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1.
J Contam Hydrol ; 191: 19-32, 2016 08.
Article in English | MEDLINE | ID: mdl-27182792

ABSTRACT

Reducing conditions are necessary for denitrification, thus the groundwater redox status can be used to identify subsurface zones where potentially significant nitrate reduction can occur. Groundwater chemistry in two contrasting regions of New Zealand was classified with respect to redox status and related to mappable factors, such as geology, topography and soil characteristics using discriminant analysis. Redox assignment was carried out for water sampled from 568 and 2223 wells in the Waikato and Canterbury regions, respectively. For the Waikato region 64% of wells sampled indicated oxic conditions in the water; 18% indicated reduced conditions and 18% had attributes indicating both reducing and oxic conditions termed "mixed". In Canterbury 84% of wells indicated oxic conditions; 10% were mixed; and only 5% indicated reduced conditions. The analysis was performed over three different well depths, <25m, 25 to 100 and >100m. For both regions, the percentage of oxidised groundwater decreased with increasing well depth. Linear discriminant analysis was used to develop models to differentiate between the three redox states. Models were derived for each depth and region using 67% of the data, and then subsequently validated on the remaining 33%. The average agreement between predicted and measured redox status was 63% and 70% for the Waikato and Canterbury regions, respectively. The models were incorporated into GIS and the prediction of redox status was extended over the whole region, excluding mountainous land. This knowledge improves spatial prediction of reduced groundwater zones, and therefore, when combined with groundwater flow paths, improves estimates of denitrification.


Subject(s)
Groundwater/chemistry , Hydrology/methods , Denitrification , Discriminant Analysis , Environmental Monitoring/methods , Geographic Information Systems , Geology , Models, Theoretical , New Zealand , Nitrates/analysis , Nitrates/chemistry , Oxidation-Reduction , Soil/chemistry , Water Wells
2.
Sci Total Environ ; 514: 281-9, 2015 May 01.
Article in English | MEDLINE | ID: mdl-25668280

ABSTRACT

Groundwater is used as a precious resource for drinking water worldwide. Increasing anthropogenic activity is putting increasing pressure on groundwater resources. One impact of increased groundwater abstraction coupled with increasing dry weather events is the lowering of groundwater levels within aquifers. Biofilms within groundwater aquifers offer protection to the groundwater by removing contaminants entering the aquifer systems from land use activities. The study presented investigated the impact of desiccation events on the biofilms present in groundwater aquifers using field and laboratory experiments. In both field and laboratory experiments a reduction in enzyme activity (glucosidase, esterase and phosphatase) was seen during desiccation compared to wet controls. However, comparing all the data together no significant differences were seen between either wet or desiccated samples or between the start and end of the experiments. In both field and laboratory experiments enzyme activity recovered to start levels after return to wet conditions. The study shows that biofilms within groundwater systems are resilient and can withstand periods of desiccation (4 months).


Subject(s)
Biofilms/growth & development , Groundwater/microbiology , Water Supply/statistics & numerical data , Desiccation , Environmental Monitoring , Laboratories
3.
J Environ Qual ; 35(2): 628-40, 2006.
Article in English | MEDLINE | ID: mdl-16510708

ABSTRACT

Accurate input data for leaching models are expensive and difficult to obtain which may lead to the use of "general" non-site-specific input data. This study investigated the effect of using different quality data on model outputs. Three models of varying complexity, GLEAMS, LEACHM, and HYDRUS-2D, were used to simulate pesticide leaching at a field trial near Hamilton, New Zealand, on an allophanic silt loam using input data of varying quality. Each model was run for four different pesticides (hexazinone, procymidone, picloram and triclopyr); three different sets of pesticide sorption and degradation parameters (i.e., site optimized, laboratory derived, and sourced from the USDA Pesticide Properties Database); and three different sets of soil physical data of varying quality (i.e., site specific, regional database, and particle size distribution data). We found that the selection of site-optimized pesticide sorption (Koc) and degradation parameters (half-life), compared to the use of more general database derived values, had significantly more impact than the quality of the soil input data used, but interestingly also more impact than the choice of the models. Models run with pesticide sorption and degradation parameters derived from observed solute concentrations data provided simulation outputs with goodness-of-fit values closest to optimum, followed by laboratory-derived parameters, with the USDA parameters providing the least accurate simulations. In general, when using pesticide sorption and degradation parameters optimized from site solute concentrations, the more complex models (LEACHM and HYDRUS-2D) were more accurate. However, when using USDA database derived parameters, all models performed about equally.


