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Symbiotic zooxanthellae enhance boring and growth rates of the tropical sponge Anthosigmella varians forma varians

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Abstract

Several species of boring sponges harbor symbiotic zooxanthellae, and it is believed that the symbiont enhances boring activity of host sponges. This hypothesis was tested using manipulative field experiments to assess the effect of intracellular zooxanthella populations on boring rates of the tropical sponge Anthosigmella varians forma varians. Portions of sponge were attached to 60 calcium carbonate blocks of known weight. Three sets of 10 blocks were grown at high light levels and three sets of 10 blocks were grown at low light levels for 105 d in the Florida Keys, Florida, USA. Boring rates, growth rates (lateral growth and within-substratum tissue penetration), and zooxanthella populations were measured at the end of the experiment. Absolute rates of boring and growth of A. varians forma varians were significantly greater when zooxanthella densities were higher. Boring rate and tissue penetration related to final surface area of sponge attachment was also enhanced when zooxanthella densities were higher, suggesting that the symbiont plays a physiological role in the decalcification process. This is in contrast to the role that zooxanthellae play in coral hosts. Based on the results of this study, it appears that the presence of zooxanthellar symbionts has important ecological and life-history consequences for host sponges. Ability to laterally overgrow competitors will be correlated with the size and activity of zooxanthella populations. In addition, the fitness of host sponges will be enhanced by algal symbionts, since greater penetration within substrata will result in an increase in production of tissue that can be converted into storage, feeding and reproductive functions.

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References

  • Alcolado PM (1990) General features of Cuban sponge communities. In: Rützler K (ed) New perspectives in sponge biology. Smithsonian Institution Press, Washington, DC, pp 351–357

    Google Scholar 

  • Barnes DJ, Chalker BE (1990) Calcification and photosynthesis in reef-building corals and algae. In: Dubinsky Z (ed) Ecosystems of the world. Vol. 25. Coral reefs. Elsevier, Amsterdam, pp 109–131

    Google Scholar 

  • Carriker MR, Chauncey HH (1974) Effect of carbonic anhydrase inhibition on shell penetration by the muricid gastropod Ursalpinx cinerea. Malacologia 12: 247–263

    Google Scholar 

  • Chalker BE, Barnes DJ, Dunlap WC, Jokiel PL (1988) Light and reef-building corals. Interdisciplinary Sci Rev 13: 222–237

    Google Scholar 

  • Chetail M, Fournie J (1969) Shell-boring mechanism of the gastropod, Purpura lapillus L.: a physiological demonstration of the role of carbonic anhydrase in the dissolution of CaCO3. Am Zool 9: 983–990

    Google Scholar 

  • Crumeyrolles-Duclaux G (1970) Sur la position systematique des zooxanthelles de Cliona viridis (Schm.), spongaire. Cr hebd Séanc Acad Sci, Paris 270: 1238–1239

    Google Scholar 

  • Gleason DF, Wellington GM (1993) Ultraviolet radiation and coral bleaching. Nature, Lond 365: 836–838

    Google Scholar 

  • Glynn PW (1973) Aspects of the ecology of coral reefs in the western Atlantic region. In: Jones OA, Endean R (eds) Biology and geology of coral reefs. Vol. 1. Biology. Academic Press, New York, pp 271–324

    Google Scholar 

  • Goreau TF, Hartman WD (1963) Boring sponges as controlling forces in the formation and maintenance of coral reefs. Publs Am Ass Advmt Sci 75: 25–54

    Google Scholar 

  • Hatch WI (1980) The implication of carbonic anhydrase in the physiological mechanism of penetration of carbonate substrata by the marine burrowing sponge Cliona celata (Demospongiac). Biol Bull mar biol Lab, Woods Hole 139: 135–147

    Google Scholar 

  • Heatfield BM (1970) Calcification in echinoderms: effects of temperature and diamox on incorporation of calcium-45 in vitro by regenerating spines of Strongylocentrotus purpuratus. Biol Bull mar biol Lab, Woods Hole 139: 151–163

    Google Scholar 

  • Hurlbert SH (1984) Psuedoreplication and the design of ecological field experiments. Ecol Monogr 54: 187–211

    Google Scholar 

  • Istin M, Girard JP (1970) Carbonic anhydrase and mobilization of calcium reserves in the mantle of lamellibranchs. Calcif Tissue Res 5: 247–260

    Google Scholar 

  • Marsh JA (1970) Primary productivity of reef building calcareous red algae. Ecology 51: 255–263

    Google Scholar 

  • Neumann AC (1966) Observations on coastal erosion in Bermuda and measurements of the boring rate of the sponge, Cliona lampa. Limnol Oceanogr 11: 92–108

    Google Scholar 

  • Pang RK (1973) The ecology of some Jamaican excavaring sponges. Bull mar Sci 23: 227–243

    Google Scholar 

  • Pomponi SA (1977) Excavation of calcium carbonate substrates by boring sponges: ultrastructure and cytochemistry. Ph.D. dissertation. University of Miami, Miami, Florida

