published_or_final_version / abstract / toc / Geography and Geology / Master / Master of Philosophy

Although silicon (Si) has not yet been recognized as an essential nutrient element, its application to sugarcane (Saccharum officinarum L.) has proved to be beneficial. Since optimum crop production depends on the maintenance of adequate plant nutrients in the soil, there is a need in the South African sugar industry for a reliable index for assessing the requirement for supplemental silicon (Si) in soils, particularly in reducing the risk of Eldana saccharina stalk borer infestation in cane. The objective of this study was to assess Si availability in soils, to select a suitable Si extraction method and a critical value for determining when a response is likely. For this purpose, five acid soils (representing. some of the most important agricultural soil groups used for sugarcane production in the sugar belt) were used in October 2004, in the lAKE WILSON glasshouse of the South African Sugarcane Research Institute (SASRI) based at Mount Edgecombe. Except for the Arcadia form soil with an initial Si content of 1.2 mmol kg- I as estimated using the O.OlM H2S04 + (NH4)zS04) extractant, soils representing the other five soil forms namely Cartref, Glenrosa, Longlands and Nomanci; exhibited a sub-optimal Si content of not more than 4.0 mmol kg-I. Sorghum was used as a plant crop and sugarcane as a ratoon crop because of their Si accumulator status. Three different Si sources: calmasil, slagment and wollastonite; with respectively 9.85, 15.20, and 5.25% Si content were applied at increasing rates of 0, 3 and 6 tons ha- 1 as Si fertilizers. Silicon (Si) was extracted from untreated and treated soils by utilizing six different extractants, (1) O.OlM H2S04 + (NH4)2S04; (2) Distilled water; (3) 0.025M H2S04; (4) 0.5M CH3COOH; (5) 0.5M CH3COONH4pH 4.8; and (6) O.OlM CaCh.2H20. The amount of soil Si extracted followed the order: 0.025M H2S04 > 0.5M CH3COOH > O.OlM H2S04 + (NH4)2S04 > O.OlM CaCh.2H20 > 0.5M CH3COON~ pH 4.8 > distilled water. Soil Si extracted by 0.025M H2S04 was significantly correlated with soil exchangeable cations,. CEC, clay content, cane biomass yield, cane Si uptake and increasing rates of applied Si. Averaged over all soil forms investigated, the increases in dry biomass yield and Si uptake ranged. from 18% to 154% for sorghum; and from 23% to 85% for cane respectively. Even though the highest increases (%) in cane biomass yield and Si uptake were obtained on a Nomanci form soil with initial poor fertility status, the highest means were obtained on an Arcadia form soil with the highest Si initial content. There was no difference between different Si sources in their ability to influence cane biomass yield and Si uptake, and therefore the supply to the soils. Even though the lower and higher Si source rates were not different from each other, they increased cane yield and Si uptake, indicating that Si was undoubtedly beneficial for sugarcane. The Si critical levels for different soils as estimated by 0.025M H2S04 were 6.0 mmol kg-1 (168 mg kg-I) for Arcadia; 2.6 mmol kg-I (64 mg kg-I) for Cartrel; 2.5 mmol kg-I (64 mg kg-I) for Glenrosa; 1.6 mmol kg-I (45 mg kg-I) for Longlands; and 2.4 mmol kg-I (67 mg kg-i) for Nomanci form soils. / Thesis (M.Sc.)-University of KwaZulu-Natal, Pietermaritzburg, 2007.

