A new scheme of nomenclature for the pyrochlore supergroup, approved by the CNMNC-IMA, is based on the ions at the A, B and Y sites. What has been referred to until now as the pyrochlore group should be referred to as the pyrochlore supergroup, and the subgroups should be changed to groups. Five groups are recommended, based on the atomic proportions of the B atoms Nb, Ta, Sb, Ti, and W. The recommended groups are pyrochlore, microlite, roméite, betafite, and elsmoreite, respectively. The new names are composed of two prefixes and one root name (identical to the name of the group). The first prefix refers to the dominant anion (or cation) of the dominant valence [or H 2 O or □] at the Y site. The second prefix refers to the dominant cation of the dominant valence [or H 2 O or □] at the A site. The prefix "keno-" represents "vacancy". Where the first and second prefixes are equal, then only one prefix is applied. Complete descriptions are missing for the majority of the pyrochlore-supergroup species. Only seven names refer to valid species on the grounds of their complete descriptions: oxycalciopyrochlore, hydropyrochlore, hydroxykenomicrolite, oxystannomicrolite, oxystibiomicrolite, hydroxycalcioroméite, and hydrokenoelsmoreite. Fluornatromicrolite is an IMA-approved mineral, but the complete description has not yet been published. The following 20 names refer to minerals that need to be completely described in order to be approved as valid species: hydroxycalciopyrochlore, fluornatropyrochlore, fluorcalciopyrochlore, fluorstrontiopyrochlore, fluorkenopyrochlore, oxynatropyrochlore, oxyplumbopyrochlore, oxyyttropyrochlore-(Y), kenoplumbopyrochlore, fluorcalciomicrolite, oxycalciomicrolite, kenoplumbomicrolite, hydromicrolite, hydrokenomicrolite, oxycalciobetafite, oxyuranobetafite, fluornatroroméite, fluorcalcioroméite, oxycalcioroméite, and oxyplumboroméite. For these, there are only chemical or crystalstructure data. Type specimens need to be defined. Potential candidates for several other species exist, but are not sufficiently well characterized to grant them any official status. Ancient chemical data refer to wet-chemical analyses and commonly represent a mixture of minerals. These data were not used here. All data used represent results of electron-microprobe analyses or were obtained by crystal-structure refinement. We also verified the scarcity of crystal-chemical data in the literature. There are crystalstructure determinations published for only nine pyrochlore-supergroup minerals:
After careful consideration of the semantics of status categories for mineral species names, minor corrections and disambiguations are presented for a recent report on the nomenclature of the pyrochlore supergroup. The names betafite, elsmoreite, microlite, pyrochlore and roméite are allocated as group names within the pyrochlore supergroup. The status of the names bindheimite, bismutostibiconite, jixianite, monimolite, partzite, stetefeldtite and stibiconite is changed from 'discredited' to 'questionable' pending further research.
The newly defined gadolinite supergroup approved by the IMA CNMNC (vote 16-A) includes mineral species that have the general chemical formula A 2 MQ 2 T 2 O 8 ' 2 and belong to silicates, phosphates and arsenates. Each site is occupied by: A À Ca, REE (Y and lanthanoids), actinoids, Pb, Mn 2þ , Bi; M À Fe, □ (vacancy), Mg, Mn, Zn, Cu, Al; Q À B, Be, Li; T À Si, P, As, B, Be, S; and ' À O, OH, F. The classification of the gadolinite supergroup is based on the occupancy of A, M, Q, T and ' sites and application of the dominant-valency and dominant-constituent rules. The gadolinite supergroup is divided into two groups defined by prevailing charge occupancy at the T site À Si 4þ in gadolinite group and P 5þ or As 5þ in herderite group. The gadolinite group is divided into the gadolinite and datolite subgroups. The A site is dominantly occupied by divalent cations in the datolite subgroup and by trivalent cations in the gadolinite subgroup. Accordingly, the Q site is dominantly occupied by B 3þ in the datolite subgroup and by Be 2þ in the gadolinite subgroup. The herderite group is divided into two subgroups. The herderite subgroup is defined by the dominant divalent cation (usually Ca 2þ ) in the A site and Be 2þ in the Q site, while the M site is vacant. The drugmanite subgroup is defined by the dominance of divalent cations (usually Pb 2þ ) in the A site, vacancy in the Q site and the occupation of the M site. Moreover, "bakerite" is discredited as mineral species because it does not meet the conditions of the dominant-constituent rule.
