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Subject: search.filters.subject.Sulphate leaching

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    Factors influencing the transformation and fate of sulphur and nitrogen in grazed hill country pastures : a thesis presented in partial fulfilment of the requirements for the degree of Doctor of Philosophy in Soil Science at Massey University
    (Massey University, 1991) Sakadevan, Karuppan
    The increasing cost of agricultural grade sulphur and the high leaching losses of sulphate sulphur(S) from superphosphate fertilized pastures in New Zealand create a need to develop more efficient S fertilization techniques. The objective of the present study was to identify the main origins of the sulphate being leached from superphosphate fertilized hill country pastures with soils (Typic Dystrachrepts) developed from underlying sedimentary parent materials. Origins of leached sulphate were categorized as S leached directly from fertilizer, from zones enriched in animal excreta and from the mineralization of soil organic matter. Mineralization studies, both in la??oratory and in field were conducted to establish the extent of and the relationship between sulphur and nitrogen mineralization and the fate of mineralized nutrients in pasture soils that contrasted in their superphosphate fertilizer history. In the preliminary laboratory study in which an open incubation technique was used to measure potential net mineralization, top soils (0-7.5cm) taken from sites that had received higher rates of superphosphate in the past, mineralized more soil organic sulphur and nitrogen than soils taken from sites that had received smaller amounts of superphosphate in the past. In addition top soils collected from low slope (0-12°) sites where a greater proportion of animal excreta is returned, mineralized more S and N than the soils from medium slope (13-25°) sites. The ratio of N to S mineralized was narrower (2. 0 to 3. 6 ) than the N to S ratio of the whole soil (7 .1 to 8. 9) suggesting that in these soils relatively more S remains in a mineral form in the soil and is more susceptible to leaching than N which is conserved in the soil. Cylindrical, mini-lysimeters with ion exchange resin traps for collecting solutes from drainage water were developed to measure the net mineralization of soil organic S and N under field conditions. Leaching losses of S and N, pasture uptake of S and N and changes in mineral S and N pools in the soil at the same site were measured simultaneously and the rate of mineralization calculated. A laboratory evaluation of the lysimeter showed that the resin trap was capable of removing all the sulphate from drainage water at several different flow rates. The main advantage of these lysimeters over the conventional methods of measuring the leaching losses of anions and cations in the field is that regular drainage collection was not necessary. By introducing mixtures of both anion and cation exchange resins in the trap in the lysimeter it was possible to monitor the amount of anions and cations in field drainage over long periods of time before it was necessary to change the resin mixtures. In the initial field lysimeter study the net mineralization and pasture uptake of N ( 119 to 251 kg N ha-1) was 10 times more than that of S ( 12 to 27.5 kg S ha-1) , yet approximately 10 times more sulphate S ( 2.0 to 17.3 kg S ha-1) than mineral N (0. 19 to 1.3 kg N ha-1) was lost by leaching. Previous fertilizer history had a marked effect on the leaching losses of sulphate with seven times more S lost ( 2.1 vs 1 5.3 kg S ha-1) from sites which received greater rates of superphosphate and had higher stocking rates. During the initial seven month period S leaching losses on the low and high fertility sites were equivalent to 1 5% and 3 3% of the annual fertilizer application. More sulphate was leached from areas identified as animal camping areas. The lack of any change in sulphate below the 150mm soil depth during a period of active plant growth and no leaching suggested that any sulphate that moved below 1 50mm of the soil could be considered to be effectively lost from the system. Increased leaching losses of calcium and magnesium were associated with increased sulphate losses. The amount of calcium lost by leaching ( 4.7 5 to 12. 5 ,kg Ca ha-1) was far greater than potassium (0.8 to 3 . 6 kg .K ha'1), although twice the amount of potassium ( 240 kg K ha·1 vs 120 kg Ca ha'1) was. cycled through the plant-animal system. The amount of magnesium lost by leaching was greater than the amount of potassium lost by leaching. In a second lysimeter study the direct effects of freshly applied fertilizer on the mineralization of S and N from soil organic matter, their plant availability and losses by leaching were studied under field conditions using 35S labelled superphosphate. Fertilizer application significantly increased the mineralization of both organic S and N. The recovery and measurement of 35S activity over a nine month period showed that major proportions of pasture S ( 8 5 and 8 6% of the pasture S for low and high fertility farmlets, respectively) and leached S (75 and 87% of the leached S for low the mineralization of soil organic matter and not recently applied fertilizer. The amounts of both S and N mineralized from soil organic matter depends upon the past fertilizer history of the site and the present fertilizer application rate (22 and 40 kg S ha-1 and 125 and 204 kg N ha-1 for low and high fertility farmlets, respectively). Further, when the net mineralization of S was greater a greater proportion (59%) of mineralized S was lost by leaching than removed by pasture (39%). Irrespective of the amount N mineralized virtually all was removed by pasture. The results suggested that low N availability was a major factor limiting carbon fixation and the formation of organic S in these pasture soils. In a third lysimeter study, field simulated sheep dung and urine events boosted pasture growth and S and N uptake by approximately (50%), whereas the leaching losses of S and N were not influenced by the their application. A preliminary computer simulation model describing the mineralization of soil organic S, pasture S uptake and leaching losses in grazed pasture was developed. The preliminary model gave reasonable predictions of the changes in soil sulphate concentrations in the soil up to a depth of 25cm, pasture uptake of S and leaching losses of S at four pasture sites varying in their fertilizer history. Further refinement of the model is necessary before it can provide the basis for predicting fertilizer S requirement for hill country pastures. The experimental results and model output confirm balance study predictions that large leaching losses of S occur and these are derived mainly from the mineralization of soil organic matter which accumulates in well fertilized soils. The extent of S losses appear to be a function of the general levels of soil productivity and the data suggested that only a small, probably less than 20% reduction in this loss could be achieved by changing to slow release S fertilizers.
