Rundqvistite-(Ce), ideally Na3(Sr3Ce)(Zn2Si8O24), is a new mineral from the Darai-Pioz alkaline massif, Tien-Shan Mountains, Tajikistan. The mineral occurs as elongated grains up to 0.1 mm long and up to 0.03 mm thick embedded in quartz–pectolite aggregate in a silexite-like peralkaline pegmatite. Associated minerals are quartz, fluorite, pectolite, baratovite, aegirine, leucosphenite, neptunite, reedmergnerite, orlovite, sokolovaite, mendeleevite-(Ce), odigitriaite, pekovite, zeravshanite, kirchhoffite and garmite. The mineral is colourless with a vitreous lustre and a white streak, brittle, Dmeas. is 3.70(2) and Dcalc. is 3.709 g/cm3. Rundqvistite-(Ce) is monoclinic, space group P21/c, a = 5.1934(16), b = 7.8934(16), c = 26.011(5) Å, β = 90.02(3)° and V = 1066.3(4) Å3. The chemical composition of rundqvistite-(Ce) is SiO2 40.17, La2O3 2.64, Ce2O3 7.55, Pr2O3 0.80, Nd2O3 2.43, Sm2O3 0.33, Eu2O3 0.09, Gd2O3 0.24, Tb2O3 0.18, Dy2O3 0.21, PbO 1.03, SrO 19.83, FeO 0.37, ZnO 13.08, CaO 2.55, Na2O 8.04, total 99.54 wt.%. The empirical formula calculated on 24 O apfu (atoms per formula unit) is Na3.10Sr2.29Ca0.54Pb0.06(Ce0.55La0.19Nd0.17Pr0.06Sm0.02Gd0.02Eu0.01Tb0.01Dy0.01)Σ1.04Zn1.92Fe0.06 Si8.00O24 Z = 2. The structural formula based on refined site-occupancies is (Na2.94Sr0.06)Σ3.00 [(Sr2.23Ca0.54Pb0.06Na0.13)Σ2.96Ln3+1.04]Σ4.00[(Zn1.92Fe2+0.06)Σ1.98Si8O24], where Ln3+1.04 = (Ce0.55La0.19Nd0.17Pr0.06Sm0.02Gd0.02Eu0.01Tb0.01Dy0.01)Σ1.04. The crystal structure of rundqvistite-(Ce) was refined to R1 = 2.76% on the basis of 3184 unique reflections [F > 4σ|F|]. In rundqvistite-(Ce), the main structural unit is a (Zn2Si8O24)12– sheet parallel to (100). In the sheet, the Si and Zn tetrahedra form four-, five- and eight-membered rings. The interstitial cations at the Na and M(1–3) sites sum to [Na3(Sr3Ce)]12– apfu. The Na and M(1–3) polyhedra share common edges to form a layer. Rundqvistite-(Ce) is a structural analogue of vladykinite, ideally Na3Sr4(Fe2+Fe3+)Si8O24. Rundqvistite-(Ce) and vladykinite are related by the following substitution: [8]Ce3+ + [4](Zn2+)2 ↔ [8]Sr2+ + [4](Fe2+Fe3+). The mineral is named after Dmitry Vasilievich Rundqvist (1930–2022), a prominent Russian geologist and an expert on the geology of ore deposits, metallogeny and mineralogy of Precambrian rocks.