Little is known regarding the effects of land use on soil organic matter and P status of South African soils. For that reason, the effects of the main agricultural land uses in the midlands region of KwaZulu-Natal [maize (Zea mays), sugarcane (Saccharum spp), annual ryegrass pasture (Lolium multiflorum), permanent kikuyu pasture (Pennisetum clandestnum), gum (Eucalyptus grandis) and pine (Pinus patula)] on soil organic matter content, microbial biomass C and P and inorganic and organic P pools derived from a modified Hedley P fractionation was investigated on two sites where the longterm history of land management was known. In comparison with undisturbed native grassland, permanent kikuyu pasture resulted in an increase in organic C, organic P and microbial biomass C and P. Maize and sugarcane production resulted in a decrease in organic C, organic P and microbial C and P. Under annual pasture, gum and pine forests, organic matter and microbial biomass concentrations remained similar to those under native grassland. Under native grassland, extractable organic P accounted for 50% or more of the total P content of soils but under agricultural management with regular applications of fertilizer P, there was an increase in the percentage of total P present as inorganic P. Agricultural management greatly affected the distribution of P among the various inorganic and organic P fractions. Resin-Pi and NaHC03-Pi (the potentially-available forms of Pi) showed similar trends with land use being greatly elevated under kikuyu pasture at both sites and sugarcane and maize at one site. This accumulated Pi was thought to have originated from recent fertilizer applications and possibly recently mineralized organic P. Trends for NaOH-Pi with land use differed greatly from those of the Resin- and NaHC03Pi fractions. Concentrations were notably high under maize and sugarcane production. Of the pools of soil organic P, the NaHC03-Po fraction was most greatly affected by land use, being elevated under kikuyu and decreased under maize and sugarcane. This supports the assertion that it is the NaHC03-Po fraction that is the most labile soil organic P pool. It was concluded that land use greatly affects soil organic C and P status, soil microbial biomass C and P contents, soil inorganic P concentrations and the distribution of P among the various P fractions. A short-term (8 weeks) laboratory incubation experiment was carried out to compare the effects of inorganic (KH2P04) and organic (cattle manure, poultry manure and maize crop residues) sources of P, applied at a rate equivalent to 30 kg P ha-1 , on soil inorganic and organic P fractions and the potential availability of soil P. Additional treatments consisted of lime [Ca(OHhl at 5 ton ha-1 and lime plus inorganic P. Applications of lime raised soil pH to a similar extent after 1, 4 and 8 weeks incubation. After 8 weeks, a small increase in soil pH was also noted for the cattle and poultry manure and maize residue treatments. For the inorganic P fractions, substantial treatment effects were observed only for the Resin-Pi fraction. The inorganic P source was more effective than the organic ones at increasing Resin-Pi after 1 and 4 weeks incubation and of the organic sources, cattle and poultry manure were more effective than maize residues. Resin-Pi concentrations generally increased between 1 and 4 weeks incubation but then declined rapidly between 4 and 8 weeks incubation. After 8 weeks incubation, treatment effects on Resin-Pi were small. Concentrations of NaHC03-Pi, dilute HCI-Pi and concentrated HCI-Pi all declined over the incubation period. There was no clear trend with incubation for NaOH-Pi although for the poultry manure and maize treatments, concentrations declined between 4 and 8 weeks incubation. In general, concentrations of NaHC03-Po were greater for organic than inorganic P sources after 8 weeks incubation suggesting microbial immobilization of P in these treatments. There were increases in NaHC03-Po and concentrated HCI-Po over the incubation period suggesting progressive immobilization of P from the Pi fractions that declined in concentration during the incubation. Concentrations of NaOH-Po were not greatly affected by incubation period. The lime treatments, however, had lower NaOH-Po concentrations than the others suggesting that liming may have stimulated microbial mineralization of Po. Residual-P concentrations increased over the incubation period. This was attributed to conversion of extractable Pi fractions into recalcitrant, non-extractable Pi forms and/or immobilization of Pinto intransigent organic forms. / Thesis (M.Sc.)-University of KwaZulu-Natal, Pietermaritzburg, 2006.

