Potassic-jeanlouisite, ideally K(NaCa)(Mg4Ti)Si8O22O2, is the first characterised species of oxo amphibole related to the sodium–calcium group, and derives from potassic richterite via the coupled exchange CMg–1W${\rm OH}_{{\rm \ndash 2}}^{\ndash}{} ^{\rm C}{\rm Ti}_1^{{\rm 4 +}} {} ^{\rm W}\!{\rm O}_2^{2\ndash} $. The mineral and the mineral name were approved by the International Mineralogical Association Commission on New Minerals, Nomenclature and Classification, IMA2018-050. Potassic-jeanlouisite was found in a specimen of leucite which is found in the lava layers, collected in the active gravel quarry on Zirkle Mesa, Leucite Hills, Wyoming, USA. It occurs as pale yellow to colourless acicular crystals in small vugs. The empirical formula derived from electron microprobe analysis and single-crystal structure refinement is: A(K0.84Na0.16)Σ1.00B(Ca0.93Na1.02Mg0.04${\rm Mn}_{{\rm 0}{\rm. 01}}^{2 +} $)Σ2.00C(Mg3.85${\rm Fe}_{{\rm 0}{\rm. 16}}^{2 +} $Ni0.01${\rm Fe}_{{\rm 0}{\rm. 33}}^{3 +} {\rm V}_{{\rm 0}{\rm. 01}}^{3 +} $Ti0.65)Σ5.01T(Si7.76Al0.09Ti0.15)Σ8.00O22W[O1.53F0.47]Σ2.00. The holotype crystal is biaxial (–), with α = 1.674(2), β = 1.688(2), γ = 1.698(2), 2Vmeas. = 79(1)° and 2Vcalc. = 79.8°. The unit-cell parameters are a = 9.9372(10), b = 18.010(2), c = 5.2808(5) Å, β = 104.955(2)°, V = 913.1(2) Å3, Z = 2 and space group C2/m. The strongest eight reflections in the powder X-ray pattern [d values (in Å) (I) (hkl)] are: 2.703 (100) (151); 3.380 (87) (131); 2.541 (80) ($\bar 2$02); 3.151 (70) (310); 3.284 (68) (240); 8.472 (59) (110); 2.587 (52) (061); 2.945 (50) (221,$\bar 1$51).

The complete mineral description of potassic-magnesio-arfvedsonite, a recently approved (IMA2016-083) new species of the amphibole supergroup is provided using electron microprobe analysis (EMPA), laser ablation inductively coupled plasma mass spectrometry, single-crystal structure refinement, Mössbauer and Raman spectroscopy, as well as measurement of optical and physical properties. The holotype material was found in syenitic and granitic dyke rocks in association with quartz, potassium feldspar and aegirine–augite from the Buhovo–Seslavtsi pluton, Bulgaria. Potassic-magnesio-arfvedsonite is monoclinic C2/m, with unit-cell parameters: a = 9.9804(11), b = 18.0127(19), c = 5.2971(6) Å, β = 104.341(2)° and V = 922.61 Å3. In transmitted plane-polarised light (λ = 590 cm–1), potassic-magnesio-arfvedsonite is pleochroic: X = yellow pale-green, Y = green and Z = dark-violet brown. It is biaxial (–), α = 1.645(2), β = 1.655(2), γ = 1.660(2) and 2Vmeas. = 60° and 2Vcalc. = 70°. The empirical unit formula obtained from EMPA and structure refinement is A(K0.86Na0.0.08)0.94B(Na1.74Ca0.25 Mn2+0.01)2.00C(Mg2.67Fe2+1.42Fe3+0.76Ti0.12Mn2+0.03)5.00TSi8O22W(OH1.58F0.22O0.20)2.00. The Fe3+/Fetot ratio (0.35) is consistent with both the Mössbauer spectra and the single-crystal structure refinement. The 10 strongest X-ray powder reflections [d values (in A°), I, (hkl)] are: 8.519, 80.5, (110); 3.402, 67.3, (131); 3.295, 41.0, (240); 3.173, 65.0, (310); 2.752, 35.6, ($\bar{3}$31); 2.715, 100.0 (151); 2.591, 44.1, (061); 2.542, 73.2, ($\bar{2}$02); 2.348, 38.5, ($\bar{3}$51); 2.174, 42.0, (261). Potassic-magnesio-arfvedsonite is the product of strongly peralkaline and potassic (perpotassic) magma compositions. Trace-element analysis shows that this amphibole did not exert significant control on trace-element distribution in the crystallising peralkaline magma.

