Skip to main content
Log in

Detrital pathways in a coral reef lagoon

II. Detritus deposition, benthic microbial biomass and production

  • Published:
Marine Biology Aims and scope Submit manuscript

Abstract

Coral reef lagoons have generally been regarded as sinks for organic matter exported from more productive reef front and reef flat zones. The object of this study was to examine the importance of detritus as a carbon source for benthic communities in the lagoon at Davies Reef, central Great Barrier Reef. We report the results of seasonal measurements, taken in 1986, of bacterial numbers and production, protozoan numbers, community primary production and respiration in the sediments of Davies Reef lagoon. Deposition rates of organic matter in the lagoon were also measured. Deposition rates (±1 SE) of carbon ranged from 9.2 (±1.5) to 140.7 (±10.3) mg Cm-2d-1. Deposition rates were highest in winter and spring, lowest in summer. Rates of bacterial production ranged from 4.7 (±0.2) pmol thymidine incorporated g-1 dry wt (DW) h-1 in winter to 23.5 (±1.0) pmol thymidine incorporated g-1 DW h-1 in spring. The number of ciliates ranged from 65 (±10) to 356 (±50) cm-3 through the year and the number of large (≥20 μm) flagellates from 38 (±7) to 108 (±16) cm-3. There were no clear relationships between the sediment organic content, detrital input or temperature and the rates of bacterial processes, community metabolism or the standing stocks of microbes in the lagoon. The relative significance of detritus and in situ primary production as sources of carbon in the lagoon varied with season. In summer and autumn, detritus was less important than primary production as a source of carbon (4 to 27% of total carbon input). In winter and spring, detritus input became more significant in supply of carbon to the sediments (32 to 67% of the total carbon input). The lagoon does not simply act as a sink for carbon exported from the reef flat. We calculate that only 5% of the net reef flat primary production reached lagoon sediments in summer, but nearly 40% in winter.

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

Literature cited

  • Alongi, D. M. (1986). Quantitative estimates of benthic protozoa in tropical marine systems using silica gel: a comparison of methods. Estuar. cstl Shelf Sci. 23: 443–450

    Google Scholar 

  • Alongi, D. M. (1989). Detritus in coral reef ecosystems: fluxes and fates. Proc. 6th. int. Symp. Coral Reefs 2: 29–36 [Choat, J. H. et al. (eds.) Sixth International Coral Reef Symposium Executive Committee, Townsville, Australia]

    Google Scholar 

  • Barnes, D. J. (1983). Profiling coral reef productivity and calcification using pH and oxygen electrodes. J. exp. mar. Biol. Ecol. 79: 213–231

    Google Scholar 

  • Barnes, D. J. (1989). Seasonality in community productivity and calcification at Davies Reef, central Great Barrier Reef. Proc. 6th int. Symp. Coral Reefs 2: 521–527 [Choat, J. H. et al. (eds.) Sixth International Coral Reef Symposium Executive Committee, Townsville, Australia]

    Google Scholar 

  • Bratbak, G., Dundas, I. (1984). Bacterial dry matter content and biomass estimations. Appl. envirl Microbiol. 48: 755–757

    Google Scholar 

  • Coffroth, M. A. (1990). Mucous sheet formation on poritid corals: an evaluation of coral mucus as a nutrient source on reefs. Mar. Biol. 105: 39–49

    Google Scholar 

  • Dobbs, F. C., Guckert, J. B., Carman, K. R. (1989). Comparison of three technique for administering radiolabeled substrates to sediments for trophic studies: incorporation by microbes. Microb. Ecol. 17: 237–250

    Google Scholar 

  • Ducklow, H. T. (1983). The production and fate of bacteria in the oceans. BioSci. 33: 494–501

    Google Scholar 

  • Findlay, R. H., Pollard, P. C., Moriarty, D. J. W., White, D. C. (1985). Qualitative determination of microbial activity and community nutritional status in estuarine sediments: evidence for a disturbance artifact. Can. J. Microbiol. 31: 493–498

    Google Scholar 

  • Folk, R. L. (1974). Petrology of sedimentary rocks. Hemphill, Austin, Texas

    Google Scholar 

  • Hamner, W. M., Jones, M. S., Carleton, J. H., Hauri, I. R., Williams, D. McB. (1988). Zooplankton, planktivorous fish, and water currents on a windward reef face: Great Barrier Reef, Australia. Bull. mar. Sci. 42: 459–479

