The REE species and their distribution in ferromanganese crusts in the Sea of Japan

Polished sections of ferromanganese crusts on underwater rises in the Sea of Japan were studied with a JXA8100 microprobe analyser. Mineral phases of REE have been detected. They have Ln₂O₃ chemical composition, where Ln is La–Ce–Pr–Nd, La–Ce–Nd, or, much more rarely, La–Ce and La–Ce–Pr. With regard to the same chemical composition of REE grains in the ore crusts and basalts from Medvedev Volcano, it has been concluded that these REE were supplied during postvolcanic gas–hydrothermal processes.     

Rare Earth Element Enrichment in Late Archean Manganese Deposits from the Iron Ore Group,East India

The major, trace and rare earth element (REE) composition of Late Archean manganese, ferromanganese and iron ores from the Iron Ore Group (IOG) in Orissa, east India, was examined. Manganese deposits, occurring above the iron formations of the IOG, display massive, rhythmically laminated or botryoidal textures. The ores are composed primarily of iron and manganese, and are low in other major and trace elements such as SiO₂, Al₂O₃, P₂O₅ and Zr. The total REE concentration is as high as 975 ppm in manganese ores, whereas concentrations as high as 345 ppm and 211 ppm are found in ferromanganese and iron ores, respectively. Heavy REE (HREE) enrichments, negative Ce anomalies and positive Eu anomalies were observed in post‐Archean average shale (PAAS)‐normalized REE patterns of the IOG manganese and ferromanganese ores. The stratiform or stratabound shapes of ore bodies within the shale horizon, and REE geochemistry, suggest that the manganese and ferromanganese ores of the IOG were formed by iron and/or manganese precipitation from a submarine, hydrothermal solution under oxic conditions that occurred as a result of mixing with oxic seawater. While HREE concentrations in the Late Archean manganese and ferromanganese ores in the IOG are slightly less than those of the Phanerozoic ferromanganese ores in Japan, HREE resources in the IOG manganese deposits appear to be two orders of magnitude higher because of the large size of the deposits. Although a reliable, economic concentration technique for HREE from manganese and ferromanganese ores has not yet been developed, those ores could be an important future source of HREE.     

β—钕褐钇铌矿(Fergusonite-beta-Nd)

至今,吐界上已经发现的褐钇铌矿族矿物中仅有钛褐钇铌矿、铈褐钇铌矿、铈-钇-褐钇铌矿……等,而未见有矿物中稀土元素以钕为最富的单斜钕褐钇铌矿的报道^[1,4,5]。     

Hydroxycalciopyrochlore,A New Mineral Species from Sichuan,China

Hydroxycalciopyrochlore, ideally(Ca,Na,U,□)2(Nb,Ti)2O6(OH), cubic, is a new mineral species(IMA2011-026) within the pyrochlore supergroup that was found occurring at the Maoniuping mine, Mianning County, Xichang prefecture, Sichuan Province, southwest China. The mineral is found in an alkali feldspar granite rare-earth ore deposit(26–27 Ma). Associated minerals include calcite, barite, celestine, albite, aegirine, aegirine-augite, fluorite, parasite-(Ce), thorite, thorianite, zircon, galena, sphalerite, magnetite, and pyrite. Crystals occur mostly as octahedra, and less often as dodecahedra and tetrahexahedra or combinations thereof. Some occur with an allotriomorphic habit with a thick triangular tabular form. Crystals generally range from 0.1 to 1 mm in size. The mineral is brownishblack, greenish-black and black on fresh sections with a brown streak. The crystal is translucent, and has a greasy lustre on fresh sections. It is metamict without any observed parting or cleavage and with a conchoidal fracture. The Vickers microhardness is 572 kg/mm2(5–6 on the Mohs hardness scale). The density measured by hydrostatic weighing is 5.10(3) g/cm3. The strongest four reflections in the X-ray powder-diffraction pattern [d in(I) hkl] are: 2.9657(100) 2 2 2, 1.8142(34) 0 4 4, 1.5463(21) 2 2 6, 2.5688(18) 0 0 4. The unit-cell parameters are a = 10.381(4), V = 1118.7(7)3, Z = 8. The structure was solved and refined in the space group Fd3m with R = 0.09. The empirical formula is(Ca0.74Na0.58U0.40Ce0.05Fe0.02□0.21)2.00(Nb1.15Ti0.80Ta0.03Al0.01Mg0.01)2.00O6.02 [(OH)1.01F0.09]1.10, on the basis of 2 atoms of B pfu; the simplified formula is(Ca,Na,U,□)2(Nb,Ti)2O6(OH). Type material is deposited in the Geological Museum of China, Beijing, People's Republic of China, catalogue number M11800.     

