Abstract
Framework cavities are the largest but least explored coral reef habitat1. Previous dive studies of caverns, spaces below plate corals, rubble and artificial cavities1,2,3 suggest that cavity-dwelling (coelobite) filter-feeders are important in the trophodynamics of reefs2,4,5. Quantitative community data are lacking, however, as the bulk of the narrow crevices interlacing the reef framework are inaccessible to conventional analysis methods6. Here we have developed endoscopic techniques to explore Red Sea framework crevices up to 4 m into the carbonate rock, revealing a large internal surface (2.5–7.4 m2 per projected m2 reef) dominated by encrusting filter-feeders. Sponges alone provided up to 60% of coelobite cover, outweighing epi-reefal filter-feeder biomass by two orders of magnitude. Coelobite community filtration removed more than 60% of the phytoplankton in the course of its less than 5-minute passage through the crevices, corresponding to an uptake of roughly 0.9 g carbon m-2 d-1. Mineralization of the largely allochthonous organic material is a principal source of nutrients supporting coral and algal growth. The supply of new material by coelobites may provide a key to understanding the ‘coral reef paradox’—a rich ecosystem thriving in nutrient-poor water.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 51 print issues and online access
$199.00 per year
only $3.90 per issue
Buy this article
- Purchase on Springer Link
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
Similar content being viewed by others
References
Ginsburg, R. N. in Perspectives on Coral Reefs (ed. Barnes, D. J.) 148–153 (Australian Institute of Marine Science, Townsville, 1983).
Buss, L. W. & Jackson, J. B. C. Planktonic food availability and suspension-feeder abundance: evidence of in situ depletion. J. Exp. Mar. Biol. Ecol. 49, 151–161 (1981).
Kobluk, D. R. Cryptic faunas in reefs: ecology and geologic importance. Palaios 3, 379–390 (1988).
Gast, G. J., Wiegmann, S., Wieringa, E., van Duyl, F. C. & Bak, R. P. M. Bacteria in coral reef water types: removal of cells, stimulation of growth and mineralization. Mar. Ecol. Prog. Ser. 167, 37–45 (1998).
Richter, C. & Wunsch, M. Cavity-dwelling suspension feeders in coral reefs - a new link in reef trophodynamics. Mar. Ecol. Prog. Ser. 188, 105–116 (1999).
Wunsch, M. & Richter, C. The CaveCam—an endoscopic underwater videosystem for the exploration of cryptic habitats. Mar. Ecol. Prog. Ser. 169, 277–282 (1998).
Jackson, J. B. C., Goreau, T. F. & Hartman, W. D. Recent brachiopod-coralline sponge communities and their paleoecological significance. Science 173, 623–625 (1971).
Mergner, H. in Proc. Symp. Coastal Marine Environ. Red Sea, Gulf of Aden and Tropical Western Indian Ocean 39–76 (ALECSO Red Sea and Gulf of Aden Environmental Programme, Jeddah (Saudi Arabia), Khartoum, Sudan, 1980).
Mergner, H. & Schuhmacher, H. in Proc. 5th Int. Coral Reef Symp. Vol. 6 (eds Gabrie, C. & Harmelin-Vivien, M.) 243–248 (Antenne Mus., EPHE, Moorea, 1985).
Yahel, G. et al. Phytoplankton distribution and grazing near coral reefs. Limnol. Oceanogr. 43, 551–563 (1998).
Erez, J. in Coral Reefs (ed. Dubinsky, Z.) 411–418 (Elsevier Science, New York, 1990).
Pawlik, J. R. Coral reef sponges: Do predatory fishes affect their distribution? Limnol. Oceanogr. 43, 1396–1399 (1998).
Wulff, J. L. Parrotfish predation on cryptic sponges of Caribbean coral reefs. Mar. Biol. 129, 41–52 (1997).
Vogel, S. Life in Moving Fluids—the Physical Biology of Flow 1–467 (Princeton Univ. Press, Princeton, 1994).
D'Elia, C. F. in Concepts of Ecosystem Ecology (eds Pomeroy, L. R. & Alberts, J. J.) 195–230 (Springer, New York, 1988).
Sorokin, Y. I. Coral Reef Ecology (Springer, Berlin, 1995).