Copies of author's previously published articles inserted. / Bibliography: leaves 195-230. / xx, 320 leaves : ill. (some col.) ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / In this study the soil aqueous phase chemistry of Zn and Cu in alkaline sodic soils are investigated. The chemistry of trace metal ions at indigenous concentrations in alkaline sodic soils are reported. Metal ions at low concentrations are measured by the graphite furnace atomic absorption spectrometry (GFAAS) technique. / Thesis (Ph.D.)--University of Adelaide, Dept. of Soil Science, 1998

The major land use in New Zealand is pastoral farming of sheep and cattle. In intensively grazed dairy-pasture systems, animals graze on nitrogen (N)-rich legume-based pastures, but do not efficiently utilize the N they ingest. On average only 10.5% of the N in forage-based animal feed is converted into milk and the remainder is excreted in dung and urine. In the pastures, a cow urine patch can typically contain up to 1000 kg N ha-1. Nitrogen input, either in the form of cow urine or fertilizer, often exceeds immediate plant requirements and hence is susceptible to losses as ammonia (NH3) volatilisation and nitrous oxide (N2O) emissions and removal in drainage water through nitrate (NO3-) leaching. This loss of N from grazed pastures causes detrimental environmental impacts in the form of acidification and eutrophication of the soil and water bodies, global warming, destruction of stratospheric ozone, and NO3- toxicity. Various approaches have been attempted to mitigate the economic and environmental impacts of N losses. One such approach is the use of Urease (UIs) and Nitrification (NIs) inhibitors. There have been extensive studies on the value of UIs in arable farming and NIs in grazed pastures. However, only limited work on the impact of UI and NI alone and in combination in influencing the N dynamics, and thus mitigating N gaseous losses from pastures, has been conducted. This thesis examines the impact of UI (Agrotain; N-(n-butyl) thiophosphoric triamide) and NI (Dicyandiamide, commonly known as DCD), when applied alone or in combination to cow urine and urea fertiliser, on N losses through NH3 and N2O emissions and NO3- leaching, and on herbage production under glasshouse conditions and a field-plot study. The degradation rate of DCD, and its effect on nitrification and on N2O emissions from four soils varying in their physical and chemical properties was also examined under laboratory incubations. The results from the field-plot study were then used to predict the effect of DCD on N2O emissions reductions from urine by adapting the process-based NZ-DNDC model. Both NH3 and N2O emissions have common sources in agriculture. Therefore, chambers were adapted to measure their emissions simultaneously using active and passive gas sampling. Active sampling involved continuous air flow and the use of acid (0.05 M H2SO4 and 2% H3BO3) traps for NH3 measurements and passive sampling involved collecting three gas samples over a one-hour period from a static chamber used for N2O emissions. The first glasshouse experiment used UI with urine or urea to assess its effect on NH3 and N2O emissions, changes in soil mineral-N and N uptake by pasture plants. The UI treatments also involved two commercial products, Sustain Yellow (urea coated with Agrotain and elemental S) and Sustain Green (urea coated with Agrotain). The use of UI effectively decreased total NH3 emissions, as well as delaying the time of maximum NH3 emissions from both urea (600 kg N ha-1) and urine (476 kg N ha-1) by 27% and 22%, respectively. The UI-induced decrease in NH3 volatilization ranged from 42-48% when urea was applied @ 100 kg N ha-1. Urease inhibitor was also effective in decreasing N2O emissions significantly from urine and urea applied @ 100 kg N ha-1. The addition of UI increased dry matter yield by 13-19% as compared to the urea-alone treatment. In the second glasshouse study, NI (DCD) was added @ 25 kg ha-1 to urea (@ 25, 50 and 75 kg N ha-1) and urine (@ 144, 290 and 570 kg N ha-1) applied at different rates. Addition of DCD reduced N2O emissions from both urea and urine and NO3- leaching from urine. Dicyandiamide reduced N2O emissions by 34-93% from the added urea and 33-80% from the added urine. However, its use increased the amount of ammonium (NH4+) present in the soil by 3 to 13% both in the urea and urine treatments, and this NH4+ was susceptible to leaching and volatilisation losses. The addition of DCD, however, resulted in a 60-65% reduction in NO3- leaching from urine applied to pasture soil cores. It also caused a significant reduction in NO3- -induced cation leaching. Leaching of K+, Mg+2 and Ca+2 ions was reduced by 36-42%, 33-50% and 72%, respectively, with DCD applied to cattle urine (290 and 