Introduction
Feldspars are traditionally considered to have the composition MT4O8, where M is a large cation such as K, Na or Ca, while T is tetrahedral Al and Si “linked in an infinite three-dimensional array” (Ribbe, Reference Ribbe and Ribbe1983). The feldspar group currently approved by the Commission on New Minerals, Nomenclature and Classification of the International Mineralogical Association (IMA–CNMNC, Back, Reference Back2022), constitutes 20 minerals, though three have an overall M:T ratio of 3:8 (for example, banalsite) instead of the more common 1:4, and dmisteinbergite is not included, presumably as it is not a framework silicate (Krivovichev, Reference Krivovichev2020). In contrast, Krivovichev (Reference Krivovichev2020) proposed that feldspars be considered a family of minerals with the composition M[T4O8], thereby following Mills et al. (Reference Mills, Hatert, Nickel and Ferraris2009, p. 1074), “mineral families apply to groups and/or supergroups having similar structural and/or chemical features that make them unique.” A prime example of a family cited by Mills et al. (Reference Mills, Hatert, Nickel and Ferraris2009) is the zeolite family, in which all members are characterised by microporous tetrahedral frameworks with large cavities containing H2O molecules, although they belong to different groups and supergroups.
Wodegongjieite, ideally KCa3(Al7Si9)O32, but with the empirical formula (K0.580Sr0.155□0.265)(Ca0.75Sr0.035□0.215)3(Al7.2Si8.8)O32, is, potentially, a new member of the feldspar family as proposed by Krivovichev (Reference Krivovichev2020), being isostructural with kokchetavite (KAlSi3O8) and topologically identical to dmisteinbergite (CaAl2Si2O8), both of which are layered silicates that are polymorphs of sanidine/orthoclase/microcline and anorthite, respectively. Similarly to these two polymorphs, wodegongjieite would be expected to have crystallised metastably in lieu of a feldspar according to Goldsmith's (Reference Goldsmith1953) ‘simplexity principle’ (e.g. Krivovichev, Reference Krivovichev2012; Reference Krivovichev2013; Reference Krivovichev2020; Zolotarev et al., Reference Zolotarev, Krivovichev, Panikorovskii, Gurzhiy, Bocharov and Rassomakhin2019).
In the present paper, we report a description of wodegongjieite from the type locality and consider how wodegongjieite can be best classified and why wodegongjieite crystallised instead of a mixture of dmisteinbergite and kokchetavite as would be expected from application of Ostwald's step rule together with Goldsmith's (Reference Goldsmith1953) ‘simplexity principle’.
The name wodegongjieite is based on the Tibetan name of a famous mountain visible from the area close to the Luobusa chromitite deposit (Fig. 1). This peak is one of the four pre-Buddhist sacred mountains of Tibet and bears the name of the father of all other Tibetan mountain deities. Our choice of spelling is based in part on the pronunciation in Tibetan. Prof. Badengzhu (personal communication) advised us that the Tibetan name of the mountain and the deity associated with the sacred mountain is ’o de gung rgyal: འོ་དེ་གུང་རྒྱལ, and that the initial transliterated Tibetan character ’O written in the conventional Tibetan transliteration as the letter O preceded by a right apostrophe, is pronounced ‘wo’ with the w pronounced as w in ‘word’, not as v in ‘volume’. The Chinese name for the mineral would be 沃德贡杰石, transliterated into English as ‘vodegongjieite’. We adopted this pronunciation for the second part of the Chinese name, 贡杰, giving ‘wodegongjieite’, which is easier to pronounce in English than alternative combinations. Transliteration into Russian is relatively easy: ‘водегонгджиеит’ as in Russian, as in German, the initial letter would be pronounced ‘V’ in any case.
Fig. 1. (a) ‘Vod-de-gung-rgyal’ (Wodegongjie) Mountain as seen from the Luobusa ophiolite, Tibet, China. Prof. Jingsui Yang at scientific drilling site LSD-2. (b) Telephoto of ‘Vod-de-gung-rgyal’ (Wodegongjie) Mountain courtesy of Fahui Xiong. View from south to north.
Both mineral and name (symbol Wgj) were approved by the IMA–CNMNC (IMA2020-036b, Xiong et al., Reference Xiong, Xu, Mugnaioli, Gemmi, Wirth, Yang and Grew2022b). Type material is deposited in the mineralogical collections of the Chinese Geological Museum, Xisiyangrouhutong 15th, Xicheng district, Beijing, China, catalogue number M16104.
