Assessment of peroxide oxidation for acid sulfate soil analysis. 1. Reduced inorganic sulfur

Soil Research ◽  
2002 ◽  
Vol 40 (3) ◽  
pp. 433 ◽  
Author(s):  
Nicholas J. Ward ◽  
Leigh A. Sullivan ◽  
Richard T. Bush ◽  
Chuxia Lin

The reduced inorganic sulfur fraction of 4 acid sulfate soil (ASS) materials was quantified using a variety of peroxide oxidation procedures. The temperature and duration of the peroxide oxidation were found to markedly affect the peroxide oxidisable sulfur determination. For 3 ASS materials with low total carbon content (i.e. <2.5% C), peroxide oxidisable sulfur underestimated the reduced inorganic sulfur fraction, with the peroxide oxidisable sulfur determinations being as low as 42% of those determined using chromium reducible sulfur technique. The precipitation of jarosite during peroxide oxidation was a major factor contributing to the underestimation of reduced inorganic sulfur in these materials. Apparent losses of sulfur of approximately 25% on average occurred during peroxide oxidation budget accounting; this also contributed towards the observed underestimation of reduced inorganic sulfur. It is most likely that these unaccounted losses are due to atmospheric losses of sulfur. In a peat ASS, one of the peroxide oxidation methods overestimated the reduced inorganic sulfur fraction and was attributed to the release of a large reserve of organic sulfur in this material by the peroxide. This study shows the peroxide oxidation methods examined here are subject to substantial interferences. Consequently these peroxide oxidation methods are unable to reliably provide accurate measurements of the reduced inorganic sulfur fraction in ASS materials. pyritic sulfur, peroxide oxidisable sulfur, chromium reducible sulfur, jarosite, sulfur budget.

Soil Research ◽  
2002 ◽  
Vol 40 (3) ◽  
pp. 443 ◽  
Author(s):  
Nicholas J. Ward ◽  
Leigh A. Sullivan ◽  
Richard T. Bush ◽  
Chuxia Lin

Total sulfidic acidity (TSA) and total potential acidity (TPA) are derived from peroxide oxidation of acid sulfate soil materials (ASS), and are measures of the sulfidic acidity and the net acidity (net acidity = sulfidic acidity + actual acidity – acid neutralising capacity), respectively. The TSA and TPA of 4 ASS materials were determined using a variety of peroxide oxidation procedures and compared with the sulfidic acidity and net acidity derived from the use of an acid–base accounting model. TSA and TPA values both varied greatly with each peroxide oxidation method used, and both measures were found to substantially underestimate (i.e. by 23–85%) both sulfidic acidity (as determined from the chromium reducible sulfur content) and net acidity (as determined by acid–base accounting). A major cause of this underestimation of acidity was the retention of acidity through the precipitation of jarosite during peroxide oxidation. Substantial clay mineral dissolution appears to have occurred during peroxide oxidation of the ASS materials, as indicated by increased soluble aluminium. Such dissolution may contribute to the underestimation of both sulfidic and net acidity for the ASS materials using peroxide oxidation methods. The loss of acidity to the atmosphere was identified as a possible additional interference. This study shows the peroxide oxidation methods examined here are subject to substantial interferences, which caused large underestimations of acidity, and consequently, are unable to reliably provide accurate measurements of sulfidic and net acidity in ASS materials. pyritic sulfur, total potential acidity, total sulfidic acidity, net acidity, jarosite, acid budget, acid neutralising capacity.


Soil Research ◽  
2002 ◽  
Vol 40 (7) ◽  
pp. 1133 ◽  
Author(s):  
Angus E. McElnea ◽  
Col R. Ahern ◽  
Neal W. Menzies

Improvements to the routine methods for the determination of actual acidity in suspension for acid sulfate soils (ASS) are introduced. The titratable sulfidic acidity (TSA) results using an improved peroxide-based method were compared with the theoretical acidity predicted by the chromium reducible sulfur method for 9 acid sulfate soils. The regression between these 2 measures of sulfidic acidity was highly significant, the slope of the regression line not significantly different from unity (P = 0.05) and the intercept not significantly different from zero. This contrasts with results of other workers using earlier peroxide oxidation methods, where TSA substantially underestimated the theoretical acidity predicted by reduced inorganic sulfur analysis. Comparison was made between the 2 principal measurements from the improved peroxide method (TSA and SPOS), with SPOS converted to theoretical sulfidic acidity to allow comparison. The relationship between these 2 measurements was highly significant. The effects of titration in suspension, as well as raising titration end points to pH 6.5, were investigated, principally with respect to the titratable actual acidity (TAA) result. TAA results obtained by KCl extraction were compared with those obtained using BaCl2, MgCl2, and water extraction. TAA in 1 M KCl suspensions titrated to pH 6.5 agreed well with titratable actual acidity measured using the 25-h extraction approach of the Lin et al. (2000a) BaCl2 method. Both BaCl2 and KCl solutions were ineffective at fully recovering acidity from synthetic jarosite without repeated extraction and titration. The application of correction factors for the estimation of total actual acidity in ASS is not supported by the results of this investigation. Acid sulfate soils that contain substantial quantities of jarosite or other acid-producing but relatively insoluble sulfate minerals continue to prove problematic to chemically analyse; however, an approach for estimating this component is discussed.


