Amorphous and Crystalline Phases in Biominerals
Abstract
Many discussions of biominerals are concerned with the formation of calcium phosphate phases and their transformations from amorphous phases to a stable crystalline form, such as apatite with various lattice substitutions [1,2,3]. Other biominerals remain amorphous notably biogenic silica [4], some calcium carbonate deposits [5] and inorganic phosphate deposits found in many invertebrates [6]. The intracellular deposits found in the hepatopancreas of the snail Helix aspersa are an example. They are amorphous and have a mineral composition of calcium magnesium pyrophosphate with ca 18% water giving a formula of CaMgP2O7.3H2O. Organic material, 5% w/w is also present [7]. A feature of these granules is their ready accumulation of dopant cations such as Mn, Fe, Co and Zn. The in vivo doped granules always remain amorphous to X-ray and electron diffraction techniques. The local atomic structures around Ca, Mn, Fe, Zn and P [8,9,10,11,12] have been determined by X-ray absorption spectroscopy using the Synchrotron Radiation Source at the SERC Daresbury Laboratory, UK. An open hydrated structure around calcium was deduced from EXAFS (Extended X-ray absorption fine structure) and density measurements [8] and it was proposed that the granules could be modelled by a modified continuous random network with metal ions cross linking the pyrophosphate chains with the water contributing to the interchain structure to allow the percolation and reaction of dopant cations [13].
Keywords
Phosphates Graphics Calcium Magnesium AluminiumPreview
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References
- [1]Nancollas GH (1989) In: Mann S, Webb J, Williams RJP (eds) Biomineralization Chemical and Biochemical Perspectives. VCH, Weinheim, pp 157–187.Google Scholar
- [2]Christofferson J, Christofferson MR, Kibalczyc W, Anderson FA (1989) J. Crys. Growth. 94: 767–777.CrossRefGoogle Scholar
- [3]Root MJ (1990) Calcif. Tissue Int. 47: 112–116.PubMedCrossRefGoogle Scholar
- [4]Mann S, Perry CC (1986) In: Silicon Biochemistry. John Wiley, Chichester pp 40–58.Google Scholar
- [5]Mason AZ, Nott JA (1981) Aquat. Toxicol. 1: 239–259.CrossRefGoogle Scholar
- [6]Taylor MG, Simkiss K, and Greaves GN (1986) Trans. Biochem. Soc. 14: 549–552.Google Scholar
- [7]Howard B, Mitchell PCH, Ritchie A, Simkiss K, Taylor MG (1981) Biochem. J. 194: 507–511PubMedGoogle Scholar
- [8]Greaves GN, Simkiss K, Taylor MG, Binsted N (1984) Biochem. J. 221: 855–868.PubMedGoogle Scholar
- [9]Taylor MG, Simkiss K, Greaves GN, Harries J (1988) Proc. R. Soc. Lond. B 234: 463–476.CrossRefGoogle Scholar
- [10]Taylor MG, Simkiss K, Greaves GN (1989) Physica B 158: 112–114CrossRefGoogle Scholar
- [11]Taylor, MG, Greaves, GN, Simkiss, K, (1990) Eur. J. Biochem.Google Scholar
- [12]Simkiss K, Taylor MG, Greaves GN (1990) J. Inorg. Biochem. 39: 17–23CrossRefGoogle Scholar
- [13]Greaves GN, (1990) Glass: Science and Technology 4B: 1–76.Google Scholar
- [14]Catlow CRA, Price GD (1990) Nature 6290: 243–248.CrossRefGoogle Scholar
- [15]Monma H, (1989) In: Kanazawa T (ed) Materials Science Monographs on Inorganic Phosphate Materials. Elsevier, Amsterdam, pp 55–77.Google Scholar
- [16]Christofferson MR, Thyregod HC, Christofferson J. (1987) Calcif Tissue Int. 41: 27–30.CrossRefGoogle Scholar
- [17]Shannon RD, Prewitt CT (1969) Acta Cryst. B25: 925–946Google Scholar
- [18]Thong N, Schwarzenbach D (1979) Acta. Cryst. A35: 658–664.Google Scholar
- [19]Crabbe MJC, Appleyard JR (1989) Desktop Molecular Mofdeller. Oxford University Press, Oxford.Google Scholar
- [20]Mandel NS (1975) Acta. Cryst. B31: 1730–1734.Google Scholar
- [21]Oka J, Kawahara A (1982) Acta. Cryst. B38: 3–5Google Scholar
- [22]Kay MI, Young RA, Posner AS (1964) Nature 204: 1050–1052PubMedCrossRefGoogle Scholar