Relevant bibliographies by topics / Acid sulfate soils

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
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Academic literature on the topic 'Acid sulfate soils'

Author: Grafiati
Published: 4 June 2021
Last updated: 20 February 2023

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Journal articles on the topic "Acid sulfate soils"

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Pupathy, UT, T. Sabrina, S. Paramananthan, and Rosazlin Abdullah. "Some important elements of soil-water relationship in managing oil palms planted on acid sulfate soils." International Journal of Hydrology 4, no. 6 (December 22, 2020): 285–91. http://dx.doi.org/10.15406/ijh.2020.04.00256.

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Oil palms (Elaeis guineensis) are generally able to grow economically and feasibly on various soil types, mostly in tropical countries. However, oil palms planted on acid sulfate soils were producing lesser Fresh Fruit Bunches (FFB) as compared to those on non-acid sulfate soils. The poor performance of oil palms planted on acid sulfate was mainly attributed to the presence of excess sulfates, which limits the FFB yields and vegetative growth.1 Generally, acid sulfate soils have significant amounts of free and absorbed sulfate. Jarosite generally occurs as pale yellow mottles along old root channels and on ped faces in acid sulfate soils. pH in these horizon is less than 4.0.2,3 These soils often are also high in Aluminium (Al), Al saturation and often with phosphorus (P) fixation capacity. These acid sulfate soils are known for having poor values for organic matter, bases, cation exchange capacity, water retention, water holding capacity and microbial activity, which contributes towards their low soil fertility and hence limitations in soil productivity. Of these limitations, Al toxicity and excess sulfates are two major constraints to FFB yields in oil palms. The important relationship of soil and water for managing a sustainable productivity of oil palms on acid sulfate soil are discussed in details in this paper.
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Hoa, Nguyen My, Trinh Thi Thu Trang, and Tran Kim Tinh. "Net N mineralisation in acid sulfate soils amended with different sources of organic matter, lime, and urea." Soil Research 42, no. 6 (2004): 685. http://dx.doi.org/10.1071/sr03081.

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Acid sulfate soils in the Mekong Delta, Vietnam, are often high in organic matter content, but net N mineralisation is low. This may be due to low soil pH or low easily decomposable organic matter content. This study aimed at investigating net N mineralisation in acid sulfate rice soil (anaerobic incubation) and acid sulfate upland soil (aerobic incubation) amended with 1% biogas sludge, 1% straw, 1% starch, 2.5‰ CaCO3 (about 10 t CaCO3/ha for acid sulfate soils), and 0.22‰ urea. Non-acid alluvial soils were used for comparison. Results showed that addition of straw and starch to acid sulfate rice soil decreased net N mineralisation, but addition of biogas sludge increased cumulative N-NH4 due to both the increase in soil pH after submergence and the supply of low C/N organic matter. Addition of biogas sludge can therefore increase N-supplying capacity in acid sulfate rice soil. During aerobic incubation of acid sulfate upland soil with biogas sludge, cumulative N (NH4 + NO3) was also increased compared with the control, although pH was not increased. It is concluded, therefore, that in acid sulfate soils in the Mekong Delta, the supply of easily decomposable organic matter with low C/N ratio can increase activity of microorganisms and hence increase net N mineralised compared with soils not supplied with biogas sludge. Liming can increase net N mineralisation in acid sulfate rice soil during anaerobic incubation, but not in acid sulfate upland soil during aerobic incubation. Addition of rice straw and starch to soil amended with urea increased N immobilisation; therefore, urea can be temporally immobilised in soils and hence may reduce loss of N in field conditions.
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Wessel, Barret M., John M. Galbraith, Mark H. Stolt, Martin C. Rabenhorst, Delvin S. Fanning, and Maxine J. Levin. "Soil taxonomy proposals for acid sulfate soils and subaqueous soils raised by the 8th International Acid Sulfate Soils Conference." South African Journal of Plant and Soil 35, no. 4 (December 11, 2017): 293–95. http://dx.doi.org/10.1080/02571862.2017.1387820.

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KIMPE, C. R. DE, M. R. LAVERDIÈRE, and R. W. BARIL. "CLASSIFICATION OF CULTIVATED ESTUARINE ACID SULFATE SOILS IN QUEBEC." Canadian Journal of Soil Science 68, no. 4 (November 1, 1988): 821–26. http://dx.doi.org/10.4141/cjss88-081.

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When drained and cultivated, acid sulfate soils developed on coastal marsh sediments lose some of their specific properties because large amounts of lime are applied before cultivation and sulfate ions are leached out of the profiles. However, these soils still contrast strongly with other Gleysolic soils and their special characteristics should be given more emphasis in the soil classification system, especially for the benefit of soil fertility specialists. Key words: de l'Anse soils, jarosite, Gleysolic soils, sulfur
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Kinsela, Andrew S., Jason K. Reynolds, and Mike D. Melville. "Agricultural acid sulfate soils: a potential source of volatile sulfur compounds?" Environmental Chemistry 4, no. 1 (2007): 18. http://dx.doi.org/10.1071/en06071.

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Environmental context. Acid sulfate soils are important contributors to global environmental problems. Agricultural acid sulfate soils have recently been shown to emit sulfur dioxide, an important gas in global issues of acid rain, cloud formation and climate change. This emission is surprising because these soils tend to be wet and the gas is extremely water-soluble. The potential origins of this gas are not yet understood within the context of acid sulfate soils. Our new study reports the measurement of two potential precursors of sulfur dioxide, dimethylsulfide and ethanethiol, from both a natural and an agricultural acid sulfate soil in eastern Australia. Abstract. Most agricultural soils are generally considered to be a sink for sulfur gases rather than a source; however, recent studies have shown significant emissions of sulfur dioxide and hydrogen sulfide from acid sulfate soils. In the current study, acid sulfate soil samples were taken in northern New South Wales from under sugarcane cropping, as well as from an undisturbed nature reserve. Using gas chromatography/flame photometric detection in conjunction with headspace solid-phase microextraction, we have now determined that these soils are a potential source of the low molecular weight volatile sulfur compounds, dimethylsulfide and ethanethiol. Although the mechanism for their production remains unclear, both compounds are important in the transfer and interconversions of atmospheric and terrestrial sulfur. Therefore, these novel findings have important implications for refining local and regional atmospheric sulfur budgets, as well as for expanding our understanding of sulfur cycling within acid sulfate soils and other sediments.
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Yli-Halla, Markku. "Acid sulfate soils: A challenge for environmental sustainability." Annales Academiae Scientiarum Fennicae 1, no. 1 (November 15, 2022): 124–41. http://dx.doi.org/10.57048/aasf.122859.