Kalyuzhnyite-(Ce), ideally NaKCaSrCeTi(Si8O21)OF(H2O)3, is a new mineral from the Darai-Pioz alkaline massif, Tien-Shan mountains, Tajikistan. It occurs as equant grains up to 0.05 × 0.07 mm in a quartz–pectolite aggregate in a silexite-like peralkaline pegmatite. Associated minerals are quartz, fluorite, pectolite, baratovite, aegirine, leucosphenite, neptunite, reedmergnerite, orlovite, sokolovaite, mendeleevite-(Ce), odigitriaite, pekovite, zeravshanite, kirchhoffite and garmite. The mineral is colourless with a vitreous lustre and a white streak, and Dcalc. is 3.120 g/cm3. Kalyuzhnyite-(Ce) is monoclinic, P2/c, a = 18.647(4), b = 11.214(2), c = 14.642(3) Å, β = 129.55(3)° and V = 2360.9(11) Å3. The chemical composition of kalyuzhnyite-(Ce) is Nb2O5 0.53, TiO2 0.16, SiO2 43.85, Er2O3 0.13, Ho2O3 0.10, Gd2O3 0.09, Sm2O3 0.47, Nd2O3 6.22, Pr2O3 1.21, Ce2O3 6.34, La2O3 0.82, PbO 4.90, BaO 0.85, SrO 11.39, CaO 1.86, Cs2O 3.80, K2O 1.59, Na2O 2.99, H2O 5.24, F 1.55, O = F –0.65, total 100.31 wt.%. The empirical formula calculated on 26.11 (O + F) apfu is Na1.07K0.37Cs0.30Sr1.21Ca0.37Pb0.24Ba0.06(Ce0.43Nd0.41Pr0.08La0.06Sm0.03Gd0.01Er0.01Ho0.01)Σ1.04(Ti0.97Nb0.04)Σ1.01Si8.06O25.21F0.90H6.42, Z = 4. The simplified formula is (Na,□)(K,Сs)(Ca,Pb,Sr,Na)SrLn3+Ti(Si8O21)OF(H2O)3, where Ce is the dominant lanthanoid. The crystal structure was solved by direct methods and refined to an R1 index of 2.74%. In kalyuzhnyite-(Ce), the main structural units are a heteropolyhedral Na–Sr–Ce–Ti sheet, ideally [NaSrCeTiOF]7+, and a double (Si8O21)10– sheet parallel to (010). In the Si–O sheet, the Si tetrahedra form ten-membered rings. This is the first occurrence of such a double Si–O sheet in a mineral. The two sheets connect via common vertices of Na-, Sr-, Ce- and Ti-polyhedra and SiO4 tetrahedra to form a framework. The interstitial cations and H2O groups, ideally [(CaK)(H2O)3]3+, occur within the Si–O sheet. The mineral is named in honour of Vasily Avksentievich Kalyuzhny (1899–1993) in recognition of his contributions to the geology of ore deposits of Komi Republic (USSR) and the mineralogy of granitic pegmatites (Tajikistan).

Letnikovite-(Ce), ideally (Na□)Ca2Ce2[Si7O17(OH)]F4(H2O)4, is a new mineral with no natural or synthetic analogues (IMA2022–132). The mineral occurs at the Darai-Pioz alkaline massif, Tien-Shan mountains, Tajikistan, in a silexite-like peralkaline pegmatite. Letnikovite-(Ce) occurs as isolated prismatic grains up to 0.03 × 0.1 mm in a quartz–pectolite aggregate. Associated minerals are quartz, fluorite, pectolite, baratovite, aegirine, leucosphenite, neptunite, reedmergnerite, orlovite, sokolovaite, mendeleevite-(Ce), odigitriaite, pekovite, zeravshanite, kirchhoffite and garmite. The mineral is colourless with a vitreous lustre and a white streak, and Dcalc. is 2.847 g/cm3. Letnikovite-(Ce) is monoclinic, C2/m, a = 7.4726(3), b = 22.9196(9), c = 13.9360(6) Å, β = 105.550(5)° and V = 2299.43(17) Å3. The chemical composition of letnikovite-(Ce) is SiO2 42.38, Gd2O3 0.16, Eu2O3 0.28, Sm2O3 0.07, Nd2O3 5.64, Pr2O3 1.69, Ce2O3 11.73, La2O3 2.24, PbO 1.22, SrO 5.77, FeO 0.32, CaO 11.87, MgO 1.14, Cs2O 0.57, K2O 0.65, Na2O 2.24, H2O 7.79, F 7.29, O = F –3.07, total 99.98 wt.