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The article discusses Mont Saint-Hilaire in Quebec, Canada, as a renowned mineral locality with over 440 distinct mineral species, attracting collectors and researchers for over fifty years. The unique geology of Mont Saint-Hilaire, specifically the East Hill Suite, has led to the discovery of exotic minerals, including carletonite. The Canadian Museum of Nature has a long history of research on Mont Saint-Hilaire, with the recent acquisition of the Gilles Haineault Collection, containing over 8,000 specimens, making it a national treasure. The museum has developed a new exhibit focusing on Mont Saint-Hilaire's mineralogy, citizen-science, and rare mineral diversity, showcasing specimens from the Haineault Collection and the national collection. [Extracted from the article]

Natromelansonite, Na3Zr[Si7AlO19]⋅4–5H2O, was found at the Poudrette (Demix) quarry, Mont Saint-Hilaire, Quebec, Canada in a highly altered pegmatite together with a clay mineral, steacyite, polylithionite and rhodochrosite. It occurs as an outer zone of tabular crystals to 0.1 × 0.3 × 1 mm in size flattened on (001). The inner zone is made of melansonite. The mineral is grey with white powder colour and vitreous lustre. The cleavage is parallel to {010}, perfect. The Mohs hardness is 3.5. The mineral has green fluorescence under short-wave ultraviolet light. The D calc is 2.31 g/cm3. The infrared spectrum is reported. The composition (wt.%, average of 8 analyses) is Na2O 10.08, K2O 1.72, CaO 0.24, BaO 0.32, MnO 0.10, Al2O3 6.86, Y2O3 0.35, Yb2O3 0.55, SiO2 56.23, ZrO2 14.78, H2O 9.52, total 100.75. The empirical formula calculated on the basis of O = 23 apfu and H = 8 apfu is Na(□Na0.38Ca0.02Mn0.01)2(Na0.70K0.28Ba0.02)Σ1.00(Zr0.91Y0.02Yb0.02)Σ0.95(Si7.08Al1.02)Σ8.10O19⋅4H2O. The mineral is monoclinic, P 21 /m , a = 6.5156(3) Å, b = 24.061(1) Å, c = 6.9759(6) Å, β = 90.453(5)° and V = 1093.61(9) Å3 and Z = 2. The strongest reflections of the powder X-ray diffraction pattern [ d ,Å(I)(hkl)] are: 12.02(100)(020), 6.97(89)(001), 6.51(39)(100), 3.416(37)(160), 3.062(42)($\bar{1}$ 61, 102, 161 and $\bar{1}$ 12), 3.018(38)(230 and 042), 2.864(40)(240 and 132). The crystal structure, solved and refined from single-crystal X-ray diffraction data (R 1 = 0.042), is based on a double sheet of tetrahedra (T) and a sheet of octahedra (O) that alternate along the [010] direction forming a TOT structure typical for members of the rhodesite mero-plesiotype series. [ABSTRACT FROM AUTHOR]

The new mckelveyite group mineral, alicewilsonite-(YLa), Na 2 Sr 2 YLa(CO 3) 6 ⋅ 3H 2 O, was found together with kamphaugite-(Y), paratooite-(Y), bastnäsite-(La), and decrespignyite-(Y) coating along fractures in dolomite at the Paratoo copper mine, South Australia, Australia. It occurs as pale pink to colourless pseudohexagonal tabular crystals up to 150 µ m in size. The streak is white; the lustre is vitreous. The mineral has no cleavage. Dcalc is 3.37 g cm -3. Alicewilsonite-(YLa) is optically biaxial (-), α = 1.556(2), β= 1.582(2), γ= 1.592(2), 2V (meas.) = 60(2)°, 2V (calc.) = 63° (589 nm). The IR spectrum is reported. The composition (wt %, average of seven analyses) is Na 2 O 7.43, CaO 2.00, SrO 18.43, BaO 1.64, Y 2 O 3 9.59, La 2 O 3 11.74, Pr 2 O 3 1.29, Nd 2 O 3 5.74, Sm 2 O 3 0.44, Eu 2 O 3 0.09, Gd 2 O 3 0.95, Dy 2 O 3 1.15, Ho 2 O 3 0.25, Er 2 O 3 0.89, Yb 2 O 3 0.29, CO 2 29.78, H 2 O 6.18, total 97.88. The empirical formula calculated on the basis of six cations with 3 H 2 O molecules is as follows: Na 2.10 Ca 0.31 Sr 1.56 Ba 0.10 Y 0.74 La 0.63 Pr 0.07 Nd 0.30 Sm 0.03 Eu 0.01 Gd 0.04 Dy 0.05 Ho 0.01 Er 0.04 Yb 0.01 (CO 3) 5.92 (H 2 O) 3. The mineral is triclinic, P 1, a= 8.9839(2), b= 8.9728(3), c= 6.7441(2) Å, α= 102.812(2)°, β= 116.424(2)°, γ= 60.128(2)°, and V= 422.17(2) Å 3 and Z= 1. The strongest reflections of the powder X-ray diffraction pattern [ d ,Å(I)(hkl)] are 6.03(43)(001), 4.355(100)(1 1‾ 0, 2‾1‾ 1, 120), 4.020(30)(1‾ 11, 210, 1‾2‾ 1), 3.188(29)(2‾1‾ 2, 1 1‾ 1, 121), 2.819(96)(002, 1‾ 12, 211, 1‾2‾ 2), 2.592(40)(3‾ 01, 030, 3‾3‾ 1), 2.228(33)(2‾ 21, 4‾2‾ 1, 2‾4‾ 1). 2.011(36)(2‾ 22, 003, 420, 2‾4‾ 2), 1.9671(32)(3‾ 03, 301, 0 3‾ 2, 032, 3‾3‾ 3, 331). The crystal structure was solved and refined from single-crystal X-ray diffraction data (R1= 0.058). [ABSTRACT FROM AUTHOR]