A New Three–Dimensional Superstructure in Bafertisite

A new superstructure was found in bafertisite [(Ba0.98Na0.02)1.00(Fe1.71Mn0.26Mg0.01)1.98 TiO[(Si1.82Ti0.04Al0.03Cr0.01)1.90O7](OH1.40F0.53Cl0.03)1.96] from Donghai County, Jiangsu Province, China. The occurrence of the superstructure reflections were observed by single crystal diffraction using a SMAR APEX CCD. The a*, b*and c* axis directions revealed extra weak reflection spots of the superstructure. The apparent 2a, 2b and 2c superstructure is monoclinic with unit cell a＝10.6502(15)?, b＝13.7233(19)?, c＝21.6897(3)?, α＝90o, β＝94.698(3)o, γ＝90o,space group Cm,Z=16. If c* extra weak reflections are ignored, the secondary supercell gave a cell a＝10.6548(15)?, b＝13.7284(19)?, c＝11.6900(17)?, α＝90o, β＝112.322(28)o, γ＝90o,space group Cm,Z=8. The basic subcell was obtained by ignoring all extra weak reflection spots and gave: a＝5.3249(17)?, b＝6.8669(22)?, c＝10.8709(36)?, α＝90o, β＝94.740(62)o, γ＝90o,space P21/m,Z=2. The superstructure has been refined to R = 0.063 for 7805 [R(int) = 0.0266] unique reflections I>2δ(I). The structure consists of an octahedra (O) sheet sandwiched between two heteropolyhedral (H) sheets. These sheets consist of Ti–octahedra and twin tetrahedral disilicate groups [Si2O7]. The O sheet comprises (Fe,Mg)O4 octahedra. The large Ba cation is located in the interlayer area. The refined structure shows Fe, Mg are partly ordered. The shifting of the TiO6 octahedron and SiO4 tetrahedron sites in the sheet may be a consequence of the superstructure.     

Crystal Structure of Natural Non-metamict Ti- and Fe~(2+)-rich Chevkinite-(Ce)

1 Introduction Chevkinite groups can be assigned to the chevkinite-(Ce) subgroup and perrierite-(Ce) subgroup in accord with the angle β : β ≈ 100o for the chevkinite subgroup and β ≈ 113o for the perrierite subgroup. Chevkinite-(Ce), polykovite-(Ce) and Maoniupingite (new mineral No. 017 of 2003) belong to the former subgroup, while renjeite and matsubaraite belong to the latter group. As strontio-chevkinite is a Sr-analogue of perrierite, usually the natural chevkinite-(Ce) group min…     

Florencite-(Sm)—(Sm,Nd)Al3(PO4)2(OH)6: A new mineral species of the alunite-jarosite group from the subpolar urals

Florencite-(Sm), a new mineral species of the florencite subgroup, was found in association with xenotime-(Y) in quartz veins of the Maldynyrd Range of the Subpolar Urals as thin zones within rhombohedral crystals of florencite-(Ce) with faceting by { 01[`1]1}\{ 01\bar 11\} and { 10[`1]2}\{ 10\bar 12\} . The thickness of particular florencite-(Sm) zones is 0.01–0.1 mm, and the total thickness of a series of such zones is 1–3 mm. Florencite-(Sm) is colorless and pale pink or pale yellow with white streaks; its Mohs hardness is 5.5–6.0. Its measured and calculated densities are 3.70 and 3.743 g/cm³, respectively. The mineral is transparent, nonpleochroic, and uniaxial (positive), and ω = 1.704(2) and ɛ = 1.713(2). The electron beam’s fluorescence spectrum was 592 nm (intense green luminescence of Sm³⁺) and 558 nm (yellow luminescence of Nd³⁺). The chemical composition was as follows (microprobe, average of 2 WDS, wt %): 0.62 La₂O₃, 3.29 Ce₂O₃, 1.05 Pr₂O₃, 10.31 Nd₂O₃, 12.62 Sm₂O₃, 0.41 Eu₂O₃, 2.30 Gd₂O₃, 0.13 Dy₂O₃, 0.71 SrO, 0.35 CaO, 29.89 Al₂O₃, 26.14 P₂O₅, 0.85 SO₃, 0.09 SiO₂, 88.76 in total; 10.74 H₂O (meas.). The empirical formula based on 14 oxygen atoms is (Sm_0.38Nd_0.32Gd_0.07Ce_0.10Pr_0.03La_0.02Eu_0.01Sr_0.04Ca_0.03)1.0Al_3.04(P_1.91S_0.05Si_0.01)_1.97O₁₄H_5.92. The idealized formula is (Sm,Nd)Al₃(PO₄)₂(OH)₆. Mineral is trigonal, space group R3m, a = 6.972(4), c = 16.182(7) ?, V = 681.2 ?³, Z = 3. The XRD pattern is as follows: dln (I) (hkl): 2.925 (10) (113), 1.881 (6) (303), 2.161 (5) (107), 5.65 (4) (101), and 3.479 (4) (110). The IR spectrum: 466, 510, 621, 1036, 1105, 1223, 2957, and 3374 cm⁻¹.     

