Hu, H., Gao, K. Impacts of CO2 enrichment on growth and photosynthesis in freshwater and marine diatoms., Chin. J. Ocean. Limnol. 26, 407–414 (2008). https://doi.org/10.1007/s00343-008-0407-7
DOI:
Hu, H., Gao, K. Impacts of CO2 enrichment on growth and photosynthesis in freshwater and marine diatoms., Chin. J. Ocean. Limnol. 26, 407–414 (2008). https://doi.org/10.1007/s00343-008-0407-7DOI:
Impacts of CO2 enrichment on growth and photosynthesis in freshwater and marine diatoms
摘要
Abstract
The physiological responses of Nitzschia palea Kützing
a freshwater diatom
to elevated CO2 were investigated and compared with those of a marine diatom
Chaetoceros muelleri Lemmermann previously reported. Elevated CO2 concentration to 700 μl/L increased the dissolved inorganic carbon (DIC) and lowered the pH in the cultures of N. palea
thus enhancing the growth by 4%–20% during the whole growth period. High CO2-grown N. palea cells showed lower levels of dark respiration rates and higher I k values. Light-saturated photosynthetic rates and photosynthetic efficiencies decreased in N. palea with the doubling CO2 concentration in airflow to the bottom of cultures
although the doubling CO2 concentration in airflow to the surface cultures had few effects on these two photosynthetic parameters. N. palea cells were found to be capable of using HCO 3 − in addition to gaseous CO2
and the CO2 enrichment decreased their affinity for HCO 3 − and CO2. Although doubled CO2 level would enhance the biomass of N. palea and C. muelleri to different extents
compared with the marine diatom
it had a significant effect on the specific growth rates of N. palea. In addition
the responses of photosynthetic parameters of N. palea to doubled CO2 concentration were almost opposite to those of C. muelleri.
关键词
Keywords
references
Badger, M. R., T. J. Andrews, S. M. Whitney, M. Ludwig, D. C. Yellowlees, W. Leggat and G. D. Price, 1998. The diversity and coevolution of Rubisco, plastids, pyrenoids, and chloroplast-based CO2-concentrating mechanisms in algae. Can. J. Bot. 76: 1 052–1 071.
Beakes, G. W., H. M. Canter and G. H. M. Jaworski, 1988. Zoospore ultrastructure of Zygorhizidium affluens and Z. planktonicum, two chytrids parasitizing the diatom Asterionella formosa. Can. J. Bot. 66: 1 054–1 067.
Burkhardt, S., G. Amoroso, U. Riebesell and D. Sültemeyer, 2001. CO2 and HCO −3 uptake in marine diatoms acclimated to different CO2 concentrations. Limnol. Oceanogr. 46: 1 378–1 391.
Chen, X. and K. Gao, 2003. Effect of CO2 concentrations on the activity of photosynthetic CO2 fixation and extracellular carbonic anhydrase in the marine diatom Skeletonema costatum. Chin. Sci. Bull. 48: 2 616–2 620.
Cole, J. J., N. F. Caraco, G. W. Kling and T. K. Kratz, 1994. Carbon dioxide supersaturation in the surface waters of lakes. Science 265: 1 568–1 570.
Falkowski, P. G., R. T. Barber and V. Smetacek, 1998. Biogeochemical controls and feedbacks on ocean primary production. Science 281: 200–206.
Giordano, M., J. Beardall and J. A. Raven, 2005. CO2 concentrating mechanisms in algae: Mechanisms, environmental modulation, and evolution. Annu. Rev. Plant Biol. 56: 99–131.
Hein, M. and K. Sand-Jensen, 1997. CO2 increases oceanic primary production. Nature 388: 526–527.
Hein, M. 1997. Inorganic carbon limitation of photosynthesis in lake phytoplankton. Freshw. Biol. 37: 545–552.
Henley, W. J. 1993. Measurement and interpretation of photosynthetic light-response curves in alga in the context of photoinhibition and diel changes. J. Phycol. 29: 729–739.
Houghton, J. T., L. G. Fiho, L. G. Meiro, B. A. Gallander, N. Harris and A. Kattenber, 1996. Climate change: the science of climate change. Cambridge University Press, Cambridge. 584p.