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Acid sulfate (AS) soils contain sulfidic compounds formed in anaerobic conditions. In aerobic conditions, they will oxidize to sulfuric acid, which commonly lowers the pH to 3 – 4. These soils cover approximately 10,000 km2 in Finland, mainly on the western coast, and over 170,000 km2 globally. Acidity and the metals dissolved from the soil matrix and leached out of the soil are serious threats to aquatic biota. Initially, AS soils were regarded as an exclusively agricultural problem, but since the 1970s nearly all studies of AS soils have been environmentally motivated. Awareness of these soils has also risen in forestry, peat mining, and in engineering projects. Liming and water management are the key methods toward the sustainable use of these soils.
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Simpson, Stuart L., Rob W. Fitzpatrick, Paul Shand, Brad M. Angel, David A. Spadaro, and Luke Mosley. "Climate-driven mobilisation of acid and metals from acid sulfate soils." Marine and Freshwater Research 61, no. 1 (2010): 129. http://dx.doi.org/10.1071/mf09066.

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The recent drought in south-eastern Australia has exposed to air, large areas of acid sulfate soils within the River Murray system. Oxidation of these soils has the potential to release acidity, nutrients and metals. The present study investigated the mobilisation of these substances following the rewetting of dried soils with River Murray water. Trace metal concentrations were at background levels in most soils. During 24-h mobilisation tests, the water pH was effectively buffered to the pH of the soil. The release of nutrients was low. Metal release was rapid and the dissolved concentrations of many metals exceeded the Australian water quality guidelines (WQGs) in most tests. The concentrations of dissolved Al, Cu and Zn were often greater than 100× the WQGs and strong relationships existed between dissolved metal release and soil pH. Attenuation of dissolved metal concentrations through co-precipitation and adsorption to Al and Fe precipitates was an important process during mixing of acidic, metal-rich waters with River Murray water. The study demonstrated that the rewetting of dried acid sulfate soils may release significant quantities of metals and a high level of land and water management is required to counter the effects of such climate change events.
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Rabenhorst, Martin C. "International Acid Sulfate Soils Conference recap." CSA News 61, no. 9 (September 2016): 24–27. http://dx.doi.org/10.2134/csa2016-61-9-8.

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Kim, Jae Hwan, So-Jeong Kim, and In-Hyun Nam. "Effect of Treating Acid Sulfate Soils with Phosphate Solubilizing Bacteria on Germination and Growth of Tomato (Lycopersicon esculentum L.)." International Journal of Environmental Research and Public Health 18, no. 17 (August 25, 2021): 8919. http://dx.doi.org/10.3390/ijerph18178919.

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Acid sulfate soils contain sulfide minerals that have adverse environmental effects because they can lead to acidic drainage and prevent the establishment of vegetation. The current study examined the effect of a novel method for the restoration of these soils and the promotion of germination and plant growth. Thus, we isolated two strains of phosphate solubilizing bacteria, Methylobacterium sp. PS and Caballeronia sp. EK, characterized their properties, and examined their effects in promoting the growth of tomato plants (Lycopersicon esculentum L.) in acid sulfate soil. Compared with untreated control soil, treatment of acid sulfate soils with these bacterial strains led to increased seed germination, growth of plants with more leaves, and plants with greater levels of total-adenosine tri-phosphate (tATP). Relative to the untreated control soil, the addition of Caballeronia sp. EK led to a 60% increase in seed germination after 52 days, growth of plants with more than 3 times as many leaves, and a 45.2% increase in tATP after 50 days. This strain has potential for use as a plant biofertilizer that promotes vegetation growth in acid sulfate soils by improving the absorption of phosphorous.
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Priatmadi, Bambang Joko, and Abdul Haris. "Reaksi Pemasaman Senyawa Pirit pada Tanah Rawa Pasang Surut." JOURNAL OF TROPICAL SOILS 14, no. 1 (January 1, 2009): 19. http://dx.doi.org/10.5400/jts.2009.v14i1.19-24.

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Most of swamp soils in tidal land are Acid Sulfate Soils. Acid sulfate soils are the common name given to soils containing iron sulfides (pyrite). The soils are characterized by very low pH and high amount of soluble S and Fe, resulted from oxidation of pyrite when soils are drained. This study was aimed to determine acidity pattern, iron and sulfate solubility as the impact of the length time of oxidized, the effect of inhibitors application to acidity rate of sulfidic materials and top soils. The materials are: (1) soils at pyritic layer (sulfidic materials) and (2) soils at 0 – 20 cm from soil surface. Soils is sampled at Barambai reclaimed area, Barito Kuala Regency, South Kalimantan Province. In the laboratory soils treated with some ameliorants, that are silica, phosphate and lime applied with dosage 2 t ha-1 with 3 replications times. The soils incubated for 2 weeks under submerged condition. After soil incubation, soil exposed to the air for 1 week, 2 weeks, 4 weeks, and 6 weeks. Parameters of soil analysis include pH, sulfate and iron soluble. Results of this study showed that (1) soil acidity rate of sulfidic materials more faster than upper soils when soils and sulfidic materials oxidized intensively, (2) at submerged soil condition or high soil water content, the application of ameliorants effective increasing the soil pH of the upper soils, (3) at further oxidized soil condition or lower soil water content, the application of ameliorants inhibited acidity rate of soils and sulfidic materials, and (4) at further oxidized soil condition or lower soil water content, the application of ameliorants increased iron solubility of soils and sulfidic materials.
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Dissertations / Theses on the topic "Acid sulfate soils"

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Yvanes-Giuliani, Yliane. "Aluminium geochemistry in coastal lowland acid sulfate soils (CLASS) : speciation, reactivity and mobility." Thesis, Aix-Marseille, 2014. http://www.theses.fr/2014AIXM4364.

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Ce projet de thèse vise à étudier les processus géochimiques de l'aluminium dans les sols acides à sulfates. Les résultats obtenus avec le dispositif de dialyse de Donnan montrent que l'aluminium dans la solution du sol est presque exclusivement (> 98%) présent sous forme de complexes de charge négative, vraisemblablement des organo-complexes d'aluminium. Les concentrations d'aluminium isotopiquement échangeables (valeurs-E) et les concentrations obtenues par extractions chimiques révèlent qu'une solution de 1 M KCl sous-estime systématiquement les valeurs E. Une méthode d'extraction séquentielle a révélé qu'une quantité importante de minéraux primaires (initialement présents dans les sols) a déjà été dissoute, comme en témoignent les concentrations élevées d'aluminium présentes en tant que minéraux secondaires d'aluminium. Ces études permettent de mieux comprendre la géochimie de l'aluminium dans les sols CLASS et de pouvoir intégrer ces connaissances dans la gestion des sols
The aim of this thesis was to further understanding on Al geochemistry in coastal lowland acid sulfate soils (CLASS). It was observed that Al was present almost solely (> 98%) as negatively charged complexes in CLASS pore-waters, presumably with natural organic matter. Isotopically exchangeable concentrations (E-values) of Al and extraction solutions used to estimate the exchangeable pool showed that 1 M KCl always underestimated isotopically exchangeable Al concentrations in these soils and that 0.2 M CuCl2 improved agreement between both methodologies but sometimes overestimated corresponding E values. A sequential extraction procedure showed that substantial amounts of Al have already been dissolved from primary aluminosilicates initially present in the soils and remain in the soils mostly as reactive secondary Al minerals. The outcomes of this thesis significantly further our understanding of Al geochemistry in CLASS environments and how this knowledge can be incorporated into land management practices
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Reynolds, Jason Kurt Faculty of Science UNSW. "Hydrogel determined metal bioaccessibility in acid sulfate-affected landscapes." Awarded by:University of New South Wales, 2008. http://handle.unsw.edu.au/1959.4/41436.

