
Aquatic Sciences Meeting, Albuquerque 2001
| PC04 Microbial Diversity |
| Date: Tuesday, February 13, 2001 |
| Location: Southwest Hall |
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| Atkins, M, S, Woods Hole Oceanographic Institution, Woods Hole, USA, matkins@whoi.edu |
| Teske, A, P, Woods Hole Oceanographic Institution, Woods Hole, USA, ateske@whoi.edu |
| Taylor, C, D, Woods Hole Oceanographic Institution, Woods Hole, USA, ctaylor@whoi.edu |
| Wirsen, C, O, Woods Hole Oceanographic Institution, Woods Hole, USA, cwirsen@whoi.edu |
| Anderson, O, R, Lamont-Doherty Earth Observatory/Columbia University, Palisades, USA, ora@ldeo.columbia.edu |
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| FLAGELLATE DIVERSITY AND ECOLOGY AT DEEP-SEA HYDROTHERMAL VENTS |
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| Eighteen strains of flagellated protists, representing 9 species from 6 taxonomic orders, were isolated and cultured from four deep-sea hydrothermal vents. Many of the vent isolates are ubiquitous members of marine, freshwater, and terrestrial ecosystems world-wide, suggesting a global distribution of these flagellate species. This discovery advanced the hypothesis that ubiquity in distribution patterns among heterotrophic flagellates implies high tolerance and/or adaptability to a wide range of environmental conditions. Experiments under vent conditions of high pressure and high concentrations of metals and sulfide showed that some of these species are very tolerant to extreme environmental conditions.
Deep-sea vent samples were both cultured to select for kinetoplastid flagellates and analyzed without culturing by denaturing gradient gel electrophoresis (DGGE) using PCR primers specific to the kinetoplastid clade. PCR and DGGE were able to specifically isolate and amplify target DNA's from all cultured kinetoplastid species in matching vent samples, thus corroborating the findings of culturing. Molecular methods had the additional ability to detect species presence where culturing did not, thereby providing a better indication of the distribution of these species. |
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