A web-based pesticide risk assessment tool for drinking water protection zones in Sweden.

To protect human health, wildlife and the aquatic environment, "safe uses" of pesticides are determined at the EU level while product authorization and terms of use are established at the national level. In Sweden, extra precaution is taken to protect drinking water, and permits are therefore required for pesticide use within abstraction zones. This paper presents MACRO-DB, a tool for assessing pesticide contamination risks of groundwater and surface water, used by authorities to support their decision-making for issuing such permits. MACRO-DB is a meta-model based on 583,200 simulations of the physically-based MACRO model used for assessing pesticide leaching risks at EU and national level. MACRO-DB is simple to use and runs on widely available input data. In a qualitative comparative assessment for two counties in Sweden, MACRO-DB outputs were in general agreement with groundwater monitoring data and matched or were more protective than the national risk assessment procedure for groundwater.

Comparative evaluation of four suspended particulate matter (SPM) sampling devices and their use for monitoring SPM quality.

Representative sampling of suspended particulate matter is fundamental for assessing river sediment quality, including the distribution and physicochemical characterisation of particles at different hydrological events. This study compares time-integrated samplers and discrete sampling methods, focusing on (a) the representativeness of the different methods and (b) the comparability between the various sampling techniques. The study investigates whether different sampling devices used under the same conditions can reproduce the annual mean. Two time-integrated sampling techniques (Binnensammler floating collector (BS); self-constructed Phillips sampler (PS)) and two discrete sampling systems (continuous-flow centrifuge (CFC); hydrocyclone (HC)) were compared. The monitoring program (August 2013 to August 2014) was conducted using a 4-week sampling frequency at two different monitoring stations in the Rhine river basin. The analysis of physicochemical parameters included total organic carbon (TOC), particulate phosphorus (PP), grain size distribution (GSD), metals, and organic pollutants (PCBs, HCB, PAH). A nested analysis of variance (ANOVA) was used to evaluate the dependence of suspended matter quality parameters on the sampling method, the sampling device, and the sampling station. According to ANOVA, physical and chemical parameters as well as persistent organic pollutants are homogenous for the time-integrated samplers PS and BS. Comparing PS and the reference technique CFC, only the mean annual concentration of TOC is significantly higher for CFC (5.91%; PS, 4.53%) due to degradation processes. With the exception of TOC, Ni, and GSD, data of BS was comparable with that of CFC. Comparing CFC and HC, there are significant differences for GSD, Zn, and Ni. An analysis of the time series of GSD < 63 µm and sum of PAHs confirms the findings of the nested ANOVA, showing that HC time series display significant differences compared with the other samplers.

Effects of sampling techniques on physical parameters and concentrations of selected persistent organic pollutants in suspended matter.

This study focusses on the effect of sampling techniques for suspended matter in stream water on subsequent particle-size distribution and concentrations of total organic carbon and selected persistent organic pollutants. The key questions are whether differences between the sampling techniques are due to the separation principle of the devices or due to the difference between time-proportional versus integral sampling. Several multivariate homogeneity tests were conducted on an extensive set of field-data that covers the period from 2002 to 2007, when up to three different sampling techniques were deployed in parallel at four monitoring stations of the River Rhine. The results indicate homogeneity for polychlorinated biphenyls, but significant effects due to the sampling techniques on particle-size, organic carbon and hexachlorobenzene. The effects can be amplified depending on the site characteristics of the monitoring stations.