Pile, A. J., Patterson, M. R., Savarese, M., Chernykh, V. I. & Fialkov, V. A. Trophic effects of sponge feeding within Lake Baikal's littoral zone. 2. Sponge abundance, diet, feeding efficiency, and carbon flux. Limnol. Oceanogr. 42, 178–184 (1997).
Reiswig, H. M. Particle feeding in natural populations of three marine demosponges. Biol. Bull. 141, 568–591 (1971).
Ferrier-Pagès, C. & Gattuso, J.-P. Biomass, production and grazing rates of pico- and nanoplankton in coral reef waters (Miyako Island, Japan). Microb. Ecol. 35, 46–57 (1998).
Andrews, J. C. & Müller, H. Space–time variability of nutrients in a lagoonal patch reef. Limnol. Oceanogr. 28, 215–227 (1983).
Tribble, G. W., Sansone, F. J., Li, Y.-H., Smith, S. V. & Buddemeier, R. W. in Proc. 6th Int. Coral Reef Symp. (eds Choat, J. H. et al.) 577–582 (Townsville, 1988).
Atkinson, M. J. & Smith, S. V. C:N:P ratios of benthic marine plants. Limnol. Oceanogr. 28, 568–574 (1983).
Rougérie, F. Nature et fonctionnement des atolls des Tuamotu (Polynésie Française). Oceanol. Acta 18, 61–78 (1995).
Shashar, N., Feldstein, T., Cohen, Y. & Loya, Y. Nitrogen fixation (acetylene reduction) on a coral reef. Coral Reefs 13, 171–174 (1994).
Meyer, J. L., Schultz, E. T. & Helfman, G. S. Fish schools: an asset to corals. Science 220, 1047–1049 (1983).
Ayukai, T. Retention of phytoplankton and planktonic microbes on coral reefs within the Great Barrier Reef, Australia. Coral Reefs 14, 141–147 (1995).
Glynn, P. W. Ecology of a Caribbean coral reef, the Porites reef flat biotope. Part II. Plankton community with evidence for depletion. Mar. Biol. 22, 1–22 (1973).
Darwin, C. The Structure and Distribution of Coral Reefs (Smith, Elder & Company, London, 1842).
Jokiel, P. L. & Morrissey, J. I. Water motion on coral reefs: evaluation of the ‘clod card’ technique. Mar. Ecol. Prog. Ser. 93, 175–181 (1993).
Parsons, T. R., Maita, Y. & Lalli, C. M. A Manual of Chemical and Biological Methods for Seawater Analysis (Pergamon, Oxford, 1984).
Acknowledgements
We thank G. Hempel and the participants of the Red Sea Programme for support; the Egyptian, Israeli and Jordanian authorities for sampling permission; A. Abu-Hilal, the staff of the Aqaba Marine Science Station, G. Yahel, R. Yahel, B. Munkes and E. Saadalla for field and laboratory support; U. Diez, I. and J. Zainer for assistance; K. Fabricius, A. Genin, B. Lazar and G. Yahel for discussions; R. van Soest for sponge determinations; and V. Ittekkot and M. Huettel for improving the manuscript. This study was funded by the German Federal Ministry of Education and Research (BMBF).
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Richter, C., Wunsch, M., Rasheed, M. et al. Endoscopic exploration of Red Sea coral reefs reveals dense populations of cavity-dwelling sponges. Nature 413, 726–730 (2001). https://doi.org/10.1038/35099547
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1038/35099547
This article is cited by
-
Crustose coralline algae can contribute more than corals to coral reef carbonate production
Communications Earth & Environment (2023)
-
Reef-building corals farm and feed on their photosynthetic symbionts
Nature (2023)
-
Poriferans rift apart: molecular demosponge biodiversity in Central and French Polynesia and comparison with adjacent marine provinces of the Central Indo-Pacific
Biodiversity and Conservation (2023)
-
Coral reef ecological pump for gathering and retaining nutrients and exporting carbon: a review and perspectives
Acta Oceanologica Sinica (2023)
-
A carbon cycling model shows strong control of seasonality and importance of sponges on the functioning of a northern Red Sea coral reef
Coral Reefs (2023)
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.