570 kg N ha-1). The combined use of UI and NI was more effective in controlling N gaseous losses than using them individually. The combination of UI and NI retarded NH3 emissions by 70% in the urea treatment and by 4% in the urine treatment (field-plot study). It also considerably reduced N2O emissions (50-51%) following the application of urea and urine (field-plot study) to pasture soil. With the combined inhibitors, there was a 14 and 38% increase in herbage yield from added urea and urine (field-plot study), respectively. A laboratory incubation experiment was undertaken to study the effect of soil types and the rate of DCD application on the degradation kinetics of DCD. The rate of degradation of DCD varied among the four soils studied. The degradation was slowest (half-life period of 6 to 11 days) in an allophanic soil with a high concentration of organic matter. The effectiveness of DCD in inhibiting nitrification also varied depending on the nature and amount of soil organic matter and clay content. The maximum inhibition was observed in a soil with low organic matter and high clay content. Finally, 'NZ-DNDC', a process-based model, was adapted and used to simulate the effect of DCD on emissions reduction using DCD inhibition values that vary according to different soil types. This model effectively simulated the effect of DCD on N2O emissions reductions in Tokomaru silt loam following urine application. However, more field data are required from a range of pasture soils with contrasting amount of soil organic matter and clay content under differing climatic conditions to further test this model modification to predict emission-reductions with DCD application in different soil types.

The soils used by the East Coast Organic Producers Trust (ECOPT; the grower group that this study is targeted towards) have exceptionally low soil Olsen P concentrations (ca. 6 mg/L). These and other limitations (e.g. poor weed and pest and disease control) result in many ECOPT growers being unable to produce economic yields on anything other than small scale gardens. Fertilisers and manures are seldom used by these growers, which exacerbates the problem. Thus, the object of this research was to provide information to ECOPT on which fertilisers and application strategies would provide the best returns on their phosphorus (P) fertiliser investment. The experimental work was carried out in two parts. A laboratory study tested a range of phosphate rock (PR) based fertilisers and application rates; Ben Guerir reactive phosphate rock (RPR; 67, 133, 267, 533 and 1,333 mg P/kg soil), BioPhos and BioSuper (267 and 1,333 mg P/kg soil) and a no fertiliser Control. Soil fertiliser mixtures were incubated for 155 days and periodic measurements of PR dissolution, soil pH and Bic-P (analogous to Olsen P but expressed in µg/g) were undertaken. The field study used fewer application rates and two application methods; banded and broadcast. Broadcast plots were applied at 678 mg P/kg soil (488 kg P/ha); banded RPR was applied at 236, 678 and 1475 mg P/kg soil (40, 115 and 250 kg P/ha respectively) and banded BioPhos and BioSuper at 678 mg P/kg soil (115 kg P/ha). A Control was also included. Fertilisers were applied in October 2004 and changes in soil pH and Bic-P were measured in the broadcast plots only over a 344 day period. Potato (Solanum tuberosum L. cv. Desiree) was the test crop. Regression analysis was used to generate exponential equations to describe the changes in Bic-P over time (∆Bic-P). Differences between fertilisers in the amount of P dissolved and pH fluxes were used to explain the differences in ∆Bic-P. BioSuper dissolved quicker and generated greater ∆Bic-P than RPR and BioPhos, which were similar. Higher application rates produced greater increases in Bic-P than lower rates but decreased the % of P applied that dissolved. The increase in Bic-P over time from fertiliser application was much slower in the field compared with the laboratory. This was put down to differences in experimental conditions; mainly soil pH and soil aggregate surface area. Potato tuber yield (mean = 35 t/ha) did not respond to any of the fertiliser treatments despite a significant increase in P concentration of the shoots mid-way through the season in all broadcast treatments (shoot P concentration was not analysed in the banded plots). Water and N availability were the main limiting factors in this season as the crop was not irrigated and soil N supply was insufficient to produce a full canopy. Phosphorus response curves generated using the fertiliser response model PARJIB (Reid, 2002), and an economic analysis, indicated that for RPR and BioPhos the optimum economic application rate was 200 kg P/ha and for BioSuper it was 100 kg P/ha (applied every third and second year respectively).

