The Canadian Mineralogist最新文献

{"title":"Application of molybdenum and thallium isotopes as indicators of paleoredox conditions and genesis of hyper-enriched black shale deposits, Peel River, Yukon, Canada","authors":"I. Crawford, D. Layton-Matthews, J. Peter, M. Gadd, A. Voinot, M. Leybourne, P. Pufahl","doi":"10.3749/canmin.2000099","DOIUrl":"https://doi.org/10.3749/canmin.2000099","url":null,"abstract":"\u0000 Hyper-enriched black shale (HEBS) deposits in northern Yukon, consist of thin (<10 cm), laterally extensive (tens of thousands of km2) stratiform sulfide mineralization layer(s) that are hyper-enriched in Ni, Mo, Zn, platinum group elements, Re, and Au. The genesis of HEBS deposits and the ambient paleoenvironment in which they formed are the subject of vigorous debate. Non-traditional stable isotopes, particularly molybdenum and thallium, are robust paleoredox indicators and we have employed these isotope systems in this study of Yukon HEBS. Systematic sampling and Mo and Tl isotopic analysis of a continuous 200 m stratigraphic section through the Yukon HEBS mineralization and footwall and hanging-wall strata at the Peel River north and south bank showings (spaced five km apart) give δ98Mo –1.24 to –0.53‰ and –8.1 to –5.2 ε-units for the mineralization and –0.70 to 0.60‰ and –6.5 to –2.0 ε-units for the unmineralized strata. These values preclude a hydrothermal origin and strongly suggest that redox processes were responsible for the Yukon HEBS mineralization. The isotopic compositions, together with rare earth element (REE) systematics (REE profile, Y positive anomalies, Ce negative anomalies, and Y/Ho values) and other bulk geochemical redox indicators (Mo, V, Re/Mo, Ni/Co, U/Th, and V/Cr) indicate that the Peel River HEBS mineralization formed because of metal scavenging from seawater in a quiescent, euxinic basinal paleoenvironment.","PeriodicalId":134244,"journal":{"name":"The Canadian Mineralogist","volume":"140 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"115236866","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Exploration geochemistry of surficial media over the high-grade McArthur River uranium deposit, Saskatchewan, Canada","authors":"S. Beyer, K. Kyser, T. Kotzer, K. Ansdell, D. Quirt","doi":"10.3749/canmin.2000081","DOIUrl":"https://doi.org/10.3749/canmin.2000081","url":null,"abstract":"\u0000 An orientation survey using surficial media was performed over the high-grade McArthur River unconformity-related U deposit (Saskatchewan, Canada) to test whether or not secondary dispersion of elements related to the ore body or alteration zone can be detected at the surface more than 500 m above the deposit. Organic-rich Ah-horizon soils, Fe-rich B-horizon soils, C-horizon soils, tree cores of Jack pine (Pinus banksiana), and glacially dispersed boulders of Manitou Falls Formation sandstone that host the U deposit were collected in four sampling grids near the mine site. Two of the grids overlaid the trace of the P2 fault that hosts the deposit and extends nearly to the surface, one grid overlaid both the P2 fault and one of the high-grade ore bodies (Zone 4), and one grid was located 2.5 km away from the ore body surface trace in the barren hanging wall of the P2 fault. The grid overlying the Zone 4 ore body had the highest proportion of samples with elevated U and low 207Pb/206Pb ratios, the latter indicative of radiogenic Pb from a high-U source, measured in two size fractions of Ah-horizon soils using Na pyrophosphate leach, pine tree cores using total digestion, and sandstone boulders using 2% HNO3 leach. A handful of pathfinder elements, such as As, Co, Ni, and Pb, are variably associated with the U and radiogenic Pb. Sandstone boulders with an assemblage of dravite + kaolinite ± illite, determined using shortwave infrared (SWIR) spectroscopy and matching the alteration mineralogy