Cervandonite-(Ce) in ores of the Berezitovoe deposit: Second finding in the world

The supposedly second finding of rare arsenosilicate cervandonite-(Ce) in the world is characterized. The mineral was recognized in the ore-bearing metasomatic rocks of the Berezitovoe gold-base metal deposit (Upper Priamurye, Russian Far East) in association with quartz, biotite, muscovite, orthoclase, garnet (almandine-spessartine), tourmaline, basic plagioclase, and sulfides. The cervandonite is represented by optically homogeneous and heterogeneous aggregates with visible crystals from 10 fum to 0.1–0.3 mm in size. Based on the microprobe analysis, the average chemical composition of the homogeneous cervandonite-(Ce) aggregates is as follows (wt %): Ce₂O₃ - 13.00, La₂O₃ - 5.70, Nd₂O₃ - 5.20, Pr₂O₃ - 1.41, Y₂O₃ - 0.77, Sm₂O₃ - 0.77, Eu₂O₃ - 0.23, Gd₂O₃ - 0.54, Dy₂O₃ - 0.31, ThO₂ - 1.12, UO₂ - 0.30, TiO₂ - 12.86, Al₂O₃ - 9.24, Fe₂O₃ - 8.93, FeO - 2.68, CaO - 0.14, SiO₂ - 19.98, As₂O₃ - 16.19. The comparative study of the cervandonite-(Ce) from the Berezitovoe deposit and the analogous minerals from the Alpine mica gneiss of Mt. Pizzo Cervandone (Central Alps) showed that the former mineral can be assigned to a new variety of cervandonite-(Ce) in terms of its compositional features. This variety is characterized by an ordered stoichiometric composition corresponding to the simpler theoretical formula (Ce,Nd,La)(Fe³⁺, Fe²⁺, Ti⁴⁺, Al)₃ (Si₂As³⁺)₃O₁₂.     

The crystal structure of galgenbergite-(Ce), CaCe2(CO3)4∙H2O

Galgenbergite-(Ce) from the type locality, the railroad tunnel Galgenberg between Leoben and St. Michael, Styria, Austria, was investigated. There it occurs in small fissures of an albite-chlorite schist as very thin tabular crystals building rosette-shaped aggregates associated with siderite, ancylite-(Ce), pyrite and calcite. Electron microprobe analyses gave CaO 9.49, Ce₂O₃ 28.95, La₂O₃ 11.70, Nd₂O₃ 11.86, Pr₂O₃ 3.48, CO₂ 30.00, H₂O 3.07, total 98.55 wt.%. CO₂ and H₂O calculated by stoichiometry. The empirical formula (based on Ca + REE ∑3.0) is $ \mathrm{C}{{\mathrm{a}}_{1.00 }}{{\left( {\mathrm{C}{{\mathrm{e}}_{1.04 }}\mathrm{L}{{\mathrm{a}}_{0.42 }}\mathrm{N}{{\mathrm{d}}_{0.42 }}\mathrm{P}{{\mathrm{r}}_{0.12 }}} \right)}_{2.00 }}{{\left( {\mathrm{C}{{\mathrm{O}}_3}} \right)}_4}\cdot {{\mathrm{H}}_2}\mathrm{O} $ , and the simplified formula is $ \mathrm{CaC}{{\mathrm{e}}_2}{{\left( {\mathrm{C}{{\mathrm{O}}_3}} \right)}_4}\cdot {{\mathrm{H}}_2}\mathrm{O} $ . According to X-ray single crystal diffraction galgenbergite-(Ce) is triclinic, space group $ P\overline{1},a=6.3916(5) $ , b?=?6.4005(4), c?=?12.3898(9) Å, α?=?100.884(4), β?=?96.525(4), γ?=?100.492(4)°, V?=?483.64(6) ų, Z?=?2. The eight strongest lines in the powder X-ray diffraction pattern are [d _calc in Å/(I)/hkl]: 5.052/(100)/011; 3.011/(70)/0-22; 3.006/(66)/004; 5.899/(59)/-101; 3.900/(51)/1-12; 3.125/(46)/-201; 2.526/(42)/022; 4.694/(38)/-102. The infrared absorption spectrum reveals H₂O (OH-stretching mode at 3,489 cm^?1, HOH bending mode at 1,607 cm^?1) and indicates the presence of distinctly non-equivalent CO₃-groups by double and quadruple peaks of their ν1, ν2, ν3 and ν4 modes. The crystal structure of galgenbergite-(Ce) was refined with X-ray single crystal data to R1?=?0.019 for 2,448 unique reflections (I?>?2σ(I)) and 193 parameters. The three cation sites of the structure Ca(1), Ce(2) and Ce(3) have a modest mixed site occupation by Ca and small amount of REE (Ce, La, Pr, Nd) and vice versa. The structure is based on double layers parallel to (001), which are composed of Ca(1)Ce(2)(CO₃)₂ single layers with an ordered chessboard like arrangement of Ca and Ce, and with a roof tile-like stacking of the CO₃ groups. Perpendicular to (001) the double layers are connected to a triclinic framework structure with good cleavage parallel to (001) by a differently organized and more open part of the structure formed by Ce(3)(CO₃)₂(H₂O). Based on the topology of the CaCe(CO₃)₂ single layer in galgenbergite-(Ce), structural relationships to rutherfordine, to aragonite and ancylite type minerals, and to lanthanite are outlined.     