Ferri-fluoro-katophorite is the second species characterised involving the rootname katophorite in the sodium–calcium subgroup of the amphibole supergroup. The mineral and its name were approved by the International Mineralogical Association Commission on New Minerals, Nomenclature and Classification, IMA2015-096. It was found in the Bear Lake diggings, Bancroft area, Ontario, Canada, where coarse euhedral crystals of amphibole, phlogopite, sanidine solid-solution (now coarsely exsolved to microcline perthite), titanite, augite, zircon and fluorapatite crystallised from a low-viscosity silicocarbonatitic magma of crustal origin. Greenish grey prismatic crystals of ferri-fluoro-katophorite generally protrude from the walls into a body of coarsely crystalline calcite, but they also occur away from the walls, completely enclosed by calcite. The empirical formula derived from electron microprobe analysis and single-crystal structure refinement is: A(Na0.55K0.32)Σ0.87B(Na0.79Ca1.18Mn2+0.03)Σ2.00C(Mg3.29Mn2+0.02Fe2+1.19Fe3+0.31Al0.09Ti4+0.08Li0.02)Σ5.00T(Si7.39Al0.61)Σ8.00O22W[F1.23 (OH)0.77]Σ2.00. Ferri-fluoro-katophorite is biaxial (–), with α = 1.640(2), β = 1.652(2), γ = 1.658(2), 2Vmeas. = 68.9(2)° and 2Vcalc.. = 70.1°. The unit-cell parameters are a = 9.887(3), b = 18.023(9), c = 5.292(2) Å, β = 104.66(3)°, V = 912.3(6) Å3, Z = 2 and space group C2/m. The strongest ten lines in the powder X-ray pattern [d values (in Å) I (hkl)] are: 2.708, 100, (151); 2.388, 74, (131); 3.139, 72, (310); 8.449, 69, (110); 2.540, 65, ($\bar{2}$02); 2.591, 53, (061); 2.739, 47, ($\bar{3}$31); 2.165, 45, (261); 3.279, 44, ($\bar{2}$40); 2.341, 43, ($\bar{3}$51).

Magnesio-hornblende (IMA2017-059) has been characterized in a specimen collected in the sand dunes of Lüderitz, Karas Region, Namibia. The empirical formula derived from electron microprobe analysis and single-crystal structure refinement is A(□0.73Na0.22K0.05)Σ1.00B(Ca1.79Fe2+0.10Mg0.04Mn2+0.03Na0.04)Σ2.00C(Mg3.48Fe2+0.97Al0.28Fe3+0.23Cr3+0.01Ti0.03)Σ5.00T(Si7.18Al0.82)Σ8.00O22W[(OH)1.93F0.05Cl0.02]Σ2.00. Magnesio-hornblende is biaxial (–), with α = 1.640(2), β = 1.654(2), γ = 1.666(2) (measured with gel-filtered Na light, λ = 589.9 nm), 2V (meas.) = 82(1)° and 2V (calc.) = 84.9°. The unit-cell parameters are a = 9.8308(7), b = 18.0659(11), c = 5.2968(4) Å, β = 104.771(6)° and V = 909.64 (11) Å3 with Z = 2 and space group C2/m. The strongest eight reflections in the X-ray powder pattern [d values (in Å), I, (hkl)] are: 2.709, 100, (151); 8.412, 74, (110); 3.121, 73, (310); 2.541, 58, ($\bar{2}$02); 3.386, 49, (131); 2.596, 45, (061); 2.338, 41, ($\bar{3}$51); and 2.164, 39, (261).

