Soil solution chemistry of contrasting soils amended with heavy metals

Soil Research ◽  
1999 ◽  
Vol 37 (5) ◽  
pp. 993 ◽  
Author(s):  
H. J. Percival ◽  
T. W. Speir ◽  
A. Parshotam
Keyword(s):  
Heavy Metals ◽  
Heavy Metal ◽  
Metal Ions ◽  
Cation Exchange ◽  
Soil Solution ◽  
Solution Chemistry ◽  
Percentage Increase ◽  
Soil Solution Chemistry ◽  
Soil Solutions ◽  
Wide Range

The soil solution chemistry of heavy metal amended soils is of great importance in assessing the bioavailability of heavy metals and their toxicity to the soil biota. Three contrasting soils were amended with Cd(II), Cu(II), Ni(II), Pb(II), Zn(II), and Cr(III) nitrate salts at rates of 10–100 mmol/kg. This concentration range was chosen to encompass a wide range of effects on sensitive soil biochemical properties as part of a larger project. Soil solutions were extracted and analysed for pH, and for concentrations of heavy metals, and major cations and anions. Heavy metal speciation was calculated with the GEOCHEM-PC model. Heavy metal concentrations in the soil solutions increased both in absolute terms and as a percentage of added heavy metal as amendment rates increased. This observation is due to decreasing specific adsorption (caused by decreasing pH induced by the amendments), and to increasing saturation of cation exchange sites. For all 3 soils, the percentage increase commonly follows the order Cr(III) < Pb < Cu < Ni < Cd < Zn. The percentage of each metal held in the soil solution increased from soil to soil as cation exchange capacity, and therefore sorptivity, decreased. Both the concentration and activity of free heavy metal ions were substantially lower than the corresponding total metal concentration. This was ascribed to ion-pairing of metal ions with anions, particularly nitrate introduced in the amending solutions, as well as to increases in ionic strength as a result of amendment. Metal-anion species were mainly inorganic but where Cu and Pb were relatively low in concentration because of strong adsorption by the soils, organic complexation was likely to be significant. Speciation trends were similar for the 3 soils but different in magnitude.

Soil and soil solution chemistry of a New Zealand pasture soil amended with heavy metal-containing sewage sludge

Soil Research ◽  
2003 ◽  
Vol 41 (1) ◽  
pp. 1 ◽  
Author(s):  
H. J. Percival
Keyword(s):  
Heavy Metals ◽  
New Zealand ◽  
Sewage Sludge ◽  
Soil Solution ◽  
Metal Ion ◽  
Solution Chemistry ◽  
Soil Solution Chemistry ◽  
Soil Solutions ◽  
Free Metal ◽  
Soil Metal

The disposal of wastewater treatment sewage sludge onto agricultural land in New Zealand has led to the development of guidelines for the upper limit concentrations for total heavy metals in the underlying soil. However, those soil biological and biochemical processes now known to be most sensitive to environmental change are being used internationally to set new soil limits. The soil solution chemistry of a pasture soil amended with heavy metals has been used to assess the bioavailability of several important heavy metals. Field trial plots were treated with both spiked (Cu, Ni, or Zn) and unspiked sewage sludge to raise total soil metal concentrations, both above and below the current New Zealand guideline values. Soils were sampled pre-amendment in 1997 and post-amendment in 1998, 1999, and 2000. Soil solutions were extracted by centrifugation and analysed for pH, for concentrations of heavy metals, major cations and anions, and dissolved organic carbon. Heavy metal speciation was calculated with the GEOCHEM-PC model.Soil solution concentrations of Cu, Ni, and Zn increased with increasing levels of metal in the spiked sludge, reflecting increases in total soil metal concentrations. Cu concentrations changed little with time, but those of Ni and Zn tended to decrease. Cu was much more adsorbed by the soil than was Ni or Zn. The free metal ions, Cu2+, Ni2+, and Zn2+ (representing the most 'bioavailable' fraction), were the dominant metal species in the soil solutions. Variations in free metal ion percentages with metal-spiking level depended on the balance between organic and sulfate complexation for Cu, but on sulfate complexation alone for Ni and Zn. Cu and Ni free metal-ion activities in soil solution were relatively low even at the highest metal loadings in the soil, but may be high enough to cause toxicity problems. Zn activities were very much higher, and at the regulatory limit for zinc likely to affect sensitive biological and biochemical properties of the soil.

