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. 1994 Aug;60(8):2677–2683. doi: 10.1128/aem.60.8.2677-2683.1994

Accumulation of selenium in a model freshwater microbial food web.

R W Sanders 1, C C Gilmour 1
PMCID: PMC201708  PMID: 8085812

Abstract

The transfer of selenium between bacteria and the ciliated protozoan, Paramecium putrinum, was examined in laboratory cultures. The population growth of the ciliate was not inhibited in the presence of the highest concentrations of dissolved selenite or selenate tested (10(3) micrograms liter-1). Experiments with radioactive 75selenite or 75selenate indicated that accumulation of selenium by ciliates through time was low when feeding and metabolism were reduced by incubating at 0 degrees C. However, selenium accumulated in ciliate biomass during incubation with dissolved 75Se and bacteria at 24 degrees C and also when bacteria prelabeled with 75Se were offered as food in the absence of dissolved selenium. When 75Se-labeled bacterial food was diluted by the addition of nonradioactive bacteria, the amount of selenite and selenate in ciliates decreased over time, indicating depuration by the ciliates. In longer-term (> 5-day) fed-batch incubations with 75selenite-labeled bacteria, the selenium concentration in ciliates equilibrated at approximately 1.4 micrograms of Se g (dry weight)-1. The selenium content of ciliates was similar to that of their bacterial food on a dry-weight basis. These data indicate that selenium uptake by this ciliate occurred primarily during feeding and that biomagnification of selenium did not occur in this simple food chain.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Besser J. M., Huckins J. N., Little E. E., La Point T. W. Distribution and bioaccumulation of selenium in aquatic microcosms. Environ Pollut. 1989;62(1):1–12. doi: 10.1016/0269-7491(89)90091-2. [DOI] [PubMed] [Google Scholar]
  2. Burton G. A., Jr, Giddings T. H., DeBrine P., Fall R. High incidence of selenite-resistant bacteria from a site polluted with selenium. Appl Environ Microbiol. 1987 Jan;53(1):185–188. doi: 10.1128/aem.53.1.185-188.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Doran J. W., Alexander M. Microbial transformations of selenium. Appl Environ Microbiol. 1977 Jan;33(1):31–37. doi: 10.1128/aem.33.1.31-37.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Hobbie J. E., Daley R. J., Jasper S. Use of nuclepore filters for counting bacteria by fluorescence microscopy. Appl Environ Microbiol. 1977 May;33(5):1225–1228. doi: 10.1128/aem.33.5.1225-1228.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Hudman J. F., Glenn A. R. Selenite uptake and incorporation by Selenomonas ruminantium. Arch Microbiol. 1984 Dec;140(2-3):252–256. doi: 10.1007/BF00454937. [DOI] [PubMed] [Google Scholar]
  6. Marshall E. Selenium Poisons Refuge, California Politics: Drainage from the San Joaquin Valley has dumped selenium into a wildlife refuge and pitted two federal agencies against each other. Science. 1985 Jul 12;229(4709):144–146. doi: 10.1126/science.229.4709.144. [DOI] [PubMed] [Google Scholar]
  7. Oremland R. S., Hollibaugh J. T., Maest A. S., Presser T. S., Miller L. G., Culbertson C. W. Selenate reduction to elemental selenium by anaerobic bacteria in sediments and culture: biogeochemical significance of a novel, sulfate-independent respiration. Appl Environ Microbiol. 1989 Sep;55(9):2333–2343. doi: 10.1128/aem.55.9.2333-2343.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Oremland R. S., Zehr J. P. Formation of methane and carbon dioxide from dimethylselenide in anoxic sediments and by a methanogenic bacterium. Appl Environ Microbiol. 1986 Nov;52(5):1031–1036. doi: 10.1128/aem.52.5.1031-1036.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Sherr B. F., Sherr E. B., Rassoulzadegan F. Rates of digestion of bacteria by marine phagotrophic protozoa: temperature dependence. Appl Environ Microbiol. 1988 May;54(5):1091–1095. doi: 10.1128/aem.54.5.1091-1095.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Stadtman T. C. Selenium biochemistry. Science. 1974 Mar 8;183(4128):915–922. doi: 10.1126/science.183.4128.915. [DOI] [PubMed] [Google Scholar]
  11. Steinberg N. A., Oremland R. S. Dissimilatory selenate reduction potentials in a diversity of sediment types. Appl Environ Microbiol. 1990 Nov;56(11):3550–3557. doi: 10.1128/aem.56.11.3550-3557.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Thompson-Eagle E. T., Frankenberger W. T., Karlson U. Volatilization of Selenium by Alternaria alternata. Appl Environ Microbiol. 1989 Jun;55(6):1406–1413. doi: 10.1128/aem.55.6.1406-1413.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]

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