Abstract
The vertical distribution of major and intermediate electron acceptors and donors was measured in a shallow stratified fjord. Peaks of zero valence sulfur, Mn(IV), and Fe(III) were observed in the chemocline separating oxic surface waters from sulfidic and anoxic bottom waters. The vertical fluxes of electron acceptors and donors (principally O2 and H2S) balanced within 5%; however, the zones of oxygen reduction and sulfide oxidation were clearly separated. The pathway of electron transfer between O2 and H2S was not apparent from the distribution of sulfur, nitrogen, or metal compounds investigated. The chemical zonation was related to bacterial populations as detected by ethidium bromide (EtBr) staining and by in situ hybridization with fluorescent oligonucleotide probes of increasing specificity. About half of all EtBr-stained cells were detectable with a general oligonucleotide probe for all eubacteria when digital image analysis algorithms were used to improve sensitivity. Both EtBr staining and hybridization indicated a surprisingly uniform distribution of bacteria throughout the water column. However, the average cell size and staining intensity as well as the abundance of different morphotypes changed markedly within the chemocline. The constant overall cell counts thus concealed pronounced population shifts within the water column. Cells stained with a delta 385 probe (presumably sulfate-reducing bacteria) were detected at the chemocline at about 5 x 10(4) cells per ml, and this concentration increased to 2 x 10(5) cells per ml beneath the chemocline. A long slim rod-shaped bacterium was found in large numbers in the oxic part of the chemocline, whereas large ellipsoid cells dominated at greater depth. Application of selective probes for known genera of sulfate-reducing bacteria gave only low cell counts, and thus it was not possible to identify the dominant morphotypes of the sulfate-reducing community.
Full Text
The Full Text of this article is available as a PDF (568.2 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Amann R. I., Binder B. J., Olson R. J., Chisholm S. W., Devereux R., Stahl D. A. Combination of 16S rRNA-targeted oligonucleotide probes with flow cytometry for analyzing mixed microbial populations. Appl Environ Microbiol. 1990 Jun;56(6):1919–1925. doi: 10.1128/aem.56.6.1919-1925.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Canfield D. E., Des Marais D. J. Aerobic sulfate reduction in microbial mats. Science. 1991 Mar 22;251:1471–1473. doi: 10.1126/science.11538266. [DOI] [PubMed] [Google Scholar]
- DeLong E. F. Archaea in coastal marine environments. Proc Natl Acad Sci U S A. 1992 Jun 15;89(12):5685–5689. doi: 10.1073/pnas.89.12.5685. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DeLong E. F., Wickham G. S., Pace N. R. Phylogenetic stains: ribosomal RNA-based probes for the identification of single cells. Science. 1989 Mar 10;243(4896):1360–1363. doi: 10.1126/science.2466341. [DOI] [PubMed] [Google Scholar]
- Ferguson R. L., Buckley E. N., Palumbo A. V. Response of marine bacterioplankton to differential filtration and confinement. Appl Environ Microbiol. 1984 Jan;47(1):49–55. doi: 10.1128/aem.47.1.49-55.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fründ C., Cohen Y. Diurnal Cycles of Sulfate Reduction under Oxic Conditions in Cyanobacterial Mats. Appl Environ Microbiol. 1992 Jan;58(1):70–77. doi: 10.1128/aem.58.1.70-77.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Giovannoni S. J., Britschgi T. B., Moyer C. L., Field K. G. Genetic diversity in Sargasso Sea bacterioplankton. Nature. 1990 May 3;345(6270):60–63. doi: 10.1038/345060a0. [DOI] [PubMed] [Google Scholar]
- Giovannoni S. J., DeLong E. F., Schmidt T. M., Pace N. R. Tangential flow filtration and preliminary phylogenetic analysis of marine picoplankton. Appl Environ Microbiol. 1990 Aug;56(8):2572–2575. doi: 10.1128/aem.56.8.2572-2575.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hahn D., Amann R. I., Ludwig W., Akkermans A. D., Schleifer K. H. Detection of micro-organisms in soil after in situ hybridization with rRNA-targeted, fluorescently labelled oligonucleotides. J Gen Microbiol. 1992 May;138(5):879–887. doi: 10.1099/00221287-138-5-879. [DOI] [PubMed] [Google Scholar]