Titanium,Ti, A New Mineral Species from Luobusha,Tibet, China

We describe the new mineral species titanium,ideally Ti,found in the podiform chromitites of the Luobusha ophiolite in Tibet,People’s Republic of China.The irregular crystals range from 0.1 to 0.6 mm in diameter and form an intergrowth with coesite and kyanite.Titanium is silver grey in colour,the luster is metallic,it is opaque,the streak is grayish black,and it is non-fluorescent.The mineral is malleable,has a rough to hackly fracture and has no apparent cleavage.The estimated Mohs hardness is 4,and the calculated density is 4.503 g/cm3.The composition is Ti 99.23-100.00 wt%.The mineral is hexagonal,space group P63 /mmc.Unit-cell parameters are a 2.950(2),c 4.686(1),V 35.32(5) 3,Z = 2.The five strongest powder diffraction lines [d in(hkl)(I/I0)] are: 2.569(010)(32),2.254(011)(100),1.730(012)(16),1.478(110)(21),and 0.9464(121)(8).The species and name were approved by the CNMNC(IMA 2010–044).     

Study on the Crystal of Daomanite

It was not possible to carry out a complete analyses of crystal, as the experiment by Ding and Shi et al.. It's analysis precision R=0.25 or more big than this, which value are not satisfied for single crystal study, but we through many test and found the best: [R(int)=14.5%]. The final fullmatix least-squares refinement on F2 converged to R1=0.0791 and wR2=0.1864 for 704 observed reflections [I 3 2s(I)]. Daomanite is orthorhombic system, space group Cmc21, a=3.7520(8))?, b=15.844(4) ?, c=5.8516(12) ?, α=β=γ=90°. V=347.86(14)?3, Z=4. Daomanite chemical formula is Cu Pt AsS 2. Idealized composition Me+M2+M2+S2=CuS ·PtA s S. There is no other similar mineral in the world.     

Lisiguangite,CuPtBiS3, a New Platinum‐Group Mineral from the Yanshan Mountains,Hebei, China

Lisiguangite, CuPtBiS3, is a new mineral species discovered in a PEG-bearing, Co-Cu sulfide vein in garnet pyroxenite of the Yanshan Mountains, Chengde Prefecture, Hebei Province, China. It is associated with chalcopyrite and bornite, galena, minor pyrite, carrolite, molybdenite and the platinum-group minerals daomanite (CuPtAsS2), Co-bearing malanite (Cu(Pt, Co)2S4) sperrylite, moncheite, cooperite and malyshevite (CuPdBiS3), rare damiaoite (Pt2In3) and yixunite (Pt3In). Lisiguangite occurs as idiomorphic crystals, tabular or lamellae (010) and elongated [100] or as aggregates, up to 2 mm long and 0.5 mm wide. The mineral is opaque, has lead-gray color, black streak and metallic luster. The mineral is non-fluorescent. The observed morphology displays the following forms: pinacoids {100}, {010}, {001}, and prism {110}. No twining is observed. The a:b:c ratio, calculated from unit-cell parameters, is 0.6010:1:0.3836. Cleavage: {010} perfect, {001} distinct, {100} may be visible. H Mohs: 21/2; VHN25=46.7-49.8 (mean 48.3) kg/mm2. Tenacity: brittle. Lisiguangite is bright white with a yellowish tint. In reflected light it shows neither internal reflections nor bireflectance or pleochroism. It has weak to moderate anisotropy (blue-greenish to brownish) and parallel-axial extinction. The reflectance values in air (and in oil) for R3, R4 and (imR3, imR4), at the standard Commission on Ore Mineralogy wavelengths are: 37.5, 35.7 (23.4, 22.3) at 470 nm; 38.6, 36.5 (23.6, 22.6) at 546 nm; 39.4, 37.5 (23.6, 22.7) at 589 nm and 40.3, 38.2 (23.7, 22.9) at 650 nm. The average of eight electron-microprobe analyses: Cu 12.98, Pt 30.04, Pd 2.69, Bi 37.65 and S 17.55, totaling 100.91%, corresponding to Cu1.10(Pt 0.83, Pd0.14)Σ0.97Bi0.97S2.96 based on six atoms apfu. The ideal formula is CuPtBiS3. The mineral is orthorhombic. Space group: P212121, a=7.7152(15)?,b=12.838(3)?, c=4.9248(10)?, V=487.80(17)?3, Z=4. The six strongest lines in the X-ray powder-diffraction pattern [d in ? (I) (h k l) are 6.40(30)(020), 3.24(80)(031), 3.03(100)(201), 2.27(40)(051), 2.14(50)(250), 1.865(60)(232).     

