Julgoldite
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| Julgoldite | |
|---|---|
| Category | Silicate mineral |
| Chemical formula | (Ca,Mn)2(Fe2+,Fe3+,Mg)(Fe3+,Al)2(SiO4)(Si2O7)(OH)2(H2O) |
| Identification | |
| Color | Black to greenish olive |
| Crystal habit | blades or prisms. |
| Crystal system | Monoclinic 2/m |
| Cleavage | [100] Good |
| Mohs Scale hardness | 4.5 |
| Luster | sub-metallic |
| Refractive index | nα=1.776 nβ=1.814 nγ=1.836 |
| Optical Properties | Biaxial (-) |
| Birefringence | δ = 0.0600 |
| Streak | greenish olive |
| Specific gravity | 3.6 |
| Fusibility | loses water |
| References | [1] |
Julgoldite is a member of the pumpellyite mineral series, a series of minerals characterized by the chemical bonding of silica tetrahedra with alkali and transition metal cations. Julgoldites, along with more common minerals like epidote and vesuvianite, belong to the subclass of sorosilicates, the rock-forming minerals that contain SiO4 tetrahedra that share a common oxygen to form Si2O7 ions with a charge of 6- (Deer et al., 1996). Julgoldite has been recognized for its importance in low grade metamorphism, forming under shear stress accompanied by relatively low temperatures (Coombs, 1953).
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[edit] Composition
The chemical formula of julgoldite is (Ca,Mn)2(Fe2+,Fe3+,Mg)(Fe3+,Al)2(SiO4)(Si2O7)(OH)2(H2O) (Moore, 1971). Pumpellyites are classified according to the prevailing metals in the X and Y sites (Moore, 1971). When Mg in the X position and Al in the Y position and both occupy greater than 50% molarity of their positions, then the mineral is identified as a pumpellyite (Moore, 1971). Julgoldites are identified when Fe2+ in the X and Fe3+ in the Y each occupy greater than 50% molarity of their positions (Moore, 1971).
[edit] Geologic Occurrence
Julgoldites were first collected as samples entrenched in large plates of apophyllite and barite, comprising a fissure inside granular hematite-magnetite ore in Långban, Sweden (Moore, 1971). Julgoldite has since been discovered in other parts of the world: Edinburgh, Scotland (in quartz dolerite) (Livingstone, 1976) and Noril’sk Russia, one of the largest nickel deposits in the world, in metamorphosed basalts and diabases associated with prehnite and laumontite (Zolotukin et al., 1965). Julgoldite has also been found exposed in basalt cavities in the Khondivili Quarry near Bombay, India along with other silicates, including pumpellyite-Fe2+, ilvaite, babingtonite, hydroandradite, prehnite, and chlorite (Wise and Moller, 1990). These minerals crystallized in the same basaltic cavities, which were primarily formed from gas bubbles in the compound lava flows; all of these Ca-Fe silicates formed in different phases of a low temperature environment (Wise and Moller, 1990).
[edit] Atomic Structure
The atomic structures of pumpellyites and julgoldites consist of chains of edge-sharing octahedra linked by SiO4 , Si2O7, and CaO7 polyhedra: in the julgoldite atomic structure, the Ca site, the W site, is a seven-coordinated site with oxygen; the X and Y are two crystallographically independent octahedral sites; and the SiO4 site is tetrahedral (Passaglia and Gottardi, 1973). Like epidote, for which the chemical formula is Ca2(Fe3+,Al)Al2(SiO4)(Si2O7)(OH), julgoldite contains additional SiO4 tetrahedra that are independent of the Si2O7 structural units (Deer et al., 1996). The octahedral sites form chains along the b axis by sharing opposite edges (Allman and Donnay, 1973). The octahedral chains are joined in the ac plane by SiO4 and Si2O6 (OH) groups, forming five-member rings of two octahedra and three tetrahedral (Allman and Donnay, 1973). Half of the rings are open ended and have a Ca2+ ion in their center; the other rings are closed, and they surround a Ca2+ ion (Allman and Donnay, 1973). The X and Y chains are parallel to the crystallographic direction [010]; therefore, the two edge sharing polyhedra cause variations in the b cell parameter. (Artioli et al., 2003) Two layers of X chains and one layer of Y chains occur along the [100] direction, whereas two layers of both X and Y chains occur along the [001] direction (Artioli et al., 2003).
