TY - JOUR
T1 - Cation ordering of (110) and (211) sectors in grandite garnet from Mali
AU - Nakamura, Yurie
AU - Kuribayashi, Takahiro
AU - Nagase, Toshiro
N1 - Funding Information:
We sincerely thank Mr. T. Ohyama for preparing the thin sections for optical observations, chemical analysis and picking up the specimens of X-ray experiments. The synchrotron XRD experiments were partially performed un-der the PAC #2014G081 and #2014G653. This study was partially supported by the Grants-in-Aid for Scientific Research of Ministry of Education (25400507 and 25400506) and the Excellent Graduate School for Earth Sciences, Tohoku University.
PY - 2016
Y1 - 2016
N2 - The cation ordering of the (110)c and (211)c growth sectors in birefringent garnet from Kayas, Mali was investigated by means of single-crystal X-ray diffraction (SC-XRD) method The chemical compositions of the (110)c and (211)c sectors were determined as (Ca2.96Mg0.04Mn0.04)Σ3.04(Fe0.97Al0.95Ti0.11)Σ2.03Si2.93O12, and (Ca2.91Mg0.05Mn0.03)Σ2.99(Fe1.01Al0.90Ti0.14)Σ2.05Si2.93O12, respectively. Reflections that violate the extinction rule for the space group Ia3d were observed, and crystal structure models for both the (110)c and (211)c sectors should have triclinic symmetry with the space group I1. The unit-cell parameters of both growth sectors were a = 11.9739(13), b = 11.9742(14), c = 11.9737(13) Å, α = 90.001(9), β = 90.098(9) and γ = 90.014 (10)° for the (110)c sector; a = 11.952(6), b = 11.952(6), c = 11.957(6) Å, α = 90.06(4), β = 90.01(4) and γ = 89.94(4)° for the (211)c sector. Structure refinements for I1 models of both sectors were convergent with R1 = 3.02 and 3.36%, respectively. There were significant differences in the Fe3+ distribution trend in the Y sites between the (110)c and (211)c sectors. The Fe3+ occupancies of the eight Y sites in the (110)c sector were 66.9(8), 66.0(8), 63.2(8), 60.0(8), 49.8(8), 49.5(8), 47.8(8), and 46.7(8)%. The octahedral Y sites of (110)c sector can be divided into two groups. In terms of symmetry, Fe3+ distribution in the Y site of the (110)c sector appeared to be pseudo-orthorhombic. In contrast, the Fe3+ distributions in the eight Y sites of the (211)c sector as follows: 60.0(10), 41.9(10), 62.7(10), 69.1(10), 55.5(10), 53.2(10), 55.7(10), and 43.5(10)%. The Fe3+ occupancies in the Y sites of the (211)c sector were random and different from that of the (110)c sector. Different cation distributions between the growth sectors in the Mali garnet indicate that cation ordering in the crystal structure was formed during growth. These observations suggest that the differences in the Fe3+ distribution between the (110)c and (211)c sectors are strongly affected by the growth process in each sector.
AB - The cation ordering of the (110)c and (211)c growth sectors in birefringent garnet from Kayas, Mali was investigated by means of single-crystal X-ray diffraction (SC-XRD) method The chemical compositions of the (110)c and (211)c sectors were determined as (Ca2.96Mg0.04Mn0.04)Σ3.04(Fe0.97Al0.95Ti0.11)Σ2.03Si2.93O12, and (Ca2.91Mg0.05Mn0.03)Σ2.99(Fe1.01Al0.90Ti0.14)Σ2.05Si2.93O12, respectively. Reflections that violate the extinction rule for the space group Ia3d were observed, and crystal structure models for both the (110)c and (211)c sectors should have triclinic symmetry with the space group I1. The unit-cell parameters of both growth sectors were a = 11.9739(13), b = 11.9742(14), c = 11.9737(13) Å, α = 90.001(9), β = 90.098(9) and γ = 90.014 (10)° for the (110)c sector; a = 11.952(6), b = 11.952(6), c = 11.957(6) Å, α = 90.06(4), β = 90.01(4) and γ = 89.94(4)° for the (211)c sector. Structure refinements for I1 models of both sectors were convergent with R1 = 3.02 and 3.36%, respectively. There were significant differences in the Fe3+ distribution trend in the Y sites between the (110)c and (211)c sectors. The Fe3+ occupancies of the eight Y sites in the (110)c sector were 66.9(8), 66.0(8), 63.2(8), 60.0(8), 49.8(8), 49.5(8), 47.8(8), and 46.7(8)%. The octahedral Y sites of (110)c sector can be divided into two groups. In terms of symmetry, Fe3+ distribution in the Y site of the (110)c sector appeared to be pseudo-orthorhombic. In contrast, the Fe3+ distributions in the eight Y sites of the (211)c sector as follows: 60.0(10), 41.9(10), 62.7(10), 69.1(10), 55.5(10), 53.2(10), 55.7(10), and 43.5(10)%. The Fe3+ occupancies in the Y sites of the (211)c sector were random and different from that of the (110)c sector. Different cation distributions between the growth sectors in the Mali garnet indicate that cation ordering in the crystal structure was formed during growth. These observations suggest that the differences in the Fe3+ distribution between the (110)c and (211)c sectors are strongly affected by the growth process in each sector.
KW - Cation ordering
KW - Garnet
KW - Sectoral structure
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U2 - 10.2465/jmps.160312
DO - 10.2465/jmps.160312
M3 - Article
AN - SCOPUS:85009360765
SN - 1345-6296
VL - 111
SP - 385
EP - 397
JO - Journal of Mineralogical and Petrological Sciences
JF - Journal of Mineralogical and Petrological Sciences
IS - 6
ER -