During systematic characterization of amphiboles that still lack a complete mineral description, fluoro-tremolite was identified in a specimen from the Limecrest-Southdown quarry, Sparta, New Jersey, USA, which was provided by the Franklin Mineral Museum. The ideal formula of fluoro-tremolite is A□ BCa2CMg5TSi8O22WF2 and the empirical formula derived for the holotype specimen, based on the results of electron-microprobe analysis and single-crystal structure refinement, is A(Na0.28K0.02)Σ0.30B(Ca1.99Na0.01)Σ2.00C(Mg4.70${\rm Fe}_{{\rm 0}{\rm. 28}}^{{\rm 2 +}} $Zn0.01${\rm Ti}_{{\rm 0}{\rm. 01}}^{{\rm 4 +}} $)Σ5.00T(Si7.68Al0.32)Σ8.00O22W(F1.16OH0.84)Σ2.00. The unit-cell dimensions in space group C2/m are a = 9.846(2), b = 18.050(3), c = 5.2769(14) Å, β = 104.80(2)° and V = 906.7 (3) Å3 and Z = 2; the a:b:c ratio is 0.545:1:0.292. Fluoro-tremolite is biaxial (+), with α = 1.5987(5), β = 1.6102(5), γ = 1.6257(5), 2V(meas.) = 85(1)o and 2V(calc.) = 82o. The strongest ten reflections in the powder X-ray pattern [d values (in Å), I, (hkl)] are: 2.706, 100, (151); 3.126, 67, (310); 2.531, 59, ($\bar 2$02); 3.381, 57, (131); 2.940, 43, ($\bar 1$51, 221); 3.276, 37, (240); 2.337, 36, ($\bar 3$51); 2.592, 35, (061); 2.731, 34, ($\bar 3$31); 2.163, 34, (261). Both the mineral and the mineral name have been approved by the Commission on New Minerals, Nomenclature and Classification of the International Mineralogical Association (IMA2016–018); the holotype has been deposited at the Franklin Mineral Museum (32 Evans Street, Franklin, 07416 New Jersey, US), under the catalogue number 7710.

Comparison with new data on tremolite and synthetic fluoro-tremolite provides a more sound crystal-chemical model of the end-member compositions and their solid-solution.

Clino-suenoite, ideally □${\rm Mn}_{2}^{2 +} $Mg5Si8O22(OH)2 is a new amphibole of the magnesium-iron-manganese subgroup of the amphibole supergroup. The type specimen was found at the Lower Scerscen Glacier, Valmalenco, Sondrio, Italy, where it occurs in Mn-rich quartzite erratics containing braunite, rhodonite, spessartine, carbonates and various accessory minerals. The empirical formula derived from electron microprobe analysis and single-crystal structure refinement is: ANa0.04B(${\rm Mn}_{1.58}^{2 +} $Ca0.26Na0.16)Σ2.00C(Mg4.21${\rm Mn}_{0. 61}^{2 +} {\rm Fe}_{0.04}^{2 +} $Zn0.01Ni0.01${\rm Fe}_{0.08}^{3 +} $Al0.04)Σ5.00TSi8.00O22W[(OH1.94F0.06)]Σ=2.00. Clino-suenoite is biaxial (+), with α = 1.632(2), β = 1.644(2), γ = 1.664(2) and 2Vmeas. = 78(2)° and 2Vcalc. = 76.3°. The unit-cell parameters in the C2/m space group are a = 9.6128(11), b = 18.073(2), c = 5.3073(6) Å, β = 102.825(2)° and V = 899.1(2) Å3 with Z = 2. The strongest ten reflections in the powder X-ray diffraction pattern [d (in Å), I, (hkl)] are: 2.728, 100, (151); 2.513, 77, ($\bar 2$02); 3.079, 62, (310); 8.321, 60, (110); 3.421, 54, (131); 2.603, 42, (061); 2.175, 42, (261); 3.253, 41, (240); 2.969, 40, (221); 9.036, 40, (020).

In this work we report on a complete crystal-chemical characterization of a near end-member riebeckite from Malawi, and use the available data to critically compare information obtained from different analytical methods. The sample occurs as well-formed and very large single crystals in pegmatitic rocks. Accurate site-populations were determined by combining single-crystal structure refinement and electron microprobe analysis (EMPA). The Fe3+/Fe2+ ratio was obtained from Mössbauer spectroscopy. Lithium was quantified by Laser Ablation Inductively Coupled Plasma Mass Spectroscopy (LA-ICP-MS).

