Skip to main content
Log in

Seasonal succession of a microphagotroph community in a small pond during litter decomposition

  • Published:
Microbial Ecology Aims and scope Submit manuscript

Abstract

Temporal dynamics of a lentic microphagotroph community were studied during leaf litter decomposition from December to May. Small plastic vessels containing leaf litter were placed on a pond bottom. They were sampled periodically to collect microphagotrophs. Three abiotic factors and abundance of two food items were also measured to analyze the autogenic and allogenic phenomena during a microphagotroph succession. Three behavior types were recognized in dominant taxa: a free-swimming type, a vagile (creeps on substratum, sometimes swims) type, and a voluntarily fixed type. Dominant taxa changed from the free-swimming to the vagile type up to mid-March, and the reverse change occurred from mid-April. Principal component analysis (PCA) indicated four factors affecting the dynamics of the community: water temperature as a seasonal factor, detritus volume on the litter surface as a habitat factor, and densities of bacteria and small flagellates as food factors. Taxa replacement appeared to occur through two mechanisms. (1) Dominance of small holotrichs, a free-swimming type, was brought about by a high bacterial density caused by seasonal events, i.e., leaf fall in December and detritus formation by litter feeders in mid-April. This is an allogenic aspect of community dynamics. (2) The free-swimming type was replaced by the vagile one during the period with high taxa diversity. This replacement occurred through intertaxa competition for scarce food and/or selective predation by larger microphagotrophs. It is an autogenic process within the community.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Bick H (1963) Vergleichende Untersuchung der Ciliatensukzession beim Abbau von Pepton und Cellulose (Modellversuche). Hydrobiologia 30:353–373

    Google Scholar 

  2. Bick H (1973) Population dynamics of protozoa associated with the decay of organic materials in fresh water. Am Zool 13:143–160

    Google Scholar 

  3. Bick H, Schmerenbeck W (1971) Vergleichende Untersuchung des Peptonabbaus und der damit verknüpften Ciliatenbesiedlung in Strömenden und stagnierenden Modellgewässern. Hydrobiologia 37:409–446

    Google Scholar 

  4. Corliss JO, Esser SC (1974) Comments on the role of the cyst in the life cycle and survival of free-living protozoa. Trans Am Micros Soc 93:578–593

    Google Scholar 

  5. Hamm A (1964) Untersuchungen uber die Okologie und Variabilität vonAspidisca costata (Hypotricha) im Belebtschlamm. Arch Hydrobiol 60:286–339

    Google Scholar 

  6. Hatano H, Watanabe Y (1981) Seasonal change of protozoa and micrometazoa in a small pond with leaf litter supply. Hydrobiologia 85:161–174

    Google Scholar 

  7. Hisai N, Sugawara T, Tanaka N (1974) Report on the qualities of water at ponds and springs in the National Park for Nature Study. Miscellaneous Reports of the National Park for Nature Study No. 5:1–7

    Google Scholar 

  8. Jackson KM, Berger J (1984) Survival of ciliate protozoa under starvation conditions and at low bacterial levels. Microb Ecol 10:47–59

    Google Scholar 

  9. Johaness RE (1964) Phosphorus excretion and body size in marine animals: microzooplankton and nutrient regeneration. Science 146:923–924

    Google Scholar 

  10. Kusano H (1985) List of microphagotrophs and their food habits in Mizutori-no-numa Pond. Rept Inst Nat Stu 16:99–112

    Google Scholar 

  11. Kusano H (1986) A sampling method for field survey of a microphagotroph community in a lentic litter layer: a litter-vessel method. Jap J Ecol 36:99–104

    Google Scholar 

  12. Münch von F (1970) Der Einfluss der Temperature auf den Peptonabbau und die damit verknüpfte Organismensukzession unter besondere Berücksichtigung der Populationsdynamik der Ciliaten. Int Revue ges Hydrobiol 55:559–594

    Google Scholar 

  13. Pielou EC (1969) An introduction to mathematical ecology. John Wiley & Sons, New York

    Google Scholar 

  14. Porter KG, Pace ML, Battey JF (1979) Ciliated protozoans as links in freshwater planktonic food chains. Nature 277:563–565

    Google Scholar 

  15. Sneath PH, Sokal RR (1973) Numerical taxonomy. WH Freeman & Company, San Francisco

    Google Scholar 

  16. Taylor WD (1978) Growth responses of ciliate protozoa to the abundance of their bacterial prey. Microb Ecol 4:207–214

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kusano, H., Kusano, T. & Watanabe, Y. Seasonal succession of a microphagotroph community in a small pond during litter decomposition. Microb Ecol 14, 55–66 (1987). https://doi.org/10.1007/BF02011570

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02011570

Keywords

Navigation