Skip to main content
Log in

Adaptation by hot spring phototrophs to reduced light intensities

  • Published:
Archives of Microbiology Aims and scope Submit manuscript

Abstract

Photosynthesis was measured by the 14C method on natural as well as low light adapted populations of Chloroflexus (a photosynthetic bacterium) and Synechococcus (a blue-green alga) from hot springs in Yellowstone National Park (Wyoming U.S.A.), to test the ability of these phototrophs to photosynthesize at a variety of light intensities. The herbicide 3-(3,4-dichlorophenyl)-1,1-dimethyl urea (DCMU) was used to distinguish uptake of the blue-green alga from that of the photosynthetic bacterium, while measurements of chlorophyll a and bacterio-chlorophyll c served to quantitate the standing crops of these organisms.

Natural populations of Synechococcus were found to be slightly inhibited by full sunlight intensities (summer values can surpass 90000 Lux), whereas the Chloroflexus populations were not. Populations of both phototrophs subjected to reduced light intensities through the use of neutral density filters were found to adapt to low light, and then become severely inhibited by high light intensities. Adaptation to various light regimes may be an important ecological phenomenon to the survival of these hot spring phototrophs.

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

  • Bauld, J., Brock, T. D.: Ecological studies of Chloroflexis, a gliding photosynthetic bacterium. Arch. Mikrobiol. 92, 267–284 (1973)

    Google Scholar 

  • Bott, T. L., Brock, T. D.: Bacterial growth rates above 90°C in Yellowstone hot springs Science 164, 1411–1412 (1969)

    Google Scholar 

  • Brock, T. D., Brock, M. L.: Temperature optima for algal development in Yellowstone and Iceland hot springs. Nature (Lond.) 209, 733–734 (1966)

    Google Scholar 

  • Brock, T. D., Brock, M. L.: Effect of light intensity on photosynthesis by thermal algae adapted to natural and reduced sunlight. Limnol. Oceanog. 14, 334–341 (1969)

    Google Scholar 

  • Cohen-Bazire, G., Sistrom, W. R.: The procaryotic photosynthetic apparatus. In: The chlorophylls (L. P. Vernon, G. R. Seely, eds.), pp. 313–341. New York: Academic Press 1966

    Google Scholar 

  • Doemel, W. N., Brock, T. D.: Bacterial stromatolites: Origin of laminations. Science 184 1083–1085 (1974)

    Google Scholar 

  • Doemel, W. N., Brock, T. D.: Vertical distribution of sulfur species in benthic algal mats. Limnol. Oceanog. 21, 237–244 (1976)

    Google Scholar 

  • Gates, D. M.: Energy exchange in the biosphere. New York Harper and Row 1962

    Google Scholar 

  • Goldman, D. R., Mason, D. T., Wood, B. J. B.: Light injury and inhibition in antarctic freshwater phytoplankton. Limnol. Oceanog 8, 313–322 (1963)

    Google Scholar 

  • Halfen, L. N., Pierson, B. K., Francis, G. W.: Carotenoids of a gliding organism, containing bacteriochlorophylls. Arch. Mikrobiol. 82, 240–246 (1972)

    Google Scholar 

  • Holt, S. C., Marr, A. G.: Effect of light intensity on the formation of intracytoplasmic membrane in Rhodospirillum rubrum. J. Bact. 89, 1421–1429 (1965)

    Google Scholar 

  • Holt, S. C., Conti, S. F., Fuller, R. C.: Effect of light intensity on the formation of the photochemical apparatus in the green bacterium Chloropseudomonas ethylicum. J. Bact. 91, 349–355 (1966)

    Google Scholar 

  • Kimball, H. H.: Records of total solar radiation intensity and their relation to daylight intensity. Monthly Weather Rev. 52, 473–479 (1924)

    Google Scholar 

  • Kok, B.: Oh inhibition of photosynthesis by intense light. Biochim. biophys. Acta (Amst.) 21, 234–244 (1956)

    Google Scholar 

  • Lowry, O. H., Rosebrough, N. J., Farr, A. L., Randall, R. J.: Protein measurement with the Folin phenol reagent. J. biol. Chem. 193, 265–275 (1951)

    Google Scholar 

  • Madigan, M. T., Brock, T. D.: Quantitative estimation of bacteriochlorophyll c in the presence of chlorophyll a in aquatic environments Limnol. Oceanog. 21, 462–467 (1976)

    Google Scholar 

  • Pfennig, N.: Photosynthetic bacteria. Ann. Rev. Microb. 21, 285–324 (1967)

    Google Scholar 

  • Pierson, B. K., Castenholz, R. W.: Bacteriochlorophylls in gliding filamentous procaryotes from hot springs. Nature New Biol 233 25–27 (1971)

    Google Scholar 

  • Pierson, B. K., Castenholz, R. W.: A phototrophic gliding filamentous bacterium in hot springs. Chloroflexus aurantiacus, gen. and sp. nov. Arch. Microbiol. 100, 5–24 (1974a)

    Google Scholar 

  • Pierson, B. K., Castenholz, R. W.: Studies of pigments and growth in Chloroflexus aurantiacus, a phototrophic filamentous bacterium. Arch. Microbiol. 100, 283–305 (1974b)

    Google Scholar 

  • Shiokawa, K., Takahashi, M., Ichimura, S.: Physiological adaptation of photosynthetic bacteria to low light and its ecological meaning. Jap. J. Limnol. 34, 1–11 (1973)

    Google Scholar 

  • Sorokin, Y. I.: Interrelations between sulphur and carbon turnover in meromictic lakes. Arch Hydrobiol. 66, 391–446 (1970)

    Google Scholar 

  • Trentini, W. C., Starr, M. P.: Growth and ultrastructure of Rhodomicrobium vannielii as a function of light intensity. J. Bact. 93, 1699–1704 (1967)

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Madigan, M.T., Brock, T.D. Adaptation by hot spring phototrophs to reduced light intensities. Arch. Microbiol. 113, 111–120 (1977). https://doi.org/10.1007/BF00428590

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00428590

Key words

Navigation