocomposite coating morphology was evaluated using scanning electron microscopy. • It was applied for HS-SPME of aliphatic hydrocarbons in water and soil samples. • Separation and determination of the hydrocarbons were performed by GC-FID. • The method is suitable for routine analysis of n-alkanes in various environmental samples. - Abstract: In this work, ZnO/PPy nanocomposite coating was fabricated on stainless steel and evaluated as a novel headspace solid phase microextraction (HS-SPME) fiber coating for extraction of ultra-trace amounts of environmental pollutants; namely, aliphatic hydrocarbons in water and soil samples. The ZnO/PPy nanocomposite were prepared by a two-step process including the electrochemical deposition of PPy on the surface of stainless steel in the first step, and the synthesis of ZnO nanorods by hydrothermal process in the pores of PPy matrix in the second step. Porous structure together with ZnO nanorods with the average diameter of 70 nm were observed on the surface by using scanning electron microscopy (SEM). The effective parameters on HS-SPME of hydrocarbons (i.e., extraction temperature, extraction time, desorption temperature, desorption time, salt concentration, and stirring rate) were investigated and optimized by one-variable-at-a-time method. Under optimized conditions (extraction temperature, 65 ± 1 °C; extraction time, 15 min; desorption temperature, 250 °C; desorption time, 3 min; salt concentration, 10% w/v; and stirring rate, 1200 rpm), the limits of detection (LODs) were found in the range of 0.08–0.5 μg L −1 , whereas the repeatability and fiber-to-fiber reproducibility were in the range 5.4–7.6% and 8.6–10.4%, respectively. Also, the accuracies obtained for the spiked n-alkanes were in the range of 85–108%; indicating the absence of matrix effects in the proposed HS-SPME method. The results

Zinc oxide/polypyrrole nanocomposite as a novel solid phase microextraction coating for extraction of aliphatic hydrocarbons from water and soil samples

Energy Technology Data Exchange (ETDEWEB)

Amanzadeh, Hatam; Yamini, Yadollah [Department of Chemistry, Tarbiat Modares University, P.O. Box 14115-175 Tehran (Iran, Islamic Republic of); Moradi, Morteza [Department of Semiconductors, Materials and Energy Research Center, Karaj (Iran, Islamic Republic of)

2015-07-16

Highlights: • ZnO/polypyrrole (ZNO/PPY) nanocomposite coating was fabricated on stainless steel. • Nanocomposite coating morphology was evaluated using scanning electron microscopy. • It was applied for HS-SPME of aliphatic hydrocarbons in water and soil samples. • Separation and determination of the hydrocarbons were performed by GC-FID. • The method is suitable for routine analysis of n-alkanes in various environmental samples. - Abstract: In this work, ZnO/PPy nanocomposite coating was fabricated on stainless steel and evaluated as a novel headspace solid phase microextraction (HS-SPME) fiber coating for extraction of ultra-trace amounts of environmental pollutants; namely, aliphatic hydrocarbons in water and soil samples. The ZnO/PPy nanocomposite were prepared by a two-step process including the electrochemical deposition of PPy on the surface of stainless steel in the first step, and the synthesis of ZnO nanorods by hydrothermal process in the pores of PPy matrix in the second step. Porous structure together with ZnO nanorods with the average diameter of 70 nm were observed on the surface by using scanning electron microscopy (SEM). The effective parameters on HS-SPME of hydrocarbons (i.e., extraction temperature, extraction time, desorption temperature, desorption time, salt concentration, and stirring rate) were investigated and optimized by one-variable-at-a-time method. Under optimized conditions (extraction temperature, 65 ± 1 °C; extraction time, 15 min; desorption temperature, 250 °C; desorption time, 3 min; salt concentration, 10% w/v; and stirring rate, 1200 rpm), the limits of detection (LODs) were found in the range of 0.08–0.5 μg L{sup −1}, whereas the repeatability and fiber-to-fiber reproducibility were in the range 5.4–7.6% and 8.6–10.4%, respectively. Also, the accuracies obtained for the spiked n-alkanes were in the range of 85–108%; indicating the absence of matrix effects in the proposed HS-SPME method. The results

Toluene removal from sandy soils via in situ technologies with an emphasis on factors influencing soil vapor extraction.

Science.gov (United States)

Amin, Mohammad Mehdi; Hatamipour, Mohammad Sadegh; Momenbeik, Fariborz; Nourmoradi, Heshmatollah; Farhadkhani, Marzieh; Mohammadi-Moghadam, Fazel

2014-01-01

The integration of bioventing (BV) and soil vapor extraction (SVE) appears to be an effective combination method for soil decontamination. This paper serves two main purposes: it evaluates the effects of soil water content (SWC) and air flow rate on SVE and it investigates the transition regime between BV and SVE for toluene removal from sandy soils. 96 hours after air injection, more than 97% removal efficiency was achieved in all five experiments (carried out for SVE) including 5, 10, and 15% for SWC and 250 and 500 mL/min for air flow rate on SVE. The highest removal efficiency (>99.5%) of toluene was obtained by the combination of BV and SVE (AIBV: Air Injection Bioventing) after 96 h of air injection at a constant flow rate of 250 mL/min. It was found that AIBV has the highest efficiency for toluene removal from sandy soils and can remediate the vadose zone effectively to meet the soil guideline values for protection of groundwater.

Toluene Removal from Sandy Soils via In Situ Technologies with an Emphasis on Factors Influencing Soil Vapor Extraction

Directory of Open Access Journals (Sweden)

Mohammad Mehdi Amin

2014-01-01

Full Text Available The integration of bioventing (BV and soil vapor extraction (SVE appears to be an effective combination method for soil decontamination. This paper serves two main purposes: it evaluates the effects of soil water content (SWC and air flow rate on SVE and it investigates the transition regime between BV and SVE for toluene removal from sandy soils. 96 hours after air injection, more than 97% removal efficiency was achieved in all five experiments (carried out for SVE including 5, 10, and 15% for SWC and 250 and 500 mL/min for air flow rate on SVE. The highest removal efficiency (>99.5% of toluene was obtained by the combination of BV and SVE (AIBV: Air Injection Bioventing after 96 h of air injection at a constant flow rate of 250 mL/min. It was found that AIBV has the highest efficiency for toluene removal from sandy soils and can remediate the vadose zone effectively to meet the soil guideline values for protection of groundwater.

Sequential Application of Soil Vapor Extraction and Bioremediation Processes for the Remediation of Ethylbenzene-Contaminated Soils

DEFF Research Database (Denmark)

Soares, António Carlos Alves; Pinho, Maria Teresa; Albergaria, José Tomás

2012-01-01

Soil vapor extraction (SVE) is an efficient, well-known and widely applied soil remediation technology. However, under certain conditions it cannot achieve the defined cleanup goals, requiring further treatment, for example, through bioremediation (BR). The sequential application of these technol......Soil vapor extraction (SVE) is an efficient, well-known and widely applied soil remediation technology. However, under certain conditions it cannot achieve the defined cleanup goals, requiring further treatment, for example, through bioremediation (BR). The sequential application...

Using DTPA-extractable soil fraction to assess the bioconcentration factor of plants in phytoremediation of urban soils

Science.gov (United States)

Rodríguez-Bocanegra, Javier; Roca, Núria; Tume, Pedro; Bech, Jaume

2017-04-01

Urban soils may be highly contaminated with potentially toxic metals, as a result of intensive anthropogenic activities. Developing cities are increasing the number of lands where is practiced the urban agriculture. In this way, it is necessary to assess the part of heavy metals that is transferred to plants in order to a) know the potential health risk that represent soils and b) know the relation soil-plant to assess the ability of these plants to remove heavy metals from soil. Nowadays, to assess the bioconcentration factor (BF) of plants in phytoremediation, the pseudototal o total concentration has been used by many authors. Two different urban soils with similar pH and carbonates content but with different pollution degree were phytoremediated with different plant species. Urban soil from one Barcelona district (Spain), the most contaminated soil, showed an extractability of Cu, Pb and Zn of 9.6, 6.7 and 5.8% of the total fraction respectively. The soil from Talcahuano city (Chile), with contents of heavy metals slightly above the background upper limit, present values of 15.5, 13.5 and 12% of the total fraction of studied heavy metals. Furthermore, a peri-urban analysed soil from Azul (Argentina) also showed an elevated extractability with values of 24, 13.5 and 14% of the Cu, Pb and Zn contents respectively. These soils presented more extractability than other disturbed soils, like for example, soils from mine areas. The urban soils present more developed soil with an interaction between solution and solid phase in polluted systems. The most important soil surface functional groups include the basal plane of phyllosilicates and metal hydroxyls at edge sites of clay minerals, iron oxyhydroxides, manganese oxyhydroxides and organic matter. The interaction between solution and solid phase in polluted urban systems tends to form labile associations and pollutants are more readily mobilized because their bonds with soil particles are weaker. Clay and organic

Estimating the extractability of potentially toxic metals in urban soils: A comparison of several extracting solutions

International Nuclear Information System (INIS)

Madrid, F.; Reinoso, R.; Florido, M.C.; Diaz Barrientos, E.; Ajmone-Marsan, F.; Davidson, C.M.; Madrid, L.

2007-01-01

Metals released by the extraction with aqua regia, EDTA, dilute HCl and sequential extraction (SE) by the BCR protocol were studied in urban soils of Sevilla, Torino, and Glasgow. By multivariate analysis, the amounts of Cu, Pb and Zn liberated by any method were statistically associated with one another, whereas other metals were not. The mean amounts of all metals extracted by HCl and by SE were well correlated, but SE was clearly underestimated by HCl. Individual data for Cu, Pb and Zn by both methods were correlated only if each city was considered separately. Other metals gave poorer relationships. Similar conclusions were reached comparing EDTA and HCl, with much lower values for EDTA. Dilute HCl extraction cannot thus be recommended for general use as alternative to BCR SE in urban soils. - Dilute HCl extraction is tested as an alternative to the BCR sequential extraction in urban soils

Measured and simulated soil water evaporation from four Great Plains soils

Science.gov (United States)

The amount of soil water lost during stage one and stage two soil water evaporation is of interest to crop water use modelers. The ratio of measured soil surface temperature (Ts) to air temperature (Ta) was tested as a signal for the transition in soil water evaporation from stage one to stage two d...

Water-soluble organo-building blocks of aminoclay as a soil-flushing agent for heavy metal contaminated soil

Energy Technology Data Exchange (ETDEWEB)

Lee, Young-Chul [Department of Chemical and Biomolecular Engineering (BK21 program), KAIST, 335 Gwahak-ro, Yuseong-gu, Daejeon 305-701 (Korea, Republic of); Kim, Eun Jung [Advanced Biomass R and D Center, KAIST, 291 Daehakno, Yuseong-gu, Daejeon 305-701 (Korea, Republic of); Ko, Dong Ah [Department of Chemical and Biomolecular Engineering (BK21 program), KAIST, 335 Gwahak-ro, Yuseong-gu, Daejeon 305-701 (Korea, Republic of); Yang, Ji-Won, E-mail: jiwonyang@kaist.ac.kr [Department of Chemical and Biomolecular Engineering (BK21 program), KAIST, 335 Gwahak-ro, Yuseong-gu, Daejeon 305-701 (Korea, Republic of); Advanced Biomass R and D Center, KAIST, 291 Daehakno, Yuseong-gu, Daejeon 305-701 (Korea, Republic of)

2011-11-30

Highlights: Black-Right-Pointing-Pointer Aminoclays have synthesized using centered metals with aminopropyl silane. Black-Right-Pointing-Pointer Developed aminoclay has unique nano-sized and water-soluble properties. Black-Right-Pointing-Pointer Aminoclay showed high heavy metal capacity with metal ions and its less toxicity. Black-Right-Pointing-Pointer Aminoclay could be used to remediate heavy metals from soils an alternative soil-flushing agent. - Abstract: We demonstrated that water-soluble aminopropyl magnesium functionalized phyllosilicate could be used as a soil-flushing agent for heavy metal contaminated soils. Soil flushing has been an attractive means to remediate heavy metal contamination because it is less disruptive to the soil environment after the treatment was performed. However, development of efficient and non-toxic soil-flushing agents is still required. We have synthesized aminoclays with three different central metal ions such as magnesium, aluminum, and ferric ions and investigated applicability of aminoclays as soil flushing agents. Among them, magnesium (Mg)-centered aminoclay showed the smallest size distribution and superior water solubility, up to 100 mg/mL. Mg aminoclay exhibited cadmium and lead binding capacity of 26.50 and 91.31 mg/g of Mg clay, respectively, at near neutral pH, but it showed negligible binding affinity to metals in acidic conditions. For soil flushing with Mg clay at neutral pH showed cadmium and lead were efficiently extracted from soils by Mg clay, suggesting strong binding ability of Mg clay with cadmium and lead. As the organic matter and clay compositions increased in the soil, the removal efficiency by Mg clay decreased and the operation time increased.

Contributions of isotopic bio-geochemistry to the analysis of water - soil - root interactions

International Nuclear Information System (INIS)

Cayet, S.

2001-07-01

The aim of this work is to study the origin of the isotopic signal of the water produced by plants transpiration. It stresses more particularly on the water movements between the soil and the plant in a context of heterogenous water availability for the root system. The use of water isotopes ( 18 O and 2 H) should allow to precise the water extraction depth of the roots and the plant strategy in front of a hydric stress of edaphic origin. The first chapter presents the place of water in the soil-plant-atmosphere continuum, the different potential sources of water accessible to the plant, the principles of water absorption and the hydric transfer in the plant in relation with the variations of water absorption and of the evaporative conditions. The isotopic method is introduced with the natural variability of the isotopic composition of the atmospheric and soil waters. Finally, the reaction of the plant in front of a hydric stress is described. The second chapter presents a series of experiments carried out in the natural environment and shows the problems encountered during the determination of water origin in heterogenous hydric availability conditions. The third chapter describes the experiments performed in controlled environment. One series of experiments is performed in homogenous hydric availability condition. The aim is to analyze the isotopic signal emitted by the plant and its significance with respect to the feeding water. The second series of experiments is performed in heterogenous hydric availability conditions and in stable or variable climatic conditions. In the last chapter, the different experiments performed in natural environment are presented, first in optimum hydric availability conditions, and second in variable hydric conditions. These experiments allow to reconstruct the isotopic signal of the soil water which is recorded by the plant and to precise the preferential areas of water extraction by the roots, and the competitive behaviour of

Measuring Soil Water Potential for Water Management in Agriculture: A Review

Directory of Open Access Journals (Sweden)

Marco Bittelli

2010-05-01

Full Text Available Soil water potential is a soil property affecting a large variety of bio-physical processes, such as seed germination, plant growth and plant nutrition. Gradients in soil water potential are the driving forces of water movement, affecting water infiltration, redistribution, percolation, evaporation and plants’ transpiration. The total soil water potential is given by the sum of gravity, matric, osmotic and hydrostatic potential. The quantification of the soil water potential is necessary for a variety of applications both in agricultural and horticultural systems such as optimization of irrigation volumes and fertilization. In recent decades, a large number of experimental methods have been developed to measure the soil water potential, and a large body of knowledge is now available on theory and applications. In this review, the main techniques used to measure the soil water potential are discussed. Subsequently, some examples are provided where the measurement of soil water potential is utilized for a sustainable use of water resources in agriculture.

The effect of tree species on seasonal fluctuations in water-soluble and hot water-extractable organic matter at post-mining sites

Czech Academy of Sciences Publication Activity Database

Cepáková, Šárka; Tošner, Z.; Frouz, Jan

2016-01-01

Roč. 275, August (2016), s. 19-27 ISSN 0016-7061 Grant - others:GA ČR(CZ) GAP504/12/1288; GAJU(CZ) GAJU/04-146/2013/P Program:GA Institutional support: RVO:60077344 Keywords : HWC * liquid-state 1H NMR * seasonality * soil organic carbon * water-extractable organic matter Subject RIV: DF - Soil Science Impact factor: 4.036, year: 2016

Evaluation of a simple, non-alkaline extraction protocol to quantify soil ergosterol

NARCIS (Netherlands)

De Ridder-Duine, A.S.; Smant, W.; Van der Wal, A.; Van Veen, J.A.; De Boer, W.

2006-01-01

Quantification of soil ergosterol is increasingly used as an estimate for soil fungal biomass. Several methods for extraction of ergosterol from soil have been published, perhaps the simplest being that described by Gong, P., Guan, X., Witter, E. [2001. A rapid method to extract ergosterol from soil

Removal of Radium-226 from Radium-Contaminated Soil using Distilled Water and Humic Acid: Effect of pH

International Nuclear Information System (INIS)

Phillips, E.; Muhammad Samudi Yasir; Muhamat Omar

2011-01-01

Effect of washing solutions' pH removal of radium-226 from radium-contaminated soil using distilled water and humic acid extracted from Malaysian peat soil was studied by batch washing method. The study encompassed the extraction of humic acid and the washing of radium-contaminated soil using distilled water and humic acid solutions of 100 ppm, both with varying pHs in the range of 3 to 11. The radioactivity concentration of radium-226 was determined by gamma spectrometer.The removal of radium-226 was greater when humic acid solutions were used compared to distilled water at the pH range studied and both washing solutions showed greater removal of radium-226 when basic solutions were used. Nevertheless, comparable removal efficiencies were observed when neutral and highly basic humic acid solutions were used. (author)

Availability of heavy metals in contaminated soil evidenced by chemical extractants

Directory of Open Access Journals (Sweden)

Maria Ligia de Souza Silva

2012-06-01

Full Text Available Heavy metals have been accumulating in Brazilian soils, due to natural processes, such as atmospheric deposition, or human industrial activities. For certain heavy metals, when in high concentrations in the soil, there is no specific extractant to determine the availability of these elements in the soil. The objective of the present study was to evaluate the availability of Cd, Cu, Fe, Mn, Pb and Zn for rice and soybeans, using different chemical extractants. In this study we used seven soil samples with different levels of contamination, in completely randomized experimental design with four replications. We determined the available concentrations of Cd, Cu, Fe, Mn, Pb and Zn extracted by Mehlich-1, HCl 0.1 mol L-1, DTPA, and organic acid extractants and the contents in rice and soybeans, which extracts were analyzed by ICP-OES. It was observed that Mehlich-1, HCl 0.1 mol L-1 and DTPA extractants were effective to assess the availability of Cd, Cu, Pb and Zn for rice and soybeans. However, the same was not observed for the organic acid extractant.

Sequential extraction procedures to ascertain the role of organic matter in the fate of iodine in soils

International Nuclear Information System (INIS)

Gavalda, D.; Colle, C.

