Thematic Issue on the Hydrological Effects of the Vegetation-Soil Complex

Peer reviewedPublisher PD

How microbial community composition, sorption and simultaneous application of six pharmaceuticals affect their dissipation in soils

Pharmaceuticals may enter soils due to the application of treated wastewater or biosolids. Their leakage from soils towards the groundwater, and their uptake by plants is largely controlled by sorption and degradation of those compounds in soils. Standard laboratory batch degradation and sorption experiments were performed using soil samples obtained from the top horizons of seven different soil types and 6 pharmaceuticals (carbamazepine, irbesartan, fexofenadine, clindamycin and sulfamethoxazole), which were applied either as single-solute solutions or as mixtures (not for sorption). The highest dissipation half-lives were observed for citalopram (average DT50,S for a single compound of 152 ± 53.5 days) followed by carbamazepine (106.0 ± 17.5 days), irbesartan (24.4 ± 3.5 days), fexofenadine (23.5 ± 20.9 days), clindamycin (10.8 ± 4.2 days) and sulfamethoxazole (9.6 ± 2.0 days). The simultaneous application of all compounds increased the half-lives (DT50,M) of all compounds (particularly carbamazepine, citalopram, fexofenadine and irbesartan), which is likely explained by the negative impact of antibiotics (sulfamethoxazole and clindamycin) on soil microbial community. However, this trend was not consistent in all soils. In several cases, the DT50,S values were even higher than the DT50,M values. Principal component analyses showed that while knowledge of basic soil properties determines grouping of soils according sorption behavior, knowledge of the microbial community structure could be used to group soils according to the dissipation behavior of tested compounds in these soils. The derived multiple linear regression models for estimating dissipation half-lives (DT50,S) for citalopram, clindamycin, fexofenadine, irbesartan and sulfamethoxazole always included at least one microbial factor (either amount of phosphorus in microbial biomass or microbial biomarkers derived from phospholipid fatty acids) that deceased half-lives (i.e., enhanced dissipations). Equations for citalopram, clindamycin, fexofenadine and sulfamethoxazole included the Freundlich sorption coefficient, which likely increased half-lives (i.e., prolonged dissipations)

Droplet infiltration dynamics and soil wettability related to soil organic matter of soil aggregate coatings and interiors

The organo-mineral coatings of soil aggregates, cracks, and biopores control sorption and macropore-matrix exchange during preferential flow, in particular in the clay-illuvial Bt-horizon of Luvisols. The soil organic matter (SOM) composition has been hypothesized to explain temporal changes in the hydraulic properties of aggregate surfaces. The objective of this research was to find relations between the temporal change in wettability, in terms of droplet infiltration dynamics, and the SOM composition of coated and uncoated aggregate surfaces. We used 20 to 40 mm sized soil aggregates from the Bt2 horizon of a Haplic Luvisol from loess that were (i) coated, (ii) not coated (both intact), and (iii) aggregates from which coatings were removed (cut). The SOM composition of the aggregate surfaces was characterized by infrared spectroscopy in the diffuse reflection mode (DRIFT). A potential wettability index (PWI) was calculated from the ratio of hydrophobic and hydrophilic functional groups in SOM. The water drop penetration times (WDPT) and contact angles (CA) during droplet infiltration experiments were determined on dry and moist aggregate samples of the three types. The decrease in the CA with time was described using the power function (CA(t) = at–b). For dry aggregates, the WDPT values were larger for coated as compared to uncoated regions on the aggregate surfaces, and increased with increasing PWI value (R2 = 0.75). The a parameter was significantly related to the WDPT (R2 = 0.84) and to the PWI (R2 = 0.64). The relations between the b parameter and the WDPT (R2 = 0.61) and the PWI (R2 = 0.53) were also significant. The WDPT values of wet soil aggregates were higher than those of dry aggregates due to high water contents, which limited the droplet infiltration potential. At the wet aggregate surfaces, the WDPT values increased with the PWI of the SOM (R2 = 0.64). In contrast to dry samples, no significant relationships were found between parameters a or b of CA(t) and WDPT or PWI for wet aggregate surfaces. The results suggest that the effect of the SOM composition of coatings on surface wettability decreases with increasing soil moisture. In addition to the dominant impact of SOM, the wettability of aggregate surfaces could be affected by different mineralogical compositions of clay in coatings and interiors of aggregates. Particularly, wettability of coatings could be decreased by illite which was the dominant clay type in coatings. However, the influence of different clay mineral fractions on surface wettability was not due to small number of measurements (2 and 1 samples from coatings and interiors, respectively) quantified

Microbial responses to selected pharmaceuticals in agricultural soils: Microcosm study on the roles of soil, treatment and time

Evaluating microbial responses to pharmaceuticals in agricultural soils is essential to improve our fundamental understanding of the fate of micropollutants and their potential implications for the environment and human health. In this study, we focused on the immediate (1 d), short- (13 d) and long-term effects (61 d) of pharmaceutical amendment on microbial communities in seven soils differing in physical chemical properties. Basal respiration was used to indicate microbial activity, while phospholipid fatty acids were used to determine microbial biomass and community structure. We identified four microbial responses to pharmaceutical amendment: stimulation, inhibition, stress and dormancy, which were highly significant in the short-term. The largest stimulatory effect accompanied by shifts in the microbial community structure towards fungi and G- bacteria was detected for sulfamethoxazole. The inhibitory effect was mainly observed for citalopram, irbesartan and pharmaceutical mixture in Cambisol Dystric with minor alterations in microbial community structure compare to a non-amended control. The stress effect was detected for all pharmaceuticals in Arenosol and Cambisol Haplic. While the dormancy effect was mainly observed in Chernozem Siltic for most of the pharmaceuticals. Microbial responses were highly dependent on the soil type, pharmaceutical compound and time, highlighting the importance to consider these parameters including a resilience of soil microbial communities to micropollutants within a long-term agricultural soil management