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|Isotopic analysis of cellular biomass has greatly improved our understanding of carbon cycling in the environment. Compound specific radiocarbon analysis (CSRA) of cellular biomass is being increasingly applied in a number of fields. However, it is often difficult to collect sufficient cellular biomass for analysis from oligotrophic waters because easy-to-use filtering methods that are free of carbon contaminants do not exist. The goal of this work was to develop a new column based filter to autonomously collect high volume samples of biomass from oligotrophic waters for CSRA using material that can be baked at 450 °C to remove potential organic contaminants. A series of filter materials were tested, including uncoated sand, ferrihydrite-coated sand, goethite-coated sand, aluminum-coated sand, uncoated glass wool, ferrihydrite-coated glass wool, and aluminum-coated glass wool, in the lab with 0.1 and 1.0 μm microspheres and Escherichia coli. Results indicated that aluminum-coated glass wool was the most efficient filter and that the retention capacity of the filter far exceeded the biomass requirements for CSRA. Results from laboratory tests indicate that for oligotrophic waters with 1 × 105 cells ml− 1, 117 l of water would need to be filtered to collect 100 μg of PLFA for bulk PLFA analysis and 2000 l for analysis of individual PLFAs. For field sampling, filtration tests on South African mine water indicated that after filtering 5955 l, 450 μg of total PLFAs were present, ample biomass for radiocarbon analysis. In summary, we have developed a filter that is easy to use and deploy for collection of biomass for CSRA including total and individual PLFAs.
|Electronic Publication Date:
|Mailloux, Brian J., Audra Dochenetz, Michael Bishop, Hailiang Dong, Lori A. Ziolkowski, K. Eric Wommack, Eric G. Sakowski, Tullis C. Onstott, and Greg F. Slater. "A carbon free filter for collection of large volume samples of cellular biomass from oligotrophic waters." Journal of Microbiological Methods 90, no. 3 (2012): 145-151. doi:10.1016/j.mimet.2012.04.016.
|145 - 151
|Type of Material:
|Journal of Microbiological Methods
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