2004-01-01

In the assessment of the radiological impact on man of radioactive substances the fate of the long-lived 129 I in soils is of special interest. In order to predict the behaviour of iodine in the environment the knowledge of soil parameters which are responsible for its sorption is necessary. Sequential extraction techniques were performed to investigate the degree of binding of iodine with soil components and more specifically with the different constituents of soil organic matter (humic acid, fulvic acid, humin) which are liable to change with time. A speciation scheme was especially developed to study the role of organic matter in iodine retention and complexation. In the first steps, several mineral fractions of iodine were extracted: water soluble (H 2 O), exchangeable (1M MgCl 2 ), carbonate bound (0.01N HCl), bound to Fe-Mn oxides (0.5 M NH 4 OH,HCl adjusted to pH=2 with HNO 3 ). After these preliminary steps, the extraction of organic matter was carried out with neutral pyrophosphate (Na 2 H 2 P 2 O 7 / K 4 P 2 O 7 1/1 0.1M pH=7) to determine iodine bound to organo-mineral complexes and sodium hydroxide (0.5 M NaOH) to quantify iodine bound to humic substances. For these extracts, the distribution of iodine between humic and fulvic acids was studied. Iodine bound to residual and insoluble organic matter (humin) was extracted with H 2 O 2 30% adjusted to pH=2 with HNO 3 . In the last step, iodine bound to the residual soil was extracted by wet digestion (H 2 SO 4 ). In this scheme, all the traditional organic reagents (acetate, acetic acid,..) were removed and replaced by mineral reagents to allow the monitoring of organic carbon in the soil extracts. (author)

Carcinogenicity of soil extracts

Energy Technology Data Exchange (ETDEWEB)

Shcherbak, N P

1970-01-01

A total of 270 3-mo-old mice, hybrids of the C57BL and CBA strains which are highly susceptible to carcinogens, were painted on the skin (2-3 admin./week) with 3-4 drops of (1) a concentrated benzene extract of soil taken near a petroleum refinery with a 3,4 benzpyrene (BP) content of 0.22%; (2) a 0.22% soln of pure BP in benzene; (3) a concentrated benzene extract of soil taken from an old residential area of Moscow (BP content 0.0004%); (4) a 0.0004% BP soln in benzene; and (5) pure benzene. Only mice in the first 2 groups developed tumors. In group (1), 8 mice had papillomas, 46 had skin cancer, 1 had a sarcoma and 2 had plasmocytomas. In group (2) all 60 animals had skin cancer. Lung metastases were present at autopsy in 5 mice in group (1) and in 10 mice in group (2); in some cases, these tumors were multiple. Lymph node metastases were found in 6 mice in group (1) and in 10 mice in group (2). Tumors developed more slowly in group (1) than in group (2).

Field Test Design Simulations of Pore-Water Extraction for the SX Tank Farm

Energy Technology Data Exchange (ETDEWEB)

Truex, Michael J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Oostrom, Martinus [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

2013-09-01

A proof of principle test of pore water extraction is being performed by Washington River Protection Solutions for the U.S. Department of Energy, Office of River Protection. This test is being conducted to meet the requirements of Hanford Federal Facility Agreement and Consent Order (HFFACO) (Ecology et al. 1989) Milestone M 045-20, and is described in RPP-PLAN-53808, 200 West Area Tank Farms Interim Measures Investigation Work Plan. To support design of this test, numerical simulations were conducted to help define equipment and operational parameters. The modeling effort builds from information collected in laboratory studies and from field characterization information collected at the test site near the Hanford Site 241-SX Tank Farm. Numerical simulations were used to evaluate pore-water extraction performance as a function of the test site properties and for the type of extraction well configuration that can be constructed using the direct-push installation technique. Output of simulations included rates of water and soil-gas production as a function of operational conditions for use in supporting field equipment design. The simulations also investigated the impact of subsurface heterogeneities in sediment properties and moisture distribution on pore-water extraction performance. Phenomena near the extraction well were also investigated because of their importance for pore-water extraction performance.

Efficiency of solvent extraction methods for the determination of methyl mercury in forest soils

Energy Technology Data Exchange (ETDEWEB)

Qian, J. [Department of Forest Ecology, Swedish University of Agricultural Sciences, Umeaa (Sweden); Dept. of Analytical Chemistry, Umeaa Univ. (Sweden); Skyllberg, U. [Department of Forest Ecology, Swedish University of Agricultural Sciences, Umeaa (Sweden); Tu, Q.; Frech, W. [Dept. of Analytical Chemistry, Umeaa Univ. (Sweden); Bleam, W.F. [Dept. of Soil Science, University of Wisconsin, Madison, WI (United States)

2000-07-01

Methyl mercury was determined by gas chromatography, microwave induced plasma, atomic emission spectrometry (GC-MIP-AES) using two different methods. One was based on extraction of mercury species into toluene, pre-concentration by evaporation and butylation of methyl mercury with a Grignard reagent followed by determination. With the other, methyl mercury was extracted into dichloromethane and back extracted into water followed by in situ ethylation, collection of ethylated mercury species on Tenax and determination. The accuracy of the entire procedure based on butylation was validated for the individual steps involved in the method. Methyl mercury added to various types of soil samples showed an overall average recovery of 87.5%. Reduced recovery was only caused by losses of methyl mercury during extraction into toluene and during pre-concentration by evaporation. The extraction of methyl mercury added to the soil was therefore quantitative. Since it is not possible to directly determine the extraction efficiency of incipient methyl mercury, the extraction efficiency of total mercury with an acidified solution containing CuSO{sub 4} and KBr was compared with high-pressure microwave acid digestion. The solvent extraction efficiency was 93%. For the IAEA 356 sediment certified reference material, mercury was less efficiently extracted and determined methyl mercury concentrations were below the certified value. Incomplete extraction could be explained by the presence of a large part of inorganic sulfides, as determined by x-ray absorption near-edge structure spectroscopy (XANES). Analyses of sediment reference material CRM 580 gave results in agreement with the certified value. The butylation method gave a detection limit for methyl mercury of 0.1 ng g{sup -1}, calculated as three times the standard deviation for repeated analysis of soil samples. Lower values were obtained with the ethylation method. The precision, expressed as RSD for concentrations 20 times

Use of sequential extraction to assess metal partitioning in soils

International Nuclear Information System (INIS)

Kaasalainen, Marika; Yli-Halla, Markku

2003-01-01

The state of heavy metal pollution and the mobility of Cd, Cu, Ni, Cr, Pb and Zn were studied in three texturally different agricultural soil profiles near a Cu-Ni smelter in Harjavalta, Finland. The pseudo-total concentrations were determined by an aqua regia procedure. Metals were also determined after division into four fractions by sequential extraction with (1) acetic acid (exchangeable and specifically adsorbed metals), (2) a reducing agent (bound to Fe/Mn hydroxides), (3) an oxidizing agent (bound to soil organic matter) and (4) aqua regia (bound to mineral structures). Fallout from the smelter has increased the concentrations of Cd, Cu and Ni in the topsoil, where 75-90% of Cd, 49-72% of Cu and 22-52% of Ni occurred in the first two fractions. Slight Pb and Zn pollution was evident as well. High proportions of mobile Cd, Cu and Ni also deeper in the sandy soil, closest to the smelter, indicated some downward movement of metals. The hydroxide-bound fraction of Pb dominated in almost all soils and horizons, while Ni, Cr and Zn mostly occurred in mineral structures. Aqua regia extraction is usefully supplemented with sequential extraction, particularly in less polluted soils and in soils that exhibit substantial textural differences within the profiles. - Sequential extraction is most useful with soils with low metal pollutant levels

Toxicity assessment using Lactuca sativa L. bioassay of the metal(loid)s As, Cu, Mn, Pb and Zn in soluble-in-water saturated soil extracts from an abandoned mining site

Energy Technology Data Exchange (ETDEWEB)

Bagur-Gonzalez, Maria Gracia [Univ. of Granada, Faculty of Sciences, Dept. of Analytical Chemistry, Granada (Spain); Univ. of Granada-CSIC, Inst. Andaluz de Ciencias de la Tierra, Faculty of Sciences, Granada (Spain); Estepa-Molina, Carmen [Univ. of Granada, Faculty of Sciences, Dept. of Mineralogy and Petrology, Granada (Spain); Martin-Peinado, Francisco [Univ. of Granada, Faculty of Sciences, Dept. of Soil Science, Granada (Spain); Morales-Ruano, Salvador [Univ. of Granada-CSIC, Inst. Andaluz de Ciencias de la Tierra, Faculty of Sciences, Granada (Spain); Univ. of Granada, Faculty of Sciences, Dept. of Mineralogy and Petrology, Granada (Spain)

2011-02-15

We used the different soluble-in-water concentrations of As, Cu, Mn, Pb and Zn from contaminated soils in an abandoned mining area (anthropogenic origin) to assess the phytotoxicity of the abandoned site using the results obtained with a Lactuca sativa L. bioassay. Material and methods The study has been carried out on potentially polluted samples from the Rodalquilar mining district (southern Spain). The area was sampled according to the different metallurgical treatments for gold extraction used in each one: dynamic cyanidation and heap leaching. The saturation extracts were obtained by filtering each saturated paste with a vacuum-extraction pump, in which measurements of metal(loid) concentrations, pH and electrical conductivity were made. The variables evaluated in the bioassay, defined as toxicity indices ranging from -1 (maximum phytotoxicity) to >0 (hormesis), were seed germination (SG) and root elongation (RE) of lettuce seeds. Results and discussion In areas with a low degree of contamination, the most sensitive toxicity index is RE, whereas in highly contaminated areas, both RE and SG are good estimators of soil toxicity. According to these results, samples from the western area showed moderate to low toxicity, which was closely related to water-soluble As concentrations. Samples from the eastern area had a high degree of toxicity in 40% of the soils. Conclusions The comparison of the two indices (SG and RE) defined using the L. sativa L. bioassay indicates that, for areas with a low degree of contamination, the most sensitive toxicity index is RE, whereas in highly contaminated areas, both RE and SG are good estimators of soil phytotoxicity. Unsupervised pattern recognition methods such as HCA and PCA enabled us to conclude that the low/moderate phytotoxicity of the soils is related to the extraction process used for the recovery of gold (mainly dynamic cyanidation in tanks located in the eastern area) and to the As and Pb contents. (orig.)

The influence of temperature, pH/molarity and extractant on the removal of arsenic, chromium and zinc from contaminated soil

Energy Technology Data Exchange (ETDEWEB)

Rastas Amofah, Lea; Maurice, Christian; Kumpiene, Jurate [Luleaa Univ. of Technology, Luleaa (Sweden). Dept. of Civil, Environmental and Natural Resources; Bhattacharya, Prosun [Royal Institute of Technology (KTH), Stockholm (Sweden). Dept. of Land and Water Resources Engineering

2011-12-15

Normal soil washing leave high residual pollutant content in soil. The remediation could be improved by targeting the extraction to coarser fractions. Further, a low/high extraction pH and higher temperature enhance the pollutant removal, but these measures are costly. In this study, the utility of NaOH, oxalate-citrate (OC) and dithionite-citrate-oxalate (DCO) solutions for extracting of arsenic, chromium and zinc from contaminated soil were assessed and compared. In addition the effects of NaOH concentration and temperature on NaOH extractions, and those of temperature and pH on OC and DCO extractions, were evaluated. A two-level, full-factorial design with a centre point was implemented. Two factors, concentration and temperature,were evaluated in NaOH extractions, and pH and temperature for OC and DCO solutions. In all cases, the extraction temperature was 20 C, 30 C and 40 C. The studied NaOH concentrations were 0.05, 0.075 and 0.1 M. The pH in OC solutions was 3, 5 and 7, and in DCO solutions, 4.7, 6.3 and 6.7. Water-washed and medium coarse soil fraction of arsenic, chromium and zinc contaminated soil was agitated for 15 min with the extraction solution. In NaOH extractions, the temperature and (less strongly) NaOH concentration significantly affected As and Cr mobilisation, but only the latter affected Zn mobilisation. Both pH and temperature significantly (and similarly) influenced As and Cr mobilisation in OC extractions, while only the pH influenced Zn mobilisation. In contrast, the extraction temperature (but not pH) influenced As, Cr and Zn mobilisation in DCO extractions. For all extractants, mobilisation was most efficient at elevated temperature (40 C). None of the extractants reduced the soil's As content to below the Swedish EPA's guideline value. Use of DCO is not recommended because dithionite has a short lifetime and residual arsenic contents in DCO-extracted soil are relatively high. Instead, sequential extraction with NaOH followed

Chemical extraction to assess the bioavailability of chlorobenzenes in soil with different aging periods

Energy Technology Data Exchange (ETDEWEB)

Song, Yang; Wang, Fang; Yang, Xinglun; Liu, Cuiying; Jin, Xin; Jiang, Xin [Chinese Academy of Sciences, Nanjing (China). State Key Lab. of Soil and Sustainable Agriculture; Kengara, Fredrick Orori [Maseno Univ. (Kenya). Dept. of Chemistry

2011-12-15

Bioavailability is mainly influenced by aging and desorption of contaminants in soil. The purpose of this study was to investigate the desorption kinetics of chlorobenzenes (CBs) in soil and to investigate whether chemical extractions are suitable for the bioavailability assessment of CBs in soil. A soil spiked with CBs and aged for different periods was extracted with Tenax, hydroxypropyl-{beta}-cyclodextrin (HPCD), and butanol to assess the bioavailability of CBs in soil, respectively. Earthworm (Eisenia foetida) accumulation was used as bioassay in parallel experiments to evaluate the chemical extractions. The results showed that desorption of CBs from soil with consecutive Tenax extraction fitted into triphasic kinetics model. Different chemical methods extracted different amounts of CBs over different aging periods. For hexachlorobenzene (HCB), the extraction efficiency was in the order of butanol > Tenax-6h > HPCD extraction, while the order of butanol > HPCD > Tenax-6h extraction for pentachlorobenzene (PeCB). The bioaccumulation by earthworm decreased with increasing aging period and was significantly higher for HCB than for PeCB (p < 0.05). Earthworm accumulated CBs correlated well with all the three chemical extracted CBs. However, HPCD extraction showed the converse extraction tendency with earthworm uptake of CBs. Chemical extraction could be used to assess the bioavailability of contaminants in soil; however, they were method and compound specific. Tenax and butanol extractions were more reliable than HPCD extraction for bioavailability assessment of the tested CBs and the soil used since they showed the consistent extraction tendency with earthworm uptake of CBs.

Characterization of soil water content variability and soil texture using GPR groundwave techniques

Energy Technology Data Exchange (ETDEWEB)

Grote, K.; Anger, C.; Kelly, B.; Hubbard, S.; Rubin, Y.

2010-08-15

Accurate characterization of near-surface soil water content is vital for guiding agricultural management decisions and for reducing the potential negative environmental impacts of agriculture. Characterizing the near-surface soil water content can be difficult, as this parameter is often both spatially and temporally variable, and obtaining sufficient measurements to describe the heterogeneity can be prohibitively expensive. Understanding the spatial correlation of near-surface soil water content can help optimize data acquisition and improve understanding of the processes controlling soil water content at the field scale. In this study, ground penetrating radar (GPR) methods were used to characterize the spatial correlation of water content in a three acre field as a function of sampling depth, season, vegetation, and soil texture. GPR data were acquired with 450 MHz and 900 MHz antennas, and measurements of the GPR groundwave were used to estimate soil water content at four different times. Additional water content estimates were obtained using time domain reflectometry measurements, and soil texture measurements were also acquired. Variograms were calculated for each set of measurements, and comparison of these variograms showed that the horizontal spatial correlation was greater for deeper water content measurements than for shallower measurements. Precipitation and irrigation were both shown to increase the spatial variability of water content, while shallowly-rooted vegetation decreased the variability. Comparison of the variograms of water content and soil texture showed that soil texture generally had greater small-scale spatial correlation than water content, and that the variability of water content in deeper soil layers was more closely correlated to soil texture than were shallower water content measurements. Lastly, cross-variograms of soil texture and water content were calculated, and co-kriging of water content estimates and soil texture

Dissolved organic carbon (DOC) in soil extracts investigated by FT-ICR-MS

Science.gov (United States)

Hofmann, D.; Steffen, D.; Jablonowski, N. D.; Burauel, P.

2012-04-01

Soil drying and rewetting usually increases the release of xenobiotics like pesticides present in agricultural soils. Besides the effect on the release of two aged 14C-labeled pesticide residues we focus on the characterisation of simultaneously remobilized dissolved organic carbon (DOC) to gain new insights into structure and stability aspects of soil organic carbon fractions. The test soil (gleyic cambisol; Corg 1.2%, pH 7.2) was obtained from the upper soil layer of two individual outdoor lysimeter studies containing either environmentally long-term aged 14C residues of the herbicide ethidimuron (0-10 cm depth; time of aging: 9 years) or methabenzthiazuron (0-30 cm depth; time of aging: 17 years). Soil samples (10 g dry soil equivalents) were (A=dry/wet) previously dried (45°C) or (B=wet/wet) directly mixed with pure water (1+2, w:w), shaken (150 rpm, 1 h), and centrifuged (2000 g). This extraction procedure was repeated several individual times, for both setups. The first three individual extractions, respectively were used for further investigations. Salt was removed from samples prior analysis because of a possible quench effect in the electrospray (ESI) source by solid phase extraction (SPE) with Chromabond C18 Hydra-cartridges (Macherey-Nagel) and methanol as backextraction solvent. The so preconcentrated and desalted samples were introduced by flow injection analysis (FIA) in a fourier transform ion cyclotron resonance mass spectrometer (FT-ICR-MS), equipped with an ESI source and a 7 T supra-conducting magnet (LTQ-FT Ultra, ThermoFisher Scientific). This technique is the key technique for complex natural systems attributed by their outstanding mass resolution (used 400.000 at m/z 400 Da) and mass accuracy (≤ 1ppm) by simultaneously providing molecular level details of thousands of compounds and was successful applied for the investigations of natural organic matter (NOM) different sources like marine and surface water, soil, sediment, bog and crude oil

Degradation of thiram in soil

International Nuclear Information System (INIS)

Raghu, K.; Murthy, N.B.K.; Kumarsamy, R.

1975-01-01

Determination of the residual 35 S labelled tetramethylthiuram disulfide showed that the fungicide persisted longer in sterilized than in unsterilized soil, while the chloroform extractable radioactivity decreased, the water extractable radioactivity increased with increase in time. However, in sterilized soil the water extractable radioactivity remained more or less constant. Degradation of the fungicide was further demonstrated by the release of C 35 S 2 from soil treated with labelled thiram. Dimethylamine was found to be one of the degradation products. A bacterium isolated from thiram-enriched soil could degrade the fungicide in shake culture. The degradation pathways of thiram in sterilized and unsterilized soils are discussed. (author)

Non-invasive detection of soil water content at intermediate field scale using natural neutrons from cosmic radiation

Energy Technology Data Exchange (ETDEWEB)

Oswald, Sascha; Rivera Villarreyes, Carlos; Baroni, Gabriele [Universitaet Potsdam, Institut fuer Erd und Umweltwissenschaften (Germany)

2011-07-01

The amount of water in the subsurface is a key factor influencing soil hydrology, run-off, evapotranspiration and plant development. A new measurement method is the so called cosmic ray method, recently introduced for soil moisture measurements by Zreda and coworkers. Secondary neutron fluxes, product of the interaction of primary cosmic-rays at the land surface, are strongly moderated by the presence of water in or above soil (soil moisture, snow and biomass water). Neutron counts at the ground/air interface represent a valuable observation at intermediate spatial scale which can be used to quantify stored water while distinguishing different water holding compartments at the land surface. We have performed such measurements in an agricultural field, in comparison with classical soil moisture measurement at a number of point locations. We discuss how to extract soil moisture values from the neutron counts, drawbacks of the method, but also that the results show a temporal development supported by the accompanying data.