in the Manitou Falls Formation above the U deposit, were prevalent in the grid above the Zone 4 ore body and in the adjacent grid in the direction of glacial dispersion. A coarse fraction of the B-horizon soils, leached with 5% HNO3, highlighted the grid above the Zone 4 ore body to a lesser extent, whereas HNO3 leaches and aqua regia digests of C-horizon soil separates did not highlight the P2 fault or ore body trace due to influence by parent till mineralogy. Results of environmental monitoring at the mine site, which was active at the time of sampling, suggest that dust containing U, Pb, and radionuclides from waste rock piles and a ventilation shaft could influence A-horizon soil geochemistry near the mine site, and that U and radiogenic Pb anomalies in B- and C-horizon soils near the water table are close to a treated mine effluent discharge point. However, older trees that record elevated U and radiogenic Pb in annual rings that pre-date mining activity, and alteration mineralogy and geochemistry of boulders that are less susceptible to the influences of mining activity, add confidence that the geochemical anomaly in diverse surficial media above the Zone 4 ore body represents secondary dispersion from the underlying U deposit.","PeriodicalId":134244,"journal":{"name":"The Canadian Mineralogist","volume":"67 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125187833","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Alteration mineralogy and pathfinder element inventory in the footprint of the McArthur River unconformity-related uranium deposit, Canada","authors":"N. Joyce, D. Layton-Matthews, K. Kyser, M. Leybourne, K. Ansdell, T. Kotzer, D. Quirt, G. Zaluski","doi":"10.3749/canmin.2000067","DOIUrl":"https://doi.org/10.3749/canmin.2000067","url":null,"abstract":"\u0000 Pathfinder elements associated with the exploration footprint of the McArthur River unconformity-related U deposit include U, radiogenic Pb, V, Ni, Co, Cu, Mo, As, Zn, and rare earth elements. In this study, the mineralogical and paragenetic context for their occurrence was established by integrating in situ mineral chemistry and laser ablation mass spectrometry chemical mapping of interstitial assemblages, detrital grains, and cements with whole-rock analyses of drill core samples from the diagenetically altered background and the hydrothermally altered sandstone host rocks. Diagenetically altered background sandstones contain a matrix assemblage of illite and dickite, with trace to minor aluminum-phosphate-sulfate (APS) minerals, apatite, and Fe-Ti oxide minerals. Aluminum-phosphate-sulfate minerals account for the majority of the Sr and light rare earth element concentrations, whereas early diagenetic apatite, monazite, and apatite inclusions in detrital quartz and detrital zircon contribute significant U and heavy rare earth elements to samples analyzed with an aggressive leach (partial digestion) such as aqua regia. Hydrothermally altered sandstone host rocks also contain variable assemblages of Al-Mg chlorite (sudoite), alkali-deficient tourmaline, APS minerals, kaolinite, illite, Fe-oxide, and sulfide minerals. Late pre-mineralization chlorite accounts for a significant portion of the observed Ni concentrations, whereas Co, Cu, Mo, and Zn occur predominantly in cryptic sub-micron sulfide and sulfarsenide inclusions within clay mineral aggregates and in association with Fe-Ti oxides. Elevated concentrations of U were observed in cryptic micro-inclusions associated with sulfides in quartz overgrowths, with Fe-Ti oxide micro-inclusions in kaolinite, and in post-mineralization Fe-oxide veins. The distribution of pathfinder elements throughout the deposit footprint appears to be less related to the primary dispersion of alteration minerals from the hydrothermal system than to the secondary dispersion of elements post-mineralization. Their