Occurrence
Wodegongjieite occurs in the Cr-11 orebody, one of several significant chromitite deposits in the Luobusa ophiolite, Tibet, China (Fig. 2), which is located ~200 km east-southeast of Lhasa. The Cr-11 orebody (Fig. 3), elevation of 5300 m, is located at 29°11′N, 92°18′E in the Kangjinla district. Wodegongjieite is found in two inclusions (Figs 4–6) of highly reduced compounds enclosed in corundum that was recovered during the processing of 1100 kg of chromitite, described in detail by Xu et al. (Reference Xu, Yang, Chen, Fang and Bai2009, Reference Xu, Yang, Robinson, Xiong, Ba and Guo2015). The mineral separation was carried out at the Institute of Multipurpose Utilization of Mineral Resources, Chinese Academy of Geological Sciences, Zhengzhou. Xu et al. (Reference Xu, Yang, Chen, Fang and Bai2009, Reference Xu, Yang, Robinson, Xiong, Ba and Guo2015) reported that before processing, all worksites and equipment were cleaned carefully to avoid contamination. Xiong et al. (Reference Xiong, Xu, Mugnaioli, Gemmi, Wirth, Grew, Robinson and Yang2020, Reference Xiong, Xu, Mugnaioli, Gemmi, Wirth, Grew and Robinson2022a) reviewed the evidence regarding the origin of the corundum and the challenges posed by Litasov et al. (Reference Litasov, Kagi and Bekker2019a, Reference Litasov, Bekker and Kagi2019b) and by Ballhaus et al. (Reference Ballhaus, Wirth, Fonseca, Blanchard, Pröll, Bragagni, Nagel, Schreiber, Dittrich, Thome, Hezel, Below and Cieszynski2017, Reference Ballhaus, Fonseca and Bragagni2018, Reference Ballhaus, Helmy, Fonseca, Wirth, Schreiber and Jöns2021), and concluded that the majority of data supports a natural and deep-seated origin for the corundum and the minerals included in it.
Fig. 2. Map of the Luobusa ophiolite, Tibet, China showing the Cr-31 and Cr-11 chromitite orebodies (stars). Wodegongjieite was recovered from Cr-11. The Zedang Formation is exposed in a small area ~5 km east of the Cr-31 orebody. Map is from Xiong et al. (2022a, figure 1). Published with permission from American Mineralogist.
Fig. 3. Exposure showing the Cr-11 chromitite orebody from which wodegongjieite was recovered, Luobusa ophiolite, Tibet, China. The chromitite is enveloped by dunite. From Xiong et al. (Reference Xiong, Xu, Mugnaioli, Gemmi, Wirth, Grew, Robinson and Yang2020, figure S1(a)).
Fig. 4. Back-scattered electron image of the corundum grain showing the source of foil #5358, studied in detail. The inset shows an enlargement of the spheroid composed of TiSi2 (zhiqinite), TiP (badengzhuite), Ti10(Si,P,□)7 (wenjiite) and Ti11(Si,P)10 (kangjinlaite). Images taken at the Center for Advanced Research on the Mantle. From Xiong et al. (Reference Xiong, Xu, Mugnaioli, Gemmi, Wirth, Grew, Robinson and Yang2020, figure 2).
Wodegongjieite is found in two parageneses. (1) In the holotype sample (foil #5358), it forms a partial overgrowth up to 1.5 μm thick around a spheroid 20 μm across of Ti–Si–P intermetallics (Figs 4 and 5). Associated minerals include zhiqinite, TiSi2 (Xiong et al., Reference Xiong, Xu, Mugnaioli, Gemmi, Wirth, Grew, Robinson and Yang2020), badengzhuite, TiP (Xiong et al., Reference Xiong, Xu, Mugnaioli, Gemmi, Wirth, Grew, Robinson and Yang2020), wenjiite, Ti10(Si,P,□)7 (Xiong et al., Reference Xiong, Xu, Mugnaioli, Gemmi, Wirth, Yang and Grew2022c) and kangjinlaite, Ti11(Si,P)10 (Xiong et al., Reference Xiong, Xu, Mugnaioli, Gemmi, Wirth, Yang and Grew2022c). Kangjinlaite and wenjiite, constitute about one third of the spheroid (brighter of two phases in the back-scattered electron (BSE) image, Fig. 4). Zhiqinite, TiSi2, constitutes much of the remainder of the spheroid (less bright phase in BSE image).
Fig. 5. High-angle annular dark-field scanning-transmission electron microscope (HAADF–STEM) image of foil #5358 showing an aggregate of zhiqinite, TiSi2, several of which have a tabular habit, enclosing globules of badengzhuite, TiP and surrounded by wenjiite (Ti10(Si,P,□)7) and kangjinlaite Ti11(Si,P)10. Al2O3 – corundum hosting the Ti silicide inclusion. Seven chemical analyses were obtained within 1 μm of the white rectangle marking the location for collecting the three-dimensional electron diffraction data. The image was obtained at the Istituto Italiano di Tecnologia. Modified from figure 1 of Xiong et al. (Reference Xiong, Xu, Mugnaioli, Gemmi, Wirth, Yang and Grew2022c). Published with permission from American Mineralogist.
An unidentified phase with the composition SiO2 53.8, Al2O3 16.2, MgO 20.1, CaO 0.3, SrO 2.0, K2O 7.6, Sum 100 wt.% (uncalibrated energy-dispersive X-ray spectroscopy (EDX) analysis) is also present with wodegongjieite in the overgrowth. The phase could be a milarite (osumilite) group mineral as the a cell parameter 10.1 Å (in hexagonal settings) fits quite well and extinctions appear consistent with P6/mcc symmetry. However, the c parameter of 15.6 Å is greater than in most milarite-group minerals (e.g. Armbruster and Oberhänsli, Reference Armbruster and Oberhänsli1988; Gagné and Hawthorne, Reference Gagné and Hawthorne2016), even allowing for errors in the measurement. Recalculating the chemical analysis assuming the phase belongs to the milarite group gives AMg2B(K0.70Sr0.19Ca0.05)Σ0.94CKT (1)Mg3T (2)(Si9.36Al3.31Mg0.23)Σ12.90O30, that is, there is an excess of cations at the A, T(1) and T(2) sites. The unidentified phase and wodegongjieite are close to having parallel orientation, but there is misalignment along c of ~10°. Further characterisation of this phase was not possible because the short tilt range and thickness of the sample in this part of the foil preclude obtaining electron diffraction data of sufficient quality.