A laboratory method to estimate the efficiency of plant extract to neutralize soil acidity

Directory of Open Access Journals (Sweden)

Marcelo E. Cassiolato

2002-06-01

Full Text Available Water-soluble plant organic compounds have been proposed to be efficient in alleviating soil acidity. Laboratory methods were evaluated to estimate the efficiency of plant extracts to neutralize soil acidity. Plant samples were dried at 65ºC for 48 h and ground to pass 1 mm sieve. Plant extraction procedure was: transfer 3.0 g of plant sample to a becker, add 150 ml of deionized water, shake for 8 h at 175 rpm and filter. Three laboratory methods were evaluated: sigma (Ca+Mg+K of the plant extracts; electrical conductivity of the plant extracts and titration of plant extracts with NaOH solution between pH 3 to 7. These methods were compared with the effect of the plant extracts on acid soil chemistry. All laboratory methods were related with soil reaction. Increasing sigma (Ca+Mg+K, electrical conductivity and the volume of NaOH solution spent to neutralize H+ ion of the plant extracts were correlated with the effect of plant extract on increasing soil pH and exchangeable Ca and decreasing exchangeable Al. It is proposed the electrical conductivity method for estimating the efficiency of plant extract to neutralize soil acidity because it is easily adapted for routine analysis and uses simple instrumentations and materials.Tem sido proposto que os compostos orgânicos de plantas solúveis em água são eficientes na amenização da acidez do solo. Foram avaliados métodos de laboratório para estimar a eficiência dos extratos de plantas na neutralização da acidez do solo. Os materiais de plantas foram secos a 65º C por 48 horas, moídos e passados em peneira de 1mm. Utilizou-se o seguinte procedimento para obtenção do extrato de plantas: transferir 3.0 g da amostra de planta para um becker, adicionar 150 ml de água deionizada, agitar por 8h a 175 rpm e filtrar. Avaliaram-se três métodos de laboratório: sigma (Ca + Mg + K do extrato de planta, condutividade elétrica (CE do extrato de planta e titulação do extrato de planta com solu

Element fractionation by sequential extraction in a soil with high carbonate content

International Nuclear Information System (INIS)

Sulkowski, Margareta; Hirner, Alfred V.

2006-01-01

The influence of carbonate and other buffering substances in soils on the results of a 3-step sequential extraction procedure (BCR) used for metal fractionation was investigated. Deviating from the original extraction scheme, where the extracts are analysed only for a limited number of metals, almost all elements in the soils were quantified by X-ray fluorescence spectroscopy, in the initial samples as well as in the residues of all extraction steps. Additionally, the mineral contents were determined by X-ray diffractometry. Using this methodology, it was possible to correlate changes in soil composition caused by the extraction procedure with the release of elements. Furthermore, the pH values of all extracts were monitored, and certain extraction steps were repeated until no significant pH-rise occurred. A soil with high dolomite content (27%) and a carbonate free soil were extracted. Applying the original BCR-sequence to the calcareous soil, carbonate was found in the residues of the first two steps and extract pH-values rose by around two units in the first and second step, caused mainly by carbonate dissolution. This led to wrong assignment of the carbonate elements Ca, Mg, Sr, Ba, and also to decreased desorption and increased re-adsorption of ions in those steps. After repetition of the acetic acid step until extract pH remained low, the carbonate was completely destroyed and the distributions of the elements Ca, Mg, Sr, Ba as well as those of Co, Ni, Cu, Zn and Pb were found to be quite different to those determined in the original extraction. Furthermore, it could be shown that the effectiveness of the reduction process in step two was reduced by increasing pH: Fe oxides were not significantly attacked by the repeated acetic acid treatments, but a 10-fold amount of Fe was mobilized by hydroxylamine hydrochloride after complete carbonate destruction. On the other hand, only small amounts of Fe were released anyway. Even repeated reduction steps did not

Microfluidic Extraction of Biomarkers using Water as Solvent

Science.gov (United States)

Amashukeli, Xenia; Manohara, Harish; Chattopadhyay, Goutam; Mehdi, Imran

2009-01-01

A proposed device, denoted a miniature microfluidic biomarker extractor (mu-EX), would extract trace amounts of chemicals of interest from samples, such as soils and rocks. Traditionally, such extractions are performed on a large scale with hazardous organic solvents; each solvent capable of dissolving only those molecules lying within narrow ranges of specific chemical and physical characteristics that notably include volatility, electric charge, and polarity. In contrast, in the mu-EX, extractions could be performed by use of small amounts (typically between 0.1 and 100 L) of water as a universal solvent. As a rule of thumb, in order to enable solvation and extraction of molecules, it is necessary to use solvents that have polarity sufficiently close to the polarity of the target molecules. The mu-EX would make selection of specific organic solvents unnecessary, because mu-EX would exploit a unique property of liquid water: the possibility of tuning its polarity to match the polarity of organic solvents appropriate for extraction of molecules of interest. The change of the permittivity of water would be achieved by exploiting interactions between the translational states of water molecules and an imposed electromagnetic field in the frequency range of 300 to 600 GHz. On a molecular level, these interactions would result in disruption of the three-dimensional hydrogen-bonding network among liquid-water molecules and subsequent solvation and hydrolysis of target molecules. The mu-EX is expected to be an efficient means of hydrolyzing chemical bonds in complex macromolecules as well and, thus, enabling analysis of the building blocks of these complex chemical systems. The mu-EX device would include a microfluidic channel, part of which would lie within a waveguide coupled to an electronically tuned source of broad-band electromagnetic radiation in the frequency range from 300 to 600 GHz (see figure). The part of the microfluidic channel lying in the waveguide would

Reliance on shallow soil water in a mixed-hardwood forest in central Pennsylvania.

Science.gov (United States)

Gaines, Katie P; Stanley, Jane W; Meinzer, Frederick C; McCulloh, Katherine A; Woodruff, David R; Chen, Weile; Adams, Thomas S; Lin, Henry; Eissenstat, David M

2016-04-01

We investigated depth of water uptake of trees on shale-derived soils in order to assess the importance of roots over a meter deep as a driver of water use in a central Pennsylvania catchment. This information is not only needed to improve basic understanding of water use in these forests but also to improve descriptions of root function at depth in hydrologic process models. The study took place at the Susquehanna Shale Hills Critical Zone Observatory in central Pennsylvania. We asked two main questions: (i) Do trees in a mixed-hardwood, humid temperate forest in a central Pennsylvania catchment rely on deep roots for water during dry portions of the growing season? (ii) What is the role of tree genus, size, soil depth and hillslope position on the depth of water extraction by trees? Based on multiple lines of evidence, including stable isotope natural abundance, sap flux and soil moisture depletion patterns with depth, the majority of water uptake during the dry part of the growing season occurred, on average, at less than ∼60 cm soil depth throughout the catchment. While there were some trends in depth of water uptake related to genus, tree size and soil depth, water uptake was more uniformly shallow than we expected. Our results suggest that these types of forests may rely considerably on water sources that are quite shallow, even in the drier parts of the growing season. © The Author 2015. Published by Oxford University Press.

Impact of interspecific interactions on the soil water uptake depth in a young temperate mixed species plantation

Science.gov (United States)

Grossiord, Charlotte; Gessler, Arthur; Granier, André; Berger, Sigrid; Bréchet, Claude; Hentschel, Rainer; Hommel, Robert; Scherer-Lorenzen, Michael; Bonal, Damien

2014-11-01

Interactions between tree species in forests can be beneficial to ecosystem functions and services related to the carbon and water cycles by improving for example transpiration and productivity. However, little is known on below- and above-ground processes leading to these positive effects. We tested whether stratification in soil water uptake depth occurred between four tree species in a 10-year-old temperate mixed species plantation during a dry summer. We selected dominant and co-dominant trees of European beech, Sessile oak, Douglas fir and Norway spruce in areas with varying species diversity, competition intensity, and where different plant functional types (broadleaf vs. conifer) were present. We applied a deuterium labelling approach that consisted of spraying labelled water to the soil surface to create a strong vertical gradient of the deuterium isotope composition in the soil water. The deuterium isotope composition of both the xylem sap and the soil water was measured before labelling, and then again three days after labelling, to estimate the soil water uptake depth using a simple modelling approach. We also sampled leaves and needles from selected trees to measure their carbon isotope composition (a proxy for water use efficiency) and total nitrogen content. At the end of the summer, we found differences in the soil water uptake depth between plant functional types but not within types: on average, coniferous species extracted water from deeper layers than did broadleaved species. Neither species diversity nor competition intensity had a detectable influence on soil water uptake depth, foliar water use efficiency or foliar nitrogen concentration in the species studied. However, when coexisting with an increasing proportion of conifers, beech extracted water from progressively deeper soil layers. We conclude that complementarity for water uptake could occur in this 10-year-old plantation because of inherent differences among functional groups (conifers

Soil Water: Advanced Crop and Soil Science. A Course of Study.

Science.gov (United States)

Miller, Larry E.

The course of study represents the fourth of six modules in advanced crop and soil science and introduces the agriculture student to the topic of soil water. Upon completing the three day module, the student will be able to classify water as to its presence in the soil, outline the hydrological cycle, list the ways water is lost from the soil,…

Remediation of uranium contaminated soils with bicarbonate extraction and microbial U(VI) reduction

Science.gov (United States)

Philips , Elizabeth J.P.; Landa, Edward R.; Lovely, Derek R.

1995-01-01

A process for concentrating uranium from contaminated soils in which the uranium is first extracted with bicarbonate and then the extracted uranium is precipitated with U(VI)-reducing microorganisms was evaluated for a variety of uranuum-contaminated soils. Bicarbonate (100 mM) extracted 20–94% of the uranium that was extracted with nitric acid. The U(VI)-reducing microorganism,Desulfovibrio desulfuricans reduced the U(VI) to U(IV) in the bicarbonate extracts. In some instances unidentified dissolved extracted components, presumably organics, gave the extract a yellow color and inhibited U(VI) reduction and/or the precipitation of U(IV). Removal of the dissolved yellow material with the addition of hydrogen peroxide alleviated this inhibition. These results demonstrate that bicarbonate extraction of uranium from soil followed by microbial U(VI) reduction might be an effective mechanism for concentrating uranium from some contaminated soils.

Remediation of uranium contaminated soils with bicarbonate extraction and microbial U(VI) reduction

International Nuclear Information System (INIS)

Phillips, E.J.P.; Landa, E.R.; Lovley, D.R.

1995-01-01

A process for concentrating uranium from contaminated soils in which the uranium is first extracted with bicarbonate and then the extracted uranium is precipitated with U(VI)-reducing microorganisms was evaluated for a variety of uranium-contaminated soils. Bicarbonate (100 mM) extracted 20-94% of the uranium that was extracted with nitric acid. The U(VI)-reducing microorganism, Desulfovibrio desulfuricans reduced the U(VI) to U(IV) in the bicarbonate extracts. In some instances unidentified dissolved extracted components, presumably organics, gave the extract a yellow color and inhibited U(VI) reduction and/or the precipitation of U(IV). Removal of the dissolved yellow material with the addition of hydrogen peroxide alleviated this inhibition. These results demonstrate that bicarbonate extraction of uranium from soil followed by microbial U(VI) reduction might be an effective mechanism for concentrating uranium from some contaminated soils. (author)

Combined in-situ and ex-situ bioremediation of petroleum hydrocarbon contaminated soils by closed-loop soil vapor extraction and air injection

International Nuclear Information System (INIS)

Hu, S.S.; Buckler, M.J.

1993-01-01

Treatment and restoration of petroleum hydrocarbon contaminated soils at a bulk petroleum above-ground storage tank (AST) site in Michigan is being conducted through in-situ and ex-situ closed-loop soil vapor extraction (SVE), soil vapor treatment, and treated air injection (AI) processes. The soil vapor extraction process applies a vacuum through the petroleum hydrocarbon affected soils in the ex-situ bio-remediation pile (bio-pile) and along the perimeter of excavated area (in-situ area) to remove the volatile or light petroleum hydrocarbons. This process also draws ambient air into the ex-situ bio-pile and in-situ vadose zone soil along the perimeter of excavated area to enhance biodegradation of light and heavy petroleum hydrocarbons in the soil. The extracted soil vapor is treated using a custom-designed air bio-remediation filter (bio-filter) to degrade the petroleum hydrocarbon compounds in the soil vapor extraction air streams. The treated air is then injected into a flush grade soil bed in the backfill area to perform final polishing of the air stream, and to form a closed-loop air flow with the soil vapor extraction perforated pipes along the perimeter of the excavated area

Sequential extraction for the speciation of some heavy metals in soils

International Nuclear Information System (INIS)

Zemberyova, M.; Zwaik, A.A.H.; Farkasovska, I.

1998-01-01

The five step sequential extraction for speciation of copper and nickel originally designed for sediments has been applied to soil samples. The extractant solutions were: 1 mol/l ammonium acetate, 1 mol/l hydroxylammonium chloride in 25% acetic acid (1:1), 0.1 mol/l hydrochlorid acid, 0.5 mol/l sodium hydroxide and 8 mol/l nitric acid. The residue was decomposed by HF and HNO 3 . Using this procedure the metal fraction bound to the organic matter can be distinguished. The concentrations of analytes were determined in the soil extracts by FAAS and ETAAS. Accuracy was assessed by comparing the sum of the contents of copper and nickel in soil extracts with the total certified values of CRMs of soils. The overall recovery values for nickel was 84-105% and for copper 105-114%. (author)

Multimedia risk-based soil cleanup at a gasoline-contaminated site using vapor extraction

International Nuclear Information System (INIS)

Mills, W.B.; Johnson, K.M.; Liu, S.; Loh, J.Y.; Lew, C.S.

1996-01-01

At a utility service center, gasoline from an underground storage tank had leaked into subsurface vadose zone soils for several years. To remediate the site, a soil vapor extraction (SVE) system was installed and operated. At the completion of the SVE operation, gasoline-containing residues in several confirmation soil borings exceeded agency-mandated cleanup levels. Rather than continue with SVE, a risk-based approach was developed to evaluate what levels of gasoline-containing residues could be left in the soil and still protect human health. The risk-based approach consisted of simulating the fate of chemical residues through the vadose zone and then into both the ground water and atmosphere. Receptor point concentrations were predicted, and health risks were assessed. The risk assessment concluded that ingestion of contaminated ground water and inhalation of air while showering were the largest potential contributors to risk, and that risks associated with inhalation of vapor-containing ambient air are small. However, all predicted risks are below the acceptable risk levels of 10 -6 individual cancer risk probability and 1.0 hazard index. Therefore, the lead agency accepted the recommendation that the site requires no further remediation. The service center continues normal operations today

Soil-Water Repellency Characteristic Curves for Soil Profiles with Organic Carbon Gradients

DEFF Research Database (Denmark)

Wijewardana, Nadeeka Senani; Muller, Karin; Moldrup, Per

2016-01-01

Soil water repellency (SWR) of soils is a property with significant consequences for agricultural water management, water infiltration, contaminant transport, and for soil erosion. It is caused by the presence of hydrophobic agents on mineral grain surfaces. Soils were samples in different depths......, and the sessile drop method (SDM). The aim to (i) compare the methods, (ii) characterize the soil-water repellency characteristic curves (SWRCC) being SWR as a function of the volumetric soil-water content (θ) or matric potential (ψ), and (iii) find relationships between SWRCC parameters and SOC content. The WDPT...... at three forest sites in Japan and three pasture sites in New Zealand, covering soil organic carbon (SOC) contents between 1 and 26%. The SWR was measured over a range of water contents by three common methods; the water drop penetration time (WDPT) test, the molarity of an ethanol droplet (MED) method...

Modeling Water Pollution of Soil

Directory of Open Access Journals (Sweden)

V. Doležel

2008-01-01

Full Text Available The government of the Czech Republic decided that in the location to the west of Prague, capital city of the Czech Republic, some deep mines should be closed because of their low efficiency of coal mined i.e. small amounts and low quality of the coal extracted in the final stage of mining. The locations near Prague influenced the decision to do maintenance on the abandoned mines, as the thread of soil pollution was unacceptably high in the neighborhood of the capital city. Before the mines were closed it was necessary to separate existed extensive horizontal location of salt water below a clay layer in order not to deteriorate the upper fresh water. The salt water could not be allowed to pollute the upper layer with the fresh water, as many wells in villages in the neighborhood of the former mines would be contaminated. Two horizontal clay layers (an insulator and a semi-insulator separated the two horizons containing salt water and fresh water. Before starting deep mining, vertical shafts had to be constructed with concrete linings to enable the miners to access the depths. The salt water was draining away throughout the existence of the mine. The drainage was designed very carefully to avoid possible infiltration of salt water into the upper horizon. Before the mines were abandoned it was necessary to prevent contact between the two kinds of waters in the shafts. Several options were put forward, the most efficient of which appeared to be one that proposed filling the shafts with spoil soil and creating a joint seal made of disparate material at the interface between the salt water and fresh water to create a reliable stopper. The material for the spoil soil was delivered from deposits located not far from the shafts. This material consisted of a variety of grains of sand, big boulders of slate, slaty clay, sandstone, etc.. Chemical admixtures were considered to improve the flocculation of the filling material. The stopper was positioned at a

Bioremediation of petroleum hydrocarbon contaminated soils using soil vapor extraction: Case study

International Nuclear Information System (INIS)

Roth, R.J.; Peterson, R.M.

1994-01-01

Soils contaminated with petroleum hydrocarbons are being remediated in situ at a site in Lakewood, New Jersey by bioremediation in conjunction with soil vapor extractions (SVE) and nutrient addition. The contaminants were from hydraulic oils which leaked from subsurface hydraulic lifts, waste oil from leaking underground storage tanks (USTs), an aboveground storage tank, and motor oil from a leaking UST. The oils contaminated subsurface soils at the site to a depth of 25 feet. Approximately 900 cubic yards of soil were contaminated. Soil sample analyses showed total petroleum hydrocarbon (TPH) concentrations up to 31,500 ppm. The design of the remedial system utilized the results of a treatability study which showed that TPH degrading microorganisms, when supplied with oxygen and nutrients, affected a 14% reduction in TPH in 30 days. A SVE system was installed which used three wells, each installed to a depth of 25 feet below grade. The SVE system was operated to achieve an extracted air flow of approximately 20 to 30 scfm from each well. Bioremediation of the TPH was monitored by measuring CO 2 and O 2 concentrations at the wellheads and vapor monitoring probes. After four months of remediation, CO 2 concentrations were at a minimum, at which point the subsurface soils were sampled and analyzed for TPH. The soil analyses showed a removal of TPH by biodegradation of up to 99.8% after four months of remediation

Gravel admix, vegetation, and soil water interactions in protective barriers: Experimental design, construction, and initial conditions

International Nuclear Information System (INIS)

Waugh, W.J.

1989-05-01

The purpose of this study is to measure the interactive effects of gravel admix and greater precipitation on soil water storage and plant abundance. The study is one of many tasks in the Protective Barrier Development Program for the disposal of Hanford defense waste. A factorial field-plot experiment was set up at the site selected as the borrow area for barrier topsoil. Gravel admix, vegetation, and enhanced precipitation treatments were randomly assigned to the plots using a split-split plot design structure. Changes in soil water storage and plant cover were monitored using neutron probe and point intercept methods, respectively. The first-year results suggest that water extraction by plants will offset gravel-caused increases in soil water storage. Near-surface soil water contents were much lower in graveled plots with plants than in nongraveled plots without plants. Large inherent variability in deep soil water storage masked any effects gravel may have had on water content below the root zone. In the future, this source of variation will be removed by differencing monthly data series and testing for changes in soil water storage. Tests of the effects of greater precipitation on soil water storage were inconclusive. A telling test will be possible in the spring of 1988, following the first wet season during which normal precipitation is doubled. 26 refs., 9 figs., 9 tabs

Heavy metals in a degraded soil treated with sludge from water treatment plant

Directory of Open Access Journals (Sweden)

Teixeira Sandra Tereza

2005-01-01

Full Text Available The application of water treatment sludge (WTS to degraded soil is an alternative for both residue disposal and degraded soil reclaim. This study evaluated effects of the application of water treatment sludge to a Typic Hapludox soil degraded by tin mining in the National Forest of Jamari, State of Rondonia, Brazil, on the content of heavy metals. A completely randomized experimental design with five treatments was used: control (n = 4; chemical control, which received only liming (n = 4; and rates D100, D150 and D200, which corresponded to 100, 150 and 200 mg of N-sludge kg-1 soil (n = 20, respectively. Thirty days after liming, period in which soil moisture was kept at 70% of the retention capacity, soil samples were taken and analyzed for total and extractable Fe, Cu, Mn, Zn, Cd, Pb, Ni, and Cr. The application of WTS increased heavy-metal contents in the degraded soil. Although heavy metals were below their respective critical limits, sludge application onto degraded areas may cause hazardous environmental impact and thus must be monitored.

