MODEL FOR PREDICTING TRANSPORT OF PESTICIDES AND THEIR METABOLITES IN THE UNSATURATED ZONE1

ABSTRACT: A finite element model based on Galerkin's upstream weighted residual technique was developed to predict the simultaneous convective-dispersion transport and transformations of pesticides and their metabolites in the unsaturated zone. Transformations of the parent compound and its metabolites were assumed to be first-order reactions for oxidation and hydrolysis, while adsorption of the pesticide species (parent compound and metabolites) to the soil components was assumed to be represented by a linear equilibrium (Freundlich type) isotherm. Volatilization and plant root uptake of pesticides in the solution phase were neglected in the analysis. The proposed model was used to simulate the transport and transformation of aldicarb and its metabolites, aldicarb sulfoxide and aldicarb sulfone, in the soil profile. Several examples are used to demonstrate the accuracy, validity, and applicability of the proposed model. Simulated results indicate that the proposed model can potentially be used to estimate the mass flux of water, and pesticide and pesticide metabolite concentrations in the subsurface environment. However, further verification of the model against actual field data is needed to fully demonstrate the model's potential.     

Trends in the Water Chemistry of High Altitude Lakes in Europe

Here we present the chemical trends of seven high altitude lakes, analysed within the AL:PE and MOLAR Projects of the EU (1999) and selected on the basis of the availability of complete and reliable data for the period 1984–1999. The lakes are representative of the Scandinavian Alps, the Cairngorm Mountains in Scotland, the Alps and the Pyrenees. Significant trends were identified for some indicators of acidification, for instance pH and alkalinity, but not all lakes reacted similarly to decreasing depositions of sulphate and base cations. Differences in lake response are discussed in relation to recent variations of atmospheric deposition chemistry and associated changes in climatic conditions. Beside individual variations of the studied lakes, depending, among other things, on altitude and morphology, catchment characteristics and climate trends play a major role for the reaction of high altitude lakes on changes in atmospheric depositions.     

Effect of water extract of the bark of Buchanania lanzan linn. on behaviour and chromatophores of a fresh water fish,Labeo rohita

Fish exposed to 150 ppm and 250 ppm doses saparately, showed eratic swimming with hyper-excitability, spiralling, convulsion and mortality. However at 350 ppm dose fish became lethargic and steady at the bottom of aquarium. This behaviour appears to be due to sedative effects of fish implicating the phychoactive nature of the plant B. Ianzan. At 150 ppm to 350 ppm doses, fish scale changed from reticulate to punctate chromatophores; and treated fish when transferred to fresh water, were slowly regained to normal behaviour after 96 h exposure. Hence doses regaining from 150 ppm to 350 ppm is considered to be psychoative in nature. In higher doses 450 ppm and 550 ppm fish could survive only 76 h and 4.30 h respectively and then died indicating toxicity of plant for the said doses. It is found that scale present on its body is most suitable test system for the study of psychoactivity and toxicity of plant extracts on fish, Labeo rohita.     

Behavior of a surface applied radionuclide and a dye tracer in structured and repacked soil monoliths

There has been increasing evidence in recent years about the impact of soil structure on vadose zone hydrology and the distribution of surface applied chemical substances. We have carried out a combined dye and radionuclide tracer study on two monoliths from the same location, one structured and one repacked, as part of an ongoing study to investigate the link between preferential flow, leaching of surface applied substances and their distribution within the soil.A tracer solution containing 1300 Bq/L (58)Co and 0.31 micromol/L Sulforhodamine B (SB) was added with roughly constant irrigation during a period of three weeks. The dye served as a tracer for water movement within the soil and thus allowed linkage of the radiotracer ((58)Co) with the flow pattern. Both were monitored in the outflow and measured within profile sections after monolith disassembly. Preferential flow in the structured monolith promoted the bypass and transport of both tracers, although transport was impeded at depths greater than 30 cm by compacted soil and reduced hydraulic conductivity. Eighty four percent of radiocobalt and 8% of SB were found in the upper 4 cm of the structured monolith. The homogenized monolith, on the other hand, showed mostly chromatographic infiltration and a more efficient soil filtering capacity with 91% of radiocobalt and 20% SB residing in the upper 4 cm. Furthermore no tracer was found in the outflow of the homogenized monolith during normal to high irrigation or at greater depth within the monolith. We have related flow characteristics and sorption of radiotracers by quantifying dye distributions and radionuclide activities throughout the profiles. Activities within the flow paths are up to 20-times higher than those measured in the soil matrix, and a fraction of radiocobalt follows the dye tracer in spite of cobalt's low mobility. The dye can thus be used to trace radionuclide distribution within the soil block.     

Sorption of polycyclic aromatic compounds to humic and fulvic acid HPLC column materials

Two different humic acids (HA) and a fulvic acid (FA) were chemically immobilized to a high performance liquid chromatography (HPLC) silica column material. The immobilization was performed by binding amino groups in HA/FA to the free aldehyde group in glutardialdehyde attached to the silica gel. The HPLC column materials were compared with a blank column material made by applying the same procedure but without immobilizing HA or FA. Also, a column was made by binding carbonyl groups in HA to amino groups attached to the silica gel. The humic substances were selected to secure appropriate variation of their structural features. The retention factors of 45 polycyclic aromatic compounds (PAC) to the four columns were determined by HPLC. The advantage of the technique is a large number of compounds can easily be studied. The binding procedure does not appear to cause a drastic selection between the HA molecules. The k' values obtained for the two Aldrich HA columns agree in general reasonably. The retention or sorption of the compounds increased with the size of the PAC and the number of lipophilic substituents, but decreased when polar substituents were present. The PAC retention was much stronger to the two HA columns than to the FA and blank column, both for hydrophobic polycyclic aromatic hydrocarbons (PAH) and the polar PAC. Other factors impacting the PAC binding may be specific interactions with HA and the ionic strength of the aqueous phase. The technique has been applied to do direct determinations of Koc.