Soil solution studies on weathered soils from tropical north Queensland

Soil Research ◽  
1978 ◽  
Vol 16 (1) ◽  
pp. 67 ◽  
Author(s):  
GP Gillman ◽  
LC Bell
Keyword(s):  
Ionic Strength ◽  
Soil Solution ◽  
Soil Extract ◽  
Ionic Ratio ◽  
Soil Extracts ◽  
Weathered Soils ◽  
Upper Limit ◽  
Soil Solutions ◽  
Solution Studies ◽  
Calcium Magnesium

Solutions obtained from six soils in tropical North Queensland after incubation at a moisture tension of 0.1 bar were analysed to obtain data on their ionic strengths. Soil extracts, at soil: solution ratios of 1:1, 1:2.5, 1:5, and 1:10 were also examined. Determinations on the aqueous phase included electrical conductivity, pH, ammonium, calcium, magnesium, potassium, sodium, bicarbonate, chloride, sulphate, and nitrate. Ionic concentrations of the soil solutions were found to be low when compared with many of the values reported in the literature. The upper limit for the ionic strength was about 0.005. Ionic strength was well correlated with the electrolytic conductivity of the soil solution itself, and also of the soil extracts. Relationships found between the soil solution and soil extracts in respect of total cation (and anion) content and also cation ratios, allow predictions about the soil solution to be made from soil extract data. Consideration of the ionic ratio of calcium to total cations in these soils suggests that the soils may have suboptimal levels of calcium for the growth of many plant species.

The chemical composition and ionic strength of soil solutions from New Zealand topsoils

Soil Research ◽  
1985 ◽  
Vol 23 (2) ◽  
pp. 151 ◽  
Author(s):  
DC Edmeades ◽  
DM Wheeler ◽  
OE Clinton
Keyword(s):  
Soil Moisture ◽  
New Zealand ◽  
Ionic Strength ◽  
Soil Solution ◽  
Soil Type ◽  
Ionic Composition ◽  
Soil Samples ◽  
Minor Effect ◽  
Solution Composition ◽  
Soil Solutions

In preliminary experiments a centrifuge method for extracting soil solutions was examined. Neither the time nor speed of centrifuging had any effect on the concentrations of cations in soil solution. The concentration of cations increased with decreasing soil moisture content, and NO3, Ca, Mg, and Na concentrations increased with increasing time of storage of freshly collected moist soils. It was concluded that to obtain soil solutions, which accurately reflect the soil solution composition and ionic strength (I) in situ, requires that soil samples are extracted immediately (<24 h) following sampling from the field. Prior equilibration of soil samples, to adjust soil moisture contents, is therefore not valid. The effect of time of sampling and soil type, and the effects of fertilizer and lime applications, on soil solution composition and ionic strength, were measured on freshly collected field moist topsoils. Concentrations of Ca, Mg, K, Na, NH, and NO, were lowest in the winter and highest in the summer. Consequently, there was a marked seasonal variation in ionic strength which ranged from 0.003 to 0.016 mol L-1 (mean, 0.005 s.d. 0.003) over time and soil type. Withholding fertilizer (P, K, S, Ca) for two years had only a minor effect on ionic composition and strength, and liming increased solution Ca, Mg and HCO3, but decreased Al, resulting in a twofold increase in ionic strength. These results suggest that the ionic strength of temperate grassland topsoils in New Zealand lie within the range 0.003-0.016 and are typically 0.005.

Chemical attributes of some Queensland acid aoils. II. Relationships between soil and soil solution phase compositions

Soil Research ◽  
1989 ◽  
Vol 27 (2) ◽  
pp. 353 ◽  
Author(s):  
RC Bruce ◽  
LC Bell ◽  
DG Edwards ◽  
LA Warrell
Keyword(s):  
Ionic Strength ◽  
Linear Relationship ◽  
Soil Water ◽  
Multiple Regression ◽  
Soil Solution ◽  
Solution Phase ◽  
Multiple Regression Equation ◽  
Soil Solutions ◽  
Chemical Attributes ◽  
Strong Linear Relationship

Relationships were sought between soil and soil solution attributes by using the data of Bruce et al. (Part I). There was a strong linear relationship between EC of soil solutions and EC of 1:5 soil : water extracts (r2 = 0.904). In subsoils, the activity of Al3 + in soil solution was dependent on soil solution ionic strength and soil Al saturation, and was described by the following multiple regression equation: loge(Al3+) = -6.97 + 1.96logeIss + 0.0777Alsat.%

Corrigenda - The chemical composition and ionic strength of soil solutions from New Zealand topsoils

