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Ferrorhodonite, CaMn3Fe[Si5O15], a new mineral species from Broken Hill, New South Wales, Australia

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Abstract

The new mineral ferrorhodonite, a Mn2+–Fe2+ ordered analogue of rhodonite with the idealized formula CaMn3Fe[Si5O15], was found in the manganese-rich metamorphic rocks of the Broken Hill Pb–Zn–Ag deposit, Yancowinna Co., New South Wales, Australia. Ferrorhodonite occurs as brownish red coarsely crystalline aggregates in association with galena, chalcopyrite, spessartine, and quartz. The mineral is brittle. Its Mohs hardness is 6. Cleavage is perfect on {201} and good on {021} and {210}. The measured and calculated values of density are 3.71 (2) and 3.701 g cm−3, respectively. Ferrorhodonite is optically biaxial positive, with α = 1.731 (4), β = 1.736 (4), γ = 1.745 (5) and 2 V (meas.) = 80 (10)°. The average chemical composition of ferrorhodonite is (electron-microprobe data, wt%): CaO 7.09, MgO 0.24, MnO 32.32, FeO 14.46, ZnO 0.36, SiO2 46.48, and total 100.95. The empirical formula calculated on 15 O apfu (Z = 2) is Ca0.81Mn2.92Fe1.29Mg0.04Zn0.03Si4.96O15. The Mössbauer and IR spectra are reported. The strongest reflections in the powder X-ray diffraction pattern [(d, Å (I, %) (hkl)] are: 3.337 (32) (−1–13), 3.132 (54) (−210), 3.091 (41) (0–23), 2.968 (100) (−2–11), 2.770 (91) (022), 2.223 (34) (−204), 2.173 (30) (−310). Ferrorhodonite is isostructural with rhodonite. The crystal structure was solved based on single-crystal X-ray diffraction data and refined to R 1 = 4.02% [for 3114 reflections with I > 2σ(I)]. The mineral is triclinic, space group P \(\bar{1}\), a = 6.6766 (5), b = 7.6754 (6), c = 11.803 (1) Å, α = 105.501 (1)°, β = 92.275 (1)°, γ = 93.919 (1)°; V = 580.44 (1). The crystal-chemical formula of ferrorhodonite inferred to be: M5(Ca0.81Mn0.19) M1−3(Mn2.52Fe0.48) M4(Fe 2+0.81 Mn0.12Mg0.04Zn0.03) [Si5O15]. .

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References

  • Back ME (2014) Fleischer’s glossary of mineral species. The Mineral Rec Inc, Tucson

    Google Scholar 

  • Birch WD (1999) Minerals of Broken Hill. Broken Hill City Council, Australia

    Google Scholar 

  • Brandenburg K, Putz H (2005) DIAMOND version 3. Crystal Impact GbR, Bonn

    Google Scholar 

  • Brown ID, Shannon RD (1973) Empirical bond strength–bond length curves for oxides. Acta Crystallogr A 29:266–282

    Article  Google Scholar 

  • Bruker (2009) APEX2 and SAINT. Bruker AXS Inc, Madison

    Google Scholar 

  • Chukanov NV (2014) Infrared spectra of mineral species: extended library. Springer, Dordrecht

    Book  Google Scholar 

  • Dickson BL (1975) The iron distribution in rhodonite. Am Mineral 60:98–104

    Google Scholar 

  • Dyar MD, Agresti DG, Schaefer MW, Grant CA, Sklute EC (2006) Mössbauer spectroscopy of earth and planetary materials. Annu Rev Earth Planet Sci 34:83–125

    Article  Google Scholar 

  • Frost RB, Mavrogenes JA, Tomkins AG (2002) Partial melting of sulfide ore deposits during medium- and high-grade metamorphism. Can Mineral 40:1–18

    Article  Google Scholar 

  • Frost RB, Swapp SM, Gregory RW (2005) Prolongedd existence of sulfide melt in the Broken Hill orebody, New South Wales, Australia. Can Mineral 43:479–493