Fourier-Transform Infrared (FTIR) spectra, collected both on powders and single crystals, are presented and discussed. FTIR spectra in the NIR region are also presented for the first time for this amphibole. The FTIR data are compatible with complete local ordering of A cations close to F, and complete Fe2+/Mg disorder at M(1,3). Polarized Raman-scattering data collected from single crystals confirm this conclusion. In addition, it was found that FTIR data collected on powders provide the best agreement with the site occupancies derived from chemical (EMPA and LA-ICP-MS) and crystal-chemical data, possibly because they do not depend on experimental issues such as orientation and polarization.

Magnesio-riebeckite from the dumps of the abandoned mine of Varenche (45°47’22’’ N, 7°29’17’’ E), Saint-Barthélemy, Nus, Aosta Valley (Italy), was studied to provide the complete mineral description (including crystal structure) and insights into the crystal-chemistry of riebeckite. The empirical formula derived from electron microprobe analysis and single-crystal structure refinement is A(Na0.09K0.01)Σ=0.10B(Na1.77Ca0.11Mg0.08Mn2+ 0:04)Σ=2.00C(Mg2.93Mn2+ 0:13Fe2+ 0:07Zn0.01Ni0.12Fe3+1:25Al0.48Ti0.01)Σ=5.00T(Si7.92Al0.08)Σ=8.00 O22W(OH1.88F0.12)Σ=2.00. Magnesio-riebeckite is biaxial (+), with α = 1.678(2), β = 1.682(2), γ = 1.688(2) and 2V (meas.) = 80.2(1.7)°, 2V (calc.) = 78.7°. The unit-cell parameters are a = 9.6481(14), b = 17.873(3), c = 5.3013(7) Å, β = 103.630(2)°, V = 888.4 (2)Å3, Z = 2, space group C2/m. The strongest ten reflections in the powder X-ray pattern [d values (in Å), I, (hkl)] are: 2.701, 100, (151); 8.303, 83, (110); 3.079, 62, (310); 3.391, 53, (131); 4.467, 50, (040,021); 2.522, 50, (̅202); 2.578, 35, (061); 2.155, 30, (261), 4.855, 30, (̅111), 2.300, 29, (̅351).

Pink-orange crystals of a composition within the ferri-obertiite compositional space were found in vesicles in a pale beige silicate vein found from a basalt quarry at Mount Rothenberg, Eifel district, Germany. Associated minerals are potassic feldspar, alpha quartz paramorphic afterbeta quartz, eifelite (the second occurrence after the Caspar quarry at Bellerberg volcano, Eifel region), tridymite, rutile, roedderite and other amphiboles. The ideal formula of ferri-obertiite is ANaBNa2C(Mg3Fe3+Ti)TSi8O22WO2; the empirical formula derived for the holotype specimen from Mount Rothenberg from the results of electron-microprobe analysis and single-crystal structure refinement is A(Na0.76K0.22)∑0.98B(Na1.61Ca0.35Mn0.042+)∑2.00C(Mg3.58Mn0.112+Fe0.623+Ti0.664+Cr0.013+Zn0.01Ni0.01)∑5.00T(Si7.82Ti0.124+Al0.06)∑8.00O22W[O1.26F0.55(OH)0.19]∑2.00. The unit-cell dimensions are a = 9.7901(7), b = 17.9354(13), c = 5.2892(4)Å, β= 104.142(2)°, V = 900.58 (11) Å3. The space group is C2/m, Z = 2. Ferri-obertiite is biaxial (+), with α = 1.664, β = 1.680, γ = 1.722, all ±0.002 and 2V (meas.) = 66.4(3)o, 2V (calc.) = 64.7o.The strongest eight reflections in the powder X-ray pattern [d values (in Å), I, (hkl)] are: 2.704, 100, (151); 3.116, 76, (310); 3.388, 72, (131); 8.931, 72, (110); 2.529, 67, (202); 2.583, 39, (061); 2.160, 38, (261); 3.260, 37, (240). Both the mineral and thename have been approved by the Commission on New Minerals, Nomenclature and Classification of the International Mineralogical Association (IMA 2015-079); the rock specimen has been deposited at the Museo di Mineralogia, Dipartimento di Scienze della Terra e dell'Ambiente, Universitàdegli Studi di Pavia, under the code 2015-02.

