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Partitioning of Sr between coexisting minerals of the hollandite- and piemontite-groups in a quartz-rich schist from the Sanbagawa metamorphic belt, Japan

Authors :
Enami, Masaki
Banno, Yasuyuki
Source :
American Mineralogist (De Gruyter); February 2001, Vol. 86 Issue: 3 p205-214, 10p
Publication Year :
2001

Abstract

Coexisting minerals of the hollandite-cryptomelane series, piemontite-group, and abswurmbachite-braunite series occur as a small nodule in a quartzose schist (metachert) from the epidote-amphibolite facies area of the Sanbagawa metamorphic belt, central Shikoku, Japan. Stron­tium, Ba. K. and Pb contents of the hollandite-cryptomelane minerals are 0.00-0.42, 0.07-0.99, 0.00-0.75 and 0.00-0.05 apfu (atoms per formula unit: O = 16), respectively. The piemontite-group minerals can be divided into common piemontite (Ca > Sr in the ten-coordinated A2-site) and strontiopiemontite (Sr > Ca). Strontium. Ba and Pb contents of the strontiopiemontite reach 0.71, 0.26 and 0.20 apfu (O = 12.5), respectively, suggesting the existence of two possible new end- members for epidote-group minerals: “Ba-piemontite [BaCa(Mn3+, Fe3+, Al)3Si3O12(OH)]” and "Pb- piemontite [PbCa(Mn3+, Fe3+, Al)3Si3O12(OH)]”. The abswunnbachite-braunite series minerals (Cu = 0.30-0.53 apfu: O = 12) contain up to 0.34 apfu Mg, indicating the exchange Mg(Mn2+, Cu)-1. Distribution coefficients for Sr between the hollandite-cryptomelane series and the piemontite-group minerals are up to 20. implying that the hollandite-type structure with its large open tunnel is more suitable for incorporation of Sr than the A2-site of the piemontite-group minerals. A synthetic alumi­nosilicate analogue of the hollandite-cryptomelane compound is stable under P > 8-10 GPa. and suggests the hollandite-type aluminosilicate may be a reservoir of Sr and other large-ion-lithophile elements in the upper mantle.

Details

Language :
English
ISSN :
0003004X and 19453027
Volume :
86
Issue :
3
Database :
Supplemental Index
Journal :
American Mineralogist (De Gruyter)
Publication Type :
Periodical
Accession number :
ejs35553002
Full Text :
https://doi.org/10.2138/am-2001-2-301