Sulphur is an important nutrient to plants, and reports of its deficiency have been increasing worldwide. Sulphur starvation causes losses in both yield and quality, and it reduces nitrogen use efficiency of plants. As the timing for fertilisation can be decisive for avoiding deleterious effects, improvements in the description of the sulphur balance in fields are a valuable contribution for assisting fertiliser management. Sulphate is the most important inorganic form of sulphur in soils. Being the mobile form, sulphate is readily available for plants, and also prone to be leached. Therefore the description of the movement of sulphate is the key component of the sulphur balance. Leaching of sulphate from the soil can be significantly delayed by its adsorption onto the soil particles. Soil type and pH are the main factors defining the sulphate adsorption capacity; although the presence of other ions in the soil solution can have a considerable effect. It has been reported that in some soils, typically volcanic and tropical soils with variable-charge characteristics, the co-presence of sulphate and calcium can substantially enhance their retention via ion-pair adsorption (IPA). To determine the influence of cations on the movement of sulphate, series of batch and miscible displacement experiments were conducted using two New Zealand soils, of contrasting ion adsorption capacities: the Taupo sandy and Egmont loam soils. These experiments demonstrated the occurrence of cooperative adsorption of sulphate and calcium in the Egmont soil, but not in the Taupo soil. Batch experiments were conducted to examine the IPA adsorption process in the Egmont soil in more detail. Based on the analyses of the results from these two series of experiments, plus the review of published data, three different mathematical approaches for evaluating the amount of solute adsorbed as ion-pairs are proposed. A computer program was built for solving an adsorption model using these three approaches, and was used to compare the model's predictions and the observed adsorption data. An extension of this program, coupling the adsorption model with a solute transport description, was used to simulate the movement of sulphate and calcium. Comparisons between the data from the miscible displacements and the results from this model are used to demonstrate the applicability of the proposed IPA description for modelling the transport of these ions in the soil. Finally, results from a pot trial with Egmont soil are used to examine the relevance of IPA for the movement of sulphate under non-equilibrium conditions, and with active plant growth. Although the results from this experiment regarding IPA were statistically non-significant, some insights could be obtained and are discussed. More studies involving IPA under non-equilibrium experiments are needed for a better understanding of the relevance of IPA in field conditions.

Thesis (M.S.)--Miami University, Dept. of Chemistry and Biochemistry, 2008. / Title from first page of PDF document. Includes bibliographical references.