The objective of this study is to investigate the efficiency of calcium carbonate bioprecipitation by Lysinibacillus sphaericus, Bacillus subtilis and Pseudomonas putida, obtained from the Coleção de Culturas do Instituto Nacional de Controle de Qualidade em Saúde (INCQS), as a first step in determining their potential to protect building materials against water uptake. Two culture media were studied: modified B4 containing calcium acetate and 295 with calcium chloride. Calcium consumption in the two media after incubation with and without the bacterial inoculum was determined by atomic absorption analysis. Modified B4 gave the best results and in this medium Pseudomonas putida INQCS 113 produced the highest calcium carbonate precipitation, followed by Lysinibacillus sphaericus INQCS 414; the lowest precipitation was produced by Bacillus subtilis INQCS 328. In this culture medium XRD analysis showed that Pseudomonas putida and Bacillus subtilis precipitated calcite and vaterite polymorphs while Lysinibacillus sphaericus produced only vaterite. The shape and size of the crystals were affected by culture medium, bacterial strain and culture conditions, static or shaken. In conclusion, of the three strains Pseudomonas putida INQCS 113 in modified B4 medium gave the best results precipitating 96% of the calcium, this strain thus has good potential for use on building materials
Hydroxycalciomicrolite, Ca 1.5 Ta 2 O 6 (OH) is a new microlite-group mineral found in the Volta Grande pegmatite, Nazareno, Minas Gerais, Brazil. It occurs as isolated octahedral and as a combination of octahedral and rhombic dodecahedral crystals, up to 1.5 mm in size. The crystals are yellow and translucent, with a white streak and vitreous to resinous lustre. The mineral is brittle, with a Mohs hardness of 5-6. Cleavage is not observed and fracture is conchoidal. The calculated density is 6.176 g cm -3 . Hydroxycalciomicrolite is isotropic, n calc. = 2.010. The infrared and Raman spectra exhibit bands due to O-H stretching vibrations. The chemical composition determined from electron microprobe analysis (n = 13) is (wt.%): Na 2 O 0.36 (8) Hydroxycalciomicrolite is cubic, with unit-cell parameters a = 10.4205(1) Å, V = 1131.53(2) Å 3 and Z = 8. It represents a pyrochlore supergroup, microlite-group mineral exhibiting P4 3 32 symmetry, instead of Fd 3m. The reduction in symmetry is due to long-range ordering of Ca and vacancies on the A sites. This is the first example of such ordering in a natural pyrochlore, although it is known from synthetic compounds. This result is promising because it suggests that other species with P4 3 32 or lower-symmetry space group can be discovered and characterized.
Fluorcalciomicrolite, (Ca, Na, ☐)2Ta2O6F, is a new microlite-group, pyrochlore supergroup mineral approved by the CNMNC (IMA 2012-036). It occurs as an accessory mineral in the Volta Grande pegmatite, Nazareno, Minas Gerais, Brazil. Associated minerals include: microcline, albite, quartz, muscovite, spodumene, “lepidolite”, cassiterite, tantalite-(Mn), monazite-(Ce), fluorite, “apatite”, beryl, “garnet” , epidote, magnetite, gahnite, zircon, “tourmaline” , bityite, hydrokenomicrolite, and other microlite-group minerals under study. Fluorcalciomicrolite occurs as euhedral, untwinned, octahedral crystals 0.1–1.5 mm in size, occasionally modified by rhombododecahedral faces. The crystals are colourless and translucent; the streak is white, and the lustre is adamantine to resinous. It does not fluoresce under ultraviolet light. Mohs' hardness is 4½–5, tenacity is brittle. Cleavage is not observed; fracture is conchoidal. The calculated density is 6.160 g/cm3. The mineral is isotropic, ncalc. = 1.992. The Raman spectrum is dominated by bands of B–X octahedral bond stretching and X–B–X bending modes. The chemical composition (n = 6) is (by wavelength dispersive spectroscopy, H2O calculated to obtain charge balance, wt.%): Na2O 4.68, CaO 11.24, MnO 0.01, SrO 0.04, BaO 0.02, SnO20.63, UO20.02, Nb2O53.47, Ta2O576.02, F 2.80, H2O 0.48, O=F–1.18, total 98.23. The empirical formula, based on 2 cations at the B site, is (Ca1.07Na0.81☐0.12)Σ2.00(Ta1.84Nb0.14Sn0.02)Σ2.00[O5.93(OH)0.07]6.00[F0.79(OH)0.21]. The strongest eight X-ray powder-diffraction lines [d in Å (I)(hkl)] are: 5.997(59)(111), 3.138(83)(311), 3.005(100)(222), 2.602(29)(400), 2.004(23)(511), 1.841(23)(440), 1.589(25)(533), and 1.504(24)(444). The crystal structure refinement (R1 = 0.0132) gave the following data: cubic, Fdm, a = 10.4191(6) Å, V = 1131.07(11) Å3, Z = 8.
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