Skip to main content
Log in

Photosynthesis in air and in water of Acanthophora najadiformis growing within a narrow zone of the intertidal

  • Published:
Marine Biology Aims and scope Submit manuscript

Abstract

In this work, we investigated photosynthetic gas exchange responses of the red alga Acanthophora najadiformis (collected in 1991 from a shore near Netanya, Israel) to heating, light, inorganic carbon and desiccation of the thalli. This was done to elucidate some of the contributing causes for its particular restricted vertical distribution within the lower intertidal zone of the Israeli Mediterranean rocky shore. In contrast to other common intertidal species, the photosynthetic performance of A. najadiformis was very sensitive to desiccation and to high temperature, and these factors may thus prevent the alga from growing above the surge zone. On the other hand, this species photosynthesized five times faster in air than in water (provided it was kept highly hydrated), and this may be the reason why it does not succeed in competing with other algae in the subtidal which use HCO -3 more efficiently.

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

Literature cited

  • Beer, S., Eshel, A. (1983a). Photosynthesis of Ulva sp. I. Effects of desiccation when exposed to air. J. exp. mar. Biol. Ecol. 70: 91–97

    Google Scholar 

  • Beer, S., Eshel, A. (1983b). Photosynthesis of Ulva sp. II. Utilization of CO2 and HCO -3 when submerged. J. exp. mar. Biol. Ecol. 70: 99–106

    Google Scholar 

  • Bolton, J. J., Luning, K. (1982). Optimal growth and maximal survival temperatures of Atlantic Laminaria species (Phaeophyta) in culture. Mar. Biol. 66: 89–94

    Google Scholar 

  • Brown, M. T. (1987). Effects of desiccation on photosynthesis of intertidal algae from a Southern New Zealand shore. Botanica mar. 30: 121–127

    Google Scholar 

  • Cubit, J. D. (1984). Herbivory and the seasonal abundance of algae on a high intertidal rocky shore. Ecology 65: 1904–1917

    Google Scholar 

  • Dawes, C. J. (1989). Temperature acclimation in cultured Eucheuma isiforme from Florida and E. alvatezii from the Philippines. J. appl. Phycol. 1: 59–65

    Google Scholar 

  • Dayton, P. K. (1975). Experimental studies of algal canopy interaction in a sea-otter dominated kelp community at Amchitka Island, Alaska. Fish Bull. U.S. 73: 230–237

    Google Scholar 

  • Dickson, D. M. J., Wyn Jones, R. G., Davenport, J. (1982). Osmotic adaptation in Ulva lactuca under fluctuating salinity regimes. Planta 155: 409–415

    Google Scholar 

  • Dring, M. J., Brown, F. A. (1982). Photosynthesis of intertidal brown algae during and after periods of immersion: a renewed search for physiological causes of zonation. Mar. Ecol. Prog. Ser. 8: 301–308

    Google Scholar 

  • Dudgeon, S. R., Davison, I. R., Vadas, R. L. (1989). Effect of freezing on photosynthesis of intertidal macroalgae: relative tolerance of Chondrus crispus and Mastocarpus stellatus (Rhodophyta). Mar. Biol. 101: 107–114

    Google Scholar 

  • Durako, M. J., Dawes, C. J. (1980). A comparative seasonal study of two populations of Hypnea musciformis from the east and west coasts of Florida, USA. II. Photosynthetic and respiratory rates. Mar. Biol. 59: 157–162

    Google Scholar 

  • FitzGerald, W. J. (1978). Environmental parameters influencing the growth of Enteromorpha clathrata (Roth) J. Ag. in the intertidal zone on Guam. Botanica mar. 23: 207–220

    Google Scholar 

  • Gattuso, J. P., Jaubert, J. (1985). Photosynthesis and respiration of Caulerpa racemosa (Chlorophyceae, Caulerpales) grown in aquaria: effect of light and temperature. Botanica mar. 28: 327–332

