scholarly journals Liming and Ionic speciation of an Oxisol under no-till system

2008 ◽  
Vol 65 (2) ◽  
pp. 190-203 ◽  
Author(s):  
Fernando Cesar Bachiega Zambrosi ◽  
Luís Reynaldo Ferracciú Alleoni ◽  
Eduardo Fávero Caires

The chemical speciation of the soil solution is an important tool for evaluating nutrient availability and aluminum phytotoxicity. The effect of liming in the composition of the soil solution under the no-till (NT) system is still not well known. We evaluated the chemical speciation of Al and nutrients in the soil solution (water extract 1:1), five years after liming at the moment of the establishment of NT in a native pasture, in Ponta Grossa, Paraná State, Brazil. Dolomitic lime was applied at a rate of 4.5 t ha-1 (either incorporated or surface-applied), or split in three annual rates of 1.5 t ha-1. Soil samples from a dystrophic clayey Rhodic Hapludox were collected at the 0 - 0.05; 0.05 - 0.1; 0.1 - 0.2; 0.2 - 0.4; 0.4 - 0.6; and 0.6 - 0.8 m layers, in May, 2003. Aluminum was mainly complexed to dissolved organic carbon (DOC) and fluoride, while the free form Al3+ was present in fewer amounts even under acidic conditions. Calcium and magnesium were found as free forms (Ca2+, Mg2+) and complexed by organic anions. Phosphorus was found as free forms (HPO4(2-), H2PO4-) and complexed with aluminum (ionic pair Al-HxPO4x) up to 0.1 m. Complexation of Al by DOC was not influenced by surface-applied or incorporated liming. Liming did not change Ca and Mg speciation in the soil solution under NT system. The presence of free forms HPO4(2-) and H2PO4-, however, was influenced by liming, because of the increase in cation associated forms.

Ceramics ◽  
2021 ◽  
Vol 4 (2) ◽  
pp. 240-248
Author(s):  
Yuki Sugiura ◽  
Masanori Horie

Octacalcium phosphate (OCP) is widely used in biomaterial fabrication by virtue of its unique crystal structure and low environmental loading. Although various ion and molecule substitution methods into the OCP unit lattice have been introduced, it remains unclear which factors and mechanisms dominate the substitution process. Experimental studies have indicated that Na alkali metal ions are substituted at the P3 PO4 conjugated site in acidic to weakly acidic conditions and the P5 PO4 conjugated site in neutral to weak basic conditions. Ionic species calculation methods have indicated that the pair ratios of Na and HPO42− (NaHPO4−) are small in acidic reacting solutions but large under weakly basic conditions. Consequently, the roles played by NaHPO4− and ionic pair formation processes are thought to dominate ion and molecule substitution into the OCP unit lattice. Such ionic pair formation strongly inhibits dicarboxylic acid substitution into the OCP unit lattice due to the replacement of the Ca ion, which conjugates P5 PO4 as an anchor of dicarboxylic acid.


Weed Science ◽  
1994 ◽  
Vol 42 (3) ◽  
pp. 462-467 ◽  
Author(s):  
Allan R. Isensee ◽  
Ali M. Sadeghi

A field study was conducted in 1987 to 1991 to determine the effect of tillage and rainfall on distribution of atrazine in soil. Soil samples (10-cm increments to 50 cm) and crop residue samples were taken at regular intervals after application each year and analyzed for atrazine. Crop residue and living vegetation on no-till plots intercepted 60 to 70% of the applied atrazine; 3 to 16% of the atrazine remained in crop residue 1 to 2 wk later. The amount of atrazine recovered in soil, 1 to 2 wk posttreatment, ranged from 22 to 59 and 47 to 73% of the amount applied for no-till and conventional till, respectively. An average of 2.6 times more atrazine was recovered in the surface 10 cm of soil under conventional till than under no-till for all samplings and years. Total amounts of atrazine in the sampled profile (0- to 50-cm depth) were also generally lower under no-till than conventional till. More leaching below 10 cm occurred under no-till than conventional till, particularly in 1988 and 1990 when rain fell soon after application. Variation in soil atrazine levels among years was related to timing and amount of the first and subsequent rainfall after application.


