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  • Mineralogical Association of Canada  (9)
  • Mineralogical Society of Great Britain and Ireland  (9)
  • American Chemical Society  (7)
  • American Association for the Advancement of Science (AAAS)  (1)
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  • 1
  • 2
    Publication Date: 2010-06-17
    Print ISSN: 1089-5639
    Electronic ISSN: 1520-5215
    Topics: Chemistry and Pharmacology , Physics
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  • 3
    Publication Date: 2008-04-01
    Print ISSN: 1089-5639
    Electronic ISSN: 1520-5215
    Topics: Chemistry and Pharmacology , Physics
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  • 4
  • 5
    Publication Date: 2015-10-17
    Description: Four factors contribute to the roles played by chance and necessity in determining mineral distribution and diversity at or near the surfaces of terrestrial planets: (1) crystal chemical characteristics; (2) mineral stability ranges; (3) the probability of occurrence for rare minerals; and (4) stellar and planetary stoichiometries in extrasolar systems. The most abundant elements generally have the largest numbers of mineral species, as modeled by relationships for Earth's upper continental crust (E) and the Moon (M), respectively: Log(NE)=0.22 Log(CE)+1.70(R2=0.34)(4861 minerals,72 elements) Log(NM)=0.19 Log(CM)+0.23(R2=0.68)(63 minerals,24 elements), where C is an element's abundance in ppm and N is the number of mineral species in which that element is essential. Several elements that plot significantly below the trend for Earth's upper continental crust ( e.g. , Ga, Hf, and Rb) mimic other more abundant elements and thus are less likely to form their own species. Other elements ( e.g ., Ag, As, Cu, Pb, S, and U) plot significantly above the trend, which we attribute to their unique crystal chemical affinities, multiple coordination and oxidation states, their extreme concentration in some ore-forming fluids, and/or frequent occurrence with a variety of other rare elements—all factors that increase the diversity of mineral species incorporating these elements. The corresponding diagram for the Moon shows a tighter fit, most likely because none of these elements, except Cu and S, are essential constituents in lunar minerals. Given the similar slopes for Earth and the Moon, we suggest that the increase in mineral diversity with element abundance is a deterministic aspect of planetary mineral diversity. Though based on a limited number of collecting sites, the Moon's observed mineralogical diversity could be close to the minimum for a rocky planet or moon comparable in size—a baseline against which diversity of other terrestrial planets and moons having radii in the same range as Earth and its Moon can be measured. Mineral-forming processes on the Moon are limited to igneous activity, meteor impacts, and the solar wind—processes that could affect any planet or moon. By contrast, other terrestrial planets and moons have been subjected to more varied physical, chemical, and (in the case of Earth) biological processes that can increase mineral diversity in both deterministic and stochastic ways. Total mineral diversity for different elements is not appreciably influenced by the relative stabilities of individual phases, e.g. , the broad pressure-temperature-composition stability ranges of cinnabar (HgS) and zircon (ZrSiO 4 ) do not significantly diminish the diversity of Hg or Zr minerals. Moreover, the significant expansion of near-surface redox conditions on Earth through the evolution of microbial oxygenic photosynthesis tripled the available composition space of Earth's near-surface environment, and resulted in a corresponding tripling of mineral diversity subsequent to atmospheric oxidation. Of 4933 approved mineral species, 34% are known from only one or two localities, and more than half are known from five or fewer localities. Statistical analysis of this frequency distribution suggests that thousands of other plausible rare mineral species await discovery or could have occurred at some point in Earth's history, only to be subsequently lost by burial, erosion, or subduction— i.e. , much of Earth's mineral diversity associated with rare species results from stochastic processes. Measurements of stellar stoichiometry reveal that stars can differ significantly from the Sun in relative abundances of rock-forming elements, which implies that bulk compositions of some extrasolar Earth-like planets likely differ significantly from those of Earth, particularly if the fractionation processes in evolving stellar nebulas and planetary differentiation are factored in. Comparison of Earth's upper continental crust and the Moon shows that differences in element ratios are reflected in ratios of mineral species containing these elements. In summary, although deterministic factors control the distribution of the most common rock-forming minerals in Earth's upper continental crust and on the Moon, stochastic processes play a significant role in the diversity of less common minerals. Were Earth's history to be replayed, and thousands of mineral species discovered and characterized anew, it is probable that many of those minerals would differ from species known today.