Subject(s)
Models, Theoretical , Pesticides/analysis , Water Pollutants, Chemical/analysis , Adsorption , Bridged Bicyclo Compounds/analysis , Bridged Bicyclo Compounds/chemistry , Carbon/analysis , Computer Simulation , Glycolates/analysis , Glycolates/chemistry , Half-Life , New Zealand , Pesticides/chemistry , Picloram/analysis , Picloram/chemistry , Research Design , Soil/analysis , Triazines/analysis , Triazines/chemistry , Water Supply
4.
J Environ Qual ; 34(1): 237-47, 2005.
Article in English | MEDLINE | ID: mdl-15647554

ABSTRACT

Colloids, including bacteria, can dramatically accelerate the transport of heavy metals in ground water. Batch and column experiments were conducted to investigate adsorption of cadmium (Cd) onto Bacillus subtilis spores or Escherichia coli vegetative cells and Cd transport in alluvial gravel aquifer media in the presence of these bacteria. Results of the batch experiments showed that adsorption of Cd onto the bacteria was (i) positively related to solution pH, bacterial concentration, and negative surface charge, but inversely related to Cd concentration and (ii) a rate-limited nonlinear process, but adsorption onto E. coli was much less. For column influent Cd concentrations of about 4 mg/L and bacterial concentrations of > or = 10(5) colony-forming units (cfu)/mL, there was a significant increase in total Cd effluent concentrations. In comparison with controls that did not have bacteria-facilitated transport, Cd traveled 17 to 20 times faster when it traveled with mobile bacteria. However, Cd traveled mostly 2 to 3 times slower during the desorption phase under the influence of bacteria retained in the column. The difference between total and dissolved Cd concentrations was significant during Cd cotransport with B. subtilis spores, but this concentration difference was very small during Cd cotransport with E. coli, suggesting an adsorption-dominant mechanism during Cd cotransport with the spores and the possibility of Cd chelation by the dissolved membrane vesicles secreted from E. coli cell walls. Bacteria-facilitated transport of heavy metals may pose a threat to ground water quality in sites such as landfills and following land disposal of industrial and domestic effluent and sludge.


Subject(s)
Cadmium/metabolism , Soil Pollutants/metabolism , Water Pollutants/metabolism , Adsorption , Bacillus subtilis , Cadmium/analysis , Colloids , Escherichia coli , Industrial Waste , Soil Microbiology , Soil Pollutants/analysis , Spores, Bacterial/chemistry , Water Pollutants/analysis
5.
Pest Manag Sci ; 57(12): 1142-50, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11802602

ABSTRACT

A field tracer experiment, simulating point source contamination, was conducted to investigate attenuation and transport of atrazine, hexazinone and procymidone in a volcanic pumice sand aquifer. Preliminary laboratory incubation tests were also carried out to determine degradation rates. Field transport of the pesticides was observed to the significant under non-equilibrium conditions. Therefore, a two-region/two-site non-equilibrium transport model, N3DADE, was used for analysis of the field data. A lump reduction rate constant was used in this paper to encompass all the irreversible reduction processes (e.g. degradation, irreversible adsorption, complexation and filtration for the pesticides adsorbed into particles and colloids) which are assumed to follow a first-order rate law. Results from the field experiment suggest that (a) hexazinone was the most mobile (retardation factor R = 1.4) and underwent least mass reduction; (b) procymidone was the least mobile (R = 9.26) and underwent the greatest mass reduction; (c) the mobility of atrazine (R = 4.45) was similar to that of rhodamine WT (R = 4.10). Hence, rhodamine WT can be used to delimit the appearance of atrazine in pumice sand groundwater. Results from the incubation tests suggest that (a) hexazinone was degraded only in the mixture of groundwater and aquifer material (degradation rate constant = 4.36 x 10(-3) day-1); (b) procymidone was degraded not only in the mixture of groundwater and aquifer material (rate constant = 1.12 x 10(-2) day-1) but also in the groundwater alone (rate constant = 2.79 x 10(-2) and-1); (c) atrazine was not degraded over 57 days incubation in either the mixture of aquifer material and groundwater or the groundwater alone. Degradation rates measured in the batch tests were much lower than the total reduction rates. This suggests that not only degradation but also other irreversible processes are important in attenuating pesticides under field conditions. Hence, the use of laboratory-determined degradation rates could underestimate reduction of pesticides in field conditions.


Subject(s)
Atrazine/metabolism , Bridged Bicyclo Compounds/metabolism , Fungicides, Industrial/metabolism , Herbicides/metabolism , Triazines/metabolism , Algorithms , Biodegradation, Environmental , Bromides/metabolism , Fluorescent Dyes/metabolism , Fresh Water/chemistry , Models, Biological , Rhodamines/metabolism , Silicates/analysis , Silicon Dioxide/analysis , Soil/analysis , Soil Pollutants/metabolism , Tritium , Water Pollutants, Chemical/metabolism
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