2013 ◽  
Vol 701 ◽  
pp. 243-248 ◽  
Author(s):  
Intan Suhada Azmi ◽  
Amizon Azizan ◽  
Ruzitah Mohd Salleh ◽  
Rafidah Jalil ◽  
Tengku Elida Tengku Zainal Mulok ◽  
...  

Over the last decade, there has been increasing research interest in the value of biosourced materials from lignocellulosic biomass. Abundant sources of lignocellulosic biomass such as palm,napiergrass,luceanatree, urban waste, municipal solid waste, agricultural waste and other waste have the potential to become a sustainable source of biofuel. In Malaysia, dissolution of cellulose from palm biomass to produce ethanol as future biofuels is very promising since palm residues from palm industry are highly abundant. In addition, cellulose contents in palm wastes or residues are relatively high for instance from empty fruit bunch or palm trunk. An efficient pretreatment is highly required prior to processes which convert the lignocellulosic palm biomass to bioethanol. The kinds of processes needed nowadays are called as green technology based techniques which are environmental friendly. Various solvents have been applied to dissolve cellulose including various types of ionic liquid as well. Previously, other method such as acid hydrolysis pretreatment process cause many drawbacks due to their low rates of hydrolysis and extreme acidic conditions. The dissolution process of the lignocellulosic biomass with ionic liquids is at its better advantage due to better dissolution as compared to by using organic or inorganic solvents. Therefore, at the moment, ionic liquid is becoming more preferable in dissolving the lignocellulosic biomass or any palm residues for instance.


1969 ◽  
Vol 75 (3) ◽  
pp. 223-231
Author(s):  
Gustavo A. Martínez ◽  
David R. Bouldin

A series of equations based on relations between exchangeable and soil solution ions were evaluated to find an appropriate procedure to determine the activity of cations in soil solution of small soil samples. The effectiveness of the developed equations was maintained even when the sample was submitted to variations in the type of salt added to the soil in the soil water ratio (SWR) used to extract the ions in solution.


2020 ◽  
Vol 45 (4) ◽  
Author(s):  
A.O. Abdullahi ◽  
A. Usman ◽  
A.H. Zakari ◽  
J.R. Tukur

This research work is aimed at determining the chemical speciation of metals Zn, Mn, Fe and Pb in soil samples from three major dumpsites within Gombe metropolis, Gombe state. The renowned five steps Tessier sequential extraction method was employed in the extraction of the heavy metals. The metals were extracted into five fractions namely: Exchangeable (F1), carbonate bound (F2), Fe-Mn oxide bound (F3), Bound to organic matter (F4) and the residual fraction (F5) in order of decreasing mobility. The elemental analysis of the fractions was carried out using atomic absorption spectrometric technique. The results showed Zn was predominantly bounded to the exchangeable fraction with 32.66±0.31 mg/kg (54.18%) and least in the Fe – Mn oxide fraction with 0.01±0.00 mg/kg (0.02%). The trend in its abundance is in the order F1> F2>F5>F4>F3. Mn was predominantly associated with the bound to carbonates fraction with the value of 103.3.±3.30 mg/kg (56.14%) and least in the exchangeable with the value of 1.30±1.85mg/kg (2.13%) its occurred in the order F2>F3>F4>F5>F1. The concentration of Fe was highest in the residual fraction with the value of 25.90±1.75mg/kg (45.45%)and least in the carbonate bound fraction wi th 5.10±0.40 mg/kg (2.13%) the order is F5>F4>F3>F2>F1. Pb was not detected in most of the fraction but highest in bond to carbonate and bond to organic matter fraction with the values of 6.64±4.12 mg/Kg (70.64 %) and 2.76±0.10 mg/Kg (29.36 %) respectively in two different samples. It was however established that Zn, Mn and Pb were mostly associated with the first three fractions thus, showed high bio-availabilty whereas Fe was found in the residual fraction and is expected to be low in mobility and less bioavailable. 


Soil Research ◽  
1985 ◽  
Vol 23 (2) ◽  
pp. 151 ◽  
Author(s):  
DC Edmeades ◽  
DM Wheeler ◽  
OE Clinton

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.