Soil solution chemistry and alfalfa response to CaCO3 and MgCO3 on an acidic Gleysol

1996 ◽  
Vol 76 (1) ◽  
pp. 41-47 ◽  
Author(s):  
Chunming Su ◽  
L. J. Evans
Keyword(s):  
Regression Analysis ◽  
Soil Solution ◽  
Solution Chemistry ◽  
Immiscible Displacement ◽  
Limiting Factor ◽  
Agricultural Practice ◽  
Soil Solution Chemistry ◽  
Mn Toxicity ◽  
The Third ◽  
Soil Solutions

Soil acidity is a limiting factor for forage production. Liming is a common agricultural practice for acid soils, yet there is limited information on the effects of soil solution chemistry in response to liming. Soil from the Ap horizon of an Orthic Humic Gleysol was amended with 0, 2.5 or 5.0 g CaCO3 kg−1 and 2.1 or 4.2 g MgCO3 kg−1 to determine the changes due to liming in soil solution composition before planting and after three cuts of alfalfa (Medicago sativa L.). The soil solution samples were extracted by immiscible displacement with C2Cl4. The low equivalent rate of CaCO3 and MgCO3 decreased the concentrations of Fe from 889 to less than 22 μM, Mn from 286 to less than 6 μM, Al from 45 μM to undetectable level before plant growth. Soil pH, dissolved organic carbon (DOC), Cu and NH4-N concentrations in the soil solutions extracted after the third cut of alfalfa were increased compared with those measured before planting. Concentrations of Ca, Mg, K, Na, Mn, Zn, Fe, Al, NO3-N, SO4 and Si were all decreased after the third cut compared with those measured before planting. Step-wise multiple regression analysis indicated that the dry matter (DM) yield of the first cut was positively correlated to NO3-N and negatively correlated to Mn concentration in the soil solutions (R2 = 0.65**); whereas the DM yield of the second and third cuts and of the roots were negatively correlated with Mn concentrations (R2 = 0.75**, 0.63**, and 0.60**, respectively). The regression analysis supported visual Mn toxicity, suggesting that Mn toxicity, not Al concentration, was the main limitation to alfalfa growth in unlimed soil. Key words: Alfalfa, liming, soil solution chemistry, immiscible displacement, plant nutrition

Solution chemistry effects on the solvation shell of metal ions

2020 ◽  
Author(s):  
Xiangwen Wang ◽  
Dimitrios Toroz ◽  
Seonmyeong Kim ◽  
Simon Clegg ◽  
Gun-Sik Park ◽  
...  
Keyword(s):  
Metal Ions ◽  
Pure Water ◽  
Solvation Shell ◽  
Solution Chemistry ◽  
Chemical Characteristics ◽  
Velocity Autocorrelation Function ◽  
Ionic Solvation ◽  
General Terms ◽  
Alkaline Earth Metal Ions ◽  
Wide Range

<div> <p>As natural aqueous solutions are far from being pure water, being rich in ions, the properties of solvated ions are of relevance for a wide range of systems, including biological and geochemical environments. We conducted ab initio and classical MD simulations of the alkaline earth metal ions Mg<sup>2+</sup> and Ca<sup>2+</sup> and of the alkali metal ions Li<sup>+</sup>, Na<sup>+</sup>, K<sup>+</sup> and Cs<sup>+</sup> in pure water and electrolyte solutions containing the counterions Cl<sup>–</sup> and SO<sub>4</sub><sup>2–</sup>. Through a detailed analysis of these simulations, this study reports on the effect of solution chemistry (composition and concentration of the solution) to the ion–water structural properties and interaction strength, and to the dynamics, hydrogen bond network, and low-frequency dynamics of the ionic solvation shell. Except for the ion–water radial distribution function, which is weakly dependent on the counter-ions and concentrations, we found that all other properties can be significantly influenced by the chemical characteristics of the solution. Calculation of the velocity autocorrelation function of magnesium ions, for example, shows that chlorine ions located in the second coordination shell of Mg<sup>2+</sup> weaken the Mg(H<sub>2</sub>O)<sub>6</sub><sup>2+</sup> hydration ‘cage’ of the cation. The result reported in this study suggest that ionic solvation shell can be significantly influenced by the interactions between other ions present in solution ions, especially those of opposite charge. In more general terms, the chemical characteristics of the solution, including the balance between ion-solvent and ion-ion interactions, could result in significant differences in behavior and function of the ionic solvation shell.</p> </div>

scholarly journals Recent developments in materials used for the removal of metal ions from acid mine drainage

2021 ◽  
Vol 11 (2) ◽  
Author(s):  
Tebogo M. Mokgehle ◽  
Nikita T. Tavengwa
Keyword(s):  
Heavy Metal ◽  
Surface Water ◽  
Acid Mine Drainage ◽  
Metal Ions ◽  
Mine Drainage ◽  
Acid Mine ◽  
Adsorption Capacities ◽  
Ion Imprinted ◽  
Wide Range ◽  
Ion Imprinted Polymers

