TY - JOUR
T1 - Biotransformation of trace organic chemicals in the presence of highly refractory dissolved organic carbon
AU - Hellauer, Karin
AU - Martínez Mayerlen, Sara
AU - Drewes, Jörg E.
AU - Hübner, Uwe
N1 - Publisher Copyright:
© 2018 Elsevier Ltd
PY - 2019/1
Y1 - 2019/1
N2 - Previous studies demonstrated that the transformation of trace organic chemicals (TOrCs) in managed aquifer recharge (MAR) systems is favored under carbon-limited and oxic redox conditions especially, if the dissolved organic carbon (DOC) serving as primary substrate has a refractory character. Since co-metabolism is suggested to be the dominant removal mechanism, it is hypothesized that TOrCs transformation is controlled by the concentration of the refractory carbon under oxic redox conditions. A laboratory-scale soil column experiment mimicking MAR was established to investigate the influence of two different concentrations of highly refractory carbon sources on TOrCs transformation, namely drinking water (DW) and drinking water augmented with humic acid (DW + HA). Oxic redox conditions and carbon-limitation were present in both systems (ΔDOCDW+HA ≈ 0.6–0.7 mg/L; ΔDOCDW ≈ 0.1 mg/L). Of the 12 TOrCs investigated seven exhibited moderate to efficient transformation in both systems with only one compound (diclofenac) showing significantly enhanced (co-metabolic) biotransformation by adding humic acids as primary growth substrate. It is postulated that transformation of some TOrCs is characterized by metabolic degradation under starving conditions (ΔDOC ≤ 0.1 mg/L). By comparing the transformation efficiency of selected TOrCs with previous studies operated under carbon-limited and oxic conditions, an inconsistent behavior of some compounds was observed. These results demonstrate that key factors triggering the transformation of TOrCs are still poorly understood and thus, further investigations regarding the biodegradation pathways of TOrCs, upregulation of key enzymes by the microbial community but also more detailed analysis of the composition of the biodegradable DOC are needed.
AB - Previous studies demonstrated that the transformation of trace organic chemicals (TOrCs) in managed aquifer recharge (MAR) systems is favored under carbon-limited and oxic redox conditions especially, if the dissolved organic carbon (DOC) serving as primary substrate has a refractory character. Since co-metabolism is suggested to be the dominant removal mechanism, it is hypothesized that TOrCs transformation is controlled by the concentration of the refractory carbon under oxic redox conditions. A laboratory-scale soil column experiment mimicking MAR was established to investigate the influence of two different concentrations of highly refractory carbon sources on TOrCs transformation, namely drinking water (DW) and drinking water augmented with humic acid (DW + HA). Oxic redox conditions and carbon-limitation were present in both systems (ΔDOCDW+HA ≈ 0.6–0.7 mg/L; ΔDOCDW ≈ 0.1 mg/L). Of the 12 TOrCs investigated seven exhibited moderate to efficient transformation in both systems with only one compound (diclofenac) showing significantly enhanced (co-metabolic) biotransformation by adding humic acids as primary growth substrate. It is postulated that transformation of some TOrCs is characterized by metabolic degradation under starving conditions (ΔDOC ≤ 0.1 mg/L). By comparing the transformation efficiency of selected TOrCs with previous studies operated under carbon-limited and oxic conditions, an inconsistent behavior of some compounds was observed. These results demonstrate that key factors triggering the transformation of TOrCs are still poorly understood and thus, further investigations regarding the biodegradation pathways of TOrCs, upregulation of key enzymes by the microbial community but also more detailed analysis of the composition of the biodegradable DOC are needed.
KW - Biodegradable dissolved organic carbon
KW - Carbon limitation
KW - Managed aquifer recharge
KW - Oxic redox conditions
KW - Refractory carbon
KW - Trace organic chemicals
UR - http://www.scopus.com/inward/record.url?scp=85055992108&partnerID=8YFLogxK
U2 - 10.1016/j.chemosphere.2018.09.166
DO - 10.1016/j.chemosphere.2018.09.166
M3 - Article
C2 - 30308387
AN - SCOPUS:85055992108
SN - 0045-6535
VL - 215
SP - 33
EP - 39
JO - Chemosphere
JF - Chemosphere
ER -