Modelling soil water dynamics and crop water uptake at the field level

NARCIS (Netherlands)

Kabat, P.; Feddes, R.A.

1995-01-01

Parametrization approaches to model soil water dynamics and crop water uptake at field level were analysed. Averaging and numerical difficulties in applying numerical soil water flow models to heterogeneous soils are highlighted. Simplified parametrization approaches to the soil water flow, such as

Soil Water Retention Curve

Science.gov (United States)

Johnson, L. E.; Kim, J.; Cifelli, R.; Chandra, C. V.

2016-12-01

Potential water retention, S, is one of parameters commonly used in hydrologic modeling for soil moisture accounting. Physically, S indicates total amount of water which can be stored in soil and is expressed in units of depth. S can be represented as a change of soil moisture content and in this context is commonly used to estimate direct runoff, especially in the Soil Conservation Service (SCS) curve number (CN) method. Generally, the lumped and the distributed hydrologic models can easily use the SCS-CN method to estimate direct runoff. Changes in potential water retention have been used in previous SCS-CN studies; however, these studies have focused on long-term hydrologic simulations where S is allowed to vary at the daily time scale. While useful for hydrologic events that span multiple days, the resolution is too coarse for short-term applications such as flash flood events where S may not recover its full potential. In this study, a new method for estimating a time-variable potential water retention at hourly time-scales is presented. The methodology is applied for the Napa River basin, California. The streamflow gage at St Helena, located in the upper reaches of the basin, is used as the control gage site to evaluate the model performance as it is has minimal influences by reservoirs and diversions. Rainfall events from 2011 to 2012 are used for estimating the event-based SCS CN to transfer to S. As a result, we have derived the potential water retention curve and it is classified into three sections depending on the relative change in S. The first is a negative slope section arising from the difference in the rate of moving water through the soil column, the second is a zero change section representing the initial recovery the potential water retention, and the third is a positive change section representing the full recovery of the potential water retention. Also, we found that the soil water moving has traffic jam within 24 hours after finished first

Sorption of Tannin and Related Phenolic Compounds and Effects on Extraction of Soluble-N in Soil Amended with Several Carbon Sources

Directory of Open Access Journals (Sweden)

Javier M. Gonzalez

2012-02-01

Full Text Available Some tannins sorb to soil and reduce soluble-N. However, we know little about how they interact with organic amendments in soil. Soil (0–5 cm from plots, which were amended annually with various carbon substances, was treated with water (control or solutions containing tannins or related phenolic subunits. Treatments included a proanthocyanidin, catechin, tannic acid, β-1,2,3,4,6-penta-O-galloyl-D-glucose (PGG, gallic acid, and methyl gallate. We applied solutions of each of these materials to soil and measured soluble-C and -N in supernatants after application and following extraction with hot water (16 h, 80 °C. Sorption was low for non-tannin phenolics, methyl gallate, gallic acid, and catechin, and unaffected by amendment. Sorption of tannins, proanthocyanidin, tannic acid, and PGG, was higher and greater in plots amended with biosolids or manure. Extraction of soluble-N was not affected by amendment or by catechin, proanthocyanidin, or methyl gallate, but was reduced with PGG, tannic acid and gallic acid. Soil cation exchange capacity increased following treatment with PGG but decreased with gallic acid, irrespective of amendment. Tannins entering soil may thus influence soil organic matter dynamics and nutrient cycling but their impact may be influenced by the composition of soil organic matter.

SOIL PHOSPHORUS THRESHOLDS IN EVALUATING RISK OF ENVIRONMENTAL TRANSFER TO SURFACE WATERS IN SANTA CATARINA, BRAZIL

Directory of Open Access Journals (Sweden)

Luciano Colpo Gatiboni

2015-08-01

Full Text Available The State of Santa Catarina, Brazil, has agricultural and livestock activities, such as pig farming, that are responsible for adding large amounts of phosphorus (P to soils. However, a method is required to evaluate the environmental risk of these high soil P levels. One possible method for evaluating the environmental risk of P fertilization, whether organic or mineral, is to establish threshold levels of soil available P, measured by Mehlich-1 extractions, below which there is not a high risk of P transfer from the soil to surface waters. However, the Mehlich-1 extractant is sensitive to soil clay content, and that factor should be considered when establishing such P-thresholds. The objective of this study was to determine P-thresholds using the Mehlich-1 extractant for soils with different clay contents in the State of Santa Catarina, Brazil. Soil from the B-horizon of an Oxisol with 800 g kg-1 clay was mixed with different amounts of sand to prepare artificial soils with 200, 400, 600, and 800 g kg-1 clay. The artificial soils were incubated for 30 days with moisture content at 80 % of field capacity to stabilize their physicochemical properties, followed by additional incubation for 30 days after liming to raise the pH(H2O to 6.0. Soil P sorption curves were produced, and the maximum sorption (Pmax was determined using the Langmuir model for each soil texture evaluated. Based on the Pmax values, seven rates of P were added to four replicates of each soil, and incubated for 20 days more. Following incubation, available P contents (P-Mehlich-1 and P dissolved in the soil solution (P-water were determined. A change-point value (the P-Mehlich-1 value above which P-water starts increasing sharply was calculated through the use of segmented equations. The maximum level of P that a soil might safely adsorb (P-threshold was defined as 80 % of the change-point value to maintain a margin for environmental safety. The P-threshold value, in mg dm-3

Effect of soil and water environment on typeability of PowerPlex Y (Promega) in selected tissue samples.

OpenAIRE

Ewa Koc-Zorawska; Jerzy Janica; Malgorzata Skawronska; Jacek Robert Janica; Witold Pepinski; Anna Niemcunowicz-Janica; Ireneusz Stolyszewski

2008-01-01

In cases of decomposed bodies Y chromosomal STR markers may be useful in identification of a male relative. The authors assessed typeability PowerPlex Y (Promega) loci in tissue material stored in water and soil environment. Tissue material was collected during autopsies of five persons aged 20-30 years with time of death determined within the limit of 14 hours. Heart muscle, liver and lung specimens were stored in pond water, sea water, sand and peat soil. DNA was extracted by organic method...

Variation of the rare earth element concentrations in the soil, soil extract and in individual plants from the same site

International Nuclear Information System (INIS)

Wyttenbach, A.; Tobler, L.; Furrer, V.; Schleppi, P.

1998-01-01

Samples of various types (spruce needles, blackberry leaves, soils, and soil extracts) have each been taken at 6 places from the same site. In addition, 4 whirls each from 2 spruce trees were sampled. Rare earth elements (REEs) were determined in these samples by neutron activation analysis with a chemical group separation. Variations between places were found to be small with soils and soil extracts, but large with plants. Variations between whirls were small. Plants neither reflected the soil nor the soil extract. Both plant species were dissimilar, but the logarithm of their ratio was a linear function of the atomic number of the REE. A negative Ce anomaly (with respect to soil) was found in both plant species. (author)

Partitioning of Iron and Scandium in Soils Having Water Drainage Limitations

International Nuclear Information System (INIS)

Aide, M.; Braden, I.; Mueller, W.

2010-01-01

Soil chemistry of Fe includes weathering reactions, adsorption, hydrolysis, complexation, and oxidation-reduction reactions. Soil chemistry for scandium (Sc) is similar, but Sc does not include oxidation-reduction reactions. To determine if geochemical analysis may be used to identify Sc partitioning with respect to Fe among the particle size fractions, two Alfisol and two Ultisol soils were assessed using an aqua-regia digestion to estimate Sc and Fe concentrations for whole soil and particle size separates. Aqua-regia digestion data showed Sc depletion relative to Fe in sand separate. Sand separate is largely composed on quartz sand and Fe-Mn-bearing nodules, which are redoximorphic features produced by alternating oxic and suboxic/anoxic conditions associated with seasonally fluctuating water tables. Relative partitioning of Fe and Sc in these soils warrants further study to assess if selective extractions could quantify the extent of modern or ancestral oxidation-reduction processes responsible in some soil features involved in soil genesis.

Effect of water treatment residuals on soil phosphorus, copper and aluminium availability and toxicity

Energy Technology Data Exchange (ETDEWEB)

Lombi, E., E-mail: enzo.lombi@unisa.edu.a [CSIRO Land and Water, Centre for Environmental Contaminant Research, PMB 2, Glen Osmond, SA 5064 (Australia); Centre for Environmental Risk Assessment and Remediation, University of South Australia, Building X, Mawson Lakes Campus, Mawson Lakes, SA 5095 (Australia); CRC CARE, PO Box 486, Salisbury, SA 5106 (Australia); Stevens, D.P. [CSIRO Land and Water, Centre for Environmental Contaminant Research, PMB 2, Glen Osmond, SA 5064 (Australia); Arris Pty Ltd, PO Box 5143, Burnley, Victoria 3121 (Australia); McLaughlin, M.J. [CSIRO Land and Water, Centre for Environmental Contaminant Research, PMB 2, Glen Osmond, SA 5064 (Australia); Soil and Land Systems, University of Adelaide, PMB 1, Glen Osmond, SA 5064 (Australia)

2010-06-15

Water treatment residuals (WTRs) are produced by the treatment of potable water with coagulating agents. Beneficial recycling in agriculture is hampered by the fact that WTRs contain potentially toxic contaminants (e.g. copper and aluminium) and they bind phosphorus strongly. These issues were investigated using a plant bioassay (Lactuca sativa), chemical extractions and an isotopic dilution technique. Two WTRs were applied to an acidic and a neutral pH soil at six rates. Reductions in plant growth in amended soils were due to WTR-induced P deficiency, rather than Al or Cu toxicity. The release of potentially toxic Al from WTRs was found to be mitigated by their alkaline nature and pH buffering capacity. However, acidification of WTRs was shown to release more soluble Al than soil naturally high in Al. Copper availability was relatively low in all treatments. However, the lability of WTR-Cu increased when the WTR was applied to the soil. - The effect of water treatment residue application to soil was investigated in relation to phosphorus availability, and copper and aluminium phytotoxicity.

Effect of water treatment residuals on soil phosphorus, copper and aluminium availability and toxicity

International Nuclear Information System (INIS)

Lombi, E.; Stevens, D.P.; McLaughlin, M.J.

2010-01-01

Water treatment residuals (WTRs) are produced by the treatment of potable water with coagulating agents. Beneficial recycling in agriculture is hampered by the fact that WTRs contain potentially toxic contaminants (e.g. copper and aluminium) and they bind phosphorus strongly. These issues were investigated using a plant bioassay (Lactuca sativa), chemical extractions and an isotopic dilution technique. Two WTRs were applied to an acidic and a neutral pH soil at six rates. Reductions in plant growth in amended soils were due to WTR-induced P deficiency, rather than Al or Cu toxicity. The release of potentially toxic Al from WTRs was found to be mitigated by their alkaline nature and pH buffering capacity. However, acidification of WTRs was shown to release more soluble Al than soil naturally high in Al. Copper availability was relatively low in all treatments. However, the lability of WTR-Cu increased when the WTR was applied to the soil. - The effect of water treatment residue application to soil was investigated in relation to phosphorus availability, and copper and aluminium phytotoxicity.

The variations of aluminium species in mountainous forest soils and its implications to soil acidification.

Science.gov (United States)

Bradová, Monika; Tejnecký, Václav; Borůvka, Luboš; Němeček, Karel; Ash, Christopher; Šebek, Ondřej; Svoboda, Miroslav; Zenáhlíková, Jitka; Drábek, Ondřej

2015-11-01

Aluminium (Al) speciation is a characteristic that can be used as a tool for describing the soil acidification process. The question that was answered is how tree species (beech vs spruce) and type of soil horizon affect Al speciation. Our hypotesis is that spruce and beech forest vegetation are able to modify the chemical characteristics of organic horizon, hence the content of Al species. Moreover, these characteristics are seasonally dependent. To answer these questions, a detailed chromatographic speciation of Al in forest soils under contrasting tree species was performed. The Jizera Mountains area (Czech Republic) was chosen as a representative mountainous soil ecosystem. A basic forestry survey was performed on the investigated area. Soil and precipitation samples (throughfall, stemflow) were collected under both beech and spruce stands at monthly intervals from April to November during the years 2008-2011. Total aluminium content and Al speciation, pH, and dissolved organic carbon were determined in aqueous soil extracts and in precipitation samples. We found that the most important factors affecting the chemistry of soils, hence content of the Al species, are soil horizons and vegetation cover. pH strongly affects the amount of Al species under both forests. Fermentation (F) and humified (H) organic horizons contain a higher content of water extractable Al and Al(3+) compared to organo-mineral (A) and mineral horizons (B). With increasing soil profile depth, the amount of water extractable Al, Al(3+) and moisture decreases. The prevailing water-extractable species of Al in all studied soils and profiles under both spruce and beech forests were organically bound monovalent Al species. Distinct seasonal variations in organic and mineral soil horizons were found under both spruce and beech forests. Maximum concentrations of water-extractable Al and Al(3+) were determined in the summer, and the lowest in spring.

Three Principles of Water Flow in Soils

Science.gov (United States)

Guo, L.; Lin, H.

2016-12-01

Knowledge of water flow in soils is crucial to understanding terrestrial hydrological cycle, surface energy balance, biogeochemical dynamics, ecosystem services, contaminant transport, and many other Critical Zone processes. However, due to the complex and dynamic nature of non-uniform flow, reconstruction and prediction of water flow in natural soils remain challenging. This study synthesizes three principles of water flow in soils that can improve modeling water flow in soils of various complexity. The first principle, known as the Darcy's law, came to light in the 19th century and suggested a linear relationship between water flux density and hydraulic gradient, which was modified by Buckingham for unsaturated soils. Combining mass balance and the Buckingham-Darcy's law, L.A. Richards quantitatively described soil water change with space and time, i.e., Richards equation. The second principle was proposed by L.A. Richards in the 20th century, which described the minimum pressure potential needed to overcome surface tension of fluid and initiate water flow through soil-air interface. This study extends this principle to encompass soil hydrologic phenomena related to varied interfaces and microscopic features and provides a more cohesive explanation of hysteresis, hydrophobicity, and threshold behavior when water moves through layered soils. The third principle is emerging in the 21st century, which highlights the complex and evolving flow networks embedded in heterogeneous soils. This principle is summarized as: Water moves non-uniformly in natural soils with a dual-flow regime, i.e., it follows the least-resistant or preferred paths when "pushed" (e.g., by storms) or "attracted" (e.g., by plants) or "restricted" (e.g., by bedrock), but moves diffusively into the matrix when "relaxed" (e.g., at rest) or "touched" (e.g., adsorption). The first principle is a macroscopic view of steady-state water flow, the second principle is a microscopic view of interface

Effects of seasonal and well construction variables on soil vapor extraction pilot tests

International Nuclear Information System (INIS)

Campbell, R.; Hudon, N.; Bass, D.

1995-01-01

The selection and design of an effective soil vapor extraction system is dependent upon data generated from pilot testing. Therefore, it is critical to understand factors that may affect the testing prior to selecting or designing a system. In Sebago Lake Village, Maine, two adjacent gasoline stations experienced a release. Gasoline migrated through fine sand into the groundwater and discharged to a small stream. Soil vapor extraction was investigated as a remedial alternative to reduce volatile organic compounds in the unsaturated soil. Three soil vapor extraction pilot tests were performed at one of the sites and one test at the other site. The results of the testing varied. Data collected during a summer test indicated soil vapor extraction was less likely to work. The wells tested were installed using an excavator. An adequate surface seal was not present in any of the tested wells. An additional test was performed in the winter using wells installed by a drill rig. Winter test results indicated that soil vapor extraction could be effective. Another test was performed after a horizontal soil vapor extraction system with a surface seal was installed. The results of this testing indicated that soil vapor extraction was more effective than predicted by the earlier tests. Tests performed on the other property indicated that the horizontal wells were more effective than the vertical wells. Testing results were affected by the well installation method, well construction, proximity to manmade structures, and the season in which testing was performed. Understanding factors that affect the testing is critical in selecting and designing the system

Distributions and concentrations of thallium in Korean soils determined by single and sequential extraction procedures.

Science.gov (United States)

Lee, Jin-Ho; Kim, Dong-Jin; Ahn, Byung-Koo

2015-06-01

The objectives of this study were to investigate the distribution of thallium in soils collected near suspected areas such as cement plants, active and closed mines, and smelters and to examine the extraction of thallium in the soils using 19 single chemical and sequential chemical extraction procedures. Thallium concentrations in soils near cement plants were distributed between 1.20 and 12.91 mg kg(-1). However, soils near mines and smelters contained relatively low thallium concentrations ranging from 0.18 to 1.09 mg kg(-1). Thallium extractability with 19 single chemical extractants from selected soils near cement plants ranged from 0.10% to 8.20% of the total thallium concentration. In particular, 1.0 M NH4Cl, 1.0 M (NH4)2SO4, and 1.0 M CH3COONH4 extracted more thallium than other extractants. Sequential fractionation results of thallium from different soils such as industrially and artificially contaminated soils varied with the soil properties, especially soil pH and the duration of thallium contamination.

Soil water capture trends over 50 years of single-cross maize (Zea mays L.) breeding in the US corn-belt.

Science.gov (United States)

Reyes, Andres; Messina, Carlos D; Hammer, Graeme L; Liu, Lu; van Oosterom, Erik; Lafitte, Renee; Cooper, Mark

2015-12-01

Breeders have successfully improved maize (Zea mays L.) grain yield for the conditions of the US corn-belt over the past 80 years, with the past 50 years utilizing single-cross hybrids. Long-term improvement for grain yield under water-limited conditions has also been reported. Grain yield under water-limited conditions depends on water use, water use efficiency, and harvest index. It has been hypothesized that long-term genetic gain for yield could be due, in part, to increased water capture from the soil. This hypothesis was tested using a set of elite single-cross hybrids that were released by DuPont Pioneer between 1963 and 2009. Eighteen hybrids were grown in the field during 2010 and 2011 growing seasons at Woodland, CA, USA. Crops grew predominantly on stored soil water and drought stress increased as the season progressed. Soil water content was measured to 300cm depth throughout the growing season. Significant water extraction occurred to a depth of 240-300cm and seasonal water use was calculated from the change in soil water over this rooting zone. Grain yield increased significantly with year of commercialization, but no such trend was observed for total water extraction. Therefore, the measured genetic gain for yield for the period represented by this set of hybrids must be related to either increased efficiency of water use or increased carbon partitioning to the grain, rather than increased soil water uptake. © The Author 2015. Published by Oxford University Press on behalf of the Society for Experimental Biology.

Electrokinetic extraction of chromate from unsaturated soils

International Nuclear Information System (INIS)

Mattson, E.D.; Lindgren, E.R.

