Coral cavities are sinks of dissolved organic carbon (DOC)

We studied the removal of dissolved organic carbon (DOC) by coral cavities of 50-250 dm3 at a depth range of 5-17 m along the coral reefs of Curacao, Netherlands Antilles, and the Berau area, East Kalimantan, Indonesia. We found significantly lower DOC concentrations in cavity water compared with ambient reef water. On average, DOC concentrations in cavity water were 15.1 ± 6.0 µmol L−1 (Curacao) and 4.0 ± 2.4 µmol L−1 (Berau) lower than in reef water. When the cavities were closed, DOC concentrations in the cavities declined by 22% ± 8% and 11% ± 4% in Curacao and Berau, respectively, within 30 min. This corresponded to average DOC removal rates per cavity surface area of 342 ± 82 mmol C m−2 d−1 in Curacao and 90 ± 45 mmol C m−2 d−1 in Berau. Bioassays showed that bacterioplankton are not responsible for this DOC removal by coral cavities. DOC fluxes exceeded bacterioplankton carbon (BC) fluxes into cavities by two orders of magnitude. On average BC fluxes per cavity surface area were 3.6 ± 1.3 mmol C m−2 d−1 (Curacao) and 1.9 ± 1.3 mmol C m−2 d−1 (Berau area). The net DOC removal per square meter of cryptic surface likely exceeded the gross primary production per square meter of planar reef area. We conclude that coral cavities and their biota are net sinks of DOC and play an important role in the energy budget of coral reefs.

[1]  R. E. Johannes ECOLOGY OF ORGANIC AGGREGATES IN THE VICINITY OF A CORAL REEF1 , 1967 .

[2]  Mohammed Rasheed,et al.  Endoscopic exploration of Red Sea coral reefs reveals dense populations of cavity-dwelling sponges , 2001, Nature.

[3]  Markus Huettel,et al.  Coral mucus functions as an energy carrier and particle trap in the reef ecosystem , 2004, Nature.

[4]  F. Thomas,et al.  The effect of water exchange on bacterioplankton depletion and inorganic nutrient dynamics in coral reef cavities , 2006, Coral Reefs.

[5]  D. Vaulot,et al.  Phytoplankton distribution and grazing near coral reefs , 1998 .

[6]  J. G. Field,et al.  The Ecological Role of Water-Column Microbes in the Sea* , 1983 .

[7]  A. Logan,et al.  Sessile invertebrate coelobite communities from reefs of Bermuda: Species composition and distribution , 1984, Coral Reefs.

[8]  J. Cole,et al.  Uptake of dissolved organic matter (DOM) and its importance to metabolic requirements of the zebra mussel, Dreissena polymorpha , 2005 .

[9]  Yossi Loya,et al.  The rate of mucus production by corals and its assimilation by the coral reef copepod Acartia negligens1 , 1975 .

[10]  H. Reiswig Bacteria as food for temperate-water marine sponges , 1975 .

[11]  C. Jørgensen AUGUST PÜTTER, AUGUST KROGH, AND MODERN IDEAS ON THE USE OF DISSOLVED ORGANIC MATTER IN AQUATIC ENVIRONMENTS* , 1976 .

[12]  F. C. V. Duyl,et al.  Linkage of small-scale spatial variations in DOC, inorganic nutrients and bacterioplankton growth with different coral reef water types , 2001 .

[13]  C. Richter,et al.  Cavity-dwelling suspension feeders in coral reefs--a new link in reef trophodynamics , 1999 .

[14]  D. Vaulot,et al.  Enumeration of Phytoplankton, Bacteria, and Viruses in Marine Samples , 1999, Current Protocols in Cytometry.

[15]  L. Buss,et al.  Bryozoan overgrowth interactions—the interdependence of competition for space and food , 1979, Nature.

[16]  S. Fitzwater,et al.  Dissolved organic carbon in the Atlantic, Southern and Pacific oceans , 1992, Nature.

[17]  R. Bak,et al.  The cave-profiler: a simple tool to describe the 3-D structure of inaccessible coral reef cavities , 2003, Coral Reefs.

[18]  R. Bak,et al.  Removal of bacteria and nutrient dynamics within the coral reef framework of Curaçao (Netherlands Antilles) , 2004, Coral Reefs.