occurrence throughout pre-, syn-, and post-mineralization assemblages further demonstrates the limitations to defining geochemical footprints from pathfinder element concentrations expressed in lithogeochemical data sets without structural, lithological, and mineralogical context.","PeriodicalId":134244,"journal":{"name":"The Canadian Mineralogist","volume":"8 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"115466192","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Mineralogy and petrogenesis of fracture coatings in Athabasca Group sandstones from the McArthur River uranium deposit","authors":"M. Valentino, T. K. Kyser, M. Leybourne, T. Kotzer, D. Quirt, P. Lypaczewski, D. Layton-Matthews, N. Joyce","doi":"10.3749/canmin.2000098","DOIUrl":"https://doi.org/10.3749/canmin.2000098","url":null,"abstract":"\u0000 The McArthur River unconformity-related uranium deposit, located in the Athabasca Basin of Saskatchewan, Canada, is structurally hosted near the unconformity between Archean to Paleoproterozoic metasedimentary basement and the Proterozoic Athabasca Group sandstones. In this study, the mineralogy and geochemistry of fracture materials within the entire ca. 550 m thickness of the Athabasca Group sandstones and the metasedimentary (host) rocks from the McArthur River area were used to determine the paragenetic sequence and origin of minerals in and near the fractures. Our work sought to determine if the host minerals record elements associated with the uranium deposit at depth and if they could be used to guide exploration (vectoring). Fracture orientations indicate that most are moderately dipping (<50°) and provided permeable pathways for fluid movement within the basin, from below, and through the overlying sedimentary rocks. Many of the fractures and adjacent wall rocks record evidence of multiple distinct fluid events.\u0000 Seven types of fracture fillings were identified from drill core intersecting the Athabasca Basin and present distinct colors, mineralogy, and chemical features. Brown (Type 1) and pink (Type 7) fractures host paragenetically late botryoidal goethite, Mn oxide minerals, and poorly crystallized kaolinite that formed from relatively recent low-temperature meteoric fluids, as indicated by poor crystallinity and low δ2H values of –198 to –115‰. These minerals variably replaced higher temperature minerals that are rarely preserved on the fractures or in wall rock near the fractures. Hydrothermal alteration associated with the mineralizing system at ca. 200 °C is recorded in assemblages of dickite, well-crystallized kaolinite, and spherulitic dravite in some white and yellow (Type 2) and white (Type 3) fractures, as reflected by the crystal habits and variable δ2H values of –85 to –44‰. Fibrous goethite in white and yellow (Type 2) and black and orange (Type 5) fractures and microfibrous Mn oxy-hydroxide minerals in black (Type 4) fractures also crystallized from hydrothermal fluids, but at temperatures less than 200 °C.\u0000 White and yellow fractures (Type 2) containing fibrous goethite reflect fracture networks indicative of hydrothermal fluids associated with the mineralizing system during primary dispersion of pathfinder elements and therefore extend the deposit footprint. Brown (Type 1) and pink (Type 7) fractures have low δ2H values in botryoidal goethite and poorly crystallized kaolinite and are indicative of the movement of meteoric waters. Secondary dispersion of elements from the deposit to the surface on some fractures is evidence that fractures are pathways for element migration from the deposit to the surface, over distances exceeding ∼500 m.","PeriodicalId":134244,"journal":{"name":"The Canadian Mineralogist","volume":"6 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"122797414","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Metal Sources in the