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Gliding motility of Peloploca spp., and their distribution in the sediment and water column of a eutrophic lake

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Abstract

Observations indicating gliding motility in the gas-vacuolate, filamentous organism Peloploca were made using microcapillary tubes. Tubes containing semi-solid agar, incubated in sediment cores gave good enrichments of Peloploca spp. The organisms, which had the form of helical bundles of filaments, were seen to corkscrew through the agar at up to 2–3 μm s-1.

The vertical distribution of Peloploca spp. in the sediment and water column of a eutrophic lake was examined periodically during summer stratification. The organisms were confined to anoxic conditions in the sediment prior to stratification. With increasing anoxia in the hypolimnion, the population shifted upwards in the sediment, and towards the end of stratification, in the most reducing conditions, appeared in the lower hypolimnion. Anaerobically incubated sediment cores also showed the movement of the Peloploca population from sediment into the overlying water.

It is suggested that the gliding motility and helical morphology of Peloploca bundles enable them to migrate through sediment in response to oxygen and Eh gradients, in addition to their use of gas vacuoles to adjust their position in the water column. The taxonomic implications of gliding motility in Peloploca spp. are discussed.

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References

  • Clark AE, Walsby AE (1978a) The occurrence of gas-vacuolate bacteria in lakes. Arch Microbiol 118:223–228

    Google Scholar 

  • Clark AE, Walsby AE (1978b) The development and vertical distribution of populations of gas-vacuolate bacteria in a eutrophic, monomictic lake. Arch Microbiol 118:229–233

    Google Scholar 

  • Cohen-Bazire G, Kunisawa R, Pfennig N (1969) A comparative study of the structure of gas vacuoles. J Bacteriol 100:1049–1061

    PubMed  Google Scholar 

  • Cyrus Z, Sladka A (1970) Several interesting organisms present in activated sludge. Hydrobiol 35:383–396

    Google Scholar 

  • Godinho-Orlandi MJL (1980) Microbiology of sediments in lakes of differing degrees of eutrophication. PhD. Thesis, University of Durham

  • Godinho-Orlandi MJL, Jones JG (1981a) Filamentous bacteria in sediments of lakes of differing degrees of enrichment. J Gen Microbiol 123:81–90

    Google Scholar 

  • Godinho-Orlandi MJL, Jones JG (1981b) The distribution of some genera of filamentous bacteria in littoral and profundal lake sediments. J Gen Microbiol 123:91–101

    Google Scholar 

  • Gorlenko VM, Lokk SI (1979) Vertical distribution and characteristics of the species composition of microorganisms in several stratified lakes in Estonia, USSR. Microbiol 48:283–290

    Google Scholar 

  • Hirsch P (1981) The family Pelonemataceae. In: Starr MP, Stolp H, Trüper HG, Balows A, Schlegel HG (eds) The Prokaryotes, Springer, Berlin Heidelberg New York, Vol I. Ch. 26, pp 412–421

    Google Scholar 

  • Jones JG (1976) The microbiology and decomposition of seston in open water and experimental enclosures in a productive lake. J Ecol 64:241–278

    Google Scholar 

  • Jørgensen BB (1977) Distribution of colourless sulphur bacteria (Beggiatoa spp.) in a coastal marine sediment. Mar Biol 41:19–28

    Google Scholar 

  • Lauterborn R (1913) Zur Kenntnis einiger sapropelischer Schizomyceten. Al Bot Z 79:97–100

    Google Scholar 

  • Maiden MFJ (1983) The biology of filamentous bacteria in fresh-water sediments. PhD. Thesis, University of Wales

  • Ohnstad FR, Jones JG (1982) The Jenkin surface-mud sampler user manual. Freshwater Biological Association Occasional Publication No. 15. Ambleside

  • Perfil'ev BV, Gabe DR (1961) Capillary methods of investigating microorganisms. Akad Nauk, SSSR, pp 1–534

    Google Scholar 

  • Skuja H (1956) Taxonomische und biologische Studien über das Phytoplankton schwedischer Binnengewässer. Nova Acta Regiae Soc Sci Upsal IV, 16:1–404

    Google Scholar 

  • Skuja H (1974) Family Pelonemataceae. In: Buchanan RE, Gibbons NE (eds) Bergey's Manual of Determinative Bacteriology. Williams & Wilkins, Baltimore 8th Edition. pp 122–127

    Google Scholar 

  • Walsby AE (1978) The gas vesicles of aquatic prokaryotes. In: Relations between structure and function in the prokaryotic cell. Symp Soc Gen Microbiol 28, pp 327–359

    Google Scholar 

  • Walsby AE (1981) Gas-vacuolate bacteria (apart from Cyanobacteria). In: Starr MP, Stolp H, Trüper HG, Balows A, Schlegel HG (eds) The Prokaryotes. Springer Berlin Heidelberg New York, Vol I, Ch. 28, pp 441–447

    Google Scholar 

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Authors and Affiliations

  1. Windermere Laboratory, The Ferry House, Freshwater Biological Association, Far Sawrey, LA22 0LP, Ambleside, Cumbria, UK

    Mark F. J. Maiden & J. Gwynfryn Jones

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  1. Mark F. J. Maiden
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  2. J. Gwynfryn Jones
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Maiden, M.F.J., Jones, J.G. Gliding motility of Peloploca spp., and their distribution in the sediment and water column of a eutrophic lake. Arch. Microbiol. 140, 44–49 (1984). https://doi.org/10.1007/BF00409770

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  • DOI: https://doi.org/10.1007/BF00409770

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