Soil Research ◽  
1985 ◽  
Vol 23 (2) ◽  
pp. 151
Author(s):  
DC Edmeades ◽  
DM Wheeler ◽  
OE Clinton
Keyword(s):  
Soil Moisture ◽  
New Zealand ◽  
Ionic Strength ◽  
Soil Solution ◽  
Soil Type ◽  
Ionic Composition ◽  
Soil Samples ◽  
Minor Effect ◽  
Solution Composition ◽  
Soil Solutions

In preliminary experiments a centrifuge method for extracting soil solutions was examined. Neither the time nor speed of centrifuging had any effect on the concentrations of cations in soil solution. The concentration of cations increased with decreasing soil moisture content, and NO3, Ca, Mg, and Na concentrations increased with increasing time of storage of freshly collected moist soils. It was concluded that to obtain soil solutions, which accurately reflect the soil solution composition and ionic strength (I) in situ, requires that soil samples are extracted immediately (<24 h) following sampling from the field. Prior equilibration of soil samples, to adjust soil moisture contents, is therefore not valid. The effect of time of sampling and soil type, and the effects of fertilizer and lime applications, on soil solution composition and ionic strength, were measured on freshly collected field moist topsoils. Concentrations of Ca, Mg, K, Na, NH, and NO, were lowest in the winter and highest in the summer. Consequently, there was a marked seasonal variation in ionic strength which ranged from 0.003 to 0.016 mol L-1 (mean, 0.005 s.d. 0.003) over time and soil type. Withholding fertilizer (P, K, S, Ca) for two years had only a minor effect on ionic composition and strength, and liming increased solution Ca, Mg and HCO3, but decreased Al, resulting in a twofold increase in ionic strength. These results suggest that the ionic strength of temperate grassland topsoils in New Zealand lie within the range 0.003-0.016 and are typically 0.005.

scholarly journals Prediction of molybdenum availability to plants in differentiated soil conditions

2017 ◽  
Vol 63 (No. 11) ◽  
pp. 491-497 ◽  
Author(s):  
Rutkowska Beata ◽  
Szulc Wiesław ◽  
Spychaj-Fabisiak Ewa ◽  
Pior Natalia
Keyword(s):  
Soil Solution ◽  
Soil Ph ◽  
Sandy Soils ◽  
Soil Samples ◽  
Soil Conditions ◽  
Soil Parameters ◽  
Displacement Method ◽  
Soil Solutions ◽  
Solution Studies ◽  
Positive Correlations

The aim of the study was to assess of plant available molybdenum (Mo) resources in the solutions of soils as well as to evaluate the effects of selected soil properties on changes of the Mo concentration in the soil solution. Sixty-two soil samples were investigated. The soil solutions were obtained by modified vacuum displacement method. The results showed that Mo concentrations in the soil solutions were much differentiated, ranging from 0.002 to approximately 0.100 µmol/L. Positive correlations were found between soil solution Mo concentration and soil pH as well as the contents of available phosphorous and organic carbon in soil. At the same time, Mo concentration was higher in the soil solutions obtained from soils with larger amounts of soil particles with diameter lesser than<br /> 0.02 mm. Among the analysed soil parameters in this study, soil pH is the most important factor that influences the Mo concentration in soil solution. Studies have shown that in acid sandy soils the amount of molybdenum found in the soil solution is too small to cover the nutritional requirements of the plants. This indicates the need of fertilization with this element. Regular liming of soils and fertilization with phosphorus can improve the availability of molybdenum to plants.

Amelioration of subsurface acidity in sandy soils in low rainfall regions .2. Changes to soil solution composition following the surface application of gypsum and lime

Soil Research ◽  
1994 ◽  
Vol 32 (4) ◽  
pp. 847 ◽  
Author(s):  
CDA Mclay ◽  
GSP Ritchie ◽  
WM Porter ◽  
A Cruse
Keyword(s):  
Ionic Strength ◽  
Soil Solution ◽  
Ion Pairs ◽  
Chemical Properties ◽  
Sandy Soils ◽  
Soil Surface ◽  
Field Trials ◽  
Annual Rainfall ◽  
First Year ◽  
Solution Composition

