Skip to main content
Log in

Time-course of photoadaptation in the symbiotic sea anemone Anemonia viridis

  • Published:
Marine Biology Aims and scope Submit manuscript

Abstract

The time-course of photoadaptation in the symbiotic sea anemone Anemonia viridis (Forskäl) was determined on freshly collected anemones which were maintained under low light (LL: 10 μE m-2s-1) or high light (HL: 300 μE m-2s-1) over a period of 35 d. Photosynthesis versus irradiance curves (P vs I) normalised to anemone dry weight were determined for anemones at the start of the experiment and for both groups at 7 d intervals. Photosynthetic parameters derived from the P vs I curves, P grossmax (the maximum photosynthetic capacity of the zooxanthellae), α (an estimate of photosynthetic efficiency) and I k(the light-saturating irradiance), and the respiration rate, showed that anemones were high-light adapted before the experiment began. Thereafter, any observed changes occurred only in anemones adapting to the low-light regime. P grossmax remained relatively constant over 35 d and there was no significant difference between LL and HL groups. In the LL group α increased and both I kand the respiration rate decreased significantly. These photoadaptive responses were most rapid in the first 7 d, after which change was gradual until about Day 28, when photoadaptation appeared to be complete. In order to predict the physiological mechanisms of photoadaptation to low light, P gross vs I curves normalised to zooxanthellae biomass were constructed for LL and HL anemones at 35 d. Zooxanthellae density and photosynthetic pigment content were also analysed. For LL-adapted anemones, α and chlorophyll a were higher, there were no differences in algal density and chlorophyll c 2 and I kwas lower. It is proposed that the size of the peridinin-chlorophyll a-protein complex (PCP) of the light-harvesting complex was increased to facilitate photoadaptation. Plotting P net vs I normalised to anemone dry weight on the 35 d-photoadapted anemones gave a measure of changes in the excess photosynthetically fixed carbon that was potentially available to the host. Net photosynthesis of the LL group was higher at subsaturating light intensities as a result of the increase in α, and at saturating light intensities P netmax was higher as a result of a decrease in the rate of respiration of the whole symbiotic association.

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

  • Achituv Y, Dubinsky Z (1990) The adaptation of symbiotic associations between zooxanthellae and corals at different light levels. In: Lesel R (ed) Microbiology in poecilotherms. Elsevier Science Publishers, BV, Amsterdam, pp 43–46

    Google Scholar 

  • Al-Sofyani, Davies PS (1994) Seasonal variation in production and respiration in Red Sea corals. Proc 7th int coral Reef Symp [Richmond RH (ed) University of Guam in Mangilao, Guam] (in press)

    Google Scholar 

  • Battey JF, Porter JW (1989) Photoadaptation as a whole organism response in Montastrea annularis. Proc 6th int coral Reef Symp 3:79–86 [Choat JH, et al (eds) Sixth International Coral Reef Symposium Executive Committee, Townsville]

  • Chalker BE (1981) Simulating light-saturation curves for photosynthesis and calcification by reef-building corals. Mar Biol 63: 135–141

    Google Scholar 

  • Chalker BE, Dunlap WC, Oliver JK (1983) Bathymetric adaptations of reef building corals at Davies Reef, Great Barrier Reef, Australia. II. Light saturation curves for photosynthesis and respiration. J exp mar Biol Ecol 73:37–56

    Google Scholar 

  • Chang SS, Prézelin BB, Trench RK (1983) Mechanisms of photoadaptation in three strains of the symbiotic dinoflagellate Symbiodinium microadriaticum. Mar Biol 76:219–229

    Google Scholar 

  • Clayton WS, Lasker HR (1984) Host feeding regime and zooxanthellal photosynthesis in the anemone Aiptasia pallida (Verrill). Biol Bull mar biol Lab, Woods Hole 167:590–600

    Google Scholar 

  • Davies PS (1977) Carbon budgets and vertical zonation of Atlantic reef corals. Proc 3rd int coral Reef Symp 1:391–396 [Taylor DL (ed) Rosenstiel School of Marine and Atmospheric Science, University of Miami]