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Exposure of sulfidic sediments to atmospheric conditions can under various environmental and anthropogenic influences. The oxidation of sulfides results in the production of acidity, dissolution of aluminosilicates and pedogenci development. This process has acid sulfate landscapes throughout the world identified as major emitters of elevated concentrations of chemical metals. This emission of acidity and metals alters the bioaccessibility and subsequently has a deleterious impact on the surrounding biologic environment. Despite this, the examination of the biologic impact in these landscapes has received only minimal attention. Passive and dynamic hydrogel techniques were used to measure the bioaccessibility of metals in sediments and waters. The technique involved the construction of a restricted pore-size thin-film hydrogel that allowed for the diffusion of the bioaccessible fraction, composed of the free-ion and easily dissociable metal-complexes. The dynamic hydrogel technique contained a resin sink, which allowed for a time-integrated flux concentration to be calculated. The dynamic hydrogel technique was trialled and found to correlate with the pygmy mussel (Xenostrobus securis) aluminium uptake for short exposure periods (24 hours).The dynamic hydrogel metal concentration was also found to correlate to indpendantly measured pore water and simultaneously extracted metal (SEM) concentrations. The hydrogel techniqe was further applied to investigate the sediment-water interface in drained and non-drained acid suflate landscapes. The studied Australian and Finnish acid sulfate landscapes showed contrasting relationships between the acid volatile sulfides (AVS) and SEM fractions. In the Australian sediments, a conversion of AVS-S to FeS2-S occurs with depth driven by a polysulfide pathway, whilst the Finnish sediments displayed a persistence of AVS-S with depth with limited conversion to FeS2-S. Distinct variations exist at the sediment-water interface of the two contrasting landscapes, with AVS-S to FeS2-S ratios of 2.5 for the Australian and 0.2 in the Finnish sediments. The sediment geochemistry regulated metal mobility. A two-dimensional passive and dynamic hydrogel approach illustrated microniches and supply zones of aluminium iron, manganese and zinc at varying depths near the sediment-water interface. The measurement of bioaccessibility using an in situ technique in acid sulfate landscapes is a first for both Australia and Finland, and this research provides an important avenue for future water and sediment quality monitoring.
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Karczewska, Hanna. "The effects of acid leaching on some physico-chemical properties of Quebec soil /." Thesis, McGill University, 1987. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=64017.

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Gunnarsson, Niklas. "Mineralogical speciation of sulfur in acid sulfate soils from Luleå, Sweden." Thesis, Luleå tekniska universitet, Geovetenskap och miljöteknik, 2018. http://urn.kb.se/resolve?urn=urn:nbn:se:ltu:diva-71759.

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Marine sulfide – bearing sediments that oxidize when in contact with oxygen and leach outelements in high concentrations to small watercourses have been a problem for many years allover the world especially around the Bothnian Bay. The purpose of this study was to furtherinvestigate the sulfur mineralogy present in acid sulfate soils in the area of Luleå, Sweden. Asecondary aim was to see if elements leach out and accumulate in an acid sulfate soil closer tothe recipient. Samples were taken in two profiles (one oxidized and one waterlogged) fromfour sites (sites A-D) and were analyzed for whole rock geochemistry. Two sites were furtherinvestigated for mineralogy in polished samples with an optical microscope, Ramanspectroscopy and SEM-EDS. Each profile consisted of three layers: oxidation zone, transitionzone and reduced zone. The oxidation zone above the groundwater table was light grey withbrown iron hydroxide staining. Parts that lied under the water table were dark grey-black within general strong odor (“rotten eggs”) due to its sulfur content. It was usually straightforwardto distinguish and separate the layers from each other directly in the field, however in somecases pH was needed for confirmation.A general feature of investigated polished samples is the presence of abundant framboidalpyrites that are common in reduced marine sediments. The transition zone was formed in suboxicconditions and this feature is reflected by the mineralogy. Many morphologies of theframboidal pyrite were observed in this layer and signs of both dissolution and formationoccur. In the sample from site C one could observe elemental sulfur in form of large (up to 50μm) euhedral crystals. In the samples with pH<4, no sulfides occur as they have been replacedby jarosite (site B). Site C lacks these sulfur-bearing hydroxides which is thought to be due toa sulfur concentration of <0.2 %. Sulfur shows extensive leaching at most sites but at site B andD1, it accumulates in the transition zone. Elements like cobalt (Co), nickel (Ni) and zinc (Zn)are leached out or are accumulated further down in the profile. Elements that could have beentransported and have accumulated in the waterlogged profiles are Co, Ni, Zn and chromium(Cr) and in some profiles also copper (Cu) and vanadium (V).
Coastal watercourses in Bottenviken: Method development and ecological restoration- A cross-border Swedish-Finnish cooperation project
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Mustafa, Akhmad Biological Earth &amp Environmental Sciences Faculty of Science UNSW. "Improving acid sulfate soils for brackish water aquaculture ponds in South Sulawesi, Indonesia." Awarded by:University of New South Wales. Biological, Earth & Environmental Sciences, 2007. http://handle.unsw.edu.au/1959.4/40619.

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Brackish water aquaculture is one of the largest coastal industries in Indonesia. This farming system involves the construction of ponds m coastal sediments. Many ponds in Indonesia have been abandoned due to past development of ponds in acid 8ulfate soils (ASS); these soils produce sulfuric acid through the oxidation of pyrite du ring and after the sediments have been excavated. The soils also contain elevated concentrations of metal such as iron and aluminium which are harmful to farmed fish and shrimp. Acidification of pond soil causes recurrent fish and shrimp mortalities, poor growth rate in fish and shrimp, soft shell syndrome in shrimp and low plankton densities, Pond maintenance costs in ASS are also significantly higher than non-ASS ponds. There are over 6.7 million ha of ASS In Indonesia of which 35% has been developed for brackish water aquaculture. This study developed and trialled methods of soil remediation to restore abandoned ASS-affected ponds. The main objective was to develop methods at remediation that were scientifically sound but also practical and inexpensive for farmers. The research involved characterising, in detail, the chemical and physical properties of ponds soil followed by laboratory-based experiments to improve soil properties. The results of laboratory trials were the basis for large-scale field experiments to test soil remediation strategies. The study showed that pond bottoms could be improved by forced oxidation, flooding and water exchange followed by Iiming and fertilising. Up to 500% increases in productivity were achieved by this method and soils conditions Improved significantly. A further twofold productivity increase was achieved by an integrated liming method in which lime is added to rebuilt or new dykes in layers. A juvenile shrimp production system was developed for ponds that were too severely degraded or costly to remediate. The research developed methods of preventing metal toxicity in Juvenile shrimp. The study showed that aquaculture ponds built in ASS could be remediated and returned to viable production systems. Importantly, the study has developed a more detailed understanding of chemical properties In ASS-affected ponds.
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Nguyen, Nga. "Multivariate analysis and GIS in generating vulnerability map of acid sulfate soils." Thesis, KTH, Mark- och vattenteknik, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-170472.