(2) In foil #6034, wodegongjieite fills interstices up to 0.25 μm wide between wenjiite, jingsuiite, TiB2 (Xiong et al., Reference Xiong, Xu, Mugnaioli, Gemmi, Wirth, Grew and Robinson2022a), osbornite–khamrabaevite and corundum (Fig. 6). Identification as wodegongjieite in foil #6034 was confirmed by an EDX spectrum showing the presence of Si, Al, K and Ca, as well as diffraction data indicating that it has the cell of holotype wodegongjieite.
Fig. 6. (a) Bright-field and (b) high-angle annular dark-field scanning-transmission electron microscope (HAADF–STEM) images of foil #6034 showing a portion of a lamellar intergrowth of osbornite–khamrabaevite, Ti(C,N), jingsuiite, TiB2, and wenjiite, Ti10(Si,P,□)7. Al2O3 – corundum hosting the lamellar intergrowth. Wodegongjieite forms pools between corundum and wenjiite, Ti10(Si,P,□)7. Its identification was confirmed by diffraction data, and the chemical composition is similar to that in foil #5358, but the small size precludes meaningful quantitative analysis. The images were obtained at the GFZ German Research Centre for Geosciences. Modified from figure 7 of Xiong et al. (Reference Xiong, Xu, Mugnaioli, Gemmi, Wirth, Grew and Robinson2022a). Published with permission from American Mineralogist.
Optical and physical properties
As in the case of the closely related mineral kokchetavite (Hwang et al., Reference Hwang, Shen, Chu, Yui, Liou, Sobolev, Zhang, Shatsky and Zayachkovsky2004), wodegongjieite is too fine-grained for optical and physical properties to be determined. However, it is expected to have some of the properties reported for the next most closely related mineral, dmisteinbergite, from the type locality (Chesnokov et al., Reference Chesnokov, Lotova, Nigmatullina, Pavlutchenko and Bushmakin1990; Zolotarev et al., Reference Zolotarev, Krivovichev, Panikorovskii, Gurzhiy, Bocharov and Rassomakhin2019) and from syntheses (Davis and Tuttle Reference Davis and Tuttle1952), e.g. presumably transparent, uniaxial (+) with birefringence ≈ 0.005 and refractive indices ≈ 1.57–1.59; colour presumably whitish to colourless; lustre presumably vitreous; Mohs hardness presumably ~6 and tenacity presumably brittle. Density was calculated to be 2.694 g⋅cm–3 from the dynamical structure refinement constrained by the EDX analyses.
Chemical composition
Spectra of wodegongjieite revealed that the major constituents are Al2O3, SiO2, K2O, CaO and SrO, which were measured with transmission electron microscopy operating at 120 kV and equipped with a Bruker EDX XFlash6T-60 detector. (acceleration voltage = 120 kV). Our EDX uses the thin-specimen approximation by Cliff and Lorimer (Reference Cliff and Lorimer1975). Because of the overlap between SiKα and SrLα lines, the SrKα lines were used to establish the presence of Sr and to measure its content. Quantification software on an earlier set of four analyses gave a trace of Na in one, but below the 1σ value, and no Na in the other three, and thus the amount of Na was assumed to be below the detection limit. Solution and refinement of the crystal structure did not reveal any evidence for OH, H2O or CO2.
Because the EDX analyses were not calibrated with standards, within 9 days of analysing wodegongjieite (Table 1; Supplementary Table S1), we analysed K-feldspar and cowlesite, ideally KAlSi3O8 and Ca(Al2Si3)O10⋅5–6H2O, respectively, by the same method, that is, also without standards (Supplementary Table S2). No drift is expected to occur over the 9 day interval, as no drift was reported during the 6 months involved in the analysis of wenjiite and kangjinlaite (Xiong et al., Reference Xiong, Xu, Mugnaioli, Gemmi, Wirth, Yang and Grew2022c). The standardless EDX analyses gave a good stoichiometry and charge balance for both K-feldspar and cowlesite in terms of the four most abundant constituents, Al, Si, K and Ca if one includes Na in the total for Ca in cowlesite. Although the analyses were not standardised, we are confident that the EDX analyses of wodegongjieite also give a reasonable stoichiometry.
Table 1. Chemical composition (in wt.%) of wodegongjieite in foil #5358.*
* Note: Mean, range and standard deviation (S.D.) of 7 determinations.
The empirical formula based on the average composition (Table 1) and normalised to Si + Al = 16 cations is K0.58Sr0.26Ca2.25Al7.20Si8.80O31.20 (Supplementary Table S1). Although analytical data on the internal standards yielded near ideal charge balance (Supplementary Table S2), the empirical formula shows a deficiency in positive charges: O should be 32. The simplified formula is (K,□,Sr)(Ca,□,Sr)3(Si,Al)16O32 and the ideal formula is KCa3(Al7Si9)O32, which requires SiO2 48.59, Al2O3 32.06, K2O 4.23, CaO 15.12, Total 100 wt.%.