Microcline, KAlSi3O8 Along with quartz and albite, perthitic microcline is one of the dominant minerals in the pegmatites at Phnom Bayong. Late-stage hydrothermal quartz occurs in the pegmatites and miarolitic cavities as fine-grained (1-3-mm), translucent, white to yellow, euhedral, doubly terminated crystals on top of microcline and primary quartz. Multiple smaller tabular golden-white muscovite crystals to 6 mm form crusts on the larger muscovite crystals, feldspar, and quartz (fig. 16). Miarolitic Pegmatites The pegmatite mineralogy is dominated by quartz, microcline, albite (variety cleavelandite), two micas (zinnwaldite and muscovite), and chamosite. [Extracted from the article]

The new mineral bounahasite, Cu+Cu2+2(OH)3Cl2, was found in the oxidation zone of the Bou Nahas Mine, Morocco. It forms pseudo-hexagonal plates up to 3 × 30 × 40 μm in size combined in loose clusters with native copper and paratacamite. The mineral is green with vitreous lustre. The cleavage is parallel to {110}, perfect. D calc is 3.90 g/cm3. The infrared spectrum is reported. The composition (wt.%) is Cu2O 23.26, CuO 51.72, Cl 23.36, H2O 8.71, O = Cl2 –5.27, total 101.78. The empirical formula calculated on the basis of 3 Cu atoms per formula unit is: Cu+Cu2+2(OH)2.97Cl2.03. The mineral is monoclinic, P 21 /n, a = 8.5925(1), b = 6.4189(1), c = 10.4118(2) Å, β = 111.804(2)°, V = 533.17(2) Å3 and Z = 4. The strongest reflections of the powder X-ray diffraction pattern [ d ,Å(I)(hkl)] are: 7.71(70)($\bar{1}$ 01), 5.34(22)(011), 3.856(100)(012, $\bar{2}$ 02), 2.673(36)(022), 2.665 (30)(103) and 2.350 (71)($\bar{1}$ 23, 301, $\bar{2}$ 14). The crystal structure, refined from single-crystal X-ray diffraction data (R 1 = 0.028), is based on two alternating sheets coplanar to (110): one consists of alternating edge-sharing Cu2+(OH)6 octahedra and two Cu2+(OH)4Cl2 octahedra, whereas the other one is based on Cu+Cl4 tetrahedra forming edge-sharing Cu+2Cl6 dimers. [ABSTRACT FROM AUTHOR]

The new högbomite-group mineral magnesiohögbomite-6N12S, ideally Mg5Al11TiO23(OH), was found in calcite "vein-dikes" at the DeWitts Corners occurrence, lots 10 and 11, concession 1, Bathurst Township, Ontario, Canada. It forms tabular and short-prismatic crystals up to 5 mm in size. The major forms are pinacoid {0001} and hexagonal pyramid {11 ${\bar 2}$ 1}, sometimes modified by hexagonal prism {11 ${\bar 2}$ 0}. The associated minerals are magnesiohögbomite-2N3S, spinel, corundum, diopside, magnesio-hastingsite, pargasite, clinochlore and calcite. Magnesiohögbomite-6N12S is dark brown to black with brown streak and vitreous lustre. It has no cleavage and its fracture is uneven. The Mohs hardness is 6½. Dcalc is 3.87 g/cm3. The infrared spectrum is reported. The composition (wt.%) is MgO 13.09, ZnO 0.46, FeO 11.91, Fe2O3 6.84, Al2O3 62.70, TiO2 4.44, H2O 0.99, total 100.43. The empirical formula calculated on the basis of 17 cations, excluding H+, is (Mg2.95Fe2+1.51Al0.49Zn0.05)Σ5(Al10.71Fe3+0.78Ti0.51)Σ12O23(OH). The simplified formula is (Mg,Fe)5(Al,Fe,Ti)12O23(OH). The mineral is trigonal, R ${\bar 3}$ m, a = 5.7194(2), c = 83.069(5) Å, V = 2353.3(2) Å3 and Z = 6. The strongest reflections of the powder X-ray diffraction pattern [d,Å(I)(hkl)] are: 2.921(26)(0.1.23), 2.863(49)(110), 2.687(29)(0.1.26), 2.547(31)(0.1. $\overline{28}$) and 2.434(100)(1.1.18). The crystal structure was solved and refined from single-crystal X-ray diffraction data to R1 = 0.022. It is composed of alternating spinel (S) and nolanite (N) modules in the sequence 3 × (NSSNSS). The sequence of cubic 'c' and hexagonal 'h' closed-packed oxygen layers is 3 × (cccccchcccch). It is the first polysome in the högbomite supergroup with such a sequence. [ABSTRACT FROM AUTHOR]

