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Newsletter 70 70年时事通讯
IF 2.7 3区 地球科学 Q2 MINERALOGY Pub Date : 2023-01-09 DOI: 10.1180/mgm.2022.135
Ritsuro Miyawaki, Frédéric Hatert, Marco Pasero, Stuart J. Mills
Ritsuro Miyawaki, (Chairman, CNMNC)1, Frédéric Hatert, (Vice-Chairman, CNMNC)2, Marco Pasero, (Vice-Chairman, CNMNC)3 and Stuart J. Mills, (Secretary, CNMNC)4 1 Department of Geology, National Museum of Nature and Science, 4-1-1 Amakubo, Tsukuba 305-0005, Japan – miyawaki@kahaku.go.jp; 2 Laboratoire de Minéralogie, Université de Liège, Bâtiment B18, Sart Tilman, 4000 Liège, Belgium – fhatert@uliege.be; 3 Dipartimento di Scienze della Terra, Università di Pisa, Via Santa Maria 53, 56126 Pisa, Italy – marco.pasero@unipi.it; and 4 Geosciences, Museums Victoria, PO Box 666, Melbourne, Victoria 3001, Australia – smills@museum. vic.gov.au
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引用次数: 1
Alumolukrahnite, CaCu2+Al(AsO4)2(OH)(H2O), the aluminium analogue of lukrahnite from the Jote mine, Copiapó Province, Chile alololuhnite, cucu2 +Al(AsO4)2(OH)(H2O), alololuhnite的类似物,产自智利Copiapó省Jote矿
IF 2.7 3区 地球科学 Q2 MINERALOGY Pub Date : 2022-12-28 DOI: 10.1180/mgm.2022.142
A. R. Kampf, S. Mills, B. Nash, M. Dini, A. A. M. Donoso
Abstract The new mineral alumolukrahnite (IMA2022–059), CaCu2+Al(AsO4)2(OH)(H2O), was found at the Jote mine, Copiapó Province, Chile, where it is a secondary alteration phase associated with conichalcite, coronadite, gypsum, olivenite, pharmacosiderite, rruffite and scorodite. Alumolukrahnite occurs as crude diamond-shaped tablets up to ~0.1 mm, intergrown in crude spherical aggregates. Crystals are apple green and transparent to translucent, with vitreous lustre and a white streak. The Mohs hardness is 3½. The mineral is brittle with irregular fracture and no cleavage. The calculated density is 4.094 g cm–3. Optically, alumolukrahnite is biaxial (+) with α = 1.73(1), β = 1.74(1) and γ = 1.76(1) (white light). The empirical formula, determined from electron microprobe analyses, is Ca1.01(Cu0.92Zn0.13)Σ1.05(Al0.96Fe0.01)Σ0.97(As0.985O4)2(OH)0.88(H2O)1.12. Alumolukrahnite is triclinic, P$bar{1}$, a = 5.343(5), b = 5.501(5), c = 7.329(5) Å, α = 67.72(2), β = 69.06(2), γ = 69.42(2)°, V = 180.3(3) Å3 and Z = 1. Alumolukrahnite is a member of the tsumcorite group and is the Al analogue of lukrahnite.