    Print ISSN: 0008-4476
    Topics: Geosciences
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  • 6
    Publication Date: 2011-12-01
    Description: The new mineral anorpiment, As2S3, the triclinic dimorph of orpiment, has space group P1I and cell parameters a = 5.7577(2), b = 8.7169(3), c = 10.2682(7) Å, a = 78.152(7), ß = 75.817(7), ? = 89.861(6)°, V = 488.38(4) Å3 and Z = 4. It occurs at the Palomo mine, Castrovirreyna Province, Huancavelica Department, Peru. It is a low-temperature hydrothermal mineral associated with dufrénoysite, muscovite, orpiment, pyrite and realgar. It occurs in drusy crusts of wedge-shaped, transparent, greenish yellow crystals. The streak is yellow. The lustre is resinous on crystal faces, but pearly on cleavage surfaces. The Mohs hardness is about 1. The mineral is sectile with an irregular fracture and one perfect and easy cleavage on {001}. The measured and calculated densities are 3.33 and 3.321 g cm-3, respectively. All indices of refraction are greater than 2. The mineral is optically biaxial (–) with 2V = 35–40° and no observed dispersion. The acute bisectrix (X) is approximately perpendicular to the {001} cleavage. Electron microprobe analyses yielded the averages and ranges in wt.%: As 58.21 (57.74–59.03), S 38.72 (38.33 39.00), total 96.94 (96.07 97.75), providing the empirical formula (based on 5 atoms) As1.96S3.04. The strongest powder X-ray diffraction lines are [d (hkl) I] 4.867(002) 97, 4.519 (110,11I1) 77, 3.702 (1I1I1) 46, 3.609 (022,11I2) 82, 2.880 (201,02I2,1I2I1,023) 75, 2.552 (1I13,1I31,132) 100, 2.469 (114,130,13I1) 96. The structure of anorpiment [R1 = 0.021 for 1484 reflections with Fo 〉 4s(F)] consists of layers of covalently bonded As and S atoms. Each S atom bonds to two As atoms at As–S–As angles between 100.45 and 104.15°. Each As atom is strongly bonded to three S atoms at S–As–S angles between 91.28 and 103.59°, forming an AsS3 pyramid with As at its apex. The As–S linkages within the layers form rings of six AsS3 pyramids. Interlayer bonding forces are interpreted as van der Waals. The structure of anorpiment is similar to that of orpiment in that it is composed of layers of As2S3 macromolecules, but arranged in a different stacking sequence.
    Print ISSN: 0026-461X
    Electronic ISSN: 1471-8022
    Topics: Geosciences
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  • 7
    Publication Date: 2012-06-01
    Description: The crystal structure and chemical composition of two samples of fettelite from the type locality, including a portion of the holotype material, was investigated to verify if a previously proposed revision of the chemical formula was applicable, and to study the role of cation substitution for Hg that would suggest new members of the fettelite family. The crystal structure of fettelite from the type locality was found to be equivalent to that reported previously for the Chilean occurrence, and consists of an alternation of two kinds of layers along c: layer A with general composition [Ag6As2S7]2− and layer B with general composition [Ag10HgAs2S8]2+. In this structure, the Ag atoms occur in various coordination configurations, varying from quasi-linear to quasi-tetrahedral, the AsS3 groups form pyramids as are typically observed in sulfosalts, and Hg links two sulfur atoms in a linear coordination. The refined compositions for the crystals in this study, [Ag6As2S7][Ag10(Fe0.53Hg0.47)As2S8] (R100124) and [Ag6As2S7][Ag10(Hg0.79Cu0.21)As2S8] (R110042), clearly indicate that new mineral species related to fettelite are likely to be found in nature.
