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Photoecology of the coral Leptoseris fragilis in the Red Sea twilight zone (an experimental study by submersible)

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Summary

Depth-dependent photoadaptational responses of the Red Sea zooxanthellate coral (Leptoseris fragilis) were studied down to 160 m from the research submersible GEO. Light saturation curves for photosynthesis revealed, with I C=1-2, I K=10.9 and I sat=20 μE·cm−2·sec−1, the lowest values of photokinetic parameters ever reported for a symbiotic coral. In summer, positive net production occurs only around noon at approx. 100m depth. Biomass parameters of corals at 100–135 m are negatively correlated with depth in algal cell density, protein, chlorophyll and carotenoid but not in pigment ratios or cell based pigment content. Coral size decreased with depth. Corals transplanted from 110–120 m original depth to 40, 70, 90 and 160 m showed high survival after one year. O2-production and dark O2-uptake increased with decreasing transplantation depth. After one year, transplants at 70 and 90 m but not at 40 m had higher algae density and pigment concentrations. The host light-harvesting systems described by Schlichter, Fricke and Weber (1986) are partially destroyed in 40 m but not in 70 and 90 m transplants. Different light exposures alter P-I-responses (P max, I C, I K, I sat) but not biomass parameters, indicating molecular or biochemical adaptation. The coraal's optimal light fields lie between 70 to 90 m. Its exceptional bathymetric distribution is linked with the newly discovered host light-harvesting systems which probably enhance photosynthetic performance in a dim environment.

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References

  • Buddemeier RW, Kinzie RA (1976) Coral growth. Oceanogr Mar Biol Ann Rev 14:183–225

    Google Scholar 

  • 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, Perzelin BB, Trench RK (1983) Mechanisms of photoadaptation in three strains of the symbiotic dinoflagelate Symbodinium microadriaticum. Mar Biol 76:219–229

    Google Scholar 

  • Crossland CJ, Barnes DJ (1977) Gas-exchange studies with the staghorn coral Acropora acuminata and its zooxanthellae. Mar Biol 40:185–194

    Google Scholar 

  • Dinesen ZD (1980) A revision of the coral genus Leptoseris (Scleractinia, Fungiidae, Agaricidae). Mem Queensl Mus 20:181–235

    Google Scholar 

  • Drew EA (1972) The biology and physiology of algae-invertebrate symbiosis. II. The density of symbiotic algal cells in a number of hermatypic hard corals and alcyonarians from various depth. J Exp Mar Biol Ecol 9:71–75

    Google Scholar 

  • Dubinsky Z, Falkowski PG, Porter JW, Muscatine L (1984) Absorption and utilization of radiant energy by light and shadeadapted colonies of the hermatypic coral Stylophora pistillata Proc R Soc Lon B 222:203–214

    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 coral reef. Bull Mar Sci 29:79–95

    Google Scholar 

  • Dustan P (1982) Depth-dependent photoadaptation by zooxanthellae of the reef coral Motastrea annularis. Mar Biol 68:253–264

    Google Scholar 

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

    Google Scholar 

  • Fricke HW, Schuhmacher H (1983) The depth limits of Red Sea stony corals: An ecophysiological problem (a deep diving survey by submersible) PSZNI Mar Ecol4:163–194

    Google Scholar 

  • Fricke HW, Knauer B (1986) Diversity and spatial pattern of coral communities in the Red Sea upper twilight zone (a quantitative assessment study by submersible). Oecologia (Berlin) 71:29–37

    Google Scholar 

  • Goreau TF (1959) The ecology of Jamaican coral reefs. I. Species composition and zonation. Ecology 40:67–90

    Google Scholar 

  • Goreau TF (1963) Calcium carbonate deposition by coralline algae and corals in relation to their role as reef builders. Ann NY Acad Sci 109:127–167

    PubMed  Google Scholar 

  • Goreau TF, Wells JW (1967) The shallow water scleractinia of Jamaica: Revised list of species and their vertical distribution range. Bull Mar Sci 17:442–453

    Google Scholar 

  • Graus RR, MacIntyre IG (1982) Variation in growth forms of the reef coral Montastrea annularis (Ellis and Solander). A quantitative evaluation of growth response to light distribution using computer simulation. In: Rützler K, MacIntyre G (eds) The atlantic Barrier Reef ecosystem at Carrie Bow Cay, Belize. I. Structure and communities, vol. 12, Smithson Contrib Mar Sci, pp 441–464

  • Jaques TG, Pilson MEQ (1980) Experimental ecology of the temperate scleractinian coral Astrangia danae. I. Partion of respiration, photosynthesis and calcification between host and symbionts. Mar Biol 60:167–178

    Google Scholar 

  • Jeffrey SW, Humphrey GF (1975) New spectrophotometric equations for determining chlorophylls a, b, c1 and c2 in higher plants, algae and natural phytoplancton. Biochem Physiol Pflanz 167:191–194

    Google Scholar 

  • Jerlov NG (1976) Marine optics. Elsevier, Amsterdam Oxford New York

    Google Scholar 

  • Jokiel PL, Morrissey JI (1986) Influence of size on primary production in the reef coral Pocillopora damicornis and the macroalgae Acanthopleura spicifera. Mar Biol 91:15–26

    Google Scholar 

  • Kawaguti S (1937) On the physiology of reef corals. The effect of light on colour and form of reef corals. Palao Trop Biol Stat Stud 1:199–208