Submitted by Johnny Rodrigues (johnnyrodrigues@ufcg.edu.br) on 2018-06-15T19:05:07Z No. of bitstreams: 1 ARMINDO BEZERRA LEÃO - DISSERTAÇÃO PPGEA 2006..pdf: 18036151 bytes, checksum: 3c7202f8b76aca90d252e37405bcede3 (MD5) / Made available in DSpace on 2018-06-15T19:05:07Z (GMT). No. of bitstreams: 1 ARMINDO BEZERRA LEÃO - DISSERTAÇÃO PPGEA 2006..pdf: 18036151 bytes, checksum: 3c7202f8b76aca90d252e37405bcede3 (MD5) Previous issue date: 2006-05 / O solo pode apresentar ampla variação dos seus atributos, estando esta relacionada a fatores ligados à sua formação ou manejo de práticas agrícolas, a exemplo da irrigação que tem, como efeito nocivo se mal empregada, problemas de salinidade. A estatística clássica considera que a variabilidade do solo ocorre de forma inteiramente aleatória; entretanto, vários estudos têm revelado que seus atributos apresentam grande dependência espacial necessitando, portanto, de uma análise geoestatística Neste trabalho se propôs como objetivo geral, estudar as variáveis que caracterizam a salinidade do solo através da estatística clássica e geoestatística e, como metas específicas avaliar a variabilidade espacial, a existência de dependência espacial entre amostras, a validação cruzada do método de interpolação utilizado (krigagen) e construir mapas de isolinhas das variáveis da área em estudo. O estudo foi conduzido no perímetro Irrigado Engenheiro Arcoverde, localizado no Município de Condado, PB, o qual se situa na Bacia do Alto Piranhas, cuja área experimental tinha 42 hectares e se constituía de solos Neossolos Flúvicos, onde se coletaram 53 amostras, nas profundidades de 0-20, 20-40 e 40-60 cm. A malha de amostragem foi irregular, os pontos de coleta se distanciaram de lOOm entre si. De início se utilizaram para avaliação da variabilidade espacial, métodos de estatística clássica a fim de se verificar medidas de posição, dispersão e geostatística, analisando-se os variogramas e se realizando, também, a validação cruzada como meio de conhecer os melhores ajustes para os modelos encontrados. Após a realização de interpolação por krigagem, construíram-se mapas de isolinhas revelando os problemas de salinidade e sodicidade, em que os resultados obtidos indicaram grande variabilidade justificando, assim, o uso da geoestatística, principalmente para os atributos CE e PST do solo, reconhecendo-se a geoestatística como uma poderosa ferramenta indicadora da dependência espacial entre amostras e a distância, a partir dos quais elas se tornam independentes. Os atributos estudados, indicadores de salinidade, apresentaram estrutura de dependência espacial, o que permitiu o seu mapeamento. A validação cruzada demonstrou forte relação entre os valores observados e os estimados, comprovando que a Krigagem ordinária é um bom interpolador. A identificação de compartimentos como sub-regiões da paisagem na área de estudo, mostrou-se eficiente na caracterização da salinidade do solo. A técnica de interpolação por krigagem permitiu verificar que a salinidade do solo aumentou em profundidade, além de distribuição diferenciada dos sais na área, com maiores teores em sub-região específica. / The soil atributes may present a great variability, due to formation and management factores, such as an inadequate irrigation that coutj produce salinity problems. The classical statistics consider that soil variability occurs in a randomized form, however several studies have shown that the attributes present an strong spatial dependence, nedding thus geoestatical analises. The objective of this work was to study the variables that characterize the soil salinity by classical statistics and geostatistics and also to evaluate the spatial variability, the spatial dependence amongst samples, to verify the crossed validation of the interpolation method (Kriging) and to build maps of isolines of the ali variables. The present work was conducted at the Engenheiro Arcoverde irrigated perimeter located at Condado, Paraíba, aiming to measure the soil parameters that define the soil salinity, to study the spatial variability of them throughout geoestatical analyses, to study the liability of the Kriging interpolation method and to construct salinity and sodicity maps, furnishing subsides for an adequate soil management which could allows their reclamation. For this, 159 soil samples were collected at 0-20, 20-40 and 40-60 cm depth intervals, on an irregular grid with the sampling points separated at approximately 100 m. To evaluate the spatial variability initially it was used classical statistics to verify position and dispersion measures and afterwards geoestatistics to analise the semivariograms, crossed validation and to obtain the best adjusted models. After interpolation by kriging, isoline maps were constructed showing the salinity and sodicity situation of the area. The results obtained allowed to observe a great spatial variability of eletrical conductivity and exchange sodium percentage. The pH variable showed a low spatial variability. The spatial dependence of the studied attributes permitted their mapping using kriging techniques. The crossed validation offered an excellent precision to estimate data. The compartments identification, sub-regions of the studied area, was excellent to characterize the soil salinity. Small variations on the soil relief, on the soil formation and management conditioned the variability found for the studied attributes. Finally, the geoestatistics showed the possibility to obtain a greater volume of information from a small volume of data, which means efficience, saving of time and resource

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