    Print ISSN: 0026-461X
    Electronic ISSN: 1471-8022
    Topics: Geosciences
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  • 8
    Publication Date: 2017-06-27
    Description: A new mineral, petersite-(Ce), ideally Cu 2+ 6 Ce(PO 4 ) 3 (OH) 6 ·3H 2 O (IMA2014-002), has been found in the Cherry Creek District of Yavapai County, Arizona, USA. It is a secondary alteration mineral associated with malachite, chlorite, a biotite phase, quartz, albite, orthoclase, hematite, chalcopyrite, and an uncharacterized hisingerite-like mineral. Petersite-(Ce) occurs as sprays of yellowish-green, acicular crystals approximately 20 x 20 x 50 μm in size. It has a white streak with vitreous luster. The mineral is brittle and has a Mohs hardness of ~3.5; no cleavage or parting was observed. The calculated density is 3.424 g/cm 3 . An electron microprobe analysis resulted in an empirical chemical formula of Cu 6.05 (Ce 0.18 Y 0.16 La 0.12 Nd 0.09 Gd 0.03 Pr 0.02 Dy 0.01 Sm 0.01 Ca 0.42 ) 1.04 [(PO 4 ) 2.54 (SiO 4 ) 0.14 (PO 3 OH) 0.32 (OH) 6 ]·3.65H 2 O. Petersite-(Ce) is hexagonal, with space group P 6 3 / m and unit-cell parameters a 13.2197(18) Å, c 5.8591(9) Å, and V 886.8(4) Å 3 , Z = 2. It is the Ce analogue of petersite-(Y) and exhibits the mixite structure type. The mixite group can be expressed by the general formula Cu 2+ 6 A ( T O 4 ) 3 (OH) 6 · 3H 2 O, where nine-coordinated A is a rare earth element, Al, Ca, Pb, or Bi, and T is P or As. The structure of petersite-(Ce) is characterized by chains of edge-sharing CuO 5 square-pyramids along c . These chains are connected in the a-b plane by edge-sharing CeO 9 polyhedra and corner-sharing PO 4 tetrahedra. Hydroxyl groups occupy each corner of the CuO 5 polyhedra not shared by a neighboring P or Ce atom. Each CeO 9 polyhedron is surrounded by three zeolitic channels. The walls of the channels, parallel to c , are six-membered, hexagonal rings composed of CuO 5 and PO 4 polyhedra in a ratio of 2:1, respectively, and contain H 2 O molecules. In our model of petersite-(Ce), we defined one distinct H 2 O site positioned to form a ring inside the channel, although there are many statistically possible locations.
    Print ISSN: 0008-4476
    Topics: Geosciences
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  • 9
    Publication Date: 2017-08-08
    Description: Hemihedrite from the Florence Lead-Silver mine in Pinal County, Arizona, USA was first described and assigned the ideal chemical formula Pb 10 Zn(CrO 4 ) 6 (SiO 4 ) 2 F 2 , based upon a variety of chemical and crystal-structure analyses. The primary methods used to determine the fluorine content for hemihedrite were colorimetry, which resulted in values of F that were too high and inconsistent with the structural data, and infrared (IR) spectroscopic analysis that failed to detect OH or H 2 O. Our reinvestigation using electron microprobe analysis of the type material, and additional samples from the type locality, the Rat Tail claim, Arizona, and Nevada, reveals the absence of fluorine, while the presence of OH is confirmed by Raman spectroscopy. These findings suggest that the colorimetric determination of fluorine in the original description of hemihedrite probably misidentified F due to the interferences from PO 4 and SO 4 , both found in our chemical analyses. As a consequence of these results, the study presented here proposes a redefinition of the chemical composition of hemihedrite to the ideal chemical formula Pb 10 Zn(CrO 4 ) 6 (SiO 4 ) 2 (OH) 2 . Hemihedrite is isotypic with iranite with substitution of Zn for Cu, and raygrantite with substitution of Cr for S. Structural data from a sample from the Rat Tail claim, Arizona, indicate that hemihedrite is triclinic in space group P 1 , a = 9.4891(7), b = 11.4242(8), c = 10.8155(7) Å, α = 120.368(2)°, β = 92.017(3)°, = 55.857(2)°, V = 784.88(9) Å 3 , Z = 1, consistent with previous investigations. The structure was refined from single-crystal X-ray diffraction data to R 1 = 0.022 for 5705 unique observed reflections, and the ideal chemical formula Pb 10 Zn(CrO 4 ) 6 (SiO 4 ) 2 (OH) 2 was assumed during the refinement. Electron microprobe analyses of this sample yielded the empirical chemical formula Pb 10.05 (Zn 0.91 Mg 0.02 ) = 0.93 (Cr 5.98 S 0.01 P 0.01 ) = 6.00 Si 1.97 O 34 H 2.16 based on 34 O atoms and six (Cr + S + P) per unit cell.
    Print ISSN: 0026-461X
    Electronic ISSN: 1471-8022
    Topics: Geosciences
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  • 10
    Publication Date: 2017-05-10
    Description: 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), CaO 15.64(13), SnO 2 0.26(3), Nb 2 O 5 2.82(30), Ta 2 O 5 78.39(22), MnO 0.12(2), F 0.72(12) and H 2 O 1.30 (from the crystal structure data), O = F –0.30, total 99.31(32), yielding an empirical formula, (Ca 1.48 Na 0.06 Mn 0.01 ) 1.55 (Ta 1.88 Nb 0.11 Sn 0.01 ) 2.00 O 6.00 [(OH) 0.76 F 0.20 O 0.04 ]. 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 P 4 3 32 symmetry, instead of Fd m . 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 P 4 3 32 or lower-symmetry space group can be discovered and characterized.
    Print ISSN: 0026-461X
    Electronic ISSN: 1471-8022
    Topics: Geosciences
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