Crystallography
Powder X-ray diffraction
It was not possible to obtain a powder X-ray diffraction pattern for this mineral. As this is normally required for new minerals to be approved by the IMA–CNMNC a simulated pattern was obtained (Supplementary Table S3) with GSAS II in Debye Scherrer geometry with a monochromatic CuKα1 radiation (λ = 1.540598 Å) using the software PowderCell 2.4 (Kraus and Nolze, Reference Kraus and Nolze1996). The angular limit is 80° (~1.2 Å).
Single-crystal three-dimensional electron diffraction
Method
Three dimensional-electron diffraction (3DED) data (Kolb et al., Reference Kolb, Gorelik, Kübel, Otten and Hubert2007; Mugnaioli and Gemmi Reference Mugnaioli and Gemmi2018; Gemmi et al., Reference Gemmi, Mugnaioli, Gorelik, Kolb, Palatinus, Boullay, Hovmöller and Abrahams2019) on wodegongjieite in foil #5358 were collected at the Center for Nanotechnology Innovation@NEST by a Zeiss Libra TEM operating at 120 kV and equipped with a LaB6 source and a Bruker EDX detector XFlash6T-60. 3DED acquisitions were performed in STEM mode after defocussing the beam in order to have a pseudo-parallel illumination on the sample. A beam size of ~150 nm in diameter was obtained by inserting a 5 μm C2 condenser aperture. An extremely mild illumination was adopted to avoid any alteration or amorphatisation of the sample.
3DED data were taken in discrete steps of 1° with a precessing beam (Vincent and Midgley, Reference Vincent and Midgley1994; Mugnaioli et al., Reference Mugnaioli, Gorelik and Kolb2009) obtained by a Nanomegas Digistar P1000 device. The precession semi-angle was kept at 1°. An in-column Ω-filter was used to filter-out the inelastic scattering contribution. The total tilt range was 90°, slightly limited by the thickness of the FIB lamellae. Camera lengths was 180 mm, with a theoretical resolution limit of 0.75 Å. Electron diffraction data were recorded by an ASI Timepix detector (van Genderen et al., Reference van Genderen, Clabbers, Das, Stewart, Nederlof, Barentsen, Portillo, Pannu, Nicolopoulos, Gruene and Abrahams2016), able to record the arrival of single electrons and deliver a pattern that is virtually background-free. Data were analysed using ADT3D (Kolb et al., Reference Kolb, Mugnaioli and Gorelik2011) for cell and space group determination and for intensity integration. Ab initio structure determination and refinement were obtained using direct methods implemented in the software SIR2014 (Burla et al., Reference Burla, Caliandro, Carrozzini, Cascarano, Cuocci, Giacovazzo, Mallamo, Mazzone and Polidori2015). Data were treated with the kinematical approximation (I hkl proportional to F 2hkl).
The structure was refined by taking into account the dynamical effects, as proposed by Palatinus et al. (Reference Palatinus, Petříček and Corrêa2015a, Reference Palatinus, Corrêa, Steciuk, Jacob, Roussel, Boullay, Klementová, Gemmi, Kopeček, Domeneghetti, Cámara and Petříček2015b, Reference Palatinus, Brázda, Boullay, Perez, Klementová, Petit, Eigner, Zaarour and Mintova2017). These authors presented the theory and practice of dynamical refinements of 3DED data, which is now fully implemented in the PETS2 (Palatinus et al., Reference Palatinus, Brázda, Jelinek, Hrda, Steciuk and Klementová2019) and JANA software (Petříček et al., Reference Petříček, Dusek and Palatinus2014). In this procedure, each diffraction pattern is refined separately using Bloch wave formalism. Together with the structure, the sample thickness and the geometrical orientation of each pattern are also refined using a simple platelet model for the sample shape.
Procedure for refining the structure
The 3DED data set collected after energy-filtering the inelastic scattering gave a nice ab initio structure solution in the hexagonal space group P6/mcc (#192) with a = 10.2(2) Å, c = 14.9(3) Å, V = 1340(50) Å3 and Z = 2 (Fig. 7). The empirical formula was used for modelling except that O was set equal to 32: K0.58Sr0.26Ca2.25Al7.20Si8.80O32 instead of 31.20 as calculated from charge balance. The structure was solved ab initio by direct methods. The four cation and four oxygen positions were clearly spotted in the first potential map.
Fig. 7. Three-dimensional reconstruction of electron diffraction data taken from wodegongjieite in foil #5358 (Fig. 4). Cell edges are sketched in yellow. Red arrow indicates a* direction, green arrow indicates b* direction and blue vector indicates c* direction. Note that these panels show projections of a three-dimensional diffraction volume and are not conventional two-dimensional electron diffraction patterns. Each apparent reflection is indeed a column of reflections piled along the viewing direction. Data were obtained at the Istituto Italiano di Tecnologia.
The empirical formula was used for the dynamical refinement except that O was set equal to 32: K0.58Sr0.26Ca2.25Al7.20Si8.80O32 instead of 31.20 as calculated from charge balance. In an earlier refinement of the structure, we attempted to refine Al and Si occupancy of the tetrahedral sites. An unconstrained refinement gave Si2 to be nearly 100% Si and Si1 to be ~50% Si and 50% Al, whereas the average T1–O and T2–O bond lengths came out to be 1.66 Å and 1.65 Å, respectively. That is, ordering of Si and Al at the T sites is not evident in the (Si,Al)–O bond lengths.
