Tomsquarryite, NaMgAl 3 (PO 4 ) 2 (OH) 6 (cid:113) 8H 2 O, a new crandallite-derivative mineral from Tom’s phosphate quarry, Kapunda, South Australia

. Tomsquarryite, NaMgAl 3 (PO 4 ) 2 (OH) 6 (cid:113) 8H 2 O, is a new secondary phosphate mineral from Tom’s phosphate quarry, Kapunda, South Australia. It occurs as colourless, talc-like hexagonal platelets, with diameters of a few tens of micrometres when formed from the decomposition of minyulite and as thicker ( ∼ 10 µm) hexagonal crystals when formed from alteration of gordonite. Associated minerals are penriceite, elliottite, minyulite, angastonite and wavellite. The calculated density is 2.22 g cm − 3 . Tomsquarryite crystals are uniaxial ( + ) with ω = 1 . 490 ( 3 ) , ε = 1 . 497 ( 3 ) (white light). Dispersion was not observed. The par-tial orientation is Z ≈ c . Electron microprobe analyses of the holotype specimen give the empirical formula Na 1 . 02 K 0 . 02 Ca 0 . 08 Mg 1 . 26 Al 2 . 86 (PO 4 ) 2 . 00 (OH) 3 . 82 F 2 . 48 (cid:113) 7.70H 2 O, based on 22 anions. Tomsquarryite be-longs to the trigonal crystal system, space group R –3 m , with hexagonal unit-cell parameters a = 6 . 9865 ( 5 ) Å, c = 30 . 634 ( 3 ) Å and V = 1294 . 9 ( 4 ) Å 3 and with Z = 3. The crystal structure was reﬁned using single-crystal diffraction data; R 1 = 0 . 069 for 303 reﬂections with I > 2 σ(I) to a resolution of 0.80 Å. The crystal structure is a derivative of the crandallite structure, with Ca 2 + cations replaced by hydrated magnesium ions, [Mg(H 2 O) 6 ] 2 + , resulting in an expansion of the interlayer separation from 5.4 Å in crandallite to 10.2 Å in tomsquarryite. The results for tomsquarryite are compared with those for the chemically and structurally related minerals penriceite and elliottite.

The name is for the location. The holotype and cotype specimens from Tom's quarry and the cotype from the Penrice marble quarry are housed in the mineralogical collections of the South Australian Museum, catalogue numbers G35033, G35034 and G35031, respectively.

Occurrence and paragenesis
Tomsquarryite was found in hand specimens collected by one of the authors (PE) in the mid 2000s at Tom's phosphate quarry, Kapunda, South Australia (34 • 21 S, 138 • 55 E) and in specimens collected by Vince Peisley in 1988-1989 at the Penrice marble quarry, located about 15 km southeast of Tom's quarry. In the specimens from both localities, thin layers of tomsquarryite and other intimately mixed fine-grained secondary phosphates coat a goethite-clay matrix (Tom's quarry) and a goethite, Mn oxide, muscovite matrix (Penrice quarry) (Fig. 2). Tomsquarryite is most commonly associated with angastonite (Grey et al., 2022a). Other closely associated minerals are penriceite (Elliott et al., 2022), elliottite (Grey et al., 2022b), minyulite and wavellite. The formation of tomsquarryite at the Penrice quarry is related to the alteration of minyulite, KAl 2 F(PO 4 ) 2 q 4H 2 O, in a nearneutral solution (Grey et al., 2022c). K is leached, and the leach product takes up solution species Mg 2+ , Ca 2+ and Na + to form an amorphous phase that subsequently crystallises as tomsquarryite, elliottite and penriceite. At Tom's quarry, an alternative paragenesis was noted in South Australian Museum specimen G35033, involving progressive surface alteration of gordonite, MgAl 2 (PO 4 ) 2 (OH) 2 q 8H 2 O, most likely by a dissolution/reprecipitation mechanism in a Na-and Fbearing solution.
3 Description and experimental procedures

Appearance and properties
Tomsquarryite at the Penrice quarry occurs most commonly as talc-like platelets, with diameters of a few tens of micrometres and thicknesses of only ∼ 1 µm (Fig. 3). At Tom's quarry, when formed from gordonite, it occurs as thicker (∼ 10 µm) pseudohexagonal crystals flattened on {001} (Fig. 4). The crystals are colourless with a white streak. They exhibit the forms {001}, {100} and {110} and have perfect cleavage on {001}. The density was not measured due to paucity of material. The calculated density, based on the empirical formula for specimen G35033 and single-crystal unit-cell parameters, is 2.22 g cm −3 . Tomsquarryite crystals are uniaxial (+) with ω = 1.490(3) and ε = 1.497(3) (white light). Dispersion was not observed. The partially determined orientation is Z ≈ c. Application of the Gladstone-Dale relationship (Mandarino, 1981) using the measured parameters for holotype specimen G35033 gives a compatibility index of 0.019 (superior).

