Epilithic biofilms as a discriminating matrix for long-term and growing season pesticide contamination in the aquatic environment: Emphasis on glyphosate and metabolite AMPA.

The indiscriminate use of pesticides represents high ecological risk in aquatic systems. Recently, the inclusion of epilithic biofilms as a reactive matrix has shown potential in diagnosing the health of water resources. The objective of this study was to use multiple matrices (water, suspended sediments, and biofilms) to discriminate contamination degrees in catchments with long and recent history of intensive pesticide use and to monitor growing season pesticides transfer to watercourses. Two catchments were monitored: one representative of "modern agriculture" in a subtropical environment, and another representative of recent agricultural expansion over the Pampa Biome in subtropical Brazil. Glyphosate and AMPA were accumulated in the biofilms and were detected at all sites and at all monitoring times, in concentrations ranging from 195 to 7673 µg kg-1 and from 225 to 4180 µg kg-1, respectively. Similarly, the fungicide tebuconazole has always been found in biofilms. The biofilms made it possible to discriminate the long-term history of pesticide use in the catchments and even to identify the influx pulses of pesticides immediately after their application to crops, which was not possible with active water sampling and even with suspended sediment monitoring. It is strongly recommended that, in regions with intensive cultivation of soybeans and other genetically modified crops, the presence of glyphosate and its metabolite AMPA be permanently monitored, a practice still very scarce in the literature.

Epilithic biofilms, POCIS, and water samples as complementary sources of information for a more comprehensive view of aquatic contamination by pesticides and pharmaceuticals in southern Brazil.

Spatial-temporal monitoring of the presence of pesticides and pharmaceuticals in water requires rigor in the choice of matrix to be analyzed. The use of matrices, isolated or combined, may better represent the real state of contamination. In this sense, the present work contrasted the effectiveness of using epilithic biofilms with active water sampling and with a passive sampler-POCIS. A watershed representative of South American agriculture was monitored. Nine sites with different rural anthropic pressures (natural forest, intensive use of pesticides, and animal waste), and urban areas without sewage treatment, were monitored. Water and epilithic biofilms were collected during periods of intensive pesticide and animal waste application. After the harvest of the spring/summer crop, a period of low agrochemical input, the presence of pesticides and pharmaceuticals was monitored using the POCIS and epilithic biofilms. The spot water sampling leads to underestimation of the level of contamination of water resources as it does not allow discrimination of different anthropic pressures in rural areas. The use of endogenous epilithic biofilms as a matrix for the analysis of pesticides and pharmaceuticals is a viable and highly recommended alternative to diagnose the health of water sources, especially if associated with the use of POCIS.

Glyphosate, AMPA, and metsulfuron-methyl retention in the main horizons of a Typic Argiudoll.

Retention is one of the processes controlling the behavior and fate of pesticides in soil. The objective of this work was to evaluate the adsorption and desorption of glyphosate, AMPA, and metsulfuron-methyl in the main horizons of a Typic Argiudoll destined for agricultural use. For this purpose, the batch equilibrium method was used at a range of concentrations for each compound. Desorption was performed in three consecutive steps after the adsorption experiment. The results obtained showed strong adsorption of glyphosate and AMPA in the three horizons, following the trend B > A > C, with weak desorption. Metsulfuron-methyl, on the other hand, showed weak adsorption in the three horizons, following the trend A > B > C, with relevant desorption. Our results allow us to identify metsulfuron-methyl as the compound that poses the greatest environmental risk in terms of the potential contamination of other areas and groundwater. However, despite their strong adsorption and weak desorption, glyphosate and AMPA also represent potential contaminants of other environmental matrices.

Pesticide bioaccumulation in epilithic biofilms as a biomarker of agricultural activities in a representative watershed.

Brazil is one of the largest consumers of pesticides in the world. The high rainfall rate and inadequate soil use and management promote the transfer of these compounds to the aquatic system. The aim of this study was to identify and quantify pesticides present in epilithic biofilms in order to evaluate the effectiveness of this matrix as a bioindicator able to discriminate areas and periods with different inputs of pesticides. Among the 25 pesticides analyzed in the biofilms, 20 compounds were detected. The epilithic biofilms picked up pesticides independent of their polarities, even in the period of lower use. The frequency and median concentration of five herbicides (2,4-D, atrazine, desethyl-atrazine, simazine, nicosulfuron), three fungicides (carbendazim, epoxiconazole, tebuconazole), and one insecticide (imidacloprid) were highest in biofilms sampled in summer crops during the growing period. Biofilms collected in the upper region of the catchment, where genetically modified soybean and corn cultivated in a no-tillage system prevail, the highest frequency and median concentration of three herbicides (2,4-D, thifensulfuron, isoproturon), four fungicides (carbendazim, epoxiconazole, tebuconazole, metconazole), and one insecticide (imidacloprid) were observed. Despite the excessive amounts of pesticides used in the catchment, the median values of all pesticides in the epilithic biofilm were considered low. The lower diversity and concentration of pesticides observed in the autumn/winter season is representative of lower use of pesticides, barriers to pesticide transfer from soil to water, and the biofilm's resilience capacity to decompose pesticides.

Prospective modeling with Hydrus-2D of 50 years Zn and Pb movements in low and moderately metal-contaminated agricultural soils.

Results of detailed modeling of in situ redistribution of heavy metals in pedological horizons of low and moderately metal contaminated soils, considering distinctly different long-term land use, are scarcely reported in literature. We used Hydrus-2D software parameterized with abundant available local soil data to simulate future Zn and Pb movements in soils contaminated by metallurgical fallout in the 20th century. In recent work on comparing different modeling hypotheses, we validated a two-site reactive model set with adjusted chemical kinetic constant values by fitting the 2005 Zn and Pb concentration profiles in soils, with estimated 1901-1963 airborne Zn and Pb loads (Mallmann et al., 2012a). In the present work, we used the same approach to simulate 2005-2055 changes in Zn and Pb depth-distribution and soil-solution concentrations, comparing two hypotheses of chemical equilibrium: i) the validated two-site model (one site at equilibrium and the other involved in kinetic reactions with pore water) set with adjusted kinetic EDTA extraction constants, and ii) a non-linear one-surface site adsorption equilibrium model. Simulated transfers were found generally lower and more realistic when using the two-site model. Simulations showed that consistent Zn redistribution and loss occurred in the moderately contaminated soil until 2055, i.e., more than one century after the main metal deposition, but negligible in low contaminated soils. Transfer of Pb was small in the three soils and under both hypotheses. In 2055, simulated Zn outflow concentrations remained under threshold values for drinking water.