    Google Scholar 

  • Johnson, W. S., Gigon, A., Gulmon, S. L., Mooney, H. A. (1974). Comparative photosynthetic capacities of intertidal algae under exposed and submerged conditions. Ecology 55: 450–453

    Google Scholar 

  • Kirst, G. O. (1990). Salinity tolerance of eukaryotic marine algae. A. Rev. Pl. Physiol. Pl. molec. Biol. 41: 21–53

    Google Scholar 

  • Lapointe, B. E., Tenore, K. R., Dawes, C. J. (1984). Interaction between light and temperature on the physiological ecology of Gracilaria tikvahiae. I. Growth, photosynthesis and respiration. Mar. Biol. 80: 161–170

    Google Scholar 

  • Lundberg, B. (1981). The algal vegetation at a platform shore at Mikhmoret. Proc., 10th int. Seaweed Symp. (Göteborg): 315–320 [Leviny, T. (ed.) Walter de Gruyter, Berlin]

    Google Scholar 

  • Madsen, T., Maberly, S. (1990). A comparison of air and water as environments for photosynthesis by the intertidal alga Fucus spiralis (Phaeophyta). J. Phycol. 26: 24–30

    Google Scholar 

  • McQuaid, C. D. (1985). Seasonal variation in biomass and zonation of nine intertidal algae in relation to changes in radiation, sea temperature and tidal regime. Botanica mar. 28: 539–544

    Google Scholar 

  • Murray, S. M., Horn, M. H. (1989). Seasonal dynamics of macrophyte population from an eastern North Pacific rocky-intertidal habitat. Botanica mar. 32: 457–473

    Google Scholar 

  • Murthy, M. S., Bhattacharya, M., Radia, P. (1978). Ecological studies on the intertidal algae at Okha (India). Botanica mar. 21: 381–386

    Google Scholar 

  • Niemeck, R. A., Mathieson, A. C. (1978). Physiological studies of intertidal fucoid algae. Botanica mar. 21: 221–227

    Google Scholar 

  • Quadir, A., Harrison, P. J., DeWreede, D. E. (1979). The effects of emergence and submergence on the photosynthesis and respiration of marine macrophytes. Phycologia 18: 83–88

    Google Scholar 

  • Reed, R. H., Collins, J. C., Russell, G. (1980). The effects of salintiy upon galactosyl-glycerol content and concentration of the marine red alga Porphyra purpurea (Roth) C. Ag. J. exp. Bot. 31: 1539–1554

    Google Scholar 

  • Reiskind, J. B., Beer, S., Bowes, G. (1989). Photosynthesis, photorespiration and ecophysiological interaction in marine macroalgae. Aquat. Bot. 34: 131–152

    Google Scholar 

  • Smith, C. M., Berry, A. (1986). Recovery of photosynthesis after exposure of intertidal algae to osmotic and temperature stresses: comparative studies of species with differing distributional limits. Oecologia 70: 6–12

    Google Scholar 

  • Yarish, C., Breeman, A. M., Hoek, C. van den (1986). Survival strategies and temperature responses of seaweeds belonging to different biogeographic distribution groups. Botanica mar. 29: 215–230

    Google Scholar 

  • Zimmerman, M. S., Livingston, R. J. (1976). Seasonal and physicochemical ranges of benthic macrophytes from a north Florida estuary (Apalachee Bay). Mar. Sci. 20: 33–45

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Communicated by T. M. Fenchel, Helsingør

This paper is in partial fulfillment of a Ph.D. study by R. Einav in cooperation with the Department of Ecology, University of Bielefeld (under supervision of Prof. Dr. S. W. Breckle), under a cooperative arrangement between Tel Aviv and Bielefeld Universities

Rights and permissions

Reprints and permissions

About this article

Cite this article

Einav, R., Beer, S. Photosynthesis in air and in water of Acanthophora najadiformis growing within a narrow zone of the intertidal. Marine Biology 117, 133–138 (1993). https://doi.org/10.1007/BF00346435

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00346435

Keywords

Navigation