- Hahn D., Amann R. I., Zeyer J. Whole-Cell Hybridization of Frankia Strains with Fluorescence- or Digoxigenin-Labeled, 16S rRNA-Targeted Oligonucleotide Probes. Appl Environ Microbiol. 1993 Jun;59(6):1709–1716. doi: 10.1128/aem.59.6.1709-1716.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hicks R. E., Amann R. I., Stahl D. A. Dual staining of natural bacterioplankton with 4',6-diamidino-2-phenylindole and fluorescent oligonucleotide probes targeting kingdom-level 16S rRNA sequences. Appl Environ Microbiol. 1992 Jul;58(7):2158–2163. doi: 10.1128/aem.58.7.2158-2163.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jørgensen B. B., Bak F. Pathways and microbiology of thiosulfate transformations and sulfate reduction in a marine sediment (kattegat, denmark). Appl Environ Microbiol. 1991 Mar;57(3):847–856. doi: 10.1128/aem.57.3.847-856.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kogure K., Simidu U., Taga N. A tentative direct microscopic method for counting living marine bacteria. Can J Microbiol. 1979 Mar;25(3):415–420. doi: 10.1139/m79-063. [DOI] [PubMed] [Google Scholar]
- Kogure K., Simidu U., Taga N. Distribution of viable marine bacteria in neritic seawater around Japan. Can J Microbiol. 1980 Mar;26(3):318–323. doi: 10.1139/m80-052. [DOI] [PubMed] [Google Scholar]
- Lovley D. R., Phillips E. J. Novel processes for anaerobic sulfate production from elemental sulfur by sulfate-reducing bacteria. Appl Environ Microbiol. 1994 Jul;60(7):2394–2399. doi: 10.1128/aem.60.7.2394-2399.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Maidak B. L., Larsen N., McCaughey M. J., Overbeek R., Olsen G. J., Fogel K., Blandy J., Woese C. R. The Ribosomal Database Project. Nucleic Acids Res. 1994 Sep;22(17):3485–3487. doi: 10.1093/nar/22.17.3485. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Poulsen L. K., Ballard G., Stahl D. A. Use of rRNA fluorescence in situ hybridization for measuring the activity of single cells in young and established biofilms. Appl Environ Microbiol. 1993 May;59(5):1354–1360. doi: 10.1128/aem.59.5.1354-1360.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ramsing N. B., Kühl M., Jørgensen B. B. Distribution of sulfate-reducing bacteria, O2, and H2S in photosynthetic biofilms determined by oligonucleotide probes and microelectrodes. Appl Environ Microbiol. 1993 Nov;59(11):3840–3849. doi: 10.1128/aem.59.11.3840-3849.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Repeta D. J., Simpson D. J., Jorgensen B. B., Jannasch H. W. Evidence for anoxygenic photosynthesis from the distribution of bacteriochlorophylls in the Black Sea. Nature. 1989 Nov 2;342(6245):69–72. doi: 10.1038/342069a0. [DOI] [PubMed] [Google Scholar]
- Risatti J. B., Capman W. C., Stahl D. A. Community structure of a microbial mat: the phylogenetic dimension. Proc Natl Acad Sci U S A. 1994 Oct 11;91(21):10173–10177. doi: 10.1073/pnas.91.21.10173. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Roden E. E., Lovley D. R. Dissimilatory Fe(III) Reduction by the Marine Microorganism Desulfuromonas acetoxidans. Appl Environ Microbiol. 1993 Mar;59(3):734–742. doi: 10.1128/aem.59.3.734-742.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Teske A., Wawer C., Muyzer G., Ramsing N. B. Distribution of sulfate-reducing bacteria in a stratified fjord (Mariager Fjord, Denmark) as evaluated by most-probable-number counts and denaturing gradient gel electrophoresis of PCR-amplified ribosomal DNA fragments. Appl Environ Microbiol. 1996 Apr;62(4):1405–1415. doi: 10.1128/aem.62.4.1405-1415.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thamdrup B., Finster K., Hansen J. W., Bak F. Bacterial disproportionation of elemental sulfur coupled to chemical reduction of iron or manganese. Appl Environ Microbiol. 1993 Jan;59(1):101–108. doi: 10.1128/aem.59.1.101-108.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Viles C. L., Sieracki M. E. Measurement of marine picoplankton cell size by using a cooled, charge-coupled device camera with image-analyzed fluorescence microscopy. Appl Environ Microbiol. 1992 Feb;58(2):584–592. doi: 10.1128/aem.58.2.584-592.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Williamson F. A., Palframan K. R. An improved method for collecting and staining microorganisms for enumeration by fluorescence light microscopy. J Microsc. 1989 Jun;154(Pt 3):267–272. doi: 10.1111/j.1365-2818.1989.tb00589.x. [DOI] [PubMed] [Google Scholar]