Canadian Mineralogist最新文献

{"title":"Carbonate-bearing phosphohedyphane–“Hydroxylphosphohedyphane” and cerussite: Supergene products of galena alteration in Permian aplite (Western Carpathians, Slovakia)","authors":"M. Ondrejka, P. Bačík, M. Putiš, P. Uher, T. Mikuš, J. Luptáková, Š. Ferenc, A. Smirnov","doi":"10.3749/canmin.1900082","DOIUrl":"https://doi.org/10.3749/canmin.1900082","url":null,"abstract":"\u0000 A unique assemblage of hedyphane-group minerals of the apatite supergroup associated with galena, cerussite, and calcite occurs in a Permian aplite dike crosscutting orthogneisses belonging to the pre-Alpine basement of the Veĺký Zelený Potok Valley in the Veporic Unit, Western Carpathians, Central Slovakia. The secondary Ca-Pb phosphates include phosphohedyphane Ca2Pb3(PO4)3Cl and (OH)-dominant “hydroxylphosphohedyphane” Ca2Pb3(PO4)3OH. Detailed EPMA and Raman spectroscopy of the hedyphane-group minerals reveal the presence of Pb, Ca, P, and Cl as major constituents; the systematic presence of (CO3)2– (up to 2.6 wt.% CO2calc; 0.65 apfu C) substituting for (PO4)3– (B-type) is the first reported carbonate-bearing phosphohedyphane in nature. There is also significant localized halogen deficiency (0.38–0.49 apfu Cl+F) which suggests the potential for a new mineral, “hydroxylphosphohedyphane”. The secondary assemblage described herein results from very low-temperature sulfide-carbonate reactions and further near-surface supergene alteration of primary magmatic or metamorphic phosphate minerals (mainly apatite) and hydrothermal galena in the alkaline CO2-rich groundwater.","PeriodicalId":9455,"journal":{"name":"Canadian Mineralogist","volume":"58 1","pages":"347-365"},"PeriodicalIF":0.9,"publicationDate":"2020-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3749/canmin.1900082","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44992551","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Viteite, Pd5InAs, a new mineral from the Monchetundra layered intrusion, Kola Peninsula, Russia","authors":"A. Vymazalová, F. Laufek, Tatiana L. Grokhovskaya, C. Stanley","doi":"10.3749/canim.1900080","DOIUrl":"https://doi.org/10.3749/canim.1900080","url":null,"abstract":"\u0000 Viteite, Pd5InAs, is a new mineral discovered in the Monchetundra layered intrusion, Kola Peninsula, Russia. It forms euhedral grains about 0.5 to 10 μm in size intergrown with irarsite (IrAsS), hollingworthite (RhAsS), zvyagintsevite (Pd3Pb), Au-Ag alloys, and tulameenite (Pt2CuFe), that are replaced by Pt-Pd-Fe-Cu alloys and Pt-Pd-Fe-Cu oxygenated compounds, all of which are embedded in chalcocite, goethite, and covellite. Viteite is brittle and has a metallic luster. In plane-polarized light, viteite is bright pinkish-white. The mineral is weakly anisotropic with rotation tints blue to pinkish brown; it exhibits no internal reflections. Reflectance values of viteite in air (R1, R2 in %) are 55.7, 54.0 at 470 nm; 59.2, 58.4 at 546 nm; 60.0, 60.4 at 589 nm; and 60.0, 62.6 at 650 nm. Eight electron-microprobe analyses of viteite give an average composition of Pd 71.90, Pt 1.60, Fe 0.98, Cu 0.59, In 11.48, Hg 1.42, Pb 0.40, As 10.70, total 99.07 wt.%, corresponding to the empirical formula (Pd4.92Pt0.06)Σ4.98(In0.73Fe0.12Cu0.07Hg0.05Pb0.01)Σ0.98As1.04 based on 7 atoms; the average of 12 analyses of its synthetic analogue is: Pd 73.72, In 16.37, As 9.80, total 99.90 wt.%, corresponding to Pd5.02In1.03As0.95. The density, calculated on the basis of the empirical formula, is 10.78 g/cm3. The mineral is tetragonal, space group P4/mmm, with a 3.98600(3), c 6.98385(8) Å, V 110.961(2) Å3, and Z = 1. The crystal structure of synthetic Pd5InAs was solved and refined using powder X-ray-diffraction data from synthetic Pd5InAs. Viteite crystallizes with the Pd5TlAs structure type. The strongest lines in the X-ray powder diffraction pattern of synthetic Pd5InAs [d in Å (I) (hkl)] are: 2.3281(45)(003), 2.1932(100)(112), 1.9928(33)(020), 1.2515(17)(115), 1.1857(25)(132). The mineral is named for the Vite river, which flows near the Monchetundra intrusion.","PeriodicalId":9455,"journal":{"name":"Canadian Mineralogist","volume":"58 1","pages":"395-402"},"PeriodicalIF":0.9,"publicationDate":"2020-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3749/canim.1900080","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48399150","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Helvine-group