AbstractAcid mine drainage is the reaction of surface water with sub-surface water located on sulfur bearing rocks, resulting in sulfuric acid. These highly acidic conditions result in leaching of non-biodegradeable heavy metals from rock which then accumulate in flora, posing a significant environmental hazard. Hence, reliable, cost effective remediation techniques are continuously sought after by researchers. A range of materials were examined as adsorbents in the extraction of heavy metal ions from acid mine drainage (AMD). However, these materials generally have moderate to poor adsorption capacities. To address this problem, researchers have recently turned to nano-sized materials to enhance the surface area of the adsorbent when in contact with the heavy metal solution. Lately, there have been developments in studying the surface chemistry of nano-engineered materials during adsorption, which involved alterations in the physical and chemical make-up of nanomaterials. The resultant surface engineered nanomaterials have been proven to show rapid adsorption rates and remarkable adsorption capacities for removal of a wide range of heavy metal contaminants in AMD compared to the unmodified nanomaterials. A brief overview of zeolites as adsorbents and the developent of nanosorbents to modernly applied magnetic sorbents and ion imprinted polymers will be discussed. This work provides researchers with thorough insight into the adsorption mechanism and performance of nanosorbents, and finds common ground between the past, present and future of these versatile materials.

Soil-solution chemistry in a low-elevation spruce-fir ecosystem, Howland, Maine

1995 ◽  
Vol 84 (1-2) ◽  
pp. 129-145 ◽  
Author(s):  
Ivan J. Fernandez ◽  
Gregory B. Lawrence ◽  
Yowhan Son
Keyword(s):  
Soil Solution ◽  
Solution Chemistry ◽  
Soil Solution Chemistry

scholarly journals Estimation of the Concentration of Some Heavy Metals in Groundwater in Rutba City

2021 ◽  
Vol 904 (1) ◽  
pp. 012009
Author(s):  
A W Abd Byty ◽  
M A Gharbi ◽  
A H Assaf
Keyword(s):  
Heavy Metals ◽  
Heavy Metal ◽  
Metal Ions ◽  
Heavy Metal Ions ◽  
Large Scale ◽  
Toxic Metal ◽  
Scale Production ◽  
Future Health ◽  
Distribution Maps ◽  
Guideline Values

Abstract Toxic metal pollutants in groundwater should be identified to prevent future health risks. In this paper, the presence of heavy metals in groundwater in the western region of Iraq was investigated. The heavy metals concentrations, including Ni2+, Co2+, Zn2+, Pb2+, Cr3+, Cd2+, As3+ and Hg2+ were explored in twenty selected aquifers near Rutba City and the results were presented as spatial distribution maps. Findings indicate that contamination with the investigated heavy metal ions possesses a serious threat to the study area’s groundwater quality when compared to WHO and IEPA guideline values. Thus, a new approach to remove or adsorb heavy metal ions can be developed for large-scale production and the safe use of these aquifers water. Results revealed that the highest concentrations in mg/L1 of 2.312 in w19, 1.098 in w2, 5.78 in w17, 0.292 in w9, 3.349 in w5, 0.32 in w13, 0.074 in w11 and 5.622 in w1 for Zn2+, Cr3+, As3+, Pb2+, Ni2+, Co2+, Cd2+ and Hg2+ were recorded, respectively.

scholarly journals The Influence of Heavy Metal Ions on the Viability and Metabolic Enzyme Activity of the Marbled Crayfish Procambarus virginalis (Lyko, 2017)

2018 ◽  
Vol 70 ◽  
pp. 11-23 ◽  
Author(s):  
Oleg Marenkov ◽  
Mykola V. Prychepa ◽  
Julia Kovalchuk
Keyword(s):  
Heavy Metals ◽  
Heavy Metal ◽  
Enzyme Activity ◽  
Metal Ions ◽  
Heavy Metal Ions ◽  
Physiological State ◽  
Metabolic Enzyme ◽  
Nickel Ions ◽  
The Individual ◽  
Marbled Crayfish

In the experiment with marbled crayfishProcambarusvirginalis(Lyko, 2017), chronic effects of various concentrations of heavy metal ions on the physiological state and enzyme activity were investigated. The obtained results showed that among the investigated heavy metals nickel ions influenced the weight indexes and mortality of crustaceans the most negatively. According to the results of the research, significant changes were noted in the individual biochemical parameters of marbled crayfish under the influence of manganese, lead and nickel ions. The most significant changes in the activity of lactate dehydrogenase were detected in muscle tissues affected by manganese and nickel ions. A significant decrease in the activity of succinate dehydrogenase in muscle of marbled crayfish was determined after the action of heavy metal ions. Investigation of changes in the activity of alkaline phosphatase under the influence of the ions of manganese, lead and nickel has its own characteristics, which indicates certain violations in the tissues of cell membranes. Changes in the activity of enzymes were also reflected in the overall protein content. Changes in these parameters may indicate a rapid biochemical response of crustaceans to the toxic effects of heavy metals.

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