1993-01-01

Heavy-metal contamination of soil and groundwater is a widespread problem in industrial nations. Remediation by excavation of such sites may not be cost effective or politically acceptable. Electrokinetic remediation is one possible remediation technique for in situ removal of such contaminants from unsaturated soils. Previous papers discussing the work performed by researchers at Sandia National Laboratories (SNL) and Sat-Unsat, Inc. (SUI) (Lindgren et al., 1991, 1992, 1993) focused on the transport of contaminants and dyes by electrokinetics in unsaturated soils. These experiments were conducted with graphite electrodes with no extraction system. As the contaminants migrated through the soil, they increased in concentration at the electrode creating a diffusion flux in the opposite direction. This paper discusses a technique to remove the contaminants from unsaturated soils once they have reached an electrode

Electrokinetic extraction of chromate from unsaturated soils

Energy Technology Data Exchange (ETDEWEB)

Mattson, E.D. [SAT-UNSAT, Inc., Albuquerque, NM (United States); Lindgren, E.R. [Sandia National Labs., Albuquerque, NM (United States)

1993-11-01

Heavy-metal contamination of soil and groundwater is a widespread problem in industrial nations. Remediation by excavation of such sites may not be cost effective or politically acceptable. Electrokinetic remediation is one possible remediation technique for in situ removal of such contaminants from unsaturated soils. Previous papers discussing the work performed by researchers at Sandia National Laboratories (SNL) and Sat-Unsat, Inc. (SUI) (Lindgren et al., 1991, 1992, 1993) focused on the transport of contaminants and dyes by electrokinetics in unsaturated soils. These experiments were conducted with graphite electrodes with no extraction system. As the contaminants migrated through the soil, they increased in concentration at the electrode creating a diffusion flux in the opposite direction. This paper discusses a technique to remove the contaminants from unsaturated soils once they have reached an electrode.

Soil water diffusivity as a function of water content and time

International Nuclear Information System (INIS)

Guerrini, I.A.

1976-04-01

The soil-water diffusivity has been studied as a function of water content and time. From the idea of studying the horizontal movement of water in swelling soils, a simple formulation has been achieved which allows for the diffusivity, water content dependency and time dependency, to be estimated, not only of this kind of soil, but for any other soil as well. It was observed that the internal rearrangement of soil particles is a more important phenomenon than swelling, being responsible for time dependency. The method 2γ is utilized, which makes it possible to simultaneously determine the water content and density, point by point, in a soil column. The diffusivity data thus obtained are compared to those obtained when time dependency is not considered. Finally, a new soil parameter, α, is introduced and the values obtained agrees with the internal rearrangment assumption and time dependency for diffusivity (Author) [pt

Chemical composition and Zn bioavailability of the soil solution extracted from Zn amended variable charge soils.

Science.gov (United States)

Zampella, Mariavittoria; Adamo, Paola

2010-01-01

A study on variable charge soils (volcanic Italian and podzolic Scottish soils) was performed to investigate the influence of soil properties on the chemical composition of soil solution. Zinc speciation, bioavailability and toxicity in the soil solution were examined. The soils were spiked with increasing amounts of Zn (0, 100, 200, 400 and 1000 mg/kg) and the soil solutions were extracted using rhizon soil moisture samplers. The pH, total organic carbon (TOC), base cations, anions, total Zn and free Zn2+ in soil solution were analysed. A rapid bioassay with the luminescent bacterium Escherichia coli HB101 pUCD607 was performed to assess Zn toxicity. The influence of soil type and Zn treatments on the chemical composition of soil solution and on Zn toxicity was considered and discussed. Different trends of total and free Zn concentrations, base cations desorption and luminescence of E. coli HB101 pUCD607 were observed. The soil solution extracted from the volcanic soils had very low total and free Zn concentrations and showed specific Zn2+/Ca2+ exchange. The soil solution from the podzolic soil had much higher total and free Zn concentrations and showed no evidence of specific Zn2+/Ca2+ exchange. In comparison with the subalkaline volcanic soils, the acidic podzol showed enhanced levels of toxic free Zn2+ and consequently stronger effects on E. coli viability.

A dual phased approach for bioremediation of petroleum contaminated soil and ground water

International Nuclear Information System (INIS)

Kennel, N.D.; Maher, A.; Buckallew, B.

1994-01-01

A case study will be presented to demonstrate an effective and timely method of site remediation which yields complete contaminant destruction rather than the contaminant transfer that traditional ground water extraction and treatment techniques result in. By utilizing bioremediation at this site, the client was able to completely degrade the contamination beneath the property, and in the process avoid future liability from transfer of the contamination to another party (i.e. landfill) or phase (i.e. liquid to vapor through air stripping). The provisions of a real estate transaction involving a former service station site in Central Iowa stipulated that the site be remediated prior to title transfer. Previous Environmental Investigative activities revealed significant soil and ground water contamination resulting from over 50 years of diesel and gasoline fuel storage and dispensing operations at the site. Microbial Environmental Services, Inc. (MES) utilized a dual phased bioremediation approach to meet regulatory clean-up guidelines in order for a timely property transfer to occur. To facilitate and expedite ground water remediation, contaminated soil was excavated and remediated via Advanced Biological Surface Treatment (ABST) techniques. ABST techniques are utilized by MES to treat excavated soil in closed cell to control emissions and treatment conditions. Following contaminant source removal, ground water was extracted and treated in a submerged, fixed film, flow through 1,000 gallon fixed film bioreactor at a rate of 2.5 gallons per minute

Chelant extraction and REDOX manipulation for mobilization of heavy metals from contaminated soils

International Nuclear Information System (INIS)

Brewster, M.D.; Peters, R.W.; Miller, G.A.; Patton, T.L.; Martino, L.E.

1994-01-01

Was the result of open burning and open detonation of chemical agents and munitions in the Toxic Burning Pits area at J-Field, located in the Edgewood Area of Aberdeen Proving Ground in Harford County, Maryland, soils have been contaminated with heavy metals. Simultaneous extraction is complicated because of the multitude of contaminant forms that exist. This paper uses data from a treatability study performed at Argonne National Laboratory to discuss and compare several treatment methods that were evaluated for remediating metals-contaminated soils. J-Field soils were subjected to a series of treatability experiments designed to determine the feasibility of using soil washing/soil flushing, enhancements to soil washing/soil flushing, solidification/stabilization, and electrokinetics for remediating soils contaminated with metals. Chelating and mobilizing agents evaluated included ammonium acetate, ethylenediaminetetraacetic acid, citric acid, Citranox, gluconic acid, phosphoric acid, oxalic acid, and nitrilotriacetic acid, in addition to pH-adjusted water. REDOX manipulation can maximize solubilities, increase desorption, and promote removal of heavy metal contaminants. Reducing agents that were studied included sodium borohydride, sodium metabisulfite, and thiourea dioxide. The oxidants studied included hydrogen peroxide, sodium percarbonate, sodium hypochlorite, and potassium permanganate. This paper summaries the results from the physical/chemical characterization, soil washing/soil flushing, and enhancements to soil washing/soil flushing portions of the study

Stochastic estimation of plant-available soil water under fluctuating water table depths

Science.gov (United States)

Or, Dani; Groeneveld, David P.

1994-12-01

Preservation of native valley-floor phreatophytes while pumping groundwater for export from Owens Valley, California, requires reliable predictions of plant water use. These predictions are compared with stored soil water within well field regions and serve as a basis for managing groundwater resources. Soil water measurement errors, variable recharge, unpredictable climatic conditions affecting plant water use, and modeling errors make soil water predictions uncertain and error-prone. We developed and tested a scheme based on soil water balance coupled with implementation of Kalman filtering (KF) for (1) providing physically based soil water storage predictions with prediction errors projected from the statistics of the various inputs, and (2) reducing the overall uncertainty in both estimates and predictions. The proposed KF-based scheme was tested using experimental data collected at a location on the Owens Valley floor where the water table was artificially lowered by groundwater pumping and later allowed to recover. Vegetation composition and per cent cover, climatic data, and soil water information were collected and used for developing a soil water balance. Predictions and updates of soil water storage under different types of vegetation were obtained for a period of 5 years. The main results show that: (1) the proposed predictive model provides reliable and resilient soil water estimates under a wide range of external conditions; (2) the predicted soil water storage and the error bounds provided by the model offer a realistic and rational basis for decisions such as when to curtail well field operation to ensure plant survival. The predictive model offers a practical means for accommodating simple aspects of spatial variability by considering the additional source of uncertainty as part of modeling or measurement uncertainty.

Enzymatic vegetable organic extracts as soil biochemical biostimulants and atrazine extenders.

Science.gov (United States)

García-Martínez, Ana María; Tejada, Manuel; Díaz, Ana Isabel; Rodríguez-Morgado, Bruno; Bautista, Juan; Parrado, Juan

2010-09-08

The purpose of this study was to gather information on the potential effects of organic biostimulants on soil activity and atrazine biodegradation. Carob germ enzymatic extract (CGEE) and wheat condensed distiller solubles enzymatic extract (WCDS-EE) have been obtained using an enzymatic process; their main organic components are soluble carbohydrates and proteins in the form of peptides and free amino acids. Their application to soil results in high biostimulation, rapidly increased dehydrogenase, phosphatase and glucosidase activities, and an observed atrazine extender capacity due to inhibition of its mineralization. The extender capacity of both extracts is proportional to the protein/carbohydrate ratio content. As a result, these enzymatic extracts are highly microbially available, leading to two independent phenomena, fertility and an atrazine persistence that is linked to increased soil activity.

Remediation of cadmium contaminated water and soil using vinegar residue biochar.

Science.gov (United States)

Li, Yuxin; Pei, Guangpeng; Qiao, Xianliang; Zhu, Yuen; Li, Hua

2018-06-01

This study investigated a new biochar produced from vinegar residue that could be used to remediate cadmium (Cd)-contaminated water and soil. Aqueous solution adsorption and soil incubation experiments were performed to investigate whether a biochar prepared at 700 °C from vinegar residue could efficiently adsorb and/or stabilize Cd in water and soil. In the aqueous solution adsorption experiment, the Cd adsorption process was best fitted by the pseudo-second-order kinetic and Freundlich isotherm models. If the optimum parameters were used, i.e., pH 5 or higher, a biochar dosage of 12 g L -1 , a 10 mg L -1 Cd initial concentration, and 15-min equilibrium time, at 25 °C, then Cd removal could reach about 100%. The soil incubation experiment evaluated the biochar effects at four different application rates (1, 2, 5, and 10% w/w) and three Cd contamination rates (0.5, 1, and 2.5 mg kg -1 ) on soil properties and Cd fractionation. Soil pH and organic matter increased after adding biochar, especially at the 10% application rate. At Cd pollution levels of 1.0 or 2.5 mg kg -1 , a 10% biochar application rate was most effective. At 0.5 mg Cd kg -1 soil, a 5% biochar application rate was most efficient at transforming the acid extractable and easily reducible Cd fractions to oxidizable and residual Cd. The results from this study demonstrated that biochar made from vinegar residue could be a new and promising alternative biomass-derived material for Cd remediation in water and soil.

Evaluation of multi-walled carbon nanotubes as solid-phase extraction adsorbents of pesticides from agricultural, ornamental and forestal soils.

Science.gov (United States)

Asensio-Ramos, M; Hernández-Borges, J; Borges-Miquel, T M; Rodríguez-Delgado, M A

2009-08-11

A new, simple and cost-effective method based on the use of multi-walled carbon nanotubes (MWCNTs) as solid-phase extraction stationary phases is proposed for the determination of a group of seven organophosphorus pesticides (i.e. ethoprophos, diazinon, chlorpyriphos-methyl, fenitrothion, malathion, chlorpyriphos and phosmet) and one thiadiazine (buprofezin) in different kinds of soil samples (forestal, ornamental and agricultural) using gas chromatography with nitrogen phosphorus detection. Soils were first ultrasound extracted with 10 mL 1:1 methanol/acetonitrile (v/v) and the evaporated extract redissolved in 20 mL water (pH 6.0) was passed through 100 mg of MWCNTs of 10-15 nm o.d., 2-6 nm i.d. and 0.1-10 microm length. Elution was carried out with 20 mL dichloromethane. The method was validated in terms of linearity, precision, recovery, accuracy and selectivity. Matrix-matched calibration was carried out for each type of soil since statistical differences between the calibration curves constructed in pure solvent and in the reconstituted soil extract were found for most of the pesticides under study. Recovery values of spiked samples ranged between 54 and 91% for the three types of soils (limits of detection (LODs) between 2.97 and 9.49 ngg(-1)), except for chlorpyrifos, chlorpyrifos-methyl and buprofezin which ranged between 12 and 54% (LODs between 3.14 and 72.4 ngg(-1)), which are the pesticides with the highest soil organic carbon sorption coefficient (K(OC)) values. Using a one-sample test (Student's t-test) with fortified samples at two concentration levels in each type of soil, no significant differences were observed between the real and the experimental values (accuracy percentages ranged between 87 and 117%). It is the first time that the adsorptive potential of MWCNTs for the extraction of organophosphorus pesticides from soils is investigated.

Characterization of extractable soil organic matter pools from African Dark Earths (AfDE): A case study in historical biochar and organic waste amendments

Science.gov (United States)

Fujiu, Manna; Plante, Alain; Ohno, Tsutomu; Solomon, Dawit; Lehmann, Johannes; Fraser, James; Leach, Melissa; Fairhead, James

2014-05-01

Anthropogenic Dark Earths are soils generated through long-term human inputs of organic and pyrogenic materials. These soils were originally discovered in the Amazon, and have since been found in Australia and in this case in Africa. African Dark Earths (AfDE) are black, highly fertile and carbon-rich soils that were formed from the original highly-weathered infertile yellowish to red Oxisols and Ultisols through an extant but hitherto overlooked climate-smart sustainable soil management system that has long been an important feature of the indigenous West African agricultural repertoire. Studies have demonstrated that ADE soils in general have significantly different organic matter properties compared to adjacent non-DE soils, largely attributable to the presence of high concentrations of ash-derived carbon. Quantification and characterization of bulk soil organic matter of several (n=11) AfDE and non-AfDE pairs of surface (0-15 cm) soils using thermal analysis techniques (TG-DSC-EGA) confirmed substantial differences in SOM composition and the presence of pyrogenic C. Such pyrogenic organic matter is generally considered recalcitrant or relatively stable, but the goal of the current study was to characterize the presumably labile, more rapidly cycling, pools of C in AfDEs through the characterization of hot water- and pyrophosphate-extractable fractions, referred to as HWEOC and PyroC respectively. Extracts were analyzed for carbon content, as well as composition using fluorescence (EEM/PARAFAC) and high resolution mass spectrometry (FTICR-MS). The amount of extractable C as a proportion of total soil C was relatively low: less than ~0.8% for HWEOC and 2.8% for PyroC. The proportion of HWEOC did not differ (P = 0.18, paired t-test) between the AfDE and the non-AfDE soils, while the proportions of PyroC were significantly larger (P = 0.001) in the AfDE soils compared to the non-AfDE soils. Preliminary analysis of the EEM/PARAFAC data suggests that AfDE samples had

Soil clean up by vapour extraction: parametrical study; Depollution des sols par extraction sous pression reduite: etude de quelques parametres

Energy Technology Data Exchange (ETDEWEB)

Dutheil, C.

2003-05-15

Soil vapour extraction is a treatment process for soils polluted by volatile organic compounds. Its principle relies on the circulation of gaseous flow in soil by the application of a depression of some hundreds milli-bars. A parametrical study has been led on a soil artificially polluted by tri-chloro-ethene. It shows that the gaseous flow rate has a slight influence on pollutants extraction yield. This is due to rate limited mass transfer processes. Soil moisture plays a negative role on treatment efficiency because of the reduction of the porosity available for the gas circulation. Tests have been performed on a soil polluted by a complex mixture of organic pollutants to elaborate a methodology of technical feasibility assessment. This methodology aims at identifying and limiting risks of site rehabilitation failure. Tests results show that soil vapour extraction was inadequate to treat the soil tested in this study because of the strong affinity between a dense organic phase (grease) and chlorinated solvents. (author)

Validation of methods for the determination of radium in waters and soil

International Nuclear Information System (INIS)

Decaillon, J.-G.; Bickel, M.; Hill, C.; Altzitzoglou, T.

2004-01-01

This article describes the advantages and disadvantages of several analytical methods used to prepare the alpha-particle source. As a result of this study, a new method combining commercial extraction and ion chromatography prior to a final co-precipitation step is proposed. This method has been applied and validated on several matrices (soil, waters) in the framework of international intercomparisons. The integration of this method in a global procedure to analyze actinoids and radium from a single solution (or digested soil) is also described

Change of the Extractability of Cadmium Added to Different Soils: Aging Effect and Modeling

Directory of Open Access Journals (Sweden)

Xi Zhang

2018-03-01

Full Text Available Ethylenediaminetetraacetic acid (EDTA is known to be a chelating agent and has been widely used for estimating the total extractable metals in soil. The effect of aging on EDTA-extractable cadmium (Cd was investigated in five different soils at three Cd concentrations incubated for 180 days. The EDTA-extractable Cd rapidly decreased after incubated during 30–60 days, followed by slow processes, and for 90 days the EDTA-extractable Cd tended to be stable. The decrease in EDTA-extractable Cd may be due to precipitation/nucleation processes, diffusion of Cd into the micropores/mesopores, and occlusion within organic matter in soils. A semi-mechanistic model to predict the extractability of Cd during incubation, based on processes of Cd precipitation/nucleation, diffusion, and occlusion within organic matter, was developed and calibrated. The results showed that the processes of micropore/mesopore diffusion were predominant processes affecting the extractability of Cd added to soils, and were slow. However, the proportions of the processes of precipitation/nucleation and occlusion within organic matter to the non-EDTA-extractable Cd added to soils were only 0.03–21.0% and 0.41–6.95%, respectively. The measured EDTA-extractable Cd from incubated soils were in good agreement with those predicted by the semi-mechanistic model (R2 = 0.829. The results also indicated that soil pH, organic matter, and incubation time were the most important factors affecting Cd aging.

Proposal of new convenient extractant for assessing phytoavailability of heavy metals in contaminated sandy soil.

Science.gov (United States)

Korzeniowska, Jolanta; Stanislawska-Glubiak, Ewa

2017-06-01

The aim of the study was to compare the usefulness of 1 M HCl with aqua regia, EDTA, and CaCl 2 for the extraction of phytoavailable forms of Cu, Ni, and Zn on coarse-textured soils contaminated with these metals. Two microplot experiments were used for the studies. Reed canary grass (Phalaris arundinacea), maize (Zea mays), willow (Salix viminalis), spartina (Spartina pectinata), and miscanthus (Miscanthus × giganteus) were used as test plants. They were grown on soil artificially spiked with Cu, Ni, and Zn. The experimental design included a control and three increasing doses of metals. Microplots (1 m 2  × 1 m deep) were filled with sandy soil (clay-6%, pH 5.5, Corg-0.8%). Metals in the form of sulfates were dissolved in water and applied to the plot using a hand liquid sprayer. During the harvest, samples were collected from aboveground parts, roots, and the soil and then tested for their Cu, Zn, and Ni contents. The metal content of the soil was determined using four tested extractants. It was found that Cu and Ni were accumulated in roots in bigger amounts than Zn. The usefulness of the extractants was evaluated based on the correlation between the content of metals in the soil and the plant (n = 32). This study demonstrated that 1 M HCl, aqua regia, and EDTA were more efficient or equally useful for the assessment of the phytoavailability of Cu, Ni, and Zn as CaCl 2 . Due to the ease of performing determinations and their low cost, 1 M HCl can be recommended to assess the excess of Cu, Ni, and Zn in the coarse-textured soils.

