Cell abundance is usually determined using epifluorescent microscopy and has demonstrated that bioturbation stimulates microbial proliferation (Table. 1). Cell counts alone, however, provide no information on the presence, growth, or activity of key functional groups that mediate biogeochemical processes. Therefore, various culture-based methods to assess abundances of specific microbial groups, such as sulphate-reducing bacteria (SRB), have been developed (Table. 1). Yet, these culture-dependent techniques are biased by the presence of uncultivatable bacteria (Teske et al., 1996, Naslund et al., 2010), with typically only 1-10% of the total community being assessed (Jenkins and Kemp, 1984, Katayama et al., 2003, Lucas et al., 2003). Overreliance on these abundance-based techniques will limit the amount of data available to understand bioturbation effects on microbially mediated processes (Nicolaisen and Ramsing,
Cell abundance is usually determined using epifluorescent microscopy and has demonstrated that bioturbation stimulates microbial proliferation (Table. 1). Cell counts alone, however, provide no information on the presence, growth, or activity of key functional groups that mediate biogeochemical processes. Therefore, various culture-based methods to assess abundances of specific microbial groups, such as sulphate-reducing bacteria (SRB), have been developed (Table. 1). Yet, these culture-dependent techniques are biased by the presence of uncultivatable bacteria (Teske et al., 1996, Naslund et al., 2010), with typically only 1-10% of the total community being assessed (Jenkins and Kemp, 1984, Katayama et al., 2003, Lucas et al., 2003). Overreliance on these abundance-based techniques will limit the amount of data available to understand bioturbation effects on microbially mediated processes (Nicolaisen and Ramsing,