In the transition zone between aquifers and basal aquitards, the perchloroethene pools at an early time in their evolution are more recalcitrant than those elsewhere in the aquifer. The aim of this study is to demonstrate that the biodegradation of chloroethenes from aged pools (i.e., pools after decades of continuous groundwater flushing and dissolution) of perchloroethene is favored in the transition zone. A field site was selected where an aged pool exists at the bottom of a transition zone. Two boreholes were drilled to obtain sediment and groundwater samples to perform chemical, isotopic, molecular, and clone library analyses and microcosm experiments. The main results were as follows: (i) the transition zone is characterized by a high microbial richness; (ii) reductively dechlorinating microorganisms are present and partial reductive dechlorination coexists with denitrification, Fe and Mn reduction, and sulfate reduction; (iii) reductively dechlorinating microorganisms were also present in the zone of the aged pool; (v) the high concentrations of perchloroethene in this zone resulted in a decrease in microbial richness; (vi) however, the presence of fermenting microorganisms supplying electrons for the reductively dechlorinating microorganisms prevented the reductive dechlorination to be inhibited. These findings suggest that biostimulation and/or bioaugmentation could be applied to promote complete reductive dechlorination and to enhance the dissolution of more nonaqueous phase liquids (DNAPL).

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The soils of Puchuncaví and Quintero, in the coastal area of central Chile, have been exposed to atmospheric deposition of sulfur dioxide (SO 2 ) and metal-rich particles from the Ventanas Industrial Complex. The objective of this study was to determine, using geostatistical tools, the spatial distribution of copper and pH in these soils. Using Universal Kriging tool for geostatistical interpolation, we generated maps of continuous distribution of Cu and pH in the soils. The distribution of these variables was related to the distance from the industrial complex and to the direction of the winds. The concentrations of Cu and acidity were higher in the surroundings to the industrial complex and in the direction of the dominant winds. Although the distributions of both variables were similar, there was no correlation between the distribution of Cu and pH, which could be due to the distinct aerial dispersion dynamics of the compounds, which causes a divergence in their deposition on the soil. Specifically, this could be due to the fact that SO 2 is smaller than the particulate matter that contains copper, so that it is capable of being dispersed over greater distances without being deposited on the soil.

Nonionic surfactants e.g. alcohol ethoxylates (AEOs) and alkylamine ethoxylates (ANEOs) are commonly utilised as adjuvants in pesticide formulations to enhance their effectiveness. In this study, analytical methods for AEO and ANEO determination in soil samples using pressurised liquid extraction (PLE) were developed and used in connection with LC-MS. The recovery of the method, which was highly dependent on the soil properties, varied in the range 47-106% for AEO and 27-109% for ANEO. Detection limits (LOD) were 7-13 microg kg(-1) for AEO and 24-43 microg kg(-1) for ANEO. The developed method has been applied to determine AEOs and ANEOs in surface soil samples from fields sprayed with glyphosate herbicides. Tallowalkylamine ethoxylates (an ANEO) were detected in the soil before and after pesticide application, with increasing concentrations after treatment. The highest concentration in the soil samples was observed for the ANEO homologues with the longest ethoxy chains; in the clay soil the concentration decreased with the length of the ethoxy chain. ANEOs added to pesticide formulations as a technical mixture will, as demonstrated in this study, behave as individual homologues, which is reflected in their behaviour in the environment.