Accelerated solvent extraction method with one-step clean-up for hydrocarbons in soil

International Nuclear Information System (INIS)

Nurul Huda Mamat Ghani; Norashikin Sain; Rozita Osman; Zuraidah Abdullah Munir

2007-01-01

The application of accelerated solvent extraction (ASE) using hexane combined with neutral silica gel and sulfuric acid/ silica gel (SA/ SG) to remove impurities prior to analysis by gas chromatograph with flame ionization detector (GC-FID) was studied. The efficiency of extraction was evaluated based on the three hydrocarbons; dodecane, tetradecane and pentadecane spiked to soil sample. The effect of ASE operating conditions (extraction temperature, extraction pressure, static time) was evaluated and the optimized condition obtained from the study was extraction temperature of 160 degree Celsius, extraction pressure of 2000 psi with 5 minutes static extraction time. The developed ASE with one-step clean-up method was applied in the extraction of hydrocarbons from spiked soil and the amount extracted was comparable to ASE extraction without clean-up step with the advantage of obtaining cleaner extract with reduced interferences. Therefore in the developed method, extraction and clean-up for hydrocarbons in soil can be achieved rapidly and efficiently with reduced solvent usage. (author)

Green Remediation Best Management Practices: Soil Vapor Extraction & Air Sparging

Science.gov (United States)

Historically, approximately one-quarter of Superfund source control projects have involved soil vapor extraction (SVE) to remove volatile organic compounds (VOCs) sorbed to soil in the unsaturated (vadose) zone.

Dynamics of dissolved and extractable organic nitrogen upon soil amendment with crop residues

NARCIS (Netherlands)

Ros, G.H.; Hoffland, E.

2010-01-01

Dissolved organic nitrogen (DON) is increasingly recognized as a pivotal pool in the soil nitrogen (N) cycle. Numerous devices and sampling procedures have been used to estimate its size, varying from in situ collection of soil solution to extraction of dried soil with salt solutions. Extractable

Using in situ pore water concentrations to estimate the phytotoxicity of nicosulfuron in soils to corn (Zea mays L.).

Science.gov (United States)

Liu, Kailin; Cao, Zhengya; Pan, Xiong; Yu, Yunlong

2012-08-01

The phytotoxicity of an herbicide in soil is typically dependent on the soil characteristics. To obtain a comparable value of the concentration that inhibits growth by 50% (IC50), 0.01 M CaCl(2) , excess pore water (EPW) and in situ pore water (IPW) were used to extract the bioavailable fraction of nicosulfuron from five different soils to estimate the nicosulfuron phytotoxicity to corn (Zea mays L.). The results indicated that the phytotoxicity of nicosulfuron in soils to corn depended on the soil type, and the IC50 values calculated based on the amended concentration of nicosulfuron ranged from 0.77 to 9.77 mg/kg among the five tested soils. The range of variation in IC50 values for nicosulfuron was smaller when the concentrations of nicosulfuron extracted with 0.01 M CaCl(2) and EPW were used instead of the amended concentration. No significant difference was observed among the IC50 values calculated from the IPW concentrations of nicosulfuron in the five tested soils, suggesting that the concentration of nicosulfuron in IPW could be used to estimate the phytotoxicity of residual nicosulfuron in soils. Copyright © 2012 SETAC.

Mitigation of dimethazone residues in soil and runoff water from agricultural field.

Science.gov (United States)

Antonious, George F

2011-01-01

Dimethazone, also known as clomazone [2-[(2-chlorophenyl) methyl]- 4,4-dimethyl-3-isoxaolidinone] is a pre-emergent nonionic herbicide commonly used in agriculture. A field study was conducted on a silty-loam soil of 10 % slope to monitor off-site movement and persistence of dimethazone in soil under three management practices. Eighteen plots of 22 x 3.7 m each were separated using stainless steel metal borders and the soil in six plots was mixed with municipal sewage sludge (MSS) and yard waste (YW) compost (MSS+YW) at 15 t acre⁻¹ on dry weight basis, six plots were mixed with MSS at 15 t acre⁻¹, and six unamended plots (NM) were used for comparison purposes. The objectives of this investigation were to: (i) monitor the dissipation and half-life (T₁/₂) of dimethazone in soil under three management practices; (ii) determine the concentration of dimethazone residues in runoff and infiltration water following natural rainfall events; and (iii) assess the impact of soil amendments on the transport of NO₃, NH₄, and P into surface and subsurface water. Gas chromatography/mass spectrometery (GC/MS) analyses of soil extracts indicated the presence of ion fragments at m/z 125 and 204 that can be used for identification of dimethazone residues. Intitial deposits of dimethazone varied from 1.3 μg g⁻¹ dry native soil to 3.2 and 11.8 μg g⁻¹ dry soil in MSS and MSS+YW amended soil, respectively. Decline of dimethazone residues in the top 15 cm native soil and soil incorporated with amendments revealed half-life (T₁/₂) values of 18.8, 25.1, and 43.0 days in MSS+YW, MSS, and NM treatments, respectively. Addition of MSS+YW mix and MSS alone to native soil increased water infiltration, lowering surface runoff water volume and dimethazone residues in runoff following natural rainfall events.

Biotoxicity of Mars soils: 2. Survival of Bacillus subtilis and Enterococcus faecalis in aqueous extracts derived from six Mars analog soils

Science.gov (United States)

Schuerger, Andrew C.; Ming, Doug W.; Golden, D. C.

2017-07-01

The search for an extant microbiota on Mars depends on exploring sites that contain transient or permanent liquid water near the surface. Examples of possible sites for liquid water may be active recurring slope lineae (RSL) and fluid inclusions in ice or salt deposits. The presence of saline fluids on Mars will act to depress the freezing points of liquid water to as low as ‒60 °C, potentially permitting the metabolism and growth of halophilic microorganisms to temperatures significantly below the freezing point of pure water at 0 °C. In order to predict the potential risks of forward contamination by Earth microorganisms to subsurface sites on Mars with liquid brines, experiments were designed to characterize the short-term survival of two bacteria in aqueous soil solutions from six analog soils. The term ''soil'' is used here to denote any loose, unconsolidated matrix with no implications for the presence or absence of organics or biology. The analog soils were previously described (Schuerger et al., 2012, Planetary Space Sci., 72, 91-101), and represented crushed Basalt (benign control), Salt, Acid, Alkaline, Aeolian, and Phoenix analogs on Mars. The survival rates of spores of Bacillus subtilis and vegetative cells of Enterococcus faecalis were tested in soil solutions from each analog at 24, 0, or ‒70 °C for time periods up to 28 d. Survival of dormant spores of B. subtilis were mostly unaffected by incubation in the aqueous extracts of all six Mars analogs. In contrast, survival rates of E. faecalis cells were suppressed by all soil solutions when incubated at 24 °C but improved at 0 and ‒70 °C, except for assays in the Salt and Acid soil solutions in which most cells were killed. Results suggest that Earth microorganisms that form spores may persist in liquid brines on Mars better than non-spore forming species, and thus, spore-forming species may pose a potential forward contamination risk to sites with liquid brines.

Validation of a spatial–temporal soil water movement and plant water uptake model

KAUST Repository

HEPPELL, J.

2014-06-01

© 2014, (publisher). All rights reserved. Management and irrigation of plants increasingly relies on accurate mathematical models for the movement of water within unsaturated soils. Current models often use values for water content and soil parameters that are averaged over the soil profile. However, many applications require models to more accurately represent the soil–plant–atmosphere continuum, in particular, water movement and saturation within specific parts of the soil profile. In this paper a mathematical model for water uptake by a plant root system from unsaturated soil is presented. The model provides an estimate of the water content level within the soil at different depths, and the uptake of water by the root system. The model was validated using field data, which include hourly water content values at five different soil depths under a grass/herb cover over 1 year, to obtain a fully calibrated system for plant water uptake with respect to climate conditions. When compared quantitatively to a simple water balance model, the proposed model achieves a better fit to the experimental data due to its ability to vary water content with depth. To accurately model the water content in the soil profile, the soil water retention curve and saturated hydraulic conductivity needed to vary with depth.

Chemical and plant extractability of metals and plant growth on soils amended with sludge

Energy Technology Data Exchange (ETDEWEB)

Gaynor, J.D.; Halstead, R.L.

1976-02-01

The addition of sludge to a Fox sandy loam (sl), Granby sl and Rideau clay (c) soil increased soil pH, total C, NaHCO3 extractable P, cation exchange capacity and exchangeable Ca. Sludge application increased DTPA-extractable Cd 2 to 5 times, Pb 2 to 3 times, Cu 3 to 7 times and Zn 7 to 31 times. Metal extractability in Granby and Fox sl soils was not greatly changed after 11 mo incubation but extractable Zn, Cu, Pb and Cd were reduced in the clay soil following incubation. Cropping to lettuce reduced the quantity of metal extracted from Fox sl soil and to a lesser extent from Rideau c soil but not from Granby sl soil. Lettuce (Lactuca sativa L.) yields were significantly reduced for the first crop grown on sludge + fertilizer-treated Rideau c and Granby sl soils and for all three harvests from similarly treated Fox s 1 soil compared to harvests from soils treated with fertilizer only. Yield reduction for the first crop was attributed to a salt effect, as subsequent yields on Rideau c and Granby sl soils were similar to harvests from fertilized treatments. Saturation extract conductivities for all sludge treatments were higher for incubated than for cropped soils. Generally Zn, Cu and Pb tissue concentrations in lettuce harvested from sludge + fertilizer-treated Fox and Granby sl soils were significantly increased but total uptake was only increased for Zn. Metal uptake and tissue concentrations for lettuce grown on similarly treated Rideau c soil were equal to or less than those found in lettuce harvested from the fertilizer-only treatment. To a lesser extent similar trends were observed with the tomato (Lycospersicon esculentum Mill.) crop. 27 references, 3 tables.

Anaerobic N mineralization in paddy soils in relation to inundation management, physicochemical soil fractions, mineralogy and soil properties

Science.gov (United States)

Sleutel, Steven; Kader, Mohammed Abdul; Ara Begum, Shamim; De Neve, Stefaan

2013-04-01

Anaerobic N mineralization measured from (saturated) repacked soil cores from 25 paddy fields in Bangladesh and was previously found to negatively related to soil N content on a relative basis. This suggests that other factors like soil organic matter (SOM) quality or abiotic factors instead control the anaerobic N mineralization process. We therefore assessed different physical and chemical fractions of SOM, management factors and various soil properties as predictors for the net anaerobic N mineralization. 1° First, we assessed routinely analyzed soil parameters (soil N and soil organic carbon, texture, pH, oxalate- and pyrophosphate-extractable Fe, Al, and Mn, fixed-NH4 content). We found no significant influences of neither soil mineralogy nor the annual length of inundation on soil N mineralization. The anaerobic N mineralization correlated positively with Na-pyrophosphate-extractable Fe and negatively with pH (both at Presistant OM fraction, followed by extraction of mineral bound OM with 10%HF thereby isolating the HF-resistant OM. None of the physicochemical SOM fractions were found useful predictors anaerobic N mineralization. The linkage between these chemical soil N fractions and N supplying processes actually occurring in the soil thus appears to be weak. Regardless, we hypothesize that variation in strength of N-mineral and N-OM linkages is likely to explain variation in bio-availability of organic N and proneness to mineralization. Yet, in order to separate kinetically different soil N fractions we then postulated that an alternative approach would be required, which instead isolates soil N fractions on the basis of bonding strength. In this respect bonding strength should be seen as opposite of proneness to dissolution of released N into water, the habitat of soil microorganisms mediating soil N mineralization. We hypothesize that soil N extracted by water at increasing temperatures would reflect such N fractions with increasing bonding strength, in

Barrier erosion control test plan: Gravel mulch, vegetation, and soil water interactions

Energy Technology Data Exchange (ETDEWEB)

Waugh, W.J.; Link, S.O. (Pacific Northwest Lab., Richland, WA (USA))

1988-07-01

Soil erosion could reduce the water storage capacity of barriers that have been proposed for the disposal of near-surface waste at the US Department of Energy's Hanford Site. Gravel mixed into the top soil surface may create a self-healing veneer that greatly retards soil loss. However, gravel admixtures may also enhance infiltration of rainwater, suppress plant growth and water extraction, and lead to the leaching of underlying waste. This report describes plans for two experiments that were designed to test hypotheses concerning the interactive effects of surface gravel admixtures, revegetation, and enhanced precipitation on soil water balance and plant abundance. The first experiment is a factorial field plot set up on the site selected as a soil borrow area for the eventual construction of barriers. The treatments, arranged in a a split-split-plot design structure, include two densities of gravel admix, a mixture of native and introduced grasses, and irrigation to simulate a wetter climate. Changes in soil water storage and plant cover are monitored with neutron moisture probes and point intercept sampling, respectively. The second experiment consists of an array of 80 lysimeters containing several different barrier prototypes. Surface treatments are similar to the field-plot experiment. Drainage is collected from a valve at the base of each lysimeter tube, and evapotranspiration is estimated by subtraction. The lysimeters are also designed to be coupled to a whole-plant gas exchange system that will be used to conduct controlled experiments on evapotranspiration for modeling purposes. 56 refs., 6 figs., 8 tabs.

Beyond clay - using selective extractions to improve predictions of soil carbon content

Science.gov (United States)

Rasmussen, C.; Berhe, A. A.; Blankinship, J. C.; Crow, S. E.; Druhan, J. L.; Heckman, K. A.; Keiluweit, M.; Lawrence, C. R.; Marin-Spiotta, E.; Plante, A. F.; Schaedel, C.; Schimel, J.; Sierra, C. A.; Thompson, A.; Wagai, R.; Wieder, W. R.

2016-12-01

A central component of modern soil carbon (C) models is the use of clay content to scale the relative partitioning of decomposing plant material to respiration and mineral stabilized soil C. However, numerous pedon to plot scale studies indicate that other soil mineral parameters, such as Fe- or Al-oxyhydroxide content and specific surface area, may be more effective than clay alone for predicting soil C content and stabilization. Here we directly address the following question: Are there soil physicochemical parameters that represent mineral C association and soil C content that can replace or be used in conjunction with clay content as scalars in soil C models. We explored the relationship of soil C content to a number of soil physicochemical and physiographic parameters using the National Cooperative Soil Survey database that contains horizon level data for > 62,000 pedons spanning global ecoregions and geographic areas. The data indicated significant variation in the degree of correlation among soil C, clay and Fe-/Al-oxyhydroxides with increasing moisture variability. Specifically, dry, water-limited systems (PET/MAP > 1) presented strong positive correlations between clay and soil C, that decreased significantly to little or no correlation in wet, energy-limited systems (PET/MAP soil C to oxalate extractable Al+Fe increased significantly with increasing moisture availability. This pattern was particularly well expressed for subsurface B horizons. Multivariate analyses indicated similar patterns, with clear climate and ecosystem level variation in the degree of correlation among soil C and soil physicochemical properties. The results indicate a need to modify current soil C models to incorporate additional C partitioning parameters that better account for climate and ecoregion variability in C stabilization mechanisms.

Geophysical surveys combined with laboratory soil column experiments to identify and explore risk areas for soil and water pollution in feedlots

Science.gov (United States)

Espejo-Pérez, Antonio Jesus; Sainato, Claudia Mabel; Jairo Márquez-Molina, John; Giráldez, Juan Vicente; Vanderlinden, Karl

2014-05-01

Changes of land use without a correct planning may produce its deterioration with their social, economical and environmental irreversible consequences over short to medium time range. In Argentina, the expansion of soybean fields induced a reduction of the area of pastures dedicated to stockbreeding. As cattle activity is being progressively concentrated on small pens, at feedlots farms, problems of soil and water pollution, mainly by nitrate, have been detected. The characterization of the spatial and temporal variability of soil water content is very important because the mostly advective transport of solutes. To avoid intensive soil samplings, very expensive, one has to recur to geophysical exploration methods. The objective of this work was to identify risk areas within a feedlot of the NW zone of Buenos Aires Province, in Argentina through geophysical methods. The surveys were carried out with an electromagnetic induction profiler EMI-400 (GSSI) and a Time domain Reflectometry (TDR) survey of depth 0-0.10 m with soil sampling and measurement of moisture content with gravimetric method (0-1.0 m). Several trenches were dug inside the pens and also at a test site, where texture, apparent density, saturated hydraulic conductivity (Ks), electrical conductivity of the saturation paste extract and organic matter content (OM) were measured. The water retention curves for these soils were also determined. At one of the pens undisturbed soil columns were extracted at 3 locations. Laboratory analysis for 0-1.0 m indicated that soil texture was classified as sandy loam, average organic matter content (OM) was greater than 2.3% with low values of apparent density in the first 10 cm. The range of spatial dependence of data suggested that the number of soil samples could be reduced. Soil apparent electrical conductivity (ECa) and soil moisture were well correlated and indicated a clear spatial pattern in the corrals. TDR performance was acceptable to identify the spatial

Soil water repellency at old crude oil spill sites

International Nuclear Information System (INIS)

Roy, J.L.

1999-08-01

This thesis presents the current state of knowledge regarding the cause of soil water repellency and characterizes disaggregated nonwettable surface soils found at old crude oil spill sites. Pollution-induced water repellency generally develops following prolonged exposures of soil to liquid- or vapour-phase petroleum hydrocarbons. The condition varies significantly in terms of severity and persistence. Soil water repellency retards plant growth and disturbs the hydrological balance of ecosystems. Disaggregated water-repellent soils are also very susceptible to dispersal by erosion, posing a threat to the productivity of surrounding soils. The author described the probable causes of soil water repellency under the following three main themes: (1) accumulation of hydrophobic organic material in soil, (2) redistribution and re-organisation of this material in soil, and (3) stabilisation of the hydrophobic organic material. This final process is necessary to ensure persistence of induced water repellency symptoms. Petroleum residues as water-repellent substances in weathered nonwettable oil-contaminated soils were also discussed and a hypothesis about soil water repellency was presented which deals with flexible conformation in organic matter coatings. Processes leading to the development of soil water repellency following crude oil contamination were also described. It was determined that soil water repellency is a function of the packing density and the chain conformation of amphiphilic organic molecules in the outermost layer of soil organic matter coatings. This research suggests that the fractional coverage of alkyl chains on soil particle surfaces determines the degree of water repellency that is displayed by soil. It was shown that prompt remediation of some oil-contaminated plots can effectively prevent the development of soil water repellency. 4 refs., 32 tabs., 22 figs., 5 appendices

Determination of Wastewater Compounds in Sediment and Soil by Pressurized Solvent Extraction, Solid-Phase Extraction, and Capillary-Column Gas Chromatography/Mass Spectrometry

Science.gov (United States)

Burkhardt, Mark R.; Zaugg, Steven D.; Smith, Steven G.; ReVello, Rhiannon C.