Infrared spectroscopy
The infrared absorption spectrum of specimen G35031 of tomsquarryite ( Fig. 5) was obtained on ground crystals using a Nicolet 5700 FTIR (Fourier-transform infrared) spectrometer (range 4000 to 700 cm −1 , transmission mode) equipped with a Nicolet Continuum IR microscope and a diamondanvil cell. A broad band is observed in the OH-stretching region with a split maximum at 3240 and 3350 cm −1 and with shoulders at 3050 and 3600 cm −1 . The first three bands correspond to H-bonded O. . . O distances in the range 2.65 to 2.80 Å (Libowitzky, 1999), consistent with results from the crystal structure refinement. The band at 3600 cm −1 corresponds to very weak H bonding, also consistent with the structure determination. The H-O-H bending vibrations of H 2 O are represented by a broad peak at 1650 cm −1 . By analogy with the IR spectrum for crandallite (Frost et al., 2011), with the same topology of PO 4 tetrahedra, the symmetric P-O stretching modes are represented by peaks at 1025 and 1045 cm −1 and a shoulder at 975 cm −1 , whereas shoulders at 1120 and 1180 cm −1 correspond to antisymmetric P-O stretching modes. A weak broad peak at 1450 cm −1 may correspond to carbonate impurity .

Chemical composition
Crystals of tomsquarryite from Tom's quarry (specimens G35033 and G35034) were analysed using wavelengthdispersive spectrometry on a JEOL JXA-8500F Hyperprobe operated at an accelerating voltage of 15 kV and a beam current of 2 nA. Aggregates of edge-on platelets were analysed, and the beam was defocused to 5 µm to minimise beam  damage. Analytical results are given in Table 1. The H 2 O content in Table 1 is based on the formula from the crystal structure refinement, NaMgAl 3 (PO 4 ) 2 X 6 q 8H 2 O, with X equal to F and OH. The quantification was applied using the library of Stratagem ® , a commercial software based on the work of Pichoir (1991, 1993). The H 2 O was included in the matrix correction. For comparison, the analyses of tomsquarryite from the Penrice marble quarry (specimen G35031) are also given in Table 1. As shown in Fig. 3, the crystals in this specimen were ultra-thin, talclike platelets in an amorphous matrix, and low analysis totals were obtained. The analyses were scaled to give a total of 100 % for the calculation of the empirical formula.
Empirical formulae, normalised to 22 anions, are the following.

Powder X-ray diffraction
Powder X-ray diffraction (PXRD) data were collected on ground samples of Penrice specimen G35031 and Tom's quarry specimen G35033. The patterns were obtained at room temperature using a Panalytical Aeris diffractometer employing CoKα radiation.
Step-scan data were collected in the 2-theta range 5 to 80 • using a step size of 0.022 • . Tomsquarryite was the major phase in the PXRD of G35031 together with minor quartz, wavellite and penriceite, whereas the PXRD for G35033 contained tomsquarryite and penriceite as co-majors. Refinement of the PXRD data using Full-Prof (Rodriguez-Carvajal, 1990) gave the following hexagonal cell parameters. Observed and calculated d values, intensities and indices for G35031 are given in Table 2.

Single-crystal structure analysis
Crystals of tomsquarryite are usually minute talc-like platelets with thicknesses of ∼ 1 µm that are unsuitable for single-crystal (SC) diffraction data collections. The specimen G35033, however, contains platelets that are typically 10 µm thick (Fig. 4), and they give sharp diffraction spots. A crystal with dimensions 0.055 × 0.055 × 0.010 mm was mounted for a data collection using an Oxford Diffraction Xcalibur E diffractometer equipped with a EOS (electrooptical system) CCD (charge-coupled device) detector. An ω scan was used to collect intensity data at room temperature using MoKα radiation (λ = 0.71073 Å). The diffraction data displayed trigonal symmetry, with possible space groups R-3m (no. 166) or its non-centrosymmetric subgroups. Refined unit-cell parameters from the SC data are a = 6.9865(5) Å, c = 30.634(3) Å and V = 1294.9(4) Å 3 . A structure solution for tomsquarryite in space group R-3m was obtained using SHELXT (Sheldrick, 2015). The solution had one Al, one P and three O sites that formed a crandallite-type layer (Blount, 1974), together with a Na atom at the centre of the hexagonal rings in the crandallite layers, and a Mg atom in the interlayer region at (0, 0, 1/2). Difference Fourier maps gave three partially occupied anion sites with distances to Mg in the range 2.02 to 2.15 Å and an anion site that completed eight coordination to Na. SHELXL refinement (Sheldrick, 2015) with anisotropic displacement parameters for the metal atoms and with refinement of the occupancies of the anions in the partially occupied sites converged at R 1 = 0.069 for 303 independent reflections with I > 2σ (I ) to a resolution of 0.80 Å. Further details of the data collection and refinement are given in Table 3. The refined atom coordinates, equivalent isotropic displacement parameters and calculated bond valence sums (BVSs, Gagné and Hawthorne, 2015) are reported in Table 4, and polyhedral bond distances and likely H-bonded O-O pairs are given in Table 5.

