Skip to main content
Log in

In vivo light-microscopic documentation for primary calcification processes in the hermatypic coral Stylophora pistillata

  • Regular Article
  • Published:
Cell and Tissue Research Aims and scope Submit manuscript

Abstract

Skeletogenesis in the hermatypic coral Stylophora pistillata was studied by using the lateral skeleton preparative (LSP) assay, viz., a coral nubbin attached to a glass coverslip glued to the bottom of a Petri dish. Observations on tissue and skeletal growth were made by polarized microscopy and by using vital staining. The horizontal distal tissue edges developed thin transparent extensions of ectodermal and calicoblastic layers only. Four stages (I-IV) of skeletogenesis were observed at these edges, underneath the newly developed tissue. In stage I, a thin clear layer of coral tissue advanced 3–40 μm beyond the existing LSP peripheral zone, revealing no sign of spiculae deposition. At stage II, primary fusiform crystals (1 μm each) were deposited, forming a primary discontinuous skeletal front 5–30 μm away from the previously deposited skeleton. During stage III, needle-like crystals appeared, covering the primary fusiform crystals. Stage IV involved further lengthening of the needle-like crystals, a process that resulted in occlusion of the spaces between adjacent crystals. Calcification stages I-III developed within hours, whereas stage IV was completed in several days to weeks. Two basic skeletal structures, “scattered” and “laminar” skeletons, were formed, integrating the growth patterns of the needle-like crystals. High variation was recorded in the expression of the four calcification stages, either between different locations along a single LSP or between different preparations observed at the same diurnal time. All four skeletogenesis stages took place during both day and night periods, indicating that an intrinsic process controls S. pistillata calcification.

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.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  • Allemand D, Furla P, Bénazet-Tambutté S (1998) Mechanisms of carbon acquisition for endosymbiont photosynthesis in Anthozoa. Can J Bot 76:925–941

    Article  CAS  Google Scholar 

  • Al-Horani FA, Al-Moghrabi SM, Beer D de (2003) Microsensor study of photosynthesis and calcification in the scleractinian coral, Galaxea fascicularis: active internal carbon cycle. J Exp Mar Biol Ecol 288:1–15

    Article  Google Scholar 

  • Barnes DJ (1970) Coral skeletons: an explanation of their growth and structure. Science 170:1305–1308

    Article  PubMed  CAS  Google Scholar 

  • Barnes DJ (1972) The structure and function of growth ridges in scleractinian coral skeletons. Proc R Soc Lond (Biol) 182:331–350

    Google Scholar 

  • Chalker BE, Taylor DL (1975) Light enhanced calcification, and the role of oxidative phosphorylation in calcification of the coral Acropora cervicornis. Proc R Soc Lond (Biol) 190:323–331

    Article  CAS  Google Scholar 

  • Clode PL, Marshall AT (2003a) Skeletal microstructure of Galaxea fascicularis exert septa: a high-resolution SEM study. Biol Bull 204:146–154

    Article  PubMed  Google Scholar 

  • Clode PL, Marshall AT (2003b) Calcium associated with a fibrillar organic matrix in the scleractinian coral Galaxea fascicularis. Protoplasma 220:153–161

    Article  PubMed  CAS  Google Scholar 

  • Constantz BR (1986) Coral skeleton construction: a physiochemically dominated process. Palaios 1:152–157

    Article  Google Scholar 

  • Constantz BR (1989) Skeletal organization in Caribbean Acropora spp. (Lamarck). In: Crick RE (ed) Origin evolution and modern aspects of biomineralization in plants and animals. Plenum, New York, pp 175–199

    Google Scholar 

  • Cuif JP, Dauphin Y (2005) The two-step mode of growth in the scleractinian coral skeletons from the micrometer to the overall scale. J Struct Biol 150:319–331

    Article  PubMed  Google Scholar 

  • Cuif JP, Dauphin Y, Gautert P (1999) Compositional diversity of soluble mineralizing matrices in some recent coral skeletons compared to fine-scale growth structures of fibers: discussion of consequences for biomineralization and diagenesis. Int J Earth Sci 88:582–592

    Article  CAS  Google Scholar 

  • Furla P, Galgani I, Durand I, Allemand D (2000) Sources and mechanisms of inorganic carbon transport for coral calcification and photosynthesis. J Exp Biol 203:3445–3457

    PubMed  CAS  Google Scholar 

  • Gattuso JP, Allemand D, Frankignoulle M (1999) Photosynthesis and calcification at cellular, organismal and community levels in coral reefs: a review on interaction and control by carbonate chemistry. Am Zool 39:160–183

    CAS  Google Scholar 

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

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Goreau TF (1959) The physiology of skeleton formation in corals. I. A method for measuring the rate of calcium deposition by corals under different conditions. Biol Bull 116:59–75

    Article  CAS  Google Scholar 

  • Hidaka M (1991) Deposition of fusiform crystals without apparent diurnal rhythm at the growing edge of septa of the coral Galaxea fascicularis. Coral Reefs 10:41–45

    Article  Google Scholar 

  • Hidaka M, Shirasaka S (1992) Mechanism of phototropism in young corallites of the coral Galaxea fascicularis (L.). J Exp Mar Biol Ecol 157:69–77

    Article  Google Scholar 

  • Howe SA, Marshall AT (2002) Temperature effects on calcification rate and skeletal deposition in the temperate coral Plesiastrea versipora (Lamark). J Exp Mar Biol Ecol 275:63–81