Petrogenesis of Late Cretaceous Jiangla’angzong I-Type Granite in Central Lhasa Terrane, Tibet, China: Constraints from Whole-Rock Geochemistry, Zircon U-Pb Geochronology, and Sr-Nd-Pb-Hf Isotopes

The Jiangla'angzong granite in the northern part of the Central Lhasa Terrane is composed of syenogranite and adamellite. LA-ICP-MS zircon U-Pb analyses suggest that syenogranite has a weighted mean ~(206) Pb/~(238) U age of 86±1 Ma(mean square weighted deviation=0.37), which is in accordance with the muscovite Ar-Ar age(85±1 Ma) of Cu-Au ore-bearing skarns and the zircon U-Pb age(84±1 Ma) of adamellite. This suggests that the Jiangla'angzong magmatism and Cu–Au mineralization events took place during the Late Cretaceous. The granite contains hornblende, biotite, and pyroxene, and does not contain Al-bearing minerals, such as muscovite, cordierite, and garnet. It has high contents of SiO_2(65.10–70.91 wt%), K_2O(3.44–5.17 wt%), and total K_2O+Na_2O(7.13–8.15 wt%), and moderate contents of A_(12)O_3(14.14–16.45 wt%) and CaO(2.33–4.11 wt%), with a Reitman index(σ43) of 2.18 to 2.33, and A/CNK values of 0.88 to 1.02. The P_2O_5 contents show a negative correlation with SiO_2, whereas Pb contents show a positive correlation with SiO_2. Th and Y contents are relatively low and show a negative correlation with the Rb contents. These characteristics suggest that the Jiangla'angzong granite is a high K calc–alkaline metaluminous I–type granite. It is enriched in light rare earth elements(LREE) and large ion lithofile elements(LILE), and depleted in heavy rare earth elements(HREE) and high field strength elements(HFSE), with LREE/HREE ratios of 11.7 to 18.1. The granite has negative Eu anomalies of 0.58 to 0.94 without obvious Ce anomalies(δCe=1.00–1.04). The relatively low initial 87 Sr/86 Sr ratios of 0.7106 to 0.7179, positive εHf(t) values of 1.0 to 4.1, and two-stage Hf model ages(TDM2) ranging from 889 Ma to 1082 Ma, These geochemical features indicate that the granite derived from a juvenile crust. The(~(143) Nd/~(144) Nd)_t values from the Jiangla'angzong granite range from 0.5121 to 0.5123, its εNd(t) values range from-10.17 to-6.10, its(~(206) Pb/~(204) Pb)_t values range from 18.683 to 18.746, its(~(207) Pb/~(204) Pb)_t values range from 15.695 to 15.700, and its(~(208) Pb/~(204) Pb)_t values range from 39.012 to 39.071. These data indicate that the granite was formed by melting of the upper crust with the addition of some mantle materials. We propose that the Jiangla'angzong granite was formed during the postcollision extension of the Qiangtang and Lhasa terranes.     