The current refinement, which assumes complete Si–Al disorder, gives average T1–O and T2–O bond lengths of 1.65 Å (Table 2, crystallographic information file deposited as Supplementary material), which are sufficiently close to exclude the possibility of measurable order. These average T–O bond lengths are consistent within the uncertainties of the measurements with a T–O length = 1.673 Å calculated for complete disorder and Si–O = 1.61 Å and Al–O = 1.75 Å for feldspars (Smith and Bailey, Reference Smith and Bailey1963). The total charge received by Si1 is somewhat higher than the formal charge, whereas total charge received by Si2 is somewhat lower (Table 3), which could indicate some ordering of Si and Al, but not enough to affect average bond lengths.
Table 2. Coordinates and isotropic displacement parameters (U iso, Å2) of atoms in wodegongjieite.
Table 3. Polyhedra in wodegongjieite.*
* Note: Q: Total charge received by the ion, q: Formal charge (oxidation number)
In principle, it would be best to refine the occupancies of the large cation sites 6f and 2a with no assumptions. However, we are dealing with four constituents: Ca, K, Sr and vacancy (□), and such an unconstrained refinement is not practical with electron diffraction data. Nonetheless, the ab initio model clearly shows that the 2a and 6f sites have different sizes and coordination. Consequently, we imposed the condition that all the K occupies the 2a site as the average K–O bond length of 3.07 Å is close to the average K–O bond lengths reported in kokchetavite, 3.1453 Å and 3.144 Å for K1–O and K2–O, respectively (Romanenko et al., Reference Romanenko, Raschchenko, Sokol, Korsakov, Seryotkin, Glazyrin and Musiyachenko2021). We also imposed the condition that all the Ca occupies the 6f site as the average Ca–O bond length of 2.60 Å (2.36 Å and 2.84 Å for Ca–O1 and Ca–O3, respectively) is reasonable for Ca–O, e.g. dmisteinbergite has 2.429–2.461 Å (Zolotarev et al., Reference Zolotarev, Krivovichev, Panikorovskii, Gurzhiy, Bocharov and Rassomakhin2019). For the final refinement, Al:Si was fixed to the same ratio for the two tetrahedral sites. K and Ca are fixed to the values from EDX and assigned to the 2a and 6f sites, respectively. Total Sr was constrained to the EDX value, but free to occupy either the 2a site or the 6f site or both. We emphasise that K and Ca occupancies were not assumed but determined from the bond lengths. All thermal parameters were refined free of constraints and converge to positive and reasonable values, supporting the correctness of our approach.
Description of the crystal structure.
Wodegongjieite is a sheet silicate (Hawthorne et al., Reference Hawthorne, Uvarova and Sokolova2019) in which the layers comprise rings of tetrahedra joined alternatively by large cations and apical oxygens (Fig. 8). The structure most closely resembles that of kokchetavite, in which K occupies two sites (Romanenko at al., Reference Romanenko, Raschchenko, Sokol, Korsakov, Seryotkin, Glazyrin and Musiyachenko2021). One K site is close to perfectly hexagonal (2a), whereas the second K site (6f) is slightly distorted; six of the distorted rings surround an undistorted ring (Fig. 9). As in kokchetavite, there are two crystallographically distinct sites for the large cations K, Ca and Sr in wodegongjieite. However, substitution of K by Ca at the 6f site is associated with marked rotation of the (Si,Al) tetrahedra and a collapse of the structure to accommodate the smaller Ca ion (Fig. 9). Coordination of Ca at 6f becomes four short (2.37Å) and four long (2.85Å) Ca–O bonds (Table 3). As viewed down [001], the tetrahedral framework in wodegongjieite resembles a pinwheel consisting of six wings of the tetrahedra coordinated to Ca surrounding a central hexagon around K (Fig. 9).
Fig. 8. View of the wodegongjieite structure along [1$\bar{1}$
0]. Drawn using Vesta (Momma and Izumi, Reference Momma and Izumi2011).
Fig. 9. Comparison of the wodegongjieite (this study) with kokchetavite (Romanenko et al., Reference Romanenko, Raschchenko, Sokol, Korsakov, Seryotkin, Glazyrin and Musiyachenko2021) and dmisteinbergite (Dimitrijević et al., Reference Dimitrijević, Dondur and Kremenović1996) viewed along [001]. The layers for wodegongjieite and kokchetavite were cut for z/c ranging from 0 to 1, whereas that for dmisteinbergite was cut for z/c ranging from 0.25 to 1.25. Drawn using Momma and Izumi (Reference Momma and Izumi2011).
The collapsed ring around Ca in wodegongjieite differs from the rings surrounding Ca in dmisteinbergite, in which there is only one type of tetrahedral ring and this has a nearly triangular outline (Fig. 9).
Discussion
Distinction of wodegongjieite from closely related minerals and synthetics
The minerals closest to wodegongjieite in terms of crystal structure and composition are dmisteinbergite, CaAl2Si2O8, and kokchetavite, KAlSi3O8, both sheet silicates that are polymorphs of feldspar (Hawthorne et al., Reference Hawthorne, Uvarova and Sokolova2019; Krivovichev, Reference Krivovichev2020). The recent crystal structure refinement of synthetic kokchetavite (Romanenko et al., Reference Romanenko, Raschchenko, Sokol, Korsakov, Seryotkin, Glazyrin and Musiyachenko2021) was critical to recognising wodegongjieite as a new mineral distinct from dmisteinbergite and kokchetavite because this refinement enabled comparison of the three minerals with greater clarity as follows:
(1) Wodegongjieite and kokchetavite are isostructural in space group P6/mcc (#192). The two large-cation sites 2a and 6f are present within each and every layer of both minerals. However, the two minerals differ in occupancies of the 6f site – dominantly Ca in wodegongjieite and entirely K in kokchetavite. Ordering of the layers does not affect this distinction.
