Decreased water retention and increased runoff and soil loss are of special importance concerning soil degradation of hilly crop fields. In this study, plots under ploughing (conventional) tillage (PT) and conservation tillage (CT; 15 years) were compared. Rainfall simulation on 6 m² plots was applied to determine infiltration and soil loss during the growing season. Results were compared with those measured from 1200 m² plots exposed to natural rainfalls in 2016. Infiltration was always higher under CT than PT, whereas the highest infiltration was measured under the cover crop condition. Infiltration under seedbed and stubble resulted in uncertainties, which suggests that natural pore formation can be more effective at improving soil drainage potential than can temporary improvements created by soil tillage operations. Soil erodibility was higher under PT for each soil status; however, the seedbed condition triggered the highest values. For CT, soil loss volume was only a function of runoff volume at both scales. Contrarily, on PT plots, some extreme precipitation events triggered extremely high soil loss owing to linear erosion, which meant no direct connection existed between the scales. Improved soil conditions due to conservation practice are more important for decreasing soil loss than the better surface conditions.

The role of the chemical properties of Pharmaceutically Active Compounds (PhACs) in their sorption behaviour and consequently in their fate and mobility is of major environmental interest, but a comprehensive evaluation is still lacking. The sorption of nine PhAC molecules with distinct physico-chemical properties on soils and goethite was described using linear, Freundlich and Langmuir models and the relationship between the chemical structures of the compounds and the parameters of the adsorption was evaluated using redundancy analysis (RDA). The latter showed that the sorption of the pharmaceuticals was determined by the intrinsic chemical characteristics of the molecules, as shown by the 35% value of constrained variability. For the hydrophobic estrogens, E1, E2 and EE2, the logD value and the number of hydrogen bond sites were found to be the main controlling factors for adsorption, indicating that hydrophobic interaction and hydrogen bonding are the dominant sorption mechanisms. The π energy of the molecules also proved a very important parameter, governing the retention of PhACs in soils, especially in the case of carbamazepine, oxazepam and lamotrigine. The main controlling factor for ionic compounds, such as diclofenac sodium, tramadol or lidocaine, is the fraction of PhACs present as charged species, revealing the importance of Coulomb forces. The results of this study will allow semi-quantitative predictions to be made on how the molecular structure governs the sorption of PhACs and which sorption mechanism could be involved.