    Google Scholar 

  • Pomponi SA (1980) Cytological mechanisms of calcium carbonate excavation by boring sponges. Int Rev Cytol 65: 301–319

    Google Scholar 

  • Rosell D, Uriz MJ (1991) Cliona virids (Schmidt, 1862) and Cliona nigricans (Schmidt, 1862) (Porifera: Hadromerida): evidence which shows they are the same species. Ophelia 33: 45–53

    Google Scholar 

  • Rosell D, Uriz MJ (1992) Do associated zooxanthellae and the nature of the substratum affect survival, attachment and growth of Cliona viridis (Porifera: Hadromerida)? An experimental approach. Mar Biol 114: 503–507

    Google Scholar 

  • Rüzler K (1975) The role of burrowing sponges in bioerosion. Oecologia 19: 203–216

    Google Scholar 

  • Rützler K (1990) Associations between Caribbean sponges and photosynthetic organisms. In: Rützler K (ed) New perspectives in sponge biology. Smithsonian Institution Press, Washington, DC, pp 455–466

    Google Scholar 

  • Sara M, Liaci L (1964) Symbiotic associations between zooxanthelae and two marine sponges of the genus Cliona. Nature, Lond 203: p. 321

    Google Scholar 

  • Schmahl, G (1990) Community structure and ecology of sponges associated with four southern Florida coral reefs. In: Rützler K (ed) New perspectives in sponge biology. Smithsonian Institution Press, Washington, DC, pp 376–383

    Google Scholar 

  • Smarsh A, Chauncey HH, Carriker MR, Person P (1969) Carbonic anhydrase in the accessory boring organ in the gastropod Urosalpinx. Am Zool 9: 967–982

    Google Scholar 

  • Sullivan KM, M Chiappone (1992) A comparison of belt quadrat and species presence/absence sampling of stony coral (Scleractinia and Milleporina) and sponges for evaluating species patterning on patch reefs of the central Bahamas. Bull mar Sci 50: 464–488

    Google Scholar 

  • Turquier Y (1968) Recherches sur la biologie des cirripèdes acrothoraciques. I. L'anhydrase carbonique et le méchanisme de perforation du substrat par Trypetesa nassarioides Turq. Archs Zool exp gén 109: 113–122

    Google Scholar 

  • Vacelet J (1981) Algalsponge symbioses in the coral reefs of New-Caledonia: morphological study. (Proc 4th int coral Reef Symp 2: 713–719) [Gomez EJ et al. (eds) Marine Sciences Center, University of the Philippines, Quezon City, Philippines]

    Google Scholar 

  • Vicente VP (1978) An ecological evaluation of the West Indian demosponge Anthosigmella varians (Hadromerida: Spirastrellidae). Bull mar Sci 28: 771–777

    Google Scholar 

  • Weis VM (1991) The induction of carbonic anhydrase in the symbiotic sea anemone Aiptasia puchella. Biol Bull mar biol Lab, Woods Hole 180: 496–504

    Google Scholar 

  • Weis VM, Smith GJ, Muscatine L (1989) A “CO2 supply” mechanism in zooxanthellate cnidarians: role of carbonic anhydrase. Mar Biol 100: 195–202

    Google Scholar 

  • Wellington, GM (1982) An experimental analysis of the effects of light and zooplankton on coral zonation. Oecologia 52: 311–320

    Google Scholar 

  • Wiedenmayer F (1977) Shallow water sponges of the western Bahamas. Birkhauser Verlag, Basel

    Google Scholar 

  • Wilkinson CR (1987) Significance of microbial symbionts in sponge evolution and ecology. Symbiosis 4: 135–146

    Google Scholar 

  • Wilkinson CR (1992) Symbiotic interactions between marine sponges and algae. In: Reisser W (ed) Algae and symbioses: plants, animals, fungi and viruses, interactions explored. Bio-press Ltd., Bristol, pp 112–151

    Google Scholar 

  • Yellowlees D, Dionisio-Sese ML, Masuda K, Maruyama T, Abe T, Baillie B, Tsuzuki M, Miyachi S (1993) Role of carbonic anhydrase in the supply of inorganic carbon to the giant clam-zooxanthellate symbiosis. Mar Biol 115: 605–611

    Google Scholar 

  • Zar JH (1984) Biostatistical analysis. 2nd edn. Prentice-Hall, Engle-wood Cliffs, New Jersey

    Google Scholar 

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  1. M. S. Hill

    Present address: Department of Biology, University of Massachusetts, 02125, Boston, Massachusetts, USA

Authors and Affiliations

  1. Program in Evolutionary Biology and Ecology Department of Biology, University of Houston, 77204-5513, Houston, Texas, USA

    M. S. Hill

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Communicated by N. H. Marcus, Tallahassee

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Hill, M.S. Symbiotic zooxanthellae enhance boring and growth rates of the tropical sponge Anthosigmella varians forma varians . Marine Biology 125, 649–654 (1996). https://doi.org/10.1007/BF00349246

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  • DOI: https://doi.org/10.1007/BF00349246

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