2006-01-01

A method for the determination of 61 compounds in environmental sediment and soil samples is described. The method was developed in response to increasing concern over the effects of endocrine-disrupting chemicals in wastewater and wastewater-impacted sediment on aquatic organisms. This method also may be used to evaluate the effects of combined sanitary and storm-sewer overflow on the water and sediment quality of urban streams. Method development focused on the determination of compounds that were chosen on the basis of their endocrine-disrupting potential or toxicity. These compounds include the alkylphenol ethoxylate nonionic surfactants and their degradates, food additives, fragrances, antioxidants, flame retardants, plasticizers, industrial solvents, disinfectants, fecal sterols, polycyclic aromatic hydrocarbons, and high-use domestic pesticides. Sediment and soil samples are extracted using a pressurized solvent extraction system. The compounds of interest are extracted from interfering matrix components by high-pressure water/isopropyl alcohol extraction. The compounds were isolated using disposable solid-phase extraction (SPE) cartridges containing chemically modified polystyrene-divinylbenzene resin. The cartridges were dried with nitrogen gas, and then sorbed compounds were eluted with methylene chloride (80 percent)-diethyl ether (20 percent) through Florisil/sodium sulfate SPE cartridge, and then determined by capillary-column gas chromatography/mass spectrometry. Recoveries in reagent-sand samples fortified at 4 to 72 micrograms averaged 76 percent ?13 percent relative standard deviation for all method compounds. Initial method reporting levels for single-component compounds ranged from 50 to 500 micrograms per kilogram. The concentrations of 20 out of 61 compounds initially will be reported as estimated with the 'E' remark code for one of three reasons: (1) unacceptably low-biased recovery (less than 60 percent) or highly variable method performance

Trace Element Concentration and Speciation in Selected Mining-Contaminated Soils and Water in Willow Creek Floodplain, Colorado

Directory of Open Access Journals (Sweden)

R. Burt

2011-01-01

Full Text Available Long-term mining activities in the mountains around Creede, Colorado have resulted in significant contamination in soils and water in the Willow Creek floodplain. Total major and trace were determined for soils and water and sequential chemical extraction for soils. Objectives were to determine concentrations and potential reactivity of trace elements and investigate their relationship with other soil and water properties. Water trace elements showed significant variability among sites, ranging from 347 to 12108 μg/L. Relative trend showed (Zn > Sr > Ba > (Mn > W > Cd > (Sn > V ≈ Ni ≈ Cu > Co > (Ag. Soil trace elements showed significant short-range spatial variability, ranging from 2819 to 19274 mg/kg. Relative trend showed (Pb ≈ Zn > Mn > Ba > P > (As > Cu > Sr > V > Cd > Sb ≈ Ag > (Co ≈ Cr > Mo ≈ Sn ≈ Ni > (Be ≈ W > Se ≈ Hg. Predominant fractions were oxide, specifically-sorbed/carbonate bound, and residual. Water soluble and exchangeable fractions showed (Zn ≈ Cd > Pb and Cd > Zn > Pb, respectively. Mobility factors for highly contaminated soils showed Cd ≈ Zn > Pb > Cu > As.

Water balance creates a threshold in soil pH at the global scale

Science.gov (United States)

Slessarev, E. W.; Lin, Y.; Bingham, N. L.; Johnson, J. E.; Dai, Y.; Schimel, J. P.; Chadwick, O. A.

2016-12-01

Soil pH regulates the capacity of soils to store and supply nutrients, and thus contributes substantially to controlling productivity in terrestrial ecosystems. However, soil pH is not an independent regulator of soil fertility—rather, it is ultimately controlled by environmental forcing. In particular, small changes in water balance cause a steep transition from alkaline to acid soils across natural climate gradients. Although the processes governing this threshold in soil pH are well understood, the threshold has not been quantified at the global scale, where the influence of climate may be confounded by the effects of topography and mineralogy. Here we evaluate the global relationship between water balance and soil pH by extracting a spatially random sample (n = 20,000) from an extensive compilation of 60,291 soil pH measurements. We show that there is an abrupt transition from alkaline to acid soil pH that occurs at the point where mean annual precipitation begins to exceed mean annual potential evapotranspiration. We evaluate deviations from this global pattern, showing that they may result from seasonality, climate history, erosion and mineralogy. These results demonstrate that climate creates a nonlinear pattern in soil solution chemistry at the global scale; they also reveal conditions under which soils maintain pH out of equilibrium with modern climate.

Remediation of lead-contaminated soil with non-toxic biodegradable natural ligands extracted from soybean.

Science.gov (United States)

Lee, Yong-Woo; Kim, Chulsung

2012-01-01

Bench-scale soil washing studies were performed to evaluate the potential application of non-toxic, biodegradable extracted soybean-complexing ligands for the remediation of lead-contaminated soils. Results showed that, with extracted soybean-complexing ligands, lead solubility extensively increased when pH of the solution was higher than 6, and approximately 10% (500 mg/kg) of lead was removed from a rifle range soil. Two potential primary factors controlling the effectiveness of lead extraction from lead-contaminated soils with natural ligands are adsorption of extracted aqueous lead ions onto the ground soybean and the pH of the extraction solution. More complexing ligands were extracted from the ground soybean as the reaction pH increased. As a result, significantly higher lead extraction efficiency was observed under basic environments. In addition, less adsorption onto soybean was observed when the pH of the solution was higher than 7. Among two available Lewis base functional groups in the extracted soybean-complexing ligands such as carboxylate and the alpha-amino functional groups, the non-protonated alpha-amino functional groups may play an important role for the dissolution of lead from lead-contaminated soil through the formation of soluble lead--ligand complexes.

Necessity of purification during bacterial DNA extraction with environmental soils

Directory of Open Access Journals (Sweden)

Hyun Jeong Lim

2017-08-01

Full Text Available Complexity and heterogeneity of soil samples have often implied the inclusion of purification steps in conventional DNA extraction for polymerase chain reaction (PCR assays. Unfortunately the purification steps are also time and labor intensive. Therefore the necessity of DNA purification was re-visited and investigated for a variety of environmental soil samples that contained various amounts of PCR inhibitors. Bead beating and centrifugation was used as the baseline (without purification method for DNA extraction. Its performance was compared with that of conventional DNA extraction kit (with purification. The necessity criteria for DNA purification were established with environmental soil samples. Using lysis conditions at 3000 rpm for 3 minutes with 0.1 mm glass beads, centrifugation time of 10 minutes and 1:10 dilution ratio, the baseline method outperformed conventional DNA extraction on cell seeded sand samples. Further investigation with PCR inhibitors (i.e., humic acids, clay, and magnesium [Mg] showed that sand samples containing less than 10 μg/g humic acids and 70% clay may not require purifications. Interestingly, the inhibition pattern of Mg ion was different from other inhibitors due to the complexation interaction of Mg ion with DNA fragments. It was concluded that DNA extraction method without purification is suitable for soil samples that have less than 10 μg/g of humic acids, less than 70% clay content and less than 0.01% Mg ion content.

Soils and water [Chapter 18

Science.gov (United States)

Goran Berndes; Heather Youngs; Maria Victoria Ramos Ballester; Heitor Cantarella; Annette L. Cowie; Graham Jewitt; Luiz Antonio Martinelli; Dan Neary

2015-01-01

Bioenergy production can have positive or negative impacts on soil and water. To best understand these impacts, the effects of bioenergy systems on water and soil resources should be assessed as part of an integrated analysis considering environmental, social and economic dimensions. Bioenergy production systems that are strategically integrated in the landscape to...

Extraction and Capture of Water from Martian Regolith Experimental Proof-of-Concept

Science.gov (United States)

Linne, Diane; Kleinhenz, Julie; Bauman, Steve; Johnson, Kyle

2016-01-01

Mars Design Reference Architecture 5.0:Lists in-situ resource utilization (ISRU) as enabling for robust human Mars missionsLO2LCH4 ascent propulsion 25,000 kg oxygen from atmosphere for ascent and life support Atmospheric based ISRU processes less operationally complex than surface based limited concept evaluation to date and Mars surface water property and distribution uncertainty would not allow [Mars soil water processing] to be base lined at this time Limited Concept Evaluation to Date Lunar regolith O2 extraction processing experience Lunar regolith is fluidized and heated to high temperatures with H2 to produce H2O from iron-bearing minerals Mars similarity concept: Soil placed in fluidized bed reactor Heated to moderate temperatures Inert gas flow used to fluidize the bed and help with water desorption Challenges: High-temperature dusty seals Working gas requires downstream separation and recycling to reduce consumables loss Batch process heating thermally inefficient.

Using soil water sensors to improve irrigation management

Science.gov (United States)

Irrigation water management has to do with the appropriate application of water to soils, in terms of amounts, rates, and timing to satisfy crop water demands while protecting the soil and water resources from degradation. In this regard, sensors can be used to monitor the soil water status; and som...

Prediction of the Soil Water Characteristic from Soil Particle Volume Fractions

DEFF Research Database (Denmark)

Naveed, Muhammad; Møldrup, Per; Tuller, Markus

2012-01-01

Modelling water distribution and flow in partially saturated soils requires knowledge of the soil-water characteristic (SWC). However, measurement of the SWC is challenging and time-consuming, and in some cases not feasible. This study introduces two predictive models (Xw-model and Xw......*-model) for the SWC, derived from readily available soil properties such as texture and bulk density. A total of 46 soils from different horizons at 15 locations across Denmark were used for models evaluation. The Xw-model predicts the volumetric water content as a function of volumetric fines content (organic matter...... (organic matter, clay, silt, fine and coarse sand), variably included in the model depending on the pF value. The volumetric content of a particular soil particle size fraction was included in the model if it was assumed to contribute to the pore size fraction still occupied with water at the given p...

Estimation of water transit time in soils under Amazon forest cover using variations in delta18O values

International Nuclear Information System (INIS)

Leopoldo, P.R.; Matsui, E.; Salati, E.

1984-01-01

The work was carried out at the forest reserve of the Instituto Nacional de Pesquisas da Amazonia, located at km 45 of Manaus, in an area characterized by Amazon vegetation of the 'terra-firme' type. To extract the soil water, four soil-water collecting stations were installed, and in each the porous cups were placed at 15, 25, 50, 80 and 120 cm depth from the soil surface. The rain-water and soil-water samples were collected only weekly for analysis of the 18 O content. In an attempt to estimate the soil-water transit time using the variation in 18 O values, a statistical model was used. This model is based on linear regression analysis applied to the values observed for soil water and rain water. From this analysis, regression coefficients are obtained which vary according to time. The values of the coefficients obtained can be adjusted generally, according to a quadratic regression, with the maximum value of the function representing the time in which the best statistical correlation between the observed delta 18 O values occurs. The time obtained from these correlations represents the mean time necessary for the water to run from one collecting point to the next. (author)

Subcritical water extraction combined with molecular imprinting technology for sample preparation in the detection of triazine herbicides.

Science.gov (United States)

Zhao, Fengnian; Wang, Shanshan; She, Yongxin; Zhang, Chao; Zheng, Lufei; Jin, Maojun; Shao, Hua; Jin, Fen; Du, Xinwei; Wang, Jing

2017-09-15

A selective, environmentally friendly, and cost-effective sample extraction method based on a combination of subcritical water extraction (SWE) and molecularly imprinted solid-phase extraction (MISPE) was developed for the determination of eight triazine herbicides in soil samples by liquid chromatography-tandem mass spectrometry (LC-MS/MS). In SWE, the highest extraction yields of triazine herbicides were obtained under 150°C for 15min using 20% ethanol as the organic modifier. Addition of MIP during SWE increased the extraction efficiency, and using MIP as a selective SPE sorbent improved the enrichment capability. Soil samples were treated with the optimized extraction MIP/SWE-MISPE method and analyzed by LC-MS/MS. The novel technique was then applied to soil samples for the determination of triazine herbicides, and better recoveries (78.9%-101%) were obtained compared with using SWE-MISPE (30%-67%). Moreover, this newly developed method displayed good linearity (R 2 >0.99) and precision (2.7-9.8%), and low enough detection limits (0.4-3.3μgkg -1 ). This combination of SWE and MIP technology is a simple, effective and promising method to selectively extract class-specific compounds in complex samples. Copyright © 2017 Elsevier B.V. All rights reserved.

Governing equations of transient soil water flow and soil water flux in multi-dimensional fractional anisotropic media and fractional time

OpenAIRE

M. L. Kavvas; A. Ercan; J. Polsinelli

2017-01-01

In this study dimensionally consistent governing equations of continuity and motion for transient soil water flow and soil water flux in fractional time and in fractional multiple space dimensions in anisotropic media are developed. Due to the anisotropy in the hydraulic conductivities of natural soils, the soil medium within which the soil water flow occurs is essentially anisotropic. Accordingly, in this study the fractional dimensions in two horizontal and one vertical di...

MICHIGAN SOIL VAPOR EXTRACTION REMEDIATION (MISER) MODEL: A COMPUTER PROGRAM TO MODEL SOIL VAPOR EXTRACTION AND BIOVENTING OF ORGANIC CHEMICALS IN UNSATURATED GEOLOGICAL MATERIAL

Science.gov (United States)

Soil vapor extraction (SVE) and bioventing (BV) are proven strategies for remediation of unsaturated zone soils. Mathematical models are powerful tools that can be used to integrate and quantify the interaction of physical, chemical, and biological processes occurring in field sc...

The variability of standard artificial soils: Behaviour, extractability and bioavailability of organic pollutants

International Nuclear Information System (INIS)

Hofman, Jakub; Hovorková, Ivana; Semple, Kirk T.

2014-01-01

Highlights: • Artificial soils from different laboratories revealed different fates, behaviour and bioavailability of lindane and phenanthrene. • Lindane behaviour was related to organic carbon. • Phenanthrene behaviour was significantly affected by degrading microorganisms from peat. • Sterilization of artificial soils might reduce unwanted variability. -- Abstract: Artificial soil is an important standard medium and reference material for soil ecotoxicity bioassays. Recent studies have documented the significant variability of their basic properties among different laboratories. Our study investigated (i) the variability of ten artificial soils from different laboratories by means of the fate, extractability and bioavailability of phenanthrene and lindane, and (ii) the relationships of these results to soil properties and ageing. Soils were spiked with 14 C-phenanthrene and 14 C-lindane, and the total residues, fractions extractable by hydroxypropyl-β-cyclodextrin, and the fractions of phenanthrene mineralizable by bacteria were determined after 1, 14, 28 and 56 days. Significant temporal changes in total residues and extractable and mineralizable fractions were observed for phenanthrene, resulting in large differences between soils after 56 days. Phenanthrene mineralization by indigenous peat microorganisms was suggested as the main driver of that, outweighing the effects of organic matter. Lindane total residues and extractability displayed much smaller changes over time and smaller differences between soils related to organic matter. Roughly estimated, the variability between the artificial soils was comparable to natural soils. The implications of such variability for the results of toxicity tests and risk assessment decisions should be identified. We also suggested that the sterilization of artificial soils might reduce unwanted variability

The variability of standard artificial soils: Behaviour, extractability and bioavailability of organic pollutants

Energy Technology Data Exchange (ETDEWEB)

Hofman, Jakub, E-mail: hofman@recetox.muni.cz [Research Centre for Toxic Compounds in the Environment (RECETOX), Faculty of Science, Masaryk University, Kamenice 753/5, Brno CZ-62500 (Czech Republic); Hovorková, Ivana [Research Centre for Toxic Compounds in the Environment (RECETOX), Faculty of Science, Masaryk University, Kamenice 753/5, Brno CZ-62500 (Czech Republic); Semple, Kirk T. [Lancaster Environment Centre, Lancaster University, Lancaster LA1 4YQ (United Kingdom)

2014-01-15

Highlights: • Artificial soils from different laboratories revealed different fates, behaviour and bioavailability of lindane and phenanthrene. • Lindane behaviour was related to organic carbon. • Phenanthrene behaviour was significantly affected by degrading microorganisms from peat. • Sterilization of artificial soils might reduce unwanted variability. -- Abstract: Artificial soil is an important standard medium and reference material for soil ecotoxicity bioassays. Recent studies have documented the significant variability of their basic properties among different laboratories. Our study investigated (i) the variability of ten artificial soils from different laboratories by means of the fate, extractability and bioavailability of phenanthrene and lindane, and (ii) the relationships of these results to soil properties and ageing. Soils were spiked with {sup 14}C-phenanthrene and {sup 14}C-lindane, and the total residues, fractions extractable by hydroxypropyl-β-cyclodextrin, and the fractions of phenanthrene mineralizable by bacteria were determined after 1, 14, 28 and 56 days. Significant temporal changes in total residues and extractable and mineralizable fractions were observed for phenanthrene, resulting in large differences between soils after 56 days. Phenanthrene mineralization by indigenous peat microorganisms was suggested as the main driver of that, outweighing the effects of organic matter. Lindane total residues and extractability displayed much smaller changes over time and smaller differences between soils related to organic matter. Roughly estimated, the variability between the artificial soils was comparable to natural soils. The implications of such variability for the results of toxicity tests and risk assessment decisions should be identified. We also suggested that the sterilization of artificial soils might reduce unwanted variability.

The application of in situ air sparging as an innovative soils and ground water remediation technology

International Nuclear Information System (INIS)

Marley, M.C.; Hazebrouck, D.J.; Walsh, M.T.

1992-01-01

Vapor extraction (soil venting) has been demonstrated to be a successful and cost-effective remediation technology for removing VOCs from the vadose (unsaturated) zone. However, in many cases, seasonal water table fluctuations, drawdown associated with pump-and-treat remediation techniques, and spills involving dense, non-aqueous phase liquids (DNAPLS) create contaminated soil below the water table. Vapor extraction alone is not considered to be an optimal remediation technology to address this type of contamination. An innovative approach to saturated zone remediation is the use of sparging (injection) wells to inject a hydrocarbon-free gaseous medium (typically air) into the saturated zone below the areas of contamination. The contaminants dissolved in the ground water and sorbed onto soil particles partition into the advective air phase, effectively simulating an in situ air-stripping system. The stripped contaminants are transported in the gas phase to the vadose zone, within the radius of influence of a vapor extraction and vapor treatment system. In situ air sparging is a complex multifluid phase process, which has been applied successfully in Europe since the mid-1980s. To date, site-specific pilot tests have been used to design air-sparging systems. Research is currently underway to develop better engineering design methodologies for the process. Major design parameters to be considered include contaminant type, gas injection pressures and flow rates, site geology, bubble size, injection interval (areal and vertical) and the equipment specifications. Correct design and operation of this technology has been demonstrated to achieve ground water cleanup of VOC contamination to low part-per-billion levels

Remediation of soils contaminated with particulate depleted uranium by multi stage chemical extraction

Energy Technology Data Exchange (ETDEWEB)

Crean, Daniel E. [Immobilisation Science Laboratory, Department of Materials Science and Engineering, The University of Sheffield (United Kingdom); Centre for Radiochemistry Research, School of Chemistry, The University of Manchester (United Kingdom); Livens, Francis R.; Sajih, Mustafa [Centre for Radiochemistry Research, School of Chemistry, The University of Manchester (United Kingdom); Stennett, Martin C. [Immobilisation Science Laboratory, Department of Materials Science and Engineering, The University of Sheffield (United Kingdom); Grolimund, Daniel; Borca, Camelia N. [Swiss Light Source, Paul Scherrer Institute, Villigen (Switzerland); Hyatt, Neil C., E-mail: n.c.hyatt@sheffield.ac.uk [Immobilisation Science Laboratory, Department of Materials Science and Engineering, The University of Sheffield (United Kingdom)

2013-12-15

Highlights: • Batch leaching was examined to remediate soils contaminated with munitions depleted uranium. • Site specific maximum extraction was 42–50% total U in single batch with NH{sub 4}HCO{sub 3}. • Analysis of residues revealed partial leaching and secondary carbonate phases. • Sequential batch leaching alternating between NH{sub 4}HCO{sub 3} and citric acid was designed. • Site specific extraction was increased to 68–87% total U in three batch steps. -- Abstract: Contamination of soils with depleted uranium (DU) from munitions firing occurs in conflict zones and at test firing sites. This study reports the development of a chemical extraction methodology for remediation of soils contaminated with particulate DU. Uranium phases in soils from two sites at a UK firing range, MOD Eskmeals, were characterised by electron microscopy and sequential extraction. Uranium rich particles with characteristic spherical morphologies were observed in soils, consistent with other instances of DU munitions contamination. Batch extraction efficiencies for aqueous ammonium bicarbonate (42–50% total DU extracted), citric acid (30–42% total DU) and sulphuric acid (13–19% total DU) were evaluated. Characterisation of residues from bicarbonate-treated soils by synchrotron microfocus X-ray diffraction and X-ray absorption spectroscopy revealed partially leached U(IV)-oxide particles and some secondary uranyl-carbonate phases. Based on these data, a multi-stage extraction scheme was developed utilising leaching in ammonium bicarbonate followed by citric acid to dissolve secondary carbonate species. Site specific U extraction was improved to 68–87% total U by the application of this methodology, potentially providing a route to efficient DU decontamination using low cost, environmentally compatible reagents.