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    Measurement and modelling of chloride and sulphate leaching from a mole-drained soil : a thesis presented in partial fulfilment of the requirements for the degree of Doctor of Philosophy in Soil Science at Massey University
    (Massey University, 1991) Heng, Lee Kheng
    A study of the leaching of sulphate, chloride, nitrate and the associated cations was carried out over two winter periods on three mole-drained paddocks on a yellow-grey earth (Tokomaru silt loam). The paddocks were occasionally grazed by sheep. At the beginning of each drainage season potassium chloride (KCl) and sulphur fertilizer, as either single superphosphate (SSP) or elemental sulphur (S°), were applied to two of the paddocks, while the third served as a control. The amount of KCl applied was 200 kg ha-1 yr-1, while sulphur was applied at 50 kg S ha-1 in 1988 and 30 kg S ha-1 1989. Drain flow from the fertilized paddocks was measured with V-notch weirs, and sampled using proportional samplers. Large differences in the total drainage flow were measured in the two years, with values of approximately 280 mm in 1988 and 110 mm in 1989. Significant amounts of the chloride added through both fertilizer and rainfall were leached, amounting to approximately 105 kg Cl ha-1 yr-1. The leaching of sulphate-S depended on the form of S fertilizer applied, the quantity of drainage, and the rate of mineralization. Leaching losses of 17 and 3.4 kg S ha-1 were measured from the SSP and S° fertilized paddocks, respectively, in 1988, and 9.4 and 3.5 kg S ha-1 in 1989. The study showed that applying SSP just before the drainage season increased leaching losses of sulphate-S substantially. Although the particle sizes of S° used in both years were much bigger than those specified by the Ministry of Agriculture and Fisheries of New Zealand, there appeared to be no difference in the yield response to S applied either as SSP or as S°. The reduced leaching of S when applied as S° resulted from the slow oxidation of S° to sulphate-S. Relatively little nitrate-N was leached, the amount ranging from 11 to 17 kg N ha-1 yr-1. Losses of potassium were less than 10 kg K ha-1 yr-1, despite the large quantity applied as KCl fertilizer immediately before winter. However a large amount of calcium was leached, between 31 and 52 kg ha-1 yr-1. The amount of magnesium leached was between 9 and 15 kg ha-1 yr-1. A considerable quantity of sodium was leached, around 58 kg ha-1 in 1988, and 31 kg Na ha-1 in 1989, roughly equal to the input in rainfall. Good mass balances were obtained for both chloride and sulphate. The measured moles of negative and positive charge from cations and anions in the leachate were also almost equal. Three models were developed for the leaching of chloride and sulphate-S. An approach dividing the soil water into mobile-immobile phases, and using a fairly detailed soil water flow model was developed. The model was able to simulate the concentration of chloride in the drainage closely, even just after the application of chloride fertilizer, and during highly preferential flow conditions induced by heavy rain. A transfer function model, assuming a log-normal probability density function (pdf) of solute travel pathway lengths, was able to simulate the leaching of chloride reasonably well in 1988. The prediction was less satisfactory in 1989 and during highly preferential flow. By adapting the pdf for chloride to sulphate and by taking adsorption of sulphate into account, the model could predict the sulphate concentration in the drainage quite successfully. A simpler model, using the idea that the two-dimensional flow geometry to the mole drain implies that the drainage concentration approximately equals the average soil solution concentration, was also developed. Despite its simplicity it was able to simulate the leaching of chloride and sulphate as well as the transfer function model. Irrespective of the model being used, the net mineralization rate of soil organic sulphur emerged as an important factor in predicting the leaching of sulphate.