(2) Wodegongjieite and dmisteinbergite are not isostructural, although topologically identical. Stacking disorder of the layers in dmisteinbergite can produce two independent Ca sites, but stacked along c, whereas the tetrahedral rings around Ca are the same from one layer to the next, albeit rotated relative to one another. Thus, the two sites for large cations in dmisteinbergite are different from the two sites for large cations in kokchetavite and wodegongjieite, which are present in each and every layer.
(3) Converting wodegongjieite to a dmisteinbergite containing 21% KAlSi3O8 in solid solution with CaAl2Si2O8, that is, without changing the bulk K/Ca ratio in wodegongjieite, would require disordering of Ca and K at the 6f and 2a sites to such an extent that distinction between the two sites would no longer be significant. This requirement seems to be sufficient to distinguish wodegongjieite from a ‘potassian dmisteinbergite’ containing 21% KAlSi3O8 in solid solution. Significant KAlSi3O8 solid solution in dmisteinbergite has not been reported from other localities, the maximum K2O reported is 0.12 wt.% (Chesnokov et al., Reference Chesnokov, Lotova, Nigmatullina, Pavlutchenko and Bushmakin1990; Simakin et al., Reference Simakin, Eremyashev and Kucherinenko2010; Ma et al., Reference Ma, Krot and Bizzarro2013; Fintor et al., Reference Fintor, Park, Nagy, Pál-Molnár and Krot2014, Di Pierro and Gnos, Reference Di Pierro and Gnos2016).
(4) Plotting the cell parameters and cell volume versus K/(K+Ca) ratio in dmisteinbergite, wodegongjieite (K/(K+Ca) = 0.21) and kokchetavite yield a nearly perfect linear fit for the c parameter (Fig. 10), implying layer thickness is largely influenced by the size of the cations occupying the 6f and 2a sites. Allowing for the large uncertainties in the cell parameters for wodegongjieite, the plot suggests that the a parameter and cell volume for dmisteinbergite plot somewhat above extensions of the lines linking wodegongjieite and kokchetavite, that is, the P6/mcc structure with two sites for Ca and K is slightly more compact at a given K/Ca ratio than the P63/mcm structure with only a single site for Ca and K. In the Ca free-system, the cell volume for kokchetavite is 0.71% smaller than the corresponding cell volume for ‘K-cymrite', which like dmisteinbergite, has but a single site for the large cation (Romanenko et al., Reference Romanenko, Raschchenko, Sokol, Korsakov, Seryotkin, Glazyrin and Musiyachenko2021). However, the small reduction in cell volume on dehydration of ‘K-cymrite' to kokchetavite (Fig. 10) differs in that it is achieved through a simultaneous decrease in the c cell parameter and increase in the a cell parameter.
Fig. 10. Plot of cell parameters and volumes of kokchetavite, wodegongjieite, dmisteinbergite and K-cymrite as a function of the K/(K+Ca) ratio. The a cell parameter has been doubled and the cell volume quadrupled in dmisteinbergite so as to be directly comparable with the corresponding parameters in wodegongjieite and kokchetavite; those of ‘K-cymrite' multiplied 8-fold. The linear fit (R 2 = 0.999) to the c parameter applies to kokchetavite, wodegongjieite and dmisteinbergite, whereas the linear fits to the a parameter and cell volume apply only to the P6/mcc structure. Sources of data are Zolotarev et al. (Reference Zolotarev, Krivovichev, Panikorovskii, Gurzhiy, Bocharov and Rassomakhin2019), Romanenko et al. (Reference Romanenko, Raschchenko, Sokol, Korsakov, Seryotkin, Glazyrin and Musiyachenko2021) and this study for: dmisteinbergite; kokchetavite and K-cymrite; and wodegongjieite, respectively. The parameters reported by Dimitrijevic et al. (Reference Dimitrijević, Dondur and Kremenović1996) for synthetic dmisteinbergite (not shown) are close to the plotted values.
In summary, the distinction between wodegongjieite and dmisteinbergite is both structural and compositional. Structural because the wodegongjieite has two distinct large-cation sites in each layer, whereas dmisteinbergite has only one such site. Compositional because one of the two sites, namely 2a, is occupied dominantly by K in wodegongjieite. That is, wodegongjieite is closer structurally to kokchetavite than to dmisteinbergite despite its being closer to dmisteinbergite in terms of bulk K/(K+Ca) ratio. We have chosen a completely new name ‘wodegongjieite’ in order to reflect this interpretation of the relationship among the three minerals.
Wodegongjieite has not yet been synthesised. As far we are aware, kokchetavite has only been synthesised by dehydrating the K-analogue of cymrite, KAlSi3O8⋅H2O (Thompson et al., Reference Thompson, Parsons, Graham and Jackson1998; Kanzaki et al., Reference Kanzaki, Xue, Amalberti and Zhang2012; Romanenko et al., Reference Romanenko, Raschchenko, Sokol, Korsakov, Seryotkin, Glazyrin and Musiyachenko2021); no direct synthesis from the oxides or from a melt has been reported.