Author(s):  
Yuriy Yuryi Kravchenko ◽  
Zhang Xingyi ◽  
Song Chun-yu ◽  
Yarosh Anna Viyacheslavivna ◽  
Voitsekhivska Olena Vasilivna

The main purpose of this study was to determine the size and direction of the seasonal dynamics of organic carbon (Сmicro) and nitrogen (Nmicro) biomass of microorganisms and microbial index (Cmicro : Corg) of natural and agrocenoses with their different uses. Field research methods involved taking of soil samples in 0-10-, 10-20- and 20-40 сm layers. Under laboratory conditions, the content of total soil carbon was determined by dry oxygen combustion on a Vario EL III analyzer (Elementar Analyzensysteme, Hanau, Germany). The carbon content of microbial biomass (Сmicro) was determined by chloroform fumigation extraction method (CFE). To freshly taken soil samples (2 hours) and soil samples after their 24-hour fumigation with chloroform vapors, 0.5 M K2SO4 was added to extract biomass lysis products of soil microorganisms. The content of organic carbon and nitrogen in the biomass of microorganisms in the obtained filtrates was determined on the Elementar Liqui TOC II, Analyzensysteme GmbH, Germany. The carbon content of microbial biomass was calculated from the difference between carbon in fumigated and control samples using a factor of 0,45 - for carbon and 0,54 &ndash; for nitrogen. The microbial index of soils was determined by the ratio between the carbon of microorganisms and the total organic carbon of the soil &ndash; Cmicro : Corg &bull; 100 (%). Average values and confidence intervals were determined for each defined indicator. The Bonferoni method was used to correct the errors of multiple comparative samples of a one-way ANOVA analyze. K. Pearson&rsquo;s linear correlation analysis was used to establish the relationships between the dynamics of carbon biomass of microorganisms and organic carbon of the soil during the growing season. Our research has shown the dynamics of Сmicro, Nmicro, Сmicro : Nmicro and Cmicro : Corg during the growing season. Analysis of the box plot showed the largest amplitude of Сmicro changes in the upper 0-10 cm layer of izogumusol. The smallest difference in the quartile range (IQR0,25-0,75) was for no-till and overhang (Ab) in the upper 0-10-, no-till (NT) and fallow (F) - in the layer 10-20- and plowing (CT) - in a layer of 20-40 cm. The content of organic carbon biomass of microorganisms in the upper layer of izogumusol at the beginning of the growing season had the highest values of Ab (577,79  1,64 mg/kg), NT (485,43  1,97 mg/kg) and CT (470,43  0,77 mg/kg), the smallest - for F (370,15  2,18 mg/kg). The content of Nmicro during this period decreased from Ab to Comb (combined tillage), NT, CT, Rot (rotary tillage), RT (reduced (ridge) tillage) and F, respectively. In the 20-40 cm layer, the highest values of Сmicro and Nmicro were observed in mid-July. The lowest values of Сmicro and Nmicro and the largest &ndash; Сmicro : Nmicro were found in late August for all variants and layers of the study. The dynamics of the microbial index resembled the trends of Сmicro and Nmicro. The largest share of Smicro in Sorghum during the growing season, on average was: - Ab (1,82  1,85 %) and NT (1,66  1,52 %) - in the layer 0-10-, - Ab (1,23  1,27 %) and NT (1,29  1,32 %) - in the layer 10-20- and - Ab (1,19  1,09 %) and F (1,11  1,077 %) - in a layer of 20-40 cm. Different use of izogumusol affected the amplitude of seasonal changes of Сmicro and Nmicro and did not affect on their direction. The maximum content of Сmicro and Nmicro was observed at the beginning of the growing season - in a layer of 0-10 cm and in mid-July - in a layer of 20-40 cm, the minimum - at the end of the summer period. During this period, the widest ratio of Сmicro : Nmicro was for F and CT - in the layer 0-20 cm and CT and Rot - in the layer 20-40 cm. The Pearson&rsquo;s correlation coefficient between Сmicro and Corg increased from the upper 0-10- to the lower 20-40 cm layer of izogumusol. "Strong" and "high" negative correlations have been established between Сmicro and Corg, but no pattern has been found between the correlation coefficient and tillage technologies.


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