A new alluaudite-group mineral zincobradaczekite, a Zn–Cu ordered highly zincian analogue of bradaczekite, was discovered in sublimates of the Yadovitaya fumarole at the Second scoria cone of the Northern Breakthrough of the Great Tolbachik Fissure Eruption, Tolbachik volcano, Kamchatka, Russia. It is associated with bradaczekite, lammerite, lammerite-β, borisenkoite, mcbirneyite, sanidine, hematite, tenorite, pseudolyonsite, lyonsite, starovaite, rutile, tripuhyite, pseudobrookite, piypite, langbeinite, calciolangbeinite, aphthitalite, alumoklyuchevskite, and palmierite. Zincobradaczekite forms oblique-angled prismatic crystals up to 0.02 × 0.02 × 0.08 mm3 and equant or tabular crystals up to 0.05 mm. It is transparent, blue, greenish-blue, grey-blue or bluish-grey. The lustre is vitreous. Dcalc is 4.71 g cm−3. Zincobradaczekite is optically biaxial (–), α 1.786(5), β 1.846(8), γ 1.90(1), 2Vmeas. 80(5)º. Chemical composition (wt%, electron microprobe) is Na2O 4.07, K2O 0.53, CaO 0.01, MgO 0.71, MnO 0.01, CuO 19.89, ZnO 24.21, Al2O3 0.02, Fe2O3 0.90, TiO2 0.03, P2O5 0.41, V2O5 1.05, As2O5 47.10, SO3 1.01, and total 99.95. The empirical formula based on 12 O apfu is Na0.90K0.08Cu1.70Mg0.12Zn2.03Fe3+0.08(As2.79S0.09V0.08P0.04)Σ3.00O12. The simplified chemical formula is NaCu2Zn2(AsO4)3. Zincobradaczekite is monoclinic, C2/c, a 12.0375(13), b 12.4500(13), c 7.2213(8) Å, β 117.506(7)º, V 959.90(18) Å3 and Z 4. The strongest reflections of the powder XRD pattern [d,Å(I)(hkl)] are 6.21(31)(020), 3.416(70)(310, − 112), 3.200(17)(002), 2.779(23)(− 402), 2.691(100)(− 132, 240), 1.841(20)(152) and 1.680(14)(− 642). The crystal structure was solved (single-crystal XRD, R = 4.38%). The simplified crystal chemical formula is A(1)□A(1)ʹCuA(2)□A(2)ʹNaM(1)CuM(2)Zn2(AsO4)3 (□—vacancy) and the end-member formula is NaCuCuZn2(AsO4)3. Zincobradaczekite and bradaczekite, ideally NaCuCuCu2(AsO4)3, are isostructural. In the Yadovitaya fumarole, Mg-poor bradaczekite forms an isomorphous series with zincobradaczekite, whilst in the neighbouring Arsenatnaya fumarole only a Zn-depleted and Mg-enriched variety of bradaczekite occurs. Zincobradaczekite and bradaczekite differ from other anhydrous alluaudite-group arsenates by increased values of the c and β unit-cell parameters due to the strong Jahn–Teller distortion of M(1)O6 octahedron predominantly occupied with Cu2+. [ABSTRACT FROM AUTHOR]