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The study employed multi-variate methods to generate vulnerability maps for acid sulfate soils (AS) in the Norrbotten county of Sweden. In this study, the relationships between the reclassified datasets and each biogeochemical element was carefully evaluated with ANOVA Kruskal Wallis and PLS analysis. The sta-tistical results of ANOVA Kruskall-Wallis provided us a useful knowledge of the relationships of the preliminary vulnerability ranks in the classified datasets ver-sus the amount of each biogeochemical element. Then, the statistical knowledge and expert knowledge were used to generate the final vulnerability ranks of AS soils in the classified datasets which were the input independent variables in PLS analyses. The results of Kruskal-Wallis one way ANOVA and PLS analyses showed a strong correlation of the higher levels total Cu2+, Ni2+ and S to the higher vulnerability ranks in the classified datasets. Hence, total Cu2+, Ni2+ and S were chosen as the dependent variables for further PLS analyses. In particular, the Variable Importance in the Projection (VIP) value of each classified dataset was standardized to generate its weight. Vulnerability map of AS soil was a result of a lineal combination of the standardized values in the classified dataset and its weight. Seven weight sets were formed from either uni-variate or multi-variate PLS analyses. Accuracy tests were done by testing the classification of measured pH values of 74 soil profiles with different vulnerability maps and evaluating the areas that were not the AS soil within the groups of medium to high AS soil probability in the land-cover and soil-type datasets. In comparison to the other weight sets, the weight set of multi-variate PLS analysis of the matrix of total Ni2+& S or total Cu2+& S had the robust predictive performance. Sensitivity anal-ysis was done in the weight set of total Ni2+& S, and the results of sensitivity analyses showed that the availability of ditches, and the change in the terrain sur-faces, the altitude level, and the slope had a high influence to the vulnerability map of AS soils. The study showed that using multivariate analysis was a very good approach methodology for predicting the probability of acid sulfate soil.
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Diallo, Ndeye Helene. "Improved Management of Acid Sulfate Soils for Rice Production in Casamance, Senegal." Thesis, Virginia Tech, 2016. http://hdl.handle.net/10919/81697.

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Casamance is a region in southern Senegal that traditionally produces rainfed rice, but Senegal produces only 1/3 of its rice consumption. Lowland areas, where rice is primarily produced, have acid sulfate soils with low pH and potential aluminum and iron toxicity. The goal of this work was to determine if soil amendments can alleviate soil acidity, counteract the negative biogeochemical effects that occur in flooded conditions, and increase rice yield. A two-year experiment was conducted to test the following soil treatments – agricultural lime, pulverized oyster shell, biochar, and control (no amendment) – in flat and raised beds. Plots amended with lime and shell materials had increased soil pH, base saturation, Ca, and cation exchange capacity. Meanwhile, biochar elevated particulate organic matter and C:N ratios. Exchangeable Fe and Al were negatively correlated with soil pH, while Geobacteraceae populations (Fe reducing bacteria) increased with pH. A greater proportion of the total Fe was strongly bound in fractions that were less bioavailable in plots amended with shell or lime, and overall rice yields were significantly higher following amendment with shell or lime. During the second growing year these effects diminished, suggesting that liming effects did not persist as expected. These results demonstrate the benefits of soil amendments that raise soil pH and suggest that this effect operates by influencing overall soil nutrient availability to rice plants, but further research is needed regarding the timing and sustainability of the beneficial liming effect.
Master of Science
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Bryson, Autumn Leah. "Sulfate sorption of acidified forest soils in the Otter Creek Wilderness area." Morgantown, W. Va. : [West Virginia University Libraries], 2006. https://eidr.wvu.edu/etd/documentdata.eTD?documentid=4900.

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Thesis (M.S.)--West Virginia University, 2006.
Title from document title page. Document formatted into pages; contains vi, 36 p. : ill. (some col.), col. maps. Includes abstract. Includes bibliographical references (p. 31-36).
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Lindström, Carola. "Acid Sulfate Soils and Metal Accumulation in Sediments in Rosån Catchment, Northern Sweden." Thesis, Uppsala universitet, Institutionen för geovetenskaper, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-325213.

