Paratacamite-(Mg) (IMA 2013-014), Cu 3 (Mg,Cu)Cl 2 (OH) 6 , is the new Mg-analogue of paratacamite. It was found near the village of Cuya in the Camarones Valley, Arica Province, Chile. The mineral is a supergene secondary phase occurring in association with anhydrite, atacamite, chalcopyrite, copiapite, dolomite, epsomite, haydeeite, hematite, magnesite and quartz. Paratacamite-(Mg) crystals are rhombs and thick to thin prisms up to 0.3 mm in size exhibiting the forms {201} and {001}. Twinning by reflection on {101} is common. The mineral is transparent with a vitreous lustre, with medium to deep-green colour and light-green streak. Mohs hardness is 3À3Ý, the tenacity is brittle and the fracture is conchoidal. Paratacamite-(Mg) has one perfect cleavage on {201}. The measured and calculated densities are 3.50(2) and 3.551 g cm À3 , respectively. The mineral is optically uniaxial (À) with e = 1.785(5) and o > 1.8 and slight pleochroism: O (bluish green) > E (green). Electron-microprobe analyses provided the empirical formula Cu 3 (Mg 0.60 Cu 0.38 Ni 0.01 Mn 0.01 )Cl 2 (OH) 6 . The mineral is easily soluble in dilute HCl. Paratacamite-(Mg) is trigonal, R3, with cell parameters a = 13.689(1), c = 14.025(1) Å , V = 2275.8(3) Å 3 and Z = 12. There is a pronounced sub-cell corresponding to a' & Ýa, c' & c in space group R3m. The eight strongest lines in the X-ray powder diffraction pattern are [d obs Å (I)(hklThe structure was refined to R 1 = 0.039 for 480 F o > 4sF reflections. Refinement using interlayer Mg-Cu site scattering factors indicated that Mg is distributed statistically between both interlayer octahedra M1O 6 and M2O 6 . A comparison of the distortions associated with M1O 6 and M2O 6 octahedra suggest that the sample is near the upper compositional limit for stability of the R3 phase.
Tondiite, with the simplified formula Cu3Mg(OH)6Cl2, occurs as a rare supergene mineral in a phonolitic tephrite from the type locality, Vesuvius volcano, Italy, as well as associated with haydeeite in the Santo Domingo Mine, Arica Province, Chile. It is emerald green to bright green in colour and occurs in irregularly shaped crystals, often with stepped faces. Its calculated density is 3.503 g cm−3. Tondiite crystallizes with the herbertsmithite structure type, space group Rm. Lattice parameters are a = 6.8377(7) Å and c = 14.088(2)Å for the holotype material. The c parameter may vary with Mg/Cu ratio and the presence of impurity atoms. The five strongest lines in the calculated powder diffraction pattern are [d in Å(I)(hkil)]: 5.459(88)(101), 3.419(22)(110), 2.764(100)(112 3), 2.266(54)(024), 1.706(26)(220). Several tondiite crystals have been examined by single-crystal X-ray diffraction and by electron microprobe analysis. The observed Mg content ranges between 0.6 and 0.7 atoms per formula unit. The structural role of Mg is discussed.
The new mineral torrecillasite (IMA2013-112), Na(As,Sb)43+O6Cl, was found at the Torrecillas mine, Iquique Province, Chile, where it occurs as a secondary alteration phase in association with anhydrite, cinnabar, gypsum, halite, lavendulan, magnesiokoritnigite, marcasite, quartz, pyrite, scorodite, wendwilsonite and other potentially new As-bearing minerals. Torrecillasite occurs as thin colourless prisms up to 0.4 mm long in jack-straw aggregates, as very thin fibres in puff balls and as massive intergrowths of needles. Prisms are elongated on [100] with diamond-shaped cross-section and irregular terminations. Crystals are transparent, with adamantine lustre and white streak. The Mohs hardness is 2½, tenacity is brittle and fracture is irregular. Cleavage on (001) is likely. The calculated density is 4.056 g cm−3. Optically, torrecillasite is biaxial (−) with α = 1.800(5), β = 1.96(1), γ = 2.03(calc.) (measured in white light). The measured 2V is 62.1(5)°, no dispersion or pleochroism were observed, the optical orientation isX=c,Y=b,Z=a. The mineral is very slowly soluble in H2O, slowly soluble in dilute HCl and rapidly soluble in concentrated HCl. The empirical formula, determined from electron-microprobe analyses, is (Na1.03Mg0.02)∑1.05(As3.39Sb0.62)∑4.01O6.07Cl0.93. Torrecillasite is orthorhombic,Pmcn, a= 5.2580(9),b= 8.0620(13),c= 18.654(3) Å,V= 790.7(2) Å3andZ= 4. The eight strongest X-ray powder diffraction lines are [dobsÅ(I)(hkl)]: 4.298(33)(111), 4.031(78)(014,020), 3.035(100)(024,122), 2.853(39)(115,123), 2.642(84)(124,200), 2.426(34)(125), 1.8963(32)(225) and 1.8026(29)(0·1·10,233). The structure, refined toR1= 4.06% for 814Fo>4σFreflections, contains a neutral, wavy As2O3layer parallel to (001) consisting of As3+O3pyramids that share O atoms to form six-membered rings. Successive layers are flipped relative to one another and successive interlayer regions contain alternately either Na or Cl atoms. Torrecillasite is isostructural with synthetic orthorhombic NaAs4O6Br.