minerals from Norwegian granitic pegmatites and some other granitic rocks: Cases of significant Sc and Sn contents","authors":"G. Raade","doi":"10.3749/canmin.1900099","DOIUrl":"https://doi.org/10.3749/canmin.1900099","url":null,"abstract":"Helvine-group minerals from two granitic pegmatites have disparate compositions, from nearly pure helvine (Ågskardet, northern Norway; Devonian) to helvine close to ternary compositions (Heftetjern, southern Norway; Precambrian). Metagranite from Høgtuva (northern Norway; Precambrian with Caledonian metamorphic overprint) contains Zn-rich danalite. The Ågskardet helvine contains up to 0.46 wt.% SnO2, and the Heftetjern ternary helvine shows a maximum of 1.74 wt.% Sc2O3. Helvine minerals were also analyzed from three occurrences connected to peralkaline granite (ekerite) of the Permian Oslo Rift. Nearly pure genthelvite (99.19 mol.%) occurs in miarolitic cavities at Gjerdingselva. Two mineralogically different granitic pegmatites derived from the same ekerite pluton in the southern part of the Oslo Rift show quite distinct helvine compositions, from nearly continuous solid solution between helvine and genthelvite in crystals with oscillatory zonation (Rundemyr) to solid solutions midway between danalite and genthelvite (Bakstevalåsen). The Rundemyr crystals have a maximum SnO2 content of 1.28 wt.%. The incorporation of minor elements (Ca, Mg, Al, Sn, Sc) in helvine-group minerals is discussed with emphasis on their chalcophilicity characteristics. For stereochemical reasons, Sn in helvine minerals must be tetravalent, even if Sn2+ is more chalcophile than Sn4+.","PeriodicalId":9455,"journal":{"name":"Canadian Mineralogist","volume":"58 1","pages":"367-379"},"PeriodicalIF":0.9,"publicationDate":"2020-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3749/canmin.1900099","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42191849","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Experimental fluid-mediated alteration of zircon under lower greenschist facies conditions","authors":"C. J. Kelly, D. Harlov, D. Schneider, S. Jackson, R. Dubosq","doi":"10.3749/canmin.1900041","DOIUrl":"https://doi.org/10.3749/canmin.1900041","url":null,"abstract":"\u0000 The use of zircon in the dating of geological processes and tectonic events has become a standard approach in many aspects of Earth science research. As a result, understanding how zircon interacts with aqueous fluids during metasomatism has become increasingly important. The alteration of natural zircon is driven primarily by coupled dissolution–reprecipitation or by ion-exchange with an aqueous fluid. In this study, whole and intact, euhedral light-brown zircon crystals (100–250 μm in length; 2 mg) from the Oligocene Fish Canyon Tuff (FCT) were experimentally reacted with an alkali-bearing reactive fluid and a REE + P source (0.5 mg CePO4 or 0.5 mg YPO4). Experiments were conducted in sealed Au metal capsules at 350 °C and 100 MPa for 182 days. During the experiment, the zircon became colorless, indicating annealing of the radiation damage in the crystal. Two-dimensional element maps of the outermost 3 μm of unpolished zircon crystal surfaces were produced using a grind of contiguous 7 μm analytical spots via laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). The chemical maps indicate that the surface of the zircon crystals from each experiment heterogeneously reacted with the fluid, such that the Ce and Y concentration of chemically modified areas increased (by an order of magnitude) in the CePO4-bearing and YPO4-bearing experiments, respectively, when compared with the chemical maps of unaltered zircon grain surfaces. Helium ion microscopy of polished crystals revealed discontinuous micron-scale altered domains at the crystal margin, consistent with the findings of the unpolished mapping technique. Interestingly, the Th and U concentration of the altered zircon grain surfaces were consistent with the unaltered zircon regardless of the experiment. Incorporation of REEs on the zircon grain surface likely occurred via the coupled substitution REE3+ + P5+ ↔ Zr4+ + Si4+. The results from these experiments imply that the surfaces of