    Google Scholar 

  • Loya Y, Slobodkin LB (1971) the coral reefs of Eilat (Gulf of Eilat, Red Sea). Symp Zool Soc Lond 28:117–139

    Google Scholar 

  • Marquardt DW (1963) An algorithm for least-squares estimation of nonlinear parameters. J Soc Ind Appl Math 11:431–441

    Google Scholar 

  • McCloskey LR, Muscatine L (1984) Production and respiration in the Red Sea coral Stylophora pistillata as a function of depth. Proc R Soc Lond B 222:215–230

    Google Scholar 

  • Mergner H, Svoboda A (1977) Productivity and seasonal changes in selected reef areas in the Gulf of Aqaba (Red Sea). Helgoländer Wiss Meeresunters 30:383–399

    Google Scholar 

  • Muscatine L, Porter JW (1977) Reef corals: Mutualistic symbioses adapted to nutrient-poor environments. Bio Science 27:454–460

    Google Scholar 

  • Muscatine L, McCloskey LR, Marian RE (1981) Estimating the daily contribution of carbon from zooxanthellae to coral animal respiration. Limnol Oceanogr 26:601–611

    Google Scholar 

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

    Google Scholar 

  • Osborne BA, Raven JA (1986) Light absorption by plants and its implications for photosynthesis. Biol Rev 61:1–61

    Google Scholar 

  • Parson TR, Strickland JDH (1963) Discussion of spectrophotometric determination of marine-plant pigments, with revised equations of ascertaining chlorophylls and carotenoids. J Mar Res 21:155–163

    Google Scholar 

  • Peterson GL (1977) A simplification of the protein assay method of Lowry et al. which is more generally applicable. Analyt Biochem 83:346–356

    Google Scholar 

  • Porter JW (1976) Autotrophy, heterotrophy, and resource partitioning in Caribbean reef-building corals. Am Nat 110:731–742

    Google Scholar 

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

    Google Scholar 

  • Redalje R (1976) Light adaptation strategies of hermatypic corals. Pac Sci 30:212

    Google Scholar 

  • Reiss Z, Hottinger L (1984) The Gulf of Aqaba. Ecological micropaleontology. Springer, Berlin Heidelberg New York Tokyo

    Google Scholar 

  • Scheer G, Pillai CSG (1983) Report on the stony corals from the Red Sea. Zoologica 133:1–198

    Google Scholar 

  • Schlichter D, Weber W, Fricke HW (1985) A chromatophore system in the hermatypic, deep water coral Leptoseris fragilis (Anthozoa: Hexacorallia). Mar Biol 89:143–147

    Google Scholar 

  • Schlichter D, Fricke HW, Weber W (1986) Light harvesting by wavelength transformation in a symbiotic coral of the Red Sea twilight zone. Mar Biol 91:403–407

    Google Scholar 

  • Schoenberg DA, Trench RK (1980) Genetic variation in Symbiodinium (=Gymnodinium) microadriaticum Freudenthal, and specificity in its symbiosis with marine invertebrates. II. Morphological variation in Symbiodinium microadriaticum. Proc R Soc Lond B 207:429–444

    Google Scholar 

  • Svoboda A, Poormann TP (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, Oxford, pp 87–99

    Google Scholar 

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

    Google Scholar 

  • Titlyanov EA, Zvalinskii WI, Leletkin WA, Schanownikowa MG (1983) Photosynthesis of zooxanthellae of reef-building corals under different light conditions. In: Biology of coral reefs. Science Academy of the USSR, Fareast Science Center, Wladiwostok (free translation of H. Fricke) pp 51–74

    Google Scholar 

  • Trench RK, Fisher CR (1983) Carbon dioxid fixation in Symbiodinium microadriaticum: problems with mechanism and pathways. In: Gruyter de W (ed) Endocytobiology vol 2, Berlin New York, pp 659–673

  • Tyler JE (1975) The in-situ quantum efficiency of natural phytoplankton populations. Limnol Oceanogr 20:976–980

    Google Scholar 

  • Tyler JE, Preisendorfer RW (1962) Transmission of energy within the sea. In: Hill MN (ed) Interscience, New York, pp 397–451

    Google Scholar 

  • Vareschi E, Fricke HW (1986) Light responses of a scleractinian coral (Plerogyra sinuosa). Mar Biol 90:395–402

    Google Scholar 

  • Wainwright SA (1964) Studies of the mineral phase of a coral skeleton. Experimental Cell Research 34:213–230

    Google Scholar 

  • Weinberg S (1976) Submarine daylight and ecology. Mar Biol 37:291–304

    Google Scholar 

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

    Google Scholar 

  • Yamazato K (1972) Bathymetric distribution of corals in the Ryukyu Islands. Proc Symp Coralsand Coral Reefs 1969, Mar Biol Assoc India: 121–133

  • Zvalinskii VI, Leletkin VA, Titlyanov EA, Shaposhinikova MG (1980) Photosynthesis and adaptation of corals to irradiance. 2. Oxygen exchange. Photosynthetica 14:422–430

    Google Scholar 

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Fricke, H.W., Vareschi, E. & Schlichter, D. Photoecology of the coral Leptoseris fragilis in the Red Sea twilight zone (an experimental study by submersible). Oecologia 73, 371–381 (1987). https://doi.org/10.1007/BF00385253

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