    Google Scholar 

  • Davies P (1980) Respiration in some Atlantic reef corals in relation to vertical distribution and growth form. Biol Bull mar biol Lab, Woods Hole 158:187–194

    Google Scholar 

  • Davies PS (1990) A rapid method for assessing growth rates of corals in relation to water pollution. Mar Pollut Bull 21:346–348

    Google Scholar 

  • Davies PS (1991) Effect of daylight variations on energy budgets of shallow-water corals. Mar Biol 108:137–144

    Google Scholar 

  • Dustan P (1979) Distribution of zooxanthellae and photosynthetic chloroplast pigments of the reef-building coral Montastrea annularis, Ellis and Solander, in relation to depth on a West Indian reef. Bull mar Sci 29:79–95

    Google Scholar 

  • Edmunds PJ, Davies PS (1988) Post-illumination stimulation of respiration rate in the coral Porites porites. Coral Reefs 7:7–9

    Google Scholar 

  • Edmunds PJ, Davies PS (1989) An energy budget for Porites porites (Scleractinia) growing in a stressed environment. Coral Reefs 8:37–43

    Google Scholar 

  • Falkowski PG (1990) Irradiance and corals. In: Dubinsky Z (ed) Coral reefs. Elsevier Science Publishers BV, Amsterdam, pp 89–107

    Google Scholar 

  • Falkowski PG, Dubinsky Z (1981) Light-shade adaptation of Stylophora pistillata, a hermatypic coral from the Gulf of Eilat. Nature, Lond 289:172–174

    Google Scholar 

  • Gattuso JP (1985) Features of depth effects on Stylophora pistillata, an hermatypic coral in the Gulf of Aqaba (Jordan, Red Sea). Proc 5th int coral Reef Congr 6:95–100 [Gabrié C, et al. (eds) Antenne Museum-EPHE, Moorea, French Polynesia]

    Google Scholar 

  • Green EJ, Carritt DE (1967) New tables for oxygen saturation of sea water. J mar Res 25:140–147

    Google Scholar 

  • Harland AD, Fixter LM, Davies PS, Anderson RA (1992) Effect of light on the total lipid content and storage lipids of the symbiotic sea anemone Anemonia viridis. Mar Biol 112:253–258

    Google Scholar 

  • Hoegh-Guldberg O, Smith GJ (1989) Influence of the population density of zooxanthellae and supply of ammonium on the biomass and metabolic characteristics of the reef corals Seriatopora hystrix and Stylophora pistillata. Mar Ecol Prog Ser 57:173–186

    Google Scholar 

  • Iriarte A, Purdie D (1993) Photosynthesis and growth response of the oceanic picoplankter Pycnococcus provasolii Guillard (clone ω48–23) (Chlorophyta) to variations in irradiance, photoperiod and temperature. J exp mar Biol Ecol 168:239–257

    Google Scholar 

  • Janssen HH, Möller H (1981) Effects of various feeding conditions on Anemonia sulcata. Zool Anz 206:161–170

    Google Scholar 

  • Jeffrey SW, Humphrey GF (1975) New spectrophotometric equations for determining chlorophylls a, c, c 1 and c 2 in higher plants, algae and natural phytoplankton. Biochem Physiol Pfl 167: 191–194

    Google Scholar 

  • Muller-Parker G (1985) Effect of feeding regime and irradiance on the photophysiology of the symbiotic sea anemone Aiptasia pulchella. Mar Biol 90:65–74

    Google Scholar 

  • Muller-Parker G (1987) Seasonal variation in light-shade adaptation of natural populations of the symbiotic sea anemone Aiptasia pulchella (Carlgren, 1943) in Hawaii. J exp mar Biol Ecol 112:165–183

    Google Scholar 

  • Muscatine L, Falkowski PG, Dubinsky Z, Cook PA, McCloskey LR (1989) The effect of external nutrient resources on the population dynamics of zooxanthellae in a reef coral. Proc R Soc (Ser B) 236:311–324

