Hostname: page-component-76fb5796d-22dnz Total loading time: 0 Render date: 2024-04-25T18:48:58.773Z Has data issue: false hasContentIssue false

Structural, Mineralogical, and Biochemical Diversity in the Lower Part of the Pearl Layer of Cultivated Seawater Pearls from Polynesia

Published online by Cambridge University Press:  16 September 2008

Jean-Pierre Cuif*
Affiliation:
University Paris-Sud, Faculty of Sciences, UMR 8148 IDES, Bat 504 Geology, 91405 Orsay, France
Alexander D. Ball
Affiliation:
Natural History Museum, Department of Mineralogy, Cromwell Road, London SW7 5BD, UK
Yannicke Dauphin
Affiliation:
University Paris-Sud, Faculty of Sciences, UMR 8148 IDES, Bat 504 Geology, 91405 Orsay, France
Bastien Farre
Affiliation:
University Paris-Sud, Faculty of Sciences, UMR 8148 IDES, Bat 504 Geology, 91405 Orsay, France
Julius Nouet
Affiliation:
University Paris-Sud, Faculty of Sciences, UMR 8148 IDES, Bat 504 Geology, 91405 Orsay, France
Alberto Perez-Huerta
Affiliation:
University of Glasgow, Department of Geographical & Earth Sciences, Gregory Building, Glasgow G12 8QQ, UK
Murielle Salomé
Affiliation:
European Synchrotron Radiation Facility, 6 rue J. Horowitz, BP 220, 38043 Grenoble, France
C. Terry Williams
Affiliation:
Natural History Museum, Department of Mineralogy, Cromwell Road, London SW7 5BD, UK
*
Corresponding author. E-mail: jean-pierre.cuif@u-psud.fr
Get access

Abstract

A series of Polynesian pearls has been investigated with particular attention to the structural and compositional patterns of the early developmental stages of the pearl layer. These initial steps in pearl formation bear witness of the metabolic changes that have occurred during the pearl-sac formation. The resulting structurally and biochemically complex structures have been investigated using a variety of techniques that provide us with information concerning both mineral phases and the organic components. Results are discussed with respect to our understanding of the biomineralization mechanisms, as well as for the grafting process.

Type
Biological Applications
Copyright
Copyright © Microscopy Society of America 2008

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Gervis, M.H. & Sims, N.A. (1992). The Biology and Culture of Pearl Oysters (Bivalvia, Pteriidae). Makati, Manilla, Philippines: International Center of Living Aquatic Resources Management.Google Scholar
Jabbour-Zahab, R., Chagot, D., Blanc, F. & Grozel, H. (1992). Mantle histology, histochemistry and ultrastructure of the pearl oyster Pinctada margaritifera. Aquat Liv Res 5, 285297.CrossRefGoogle Scholar
Kawakami, I.K. (1952). Mantle regeneration in pearl oyster (Pinctada martensii). J Fuji Pearl Inst 2, 14.Google Scholar
Loreau, J.P. (1982). Sédiments aragonitiques et leur genèse. Mém Mus ntnl hist nat N.S. C47, 1312.Google Scholar
Ma, H., Zhang, B., Lee, I.S., Quin, Z., Tong, Z. & Qui, S. (2007). Aragonite observed in the prismatic layer of the seawater-cultured pearls. Front Mat Sci China 1, 326329; DOI 10.1007/s11706-007-0061-6.CrossRefGoogle Scholar
Milliman, J.D. (1974). Marine Carbonates. New York, Heidelberg, Berlin: Springer Verlag.Google Scholar
Takeuchi, T. & Endo, K. (2006). Biphasic and dually coordinated expression of the genes encoding major shell matrix proteins in the pearl oyster Pinctada fucata. Mar Biotech 8, 5261.CrossRefGoogle ScholarPubMed
Weiner, S. & Dove, P.M. (2003). An overview of biomineralization processes and the problem of the vital effect. In Biomineralization, Dove, P.M., De Yoreo, J.J. & Weiner, S. (Eds.), S54, pp. 129.Google Scholar