%. The empirical formula calculated on 7 Si apfu is Na0.72K0.14Cs0.04Ca2.10Sr0.55Mg0.28Pb0.05Fe0.04(Ce0.71Nd0.33La0.14Pr0.10Eu0.02Gd0.01)Σ1.31Si7O21.84F3.81H8.58 for Z = 4. The structural formula is (Na0.72Ca0.16□1.12)Σ2(Cs0.04□0.96)Σ1(Ca1.83□0.17)Σ2(Mg0.28Fe0.04□0.68)Σ1(Ln3+1.31Sr0.55Ca0.09Pb0.05)Σ2[Si7O17(OH)]F3.81(H2O)3.79, where Ln3+1.31 = (Ce0.71Nd0.33La0.14Pr0.10Eu0.02Gd0.01)Σ1.31. The simplified formula is (Na,□)2Ca2(Ln3+,Sr)2[Si7O17(OH)]F4(H2O)4, where Ce is the dominant lanthanoid. The crystal structure was solved by direct methods and refined to an R1 index of 4.2%. In letnikovite-(Ce), the main structural unit is a layer which consists of the central heteropolyhedral Ca–Ce sheet and two adjacent single [Si7O17(OH)] sheets parallel to (001). In the Si–O–OH sheet, the Si tetrahedra form five-membered and ten-membered rings. This is the first occurrence of a single [Si7O17(OH)]7– sheet in a mineral. The layers connect via Na and Cs at the interstitial A(1,2) sites, H2O groups and hydrogen bonding. The mineral is named in honour of Felix Artem'evich Letnikov (born October 3rd,1934) in recognition of his outstanding contributions to the field of petrology and geochemistry of Precambrian rocks.

In terrestrial rocks, Br minerals are extremely rare with only nine minerals known where Br is a dominant component. A new arsenite bromide mineral ermakovite, (NH4)(As2O3)2Br, was discovered at the tract of Kukhi-Malik, Fan-Yagnob coal deposit, ca. 75 km N of Dushanbe, Tajikistan. Ermakovite is a fumarolic mineral formed directly from gas from a natural underground coal fire. Associated minerals are sulfur, realgar, amorphous As-sulfides, salammoniac, alacránite, bonazziite and thermessaite-(NH4). In addition, there are amorphous As2S3 intergrowths associated with ermakovite. The mineral typically occurs as tabular or prismatic hexagonal crystals up to 200 μm with the following forms: c (001), m (010) and p (014). Spherulites and multi-twinned intergrowths are very common. The mineral is optically uniaxial (–), ω = 1.960 (5) and ɛ = 1.716(3) (589 nm). The measured density is 3.64(2) g/cm3. The mineral is insoluble in water, HCl, HNO3 and organic solvents. The empirical formula calculated on the basis of (As+Sb) = 4 atoms per formula unit is [(NH4)0.92Na0.01]0.93(As3.94Sb0.06)4.00O6.02(Br0.97Cl0.08I0.01)1.06. The strongest lines in the powder X-ray diffraction pattern are [d, Å (I, %) (hkl)]: 9.160 (80)(001); 4.560(90)(002); 3.228(100) (102); 2.629(80)(110); and 2.522(60)(103). Ermakovite is hexagonal, P6/mmm, a = 5.271(3), c = 9.157(6) Å, V = 220.3(3) Å3 and Z = 1. The sandwich-type structure of ermakovite is based on three types of layers: (1) a honeycomb [As2O3] arsenite layer; (2) an NH4+ layer; and (3) a Br layer. The layer stacking sequence is ⋅⋅⋅NH4–As2O3–Br–As2O3–NH4⋅⋅⋅. Ermakovite has a synthetic analogue. Infrared and Raman spectra are also reported.

An overview of the processes that give rise to high concentrations of Br, leading to the formation of exotic Br minerals, is given.