Magnesio-arfvedsonite, the CFe3+-dominant analogue of eckermannite, has been found in a sample of “szechenyite” in the mineral collection of the American Museum of Natural History (AMNH H35024). It comes from the northern part of the Jade Mine Tract near Hpakan, Kachin State, Myanmar. Associated minerals are kosmochlor–jadeite solid-solution pyroxene and clinochlore. The ideal formula of magnesio-arfvedsonite is ANaBNa2C(Mg4Fe3+)TSi8O22W(OH)2, and the empirical formula derived from electron microprobe analysis and single-crystal structure refinement for the sample of this work is A(Na0.96K0.04)Σ=1.00B(Na1.57Ca0.40Fe0.022+Mn0.01)Σ=2.00C(Mg4.26Fe0.192+Fe0.413+Al0.11Ti0.034+)Σ=5.00T(Si7.99Al0.01)Σ=8.00O22W[F0.02(OH)1.98]Σ=2.00. The unit-cell dimensions are a = 9.867(1), b = 17.928(2), c = 5.284(1) Å, β = 103.80(2)°, V = 907.7 (2) Å3, Z = 2. Magnesio-arfvedsonite is biaxial (–), with α = 1.624, β = 1.636, γ = 1.637, all ± 0.002 and 2Vobs = 36(1)°, 2Vcalc = 32°. The ten strongest reflections in the X-ray powder pattern [d values (in Å), I, (hkl)] are: 2.708, 100, (151); 3.399, 68, (131); 3.144, 63, (310); 2.526, 60, (202); 8.451, 46, (110); 3.273, 39, (240); 2.167, 37, (261); 2.582, 34, (061); 2.970, 34, (221); 2.326, 33, [(251) (421)].

Katophorite has the ideal formula ANaB(NaCa)C(Mg4Al)T(Si7Al)O22W(OH)2 (Hawthorne et al., 2012). No published analyses of amphiboles fall in the katophorite compositional field, except that of Harlow and Olds (1987) for an amphibole from near Hpakan in the Jade Mine Tract, Myanmar. This amphibole was approved by the International Mineralogical Association Commission on New Minerals, Nomenclature and Classification (vote 2013-140) as katophorite, and is reported here. Holotype katophorite is monoclinic, space group C2/m, a = 9.8573(8), b = 17.9617(15), c = 5.2833(4) Å, β = 104.707(2)°, V = 904.78(13) Å3, Z = 2. The calculated density is 3.091 g cm–3. In plane-polarized light, katophorite is pleochroic, X = pale blue (medium), Y = light blue-green (strongest), Z = colourless; X ∧ a = 30.6° (β obtuse), Y || b, Z ∧ c = 15.8 (β acute). It is biaxial negative, α = 1.638, β = 1.642, γ = 1.644, all ± 0.002; 2Vobs = 73(1)°, 2Vcalc = 70°. The eight strongest lines in the powder X-ray diffraction pattern are [d in Å (I)(hkl)]: 2.700 (100)(151), 3.129 (69)(310), 2.536 (65)(202), 3.378 (61)(131), 8.421 (55)(110), 2.583 (46)(061), 2.942 (43)(221) and 2.334 (41)(351). Electron-microprobe analysis of the refined crystal gave SiO251.74, Al2O37.38, TiO2 0.14, FeO 1.55, Fe2O3 2.82, MgO 18.09, CaO 8.17, Na2O 6.02, K2O 0.24, F 0.06, H2Ocalc. 1.80, Li2Ocalc. 0.09, sum 100.55 wt.% (Li2O and H2O based on the results of single-crystal structure refinement). The formula unit, calculated on the basis of 24 (O,OH,F) with (OH + F + O) = 2 is: A(Na0.85K0.04)Σ=0.89B(Ca1.22Na0.78)Σ=2.00C(Mg3.76Al0.43Fe0.303+Cr0.273+Fe0.182+Li0.05Ti0.014+)Σ=5.00T(Si7.21Al0.79)Σ=8.00O22W[(OH)1.67O0.30F0.03)]Σ=2.00.