Proterozoic Vazante-Paracatu Sediment-Hosted Zn District, Brazil: Constraints from Pb Isotope Compositions of Meta-Siliciclastic Units","authors":"Neil A. Fernandes, G. Olivo, D. Layton-Matthews, A. Voinot, D. Chipley, M. Leybourne, W. Reith, E. Leduc, Gustavo Diniz-Oliveira, T. Kyser","doi":"10.3749/CANMIN.2000055","DOIUrl":"https://doi.org/10.3749/CANMIN.2000055","url":null,"abstract":"\u0000 Different types of sediment-hosted whole-rock Pb isotope (206Pb/204Pb, 207Pb/204Pb, 208Pb/204Pb) compositions were determined from phyllites, carbonaceous phyllites (>1% TOC), and meta-litharenites belonging to the Serra do Garrote Formation, which is part of the Proterozoic Vazante Group, Brazil. Results were integrated with lithogeochemistry in order to identify the Pb isotopic signature of Zn enrichment (up to 0.24 wt.% Zn) associated with meta-siliciclastic-hosted sulfide mineralization that formed prior to the Brasiliano Orogeny (850 to 550 Ma) in order to (1) understand the nature of siliciclastic sediment sources, (2) identify possible metal sources in pre-orogenic meta-siliciclastic-hosted Zn mineralization, and (3) evaluate the genetic links between the Zn enrichment in the relatively reduced phyllite package, and different styles of syn-orogenic Zn ± Pb mineralization (hypogene Zn-silicate and Zn-Pb sulfide) in overlying dolomitic carbonates throughout the Vazante-Paracatu Zn District, Brazil.\u0000 The whole-rock 206Pb/204Pb and 207Pb/204Pb isotope ratios of meta-siliciclastic rocks plot as positively sloping, sub-parallel arrays with radiogenic, upper continental crust compositions, which could represent a detrital contribution from at least two upper continental crust sources. However, the 206Pb/204Pb versus 207Pb/204Pb isotope system does not distinguish between Zn-enriched samples and un-mineralized samples. In the whole-rock 206Pb/204Pb–208Pb/204Pb plot, Zn-enriched samples form a flat trend of lower 208Pb/204Pb values (38.3 to 39.5) compared to the Zn-poor ones that follow common upper crustal trends. Zinc-enriched samples have low whole-rock Th/U values (<4) and higher whole-rock U concentrations compared to unmineralized samples. These support the hypothesis that U (± Pb) was added by pre-orogenic metalliferous fluids, which were in turn derived from underlying Paleoproterozoic and Archean basement rocks. Due to U addition, the original whole-rock thorogenic and uranogenic Pb isotope systems were decoupled in mineralized samples. Pre-orogenic metalliferous fluids have similar present-day first-order characteristics, including: (1) relatively high U/Pb and (2) low Th/U values, when compared to galena in the major carbonate-hosted Zn ± Pb deposits (Vazante, Morro Agudo, Ambrosia, Fagundes) in the Vazante Group. These results support the hypothesis that Zn-rich layers and veins in mineralized carbonaceous phyllites could be linked to the same origins as carbonate-hosted mineral deposits throughout the Vazante Basin, but further data are warranted. We suggest that the tectonic evolution of the Vazante Basin saw multiple phases of Zn-rich mineralization over protracted time periods from around 1200 to 550 Ma.","PeriodicalId":134244,"journal":{"name":"The Canadian Mineralogist","volume":"49 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-07-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"122764732","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Alkaline Rocks and Carbonatites of the World Part 4: Antarctica, Asia and Europe (excluding the former USSR), Australasia and Oceanic Islands","authors":"I. Coulson","doi":"10.3749/canmin.br00006","DOIUrl":"https://doi.org/10.3749/canmin.br00006","url":null,"abstract":"","PeriodicalId":134244,"journal":{"name":"The Canadian Mineralogist","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"128556272","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Ferro-fluoro-edenite, a