A new mineral falgarite, K4(V+4O)3(SO4)5 was discovered at the tract of Kukhi-Malik, Fan-Yagnob coal deposit, ca. 75 km N of Dushanbe, Tajikistan. The new mineral is named after the Falgar, an ancient Sogdian name for an area around the Zeravshan riverhead. Falgarite is a fumarolic mineral formed directly from a gas emitted by a natural underground coal fire. Associated minerals are anhydrite, baryte, molybdite, an unidentified Tl-vanadyl sulfate, K–Mg sulfate and an anhydrous Mg-sulfate. Falgarite forms small isometric or pseudo-octahedral individual crystals (10–60 μm) of turquoise colour and spherical aggregates up to 0.5 mm in diameter. Mohs hardness is ~ 2.5, Dmeas = 2.87(2) and Dcalc = 2.89 g/cm3. Refractive indices are: α = 1.588(3), β(calc.) = 1.600(3) and γ = 1.609(2) (590 nm). In transmitted light falgarite is transparent green with a weak pleochroism. The mineral is non-soluble in H2O and 5% HNO3 at room temperature. Infrared spectra support the absence of H2O and OH–. The chemical composition determined by electron-microprobe analysis is (wt.%): Na2O 0.55, K2O 20.76, Tl2O 1.83, VO2 29.38 and SO3 46.78, total 99.29. The empirical formula (based on 23 O apfu) is: (K3.76Na0.15Tl0.07)Σ3.98V3.02S4.99O23.0. The strongest lines of the powder X-ray diffraction pattern are [d,Å(I,%)(hkl)]: 3.20(70)(202); 3.17(80)024; 3.14(70)$\bar{2}$04; 3.01(50)$\bar{1}$51; and 2.88(100)151. Falgarite is monoclinic, P21/n, a = 8.7209(5), b = 16.1777(6), c = 14.4614(7) Å, β = 106.744(5)°, V = 1953.77(17) Å3, Z = 4 and R1 = 0.05. VO6 octahedra and SO4 tetrahedra link together by sharing corners thus forming a [(VO)3(SO4)5]4– framework. K+, Na+ and Tl+ cations are located in the channels of the framework. The synthetic K4(VO)3(SO4)5 analogue is known.

Akopovaite, ideally Li2Al4(OH)12(CO3)(H2O)3, is a new hydrotalcite-supergroup mineral from the Karasu–Karavshinskoye Sn deposit, Turkestan Range, Kyrgyzstan. It occurs as white or pale yellowish rosette-like aggregates that are composed of tiny curved plates up to 20–30 μm. Akopovaite is associated with gibbsite, quartz, albite, microcline, muscovite, montebrasite, siderite, schorl and birnessite-like Fe–Mn oxides. Akopovaite has a perfect cleavage along {001}, the mineral is transparent and very soft (VHN = 24 that corresponds to Mohs hardness of ca. 1). Dmeas = 2.12(2) g/cm3 and Dcalc = 2.106 g/cm3. The Raman spectra contain bands of carbonate groups and bands of O–H stretching vibrations. The chemical composition (wt.%, electron microprobe for Al and Fe; ICP-OES for Li; CHN method for CO2 and H2O) is Li2O 6.43, Al2O3 45.79, Fe2O3 0.27, CO2 10.09, H2O 36.1, total 98.68. The empirical formula based on (Li + Al + Fe) = 6 apfu is Li1.94(Al4.05Fe0.02)Σ4.07(OH)12(CO3)1.03(H2O)3.03. The crystal structure was refined by the Rietveld method with RB = 0.006 and Rwp = 0.014. Akopovaite is monoclinic, C2/m, a = 5.0953(6), b = 8.877(1), c = 7.806(1) Å, β = 102.572(6)°, V = 344.61(8) Å3 and Z = 1. The polytype should be denoted as 1M. The strongest lines of the powder X-ray diffraction pattern [d, Å (I, %) (hkl)] are: 7.66(100)(001), 4.397(27)(020), 3.821(45)(002,021), 2.4881(27)(200), 2.2273(16)(201) and 1.9027(18)(202). Akopovaite is the first naturally occurring hydrotalcite-supergroup carbonate species of Al and Li; its synthetic analogue is known.