    Article  CAS  Google Scholar 

  • Isa Y (1986) An electron microscope study on the mineralization of the skeleton of the staghorn coral Acropora hebes. Mar Biol 93:91–101

    Article  CAS  Google Scholar 

  • Johnston IS (1980) The ultrastructure of skeletogenesis in hermatypic corals. Int Rev Cytol 67:171–214

    Article  CAS  Google Scholar 

  • Le Tissier MDÁA (1988) Diurnal patterns of skeleton formation in Pocillopora damicornis (Linnaeus). Coral Reefs 7:81–88

    Article  Google Scholar 

  • Le Tissier MDÁA (1990) The ultrastructure of the skeleton and skeletogenic tissues of the temperate coral Caryophyllia smithii. J Mar Biol Assoc UK 70:295–310

    Article  Google Scholar 

  • Le Tissier MDÁA (1991) The nature of the skeleton and skleletonic tissues in the Cnidaria. Hydrobiologia 216/217:397–402

    Article  Google Scholar 

  • Marin F, Smith M, Isa Y, Muyzer G, Westbroek P (1996) Skeletal matrices, muci, and the origin of invertebrate calcification. Proc Natl Acad Sci USA 93:1554–1559

    Article  PubMed  CAS  Google Scholar 

  • Marshall AT, Wright OP (1993) Confocal laser scanning light microscopy of extra thecal epithelia of undecalcified scleractinian corals. Cell Tissue Res 272:533–543

    Article  Google Scholar 

  • Muscatine L (1990) The role of symbiotic algae in carbon and energy flux in reef corals. In: Dubinsky Z, et al (eds) Ecosystems of the world, vol 25. Elsevier, Amsterdam, pp 75–87

    Google Scholar 

  • Ogilvie M (1896) Microscopic and systematic study of madreporarian types of corals. Philos Trans R Soc Lond Biol 187:85–345

    Article  Google Scholar 

  • Pearse VB, Muscatine L (1971) Role of symbiotic algae (zooxanthellae) in coral calcification. Biol Bull 141:350–363

    Article  CAS  Google Scholar 

  • Perrin C (2003) Compositional heterogeneity and microstructural diversity of coral skeleton: implications for taxonomy and control on early diagenesis. Coral Reefs 22:109–120

    Article  Google Scholar 

  • Reynaud-Vaganay S, Gattuso JP, Cuif JP, Jaubert J, Juillet-Leclerc A (1999) A novel culture technique for scleractinian corals: application to investigate changes in skeletal Δ18O as a function of temperature. Mar Ecol Prog Ser 180:121–130

    Article  CAS  Google Scholar 

  • Rinkevich B, Loya Y (1984) Does light enhance calcification in hermatypic corals? Mar Biol 80:1–6

    Article  CAS  Google Scholar 

  • Rowley RJ, Mackinnon DT (1995) Use of the fluorescent marker Calcein in biomineralization studies of brachiopods and other marine organisms. Bull Inst Oceanogr (Monaco) SPEC 14:111–120

    Google Scholar 

  • Shafir S, Van Rijn J, Rinkevich B (2001) Nubbing of coral colonies: a novel approach for the development of inland bloodstocks. Aquarium Sci Conserv 3:183–190

    Article  Google Scholar 

  • Shafir S, Van Rijn J, Rinkevich B (2003) The use of coral nubbins in coral reef ecotoxicology testing. Biomol Eng 20:401–406

    Article  PubMed  CAS  Google Scholar 

  • Simkiss K, Wilbur KM (1989) Biomineralization, cell biology and mineral deposition. Academic Press, San Diego

    Google Scholar 

  • Vago R, Gill E, Collingwood JC (1997) Laser measurements of coral growth. Nature 386:30–31

    Article  CAS  Google Scholar 

  • Wise SW (1972) Observations of fasciculi on developmental surfaces of scleractinian coral exoskeletons. Biomineralization 6:160–175

    Google Scholar 

  • Wainwright SA (1963) Skeletal organization in the coral Pocillopora damicornis. Q J Microsc Sci 104:169–183

    Google Scholar 

  • Wright OP, Marshall AT (1991) Calcium transport across the isolated oral epithelium of scleractinian corals. Coral Reefs 10:37–40

    Article  Google Scholar 

  • Young SD (1971) Organic material from scleratinian coral skeletons. I. Variation in composition between several species. Comp Biochem Physiol 40B:113–120

    Google Scholar 

  • Young SD (1973) Calcification and synthesis of skeletal organic material in the coral Pocillopora damicornis. Comp Biochem Physiol 44A:669–672

    Article  Google Scholar 

Download references

Acknowledgement

We thank Dr. E. Moisseva for her help with histological sections.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Baruch Rinkevich.

Additional information

This study was supported by the Israel Science Foundation (206/01 to J.E.), by the BARD, US-Israel Bi-National Agricultural Research and Development, by INCO-DEV project (REEFRES), and by CORALZOO, EC Collective Research project.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Raz-Bahat, M., Erez, J. & Rinkevich, B. In vivo light-microscopic documentation for primary calcification processes in the hermatypic coral Stylophora pistillata . Cell Tissue Res 325, 361–368 (2006). https://doi.org/10.1007/s00441-006-0182-8

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00441-006-0182-8

Keywords

Navigation