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Global environmental concerns arise when marine deposits with fine-grained iron sulfide-rich sediments (FeS and FeS2), now situated above sea level, oxidize from anthropogenic lowering of the groundwater table. The oxidation of iron sulfides decreases the soil pH and the acidic environment of these Acid Sulfate Soils (AS) soils increase weathering and mobilization of metals into adjacent watercourses, lakes and estuaries. Low pH and enhanced concentrations of metals are known to influence water quality negatively, causing fish kills and reduced aquatic diversity. Sulfide rich sediments were deposited in the Baltic Sea after the last glaciation and are now abundantly found along the coasts of for example the Bothnian Bay as a result of isostatic rebound. Recent studies from Finland have stated associations between leached (AS) soils and increased concentrations of metals in estuary sediments, thus the effects are likely to be similar in Sweden. With financial support from the Interreg Nord project “Ecological restoration in coastal river basins in the Bothnian Bay” in cooperation with the Geological Survey of Sweden (SGU), sediments from three lakes and two estuarine sites in the Rosån catchment in Norrbotten county, northern Sweden, were sampled and analyzed with fpXRF, ICP-MS and LOI methods. Elemental concentrations and organic contents were compared to establish accumulation trends over time and relationships between metal concentrations in recently deposited sediments and potential influence from previously sampled (AS) soils. Correlations in time, to anthropogenic activity, such as ditching were also considered. A primary allover trend with increasing concentrations of Aluminum (Al), Arsenic (As), Cadmium (Cd), Cobalt (Co), Cupper (Cu), Iron (Fe), Manganese (Mn), Nickel (Ni), Lead (Pb), Rare Earth Elements (REE) and Zinc (Zn), was noticed in a majority of the lake and estuary sediment samples. With some site variation, also two discrete peaks at different depth, were found in the upper 20 to 30 cm of the sampled sediments. Significant correlations to organic matter were also found for a considerable amount of the elements. Soil samples from (AS) soils in areas related to Rosån show pH values as low as 2.62 and oxidation depths down to 170 cm. Substantial elemental depletion in the oxidized zone suggest increased weathering, leaching and mobilization of Al, Cd, Co, Mn, Ni, REE, Zn and to some extent As, Cu, Fe and Pb from the soil, as a consequence of the acidic environment. A relationship between (AS) soils and increased metal concentrations is therefore likely. The sedimentation rate of roughly 0.2 cm/year was calculated from the separation age of the lakes and the sediment depth to an interpreted transition from more marine environment to lake settings. Consequently the distinct peaks of increased metal concentrations are thus suggested to be related to anthropogenic activities as for example improved drainage methods after the Second World War, but proper dating of the sediments is needed to establish any certain correlations.
På senare tid har man uppmärksammat de miljöproblem som uppstår när finkorniga sediment, innehållande järnsulfider, oxiderar på grund av mänsklig påverkan, t ex. dikning, eller annan typ av aktivitet som sänker grundvattennivån. När järnsulfiderna oxiderar bildas svavelsyra som gör att pH- värdet i marken blir väldigt lågt. Den sura miljön i dessa så kallade sura sulfatjordar, gör i sin tur att mineraler i marken vittrar fortare med påföljden att både surt vatten och ökade mängder metaller, sprids till närliggande vattendrag, sjöar och hav. Lågt pH och höga halter av metaller i vatten påverkar även vattenkvalitén negativt och har rapporterats orsaka fiskdöd och minskad akvatisk mångfald. Sura sulfatjordar är globalt förekommande och återfinns bland annat längs Bottenvikens kuster. De har kunnat bildas genom att sulfidhaltiga sediment, som avsattes i Östersjön efter den senaste istiden, nu befinner sig ovan havsnivån på grund av landhöjningen. I Finland har man i flera studier sett ett samband mellan sura sulfatjordar och ökade metallhalter i nyligen avsatta kustsediment och man kan anta att liknande förhållande gäller även i Sverige. Med finansiellt stöd från EU-projektet “Kustmynnande Vattendrag i Bottenviken-Metodutveckling och Ekologisk Restaurering” (Interreg Nord) genom Sveriges geologiska undersökning (SGU) och i samarbete med Länsstyrelsen i Norrbotten, har bottensediment från tre sjöar och två fjärdar i Rosåns avrinningsområde i Norrbotten provtagits och analyserats. För att fastställa hur koncentrationerna har förändrats över tiden har metallhalterna i de nyligen avsatta sedimenten jämförts med koncentrationerna i äldre sediment. Även jordprofiler från sura sulfatjordar i området har studerats för att kunna utvärdera ett ev. samband mellan urlakade ämnen i jordarna och ökade halter i sedimenten. Granskning av hur långt metallerna transporteras i systemet har gjorts, liksom försök att hitta kopplingar i tiden till mänsklig påverkan som t.ex. dikning. I de översta sedimenten kan man, förutom en generellt ökande trend av aluminium (Al), arsenik (As), kadmium (Cd), kobolt (Co), koppar (Cu), järn (Fe), mangan (Mn), nickel, (Ni) bly (Pb), sällsynta jordartsmetaller (REE) och zink (Zn), också se tydliga toppar med ökade halter av dessa ämnen på minst två specifika djup. De sura sulfatjordarna, som uppmätte pH-värden ner till 2,62, visade tecken på urlakning av Al, Cd, Co, Ni, Mn, REE, Zn och till viss del också As, Cu, Fe och Pb, varpå en trolig relation mellan sura sulfatjordar och ökade metallhalter i nyligen avsatta sediment kan fastställas. En uppskattning av ackumulationshastigheten, som gjordes utifrån när de provtagna sjöarna skiljdes från havet, och sedimentdjupet som visar övergången från hav till sjö, visar att de observerade topparna av ökade metallkoncentrationer i sedimenten skulle kunna vara förknippade med dikning i början av 1900-talet och efter andra världskriget. För en säker bestämning av sambandet till specifika händelser behövs dock en riktig datering.
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Courchesne, François. "Mechanisms regulating sulfate movement in some podzols from Quebec." Thesis, McGill University, 1988. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=75774.

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The reaction of sulfate with six podzolic horizons of the Southern Laurentians (Quebec) was investigated using batch reaction techniques. It was demonstrated that sulfate sorption increased with decreasing solution pH to a maximum sorption capacity at around pH 4.0; below this pH retention decreased. This drop in sorption capacity was related to the partial dissolution of Al surface coatings. Indeed, the amount of native sulfate and the maximum sorption during the experiment were positively correlated (R$ sp2$ = 0.982, 0.800) with the oxalate extractable Al content of these forested soils. In all six horizons, the increase in sulfate sorption as a function of equilibrium sulfate concentration was best described by the Gunary equation. Kinetic experiments showed the presence of two major stages in both sorption and desorption reactions with an initial quick change (first 6 h) in solution concentration being followed by a second step where the reactions between sulfate and the soil matrix were much slower. The time-dependence of these reactions emphasized the appropriateness of kinetic equation in describing field situations. Moreover, kinetics studies performed under highly acidic conditions demonstrated that the amount of sulfate sorbed decreased with time after an initial sorption step due to the partial dissolution of Al surface materials. Thermodynamic calculations further suggested the subsequent precipitation of jurbanite. It was then concluded that surface dissolution and mineral formation should be considered in the interpretation of results obtained from experiments aimed at determining the effect of pH on sulfate retention.
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Books on the topic "Acid sulfate soils"

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Acid sulfate soils in Malaysia. Serdang: Universiti Putera Malaysia Press, 2006.

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Jacobs, James A., Jay H. Lehr, and Stephen M. Testa, eds. Acid Mine Drainage, Rock Drainage, and Acid Sulfate Soils. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118749197.

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Boivin, Pascal. Caractérisation physique des sols sulfatés acides de la vallée de Katouré, Basse Casmance, Sénégal : étude de la variabilité spatiale et relation avec les caractériques pédologiques. Paris: Editions de l'ORSTOM, 1991.

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Krasilʹnikov, P. V. Sulʹfatnokislye pochvy vostochnoĭ Fennoskandii (na vneberegovykh otlozhenii͡a︡kh). Petrozavodsk: Rossiĭskai͡a︡ akademii͡a︡ nauk, Karelʹskiĭ nauch. t͡s︡entr in-t biologii, 1997.

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Võ, Quang Minh, Thị Gương Võ, and Mỹ Hoa Nguyễn. Một số kết quả nghiên cứu về sử dụng và quản lý đất phèn ở Đồng bằng Sông Cửu Long. TP. [i.e. Thành phố] Hồ Chí Minh: Nhà xuất bản Nông nghiệp, 2010.

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Nichnadowicz, Vincent F. Mitigation of acid-producing soils: Final report. [Trenton, NJ]: The Dept., 2003.

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Dent, David. Quick quantitative assessment of the acid sulphate hazard. Glen Osmond, S. Aust: CSIRO Division of Soils, 1996.

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Colley, Raymond. Constraints imposed by acid sulfate soils on the Gambia's bridge-barrage scheme. Ann Arbor, Mich: Great Lakes and Marine Waters Center, University of Michigan, 1985.

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Simposium, Nasional Pendayagunaan Tanah Masam (2003 Bandar Lampung Indonesia and Lampung Timur Indonesia). Prosiding. Bogor: Pusat Penelitian dan Pengembangan Tanah dan Agroklimat, Badan Penelitian dan Pengembangan Pertanian, Departemen Pertanian, 2004.

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Ohmann, L. F. Properties of soils and tree wood tissue across a Lake States sulfate deposition gradient. St. Paul, Minn: U.S. Dept. of Agriculture, Forest Service, North Central Forest Experiment Station, 1991.

