Skip to main content
Log in

Photosynthetic strategies in leaves and stems of Egeria densa

  • Published:
Planta Aims and scope Submit manuscript

Abstract

Photosynthetic mechanisms have been compared in leaves and, separately, in stems of Egeria densa Planch. In order to correlate the structural and functional characteristics of the two organs (1) the ultrastructural features of leaves and stems have been studied and (2) their photosynthetic activity has been evaluated by measuring in vivo both oxygen evolution and the kinetics of chlorophyll fluorescence. The results confirm the aquatic behaviour of the leaf which is able to utilize inorganic C supplied both as CO2 and HCO 3 . In this respect, the different wall organization found in the two cell layers of the leaf is particularly interesting, since it could be related to the known polar mechanism of inorganic-C uptake. The stem, by contrast, behaves rather as an aerial organ, needing very high CO2 concentrations in the aquatic environment in order to carry out photosynthesis. In the stem, the aerenchyma plays a role in supplying the green cells with gaseous respiratory CO2, thus facilitating the photosynthetic activity of the submerged stems.

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

  • APHA, AWWA, WPCF (1975) Standard methods for the examination of water and waste water. Am. Public Health Assoc., New York

    Google Scholar 

  • Badger, M.R.I. (1987) The CO2-concentrating mechanism in aquatic phototrophs. In: The biochemistry of plants, vol. 10; Photosynthesis, pp. 219–274, Hatch, M.D., Boardman, N.K., eds. Academic Press, San Diego New York London

    Google Scholar 

  • Beer, S., Israel, A. (1990) Photosynthesis of Ulva fasciata IV. pH, carbonic anhydrase and inorganic carbon conversions in the unstirred layer. Plant Cell Environ. 13, 555–560

    Google Scholar 

  • Beer, S., Eshel, A., Waisel, Y. (1977) Carbon metabolism in seagrasses. I The utilization of exogenous inorganic carbon species in photosynthesis. J. Exp. Bot. 28, 1180–1189

    Google Scholar 

  • Björkman, O., Demmig, B. (1987) Photon yield of O2 evolution and Chlorophyll fluorescence characteristics at 77 K among vascular plants of diverse origin. Planta 170, 489–504

    Google Scholar 

  • Bowes, G., Salvucci M.E. (1989) Plasticity in the photosynthetic carbon metabolism of submerged aquatic macrophytes. Aquat. Bot. 34, 233–266

    Google Scholar 

  • Elzenga, J.T.M., Prins, H.B.A. (1988) Adaptation of Elodea and Potamogeton to different inorganic carbon levels and the mechanism for photosynthetic bicarbonate utilization. Austr. J. Plant Physiol. 15, 727–735

    Google Scholar 

  • Elzenga, J.T.M., Prins, H.B.A. (1989a) Light induced polar pH changes in leaves of Elodea canadensis. I Effects of carbon concentration and light intensity. Plant Physiol. 91, 62–67

    Google Scholar 

  • Elzenga, J.T.M., Prins, H.B.A. (1989b) Light induced polar pH changes in leaves of Elodea canadensis. II Effects of ferricyanide: evidence for modulation by the redox state of the cytoplasm. Plant Physiol. 91, 68–72

    Google Scholar 

  • Falk, H., Sitte, P. (1963) Zellfeinbau bei Plasmolyse. I Der Feinbau der Elodea Blattzellen. Protoplasma 57, 290–303

    Google Scholar 

  • Franceschi, V.R., Lucas, W.J. (1980) Structure and possible function(s) of charasomes: Complex plasmalemma cell wall elaborations present in some characean species. Protoplasma 104, 253–271

    Google Scholar 

  • Harche, R., Chandly, R., Catesson, M.A. (1990) Diversity of cellulose microfibril arrangement in the cell wall of Lygeum spartumleaves. Ann. Bot. 65, 79–86

    Google Scholar 

  • Helder, R.J., Berma, J., Zanstra, P.E. (1980) Uptake pattern of carbon dioxide and bicarbonate by leaves of Potamogeton lucens L. Proc. K. Ned. Acad. Van Wet. Ser. C 83, 151–166

    Google Scholar 

  • Inskeep, W.P., Bloom, P.R. (1985) Extinction coefficients of chlorophyll a and b in N,N-dimethylformamide and 80% acetone. Plant Physiol. 77, 483–485

    Google Scholar 

  • Ishii, R., Yamagishi, T.Y., Murata, Y. (1977) On a method for measuring photosynthesis and respiration of leaf slices with an oxygen electrode. Jap. J. Crop. Sci. 46, 53–57

    Google Scholar 

  • Kadono, Y. (1980) Photosynthetic carbon sources in some Potamogeton species. Bot. Mag. Tokyo 93, 185–194

    Google Scholar 

  • Kitajima, M., Butler, W.L. (1975) Quenching of chlorophyll fluorescence and primary photochemistry in chloroplasts by dibromothymoquinone. Biochem. Biophys. Acta 376, 105–115

    Google Scholar 

  • Lucas, W.J. (1983) Photosynthetic assimilation of exogenous HCO 3 by aquatic plants. Annu. Rev. Plant Physiol. 34, 71–104

    Google Scholar 

  • Lucas, W.J., Berry, J.A. (1985) Inorganic carbon transport in aquatic photosynthetic organisms. Physiol. Plant. 65, 539–543