Conditions of crystallisation of wodegongjieite
Our current scenario for the formation of the six new minerals occurring in and around the spheroid of intermetallic phases in foil #5358 is based on the model developed by Griffin et al. (Reference Griffin, Gain, Bindi, Toledo, Cámara, Saunders and O'Reilly2018, Reference Griffin, Gain, Saunders, Huang, Alard, Toledo and O'Reilly2022) and Xiong et al. (Reference Xiong, Griffin, Huang, Gain, Toledo, Pearson and O'Reilly2017) for similar intermetallic phases at Mount Carmel, Israel. Mantle-derived CH4 + H2 fluids are believed to have interacted with basaltic magmas in the shallow lithosphere (depths of ~30–100 km), which resulted in precipitation of corundum that entrapped intermetallic melts derived from the desilication of a parental magma, presumably basaltic. These intermetallic melts crystallised to Ti–P–Si phases such as the spheroid in foil #5358 (Xiong et al., Reference Xiong, Xu, Mugnaioli, Gemmi, Wirth, Grew, Robinson and Yang2020, 2022) and the aggregate in foil #6034. It is likely that the ternary Ti–Si–P phases in foil #5358 would have crystallised at temperatures below the 1330–1600°C indicated for TiSi2 and TiP, respectively, in the Ti–Si and Ti–P binaries (Xiong et al., Reference Xiong, Xu, Mugnaioli, Gemmi, Wirth, Grew, Robinson and Yang2020, Reference Xiong, Xu, Mugnaioli, Gemmi, Wirth, Yang and Grew2022c). Traces of immiscible silicate melt of granodioritic composition (Xiong et al., Reference Xiong, Xu, Mugnaioli, Gemmi, Wirth, Grew, Robinson and Yang2020, Reference Xiong, Xu, Mugnaioli, Gemmi, Wirth, Yang and Grew2022c) that is associated with the intermetallic phases crystallised to wodegongjieite, either externally to aggregates of the intermetallic phases in association with an osumilite-like K–Mg–Al–Si–O phase (e.g. the spheroid in foil #5358) or in the interstices between larger crystals of the intermetallic phases (e.g. the aggregate in foil #6034). Potassium, an essential constituent in wodegongjieite, most probably originated in the parental melt and was concentrated in a residual silicate melt after separation of immiscible intermetallic melts.
Classification of wodegongjieite as a feldspar family mineral
Feldspars traditionally are considered to have the composition M[T4O8] where M is a large cation such as K, Na or Ca, while T is tetrahedral Al and Si. The feldspar group approved by the IMA–CNMNC (Back, Reference Back2022) has just one hierarchical level and comprises 20 minerals, including 11 minerals in the quaternary system relevant for wodegongjieite, NaAlSi3O8–CaAl2Si2O8–KAlSi3O8–SrAl2Si2O8 (Ab–An–Or–Sws), but leaves out one polymorph of anorthite, dmisteinbergite.
Krivovichev (Reference Krivovichev2020) proposed that feldspars are better considered a family that comprises mineral species with the general formula Mn +[Tk+4O8], where n is the average charge of the Mn + cation (n = 1–2) and k is the average charge of the Tk + cation (k = 4 – n/4). Banalsite, lisetite and stronalsite would not be included in the feldspar family as M:T = 3:8, not 1:4 (Krivovichev, Reference Krivovichev2020). Members of the proposed feldspar family would have a crystal structure based upon a d-dimensional network of (TOm) coordination polyhedra sharing O atoms. For the mineral species known so far, d = 2 or 3 (layers or frameworks), and m = 4 or 6, i.e. either tetrahedral or octahedral. The feldspar family proposed by Krivovichev (Reference Krivovichev2020) is far better suited for classifying wodegongjieite than is the existing feldspar group approved by the IMA–CNMNC.
Krivovichev's (Reference Krivovichev2020) feldspar family comprises several supergroups based on composition. Minerals in the quaternary system Ab–An–Or–Sws, all belong in the aluminosilicate supergroup, which comprises five groups based on four basic tetrahedral structure topologies and an octahedral topology related to the hollandite structure. Three quaternary feldspar family minerals belong to the last type, while the remaining 10 minerals belong to one of the four groups (Table 4): (1) feldspar topology in the five familiar tectosilicate Ab–An–Or feldspars anorthite, albite, microcline, orthoclase and sanidine (strictly speaking, the last three are not distinct species, but one species with different degrees of Al–Si ordering) (fsp); (2) paracelsian topology in the tectosilicate slawsonite (pcl); (3) svyatoslavite topology in the tectosilicate svyatoslavite (Krivovichev et al., Reference Krivovichev, Shcherbakova and Nishanbaev2012) and kumdykolite (bct); and (4) the dmisteinbergite topology in the sheet silicates dmisteinbergite and kokchetavite (dms). Because wodegongjieite is isostructural with kokchetavite and topologically identical to dmisteinbergite, it can be included in the sheet-silicate group (dms).