    Google Scholar 

  • Hansen, J. A., Alongi, D. M., Moriarty, D. J. W., Pollard, P. C. (1987). The dynamics of benthic microbial communities at Davies Reef, central Great Barrier Reef. Coral Reefs 6: 63–70

    Google Scholar 

  • Hatcher, B. G. (1983a). The role of detritus in the metabolism and secondary production of coral reef ecosystems. In: Baker, J. T., Carter, R. M., Sammarco, P. W., Stark, K. P. (eds.) Proceedings of the Inaugural Great Barrier Reef Conference. James Cook University Press, Townsville, p. 317–325

    Google Scholar 

  • Hatcher, B. G. (1983b). Grazing in coral reef ecosystems. In: Barnes, D. J. (ed.) Perspectives on coral reefs. Clouston, Manuka, p. 164–169

    Google Scholar 

  • Hobbie, J. E., Daley, R. J., Jasper, R. (1977). Use of Nuclepore filters for counting bacteria by fluorescence microscopy. Appl. envirl Microbiol. 33: 1225–1228

    Google Scholar 

  • Johannes, R. E., and coauthors (1972). The metabolism of some coral reef communities: a team study of nutrient and energy flux at Eniwetak. BioSci. 22: 541–543

    Google Scholar 

  • Kinsey, D. W. (1978). Productivity and calcification estimates using slack water periods and field enclosures. In: Stoddart, D. R., Johannes, R. E. (eds.) Coral reefs: research methods. UNESCO, Paris, p. 439–468

    Google Scholar 

  • Kinsey, D. W. (1979). Carbon turnover and accumulation by coral reefs. PhD thesis, University of Hawaii, Honolulu

    Google Scholar 

  • Kinsey, D. W. (1985a). The functional role of back-reef and lagoonal systems in the central Great Barrier Reef. Proc. 5th int. Symp. Coral Reefs 6: 223–228 [Gabrié, C. et al. (eds.) Antenne Museum-EPHE, Moorea, French Polynesia]

    Google Scholar 

  • Kinsey, D. W. (1985b). Metabolism, calcification and carbon production I. Systems level studies. Proc. 5th int. Symp. Coral Reefs 4: 505–526 [Gabrié, C. et al. (eds.) Antenne Museum-EPHE, Moorea, French Polynesia]

    Google Scholar 

  • Klumpp, D. W., McKinnon, A. D. (1989). Temporal and spatial patterns in primary production of a coral-reef epilithic algal community. J. exp. mar. Biol. Ecol. 131: 1–22

    Google Scholar 

  • Klumpp, D. W., Polunin, N. V. C. (1989). Partitioning among grazers of food resources within damselfish territories on a coral reef. J. exp. mar. Biol. Ecol. 125: 145–169

    Google Scholar 

  • Klumpp, D. W., Polunin, N. V. C. (1990). Algal production, grazers and habitat partitioning on a coral reef: positive correlation between grazing rate and food availability. In: Barnes, M. (ed.) Trophic relationships in the marine environment. Aberdeen University Press, Aderdeen, p. 372–388

    Google Scholar 

  • Klumpp, D. W., Pulfrich, A. (1989). Trophic significance of herbivorous macroinvertebrates on the central Great Barrier Reef. Coral Reefs 8: 135–144

    Google Scholar 

  • Koop, K., Larkum, A. W. D. (1987). Deposition of organic material in a coral reef lagoon, One Tree Island, Great Barrier Reef. Estuar. cstl Shelf Sci. 25: 1–9

    Google Scholar 

  • Lewis, J. B. (1980). Coral reef ecosystems. In: Longhurst, A. R. (ed.) Analysis of marine ecosystems. Academic Press, London, p. 127–158

    Google Scholar 

  • Lorenzen, C. J. (1967). Determination of chlorophyll and pheopigments: spectrometric equations. Limnol. Oceanogr. 12: 343–346

    Google Scholar 

  • Moriarty, D. J. W. (1986). Measurement of bacterial growth rates in aquatic systems from rates of nucleic acid synthesis. Adv. microb. Ecol. 9: 245–292