new amphibole endmember from Vulcano Island (Sicily, Italy)","authors":"I. Campostrini, F. Demartin, P. Vignola, F. Pezzotta","doi":"10.3749/canmin.2000118","DOIUrl":"https://doi.org/10.3749/canmin.2000118","url":null,"abstract":"\u0000 Ferro-fluoro-edenite, ideally NaCa2Fe2+5(Si7Al)O22F2, was found as prismatic crystals up to 1.00 mm inside cavities in ejecta of the 1873 eruption at La Fossa crater, Vulcano Island, Aeolian Archipelago, Sicily, Italy. It is associated with quartz, magnetite, and vonsenite. Crystals are dark brown to black, transparent or semitransparent with vitreous luster, and non fluorescent. The Mohs hardness is 5–6. Cleavage is fair on {110} and fracture is uneven. Density (calc.) is 3.358 g cm–3 using the empirical formula and single-crystal cell data. The mineral is biaxial negative, α = 1.629(2), β = 1.659(2), γ = 1.667(2), 2V (calc.) = –53.8°, Y = b. Dispersion is weak to very weak, r < v, pleochroism not visible. Ferro-fluoro-edenite is monoclinic, space group C2/m, a = 9.9132(10), b = 18.1736(19), c = 5.2943(6) Å, β = 104.85(1)°, V = 922.0(2) Å3, Z = 2. The strongest X-ray diffraction peaks in the powder pattern are [d(I, hkl)]: 8.54(100, 1 1 0), 4.506(16, 0 4 0), 3.154(52, 3 1 0), 2.833(43, 3 3 0), 2.057(14, 2 0 2), 1.910(12, 5 1 0), 1.662(15, 4 6 1). The FTIR spectrum shows a broad band at about 950 cm–1 and no bands in the OH stretching region. The structure refinement led to a final R = 0.0210 for 1444 observed reflections with I > 2σ(I) and allowed cation site assignment and ordering. Microprobe analysis gave the following empirical formula calculated on the basis of 24 (O + F + Cl) apfu: (Na0.69K0.23□0.08)(Ca1.69Mg0.16Mn0.10Na0.05)Σ2(Fe2+2.86Mg2.04Ti0.10)Σ5(Si6.93Al1.05Ti0.02)Σ8O22(F1.89Cl0.09OH0.02)Σ2.","PeriodicalId":134244,"journal":{"name":"The Canadian Mineralogist","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"132545174","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Liudongshengite, Zn4Cr2(OH)12(CO3)·3H2O, a new mineral of the hydrotalcite supergroup, from the 79 mine, Gila County, Arizona, USA","authors":"Hexiong Yang, R. Gibbs, Cody Schwenk, Xiande Xie, X. Gu, R. Downs, S. Evans","doi":"10.3749/canmin.2000101","DOIUrl":"https://doi.org/10.3749/canmin.2000101","url":null,"abstract":"\u0000 A new mineral species, liudongshengite, ideally Zn4Cr2(OH)12(CO3)·3H2O, has been found in the 79 mine, Gila County, Arizona, USA. It occurs as micaceous aggregates or hexagonal platy crystals (up to 0.10 × 0.10 × 0.01 mm). The mineral is pinkish and transparent with white streak and vitreous luster. It is brittle and has a Mohs hardness of ∼1.5, with perfect cleavage on (001). No twinning or parting is observed macroscopically. The measured and calculated densities are 2.95 (3) and 3.00 g/cm3, respectively. Optically, liudongshengite is uniaxial (−), with ω = 1.720 (8), ε = 1.660 (7) (white light). An electron microprobe analysis, combined with the carbon content measured using an elemental combustion system equipped with mass spectrometry, yielded the empirical formula (Zn3.25Mg0.17Cr2.58)Σ6.00(OH)12(CO3)1.29·3H2O, based on (M2+ + M3+) = 6 apfu, where M2+ and M3+ are divalent and trivalent cations, respectively.\u0000 Liudongshengite belongs to the quintinite group within the hydrotalcite supergroup and is the Cr-analogue of zaccagnaite-3R, Zn4Al2(OH)12(CO3)·3H2O. It is trigonal, with space group Rm and unit-cell parameters a = 3.1111(4), c = 22.682(3) Å, and V = 190.12(4) Å3. The crystal structure of liudongshengite is composed of positively charged brucite-like layers, [M2+1–xM3+x(OH)2]x+, alternating with negatively charged layers of (CO3)2–·3H2O. Compared to other minerals in the quintinite group, liudongshengite is remarkably enriched in M3+, with an M2+:M3+ ratio of 1.33:1. Like zaccagnaite-3R and many other hydrotalcite-type minerals, liudongshengite