Skip to main content
Log in

Skeletal development in Acropora cervicornis

III. A comparison of monthly rates of linear extension and calcium carbonate accretion measured over a year

  • Published:
Coral Reefs Aims and scope Submit manuscript

Abstract

Monthly linear extension and calcium carbonate accretion were measured over a year in the Caribbean staghorn coral, Acropora cervicornis. X-radiographs were made of cross sections of branches to analyze radial growth. Correlations were made between parameters of skeletal growth and four environmental parameters monitored over the same sampling periods: temperature, daylight hours, sun hours, plankton abundance. The results indicate that linear extension does not change during the year with the possible exception of April. It is suggested that temperatures outside an optimal range (ca. 26°–29°C for staghorn Acroporas) might cause a decrease in linear extension, however. Specific accretion (mg. mm-1) does show significant variations through the year. Calcium carbonate accretion (mean specific accretion times mean linear extension, mg. tip-1) is most strongly correlated with number of sun hours. A comparison is made between diel patterns of extension and accretion and longer term measurements. It is suggested that the accretion process is probably most influenced by some activity influenced by light. There are no annual growth bands in X-radiographs of cross-sections of the branches of A. cervicornis. This may result from secondary infilling in the skeleton.

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

References

  • Bak RPM (1974) Available light and other factors influencing growth of stony corals through the year in Curacao. Proc 2nd Int Coral Reef Symp 2:229–233

    Google Scholar 

  • Barnes DJ, Crossland CJ (1978) Diurnal productivity and apparent 14C-calcification in the staghorn coral, Acropora acuminata. Comp Biochem Physiol A 59:133–138

    Google Scholar 

  • Barnes DJ, Crossland CJ (1980) Diurnal and seasonal variations in the growth of a staghorn coral measured by time-lapse photography. Limnol Oceanogr 25:1113–1117

    Google Scholar 

  • Buddemeier RW, Maragos JE, Knutson DW (1974) Radiographic studies of coral reef exoskeletons: rates and patterns of coral growth. J Exp Mar Biol Ecol 14:179–200

    Google Scholar 

  • Crossland CS (1981) Seasonal growth of Acropora cf formosa and Pocillopora damicornis on a high latitude reef (Houtman Albrolhos, Western Australia). Proc 4th Int Coral Reef Symp 1:663–667

    Google Scholar 

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

    Google Scholar 

  • Foster AB (1983) The relationship between corallite morphology and colony shape in some massive reef-corals. Coral Reefs 2:19–26

    Google Scholar 

  • Gladfelter EH (1982) Skeletal development in Acropora cervicornis. I. Patterns of calcium carbonate accretion in the axial corallite. Coral Reefs 1:45–51

    Google Scholar 

  • Gladfelter EH (1983) Skeletal development in Acropora cervicornis. II. Diel patterns of calcium carbonate accretion. Coral Reefs 2:91–100

    Google Scholar 

  • Gladfelter EH, Gladfelter WB (1980) Environmental studies of Buck Island Reef National Monument. US Dept Interior Nat'l Park Service Report

  • Gladfelter EH, Monahan RK, Gladfelter WB (1978) Growth rates of five reef building corals in the northeastern Caribbean. Bull Mar Sci 28:728–734

    Google Scholar 

  • Goreau TF, Goreau NI (1959) The physiology of skeleton formation in Corals. II. Calcium deposition by hermatypic corals under various conditions in the reef. Biol Bull 117:239–250

    Google Scholar 

  • Highsmith RC (1979) Coral growth rates and environmental control of density banding. J Exp Mar Biol Ecol 37:105–125

    Google Scholar 

  • Hubbard DK, Scaturo DM (in press) Growth rates of Montastrea annularis along a depth gradient at Cane Bay, St Croix US Virgin Islands. Bull Mar Sci

  • Hudson JH, Shinn EA, Halley RB, Lidz B (1976) Sclerochronology: a tool for interpreting past environments. Geology 4:361–364

    Google Scholar 

  • Knutson DW, Buddemeier RW, Smith SV (1972) Coral chronometers: seasonal growth bands in reef corals. Science 177:270–272

    Google Scholar 

  • Lewis JB (1974) The importance of light and food upon the early growth of the reef coral Favia fragum. J Exp Mar Biol Ecol 15:299–304

    Google Scholar 

  • Lewis JB (1981) Estimates of secondary production of reef corals. Proc 4th Int Coral Reef Symp 2:369–377

    Google Scholar 

  • Lewis JB, Axelson F, Goodbody I, Page C, Chislett G (1968) Comparative growth rates of some corals in the Caribbean. Mar Sci Manu Rep McGill Univ No 10

  • Macintyre IG, Smith SV (1974) X-radiographic studies of skeletal development in coral colonies. Proc 2nd Int Coral Reef Symp 2:277–287

    Google Scholar 

  • McCloskey LR, Muscatine L (in press) Depth related changes in production and respiration in the Red Sea coral Stylophora pistillata. Proc R Soc Lond

  • Milliman JD (1974) Marine carbonates. Springer, New York Heidelberg Berlin

    Google Scholar 

  • Schneider RC, Smith SV (1982) Skeletal growth content and density in Porites spp in relation to environmental factors. Mar Biol 66:121–131

    Google Scholar 

  • Shinn EA (1966) Coral growth rate: an environmental indicator. J Paleontol 40:233–240

    Google Scholar 

  • Tunnicliffe VJ (1980) Biological and physical processes affecting the survival of a stony coral, Acropora cervicornis. PhD disseration, Yale University

  • Vandermeulen JH, Davis ND, Muscatine L (1972) The effect of inhibitors of photosynthesis on zooxanthellae in corals and other invertebrates. Mar Biol 16:185–191

    Google Scholar 

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

    Google Scholar 

  • Wellington GM, Glynn PW (1983) Environmental influences on Skeletal banding in (Panama) corals. Coral Reefs 1:215–222

    Google Scholar 

  • Yap HT, Gomez ED (1981) Growth of Acropora pulchra (Brook) in Bolinao, Pangasinan, Philippines. Proc 4th Int Coral Reef Symp 2:207–213

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Gladfelter, E.H. Skeletal development in Acropora cervicornis . Coral Reefs 3, 51–57 (1984). https://doi.org/10.1007/BF00306140

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00306140

Keywords

Navigation