Soil Research ◽  
2004 ◽  
Vol 42 (6) ◽  
pp. 515 ◽  
Author(s):  
Nicholas J. Ward ◽  
Leigh A. Sullivan ◽  
Richard T. Bush

Four acid sulfate soil (ASS) materials were subjected to anoxia after varying periods of oxidation to determine the geochemical response of these types of soils to flooding. The response of the partially oxidised ASS materials to the exclusion of oxygen was variable. The rate of sulfide oxidation, acidification, and the production of soluble oxidation products such as sulfate, iron, and aluminium generally decreased markedly when subjected to anoxia. However, especially in the highly acidic ASS materials (i.e. pH <3.5), sulfide oxidation and acidification generally continued (albeit at much slower rates), most probably due to oxidation by Fe3+. Rapid sulfide re-formation occurred in the peat ASS material that had been oxidised for 63 days, with 0.47% reduced inorganic sulfur (SCR) formed over 60 days of anoxia. This substantial sulfide re-formation was accompanied by only a slight increase in pH. Minimal sulfide re-formation occurred in 2 of the ASS materials when placed in anoxic conditions, most likely due to a lack of readily available organic matter in these materials. The results show that the imposition of anoxic conditions on partially oxidised ASS materials is generally effective in decreasing the rates of further sulfide oxidation, acidification, and the production of soluble sulfide oxidation products. Biogeochemical sulfide formation consumes acidity; however, sulfide re-formation was ineffective in reversing acidification under the conditions of this experiment. The results indicate that the treatment of sites containing actual ASS materials by management strategies relying on oxygen exclusion need to be accompanied by other strategies that include acidty neutralisation or containment.


2006 ◽  
Vol 40 (3) ◽  
pp. 888-893 ◽  
Author(s):  
Edward D. Burton ◽  
Richard T. Bush ◽  
Leigh A. Sullivan

Soil Research ◽  
2000 ◽  
Vol 38 (3) ◽  
pp. 729 ◽  
Author(s):  
L. A. Sullivan ◽  
R. T. Bush ◽  
D. M. McConchie

Reaction times for 16 acid sulfate soil materials analysed using a modified chromium-reducible sulfur method varied between 10 and 15 min, regardless of whether the samples had been dried and ground prior to analysis or were analysed without pretreatment. The reaction time for a ground (<63 mm) pyritic rock sample was 20 min. An optimum reaction time of 20 min is recommended for analysing acid sulfate soil using the modified method; this reaction time is much less than the 1 h reaction time used in previous methods.


2019 ◽  
Vol 646 ◽  
pp. 1489-1502 ◽  
Author(s):  
José M. Soriano-Disla ◽  
Leslie J. Janik ◽  
Sean T. Forrester ◽  
Sonia F. Grocke ◽  
Robert W. Fitzpatrick ◽  
...  

2009 ◽  
Vol 4 (1) ◽  
pp. 125
Author(s):  
Akhmad Mustafa ◽  
Rachmansyah Rachmansyah ◽  
Dody Dharmawan Trijuno ◽  
Ruslaini Ruslaini