Ferro-ferri-hornblende is a new member of the amphibole supergroup (IMA-CNMNC 2015-054). It has been found in a rock specimen from the historical collection of Leandro De Magistris, which was collected at the Traversella mine (Val Chiusella, Ivrea, Piemonte, Italy). The specimen was catalogued as ‘speziaite', and contains a wide range of amphibole compositions from tremolite/actinolite to magnesio-hastingsite. The end-member formula of ferro-ferri-hornblende is A□BCa2c(Fe+Fe3+)T(Si7Al) O22W(OH)2 , which requires SiO2 43.41, Al2O3 5.26, FeO 29.66, Fe2O3 8.24 CaO 11.57, H2O 1.86, total 100.00 wt.%. The empirical formula derived from electron microprobe analysis and single-crystal structure refinement for the holotype crystal is A(Na0.10K0.13) Σ=0.23B(Ca 1.93Na0.07)Σ=2.00C(Mg1.16Fe2+3.21Mn0.O6Fe3+0.45 Al0.12Ti 0.01)Σ=5.01T(Si7.26Al0. 74)Σ=8.00 O22W(OH1.89F0.01C10.10)Σ=2.00- Ferro-ferri-hornblende is biaxial (-), with α = 1.697(2), P = 1 .722(5), γ = 1.726(5) and 2V (meas.) = 35.7(1.4)°, 2V (calc.) = 43.1°. The unit-cell parameters are a = 9.9307(5), b = 18.2232(10), c = 5.3190(3) Å, β = 104.857(1)°, V= 930.40 (9) Å3, Z= 2, space group C2/m. The a:b:c ratio is 0.545:1:0.292. The strongest eight reflections in the powder X-ray pattern [d values (in Å), I, (hkl)] are: 8.493, 100, (110); 2.728, 69, (151); 3.151, 47, (310); 2.555, 37, (); 2.615, 32, (061); 2.359, 28, (); 3.406, 26, (131); 2.180, 25, (261). Type material is deposited in the collections of the Museo di Mineralogia, Dipartimento di Scienze della Terra e dell'Ambiente, Università di Pavia, under the catalogue number 2015-01. Sample M/U15285 from the historical collection of Luigi Colomba, presently at the Museo Regionale di Scienze Naturali di Torino, was also checked, and the presence of ferro-ferri-hornblende was confirmed.

New chemical (EMP, SIMS) and structural data are reported for a suite of crystals of oxo-mangani-leakeite and mangano-mangani-ungarettiite from their common type locality, the Hoskins mine (New South Wales, Australia). Notwithstanding the low OH content, FTIR analysis of selected sampleshas provided considerable information on short-range order in these Mn3+-rich amphiboles, and shows that Li is associated with occupied A sites and is linked to the oxo-component at the O(3) site. Comparative analysis of all available data allows us to: (1) further improveour understanding of the crystal-chemistry of these very peculiar compositions of the oxo-amphibole group; and (2) calculate reliable site-populations. The proposed limited compositional variability has been confirmed. The two amphiboles have completely different arrangements of CR3+cations. In oxo-mangani-leakeites, those CR3+ cations related to the oxocomponent occur at the M (1) site, whereas those CR3+ cations related to the leakeite charge-arrangement occur at the M (2) site. In mangano-mangani-ungarettiite,all CR3+ cations order at the M (1) and M (3) sites, and local bond-valence requirements are satisfied by the presence of Mn3+, which assumes a strongly distorted coordination due to its degenerate eg electronic state. Therefore,the inverse patterns observed for both cation-ordering and deformation of the octahedra are incompatible with solid-solution between these two species that coexist at the Hoskins mine.

