“…However, bulk DOC does not permit distinction between the different carbon pools and uniformly labeled substrates omit the understanding of the fate of single carbon atoms within a molecule that are being differently used during uptake, biosynthesis, molecular transformation, and final release of DIC. Therefore, to specifically trace the microbial conversion of DOC to cellular biomolecules and metabolites or microbial remineralization of DOC to CO 2 , novel approaches based on position-specific and dual-isotope stable isotope probing (SIP), lipid radioisotope probing (RIP), and reversed isotope labeling (RIL) have been adapted from routine labeling techniques (Figure 3) (Wegener et al, 2012;Dippold and Kuzyakov, 2013;Kellermann et al, 2016;Dong et al, 2017Dong et al, , 2019Evans et al, 2018Evans et al, , 2019Aepfler et al, 2019).…”