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Bacterial Removal and Protozoan Grazing in Biological Sand Filters

Anne-Marie Bomo*,a, Tor Kristian Stevika, Ine Hovib and Jon Fredrik Hanssenc

a Department of Mathematical Sciences and Technology, Agricultural University of Norway, P.O. Box 5003, 1432 Ås, Norway
b Technical Department of Ski County Council, P.O. Box 3010, 1402 Ski, Norway
c Department of Chemistry, Biotechnology and Food Science, Agricultural University of Norway, P.O. Box 5040, 1432 Ås, Norway



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Fig. 1. Concentration of Aeromonas hydrophila (AH water) in filter effluents (in colony forming units [CFU] mL–1) and protozoan numbers (PR) in top, middle, and bottom layers of the sand columns (protozoa g–1 dry wt. sand). Error bars = standard deviations (n = 3).

 


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Fig. 2. Concentration of Aeromonas hydrophila in sand in different layers in filter columns (colony forming units [CFU] g–1 dry wt. sand). Results are log10–transformed. Error bars = standard deviations (n = 3).

 


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Fig. 3. Concentration of culturable bacteria (HPC) in sand in different layers in filter columns (colony forming units [CFU] g–1 dry wt. sand). Results are log10–transformed. Error bars = standard deviations (n = 3).

 


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Fig. 4. Numbers of total bacterial cells in sand in different layers in filter columns (cells g–1 dry wt. sand). Results are log10–transformed. Error bars = standard deviations (n = 3). Bacterial numbers on Day 21 not determined.

 





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