Magnesio-ferri-fluoro-hornblende has the ideal formula A□B Ca2C(Mg4Fe3+)T(Si7Al)O22WF2 (Hawthorne et al., 2012). The holotype sample described in this work occurs as prismatic crystals in vugs of volcanic rocks (Seruci ignimbrites), found along the coast road ∼5.5 km northeast of Portoscuso, Cagliari, Sardinia; associated minerals are tridymite, todorokite, magnetite, and hematite. The name and the mineral were approved by the IMA CNMNC (2014-091). Holotype magnesio-ferri-fluoro-hornblende is monoclinic, space group C2/m, a = 9.839(5), b = 18.078(9), c = 5.319(3) Å, β = 104.99(3)°, V = 913.9(9) Å3, Z = 2. The density calculated from the empirical formula is 3.315 g cm–3. In plane-polarized light, magnesio-ferri-fluoro-hornblende is pleochroic, X = pale grey (least), Y = dark grey (most), Z = pale brownish grey (intermediate); X^ a = 47.6° (β obtuse), Y // b, Z^ c = 33.4° (β acute). It is biaxial negative, α = 1.669, β = 1.676, γ = 1.678, all ±0.002; 2Vobs = 74(1)°, 2Vcalc = 56°. The strongest eight lines in the powder X-ray diffraction pattern are [d in Å (I)(hkl)]: 2.711 (100)(151), 8.412 (89)(110), 3.121 (64)(310), 2.553 (61)(2̄02), 3.389 (55)(131), 2.599 (45)(061), 2.164 (36)(261), and 2.738 (34)(3̄31). Electron-microprobe analysis of the refined crystal gave SiO2 45.34, Al2O3 6.18, TiO2 1.22, FeO 15.24, Fe2O3 6.27, MgO 9.71, MnO 0.78, ZnO 0.06, CaO 10.18, Na2O 1.35, K2O 1.15, F 3.22, Cl 0.30, H2Ocalc 0.37, sum 99.95 wt.%. The empirical formula unit, calculated on the basis of 24 (O, OH, F, Cl) apfu with (OH + F + Cl) = 2 apfu is: (Na0.15K0.22)∑0.37(Na0.25Ca1.66Mn0.09)∑2.00(Mg2.20Fe2+1.94Mn0.01Zn0.01Fe3+0.72Ti0.13)∑5.01 (Al1.11Si6.89)∑8.00O22[F1.55(OH)0.37Cl0.08)∑2.00.

Oxo-mangano-leakeite, a newly approved end-member of the amphibole supergroup (IMA-CNMNC 20150-35), has been found in a rock containing manganese silicate and oxide at the Hoskins Mine, a Mn deposit 3 km west of Grenfell, New South Wales. The end-member formula of oxo-mangani-leakeite is ANaBNa2C(Mn3+4Li)TSi8 O22WO2, which would require SiO2 53.15, Mn2O3 34.91, Li2O 1.66, Na2O 10.28, total 100.00 wt.%. The empirical formula derived for the sample of this work from electron and ion microprobe analysis using constraints resulting from single-crystal structure refinement is A(Na0.65K0.36)∑ = 1.01B(Na1.94Ca0.06)∑ = 2.00C(Mg1.60Zn0.01 Li0.58)∑ = 5.01T(Si7.98Al0.02)∑ = 8.00O22W(O1.34OH0.66)∑ = 2.00. Oxo-mangano-leakeite is biaxial (–), with α = 1.681, β = 1.712, γ = 1.738, all ± 0.002, and 2V (meas.) = 81.0(4)°, 2V (calc.) = 83.5°. The unit-cell dimensions are a = 9.875(5), b = 17.873(9), c = 5.295(2) Å, β = 104.74(3)°, V = 903.8 (7) Å3; the space group is C2/m, with Z = 2. The strongest ten reflections in the powder X-ray pattern [d values (in Å), I, (hkl)] are: 8.423, 100, (110); 3.377, 46, (131); 4.461, 40, (040); 4.451, 40, (021); 3.134, 37, (310); 2.694, 37, (151); 2.282, 27, (); 2.734, 25, (31); 2.575, 24, (061); 2.331, 24, [() ()]. The holotype material is deposited in the Canadian Museum of Nature, Ottawa, under the catalogue number CMNMC 86895.