Rinkite-(Y), ideally Na2Ca4YTi(Si2O7)2OF3, is a new rinkite-group (seidozerite-supergroup) TS-block mineral from the Darai-Pioz alkaline massif, Tian-Shan mountains, Tajikistan. The mineral is of hydrothermal origin. It occurs as aggregates (up to 1.5 cm long) of acicular crystals 0.1–1.0 mm thick, and as separate elongated columnar, flattened-prismatic crystals up to 1 cm long with rectangular or rhombic sections up to 0.5 mm across. Associated minerals are quartz, aegirine, microcline, neptunite, pectolite, calcite, eudialyte-group minerals, fluorite, titanite, turkestanite, kupletskite, galena, albite and pyrochlore-group minerals. Crystals are transparent and colourless to occasionally white, with a vitreous lustre. Rinkite-(Y) has a white streak, uneven, conchoidal fracture and does not fluoresce under a cathode or ultraviolet light. Cleavage is very good on {100}, no parting was observed, Mohs hardness is ~5, and it is brittle, Dmeas. = 3.44(2) g/cm3, Dcalc. = 3.475 g/cm3. It is biaxial (+) with refractive indices (λ = 590 nm) α = 1.662(2), β = 1.666(2), γ = 1.685(5); 2Vmeas. = 50(3) and 2Vcalc. = 49.7°. It is nonpleochroic. Rinkite-(Y) is monoclinic, space group P21/c, a = 7.3934(5), b = 5.6347(4), c = 18.713(1) Å, β = 101.415(2)° and V = 764.2(2) Å3. The six strongest reflections in the X-ray powder diffraction data [d(Å), I, (hkl)] are: 3.057, 100, (006, $\bar{2}$12, 210); 2.688, 28, (016); 9.18, 24, (002); 2.929, 17, ($\bar{2}$13, 211); 3.559, 15, (104, 014) and 2.783, 14, (021). The empirical formula calculated on 18 (O + F) is Na2.11(Ca3.74Sr0.03Mn0.03)Σ3.80(Y0.50Nd0.16Ce0.16Gd0.07Dy0.06Sm0.05Pr0.03La0.03${\rm U}_{0.01}^{{\rm 4 + }} {\rm )}_{\Sigma 1.07}{\rm (T}{\rm i}_{0.85}{\rm N}{\rm b}_{0.17}{\rm W}^{6+}_{0.01}{\rm T}{\rm a}_{0.01}{\rm )}_{\Sigma 1.04}\left( {{\rm S}{\rm i}_{4.03}{\rm O}_{14}} \right){\rm O}_{1.40}{\rm F}_{2.60}$ with Z = 2. The ideal formula is Na2Ca4YTi(Si2O7)2OF3. The crystal structure was refined on a twinned crystal to R1 = 4.59% on the basis of 1489 unique reflections (F > 4σF) and is a framework of TS (Titanium-Silicate) blocks. The TS block consists of HOH sheets (H – heteropolyhedral, O – octahedral) parallel to (100). In the O sheet, the Ti-dominant [6]MO1 site ideally gives 1 Ti apfu. The [8]MO2 and [6]MO3 sites are ideally occupied by Na and (NaCa) apfu. In the H sheet, the [7]MH site is occupied by Ca1.13Y0.50REE0.37, (REE = rare-earth element), ideally (CaY), <MH–φ> = 2.415 Å and the [7]AP site is occupied by Ca1.81REE0.19, ideally Ca2, <AP–φ> = 2.458 Å. The MH + AP sites ideally give (Ca3Y) apfu. The MH and AP polyhedra and Si2O7 groups constitute the H sheet. Linkage of H and O sheets via common vertices of MH and AP polyhedra and Si2O7 groups with MO1–3 polyhedra results in a TS block. The TS block in rinkite-(Y) exhibits linkage 1 and stereochemistry typical for the rinkite group (Ti = 1 apfu) of the seidozerite supergroup. For rinkite-(Y), the ideal structural formula of the form AP2MH2MO4(Si2O7)2$ \left( {{\rm X}_{\rm M}^{\rm O} } \right)_2\left( {{\rm X}_{\rm A}^{\rm O} } \right)_2{\rm is }\;\left( {{\rm C}{\rm a}_3{\rm Y}} \right){\rm Na}\left( {{\rm NaCa}} \right){\rm Ti}\left( {{\rm S}{\rm i}_2{\rm O}_7} \right)_2\left( {{\rm OF}} \right){\rm F}_2 $ with Z = 2. The mineral is named rinkite-(Y) as it is structurally identical to rinkite-(Ce) and Y is the dominant rare-earth element.