Two field trials were sampled to investigate the changes to soil solution chemical properties of a yellow sandplain soil with an acidic subsoil following the application of gypsum and lime to the soil surface in 1989. The soils were sandy textured and located in a region of low annual rainfall (300-350 mm). Soil was sampled annually to a depth of 1 m and changes in soil solution composition were estimated by extraction of the soil with 0.005 M KCl. Gypsum leaching caused calcium (Ca), sulfate (SO4) and the ionic strength to increase substantially in both topsoil and subsoil by the end of the first year. Continued leaching in the second year caused these properties to decrease by approximately one-half in the topsoil. Gypsum appeared to have minimal effect on pH or total Al (Al-T), although the amount of Al present as toxic monomeric Al decreased and the amount present as non-toxic AlSO+4 ion pairs increased. Magnesium (Mg) was displaced from the topsoil by gypsum and leached to a lower depth in the subsoil. In contrast, lime caused pH to increase and Al to decrease substantially in the topsoil, but relatively little change to any soil solution properties was observed in the subsoil. There was an indication that more lime may have leached in the presence of gypsum in the first year after application at one site. Wheat yields were best related to the soil acidity index Al-T/EC (where EC is electrical conductivity of a 1:5 soil:water extract), although the depth at which the relationship was strongest in the subsoil varied between sites. The ratio Al-T/EC was strongly correlated with the activity of monomeric Al species (i.e. the sum of the activities of Al3+, AlOH2+ and Al(OH)+2 in the soil solution. An increase in the concentration of sulfate in the subsoil solution (which increased the ionic strength, thereby decreasing the activity of Al3+, and also increased the amount of Al present as the AlSO+4 ion pair) was probably the most important factor decreasing Al toxicity to wheat. The results indicated that gypsum could be used to increase wheat growth in aluminium toxic subsoils in sandy soils of low rainfall regions and that a simple soil test could be used to predict responses.

scholarly journals Chloroform extraction of trace nutrients as oxinates from soil extracts for spectrographic analysis

1960 ◽  
Vol 32 (1) ◽  
pp. 223-228
Author(s):  
Osmo Mäkitie
Keyword(s):  
Trace Metals ◽  
Chloroform Solution ◽  
Soil Extract ◽  
Hydrogen Ion ◽  
Ion Concentration ◽  
Spectrographic Analysis ◽  
Hydrogen Ion Concentration ◽  
Soil Extracts ◽  
Copper Manganese ◽  
The Common

The experiments show that under these conditions the common trace nutrients, cobalt, copper, manganese, molybdenum and zinc are sufficiently completely extracted as chelates by shaking the soil extract with oxine-chloroform solution. The hydrogen ion concentration of the extract and the concentration of oxine in chloroform have decisive effects on the extractability. Using the reported and discussed procedure it is possible to separate the common trace metals from the major soil extract constituents, especially for spectrographic analysis.

The Role of Dissolved CH4 in Soil Solution in the CH4 Emission from Water-Saving Irrigated Rice Fields

2011 ◽  
Vol 148-149 ◽  
pp. 977-982
Author(s):  
Dao Xi Li
Keyword(s):  
Soil Solution ◽  
Early Stage ◽  
Dominant Role ◽  
Water Layer ◽  
Water Saving ◽  
Rice Fields ◽  
Chromatography Method ◽  
Soil Layers ◽  
Soil Solutions

To examine how the dissolved CH4 in soil solution would affect the CH4 emission from rice field, fluxes of CH4 emission were measured by using a manually closed static chamber-gas chromatography method, and the dissolved CH4 in soil solution was obtained through shaking soil solutions, which were extracted from different paddy soil layers by a soil solution sampler with suction and pressure. The results show that the CH4 fluxes from rice fields and the concentration of dissolved CH4 in soil solution are both reduced significantly under the water-saving irrigation as compared to the traditional flooded irrigation. Under the water-saving irrigation, naturally receding water-layer during the early stage leads to an earlier peak of CH4 flux, but dramatically reduces the concentration of dissolved CH4 in soil solution. The maximum concentration is shifted to about 20-cm depth soil layers, and the relationship between CH4 emissions and dissolved CH4 in soil solution can be estimated using an exponential function of dissolved CH4 in soil solution at the depth of about 20 cm (R2＝0.89, p4 in soil solution plays a more dominant role in CH4 emission under the water-saving irrigation than that under continuously flooded irrigation.

Speciation of cadmium in soil solutions of saline/sodic soils and relationship with cadmium concentrations in potato tubers (Solanum tuberosum L.)

Soil Research ◽  
1997 ◽  
Vol 35 (1) ◽  
pp. 183 ◽  
Author(s):  
M. J. McLaughlin ◽  
K. G. Tiller ◽  
M. K. Smart
Keyword(s):  
Soil Solution ◽  
Soil Ph ◽  
Solanum Tuberosum L ◽  
Alkaline Soil ◽  
Sodic Soils ◽  
Chloro Complexes ◽  
Soil Solutions ◽  
High Concentrations ◽  
The Stability ◽  
Saline Solutions

Fifty commercial potato crops and associated soils were sampled. Soil solutions were extracted from rewetted soils by centrifugation, and solution composition was related to Cd concentrations in tubers. Soils were also extracted with 0·01 M Ca(NO3)2 and 0·01 M CaCl2 solutions, and Cd2+ activities in the extracts were calculated by difference using the stability constants for formation of CdCl2-nn species. The soils had saline solutions (>4 dS/m), and Cl- and SO2-4 in solution markedly affected the speciation of Cd in soil solution, with chloro-complexes, in particular, dominating. While low soil pH was associated with high (>25 nM) concentrations of Cd in soil solution, chloro-complexation also led to high concentrations of Cd in solution, even at neutral to alkaline soil pH values. Tuber Cd concentrations were not related to activities of Cd2+ in soil solution or to activities in dilute salt extracts of soil. Tuber Cd concentrations were related to the degree of chloro-complexation of Cd in solution. The relationship of tuber Cd concentrations to chloro-complexation in soil solution suggests that Cd species other than the free Cd2+ ion are involved in the transport through soil and uptake of Cd by plants.