Hu, H. and K. Gao, 2001. Effects of doubled atmospheric CO2 on the growth and photosynthesis of Chaetoceros muelleri. Acta Hydrob. Sinica 25: 636–639. (in Chinese)
Hu, H. 2001. Studies on the characteristics of food microalgae and their relationships with varied CO2 concentrations. PhD Thesis, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan. (in Chinese)
Ibelings, B. W. and S. C. Maberly, 1998. Photoinhibition and the availability of inorganic carbon restrict photosynthesis by surface blooms of cyanobacteria. Limnol. Oceanogr. 43: 408–419.
Jeffrey, S. W. and G. F. Humphrey, 1975. New spectrophotometric equations for determining chlorophylls a, b, c 1 and c 2 in higher plants, algae and natural phytoplankton. Biochem. Physiol. Pflanz. 167: 191–194.
Miller, A. G. and B. Colman, 1980. Evidence for HCO −3 transport by the blue-green alga (Cyanobacterium) Coccochloris peniocystis. Plant Physiol. 65: 397–402.
Nimer, N. A., M. X. Ling, C. Brownlee and M. J. Merrett, 1999. Inorganic carbon limitation, exofacial carbonic anhydrase activity, and plasma membrane redox activity in marine phytoplankton species. J. Phycol. 35: 1 200–1 205.
Qiu, B. and K. Gao, 2002. Effects of CO2 enrichment on the bloom-forming cyanobacterium Microcystis aeruginosa (Cyanophyceae): physiological responses and relationships with the availability of dissolved inorganic carbon. J. Phycol. 38: 721–729.
Raven, J. A. and P. G. Falkowski, 1999. Oceanic sinks for atmospheric CO2. Plant Cell Environ. 22: 741–755.
Raven, J. A. 1997. Inorganic carbon acquisition by marine autotrophs. Adv. Bot. Res. 27: 85–209.
Raymond, P. A., N. F. Caraco and J. J. Cole, 1997. Carbon dioxide concentration and atmospheric flux in the Hudson River. Estuaries 20: 381–390.
Reinfelder, J. R., A. M. L. Kraepiel and F. M. M. Morel 2000. Unicellular C4 photosynthesis in a marine diatom. Nature 407: 996–999.
Riebesell, U., D. A. Wolf-Gladrow and V. Smetacek, 1993. Carbon dioxide limitation of marine phytoplankton growth rates. Nature 361: 249–251.
Rost, B., U. Riebesell, S. Burkhardt and D. Sültemeyer, 2003. Carbon acquisition of bloom-forming marine phytoplankton. Limnol. Oceanogr. 48: 55–67.
Schippers, P., M. Lürling and M. Scheffer, 2004. Increase of atmospheric CO2 promotes phytoplankton productivity. Ecol. Lett. 7: 446–451.
Schippers, P., J. E. Vermaat, J. de Klein and W. M. Mooij, 2004. The effect of atmospheric carbon dioxide elevation on plant growth in freshwater ecosystems. Ecosystems 7: 63–74.
Stumm, W. and J. J. Morgan, 1996. Aquatic Chemistry, 3rd. John Wiley & Sons, New York. p. 171–185.
Talling, J. F. 1985. Inorganic carbon reserves of natural waters and ecophysiological consequences of their photosynthetic depletion: microalgae. In: Lucas, W. J. and J. A. Berry eds. Inorganic carbon uptake by aquatic photosynthetic organisms. American Society of Plant Physiologists, Rockville, Md. p. 403–420.
Tortell, P. D., G. H. Rau and F. M. M. Morel, 2000. Inorganic carbon acquisition in coastal Pacific phytoplankton communities. Limnol. Oceanogr. 45: 1 485–1 500.
Tortell, P. D., J. R. Reinfelder and F. M. M. Morel, 1997. Active uptake of bicarbonate by diatoms. Nature 390: 243–244.
Xia, J. and K. Gao, 2003. Effects of doubled atmospheric CO2 concentration on the photosynthesis and growth of Chlorella pyrenoidosa cultured at varied levels of light. Fish. Sci. 69: 767–771.
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