    Google Scholar 

  • Lucas, W.J., Brechignac, F., Mimura, T., Oross, J.W. (1989) Charasomes are not essential for photosynthetic utilization of exogenous HCO 3 in Chara corallina. Protoplasma 151, 106–114

    Google Scholar 

  • Maberly, S.C., Spence, D.H.N. (1983) Photosynthetic inorganic carbon use by freshwater plants. J. Ecol. 71, 705–734

    Google Scholar 

  • Marrè, M.T., Albergoni, F.G., Moroni, A., Marrè, E. (1989a) Light-induced activation of electrogenic H+ extrusion and K+ uptake in Elodea densa depends on photosynthesis and is mediated by the plasma membrane H+ ATPase. J. Exp. Bot. 40, 343–352

    Google Scholar 

  • Marrè, M.T., Albergoni, F.G., Moroni, A., Pugliarello, M.C. (1989b) Evidence that H+ extrusion in Elodea densa leaves is mediated by an ATP-driven H+ pump. Plant Sci. 62, 21–28

    Google Scholar 

  • Moran, R., Porath, D. (1980) Chlorophyll determination in intact tissues using N,N-dimethylformamide. Plant Physiol. 65, 478–479

    Google Scholar 

  • Neville, A.C. (1985) Molecular and mechanical aspects of helicoid development in plant cell walls. BioEssays 3, 4–8

    Google Scholar 

  • Pate, J.S., Gunning, B.E.S. (1977) Transfer cells. Annu. Rev. Plant Physiol. 23, 173–196

    Google Scholar 

  • Pokorny, J., Ondok, J.P., Koncalová, H. (1985) Photosynthetic response to inorganic carbon in Elodea densa (Planchon) Caspary. Photosynthetica 19, 366–372

    Google Scholar 

  • Price, G.D., Whitecross, M.I. (1983) Cytochemical localization of ATPase activity on the plasmalemma of Chara corallina. Protoplasma 116, 65–74

    Google Scholar 

  • Prins, H.B.A., Elzenga, J.T.M. (1989) Bicarbonate utilization: Function and mechanism. Aquat. Bot. 34, 59–83

    Google Scholar 

  • Prins, H.B.A., Snel, J.F.H., Zanstra, P.E., Helder, R.J. (1982) The mechanism of bicarbonate assimilation by the polar leaves of Potamogeton and Elodea. CO2 concentration at the leaf surface. Plant Cell Environ. 5, 207–214

    Google Scholar 

  • Prins, H.B.A., Zanstra, P.E. (1985) Bicarbonate assimilation in aquatic angiosperms. Significance of the apoplast and unstirred layer. Verh. Internat. Verein. Limnol. 22, 2962–2967

    Google Scholar 

  • Robert, D., Roland, J.C. (1989) Biologie Vegetale. I Organization cellulaire, Dom Editeurs, Paris

    Google Scholar 

  • Roland, J.C., Vian, B., Satiat-Jeunemaitre, B., Mosiniak, M. (1987) Morphogenesis of plant cell walls at the supramolecular level: Internal geometry and versatility of helicoidal expression. Protoplasma 140, 75–91

    Article  PubMed  Google Scholar 

  • Sand-Jensen, K. (1983) Photosynthetic carbon sources of stream macrophytes. J. Exp. Bot. 139, 198–210

    Google Scholar 

  • Schreiber, U., Schliwa, U., Bilger, W. (1986) Continuous recording of photochemical and non-photochemical chlorophyll fluorescence quenching with a new type of modulation fluorometer. Photosynth. Res. 10, 51–62

    Google Scholar 

  • Sorrell, K.B., Dromgoole, F.I. (1987) Oxygen transport in the submerged freshwater macrophyte Egeria densa Planch. I Oxygen production, storage and release. Aquat. Bot. 28, 63–80

    Google Scholar 

  • Sorrell, K.B., Dromgoole, F.I. (1988) Oxygen transport in the submerged freshwater macrophyte Egeria densa Planch. II Role of lacunar gas pressure. Aquat. Bot. 31, 93–106

    Google Scholar 

  • Staal, M., Prins, H.B.A., Van Harmelen, M., Helder, R.J. (1988) The isolation of leaf protoplasm from the submerged aquatic angiosperm Potamogeton lucens L. Plant Cell Environ. 11, 715–719

    Google Scholar 

  • Titus, J.E., Stone, W.H. (1982) Photosynthetic response of two submerged macrophytes to dissolved inorganic carbon concentration and pH. Limnol. Oceanogr. 27, 151–160

    Google Scholar 

  • Walker, N.A. (1983) The uptake of inorganic carbon by freshwater plants. Plant Cell Environ. 6, 323–328

    Google Scholar 

  • Williams, W.T., Barber, D.A. (1961) The functional significance of aerenchyma in plants. Symp. Soc. Exp. Biol. 15, 132–144

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

The authors are grateful to C.U.G.A.S. (University of Padua) for the use of the scanning electron microscope. They also wish to thank Mr. Claudio Furlan and Mr. Giorgio Varotto for helpful technical assistance. This work was supported by a grant from C.N.R. and M.P.I, and was developed within the cooperation agreement between the Universities of Padova (Italy) and Innsbruck (Austria).

Rights and permissions

Reprints and permissions

About this article

Cite this article

Rascio, N., Mariani, P., Tommasini, E. et al. Photosynthetic strategies in leaves and stems of Egeria densa . Planta 185, 297–303 (1991). https://doi.org/10.1007/BF00201047

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00201047

Key words

Navigation