Effects of grassland afforestation on exchangeable soil and soil solution aluminium

Soil Research ◽  
2001 ◽  
Vol 39 (5) ◽  
pp. 1003 ◽  
Author(s):  
M. L. Adams ◽  
M. R. Davis ◽  
K. J. Powell
Keyword(s):  
Forest Soil ◽  
Soil Solution ◽  
Base Cation ◽  
Pinus Nigra ◽  
Base Saturation ◽  
Conifer Forest ◽  
Forest Sites ◽  
Hill Slope ◽  
Soil Solutions ◽  
The Impact

The impact of land use change from grassland to conifer forest on the aluminium (Al) concentrations in soils and soil solutions was examined. Soils from grassland were compared with those from adjoining 15–19-year old forest stands at 3 contrasting pairs of sites in South Island, New Zealand. The site pairs were on a terrace [Pinus nigra/P. ponderosa, and grassland (CP)], and a hill slope [Pseudotsuga menziesii and grassland (CF)] in the Craigieburn range, Canterbury, and a hill slope in the Lammerlaw Range, Otago [P. radiata and grassland (LP)]. The sites had never been cultivated or fertilised, and for each pair the forest and grassland were similar in terms of soil and topography. The 1 M KCl exchangeable and 0.02 M CaCl 2 extractable Al levels at 0–10 cm were higher in forest than in grassland topsoil at CP and LP (P < 0.01). In soil solutions there was a trend for both ‘reactive Al’ and Al bound in labile organic complexes to be higher in forest soil at all sites, but site-pair differences were only significant at LP, and only for ‘reactive Al’. The increase in ‘reactive Al’ at this site was linked to the low pH and low base saturation. The ratios of exchangeable and soil solution Ca 2+ and Mg 2+ to ‘reactive Al’ were substantially lower in forest than grassland soils at all sites. Aluminium complexation capacity (Al-CC) values at all sites were higher in forest soil solutions than in grassland soil solutions. For the grassland and forest sites at LP, the Al-CC correlated strongly with the amount of soluble fulvic and humic matter present, as estimated from soil solution UV absorbance at 250 nm. In soils with the lowest percentage base saturation and buffering capacity (LP), afforestation of pastoral grassland with Pinus radiata significantly reduced soil pH and base cation levels, while increasing both soil and soil solution Al concentrations. Under such conditions (base saturation <20%), the increase in ‘reactive Al’ concentrations in soil solutions under fast growing conifer tree species may be sufficient to affect Mg uptake.

The orthophosphate content of bicarbonate soil extracts

Soil Research ◽  
2001 ◽  
Vol 39 (2) ◽  
pp. 415 ◽  
Author(s):  
Joanne L. Coventry ◽  
David J. Halliwell ◽  
David M. Nash
Keyword(s):  
Molecular Weight ◽  
Plant Uptake ◽  
High Performance ◽  
Average Amount ◽  
Soil Extracts ◽  
Specific Identification ◽  
Soil P ◽  
Olsen P ◽  
Soil Solutions ◽  
Future Work

The Olsen P and Colwell P bicarbonate extraction procedures are empirically derived tests that provide an estimate of the soil P that is available for plant uptake. This paper examines each procedure using high performance liquid chromatography with flow injection analysis detection (HPLC-FIA) to specifically measure orthophosphate in bicarbonate extracts. Extract solutions from 3 soils of contrasting plant-available soil P contents were analysed for orthophosphate, total filtered (<15—45 µm) P (TFP), and either Olsen P or Colwell P. The amounts of P extracted by the Olsen procedure were not statistically different from orthophosphate (HPLC-FIA) (P > 0.05), suggesting the Olsen P test was a good measure of orthophosphate, the most immediately plant-available form of P. However, the average amount of P extracted by the Colwell procedure was 14% higher (P < 0.01) than the corresponding average orthophosphate concentration, presumably due to the presence of labile organic/condensed P, colloidal associated orthophosphate, or high molecular weight reactive P. These results suggest that there is a pool of non-orthophosphate P present in the molybdate reactive Colwell P extract that is potentially plant available. Future work should focus on specific identification of P compounds extracted from soils and soil solutions to examine their role as a source of P to plants.

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