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Book chapters on the topic "Acid sulfate soils"

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Jacobs, James A. "Acid Sulfate Soils." In Acid Mine Drainage, Rock Drainage, and Acid Sulfate Soils, 191–96. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118749197.ch16.

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van Mensvoort, M. E. F., and D. L. Dent. "Acid Sulfate Soils." In Methods for Assessment of Soil Degradation, 301–35. Boca Raton: CRC Press, 2020. http://dx.doi.org/10.1201/9781003068716-16.

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Osman, Khan Towhid. "Acid Soils and Acid Sulfate Soils." In Management of Soil Problems, 299–332. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-75527-4_11.

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Fanning, D. S., and S. N. Burch. "Coastal Acid Sulfate Soils." In Agronomy Monographs, 921–37. Madison, WI, USA: American Society of Agronomy, Crop Science Society of America, Soil Science Society of America, 2015. http://dx.doi.org/10.2134/agronmonogr41.c36.

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Fanning, D. S., M. C. Rabenhorst, and J. M. Bigham. "Colors of Acid Sulfate Soils." In Soil Color, 91–108. Madison, WI, USA: Soil Science Society of America, 2015. http://dx.doi.org/10.2136/sssaspecpub31.c6.

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Downing, Bruce W. "Acid-Base Accounting Associated with Acid Rock Drainage." In Acid Mine Drainage, Rock Drainage, and Acid Sulfate Soils, 217–27. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118749197.ch19.

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Fanning, Delvin S. "Salinity problems in acid sulfate coastal soils." In Towards the rational use of high salinity tolerant plants, 491–500. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1858-3_52.

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Jacobs, James A., and David B. Vance. "Biogeochemistry of Acid Drainage." In Acid Mine Drainage, Rock Drainage, and Acid Sulfate Soils, 15–51. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118749197.ch3.

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Jacobs, James A., and Stephen M. Testa. "Acid Drainage and Sulfide Oxidation: Introduction." In Acid Mine Drainage, Rock Drainage, and Acid Sulfate Soils, 1–8. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118749197.ch1.

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Jacobs, James A. "Overview of Soil and Groundwater Sampling Methods for Acid Drainage Studies." In Acid Mine Drainage, Rock Drainage, and Acid Sulfate Soils, 119–22. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118749197.ch10.

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Conference papers on the topic "Acid sulfate soils"

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Kopackova, Veronika. "Mapping Acid Mine Drainage (AMD) and Acid Sulfate Soils Using Sentinel-2 Data." In IGARSS 2019 - 2019 IEEE International Geoscience and Remote Sensing Symposium. IEEE, 2019. http://dx.doi.org/10.1109/igarss.2019.8900505.

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"Potential of controlled drainage and sub-irrigation to manipulate groundwater table for mitigating acid loadings in Finnish acid sulfate soils." In 2016 10th International Drainage Symposium. American Society of Agricultural and Biological Engineers, 2016. http://dx.doi.org/10.13031/ids.20162521555.

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Jumar, Riza Adrianoor Saputra, Muhammad Imam Nugraha, and Ahmad Ghazali. "The effect of composted oyster mushroom baglog waste on rice growth and productivity in acid sulfate soils." In THE 5th INTERNATIONAL CONFERENCE ON AGRICULTURE AND LIFE SCIENCE 2021 (ICALS 2021): “Accelerating Transformation in Industrial Agriculture Through Sciences Implementation”. AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0116297.

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Vasquez, P., J. Urich, A. Rodriguez, V. Gonzalez, J. Marcano, C. Lopez, and P. Colombo. "Edafic and Successional Changes Generated by Drill Wastes Application in Acid-sulfate Soils at the Upper Orinoco Delta." In SPE International Conference on Health, Safety, and Environment in Oil and Gas Exploration and Production. Society of Petroleum Engineers, 1998. http://dx.doi.org/10.2118/48922-ms.

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Taufieq, Nur Anny Suryaningsih, Sahibin Abdul Rahim, and Habibah Jamil. "Effectiveness of the bran media and bacteria inoculum treatments in increasing pH and reducing sulfur-total of acid sulfate soils." In THE 2013 UKM FST POSTGRADUATE COLLOQUIUM: Proceedings of the Universiti Kebangsaan Malaysia, Faculty of Science and Technology 2013 Postgraduate Colloquium. AIP Publishing LLC, 2013. http://dx.doi.org/10.1063/1.4858728.

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Sadao Nagasaka, Eiichi Kohno, Wesley W Wallender, Dong-Jin Kang, Shingo Ueda, Shigeo Ishikawa, and Pisoot Vijarnsorn. "Improvement of Leaching Methods for Acid Sulfate Soil." In 2009 Reno, Nevada, June 21 - June 24, 2009. St. Joseph, MI: American Society of Agricultural and Biological Engineers, 2009. http://dx.doi.org/10.13031/2013.27425.

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Pathirage, Udeshini, and Buddhima Indraratna. "A Permeable Reactive Barrier Installed in Acid Sulfate Soil Terrain." In Geo-Chicago 2016. Reston, VA: American Society of Civil Engineers, 2016. http://dx.doi.org/10.1061/9780784480144.031.

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Han, Fengxiang, Safwan Shiyab, Yi Su, David L. Monts, Charles A. Waggoner, and Frank B. Matta. "Bioavailability and Stability of Mercury Sulfide in Armuchee (USA) Soil." In The 11th International Conference on Environmental Remediation and Radioactive Waste Management. ASMEDC, 2007. http://dx.doi.org/10.1115/icem2007-7122.

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Because of the adverse effects of elemental mercury and mercury compounds upon human health, the U.S. Department of Energy (DOE) is engaged in an on-going effort to monitor and remediate mercury-contaminated DOE sites. In order to more cost effectively implement those extensive remediation efforts, it is necessary to obtain an improved understanding of the role that mercury and mercury compounds play in the ecosystem. We have conducted pilot scale experiments to study the bioavailability of mercury sulfide in an Armuchee (eastern US) soil. The effects of plants and incubation time on chemical stability and bioavailability of HgS under simulated conditions of the ecosystem have been examined, as has the dynamics of the dissolution of mercury sulfide by various extractants. The results show that mercury sulfide in contaminated Armuchee soil was still to some extent bioavailable to plants. After planting, soil mercury sulfide is more easily dissolved by both 4 M and 12 M nitric acid than pure mercury sulfide reagent. Dissolution kinetics of soil mercury sulfide and pure chemical reagent by nitric acid are different. Mercury release by EDTA from HgS-contaminated soil increased with time of reaction and soil mercury level. Chelating chemicals increase the solubility and bioavailability of mercury in HgS-contaminated soil.
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Shi, Xianzhong, Mehrooz Aspandiar, and Ian C. Lau. "Assessment of acid sulfate soil using hyperspectral data in South Yunderup, Western Australia." In IGARSS 2013 - 2013 IEEE International Geoscience and Remote Sensing Symposium. IEEE, 2013. http://dx.doi.org/10.1109/igarss.2013.6723790.