minimally metamict zircon can be chemically modified by alkali-bearing fluids via ion exchange under lower greenschist pressures and temperatures over relatively short time periods with respect to the geological time scale.","PeriodicalId":9455,"journal":{"name":"Canadian Mineralogist","volume":"58 1","pages":"247-265"},"PeriodicalIF":0.9,"publicationDate":"2020-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3749/canmin.1900041","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49324276","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Kainotropite, Cu4Fe3+O2(V2O7)(VO4), a new mineral with a complex vanadate anion from fumarolic exhalations of the Tolbachik volcano, Kamchatka, Russia","authors":"I. Pekov, N. Zubkova, V. Yapaskurt, Y. Polekhovsky, S. Britvin, A. Turchkova, E. Sidorov, D. Pushcharovsky","doi":"10.3749/canmin.1900073","DOIUrl":"https://doi.org/10.3749/canmin.1900073","url":null,"abstract":"\u0000 The new mineral kainotropite Cu4Fe3+O2(V2O7)(VO4) was found in sublimates of fumaroles related to the Tolbachik volcano, Kamchatka, Russia. The holotype specimen originates from the Yadovitaya fumarole at the Second scoria cone of the Northern Breakthrough of the Great Tolbachik Fissure Eruption; associated minerals are hematite, langbeinite, calciolangbeinite, tenorite, piypite, lyonsite, rutile, pseudobrookite, sanidine, and lammerite. In paleo-fumarolic deposits of Mountain 1004 kainotropite is associated with diopside and hematite. It forms prismatic crystals up to 0.2 × 0.2 × 0.5 mm3, isolated or combined in clusters up to 0.7 mm across. Kainotropite is iron-black to reddish-black, with semi-metallic luster. Dcalc is 4.10 g/cm3. In reflected light, kainotropite is grey, weakly anisotropic. The reflectance values [Rmax–Rmin,% (λ, nm)] are: 18.3–17.3 (470), 17.3–16.3 (546), 16.9–15.7 (589), 16.3–15.1 (650). The chemical composition of the holotype sample (wt.%, electron microprobe) is: CuO 46.69, Al2O3 1.40, Fe2O3 10.04, TiO2 0.32, V2O5 37.58, As2O5 2.55, MoO3 0.76, total 99.34. The empirical formula, based on 13 O apfu, is: Cu3.96Fe3+0.85Al0.19Ti0.03(V2.78As0.15Mo0.04)Σ2.97O13. Kainotropite is orthorhombic, Pnma, a = 14.139(2), b = 6.7102(7), c = 11.4177(15) Å, V = 1083.3(2) Å3, and Z = 4. The strongest reflections of the powder XRD pattern [d,Å(I)(hkl)] are: 8.89(100)(101), 5.728(33)(002), 3.698(35)(212), 3.357(52)(020,203), 3.034(77)(220), 2.968(60)(303), and 2.655(27)(321,204). The crystal structure was solved from single-crystal XRD data, R = 0.085. Kainotropite represents a novel structure type. Cu2+ polyhedra (distorted tetragonal pyramids and strongly distorted octahedra) and Fe3+ octahedra are connected via common edges to form zigzag ribbons. Adjacent ribbons are connected by both V2O7 and VO4 groups (isolated from each other) to form a heteropolyhedral pseudo-framework. The name kainotropite is derived from the Greek word καινóτρoπoς, unusual, in allusion to its uncommon (for natural vanadates) anionic composition: it is the first mineral containing both pyrovanadate (V2O7)4– and orthovanadate (VO4)3– anions.","PeriodicalId":9455,"journal":{"name":"Canadian Mineralogist","volume":"58 1","pages":"155-165"},"PeriodicalIF":0.9,"publicationDate":"2020-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3749/canmin.1900073","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46715468","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Ultramafic xenoliths from the 1.15 Ga Certac kimberlite, eastern Superior Craton","authors":"A. V. Rythoven, D. Schulze, D. Davis","doi":"10.3749/canmin.1900064","DOIUrl":"https://doi.org/10.3749/canmin.1900064","url":null,"abstract":"\u0000 Xenoliths and xenocrysts of mantle material from kimberlite dikes located underground at the Certac Au mine, Québec, in the eastern Superior Craton, were studied in terms of the major element composition of their constituent minerals. The kimberlite was dated at 1151 ± 46 Ma by the U-Pb perovskite method. This suite thus provides a rare glimpse into the Mesoproterozoic mantle of the Superior Craton. Two parageneses of mantle material unrelated to the kimberlite magmatism occur: (1) an olivine + ilmenite ± magnetite association characterized by relatively Fe-rich olivine (Mg# = 0.68–0.84) and ilmenite enriched in Mg and Cr (4–13 wt.