[edit] Physical Properties
Moore (1971) sampled flat prismatic or bladed crystals, with the greatest dimension of each mineral to be no more than 2mm. The julgoldites found in the basalt cavities in India were almost 10mm in length (Wise and Moller, 1990). Julgoldite is elongated parallel b [010] and flattened parallel a {100} (Moore, 1971). Allman and Donnay (1973) calculated the cell dimensions to be a 8.922(4), b 6.081(3), c 19.432 (9) Å. The color of julgoldite is usually a deep lustrous black, and it has a hardness of 4.5 and cleavage on the a-axis {100} (Moore, 1971). It has a greenish-olive powdery streak with a blue tinge (Moore, 1971). Under the petrographic microscope, a thin section of the mineral will display brilliant interference figures in greens or blues (Moore, 1971). The mineral is classified under the space group A2/m (Moore, 1971). A monoclinic mineral, julgoldite is isostructural to pumpellyite and epidote (Allman and Donnay, 1973
[edit] Biographic Sketch
Julgoldite was named in honor of Professor Julian Royce Goldsmith, an accomplished mineralogist and geochemist at the University of Chicago (Moore, 1971). Goldsmith, along with colleague Fritz Laves, first defined the crystallographic polymorphism of alkali feldspar (Newton, 1989). Goldsmith also experimented on the temperature dependence of the solid solution between calcite and dolomite (Newton, 1989). Goldsmith’s research also led him to experiment with the determination of the stability of intermediate structural states of albite (Newton, 1989). For his outstanding contributions to the study of mineralogy and geochemistry, Goldsmith was awarded the prestigious honor of the Roebling Medal by the Mineralogical Society of America in 1988 (Newton, 1989).
[edit] References
- Allmann, R. and Donnay, G. (1973) The crystal structure of julgoldite. Mineralogical Magazine 39, 271-281.
- Artioli, G., Geiger, C.A., and Dapiaggi, M. (2003) The crystal chemistry of julgoldite-Fe3+ from Bombay, India, studied using synchrotron X-ray powder diffraction and 57Fe Mössbauer spectroscopy. American Mineralogist 88, 1084-1090.
- Coombs, D.S. (1953) The pumpellyite mineral series. Mineralogical Magazine 30, 221, 113-133.
- Deer, W.A., Howie, R.A., and Zussman, J. (1996) An Introduction to the Rock-Forming Minerals. Prentice Hall, NY.
- Livingstone, A. (1976) Julgoldite, new data and occurrences; a second recording. Mineralogical Magazine 40, 761-763.
- Moore, P.B. (1971) Julgoldite, the Fe +2-Fe+3 dominant pumpellyite. A new mineral from Långban, Sweden. Lithos 4, 93-99.
- Newton, R. (1989) Presentation of the Roebling Medal of the Mineralogical Society of America for 1988 to Julian R. Goldsmith. American Mineralogist, 74, 715-716.
- Passaglia, E. and Gottardi, G. (1973) Crystal chemistry and nomenclature of pumpellyites and julgoldites. Canadian Mineralogist 12, 219-223.
- Wise, W. and Moller, W. (1990) Occurrence of Ca-Fe silicate minerals with zeolites in basalt cavities at Bombay, India. European Journal of Mineralogy. 2, 875-883.
- Zolotukin, V.V., Vasilyev, Y., Zyuzin, N. (1965) Babingtonite-prehnite-pumpellyite paragenetic association in Norilsk metasomatites. Dok. Akad. Nauk. SSSR, 161, 138-141.