The hyalotekite group has been approved by the Commission on New Minerals, Nomenclature and Classification of the International Mineralogical Association (memorandum 57–SM/16). The general formula of the minerals of the hyalotekite group may be written as: A2B2M2[Si8T4O28]W where A = Ba2+, Pb2+ or K+; B = Ba2+, Pb2+ or K+; M = Ca2+, Y3+ or REE3+; T = Si4+, B3+ or Be2+; and W = F– or □ (where REE = rare-earth elements and □ = vacancy).

Four minerals are currently known in this group: hyalotekite, Ba4Ca2[Si8B2(SiB)O28]F, triclinic, I$\bar 1$; khvorovite, Pb2+4Ca2[Si8B2(SiB)O28]F, triclinic I$\bar 1$; kapitsaite-(Y), Ba4(YCa)[Si8B2B2O28]F, triclinic, I$\bar 1$; and itsiite Ba4Ca2[Si8B4O28]□, tetragonal, I$\bar 4$2m.

We explore the possible end-member compositions within this group by conflating the properties of an end-member with the stoichiometry imposed by the bond topology of the hyalotekite structure-type and the crystal-chemical properties of its known constituents. There are two high-coordination sites in the hyalotekite structure, A and B, and occupancy of each of these sites can be determined only by crystal-structure refinement. If these two sites are considered together, there are 19 end-member compositions of the triclinic structure and six end-member compositions of the tetragonal structure involving A and B = Ba2+, Pb2+, K+; M = Ca2+, Y3+, REE3+; and T = Si4+, B3+, Be2+. There is the possibility for many other hyalotekite-group minerals, and two potential new minerals have been identified from data in the literature.

Odigitriaite, a new Cs, Na, Ca borosilicate mineral, was discovered in moraine adjacent to the Darai-Pioz alkaline massif in the upper reaches of the Darai-Pioz river at the intersection of the Turkestansky, Zeravshansky and Alaisky mountain ridges, Tajikistan. It occurs as irregular thin flakes associated with quartz, pectolite, baratovite, fluorite, pekovite, polylithionite, aegirine, leucosphenite, pyrochlore, neptunite, reedmergnerite, mendeleevite-(Ce), zeravshanite and sokolovaite. It is colourless with a white streak, is translucent and has a vitreous lustre; it does not fluoresce under ultraviolet light. Odigitriaite is brittle with an uneven fracture and a Mohs hardness of 5. The calculated density is 2.80(2) g/cm3. The indices of refraction are α = 1.502, β = 1.564, γ = 1.576; 2Vobs = 46(2)°, dispersion is weak r > v, and there is no pleochroism. The chemical composition is as follows (electron microprobe, H2O calculated from structure): SiO2 55.30, Al2O3 0.09, Y2O3 0.44, MnO 0.94, FeO 0.10, PbO 0.21, K2O 0.01 Cs2O 8.36, B2O3 4.75, H2O 0.37, F 1.74, O = F2 –0.74, total 99.43 wt.%. The empirical formula of odigitriaite is Cs0.90Na5.12Ca4.68Mn0.20Y0.06Fe0.02Pb0.01[Si13.92Al0.03B2.06O38]F1.39(OH)0.62. The end-member formula is CsNa5Ca5[Si14B2O38]F2. The strong reflections in the powder X-ray diffraction pattern are: [(d, Å), (I, %), (hkl)]: 5.45 (25) (1 1 3), 4.66 (33) (3 1 1), 4.40 (26) (0 2 2), 4.10 (36) (3 1 3), 3.95 (25) (3̄ 1 3), 2.85 (31) (2 2 2), 2.68 (40) (0 0 6), 3.62 (45) (0 2 4), 3.35 (100) (2̄ 2 4), 3.31 (30) (3̄ 1 5), 3.25 (35) (4 0 4), 3.04 (60) (4̄ 2 2), 2.925 (22) (4̄ 2 3), 1.813 (23) (9 1 0). Odigitriaite is monoclinic, space group C2/c, a = 16.652(5), b = 9.598 (3), c = 22.120(7) Å, β= 92.875(14)°, V = 3530.9(1.9) Å3, Z = 4. The crystal structure of odigitriaite was solved by direct methods and refined to an R 1 value of 2.75% based on single-crystal X-ray data. It is a double-layer sheet-borosilicate mineral; Cs and Na are intercalated within the double-layer sheet, and the double layers are linked by interstitial Ca and Na atoms.