    Google Scholar 

  • Moriarty, D. J. W. (1988). Accurate conversion factors for calculating bacterial growth rates from thymidine incorporation into DNA: elusive or illusive? In: Cappenberg, T. E., Steenbergen, C. L. M. (eds.) Proceedings of the Third International Workshop on the Measurement of Microbial Activities in the Carbon Cycle in Aquatic Ecosystems. Adv. Limnol. 31: 211–217

  • Moriarty, D. J. W. (1989). Relationships of bacterial biomass and production to primary production in marine sediments. In: Hattori, T., Ishida, Y., Maruyama, Y., Morita, R. Y., Uchida, A. (eds.) Recent advances in microbial ecology. Japan Scientific Societies Press, Tokyo, p. 349–354

    Google Scholar 

  • Moriarty, D. J. W., Pollard, P. C. (1990). Effects of radioactive labelling of macromolecules, disturbance of bacteria and adsorption of thymidine to sediment on the determination of bacterial growth rates in sediment with tritiated thymidine. J. microbiol. Meth. 11: 127–139

    Google Scholar 

  • Moriarty, D. J. W., Pollard, P. C., Hunt, W. G., Moriarty, C. M., Wassenberg, T. J. (1985). Productivity of bacteria and microalgae and the effect of grazing by holothurians on a coral reef flat. Mar. Biol. 85: 293–300

    Google Scholar 

  • Odum, E. P., Odum, H. T. (1955). Trophic structure and productivity of a windward coral reef community on Eniwetok Atoll. Ecol. Monogr. 25: 291–320

    Google Scholar 

  • Pollard, P. C. (1987). Dialysis: a simple method of separating labelled bacterial DNA and tritiated thymidine from aquatic sediments. J. Microbiol. Meth. 7: 91–101

    Google Scholar 

  • Pollard, P. C., Moriarty, D. J. W. (1984). Validity of isotope dilution of tritiated thymidine during incorporation into DNA as an estimate of bacterial growth rates. Appl. envirl Microbiol. 48: 1075–1083

    Google Scholar 

  • Rice, D. L., Tenore, K. R. (1981). Dynamics of carbon and nitrogen during the decomposition of detritus derived from estuarine macrophytes. Estuar. cstl Shelf Sci. 13: 681–690

    Google Scholar 

  • Riddle, M. J., Alongi, D. M., Dayton, P. K., Hansen, J. A., Klumpp, D. W. (1990). Detrital pathways in a coral reef lagoon. I. Macrofaunal biomass and estimates of production. Mar. Biol. 104: 109–118

    Google Scholar 

  • Roman, M. R., Furnas, M. J., Mullin, M. M. (1990). Zooplankton abundance and grazing at Davies Reef, Great Barrier Reef, Australia. Mar. Biol. 105: 73–82

    Google Scholar 

  • Russ, G. R. (1987). Is rate of removal of algae by grazers reduced inside territories of tropical damselfishes? J. exp. mar. Biol. Ecol. 110: 1–17

    Google Scholar 

  • Sandstrom, M. W., Tirendi, F., Nott, A. (1985). Direct determination of organic carbon in modern reef sediments and calcareous organisms after dissolution of carbonate. Mar. Geol. 70: 321–329

    Google Scholar 

  • Strayer, D. (1988). On the limits to secondary production. Limnol. Oceanogr. 33: 1217–1220

    Google Scholar 

  • Tenore, K. R., Hanson, R. B., McClain, J., Maccubbin, A. E., Hodson, R. E. (1984). Changes in composition and nutritional value to a benthic deposit feeder of decomposing detritus pools. Bull. mar. Sci. 35: 299–311

    Google Scholar 

  • Williams, P. J. LeB. (1984). Bacterial production in the marine food chain: the emperor's new suit of clothes? In: Fasham, M. J. R. (ed.) Flows of energy and materials in marine ecosystems. Plenum Press, New York, p. 271–300

    Google Scholar 

  • Winer, B. J. (1971). Statistical principles in experimental degign, 2nd edn. MacGraw Hill, Kogakusha, Tokyo

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Communicated by G. F. Humphrey, Sydney

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hansen, J.A., Klumpp, D.W., Alongi, D.M. et al. Detrital pathways in a coral reef lagoon. Marine Biology 113, 363–372 (1992). https://doi.org/10.1007/BF00349160

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00349160

Keywords

Navigation