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Banasiak, Laura, Punyama Pathirage, and Buddhima Indraratna. "Modeling of Chemical Armoring in a Permeable Reactive Barrier (PRB) in Acid Sulfate Soil (ASS) Terrain." In International Conference on Ground Improvement & Ground Control. Singapore: Research Publishing Services, 2012. http://dx.doi.org/10.3850/978-981-07-3560-9_05-0501.

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Reports on the topic "Acid sulfate soils"

1

Berkowitz, Jacob, and Christine VanZomeren. Approaches to identify and monitor for potential acid sulfate soils in an ecological restoration context. Engineer Research and Development Center (U.S.), February 2022. http://dx.doi.org/10.21079/11681/43349.

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Potential acid sulfate soils include materials with the capacity to generate acidity under certain environmental conditions. As such, these soils can pose challenges to ecological restoration projects occurring in wetlands and nearshore environments. To provide guidance for ecosystem restoration practitioners, the following technical note describes acid sulfate soil formation and distribution and then describes techniques for identifying and monitoring acid sulfate soil conditions prior to and following implementation of restoration activities. Finally, this technical note outlines a number of tools and recently published resources to help avoid unintended consequences of acid sulfate soil disturbance and achieve ecological restoration objectives.
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VanZomeren, Christine, Jacob Berkowitz, Candice Piercy, and Jeffrey King. Acid sulfate soils in coastal environments : a review of basic concepts and implications for restoration. Engineer Research and Development Center (U.S.), September 2020. http://dx.doi.org/10.21079/11681/38240.

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Shenker, Moshe, Paul R. Bloom, Abraham Shaviv, Adina Paytan, Barbara J. Cade-Menun, Yona Chen, and Jorge Tarchitzky. Fate of Phosphorus Originated from Treated Wastewater and Biosolids in Soils: Speciation, Transport, and Accumulation. United States Department of Agriculture, June 2011. http://dx.doi.org/10.32747/2011.7697103.bard.

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Beneficial use of reclaimed wastewater (RW) and biosolids (BS) in soils is accompanied by large input of sewage-originated P. Prolonged application may result in P accumulation up to levelsBeneficial use of reclaimed wastewater (RW) and biosolids (BS) in soils is accompanied by large input of sewage-originated P. Prolonged application may result in P accumulation up to levels that impair plant nutrition, increase P loss, and promote eutrophication in downstream waters. This study aims to shed light on the RW- and BS-P forms in soils and to follow the processes that determine P reactivity, solubility, availability, and loss in RW and BS treated soils. The Technion group used sequential P extraction combined with measuring stable oxygen isotopic composition in phosphate (δ18OP) and with 31P-NMR studies to probe P speciation and transformations in soils irrigated with RW or fresh water (FW). The application of the δ18OP method to probe inorganic P (Pi) speciation and transformations in soils was developed through collaboration between the Technion and the UCSC groups. The method was used to trace Pi in water-, NaHCO3-, NaOH-, and HCl- P fractions in a calcareous clay soil (Acre, Israel) irrigated with RW or FW. The δ18OP signature changes during a month of incubation indicated biogeochemical processes. The water soluble Pi (WSPi) was affected by enzymatic activity yielding isotopic equilibrium with the water molecules in the soil solution. Further it interacted rapidly with the NaHCO3-Pi. The more stable Pi pools also exhibited isotopic alterations in the first two weeks after P application, likely related to microbial activity. Isotopic depletion which could result from organic P (PO) mineralization was followed by enrichment which may result from biologic discrimination in the uptake. Similar transformations were observed in both soils although transformations related to biological activity were more pronounced in the soil treated with RW. Specific P compounds were identified by the Technion group, using solution-state 31P-NMR in wastewater and in soil P extracts from Acre soils irrigated by RW and FW. Few identified PO compounds (e.g., D-glucose-6-phosphate) indicated coupled transformations of P and C in the wastewater. The RW soil retained higher P content, mainly in the labile fractions, but lower labile PO, than the FW soil; this and the fact that P species in the various soil extracts of the RW soil appear independent of P species in the RW are attributed to enhanced biological activity and P recycling in the RW soil. Consistent with that, both soils retained very similar P species in the soil pools. The HUJ group tested P stabilization to maximize the environmental safe application rates and the agronomic beneficial use of BS. Sequential P extraction indicated that the most reactive BS-P forms: WSP, membrane-P, and NaHCO3-P, were effectively stabilized by ferrous sulfate (FeSul), calcium oxide (CaO), or aluminum sulfate (alum). After applying the stabilized BS, or fresh BS (FBS), FBS compost (BSC), or P fertilizer (KH2PO4) to an alluvial soil, P availability was probed during 100 days of incubation. A plant-based bioassay indicated that P availability followed the order KH2PO4 >> alum-BS > BSC ≥ FBS > CaO-BS >> FeSul-BS. The WSPi concentration in soil increased following FBS or BSC application, and P mineralization further increased it during incubation. In contrast, the chemically stabilized BS reduced WSPi concentrations relative to the untreated soil. It was concluded that the chemically stabilized BS effectively controlled WSPi in the soil while still supplying P to support plant growth. Using the sequential extraction procedure the persistence of P availability in BS treated soils was shown to be of a long-term nature. 15 years after the last BS application to MN soils that were annually amended for 20 years by heavy rates of BS, about 25% of the added BS-P was found in the labile fractions. The UMN group further probed soil-P speciation in these soils by bulk and micro X-ray absorption near edge structure (XANES). This newly developed method was shown to be a powerful tool for P speciation in soils. In a control soil (no BS added), 54% of the total P was PO and it was mostly identified as phytic acid; 15% was identified as brushite and 26% as strengite. A corn crop BS amended soil included mostly P-Fe-peat complex, variscite and Al-P-peat complex but no Ca-P while in a BS-grass soil octacalcium phosphate was identified and o-phosphorylethanolamine or phytic acid was shown to dominate the PO fraction that impair plant nutrition, increase P loss, and promote eutrophication in downstream waters. This study aims to shed light on the RW- and BS-P forms in soils and to follow the processes that determine P reactivity, solubility, availability, and loss in RW and BS treated soils. The Technion group used sequential P extraction combined with measuring stable oxygen isotopic composition in phosphate (δ18OP) and with 31P-NMR studies to probe P speciation and transformations in soils irrigated with RW or fresh water (FW). The application of the δ18OP method to probe inorganic P (Pi) speciation and transformations in soils was developed through collaboration between the Technion and the UCSC groups. The method was used to trace Pi in water-, NaHCO3-, NaOH-, and HCl- P fractions in a calcareous clay soil (Acre, Israel) irrigated with RW or FW. The δ18OP signature changes during a month of incubation indicated biogeochemical processes. The water soluble Pi (WSPi) was affected by enzymatic activity yielding isotopic equilibrium with the water molecules in the soil solution. Further it interacted rapidly with the NaHCO3-Pi. The more stable Pi pools also exhibited isotopic alterations in the first two weeks after P application, likely related to microbial activity. Isotopic depletion which could result from organic P (PO) mineralization was followed by enrichment which may result from biologic discrimination in the uptake. Similar transformations were observed in both soils although transformations related to biological activity were more pronounced in the soil treated with RW. Specific P compounds were identified by the Technion group, using solution-state 31P-NMR in wastewater and in soil P extracts from Acre soils irrigated by RW and FW. Few identified PO compounds (e.g., D-glucose-6-phosphate) indicated coupled transformations of P and C in the wastewater. The RW soil retained higher P content, mainly in the labile fractions, but lower labile PO, than the FW soil; this and the fact that P species in the various soil extracts of the RW soil appear independent of P species in the RW are attributed to enhanced biological activity and P recycling in the RW soil. Consistent with that, both soils retained very similar P species in the soil pools. The HUJ group tested P stabilization to maximize the environmental safe application rates and the agronomic beneficial use of BS. Sequential P extraction indicated that the most reactive BS-P forms: WSP, membrane-P, and NaHCO3-P, were effectively stabilized by ferrous sulfate (FeSul), calcium oxide (CaO), or aluminum sulfate (alum). After applying the stabilized BS, or fresh BS (FBS), FBS compost (BSC), or P fertilizer (KH2PO4) to an alluvial soil, P availability was probed during 100 days of incubation. A plant-based bioassay indicated that P availability followed the order KH2PO4 >> alum-BS > BSC ≥ FBS > CaO-BS >> FeSul-BS. The WSPi concentration in soil increased following FBS or BSC application, and P mineralization further increased it during incubation. In contrast, the chemically stabilized BS reduced WSPi concentrations relative to the untreated soil. It was concluded that the chemically stabilized BS effectively controlled WSPi in the soil while still supplying P to support plant growth. Using the sequential extraction procedure the persistence of P availability in BS treated soils was shown to be of a long-term nature. 15 years after the last BS application to MN soils that were annually amended for 20 years by heavy rates of BS, about 25% of the added BS-P was found in the labile fractions. The UMN group further probed soil-P speciation in these soils by bulk and micro X-ray absorption near edge structure (XANES). This newly developed method was shown to be a powerful tool for P speciation in soils. In a control soil (no BS added), 54% of the total P was PO and it was mostly identified as phytic acid; 15% was identified as brushite and 26% as strengite. A corn crop BS amended soil included mostly P-Fe-peat complex, variscite and Al-P-peat complex but no Ca-P while in a BS-grass soil octacalcium phosphate was identified and o-phosphorylethanolamine or phytic acid was shown to dominate the PO fraction.
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Chefetz, Benny, Baoshan Xing, Leor Eshed-Williams, Tamara Polubesova, and Jason Unrine. DOM affected behavior of manufactured nanoparticles in soil-plant system. United States Department of Agriculture, January 2016. http://dx.doi.org/10.32747/2016.7604286.bard.

