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Pollutant Loads Returned to the Lower Murray River from Flood-Irrigated Agriculture
2010
Mosley, Luke M. | Fleming, Nigel
Pollutant concentrations and loads returned to the lower Murray River (South Australia) from flood-irrigated agriculture were monitored over a period of 2 years at six locations. This monitoring programme was designed to provide a baseline prior to environmental improvements being undertaken to reduce pollutant loads returned to the river. Pollutant (Escherichia coli, total nitrogen, oxidised nitrogen, total phosphorus, filtered reactive phosphorus and total organic carbon) concentrations were significantly (p < 0.01) higher in the drainage water than the river water and increased during the irrigation season. Salt concentrations were also significantly (p < 0.01) higher in the drainage water than the river inflow water but decreased during the irrigation season because of dilution of the saline groundwater inputs. Pollutant loads exported to the river were significantly higher (p < 0.01-0.05) during the irrigation season for all water quality parameters except oxidised nitrogen. Levels of oxidised nitrogen, filtered reactive phosphorus and E. coli increased in the river downstream of the where the agricultural pollutant inputs begin. Load calculations indicated that this increased water pollution is likely due to the pollutant contributions from the flood-irrigated areas and biogeochemical processing of dissolved nutrients in the river.
Show more [+] Less [-]Preventing Acid Mine Drainage with an Elevated Water Table: Long-Term Column Experiments and Parameter Analysis
2010
Ouangrawa, Mariam | Aubertin, Michel | Molson, John W. | Bussière, Bruno | Zagury, Gérald J.
The elevated water table (EWT) technique for preventing acid mine drainage (AMD) was tested using instrumented laboratory columns containing reactive tailings from the Louvicourt and Sigma mines, Abitibi, Quebec. The tests were performed in short (0.4 m) and long (1.4-1.7 m) columns over 400-500 days and included periodic surface recharge and subsequent monitoring of the leached drainage water. In each column, the water table depth was adjusted relative to the air entry value (AEV or ψa) of the tailings. The influence of different water table elevations was evaluated by measuring the effluent pH, as well as the concentrations of major ions including sulphate, iron, zinc, copper and lead. Provided the water table depth below the tailings surface remained less than one half of the tailings' AEV, the observed data showed that an EWT can be very effective in reducing acid mine drainage. The principal factors controlling drainage quality were the saturated hydraulic conductivity (k sat) and the air entry value (ψa) of the tailings. A lower k sat and a higher ψa in the tailings tend to increase the performance of an elevated water table by limiting drainage-induced desaturation. Mineralogical composition had relatively little effect on the hydrogeochemical evolution provided the tailings remained highly saturated (S r ≥ 90%). The results presented here indicate that an elevated water table can be an effective means for controlling the production of AMD when the design conditions are properly selected and applied.
Show more [+] Less [-]N-Application Methods and Precipitation Pattern Effects on Subsurface Drainage Nitrate Losses and Crop Yields
2010
Bakhsh, Allah | Kanwar, Ramesh S. | Baker, J. L.
Diverting the infiltrating water away from the zone of N application can reduce nitrate-nitrogen (NO₃-N) leaching losses to groundwater from agricultural fields. This study was conducted from 2001 through 2005 to determine the effects of N-application methods using a localized compaction and doming (LCD) applicator and spoke injector on NO₃-N leaching losses to subsurface drainage water and corn (Zea mays L.)-soybean (Glycine max L.) yields. The field experiments were conducted at the Iowa State University's northeastern research center near Nashua, Iowa, on corn-soybean rotation plots under chisel plow system having subsurface drainage ‘tile' system installed in 1979. The soils at the site are glacial till derived soils. The N-application rates of 168 kg-N ha⁻¹ were applied to corn only for both the treatments each replicated three times in a randomized complete block design. For combined 5 years, the LCD N-applicator in comparison with spoke injector showed lower flow weighted NO₃-N concentrations in tile water (16.8 vs. 20.1 mg L⁻¹) from corn plots, greater tile flow (66 vs. 49 mm), almost equivalent NO₃-N leaching loss with tile water (11.5 vs. 11.3 kg-N ha⁻¹) and similar corn grain yields (11.17 vs. 11.37 Mg ha⁻¹), respectively, although treatments effects were found to be non-significant (p = 0.05) statistically. The analysis, however, revealed that amount and temporal distribution of the growing season precipitation also affected the tile flow, NO₃-N leaching loss to subsurface drain water, and corn-soybean yields. Moreover, the spatial variability effects from plot to plot in some cases, resulted in differences of tile flow and NO₃-N leaching losses in the range of three to four times despite being treated with the same management practices. These results indicate that the LCD N-applicator in comparison with spoke injector resulted in lower flow weighted NO₃-N concentrations in subsurface drain water of corn plots; however, strategies need to be developed to reduce the offsite transport of nitrate leaching losses during early spring period from March through June.