    Google Scholar 

  • Muscatine L, Falkowski PG, Porter JW, Dubinsky Z (1984) Fate of photosynthetic carbon in light- and shade-adapted colonies of Stylophora pistillata. Proc R Soc (Ser B) 222:181–202

    Google Scholar 

  • Parsons TR, Maita Y, Lalli CM (1984) A manual of chemical and biological methods for sea water analysis. Pergamon Press, Oxford

    Google Scholar 

  • Porter JW, Muscatine L, Dubinsky Z, Falkowski PG (1984) Primary production and photoadaptation in light- and shade-adapted colonies of the symbiotic coral Stylophora pistillata. Proc R Soc (Ser B) 222:161–180

    Google Scholar 

  • Prézelin BB (1987) Photosynthetic physiology of dinoflagellates. In: Taylor FJR (ed) The biology of the dinoflagellates. Blackwell Scientific Publications, Oxford, p 174–223

    Google Scholar 

  • Prézelin BB, Ley AC, Haxo FT (1976) Effect of growth irradiance on the photosynthetic action spectra of the marine dinoflagellate Glenodinium sp. Planta 130:251–256

    Google Scholar 

  • Prézelin BB, Matlick HA (1983) Nutrient-dependent low-light adaptation in the dinoflagellate Gonyaulax polyedra. Mar Biol 74: 141–150

    Google Scholar 

  • Prézelin BB, Sweeney BM (1978) Photoadaptation of photosynthesis in two bloom-forming dinoflagellates. In: Taylor DL, Seliger HH (eds) Toxic dinoflagellate blooms. Elsevier North Holland, New York, pp 101–106

    Google Scholar 

  • Sokal RR, Rohlf FJ (1981) Biometry. The principles and practice of statistics in biological research. 2nd ed. Freeman WH & Co, San Francisco

    Google Scholar 

  • Steele RD (1976) Light intensity as a factor in the regulation of the density of symbiotic zooxanthellae in Aiptasia tagetes (Coelenterata, Anthozoa). J Zool, Lond 179:387–405

    Google Scholar 

  • Svoboda A, Porrmann T (1980) Oxygen production and uptake by symbiotic Aiptasia diaphana (Rapp) (Anthozoa, Coelenterata) adapted to different light intensities. In: Smith DC, Tiffon Y (eds) Nutrition in the lower metazoa. Pergamon Press, New York, pp 87–99

    Google Scholar 

  • Thinh L-V (1991) Photo-adaption in two species of Acropora grown under controlled conditions. Photosynthetica 25:365–371

    Google Scholar 

  • Titlyanov EA, Shaposhnikova MG, Zvalinski VI (1980) Photosynthesis and adaptation of corals to irradiance. I. Contents and native state of photosynthetic pigments in symbiotic microalga. Photosynthetica 14:413–421

    Google Scholar 

  • Trench RK (1987) Dinoflagellates in non-parasitic symbiosis. In: Taylor FJR (ed) The biology of the dinoflagellates. Blackwell Scientific Publications, Oxford, pp 530–570

    Google Scholar 

  • Tytler EM (1982) The contribution of zooxanthellae to the energy requirements of the sea anemone anemonia sulcata (Pennant). PhD thesis. University of Glasgow

  • Tytler EM, Davies PS (1984) Photosynthetic production and respiratory energy expenditure in the anemone Anemonia sulcata (Pennant). J exp mar Biol Ecol 81:73–86

    Google Scholar 

  • Wethey DS, Porter JW (1976) Sun and shade differences in productivity of reef corals. Nature, Lond 262:281–282

    Google Scholar 

  • Zvalinski VI, Letekin VA, Titlyanov EA, Shaposhnikova MG (1980) Photosynthesis and adaptation of corals to irradiance. II. Oxygen exchange. Photosynthetica 14:422–430

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Communicated by J. Mauchline, Oban

Rights and permissions

Reprints and permissions

About this article

Cite this article

Harland, A.D., Davies, P.S. Time-course of photoadaptation in the symbiotic sea anemone Anemonia viridis . Marine Biology 119, 45–51 (1994). https://doi.org/10.1007/BF00350105

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00350105

Keywords

Navigation