may also possess polytypes, as a series of synthetic hydrotalcite-type compounds with a general chemical formula [Zn4Cr2(OH)12]X2·4H2O, where X = Cl–, NO3–, or ½ SO42–, but with unit-cell parameters different from those for liudongshengite, have been reported previously.","PeriodicalId":134244,"journal":{"name":"The Canadian Mineralogist","volume":"27 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134164404","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Wildcatite, CaFe3+Te6+O5(OH), the second new tellurate mineral from the Detroit district, Juab County, Utah","authors":"Owen P. Missen, S. Mills, A. Kampf, M. Coolbaugh, J. Najorka, M. Rumsey, J. Marty, J. Spratt, M. Raudsepp, J. McCormack","doi":"10.3749/canmin.2000092","DOIUrl":"https://doi.org/10.3749/canmin.2000092","url":null,"abstract":"\u0000 Wildcatite (IMA2020–019) is a new calcium–iron(III) tellurate discovered at the Wildcat prospect in the Detroit district, Juab County, Utah. Wildcatite may take on a variety of appearances, ranging from transparent orange to brown coatings or masses to earthy, white polycrystalline coatings filling jasperoid fracture surfaces. Coatings of wildcatite are generally less than 0.1 mm thick and may cover up to 5 cm2, while nanoscale crystallites of wildcatite may form translucent red-brown “crystals” up to 0.1 mm. Wildcatite is found associated with gold, calcite, aragonite, native tellurium, manganese oxides, iron oxides, rare clinobisvanite, beyerite, coronadite, the Te oxides paratellurite and tellurite, and the Te oxysalts andymcdonaldite, burckhardtite, carlfriesite, eckhardite, frankhawthorneite, khinite, mcalpineite, tlapallite, and xocolatlite. The strongest powder diffraction lines are [dobsÅ(Iobs)(hkl)]: 3.33(100)(011), 2.60(55)(110), 2.30(59)(111), 2.05(33)(021), and 1.80(88)(112). The average size of wildcatite crystallites is 13 nm, thus the crystal structure of wildcatite was solved by Rietveld refinement, converging to a final RB value of 3.14%. The empirical formula of wildcatite, as determined by electron probe microanalysis and Rietveld refinement, is Ca0.98Bi3+0.02Pb0.01Fe3+0.73Mg0.05Mn2+0.02Zn0.01Cu0.00Te6+1.15Sb5+0.02Si0.01O5.44H0.56, simplified to the ideal formula of CaFe3+Te6+O5(OH). Wildcatite is trigonal, crystallizing in the space group P1m, with a = 5.2003(14) Å, c = 4.9669(14) Å, V = 116.3(1) Å3 and Z = 1. Wildcatite is structurally very similar to rosiaite (PbSb2O6), possessing a honeycomb-like two-dimensional framework of edge-sharing Fe3+O6 and Te6+O6 octahedra, sandwiching octahedrally coordinated Ca2+ cations. Minor OH substitution (∼10%) at the O sites is required for charge balance in wildcatite.","PeriodicalId":134244,"journal":{"name":"The Canadian Mineralogist","volume":"18 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"124265870","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"The pascoite family of minerals, including the redefinition of rakovanite","authors":"A. Kampf, John M. Hughes, M. Cooper, F. Hawthorne, B. Nash, Travis A. Olds, P. Adams, J. Marty","doi":"10.3749/canmin.2000082","DOIUrl":"https://doi.org/10.3749/canmin.2000082","url":null,"abstract":"\u0000 Mineral species that contain the decavanadate isopolyanion [V10O28]6–, including its protonated and mixed-valence variants, constitute the pascoite family of minerals. Within the pascoite family, the isostructural minerals pascoite and magnesiopascoite form the pascoite group and the isostructural minerals lasalite and ammoniolasalite form the lasalite group. Rakovanite, which was originally assigned the ideal formula Na3[H3V10O28]·15H2O, is redefined with the ideal formula (NH4)3Na3[V10O28]·12H2O.","PeriodicalId":134244,"journal":{"name":"The Canadian Mineralogist","volume":"130 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"115892395","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}