Discussion
A projection of the crystal structure of tomsquarryite along [110] is shown in Fig. 6a. It is essentially the same as the structure of crandallite but with a hydrated magnesium ion, [Mg(H 2 O) 6 ] 2+ , replacing Ca in the interlayer, resulting in an increase in the interlayer separation from 5.4 Å in crandallite to 10.2 Å in tomsquarryite. The tomsquarryite structure also differs from that for crandallite in having a sodium cation at the centre of the hexagonal rings in the heteropolyhedral layers. The sodium coordinates to six intralayer OH/F anions and to two H 2 O (Ow4) perpendicular to the layer, giving eight coordination in the form of a scalenohedron. The same Na coordination occurs in penriceite (Elliott et al., 2022). The mean Mg-O distance is 2.09 Å, and the ratio of the summed site occupancies of the coordinating Ow1 to Ow3 atoms to that for Mg is 6.06; both being consistent with octahedral coordination for Mg. The octahedra display severe rotational disorder about [001]. Due to disordered, partially occupied Ow sites and the replacement of OH by F, the H atoms could not be unambiguously located in the refinement. The BVSs in Table 4 correspond to OH/F at the O3 site and H 2 O at the Ow sites. The O1 site, with a low BVS of 1.34, receives strong H bonds from both Ow2 and Ow3 (Table 5). The BVS values for the Na (1.18) and Al (2.89) sites are consistent with minor substitution of Ca and Mg, respectively, at these sites.   Tomsquarryite is closely related, both compositionally and structurally, to elliottite, NaMgAl 3 (PO 4 ) 2 F 6 q 9H 2 O (Grey et al., 2022b). The structure of elliottite is shown in projection along [010] in Fig. 6b. Both have crandallite-derivative layer structures, which are built from planer nets of trans-cornershared Al-centred octahedra, decorated with PO 4 tetrahedra. In tomsquarryite, Na atoms at the centres of the six-member rings have eight-coordinated scalenohedral coordination, whereas in elliottite, the Na is six-coordinated as a very flat octahedron with the next-nearest anions being over 3 Å away. In tomsquarryite, the interlayer Mg(H 2 O) 6 octahedra are isolated, whereas in elliottite they share edges, giving half-occupied Mg 2 (H 2 O) 10 dimers. Elliottite has a larger layer spacing, 11.0 Å, and accommodates extra H 2 O in the interlayer region.
Tomsquarryite is also chemically and structurally related to penriceite, NaMgAl 3 (PO 4 ) 2 F 6 q 9H 2 O (Elliott et al., 2022). Whereas in tomsquarryite the heteropolyhedral layers are built from planar nets of trans-corner-shared Al-centred octahedra, the layers in penriceite and the isostructural mineral aldermanite (Elliott et al., 2021) have a sawtooth shape and involve both trans-and cis-corner-sharing of octahedra, shown in Fig. 6c. The layers in penriceite can be described in terms of periodic unit-cell-scale twinning of the crandallitetype layers in tomsquarryite (and elliottite). The relationship between the two structures is similar to that between the structures of orthoenstatite and clinoenstatite, for which the orthorhombic orthoenstatite structure has been described as unit-cell twinning of the monoclinic clinoenstatite structure (Morimoto and Koto, 1969). Penriceite has a much larger layer spacing (13.5 Å), resulting in a PXRD pattern very different from those of tomsquarryite (with a 10.2 Å layer spacing) and elliottite (with an 11.0 Å layer spacing). The properties of tomsquarryite, elliottite and penriceite are compared in Table 6.
Data availability. Crystallographic data for tomsquarryite are available in the Supplement.