REE and C-O Isotopic Geochemistry of Calcites from the World-class Huize Pb-Zn Deposits, Yunnan, China: Implications for the Ore Genesis

<正>The world-class Huize Pb-Zn deposits of Yunnan province,in southwestern China,located in the center of the Sichuan-Yunnan-Guizhou Pb-Zn polymetallic metallogenic province,has Pb+Zn reserves of more than 5 million tons at Pb+Zn grade of higher than 25%and contains abundant associated metals,such as Ag,Ge,Cd,and Ga.The deposits are hosted in the Lower Carboniferous carbonate strata and the Permian Emeishan basalts which distributed in the northern and southwestern parts of the orefield.Calcite is the only gangue mineral in the primary ores of the deposits and can be classified into three types,namely lumpy,patch and vein calcites in accordance with their occurrence.There is not intercalated contact between calcite and ore minerals and among the three types of calcite,indicating that they are the same ore-forming age with different stages and its forming sequence is from lumpy to patch to vein calcites. This paper presents the rare earth element(REE) and C-O isotopic compositions of calcites in the Huize Pb-Zn deposits.From lumpy to patch to vein calcites,REE contents decrease as LREE/ HREE ratios increase.The chondrite-normalized REE patterns of the three types of calcites are characterized by LREE-rich shaped,in which the lumpy calcite shows(La)_N(Ce)_N(Pr)_N≈(Nd)_N with Eu/Eu~*1,the patch calcite has(La)_N(Ce)_N(Pr)_N≈(Nd)_N with Eu/Eu~*1,and the vein calcite displays(La)_N(Ce)_N(Pr)_N(Nd)_N with Eu/Eu~*1.The REE geochemistry of the three types of calcite is different from those of the strata of various age and Permian Emeishan basalt exposed in the orefield.Theδ~(13) C_(PDb) andδ~(18)O_(Smow) values of the three types of calcites vary from-3.5‰to-2.1‰and 16.7‰to 18.6‰,respectively,falling within a small field between primary mantle and marine carbonate in theδ~(13)C_(PDb) vsδ~(18)O_(Smow) diagram. Various lines of evidence demonstrate that the three types of calcites in the deposits are produced from the same source with different stages.The ore-forming fluids of the deposits resulted from crustal -mantle mixing processes,in which the mantle-derived fluid components might be formed from degassing of mantle or/and magmatism of the Permian Emeishan basalts,and the crustal fluid was mainly provided by carbonate strata in the orefield.The ore-forming fluids in the deposits were homogenized before mineralization,and the ore-forming environment varied from relatively reducing to oxidizing.     

Naquite,FeSi, a New Mineral Species from Luobusha,Tibet, Western China

A new mineral species, named naquite(FeSi), is found in the podiform chromitites of the Luobusha ophiolite in Qusong County, Tibet, China. The detailed composition is Fe 65.65, Si 32.57 and Al 1.78 wt%. The mineral is cubic, space group P213. The irregular crystals range from 15 to 50 μm in diameter and form an intergrowth with luobusaite. Naquite is steel grey in color, opaque, with a metallic lustre and gives a grayish-black streak. The mineral is brittle, has a conchoidal fracture and no apparent cleavage. The estimated Mohs hardness is 6.5, and the calculated density is 6.128 g/cm3. Unit-cell parameters are a 4.486 (4) ?, V 90.28 (6) ?3, Z=4. The five strongest powder diffraction lines [d in ? (hkl) (I/I0)] are: 3.1742 (110) (40), 2.5917(111) (43), 2.0076 (210) (100), 1.8307 (211) (65), and 1.1990 (321) (36). Originally called ‘fersilicite’, the species and new name have now been approved by the CNMNC (IMA 2010–010).     

Bastnäsite-(Ce) at the Nkombwa Hill carbonatite complex, Isoka District, Northeast Zambia

Summary Within the Nkombwa Hill carbonatite complex, bastnäsite-(Ce), (Ce,La)CO₃F, has been identified as an abundant mineral in xenoliths hosted by late-stage ferrocarbonatite sills and dykes. Bastnäsite-(Ce) occurs as fibrous yellow crystals, about 1 µm in size, replacing monazite and in association with baryte, in a matrix of dolomite. In common with bastnäsite-(Ce) from other locations, the bastnäsite-(Ce) of Nkombwa Hill contains up to 70% RE₂O₃, almost entirely as light rare-earth oxides. However, Nkombwa Hill bastnäsite-(Ce) is relatively deficient in La and enriched in Pr and Nd.

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Bastnäsit-(Ce) im Nkombwa Hill Karbonatit-Komplex, Isoka-Distrikt, Nordost-Sambia

Zusammenfassung Im Karbonatit-Komplex von Nkombwa Hill kommt Bastnäsit-(Ce), (Ce-La) CO₃F, als eine weitverbreitete Komponente in Xenolithen in späten Ferrokarbonatit-Lagergängen und Gängen vor. Bastnäsit-(Ce) bildet faserige gelbe Kristalle in einer Matrix aus Dolomit, die ungefähr 1 µm groß sind, Monazit verdrängen und mit Baryt assoziiert sind. Ähnlich wie Bastnäsit von anderen Lokalitäten, enthält auch dieser bis zu 70% RE₂O₃ fast ausschließlich als Oxide der Leichten Seltenen Erden. Der Bastnäsite-(Ce) von Nkombwa Hill ist jedoch relativ verarmt an La und an Pr und Nd angereichert.

