“…In contrast, by extracting transcribed RNA and reverse transcriptase polymerase chain reaction (RT-PCR) based sequencing, the active members of fungal communities can be targeted [4,13,14]. This approach can even be used for targeting the universal DNA barcode region for fungi, the nuclear ribosomal internal transcribed spacer region (ITS) [15], and the few available studies showed that rRNA derived fungal communities differ from those derived from rDNA at the levels of richness, abundance of certain taxa and overall community composition [14,16,17,18,19]. However, such studies comparing total and active fungal communities have mostly been carried out either in surface soils from different biomes [14,16,17,20], or in communities associated with different plant species [19,21], but equivalent studies in subsurface aquatic ecosystems are largely missing.…”