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CO2 gas exchange of benthic microalgae during exposure to air: a technique for the rapid assessment of primary production

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Abstract

A method of measuring CO2gas exchange (caused, for example, by microalgal photosynthesis on emersed tidal mudflats) using open flow IR gas analyzers is described. The analyzers are integrated in a conventional portable photosynthesis system (LI-6400, LI-COR, Nebraska, USA), which allows manipulation and automatic recording of environmental parameters at the field site. Special bottomless measuring chambers are placed directly on the surface sediment. Measurements are performed under natural light conditions and ambient CO2concentrations, as well as under different CO2concentrations in air, and various PAR radiation levels produced by a LED light source built into one of the measurement chambers. First results from tidal channel banks in a north Brazilian mangrove system at Bragança (Pará, Brazil) under controlled conditions show a marked response of CO2assimilation to CO2concentration and to irradiance. Photosynthesis at 100 μmol mol−1CO2in air in one sample of a well-developed algal mat was saturated at 309 μmol photons m−2s−1, but increased with increasing ambient CO2concentrations (350 and 1000 μmol mol−1CO2) in the measuring chamber. Net CO2assimilation was 0.8 μmol CO2 m−2s−1at 100 μmol mol−1CO2, 5.9 μmol CO2m−2s−1at 350 μmol mol−1CO2and 9.8 μmol CO2m−2s−1at 1000 μmol mol−1CO2. Compensation irradiance decreased and apparent photon yield increased with ambient CO2concentration. Measurements under natural conditions resulted in a quick response of CO2exchange rates when light conditions changed. We recommend the measuring system for rapid estimations of benthic primary production and as a valuable field research tool in connection with certain ecophysiological aspects under changing environmental conditions.

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References

  • Alongi, D.M. 1994. Zonation and seasonality of benthic estuarine diatoms as tested with a rapid polarographic measurement of photosynthesis. Marine Biology 39: 11–18.

    Google Scholar 

  • Anonymous, 1997. LI-6400 portable photosynthesis system - primer. LI-COR, Lincoln, Nebraska, USA. Publication number 9501-110.

    Google Scholar 

  • Asmus, R. 1982. Field measurements on seasonal variation of the activity of primary producers on a sandy tidal flat in the northern Wadden Sea. Netherlands Journal of Sea Research 16: 389–402.

    Google Scholar 

  • Blanchard, G.F. and Montagna, P.A. 1992. Photosynthetic response of natural assemblages of marine benthic microalgae to shortand long-term variations of incident irradiance in Baffin Bay, Texas. Journal of Phycology 28: 7–14.

    Google Scholar 

  • Burris, J.E. 1981. Effects of oxygen and inorganic carbon concentrations on the photosynthetic quotients in marine algae. Marine Biology 65: 215–219.

    Google Scholar 

  • Caemmerer, S. von and Farquhar, G.D. 1981. Some relationships between the biochemistry of photosynthesis and the gas exchange of leaves. Planta 153: 376–387.

    Google Scholar 

  • Catarino, F., Tenhunen, J.D., Brotas, V. and Lange, O.L. 1985. Application of CO2-porometer methods to assessment of components of photosynthetic production in estuarine ecosystems. Marine Biology 89: 37–43.

    Google Scholar 

  • Clough, B.F. and Attiwill, P.M. 1980. Primary productivity of Zostera muelleri Irmissch ex Ascher. in Westernport Bay (Victoria, Australia). Aquatic Botany 9: 1–13.

    Google Scholar 

  • Darley, W.M., Dunn, E.L., Holmes, K.S. and Larew, H.G. 1976. A 14C method for measuring epibenthic microalgal productivity in air. Journal of Experimental Marine Biology and Ecology 25: 207–217.

    Google Scholar 

  • Dring, M.J. and Brown, F.A. 1982. Photosynthesis of intertidal brown algae during and after periods of emersion: A renewed search for physiological causes of zonation. Marine Ecology Progress Series 8: 301–308.

    Google Scholar 

  • Es, F.B. van 1982. Community metabolism of intertidal flats in the Ems-Dollard Estuary. Marine Ecology Progress Series 14: 185–196.

    Google Scholar 

  • Gargas, E. 1971. 'sun-shade’ adaption in microbenthic algae from the Öresund. Ophelia 9: 107–112.

    Google Scholar 

  • Gätje, C. 1991. Artenzusammensetzung, Biomasse und Primärproduktion des Mikrophytobenthos des Elbe-Ästuars. Dissertation Universität Hamburg, pp. 1–211.

  • Hargrave, B.T., Prouse, N.J., Phillips, G.A. and Neame, P.A. 1983. Primary production and respiration in pelagic and benthic communities at two intertidal sites in the upper Bay of Fundy. Canadian Journal of Fisheries and Aquatic Science 40: 229–243.

    Google Scholar 

  • Hunding, C. and Hargrave, B.T. 1973. A comparison of benthic microalgal production measured by C14 and oxygen methods. Journal of the Fishery Research Board of Canada 30: 309–312.

    Google Scholar 

  • Leuschner, C. and Rees, U. 1993. CO2 gas exchange of two intertidal seagrass species, Zostera marina L. and Zostera noltii Hornem., during emersion. Aquatic Botany 45: 53–62.

    Google Scholar 

  • Leuschner, C., Landwehr, S. and Mehlig, U. 1998. Limitation of carbon assimilation of intertidal Zostera noltii and Z. marina by desiccation at low tide. Aquatic Botany 62: 171–176.

    Google Scholar 

  • Lignell, R. 1992. Problems in filtration and fractionation of 14C primary productivity samples. Limnology and Oceanography 37: 172–178.

    Google Scholar 

  • Megard, R.O, Berman, T., Curtis, P.J. and Vaughan, P.W. 1985. Dependence of phytoplankton assilimilation quotients of light and nitrogen source: implications for oceanic primary productivity. Journal of Plankton Research 7: 691–701.

    Google Scholar 

  • Raine, R.C.T. 1983. The effect of nitrogen supply on the photosynthetic quotient of natural phytoplankton assemblages. Botanica Marina 26: 417–423.

    Google Scholar 

  • Revsbech, N.P., Jorgensen, B.B. and Brix, O. 1981. Primary production of microalgae in sediments measured by O2 microprofiles, H14CO ?3 fixation and O2 exchange methods. Limnology and Oceanography 26: 717–730.

    Google Scholar 

  • Revsbech, N.P. and Jorgensen, B.B. 1983. Photosynthesis of benthic microflora measured with high spatial resolution by the oxygen microfile method: capabilities and limitations of the method. Limnology and Oceanography 28: 749–756.

    Google Scholar 

  • Whitney, D.E. and Darley, W.M. 1983. Effect of light intensity upon salt marsh benthic microbial photosynthesis. Marine Biology 75: 249–252.

    Google Scholar 

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Schories, D., Mehlig, U. CO2 gas exchange of benthic microalgae during exposure to air: a technique for the rapid assessment of primary production. Wetlands Ecology and Management 8, 273–280 (2000). https://doi.org/10.1023/A:1008448729277

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