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The overall goal of this project was to elucidate the role of dissolved organic matter (DOM) in soil retention, bioavailability and plant uptake of silver and cerium oxide NPs. The environmental risks of manufactured nanoparticles (NPs) are attracting increasing attention from both industrial and scientific communities. These NPs have shown to be taken-up, translocated and bio- accumulated in plant edible parts. However, very little is known about the behavior of NPs in soil-plant system as affected by dissolved organic matter (DOM). Thus DOM effect on NPs behavior is critical to assessing the environmental fate and risks related to NP exposure. Carbon-based nanomaterials embedded with metal NPs demonstrate a great potential to serve as catalyst and disinfectors. Hence, synthesis of novel carbon-based nanocomposites and testing them in the environmentally relevant conditions (particularly in the DOM presence) is important for their implementation in water purification. Sorption of DOM on Ag-Ag₂S NPs, CeO₂ NPs and synthesized Ag-Fe₃O₄-carbon nanotubebifunctional composite has been studied. High DOM concentration (50mg/L) decreased the adsorptive and catalytic efficiencies of all synthesized NPs. Recyclable Ag-Fe₃O₄-carbon nanotube composite exhibited excellent catalytic and anti-bacterial action, providing complete reduction of common pollutants and inactivating gram-negative and gram-positive bacteria at environmentally relevant DOM concentrations (5-10 mg/L). Our composite material may be suitable for water purification ranging from natural to the industrial waste effluents. We also examined the role of maize (Zeamays L.)-derived root exudates (a form of DOM) and their components on the aggregation and dissolution of CuONPs in the rhizosphere. Root exudates (RE) significantly inhibited the aggregation of CuONPs regardless of ionic strength and electrolyte type. With RE, the critical coagulation concentration of CuONPs in NaCl shifted from 30 to 125 mM and the value in CaCl₂ shifted from 4 to 20 mM. This inhibition was correlated with molecular weight (MW) of RE fractions. Higher MW fraction (> 10 kDa) reduced the aggregation most. RE also significantly promoted the dissolution of CuONPs and lower MW fraction (< 3 kDa) RE mainly contributed to this process. Also, Cu accumulation in plant root tissues was significantly enhanced by RE. This study provides useful insights into the interactions between RE and CuONPs, which is of significance for the safe use of CuONPs-based antimicrobial products in agricultural production. Wheat root exudates (RE) had high reducing ability to convert Ag+ to nAg under light exposure. Photo-induced reduction of Ag+ to nAg in pristine RE was mainly attributed to the 0-3 kDa fraction. Quantification of the silver species change over time suggested that Cl⁻ played an important role in photoconversion of Ag+ to nAg through the formation and redox cycling of photoreactiveAgCl. Potential electron donors for the photoreduction of Ag+ were identified to be reducing sugars and organic acids of low MW. Meanwhile, the stabilization of the formed particles was controlled by both low (0-3 kDa) and high (>3 kDa) MW molecules. This work provides new information for the formation mechanism of metal nanoparticles mediated by RE, which may further our understanding of the biogeochemical cycling and toxicity of heavy metal ions in agricultural and environmental systems. Copper sulfide nanoparticles (CuSNPs) at 1:1 and 1:4 ratios of Cu and S were synthesized, and their respective antifungal efficacy was evaluated against the pathogenic activity of Gibberellafujikuroi(Bakanae disease) in rice (Oryza sativa). In a 2-d in vitro study, CuS decreased G. fujikuroiColony- Forming Units (CFU) compared to controls. In a greenhouse study, treating with CuSNPs at 50 mg/L at the seed stage significantly decreased disease incidence on rice while the commercial Cu-based pesticide Kocide 3000 had no impact on disease. Foliar-applied CuONPs and CuS (1:1) NPs decreased disease incidence by 30.0 and 32.5%, respectively, which outperformed CuS (1:4) NPs (15%) and Kocide 3000 (12.5%). CuS (1:4) NPs also modulated the shoot salicylic acid (SA) and Jasmonic acid (JA) production to enhance the plant defense mechanisms against G. fujikuroiinfection. These results are useful for improving the delivery efficiency of agrichemicals via nano-enabled strategies while minimizing their environmental impact, and advance our understanding of the defense mechanisms triggered by the NPs presence in plants.
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