Mendeleevite-(Nd), (Cs,□)6(□,Cs)6(□,K)6(REE,Ca)30(Si70O175)(OH,H2O,F)35 is a new mineral from the Darai-Pioz alkaline massif, Tajikistan. Mendeleevite-(Nd) was found in a pectolite aggregate in silexites (quartz-rich rocks) which consist of fine to medium pectolite grains, quartz, aegirine and fluorite, with minor khvorovite, mendeleevite-(Ce), sokolovaite, hyalotekite, orlovite, kirchhoffite, pekovite, neptunite, zeravshanite, senkevichite, nordite-(Nd), alamosite, pyrochlore-group minerals and baratovite. Mendeleevite-(Nd) forms colourless cubic crystals 10–40 μm in size; it has a vitreous lustre and a Mohs hardness of 5–5.5; Dmeas. = 3.20(2) g/cm3, Dcalc. = 3.155 g/cm3. Mendeleevite-(Nd) is optically isotropic, with the refractive index n = 1.582(2). Mendeleevite-(Nd) is cubic, space group Pm3̄, a = 21.9106(4) Å; Z = 2. The six strongest reflections in the powder X-ray diffraction pattern are [d (Å), I (%), (h k l)] are: 11.01, 100, (0 0 2); 15.63, 55, (0 1 1); 3.47, 42, (2 0 6); 3.099, 42, (3 4 5); 2.192, 42, (0 0 10); 1.819, 41, (3 6 10). Chemical analysis by electron microprobe gave SiO2 42.30, Ce2O3 10.12, La2O3 3.60, Nd2O3 16.19, Pr2O3 2.79, Sm2O3 4.19, Gd2O3 1.69, Eu2O3 0.47, SrO 2.99, CaO 2.20, Cs2O 8.50, K2O 0.85, H2O 3.85, F 1.25, –O = F2 –0.53, sum 100.46 wt.%, with H2O calculated by analogy with mendeleevite-(Ce). The empirical formula based on 210 (O + F) apfu, with F + OH + H2O = 35 pfu, is Cs6(□4.20K1.80)∑6{[(Nd9.57Ce6.13Sm2.39La2.20Pr1.68Gd0.93Eu0.27)∑23.17(Ca3.90Sr2.87)∑6.77]∑29.94□0.06}∑30(Si70.03O175)(OH14.47F6.54)∑21.01 (H2O)14, Z = 2. The simplified and ideal formulae are (Cs,□)6 (□,Cs)6(□,K)6 (REE,Ca)30 (Si70O175)(OH, H2O,F)35 and Cs6(REE23Ca7)(Si70O175)(OH,F)19(H2O)16, respectively. The compatibility index (from measured density) = – 0.039 (excellent). Mendeleevite-(Nd) is a Nd analogue of mendeleevite-(Ce), (Cs,□)6(□,Cs)6(□,K)6(REE,Ca,□)30(Si70O175)(H2O,OH,F,□)35. Both minerals are named after Dmitri Mendeleev (1834–1907), the great Russian chemist, author of the periodic table of chemical elements, who has had a significant impact on the development of natural sciences and industry, both in Russia and around the world.