% MgO, Cr2O3 up to 3 wt.%), and (2) spinel peridotite characterized by Mg-rich olivine (Mg# = 0.91–0.94). The Fe-rich association is interpreted as a magmatic cumulate likely unrelated to the kimberlite. No mantle-derived garnet occurs in the xenoliths or as xenocrysts. The presence of Cr-rich spinel (Cr# = 0.84–0.98) in high temperature (860–953 °C) chromite peridotite indicates bulk compositions too depleted in Al for garnet to be stable, although geothermometry suggests they equilibrated at depths corresponding to garnet stability (90–131 km, depending on the geothermal gradient). Alternatively, the presence of phlogopite in two of the three high temperature (i.e., deepest) chromite peridotites suggests the absence of garnet and presence of low-Al chromite may have been caused by metasomatism from a K-rich fluid that replaced garnet with phlogopite + clinopyroxene ± chromite. Less depletion at shallower depths is indicated by a chromite (Cr# = 0.60) dunite that equilibrated at 831 °C and a low temperature (752 °C) Mg-Al-spinel lherzolite.","PeriodicalId":9455,"journal":{"name":"Canadian Mineralogist","volume":"58 1","pages":"267-286"},"PeriodicalIF":0.9,"publicationDate":"2020-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3749/canmin.1900064","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48588182","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Alkali sulfates with aphthitalite-like structures from fumaroles of the Tolbachik volcano, Kamchatka, Russia. II. A new mineral, natroaphthitalite, and new data on belomarinaite","authors":"N. V. Shchipalkina, I. Pekov, N. Chukanov, D. I. Belakovskiy, N. Zubkova, N. Koshlyakova, S. Britvin, E. Sidorov","doi":"10.3749/canmin.1900076","DOIUrl":"https://doi.org/10.3749/canmin.1900076","url":null,"abstract":"\u0000 Natroaphthitalite K(Na,K)2Na(SO4)2, a new aphthitalite-group mineral, was found in exhalations of the active Arsenatnaya fumarole at the Second scoria cone of the Northern Breakthrough of the Great Tolbachik Fissure Eruption, Tolbachik volcano, Kamchatka Peninsula, Russia. The associated minerals are anhydrite, langbeinite, hematite, tenorite, sanidine, johillerite, tilasite, and belomarinaite. Natroaphthitalite occurs as translucent yellow to colorless roundish single-crystal individuals up to 1 cm in diameter, sometimes combined in crusts up to 2 cm across, and as aqua-transparent colorless tabular to lamellar hexagonal crystals up to 2 mm across, sometimes skeletal, typically combined in parallel intergrowths or brush-like aggregates. Dcalc is 2.664 g/cm3. Natroaphthitalite is optically uniaxial (+), ω = 1.488(2), ε = 1.490(2). The chemical composition (wt.%, electron microprobe) is: Na2O 22.54, K2O 26.39, SO3 51.78, total 100.71. The empirical formula calculated based on 8 O apfu is K1.735Na2.252S2.002O8 (average of 15 spot analyses). The crystal structures of natroaphthitalite and the associated aphthitalite-group mineral belomarinaite, ideally KNaSO4, from the Arsenatnaya fumarole were solved using single-crystal X-ray diffraction and refined to R1 = 0.0283 and 0.0261, respectively. The unit-cell parameters, Z, and space groups are a = 5.6014(3), c = 7.1507(5) Å, V = 194.30(2) Å3, Z = 1, and for natroaphthitalite and a = 5.6088(3), c = 7.1858(4) Å, V = 195.77(1) Å3, Z = 2, and P3m1 for belomarinaite. The crystal chemical formulae of natroaphthitalite and belomarinaite (Z = 1) are XK1.00Y(Na1.28K0.72)Σ2.00MNa1.00(TSO4)2 and XK1.00Y1(Na0.96K0.04)Σ1.00Y2(K0.94Na0.06)Σ1.00MNa1.00(TSO4)2, respectively. Natroaphthitalite is isostructural with aphthitalite K3Na(SO4)2 = XKYK2MNa(TSO4)2 (both have centrosymmetric structures) with prevailing Na over K at the Y site of the crystal structure. Belomarinaite XKY2KY1NaMNa(TSO4)2 is the fully cation-ordered species, with acentric structure, in the series of natural aphthitalite-like K-Na sulfates.","PeriodicalId":9455,"journal":{"name":"Canadian Mineralogist","volume":"58 1","pages":"167-181"},"PeriodicalIF":0.9,"publicationDate":"2020-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3749/canmin.1900076","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47654172","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Pedogenic origin of Mezezo opal hosted in Ethiopian Miocene