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Oxygen isotope equilibrium in brachiopod shell fibres in the context of biological control

Published online by Cambridge University Press:  05 July 2018

M. Cusack*
Affiliation:
Department of Geographical and Earth Sciences, University of Glasgow, UK
A. Pérez-Huerta
Affiliation:
Department of Geographical and Earth Sciences, University of Glasgow, UK
P. Chung
Affiliation:
Department of Geographical and Earth Sciences, University of Glasgow, UK
D. Parkinson
Affiliation:
Donaldon Associates Ltd., The Pentagon Centre, 36 Washington St, Glasgow, UK
Y. Dauphin
Affiliation:
UMR IDES 8148, Bat 504, Université Paris XI-Orsay, F-91405 Orsay Cedex, France
J.-P. Cuif
Affiliation:
UMR IDES 8148, Bat 504, Université Paris XI-Orsay, F-91405 Orsay Cedex, France
*

Extract

With their long geological history and stable low-Mg calcite shells, Rhynchonelliform brachiopods are attractive sources of environmental data such as past seawater temperature (Buening and Spero, 1996; Auclair et al., 2003; Brand et al., 2003; Parkinson et al., 2005). Concerns about the influence of vital effects on the stable isotope composition of brachiopod shells (Popp et al., 1986), led to isotope analyses of different parts of brachiopod shells in order to identify those parts of the shell that are influenced by any vital effect and those parts that may be suitable recorders of seawater temperature via stable oxygen isotope composition (Carpenter and Lohmann, 1995; Parkinson et al., 2005). Such detailed studies demonstrated that the outer primary layer of acicularcalcite is isotopically light in both δ18O and δ13C while the secondary layer, composed of calcite fibres, is in oxygen-isotope equilibrium with ambient seawater(Fig. 1) (Parkinson et al., 2005).

Type
Research Article
Copyright
Copyright © The Mineralogical Society of Great Britain and Ireland 2008

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References

Addadi, L., Joester, D., Nudelman, F. and Weiner, S. (2006) Mollusk shell formation: A source of new concepts for understanding biomineralization processes. Chemistry — A European Journal, 12, 981–987.CrossRefGoogle ScholarPubMed
Auclair, A.-C, Joachimski, M.M. and Lécuyer, C. (2003) Deciphering kinetic, metabolic and environmental controls on stable isotope fractions between seawater and the shell of terebratalia transvers. (brachiopoda). Chemical Geology, 202, 59–78.CrossRefGoogle Scholar
Brand, U., Logan, A., Hiller, N. and Richardson, J. (2003) Geochemistry of modern brachiopods: Applications and implications for oceanography and paleoceanography. Chemical Geology, 198, 305–334.CrossRefGoogle Scholar
Buening, N. and Spero, HJ. (1996) Oxygen- and carbon-isotope analyses of the articulate brachiopod laqueus californianus:. recorder of environmental change in the subeuphotic zone. Marine Biology, 127, 105–114.CrossRefGoogle Scholar
Carpenter, SJ. and Lohmann, K.C. (1995) A18O and 513C values of modern brachiopod shells. Geochimica et Cosmochimica Ada, 59, 3748–3764.CrossRefGoogle Scholar
Cuif, J.P. and Dauphin, Y. (2005) The environment recording unit in coral skeletons — a synthesis of structural and chemical evidences for a biochemically driven, stepping-growth process in fibres. Biogeosciences, 2, 61–73.CrossRefGoogle Scholar
Cusack, M., Perez-Huerta, A. and Dalbeck, P. (2007) Common crystallographic control in calcite biomineralization of bivalve shells. CrystEngComm, 9, 1215–1218.CrossRefGoogle Scholar
Dauphin, Y. (2003) Soluble organic matrices of the calcitic prismatic shell layers of two pteriomorphid bivalves — pinna nobilis and pinctada margaritifera. Journal of Biological Chemistry, 278, 15168–15177.CrossRefGoogle ScholarPubMed
Dauphin, Y. (2006) Mineralizing matrices in the skeletal axes of two corallium species (alcyonacea). Comparative Biochemistry and Physiology, A145, 54–64.Google Scholar
Dauphin, Y., Cusack, M. and Ortlieb. (2007) Nanogranules in carbonate skeletons; a universal scheme? Geophysical Research Abstracts, 9, #02261.Google Scholar
Nudelman, F., Chen, H.H., Goldberg, H.A., Weiner, S. and Addadi, L. (2007) Spiers memorial lecture: Lessons from biomineralization: Comparing the growth strategies of mollusc shell prismatic and nacreous layers in atrina rigida. Farada. Discussions, 136, 9–25.Google ScholarPubMed
Parkinson, D., Curry, G.B., Cusack, M. and Fallick, A.E. (2005) Shell structure, patterns and trends of oxygen and carbon stable isotopes in modern brachiopod shells. Chemical Geology, 219, 193–235.CrossRefGoogle Scholar
Popp, B.N., Anderson, T.F. and Sandberg, P.A. (1986) Brachiopods as indicators of original isotopic compositions in some paleozoic limestones. Geological Society of America Bulletin, 97, 1262–1269.2.0.CO;2>CrossRefGoogle Scholar
Rousseau, M., Lopez, E., Stemplfle, P., Brendle, M., Franke, L., Guette, A., Naslain, R. and Bourrat, X. (2005) Multiscale structure of sheet nacre. Biomaterials, 26, 6254–6262.Google Scholar
Schmahl, W.W., Griesshaber, E., Neuser, R., Lenze, A., Job, R. and Brand, U. (2004) The microstructure of the fibrous layer of terebratulide brachiopod shell calcite. European Journal of Mineralogy, 16, 693–697.Google Scholar