Ca2Mn(AsO4)2.2H2O
Triclinic, P1 or P1, a =
5.89, b = 7.031, c = 5.64 Ć,
a = 96.77, b = 109.32, g
= 108.47o, Z = 1
| Figure 25-31. Parabrandtite crystals in parallel growth from Sterling Hill. Field of view is 0.4 mm in maximum dimension. | ||
Parabrandtite, first thought to be talmessite, was described from Sterling Hill by Dunn et al. (1987c). It has not been found at Franklin.
Parabrandtite occurs as stout, colorless, 1-2 mm aggregates of crystals which occur in parallel growth (Figures 25-31 and 25-32); the quality of available crystals did not permit goniometric measurement of the crystal forms.
Parabrandtite is transparent, has perfect cleavage on {010} and {110}, vitreous luster, and a density of 3.55 g/cm3 (meas.), 3.60 g/cm3 (calc.) Optically, parabrandtite is biaxial, positive, 2V = 79.9o, with a = 1.701, b = 1.721, and g = 1.751; dispersion is weak, r > v.
| Figure 25-32. Parabrandtite crystals in parallel growth from Sterling Hill. Field of view is 1.0 mm in maximum dimension. | ||
The optical orientation is given in detail by Dunn et al. (1987c). There is no discernible fluorescence in ultraviolet. It is best verified using X-ray and chemical methods.
Parabrandtite is a calcium manganese arsenate hydrate mineral and the Mn nalogue of talmessite. A microprobe analysis is given in Table 25, showing minimal substitution of other cations.
Parabrandtite occurs at Sterling Hill, forming crystals in a cavity in franklinite/red-willemite/calcite ore. It is associated with sarkinite and was found but once.
Parabrandtite is named for its close relation to brandtite.
|
|
||||
| Copyright © 1995 by Pete J. Dunn |
Website
by Herb Yeates
|
|||
|
|
|
|||
|
Link
to homepage
|
||||
|
|
||||
|
|
|
|||