rhyolites","authors":"D. Ayalew, R. Pik, S. Gibson, G. Yirgu, S. Ali, D. Assefa","doi":"10.3749/canmin.1900059","DOIUrl":"https://doi.org/10.3749/canmin.1900059","url":null,"abstract":"\u0000 Opals are widespread within Miocene volcanic sequences in the North Shoa province of Central Ethiopia. The opal occurs as cavity fillings in a 5 m thick seam of glassy rhyolitic ignimbrite that is sandwiched between basaltic lava flows. The opals occur over a large area (>25 km2). X-ray diffraction analyses show that they are CT-type. The opals contain lower concentrations of trace elements (up to 100 times) than the host rhyolite. Ratios of most trace elements are, however, similar in both the opals and rhyolites. The opals have high δ18O values (28.4–33.8‰) that imply a low temperature of formation, between 20.55 and 25.74 °C. We therefore propose that the opals precipitated from meteoric waters that had percolated through and interacted with the host rhyolite. Field evidence indicates that this weathering and alteration occurred immediately after emplacement of the rhyolites, but prior to the extrusion of the overlying basalt flows.","PeriodicalId":9455,"journal":{"name":"Canadian Mineralogist","volume":"58 1","pages":"231-246"},"PeriodicalIF":0.9,"publicationDate":"2020-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3749/canmin.1900059","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49416793","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"The Ag- and Au-bearing phases in the Escondida epithermal vein, Cerro Moro deposit, Santa Cruz, Argentina","authors":"A. C. M. Lobos, M. F. Márquez-Zavalía, Laura Hernández","doi":"10.3749/canmin.1900075","DOIUrl":"https://doi.org/10.3749/canmin.1900075","url":null,"abstract":"\u0000 The Cerro Moro deposit is located at 48°5′55″S, 66°39′1.6″W and 100 m.o.s.l. in Santa Cruz province, southern Argentina. It is a low sulfidation Au-Ag epithermal mineralization hosted by numerous NW–SE structurally controlled quartz veins developed in close spatial and temporal proximity to the products of Jurassic extension and magmatism. The Escondida vein is the most significant mineralized structure, as it hosts the base metal-rich and Au-Ag high grade mineralization. In this vein and the Zoe ore-shoot, ore minerals are abundant (sphalerite, galena, chalcopyrite, acanthite, and less abundant pyrite and marcasite) and frequently related to dark grey, fine-grained quartz with massive, porous, crustiform, and banded textures; variable quantities of fine-grained flakes of muscovite are locally present. The Ag- and Au-bearing mineral association is represented by acanthite, argyrodite, polybasite, pearceite, stromeyerite, mckinstryite, and jalpaite. Abundant acanthite occurs commonly associated with gold and silver; copper enrichments were detected and interpreted as nanoinclusions of Cu-bearing minerals. The occurrence of Se- and Te-enriched minerals (acanthite, argyrodite, polybasite, pearceite, stromeyerite, and mckinstryite), rather than silver selenides and/or tellurides, indicates the presence of reduced mineralizing fluids and may be ascribed to partial substitution of S by Se or Te. Polybasite and pearceite were differentiated by their chemistry. Although the presence of argyrodite in epithermal deposits with silver sulfosalts is relatively common, this first mention in Cerro Moro is highly encouraging for exploration for germanium, a critical element, which is also considered strategic by countries such as the USA and China.","PeriodicalId":9455,"journal":{"name":"Canadian Mineralogist","volume":"58 1","pages":"191-201"},"PeriodicalIF":0.9,"publicationDate":"2020-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3749/canmin.1900075","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42218531","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"In memoriam: Donald David Hogarth (1927–2019)","authors":"R. Martin","doi":"10.3749/canmin.obit00008","DOIUrl":"https://doi.org/10.3749/canmin.obit00008","url":null,"abstract":"","PeriodicalId":9455,"journal":{"name":"Canadian Mineralogist","volume":" 43","pages":"289-290"},"PeriodicalIF":0.9,"publicationDate":"2020-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3749/canmin.obit00008","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41255042","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}