     

Perrierite-(La), (La,Ce,Ca)4(Fe2+,Mn)(Ti,Fe3+,Al)4(Si2O7)2O8, a new mineral species from the Eifel volcanic district, Germany

Non-metamict perrierite-(La) discovered in the Dellen pumice quarry, near Mendig, in the Eifel volcanic district, Rheinland-Pfalz, Germany has been approved as a new mineral species (IMA no. 2010-089). The mineral was found in the late assemblage of sanidine, phlogopite, pyrophanite, zirconolite, members of the jacobsite-magnetite series, fluorcalciopyrochlore, and zircon. Perrierite-(La) occurs as isolated prismatic crystals up to 0.5 × 1 mm in size within cavities in sanidinite. The new mineral is black with brown streak; it is brittle, with the Mohs hardness of 6 and distinct cleavage parallel to (001). The calculated density is 4.791 g/cm³. The IR spectrum does not contain absorption bands that correspond to H₂O and OH groups. Perrierite-(La) is biaxial (-), α = 1.94(1), β = 2.020(15), γ = 2.040(15), 2V _meas = 50(10)°, 2V _calc = 51°. The chemical composition (electron microprobe, average of seven point analyses, the Fe²⁺/Fe³⁺ ratio determined from the X-ray structural data, wt %) is as follows: 3.26 CaO, 22.92 La₂O₃, 19.64 Ce₂O₃, 0.83 Pr₂O₂, 2.09 Nd₂O₃, 0.25 MgO, 2.25 MnO, 3.16 FeO, 5.28 Fe₂O₃, 2.59 Al₂O₃, 16.13 TiO₂, 0.75 Nb₂O₅, and 20.06 SiO₂, total is 99.21. The empirical formula is (La_1.70Ce_1.45Nd_0.15Pr_0.06Ca_0.70)_Σ4.06(Fe _0.53 ²⁺ Mn_0.38Mg_0.08)_Σ0.99(Ti_2.44Fe _0.80 ³⁺ Al_0.62Nb_0.07)_Σ3.93Si_4.04O₂₂. The simplified formula is (La,Ce,Ca)₄(Fe²⁺,Mn)(Ti,Fe³⁺,Al)₄(Si₂O₇)₂O₈. The crystal structure was determined by a single crystal. Perrierite-(La) is monoclinic, space group P2₁/a, and the unit-cell dimensions are as follows: a =13.668(1), b = 5.6601(6), c = 11.743(1) Å, β = 113.64(1)°; V = 832.2(2) ų, Z = 2. The strong reflections in the X-ray powder diffraction pattern are [d, Å (I, %) (hkl)]: 5.19 (40) (110), 3.53 (40) ( $\overline 3 $ 11), 2.96 (100) ( $\overline 3 $ 13, 311), 2.80 (50) (020), 2.14 (50) ( $\overline 4 $ 22, $\overline 3 $ 15, 313), 1.947 (50) (024, 223), 1.657 (40) ( $\overline 4 $ 07, $\overline 4 $ 33, 331). The holotype specimen of perrierite-(La) is deposited at the Fersman Mineralogical Museum, Russian Academy of Sciences, Moscow, Russia, with the registration number 4059/1.     

Ivsite,Na<Subscript>3</Subscript>H(SO<Subscript>4</Subscript>)<Subscript>2</Subscript>, a new mineral from volcanic exhalations of fumaroles of the Fissure Tolbachik Eruption of the 50th Anniversary of the Institute of Volcanology and Seismology,Far East Branch,Russian Academy of Sciences

Fine-granular (<0.1 mm) flattened colorless transparent crystals of ivsite form white aggregates. The empirical formula (Na_2.793Cu_0.056)_2.849HS_2.016O₈ is close to the ideal Na₃H(SO₄)₂. The structure was refined up to R = 0.040. Ivsite has a monoclinic symmetry, P2₁/c, a = 8.655(1) Å, b = 9.652(1) Å, c = 9.147(1) Å, β = 108.76(1)°, V = 723.61(1) ų, Z = 4. Na atoms occur at six- and seven-fold sites (NaO₆ and NaO₇); S atoms, in isolated SO₄ tetrahedrons; these polyhedrons form a three-dimensional framework. The diagnostic lines of powder diffraction patterns (d[Å]–I–hkl) are 4.010–53–12-1, 3.949–87–012, 3.768–100–210, 3.610–21–20-2, 3.022–22–031, 2.891–42–22-2, 2.764–49–31-1, and 2.732–70–13-1.     