Remediation of soils contaminated with particulate depleted uranium by multi stage chemical extraction.

Science.gov (United States)

Crean, Daniel E; Livens, Francis R; Sajih, Mustafa; Stennett, Martin C; Grolimund, Daniel; Borca, Camelia N; Hyatt, Neil C

2013-12-15

Contamination of soils with depleted uranium (DU) from munitions firing occurs in conflict zones and at test firing sites. This study reports the development of a chemical extraction methodology for remediation of soils contaminated with particulate DU. Uranium phases in soils from two sites at a UK firing range, MOD Eskmeals, were characterised by electron microscopy and sequential extraction. Uranium rich particles with characteristic spherical morphologies were observed in soils, consistent with other instances of DU munitions contamination. Batch extraction efficiencies for aqueous ammonium bicarbonate (42-50% total DU extracted), citric acid (30-42% total DU) and sulphuric acid (13-19% total DU) were evaluated. Characterisation of residues from bicarbonate-treated soils by synchrotron microfocus X-ray diffraction and X-ray absorption spectroscopy revealed partially leached U(IV)-oxide particles and some secondary uranyl-carbonate phases. Based on these data, a multi-stage extraction scheme was developed utilising leaching in ammonium bicarbonate followed by citric acid to dissolve secondary carbonate species. Site specific U extraction was improved to 68-87% total U by the application of this methodology, potentially providing a route to efficient DU decontamination using low cost, environmentally compatible reagents. Copyright © 2013 The Authors. Published by Elsevier B.V. All rights reserved.

Field soil-water properties measured through radiation techniques

International Nuclear Information System (INIS)

1984-07-01

This report shows a major effort to make soil physics applicable to the behaviour of the field soils and presents a rich and diverse set of data which are essential for the development of effective soil-water management practices that improve and conserve the quality and quantity of agricultural lands. This piece of research has shown that the neutron moisture meter together with some complementary instruments like tensiometers, can be used not only to measure soil water contents but also be extremely handy to measure soil hydraulic characteristics and soil water flow. It is, however, recognized that hydraulic conductivity is highly sensitive to small changes in soil water content and texture, being extremely variable spatially and temporally

Phytotoxicity of trace metals in spiked and field-contaminated soils: Linking soil-extractable metals with toxicity.

Science.gov (United States)

Hamels, Fanny; Malevé, Jasmina; Sonnet, Philippe; Kleja, Dan Berggren; Smolders, Erik

2014-11-01

Soil tests have been widely developed to predict trace metal uptake by plants. The prediction of metal toxicity, however, has rarely been tested. The present study was set up to compare 8 established soil tests for diagnosing phytotoxicity in contaminated soils. Nine soils contaminated with Zn or Cu by metal mining, smelting, or processing were collected. Uncontaminated reference soils with similar soil properties were sampled, and series of increasing contamination were created by mixing each with the corresponding soil. In addition, each reference soil was spiked with either ZnCl2 or CuCl2 at several concentrations. Total metal toxicity to barley seedling growth in the field-contaminated soils was up to 30 times lower than that in corresponding spiked soils. Total metal (aqua regia-soluble) toxicity thresholds of 50% effective concentrations (EC50) varied by factors up to 260 (Zn) or 6 (Cu) among soils. For Zn, variations in EC50 thresholds decreased as aqua regia > 0.43 M HNO3  > 0.05 M ethylenediamine tetraacetic acid (EDTA) > 1 M NH4 NO3  > cobaltihexamine > diffusive gradients in thin films (DGT) > 0.001 M CaCl2 , suggesting that the last extraction is the most robust phytotoxicity index for Zn. The EDTA extraction was the most robust for Cu-contaminated soils. The isotopically exchangeable fraction of the total soil metal in the field-contaminated soils markedly explained the lower toxicity compared with spiked soils. The isotope exchange method can be used to translate soil metal limits derived from soils spiked with metal salts to site-specific soil metal limits. © 2014 SETAC.

Contamination of urban garden soils with copper and boron

Energy Technology Data Exchange (ETDEWEB)

Purves, D

1966-06-04

Spectrochemical analyses of garden soils sampled in the Edinburgh and Dundee areas indicate that there is substantial contamination of urban soils with copper and boron. These soils were analyzed spectrochemically with respect to total copper and water-extractable boron content with the view of comparing the levels obtained in urban areas with levels in arable soils in rural areas. The results indicate that urban garden soils contain about four times as much copper and two to three times as much water-soluble boron as rural arable soils. The existence of such a marked disparity between the levels of two potentially toxic elements in urban and rural areas is evidence of slow poisoning of the soil environment in built-up areas and is cause for concern. While the major source of contamination of soils with copper and boron is still a matter for speculation, it is probable that the addition of soot to garden soils and the fall-out of sooty material in built-up areas where atmospheric pollution is a problem make a substantial contribution to the water-extractable boron content of urban soils. Three samples of soot from domestic chimneys, obtained from independent sources, were found on analysis to contain 640, 650 and 555 p.p.m. water-extractable boron, and it is evident that the addition to soil of even small amounts of soot with a boron content of this order would have a marked effect on its water-extractable boron content.

Novel approach to microwave-assisted extraction and micro-solid-phase extraction from soil using graphite fibers as sorbent.

Science.gov (United States)

Xu, Li; Lee, Hian Kee

2008-05-30

A single-step extraction-cleanup procedure involving microwave-assisted extraction (MAE) and micro-solid-phase extraction (micro-SPE) has been developed for the analysis of polycyclic aromatic hydrocarbons (PAHs) from soil samples. Micro-SPE is a relatively new extraction procedure that makes use of a sorbent enclosed within a sealed polypropylene membrane envelope. In the present work, for the first time, graphite fiber was used as a sorbent material for extraction. MAE-micro-SPE was used to cleanup sediment samples and to extract and preconcentrate five PAHs in sediment samples prepared as slurries with addition of water. The best extraction conditions comprised of microwave heating at 50 degrees C for a duration of 20 min, and an elution (desorption) time of 5 min using acetonitrile with sonication. Using gas chromatography (GC)-flame ionization detection (FID), the limits of detection (LODs) of the PAHs ranged between 2.2 and 3.6 ng/g. With GC-mass spectrometry (MS), LODs were between 0.0017 and 0.0057 ng/g. The linear ranges were between 0.1 and 50 or 100 microg/g for GC-FID analysis, and 1 and 500 or 1000 ng/g for GC-MS analysis. Granular activated carbon was also used for the micro-SPE device but was found to be not as efficient in the PAH extraction. The MAE-micro-SPE method was successfully used for the extraction of PAHs in river and marine sediments, demonstrating its applicability to real environmental solid matrixes.

Water transport in desert alluvial soil

International Nuclear Information System (INIS)

Kearl, P.M.

1982-04-01

Safe storage of radioactive waste buried in an arid alluvial soil requires extensive site characterization of the physical process influencing moisture movement which could act as a transport medium for the migration of radionuclides. The field portion of this study included an infiltration plot instrumented with thermocouple psychrometers and neturon moisture probe access holes. Baseline information shows a zone of higher moisture content at approximately 1.5 m (5 ft) in depth. A sprinkler system simulated a 500-year precipitation event. Results revealed water penetrated the soil to 0.9 m (2.9 ft). Due to the low moisture content, vapor transport was primarily responsible for water movement at this depth. Temperature gradients are substantially responsible for vapor transport by preferentially sorting water-vapor molecules from the surrounding air by using the soil as a molecular sieve. Adsorbed and capillary water vapor pressure increases in response to a temperature increase and releases additional water to the soil pore atmosphere to be diffused away

Impact of tree cutting on water-soluble organic compounds in podzolic soils of the European North-East

Science.gov (United States)

Lapteva, Elena; Bondarenko, Natalia; Shamrikova, Elena; Kubik, Olesya; Punegov, Vasili

2016-04-01

Water-soluble organic compounds (WOCs) and their single components, i.e. low-molecular organic acids, alcohols, and carbohydrates, attain a great deal of attention among soil scientists. WOCs are an important component of soil organic matter (SOM) and form as a results of different biological and chemical processes in soils. These processes are mainly responsible for formation and development of soils in aboveground ecosystems. The purpose of the work was identifying qualitative and quantitative composition of low-molecular organic substances which form in podzolic loamy soils against natural reforestation after spruce forest cutting. The studies were conducted on the territory of the European North-East of Russia, in the middle taiga subzone (Komi Republic, Ust-Kulom region). The study materials were soil of undisturbed bilberry spruce forest (Sample Plot 1 (SP1)) and soils of different-aged tree stands where cutting activities took place in winter 2001/2002 (SP2) and 1969/1970 (SP3). Description of soils and vegetation cover on the plots is given in [1]. Low-molecular organic compounds in soil water extracts were identified by the method of gas chromatography mass-spectrometry [2, 3]. Finally, reforestationafterspruceforestcutting was found to be accompanied by different changes in soil chemical composition. In contrast with soils under undisturbed spruce forest, organic soil horizons under different-aged cuts decreased in organic carbon reserves and production of low-molecular organic compounds, changed in soil acidity. Within the soil series of SP1→SP2→SP3, the highest content of WOCs was identified for undisturbed spruce forest (738 mg kg-1 soil). In soils of coniferous-deciduous forests on SP1 and SP3, WOC content was 294 and 441 mg kg-1 soil, correspondingly. Soils at cuts decreased in concentration of any water-soluble low-molecular SOM components as low-molecular acids, alcohols, and carbohydrates. Structure of low-molecular WOCs in the study podzolic

Extractability and bioavailability of Pb and As in historically contaminated orchard soil: Effects of compost amendments

International Nuclear Information System (INIS)

Fleming, Margaret; Tai, Yiping; Zhuang, Ping; McBride, Murray B.

2013-01-01

The availability of Pb and As in an historically contaminated orchard soil, after amendment with compost and aging in the field, was determined by single-step chemical extraction with 1.0 M ammonium acetate at pH 4.8, sequential extraction using the modified BCR test, and a redworm bioassay in the laboratory. The efficiency of soil Pb extraction by ammonium acetate was greater at higher total soil Pb but was reduced by compost amendment. Conversely, the extraction efficiency of total soil As increased with compost amendment, but was not sensitive to total soil As. The redworm bioassay indicated Pb (but not As) bioavailability to be reduced by soil amendment with compost, a result consistent with the ammonium acetate extraction test but not reflected in modified BCR test. Electron microprobe studies of the orchard soil revealed Pb and As to be spatially associated in discrete particles along with phosphorus and iron. -- Highlights: ► Soil Pb and As in an old orchard were concentrated in discrete particles. ► Compost amendment of contaminated soil reduced Pb bioavailability. ► Compost amendment of contaminated soil did not reduce As bioavailability. ► Ammonium acetate extraction test reflected bioavailability of soil Pb and As. -- Remediating metal-contaminated orchard soils with compost reduced lead bioavailability but had little effect on arsenic

Soil water regime under homogeneous eucalyptus and pine forests

International Nuclear Information System (INIS)

Lima, W.P.; Reichardt, K.

1977-01-01

Measurement of precipitation and monthly soil water content during two consecutive years, in 6-year old plantations of eucalypt and pine, and also in an open plot containing natural herbaceous vegetation, were used to compare the soil water regime of these vegetation covers. Precipitation was measured in the open plot with a recording and a non-recording rain gage. Soil water was assessed by the neutron scattering technique to a depth of 1,80 meters. Results indicate that there was, in general, water available in the soil over the entire period of study in all three vegetation conditions. The annual range of soil water in eucalypt, pine, and in natural herbaceous vegetation was essentially similar. The analysis of the average soil water regime showed that the soil under herbaceous vegetation was, generally, more umid than the soil under eucalypt and pine during the period of soil water recharge (September through February); during the period of soil water depletion, the opposite was true. Collectively, the results permit the conclusion that there were no adverse effects on the soil water regime which could be ascribed to reflorestation with eucalypt or pine, as compared with that observed for the natural herbaceous vegetation [pt

Impact of historical mining assessed in soils by kinetic extraction and lead isotopic ratios

International Nuclear Information System (INIS)

Camizuli, E.; Monna, F.; Bermond, A.; Manouchehri, N.; Besançon, S.; Losno, R.; Oort, F. van; Labanowski, J.; Perreira, A.; Chateau, C.; Alibert, P.

2014-01-01

The aim of this study is to estimate the long-term behaviour of trace metals, in two soils differently impacted by past mining. Topsoils from two 1 km 2 zones in the forested Morvan massif (France) were sampled to assess the spatial distribution of Cd, Cu, Pb and Zn. The first zone had been contaminated by historical mining. As expected, it exhibits higher trace-metal levels and greater spatial heterogeneity than the second non-contaminated zone, supposed to represent the local background. One soil profile from each zone was investigated in detail to estimate metal behaviour, and hence, bioavailability. Kinetic extractions were performed using EDTA on three samples: the A horizon from both soil profiles and the B horizon from the contaminated soil. For all three samples, kinetic extractions can be modelled by two first-order reactions. Similar kinetic behaviour was observed for all metals, but more metal was extracted from the contaminated A horizon than from the B horizon. More surprising is the general predominance of the residual fraction over the “labile” and “less labile” pools. Past anthropogenic inputs may have percolated over time through the soil profiles because of acidic pH conditions. Stable organo-metallic complexes may also have been formed over time, reducing metal availability. These processes are not mutually exclusive. After kinetic extraction, the lead isotopic compositions of the samples exhibited different signatures, related to contamination history and intrinsic soil parameters. However, no variation in lead signature was observed during the extraction experiment, demonstrating that the “labile” and “less labile” lead pools do not differ in terms of origin. Even if trace metals resulting from past mining and metallurgy persist in soils long after these activities have ceased, kinetic extractions suggest that metals, at least for these particular forest soils, do not represent a threat for biota. - Highlights: • Trace

Impact of historical mining assessed in soils by kinetic extraction and lead isotopic ratios

Energy Technology Data Exchange (ETDEWEB)

Camizuli, E., E-mail: estelle.camizuli@u-bourgogne.fr [UMR 6298, ArTeHiS, Université de Bourgogne — CNRS — Culture, 6 bd Gabriel, Bat. Gabriel, 21000 Dijon (France); Monna, F. [UMR 6298, ArTeHiS, Université de Bourgogne — CNRS — Culture, 6 bd Gabriel, Bat. Gabriel, 21000 Dijon (France); Bermond, A.; Manouchehri, N.; Besançon, S. [Institut des sciences et industries du vivant et de l' environnement (AgroParisTech), Laboratoire de Chimie Analytique, 16, rue Claude Bernard, 75231 Paris Cedex 05 (France); Losno, R. [UMR 7583, LISA, Universités Paris 7-Paris 12 — CNRS, 61 av. du Gal de Gaulle, 94010 Créteil Cedex (France); Oort, F. van [UR 251, Pessac, Institut National de la Recherche Agronomique, Centre de Versailles-Grignon, RD 10, 78026 Versailles Cedex (France); Labanowski, J. [UMR 7285, IC2MP, Université de Poitiers — CNRS, 4, rue Michel Brunet, 86022 Poitiers (France); Perreira, A. [UMR 6298, ArTeHiS, Université de Bourgogne — CNRS — Culture, 6 bd Gabriel, Bat. Gabriel, 21000 Dijon (France); Chateau, C. [UFR SVTE, Université de Bourgogne, 6 bd Gabriel, Bat. Gabriel, 21000 Dijon (France); Alibert, P. [UMR 6282, Biogeosciences, Université de Bourgogne — CNRS, 6 bd Gabriel, Bat. Gabriel, 21000 Dijon (France)

2014-02-01

The aim of this study is to estimate the long-term behaviour of trace metals, in two soils differently impacted by past mining. Topsoils from two 1 km{sup 2} zones in the forested Morvan massif (France) were sampled to assess the spatial distribution of Cd, Cu, Pb and Zn. The first zone had been contaminated by historical mining. As expected, it exhibits higher trace-metal levels and greater spatial heterogeneity than the second non-contaminated zone, supposed to represent the local background. One soil profile from each zone was investigated in detail to estimate metal behaviour, and hence, bioavailability. Kinetic extractions were performed using EDTA on three samples: the A horizon from both soil profiles and the B horizon from the contaminated soil. For all three samples, kinetic extractions can be modelled by two first-order reactions. Similar kinetic behaviour was observed for all metals, but more metal was extracted from the contaminated A horizon than from the B horizon. More surprising is the general predominance of the residual fraction over the “labile” and “less labile” pools. Past anthropogenic inputs may have percolated over time through the soil profiles because of acidic pH conditions. Stable organo-metallic complexes may also have been formed over time, reducing metal availability. These processes are not mutually exclusive. After kinetic extraction, the lead isotopic compositions of the samples exhibited different signatures, related to contamination history and intrinsic soil parameters. However, no variation in lead signature was observed during the extraction experiment, demonstrating that the “labile” and “less labile” lead pools do not differ in terms of origin. Even if trace metals resulting from past mining and metallurgy persist in soils long after these activities have ceased, kinetic extractions suggest that metals, at least for these particular forest soils, do not represent a threat for biota. - Highlights: • Trace

Comparison of DNA extraction protocols for microbial communities from soil treated with biochar

Science.gov (United States)

Leite, D.C.A.; Balieiro, F.C.; Pires, C.A.; Madari, B.E.; Rosado, A.S.; Coutinho, H.L.C.; Peixoto, R.S.

2014-01-01

Many studies have evaluated the effects of biochar application on soil structure and plant growth. However, there are very few studies describing the effect of biochar on native soil microbial communities. Microbial analysis of environmental samples requires accurate and reproducible methods for the extraction of DNA from samples. Because of the variety among microbial species and the strong adsorption of the phosphate backbone of the DNA molecule to biochar, extracting and purifying high quality microbial DNA from biochar-amended soil is not a trivial process and can be considerably more difficult than the extraction of DNA from other environmental samples. The aim of this study was to compare the relative efficacies of three commercial DNA extraction kits, the FastDNA® SPIN Kit for Soil (FD kit), the PowerSoil® DNA Isolation Kit (PS kit) and the ZR Soil Microbe DNA Kit Miniprep™ (ZR kit), for extracting microbial genomic DNA from sand treated with different types of biochar. The methods were evaluated by comparing the DNA yields and purity and by analysing the bacterial and fungal community profiles generated by PCR-DGGE. Our results showed that the PCR-DGGE profiles for bacterial and fungal communities were highly affected by the purity and yield of the different DNA extracts. Among the tested kits, the PS kit was the most efficient with respect to the amount and purity of recovered DNA and considering the complexity of the generated DGGE microbial fingerprint from the sand-biochar samples. PMID:24948928