Rumput laut (Gracilaria verrucosa) telah dibudidayakan di tambak tanah sulfat masam dengan kualitas dan kuantitas produksi yang relatif tinggi. Oleh karena itu, dilakukan penelitian yang bertujuan untuk mengetahui peubah kualitas air yang mempengaruhi laju pertumbuhan rumput laut di tambak tanah sulfat masam Kecamatan Angkona Kabupaten Luwu Timur Provinsi Sulawesi Selatan. Pemeliharaan rumput laut dilakukan di 30 petak tambak  terpilih selama 6 minggu. Bibit rumput laut dengan bobot 100 g basah ditebar dalam hapa berukuran 1,0 m x 1,0 m x 1,2 m. Peubah tidak bebas yang diamati adalah laju pertumbuhan relatif, sedangkan peubah bebas adalah peubah kualitas air yang meliputi: intensitas cahaya, salinitas, suhu, pH, karbondioksida, nitrat, amonium, fosfat, dan besi. Analisis regresi berganda digunakan untuk menentukan peubah bebas yang dapat digunakan untuk memprediksi peubah tidak bebas. Hasil penelitian menunjukkan bahwa laju pertumbuhan relatif rumput laut di tambak tanah sulfat masam berkisar antara 1,52% dan 3,63%/hari dengan rata-rata 2,88% ± 0,56%/hari. Di antara 9 peubah kualitas air yang diamati ternyata hanya 5 peubah kualitas air yaitu: nitrat, salinitas, amonium, besi, dan fosfat yang mempengaruhi pertumbuhan rumput laut secara nyata. Untuk meningkatkan pertumbuhan rumput laut di tambak tanah sulfat masam Kecamatan Angkona Kabupaten Luwu Timur dapat dilakukan dengan pemberian pupuk yang mengandung nitrogen untuk meningkatkan kandungan amonium dan nitrat serta pemberian pupuk yang mengandung fosfor untuk meningkatkan kandungan fosfat sampai pada nilai tertentu, melakukan remediasi untuk menurunkan kandungan besi serta memelihara rumput laut pada salinitas air yang lebih tinggi, tetapi tidak melebihi 30 ppt.Seaweed (Gracilaria verrucosa) has been cultivated in acid sulfate soil-affected ponds with relatively high quality and quantity of seaweed production. A research has been conducted to study water quality variables that influence the growth of seaweed in acid sulfate soil-affected ponds of Angkona Sub-district East Luwu Regency South Sulawesi Province. Cultivation of seaweed was done for six weeks in 30 selected brackishwater ponds. Seeds of seaweed with weight of 100 g were stocked in hapa sized 1.0 m x 1.0 m x 1.2 m. Dependent variable that was observed was specific growth rate, whereas independent variables were water quality variables including light intensity, salinity, temperature, pH, carbondioxide, nitrate, ammonium, phosphate, and iron. Analyses of multiple regressions were used to determine the independent variables which could be used to predict the dependent variable. Research result indicated that relative growth rate of seaweed in acid sulfate soils-affected brackishwater ponds ranged from 1.52% to 3.63%/day with 2.88% ± 0.56%/day in average. Among nine observed water quality variables, only five variables namely: nitrate, salinity, ammonium, phosphate and iron influence significantly on the growth of seaweed in acid sulfate soils-affected brackishwater ponds. The growth of seaweed in acid sulfate soils-affected brackishwater ponds of Angkona District East Luwu Regency, can be improved by using nitrogen-based fertilizers to increase ammonium and nitrate contents and also fertilizers which contain phosphorus to improve phosphate content to a certain level. Pond remediation to decrease iron content and also rearing seaweed at higher salinity (but less than 30 ppt) can also be alternatives to increase the growth of seaweed.


1999 ◽  
Vol 79 (2) ◽  
pp. 303-310 ◽  
Author(s):  
F. L. Wang ◽  
A. K. Alva

Leaching of water soluble soil carbon plays an important role in downward transport of soil nutrients and pollutants and may be influenced by soil and management factors. We examined the leaching of water soluble carbon from two sandy soils under nitrogen fertilization by adapting an intermittent leaching-incubation technique using packed soil columns (94 × 10 cm). After 30 d, cumulative amounts of water-soluble organic carbon (SOC) leached from the Candler and Wabasso sand for various treatments in mg C column−1 were: 77 and 302 (NH4NO3), 64 and 265 (control), and 45 and 239 (isobutylidene diurea, IBDU), respectively. The IBDU and NH4NO3 treatments increased the leaching of water-soluble inorganic carbon (SIC), which ranged from 2 to 38 mg C column−1 over 30 d. At the end of eight cycles of leaching/incubation, the total carbon content increased at depth (control and NH4NO3 treatment) in the Candler sand, but decreased in the Wabasso sand. In the first leaching event, the average rate of SOC leaching from the Wabasso sand was 26 mg C column−1 d−1 which dropped rapidly to about 5 mg C column−1 d−1 towards the end of the experiment. The rate of SOC leaching from the Candler sand was much lower (<8 mg C column−1 d−1) than the rate of SOC leaching from the Wabasso sand. Compared with the unamended treatments, application of NH4NO3 increased and IBDU decreased the leaching of SOC in both soils. These effects of N application were considerable during the initial two to three leaching events only. Our results suggest that the initial rainfalls that follow a dry period may be critical for transporting SOC from the upper layer of these sandy soils. Key words: C leaching, sandy soil, intermittent leaching condition, isobutylidene


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