[19]  S. Scheffers Benthic-Pelagic Coupling in Coral Reefs: Interaction Between Framework Cavities and Reef Water , 2005 .

[20]  R. Brock,et al.  A method for quantitatively assessing the infaunal community in coral rock1 , 1977 .

[21]  D. Patriquin,et al.  Physiography, Ecology, and Sediments of Two Bermuda Patch Reefs , 1971, The Journal of Geology.

[22]  A. Pile,et al.  In situ grazing on plankton 10 µm by the boreal sponge Mycale lingua , 1996 .

[23]  H. Ducklow The biomass, production and fate of bacteria in coral reefs , 1990 .

[24]  M. Ilan,et al.  Virus predation by sponges is a new nutrient‐flow pathway in coral reef food webs , 2006 .

[25]  S. Leys,et al.  Feeding in a Calcareous Sponge: Particle Uptake by Pseudopodia , 2006, The Biological Bulletin.

[26]  Z. Dubinsky,et al.  The effect of light and temperature on DOC excretion by phytoplankton , 1989 .

[27]  C. W. Carlson Production and Removal Processes , 2002 .

[28]  P. Dufour,et al.  Bacterioplankton carbon growth yield and DOC turnover in some coral reef lagoons , 1997 .

[29]  M. Veldhuis,et al.  Factors influencing the short-term variation in phytoplankton composition and biomass in coral reef waters , 2002, Coral Reefs.

[30]  R. Ginsburg,et al.  Growth and Submarine Fossilization of Algal Cup Reefs, Bermuda , 1973 .

[31]  B. Hatcher,et al.  Coral reef ecosystems: how much greater is the whole than the sum of the parts? , 1997, Coral Reefs.

[32]  Mark R. Patterson,et al.  Trophic effects of sponge feeding within Lake Baikal's littoral zone. 2. Sponge abundance, diet, feeding efficiency, and carbon flux , 1997 .

[33]  D. Schlichter,et al.  The natural release of amino acids from the symbiotic coral Heteroxenia fuscescens (Ehrb.) as a function of photosynthesis , 1991 .

[34]  R. Knijn,et al.  Sub-rubble communities of Curaçao and Bonaire coral reefs , 1991, Coral Reefs.

[35]  J. Jackson,et al.  Recent Brachiopod-Coralline Sponge Communities and Their Paleoecological Significance , 1971, Science.

[36]  B. Hatcher,et al.  Coral reef primary productivity. A hierarchy of pattern and process. , 1990, Trends in ecology & evolution.

[37]  R. Benner Chapter 3 – Chemical Composition and Reactivity , 2002 .

[38]  J. Sharp,et al.  In situ feeding and element removal in the symbiont‐bearing sponge Theonella swinhoei: Bulk DOC is the major source for carbon , 2003 .

[39]  T. Fenchel MARINE PLANKTON FOOD CHAINS , 1988 .

[40]  L. Buss,et al.  Competitive Networks: Nontransitive Competitive Relationships in Cryptic Coral Reef Environments , 1979, The American Naturalist.

[41]  H. Reiswig Partial Carbon and Energy Budgets of the Bacteriosponge Verohgia fistularis (Porifera: Demospongiae) in Barbados , 1981 .

[42]  R. Bak,et al.  Bacteria in coral reef water types: removal of cells, stimulation of growth and minaralization , 1998 .

[43]  I. Koike,et al.  Direct Determination of Carbon and Nitrogen Contents of Natural Bacterial Assemblages in Marine Environments , 1998, Applied and Environmental Microbiology.

[44]  T. Ayukai Retention of phytoplankton and planktonic microbes on coral reefs within the Great Barrier Reef, Australia , 1995, Coral Reefs.

[45]  Kazuhiro Kogure,et al.  Role of sub-micrometre particles in the ocean , 1990, Nature.

[46]  M. Ribes,et al.  Natural diet and grazing rate of the temperate sponge Dysidea avara (Demospongiae, Dendroceratida) throughout an annual cycle , 1999 .

[47]  Ian Morris,et al.  Extracellular release of carbon by marine phytoplankton; a physiological approach1 , 1980 .

[48]  R. Coma,et al.  Benthic suspension feeders: their paramount role in littoral marine food webs. , 1998, Trends in ecology & evolution.

[49]  N. Fisher,et al.  Uptake of dissolved organic carbon and trace elements by zebra mussels , 2000, Nature.