Mariinskite, BeCr2O4, a new mineral, chromium analog of chrysoberyl

A new mineral, mariinskite, BeCr₂O₄, the chromium analog of chrysoberyl, has been found at the Mariinsky (Malyshevo) deposit, the Ural Emerald Mines, the Central Urals, Russia. The mineral is named after its type locality. It was discovered in chromitite in association with fluorphlogopite, Cr-bearing muscovite, eskolaite, and tourmaline. Mariinskite occurs as anhedral grains ranging from 0.01 to 0.3 mm in size; in some cases it forms pseudohexagonal chrysoberyl-type twins. The mineral is dark-green, with a pale green streak; the Mohs’ hardness is 8.5, microhardness VHN = 1725 kg/mm². D _meas = 4.25(2) g/cm³, D _calc = 4.25 g/cm³. Microscopically, it is emerald-green, pleochroic from emerald-green (γ) to yellow-green (β) and greenish yellow (α). The new mineral is biaxial (+), γ = 2.15(1), β = 2.09(3), and α = 2.05(1), 2V _meas = 80 ± (10)°, 2V _calc = 80.5°. In reflected light, it is gray with green reflections; R _max (589) = 12.9%; R _min (589) = 12.3%, and there are strong, internal green reflections. The strongest absorption bands in the IR spectrum are as follows (cm^?1): 935, 700, 614, 534. Space group Pnma, a = 9.727(3), b = 5.619(1), c = 4.499(1) Å, V = 245.9(3) ų, Z = 4. The strongest reflections in the X-ray powder diffraction pattern are as follows (d Å, I, hkl): 4.08(40)(101), 3.31(90)(111), 2.629(50)(301), 2.434(50)(220), 2.381(40)(311), 2.139(60)(221), 1.651(100)(222). The average chemical composition of mariinskite (electron microprobe, wt %) is as follows: BeO 16.3, Al₂O₃ 23.89, Cr₂O₃ 58.67, Fe₂O₃ 0.26, V₂O₃ 0.26, TiO₂ 0.61, total is 99.98. The empirical formula, calculated on the basis of four O atoms is Be_1.03(Cr_1.22Al_0.74Ti_0.01Fe_0.01V_0.01)_1.99O₄. The compatibility index 1 ? (K_p/K_c), 0.019, is excellent. The type specimens are deposited in the Fersman Mineralogical Museum, Russian Academy of Sciences, Moscow, and the Ural Geological Museum, Yekaterinburg, Russia.     

Geochemistry and origin of Dehoo manganese deposit,south Zahedan,southeastern Iran

Dehoo manganese deposit is located 52 km to the south of Zahedan in Sistan and Baluchestan Province, southeastern Iran. This deposit that lies in the central part of the Iranian Flysch Zone is lenticular in shape and lies above the micritic limestone-radiolarite cherts of the upper Cretaceous ophiolite unit. It is hosted within the reddish to brown radiolarite cherts and in places interlinks with them, so that the radiolarite chert packages play a key role for Mn mineralization in the region. Investigated ore-paragenetic successions and the geochemical characteristics of the Dehoo deposit were studied by means of major oxide, trace, and rare earth element (REE) contents that provide information as to the mineral origin. Strong positive correlations were found between major oxides and trace elements (Al₂O₃-TiO₂, r = 0.95; TiO₂-MgO, r = 0.94; Fe₂O₃-Al₂O₃, r = 0.90; MgO-Al₂O₃, r = 0.84; MgO-Fe₂O₃, r = 0.88; Fe₂O₃-TiO₂, r = 0.91; Fe₂O₃-K₂O, r = 0.74; Al₂O₃-K₂O, r = 0.69; Al₂O₃-V, r = 0.72; TiO₂-V, r = 0.73, and MgO-V, r = 0.69) that testify to the contribution of mafic terrigenous detrital material to the deposit. Chondrite-normalized REE patterns of all ore samples are characterized by negative Ce (0.06–0.15, average 0.10) and slightly positive Eu (0.29–0.45, average 0.36) anomalies. Based on ratios of Mn/Fe (average 56.23), Co/Ni (average 0.33), Co/Zn (average 0.38), U/Th (average 3.40), La/Ce (average 1.45), La_n/Nd_n (average 2.16), Dy_n/Yb_n (average 0.33), and light REE/heavy REE (average 8.40; LREE > HREE), as well as Ba (average 920 ppm) and total REE contents (average 6.96 ppm) negative Ce and positive Eu anomalies, Dehoo could be considered a predominantly submarine hydrothermal Mn deposit complemented by terrigenous detrital mafic material.