Table 4. Shannon information (in bits) in feldspar-family minerals related to wodogongjieite.*
* Notes: Based on the Shannon information concept (e.g. Krivovichev, Reference Krivovichev2012, Reference Krivovichev2013). Structural topologies: fsp = feldspar; bct = BCT type of zeolite; pcl = paracelsian), dms = dmisteinbergite (Krivovichev, Reference Krivovichev2020). Sources of data: slawsonite, svyatoslavite, dmisteinbergite and anorthite (Krivovichev, Reference Krivovichev2020), kokchetavite calculated from Romanenko et al. (Reference Romanenko, Raschchenko, Sokol, Korsakov, Seryotkin, Glazyrin and Musiyachenko2021), wodegongjieite (this study).
However, in contrast to these 12 minerals and slawsonite (SrAl2Si2O8), the end-member composition for wodegongjieite is intermediate between other feldspar end-members, i.e. 56.2% CaAl2Si2O8, 14.6%, KAlSi3O8, 6.6% SrAl2Si2O8, and 22.6% □Si4O8, Moreover, wodegongjieite would be unique among these minerals in showing ordering of two M cations, namely, K and Ca, at two distinct M sites. Other feldspar-family minerals, e.g. kokchetavite, have more than one M site, but only one M cation at these sites.
Metastable crystallisation of wodegongjieite
It is doubtful that equilibrium was attained during crystallisation of wodegongjieite. The equilibrium assemblage expected under the conditions estimated for the spheroid (<1300°C) would comprise K-feldspar and anorthite. Instead, we have a mineral structurally much more closely related to polymorphs of feldspar that are generally considered to have crystallised under non-equilibrium conditions in accord with Ostwald's step rule and Goldsmith's (Reference Goldsmith1953) ‘simplexity principle’, whereby the least complex polymorphs of a given composition tend to crystallise first, albeit metastably. Complexity is best expressed in terms of the Shannon information concept (e.g. Krivovichev, Reference Krivovichev2012, Reference Krivovichev2013, Reference Krivovichev2020; Krivovichev et al., Reference Krivovichev, Krivovichev, Hazen, Aksenov, Avdontceva, Banaru, Gorelova, Ismagilova, Kornyakov, Kuporev, Morrison, Panikorovskii and Starova2022; Zolotarev et al., Reference Zolotarev, Krivovichev, Panikorovskii, Gurzhiy, Bocharov and Rassomakhin2019). Shannon information in bits reflects diversity of structural sites (information per atom) and both diversity of sites and the number of atoms in the unit cell (information per cell).
Wodegongjieite is structurally simpler than anorthite, but more complex (in terms of total information) than the structurally related dmisteinbergite (Table 4), not surprising given the greater chemical complexity of wodegongjieite compared to dmisteinbergite. The topological complexity of the aluminosilicate layer in wodegongjieite and dmisteinbergite is significantly less than that of the aluminosilicate framework in anorthite and other feldspars. Thus, a theoretical Ostwald sequence for crystallisation of a CaO–K2O-bearing (granodioritic) melt, is predicted to be dmisteinbergite → svyatoslavite → dmisteinbergite + kokchetavite → wodegongjieite → anorthite + sanidine. Note that two minerals, either two feldspars or two feldspar polymorphs, are needed to fully accommodate the major constituents of a granodioritic melt. As far as we are aware, the svyatoslavite stage has not been reported except at the type locality in the Urals. However, the dmisteinbergite + kokchetavite stage has been reported in inclusions of silicate melt (Wannhoff et al., Reference Wannhoff, Ferrero, Borghini, Darling and O´Brien2022), and the predicted sequence can then be simplified to dmisteinbergite → dmisteinbergite + kokchetavite → wodegongjieite → anorthite + sanidine.
However, the appearance of wodegongjieite without either dmisteinbergite or kokchetavite violates this sequence. A possible explanation is that the tolerance of the wodegongjieite structure for vacancies at the K and Ca sites (the refinement gave 21.5–26.5% vacancy) and the presence of Sr at these sites might have tipped the balance so that wodegongjieite crystallised first despite its greater complexity. Another consideration is that wodegongjieite could have a further advantage in that a single feldspar-family mineral accommodates the granodiorite composition, whereas two feldspar family members with end-member compositions would be needed to accommodate it, that is, one nucleation versus two. The number of phases to be nucleated may only come into play in a very rapid quench, more rapid than the quench of included silicate melt that resulted in the crystallisation of the dmisteinbergite + kokchetavite assemblage reported by Wannhoff et al. (Reference Wannhoff, Ferrero, Borghini, Darling and O´Brien2022).
Acknowledgements
We thank members of the IMA–CNMNC for their insightful comments on our proposal for wodegongjieite as a new mineral, which led to a vast improvement in our case, and the two reviewers, together with Peter Leverett, Structural Editor, for their thoughtful and constructive comments on an earlier version of the manuscript.
This research was co-supported by the National Natural Science Foundation of China (NNSFC; Project No. 92062215, 42172069, 41720104009), the Second Tibetan Plateau Scientific Expedition and Research Program (No. 2019QZKK0801), Key Special Project for Introduced Talents Team of Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou) (No. GML2019ZD0201), the Key Laboratory of Deep-Earth Dynamics of Ministry of Natural Resources Fund (No. J1901-28), the China Geological Survey (CGS; Project No.DD20221817, DD20221630).
Supplementary material
To view supplementary material for this article, please visit https://doi.org/10.1180/mgm.2022.107
Competing interests
The authors declare none.
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