Show more [+] Less [-]Fate and transport of chlormequat in subsurface environments
2010
Juhler, René K | Henriksen, Trine | Rosenbom, Annette E | Kjaer, Jeanne
Background, aim and scope Chlormequat (Cq) is a plant growth regulator used throughout the world. Despite indications of possible effects of Cq on mammalian health and fertility, little is known about its fate and transport in subsurface environments. The aim of this study was to determine the fate of Cq in three Danish subsurface environments, in particular with respect to retardation of Cq in the A and B horizons and the risk of leaching to the aquatic environment. The study combines laboratory fate studies of Cq sorption and dissipation with field scale monitoring of the concentration of Cq in the subsurface environment, including artificial drains. Materials and methods For the laboratory studies, soil was sampled from the A and B horizons at three Danish field research stations—two clayey till sites and one coarse sandy site. Adsorption and desorption were described by means of the distribution coefficient (K d) and the Freundlich adsorption coefficient (K F,ads). The dissipation rate was estimated using soil sampled from the A horizon at the three sites. Half life (DT₅₀) was calculated by approximation to first-order kinetics. A total of 282 water samples were collected at the sites under the field monitoring study— groundwater from shallow monitoring screens located 1.5-4.5 m b.g.s. at all three sites as well as drainage water from the two clayey sites and porewater from suction cups at the sandy site, in both cases from 1 m b.g.s. The samples were analysed using LC-MS/MS. The field monitoring study was supported by hydrological modelling, which provided an overall water balance and a description of soil water dynamics in the vadose zone. Results The DT₅₀ of Cq from the A horizon ranged from 21 to 61 days. The Cq concentration-dependant distribution coefficient (K d) ranged from 2 to 566 cm³/g (median 18 cm³/g), and was lowest in the sandy soil (both the A and B horizons). The K F,ads ranged from 3 to 23 (µg¹ ⁻ ¹/n (cm³)¹/n g⁻¹) with the exponent (1/n) ranging from 0.44 to 0.87, and was lowest in the soil from the sandy site. Desorption of Cq was very low for the soil types investigated (<10%w). Cq in concentrations exceeding the detection limit (0.01 µg/L) was only found in two of the 282 water samples, the highest concentration being 0.017 µg/L. Discussion That sorption was highest in the clayey till soils is attributable to the composition of the soil, the soil clay and iron content being the main determinant of Cq sorption in both the A and B horizons of the subsurface environment. Cq was not detected in concentrations exceeding the detection limit in either the groundwater or the porewater at the sandy site. The only two samples in which Cq was detected were drainage water samples from the two clayey till sites. The presence of Cq here was probably attributable to the hydrogeological setting as water flow at the two clayey till sites is dominated by macropore flow and less by the flow in the low permeability matrix. In contrast, water flow at the sandy site is dominated by matrix flow in the high permeability matrix, with negligible macropore flow. Given the characteristics of these field sites, Cq adsorption and desorption can be expected to be controlled by the clay composition and content and the iron content. Combining these observations with the findings of the sorption and dissipation studies indicates that the key determinant of Cq retardation and fate in the soil is sorption characteristics and bioavailability. Conclusions The leaching risk of Cq was negligible at the clayey till and sandy sites investigated. The adsorption and desorption experiments indicated that absorption of Cq was high at all three sites, in particular at the clayey till sites, and that desorption was generally very limited. The study indicates that leaching of Cq to the groundwater is hindered by sorption and dissipation. The detection of Cq in drainage water at the clayey till sites and the evidence for rapid transport through macropores indicate that heavy precipitation events may cause pulses of Cq. Recommendations and perspectives The present study is the first to indicate that the risk of Cq leaching to the groundwater and surface water is low. Prior to any generalisation of the present results, the fate of Cq needs to be studied in other soil types, application regimes and climatic conditions to determine the Cq retardation capacity of the soils. The study identifies bioavailability and heavy precipitation events as important factors when assessing the risk of Cq contamination of the aquatic environment. The possible effects of future climate change need to be considered when assessing whether or not Cq poses an environmental risk.
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