The new mineral gajardoite (IMA2015-040), KCa0.5As3+4O6Cl2·5H2O, was found at the Torrecillas mine, Iquique Province, Chile, where it occurs as a secondary alteration phase in association with native arsenic, arsenolite,chongite, talmessite and torrecillasite. Gajardoite occurs as hexagonal plates up to ∼100 μm in diameter and 5 μm thick, in rosette-like subparallel intergrowths. Crystals are transparent, with vitreous lustre and white streak. The Mohs hardness is ∼1½, tenacity is brittleand fracture is irregular. Cleavage is perfect on {001}. The measured density is 2.64 g/cm3 and the calculated density is 2.676 g/cm3. Optically, gajardoite is uniaxial (–) with ω = 1.780(3) and ε = 1.570(5) (measured in white light). The mineral is very slowly soluble in H2O and slowly soluble in dilute HCl at room temperature. The empirical formula, determined from electron-microprobe analyses, is (K0.77Ca0.71Na0.05Mg0.05)∑1.58As4O11Cl1.96H9.62.Gajardoite is hexagonal, P6/mmm, a = 5.2558(8), c = 15.9666(18) Å, V = 381.96(13) Å3 and Z = 1. The eight strongest powder X-ray diffraction lines are [dobs Å(I)(hkl)]: 16.00(100)(001), 5.31(48)(003),3.466 (31)(103), 3.013(44)(104), 2.624(51)(006,110,111), 2.353(36)(113), 1.8647(21)(116,205) and 1.4605(17) (119,303,216). The structure, refined to R1 = 3.49% for 169 Fo > 4σF reflections, contains two types of layers. One layer of formulaKAs3+4O6Cl2 consists of two neutral As2O3 sheets, between which are K+ cations and on the outside of which are Cl– anions. This layer is topologically identical to a slice of the lucabindiite structureand similar to a slice of the torrecillasite structure. The second layer consists of an edge-sharing sheet of Ca(H2O)6 trigonal pyramids with isolated H2O groups centred in the hexagonal cavities in the sheet.
The new mineral chongite (IMA2015–039), Ca3Mg2(AsO4)2(AsO3OH)2.4H2O, was found at the Torrecillas mine, Iquique Province, Chile, where it occurs as a secondary alteration phase in association with native arsenic, arsenolite, gajardoite, talmessite and torrecillasite. Chongite occurs as prismatic crystals up to ∼1 mm long grouped in tightly intergrown radial aggregates up to 2 mm in diameter. Crystals are transparent, with vitreous lustre and white streak. The Mohs hardness is∼3½,tenacity is brittle and fracture is conchoidal. Cleavage is good on ﹛100﹜. The measured density is 3.09(2) g/cm3and the calculated density is 3.087 g/cm3. Optically, chongite is biaxial (-) with α = 1.612(1), β= 1.626(1), γ= 1.635(1) and 2V = 76.9(1)° (measured in white light). Dispersion isr < v,distinct. The optical orientation isX= b;Z^a =27° in obtuse angle β. The mineral is slowly soluble in dilute HCl at room temperature. The empirical formula, determined from electron-microprobe analyses, is (Ca2.90Mg1.93Mn0.14)Σ4.97As4O20H10.07. Chongite is monoclinic,die, a =18.5879(6),b =9.3660(3),c =9.9622(7) Å, β = 96.916(7)°,V=1721.75(14) Å3and Z=4. The eight strongest powder X-ray diffraction lines are[dobsÅ(I)(hkl)]: 8.35(29)(110), 4.644(62) (3ˉ11,020,400,2̄02), 4.396(26)(311), 3.372(62)(022,312,5̄11), 3.275(100)(420,22ˉ2,421), 3.113(57)(222), 2.384(30)(711,530,7̄12) and 1.7990(22)(9̄13,334,5̄34). The structure determination(R1= 1.56% for 1849 Fo> 4σFreflections) confirms that chongite is a member of the hureaulite group.
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