The new mineral zubkovaite, Ca3Cu3(AsO4)4, was found in the Arsenatnaya fumarole at the Second scoria cone of the Northern Breakthrough of the Great Tolbachik Fissure Eruption, Tolbachik volcano, Kamchatka, Russia. It is associated with anhydrite, svabite, hematite, johillerite, tilasite, fluorophlogopite, sanidine and aphthitalite. Zubkovaite occurs as coarse prismatic crystals up to 0.01 mm × 0.01 mm × 0.2 mm combined in radiating aggregates or crusts. The mineral is transparent, bright sky-blue, turquoise-coloured or light bluish-green, with vitreous lustre. It is brittle, with imperfect cleavage. The Mohs' hardness is ca 3. D calc is 4.161 g cm–3. Zubkovaite is optically biaxial (–), α = 1.747(5), β = 1.774(5), γ = 1.792(5) and 2Vmeas = 75(10)°. Chemical composition (wt.%, electron microprobe) is: CaO 19.22, CuO 27.37, As2O5 52.54, SO3 0.67, total 99.80. The empirical formula based on 16 O apfu is Ca2.96Cu2.97(As3.945S0.07)Σ4.015O16. Zubkovaite is monoclinic, C 2, a = 16.836(3), b = 5.0405(8), c = 9.1173(17) Å, β = 117.388(13)°, V = 687.0(2) Å3 and Z = 2. The strongest reflections of the powder XRD pattern [ d ,Å (I) (hkl)] are: 7.44 (100) ($\bar 2$ 01), 3.727 (79) (400, $\bar 2$ 02, $\bar 3$ 11), 3.334 (92) ($\bar 1$ 12), 2.914 (73) (311), 2.765 (50) ($\bar 6$ 01, $\bar 6$ 02), 2.591 (96) ($\bar 3$ 13) and 2.521 (53) (020). The crystal structure is unique for minerals. It was solved from single-crystal X-ray diffraction data to R = 7.19%. The structure contains trimers of Cu2+-centred polyhedra (consisting of one distorted square CuO4 in the core and two distorted square pyramids CuO5) and two crystallographically independent As5+O4 tetrahedra playing different roles: As(2)O4 tetrahedra link neighbouring trimers into ribbons whereas As(1)O4 tetrahedra link adjacent ribbons into heteropolyhedral layers; Ca cations are located in the interlayer space. The mineral is named in honour of the Russian crystallographer and crystal chemist Natalia Vital'evna Zubkova (born 1976). [ABSTRACT FROM AUTHOR]

The new mineral anatolyite Na6(Ca,Na)(Mg,Fe3+)3Al(AsO4)6 was found in the Arsenatnaya fumarole, Tolbachik volcano, Kamchatka, Russia. It is associated with potassic feldspar, hematite, tenorite, cassiterite, johillerite, tilasite, ericlaxmanite, lammerite, arsmirandite, sylvite, halite, aphthitalite, langbeinite, anhydrite, wulffite, krasheninnikovite, fluoborite, pseudobrookite and fluorophlogopite. Anatolyite occurs as aggregates (up to 2 mm across) of rhombohedral–prismatic, equant or slightly elongated along [001] crystals up to 0.2 mm. The mineral is transparent, pale brownish–pinkish, with vitreous lustre. It is brittle, cleavage was not observed and the fracture is uneven. The Mohs' hardness is ca 4½. D calc is 3.872 g cm–3. Anatolyite is optically uniaxial (–), ω = 1.703(4) and ε = 1.675(3). Chemical composition (wt.%, electron microprobe) is: Na2O 16.55, K2O 0.43, CaO 2.49, MgO 5.80, MnO 0.16, CuO 0.69, ZnO 0.55, Al2O3 5.01, Fe2O3 7.94, TiO2 0.18, SnO2 0.17, SiO2 0.04, P2O5 0.55, As2O5 60.75, SO3 0.03, total 101.34. The empirical formula based on 24 O apfu is (Na5.90K0.10)Σ6.00(Ca0.50Na0.13Zn0.08Mn0.03)Σ0.74(Mg1.63Fe3+1.12Al0.15Cu0.10)Σ3.00(Al0.96Ti0.03Sn0.01)Σ1.00(As5.97P0.09Si0.01)Σ6.07O24. Anatolyite is trigonal, R $\bar{3}$ c , a = 13.6574(10), c = 18.2349(17) Å, V = 2945.6(4) Å3 and Z = 6. The strongest reflections of the powder XRD pattern [ d ,Å(I)(hkl)] are: 7.21(33)(012), 4.539(16)(113), 4.347(27)(211), 3.421(20)(220), 3.196(31)(214), 2.981(17)(223), 2.827(100)(125) and 2.589(18)(410). The crystal structure was solved from single-crystal XRD data to R = 4.77%. The structure is based on a 3D heteropolyhedral framework formed by M 4O18 clusters [ M 1 = Al and M 2 = (Mg,Fe3+)] linked with AsO4 tetrahedra. (Ca,Na) and Na cations centre A 1O6 and A 2O8 polyhedra in voids of the framework. Anatolyite is isostructural with yurmarinite. The new mineral is named in honour of the outstanding Russian crystallographer, mineralogist and mathematician Anatoly Kapitonovich Boldyrev (1883–1946). [ABSTRACT FROM AUTHOR]