    Article  Google Scholar 

  • Griffen DT, Nelson WR (2007) Mössbauer spectroscopy of Zn-poor and Zn-rich rhodonite. Am Mineral 92:1486–1491

    Article  Google Scholar 

  • Henderson EP, Glass JJ (1936) Pyroxmangite, a new locality: identity of sobralite and pyroxmangite. Am Mineral 21:273–294

    Google Scholar 

  • Hietanen A (1938) On the petrology of Finnish quartzites. Bull Comm Geol Finl 122:1–119

    Google Scholar 

  • Ibers JA, Hamilton WC (eds) (1974) International tables for X-ray crystallography, vol IV. The Kynoch Press, Birmingham

    Google Scholar 

  • Leverett P, Williams PA, Hibbs DE (2008) Ca-Mg-Fe-rich rhodonite from the Morro da Mina mine, Conselheiro Lafaiete, Minas Gerais, Brasil. Mineral Rec 44:149–184

    Google Scholar 

  • Liebau F, Hilmer W, Lindemann G (1959) Über die Kristallstruktur des Rhodonit (Mn, Ca)SiO3. Acta Crystallogr 12:182–187

    Article  Google Scholar 

  • Mason B (1973) Manganese silicate minerals from Broken Hill, New South Wales. J Geol Soc Aust 20:397–404

    Article  Google Scholar 

  • Nelson WR, Griffen DT (2005) Crystal chemistry of Zn-rich rhodonite (“fowlerite”). Am Mineral 90:969–983

    Article  Google Scholar 

  • Ohashi Y, Finger LW (1975) Pyroxenoids: a comparison of refined structures of rhodonite and pyroxmangite. Carnegie Inst Wash Year Book 74:564–569

    Google Scholar 

  • Peacor DR, Niizeki N (1963) The redetermination and refinement of the crystal structure of rhodonite. (Mn, Ca)SiO3. Z Kristallogr 119:98–116

    Article  Google Scholar 

  • Peacor DR, Essene EJ, Brown PE, Winter GA (1978) The crystal chemistry and petrogenesis of a magnesian rhodonite. Am Mineral 63:1137–1142

    Google Scholar 

  • Petříček V, Dušek M, Palatinus L (2006) Jana 2006. Structure determination software programs. Institute of Physics, Praha

    Google Scholar 

  • Prescher C, McCammon C, Dubrovinsky L (2012) MossA—a program for analyzing energy-domain Mössbauer spectra from conventional and synchrotrone sources. J Appl Crystallogr 45:329–331

    Article  Google Scholar 

  • Minerals. Reference book (1981) vol 3, part. 2, Nedra Publishing, Moscow (in Russian)

  • Shannon RD, Prewitt CT (1969) Effective ionic radii in oxides and fluorides. Acta Crystallogr. B 25:925–946

    Article  Google Scholar 

  • Walters SG (1998) Broken Hill-type deposits. J Aust Geol Geophys 17(4):229–237

    Google Scholar 

Download references

Acknowledgements

We are grateful to Robert F. Martin and anonymous reviewer for valuable comments. This study was supported by the Russian Science Foundation, Grant No. 14-17-00048 (in part of mineralogical studies) and Foundation of the President of the Russian Federation, Grant No. MK-8033.2016.5 (refinement of the crystal structure). The electron-microprobe analyses were performed at the Laboratory of Analytical Techniques of High Spatial Resolution, Department of Petrology, Moscow State University, using a microprobe instrument JEOL JXA-8230 purchased with the financial support by the Program for Development of MSU.

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Correspondence to Nadezhda V. Shchipalkina.

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Shchipalkina, N.V., Chukanov, N.V., Pekov, I.V. et al. Ferrorhodonite, CaMn3Fe[Si5O15], a new mineral species from Broken Hill, New South Wales, Australia. Phys Chem Minerals 44, 323–334 (2017). https://doi.org/10.1007/s00269-016-0860-3

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