Crystal chemistry of K-tourmalines from the Kumdy-Kol microdiamond deposit, Kokchetav Massif, Kazakhstan

Abstract. Selected crystals of natural K-bearing tourmalines, extracted from a quartzofeldspathic rock from the Kumdy-Kol microdiamond deposit (an ultrahigh-pressure region of Kokchetav Massif, northern Kazakhstan), were characterized using a scanning electron microscope, an electron microprobe and single-crystal X-ray diffraction to investigate the impact of K uptake on the tourmaline structure. All the studied crystals belong to the maruyamaite–oxy-dravite/dravite compositional field, with K contents ranging from 0.03 to 0.47 apfu (atoms per formula unit), and contain a minor fluor-uvite component that increases towards oxy-dravite and dravite. The compositional variability of our samples can be expressed as a sequence of substitutions ranging from maruyamaite to oxy-dravite, dravite and fluor-uvite (or vice versa). Specifically, the substitutions that lead from maruyamaite to oxy-dravite to dravite are (1) XK + AlTOT + O1O ↔ XNa + MgTOT + O1O and (2) XNa + MgTOT + O1O ↔ XNa + MgTOT + O1OH, respectively. Conversely, the substitutions that lead from oxy-dravite to dravite to fluor-uvite are (1) XNa + MgTOT + O1O ↔ XNa + MgTOT + O1OH and (2) XNa + MgTOT + O1OH ↔ XCa + MgTOT + O1F, respectively. By analysing the difference between the bond valence sum and mean formal charge at the X site, we show that an increase in the K content (K > 0.21 apfu) results in the compression of X–O bonds (overbonded cation). Conversely, lower K contents lead to the stretching of the bonds (underbonded cation). Compared to the K-dominant analogues with ZFeO6 povondraite-type framework, K-bearing tourmalines with a smaller ZAlO6 framework such as maruyamaite should only be stable at higher-pressure conditions, as pressure is necessary to squeeze the relatively large K cation into the tighter X cavity. In both cases, the essential condition for the formation of K-dominant tourmalines is the extremely high K activity in the crystallization fluid. The K-tourmaline from the Kokchetav Massif may have crystallized under high-pressure (HP) conditions, with an upper limit between 3.5–7 GPa, during retrograde metamorphism following the ultrahigh-pressure (UHP) metamorphic peak.

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Journal
European Journal of Mineralogy
Published
2024-09-12
DOI
https://doi.org/10.5194/ejm-36-797-2024
Primary Topic
Geological and Geochemical Analysis
Type
article
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article

Crystal chemistry of K-tourmalines from the Kumdy-Kol microdiamond deposit, Kokchetav Massif, Kazakhstan

Andrey V. Korsakov, Ferdinando Bosi, Kira Musiyachenko, Beatrice Celata et al.
European Journal of Mineralogy
Geological and Geochemical Analysis
article

Crystal chemistry of K-tourmalines from the Kumdy-Kol microdiamond deposit, Kokchetav Massif, Kazakhstan

Andrey V. Korsakov, Ferdinando Bosi, Kira Musiyachenko, Beatrice Celata, Giovanni B. Andreozzi
article en

Abstract

Abstract. Selected crystals of natural K-bearing tourmalines, extracted from a quartzofeldspathic rock from the Kumdy-Kol microdiamond deposit (an ultrahigh-pressure region of Kokchetav Massif, northern Kazakhstan), were characterized using a scanning electron microscope, an electron microprobe and single-crystal X-ray diffraction to investigate the impact of K uptake on the tourmaline structure. All the studied crystals belong to the maruyamaite–oxy-dravite/dravite compositional field, with K contents ranging from 0.03 to 0.47 apfu (atoms per formula unit), and contain a minor fluor-uvite component that increases towards oxy-dravite and dravite. The compositional variability of our samples can be expressed as a sequence of substitutions ranging from maruyamaite to oxy-dravite, dravite and fluor-uvite (or vice versa). Specifically, the substitutions that lead from maruyamaite to oxy-dravite to dravite are (1) XK + AlTOT + O1O ↔ XNa + MgTOT + O1O and (2) XNa + MgTOT + O1O ↔ XNa + MgTOT + O1OH, respectively. Conversely, the substitutions that lead from oxy-dravite to dravite to fluor-uvite are (1) XNa + MgTOT + O1O ↔ XNa + MgTOT + O1OH and (2) XNa + MgTOT + O1OH ↔ XCa + MgTOT + O1F, respectively. By analysing the difference between the bond valence sum and mean formal charge at the X site, we show that an increase in the K content (K > 0.21 apfu) results in the compression of X–O bonds (overbonded cation). Conversely, lower K contents lead to the stretching of the bonds (underbonded cation). Compared to the K-dominant analogues with ZFeO6 povondraite-type framework, K-bearing tourmalines with a smaller ZAlO6 framework such as maruyamaite should only be stable at higher-pressure conditions, as pressure is necessary to squeeze the relatively large K cation into the tighter X cavity. In both cases, the essential condition for the formation of K-dominant tourmalines is the extremely high K activity in the crystallization fluid. The K-tourmaline from the Kokchetav Massif may have crystallized under high-pressure (HP) conditions, with an upper limit between 3.5–7 GPa, during retrograde metamorphism following the ultrahigh-pressure (UHP) metamorphic peak.

European Journal of MineralogyVol. 36(5)
National Agency for New Technologies, Energy and Sustainable Economic Development (IT), University of British Columbia (CA), V.S. Sobolev Institute of Geology and Mineralogy (RU), Sapienza University of Rome (IT)
Openalex Percentile: Top 84%
Geological and Geochemical Analysis
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