FRANKLIN AND STERLING HILL NEW JERSEY: THE WORLD'S MOST MAGNIFICENT MINERAL DEPOSITS
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SULFATES BORATES TUNGSTATES AND MOLYBDATES ARSENATRES ARSENIDES PHOSPHATES AND VANADATES UNNAMED MINERALS


QUARTZ

 

The feldspar group

ALBITE

ANORTHITE

ANORTHOCLASE

CELSIAN

HYALOPHANE

MICROCLINE

OLIGOCLASE

ORTHOCLASE

 

The scapolite group

MARIALITE

MEIONITE

 

The zeolite group

ANALCIME

CHABAZITE

HEULANDITE

LAUMONTITE

NATROLITE

STILBITE

THOMSONITE

 

Silicates with unknown structures

BOSTWICKITE

NEOTOCITE

WAWAYANDAITE

BOSTWICKITE

CaMn3+6Si3O16.7H2O
Orthorhombic?            

 
 
 
  Figure 19-8. Thin bladed crystals of bostwickite from Franklin. Field of view is approximately 0.3 mm in maximum dimension.  
   

Bostwickite was known to mineralogists for over a century, but was undescribed, in part due to the soft and friable nature of the aggregates and the paucity of clean material. It was considered to be arseniosiderite by Palache (1935) and was shown to be a manganese silicate by Frondel (1972) and Dunn (1979c). It was described and named bostwickite by Dunn and Leavens (1983). It is known only from Franklin. The unit-cell and crystal structure are unknown. 

Description

 
 
 
  Figure 19-9. Acicular bladed crystals of bostwickite with minor rhombic calcite; these crystals are especially small compared with the common crystals. Field of view is 0.5 mm in maximum dimension.  
   

Bostwickite occurs as hemispherules and radial aggregates up to 3 mm in diameter. It is brownish-red; weathered surfaces are darker brownish-red. It has vitreous luster and is very soft. The crystals are bladed, composite units, made up of many crystallites. Representative photographs are shown in figures 19-8 and 19-9. The density is 2.93 g/cm3 or greater.

Optically, bostwickite is biaxial, negative, with 2V = 25o, a = 1.775, b = 1.798, and g = 1.800; dispersion is strong, r < v; the absorption is X = Y > Z; pleochroism is strong with X = Y = reddish brown and Z = yellowish brown. There is no discernible fluorescence in ultraviolet. Bostwickite is best distinguished using its unique X-ray diffraction data.

Composition

Bostwickite is a calcium manganese silicate hydrate mineral. The oxidation state of Mn is inferred to be trivalent, in part because of the color and in part based on Gladstone-Dale calculations. The chemical analysis yielded MgO 0.9, CaO 5.1, Mn2O3 56.3, Fe2O3 0.5, Al2O3 1.0, As2O5 1.0, SiO2 20.1, H2O (by difference) 15.1, total = 100.0 wt. percent.

Occurrence and paragenesis

Bostwickite is known from but one occurrence from which a number of specimens were saved; most of these are in the collection at Harvard University. It was found in the Taylor Mine (later part of the Franklin Mine) in l874. Bostwickite occurs as flattened hemispherules on medium-grade ore consisting of franklinite, calcite, and fluorite, with minor willemite. Bostwickite occurs directly on the ore surface and on secondary carbonates which coat the ore in part. The “back” side of the sample contains the type material for kittatinnyite, an even rarer mineral.

Name

Bostwickite is named in honor of Richard C. Bostwick, a sophisticated collector of Franklin and Sterling Hill minerals. He has contributed much to our knowledge of their fluorescence and has done much to spread the excitement of minerals from Franklin and Sterling Hill far and wide. 

 

FOOTER LBI

 
Copyright © 1995 by Pete J. Dunn
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This page created: January 11, 2001

 

CHAPTER 19. TECTOSILICATES AND SILICATES WITH UNKNOWN STRUCTURE