摘要:在智利Copiapó省Jote矿中发现了一种新矿物铝榴辉石(IMA2022-059), CaCu2+Al(AsO4)2(OH)(H2O),该矿物为次级蚀变相,与锥辉石、冠状石、石膏、橄榄石、药黄石、铁榴石和铁榴石伴生。铝榴辉石以粗菱形片剂的形式出现,片剂可达~0.1 mm,在粗球形集合体中交错生长。晶体为苹果绿色,透明至半透明,具有玻璃光泽和白色条纹。莫氏硬度是3½。该矿物易碎,呈不规则断裂,无解理。计算密度为4.094 g cm-3。光学上,铝榴辉石为双轴(+),α = 1.73(1), β = 1.74(1), γ = 1.76(1)(白光)。由电子探针分析得到的经验公式为Ca1.01(Cu0.92Zn0.13)Σ1.05(Al0.96Fe0.01)Σ0.97(As0.985O4)2(OH)0.88(H2O)1.12。Alumolukrahnite三斜,P{1} 酒吧,美元= 5.343 (5),b = 5.501 (5), c = 7.329(5),α= 67.72(2),β= 69.06(2),γ= 69.42(2)°,V = 180.3 (3) A3和Z = 1。铝榴辉石是闪长岩群的一员,是铝榴辉石的类似物。
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引用次数: 1
Crystal structures of rhodium-containing erlichmanite–laurite solid solutions (Os1–x–yRuxRhyS2: x = 0.09–0.60, y = 0.07–0.10) with unique compositional dependence 具有独特组成依赖性的含铑伊利石-月桂石固溶体(Os1–x–yRuxRhyS2:x=0.09–0.60,y=0.07–0.10)的晶体结构
IF 2.7 3区 地球科学 Q2 MINERALOGY Pub Date : 2022-12-22 DOI: 10.1180/mgm.2022.139
Ginga Kitahara, A. Yoshiasa, S. Ishimaru, Kunihisa Terai, M. Tokuda, D. Nishio–Hamane, Takahiro Tanaka, K. Sugiyama
Abstract Rh-rich and Ir-poor erlichmanite–laurite OsS2–RuS2 solid solutions have been discovered at placers in Haraigawa, Misato-machi, Kumamoto, Japan. Microprobe analysis was performed to identify solid solutions containing few sub-components other than Rh. Approximately 10 at.% Rh was found to be present in the solid-solution samples. Structural refinement was performed using four natural samples: Os0.32Ru0.61Rh0.07S2, Os0.49Ru0.43Rh0.08S2, Os0.58Ru0.33Rh0.08S2 and Os0.81Ru0.09Rh0.10S2. The unit-cell parameters for the solid solutions containing Rh from Haraigawa varied from 5.61826(6) to 5.63142(8) Å. The (Os, Ru, Rh)–S distances in the Os1–x–yRuxRhyS2 system were almost constant with a small variation of 0.001 Å. Conversely, the S–S distances varied significantly, with variations approaching 0.1 Å. Rh substitution of Os rather than Ru had a larger impact on the crystal structure. The atomic displacement ellipsoid of both cations and anions was almost spherical, and no elongation along the M–S and S–S bond directions was observed. The bulk Debye temperatures were estimated from the Debye–Waller factor for the sulfide site. The bulk Debye temperatures of pure OsS2 and RuS2 were 688 K and 661 K, respectively, which suggests that the melting point of erlichmanite is higher than that of laurite. The high Debye temperature of OsS2 is inconsistent with the crystallisation of laurite prior to erlichmanite from the primitive magma, which suggests that $f_{rm S_2}$, rather than temperature, is the main cause of the known crystallisation order. The presence of several percent Rh has a significant effect on the thermal stability of OsS2 and lowers the melting point of the erlichmanite solid solution compared to that of the laurite solid solution.
摘要在日本熊本县三户町原井川砂矿中发现了富Rh和贫Ir的二辉橄榄岩-月桂石OsS2–RuS2固溶体。进行微探针分析以鉴定含有除Rh以外的少数亚组分的固溶体。发现在固体溶液样品中存在大约10at.%Rh。使用四种天然样品进行结构细化:Os0.32Ru0.61Rh0.07S2、Os0.49Ru0.43Rh0.08S2、Os0.58Ru0.33Rh0.08S2和Os0.81Ru0.09Rh0.10S2。来自Haraigawa的含有Rh的固溶体的晶胞参数在5.61826(6)至5.63142(8)Å之间变化。Os1–x–yRuxRhyS2系统中的(Os,Ru,Rh)–S距离几乎恒定,变化很小,为0.001Å。相反,S–S距离变化很大,变化接近0.1Å。Os而不是Ru的Rh取代对晶体结构的影响更大。阳离子和阴离子的原子位移椭球几乎是球形的,并且没有观察到沿M–S和S–S键方向的延伸。根据硫化物场地的德拜-沃勒系数估算出整体德拜温度。纯OsS2和RuS2的体相德拜温度分别为688 K和661 K,这表明伊利石的熔点高于月桂石。OsS2的高德拜温度与原始岩浆中的埃尔希曼岩之前的月桂岩结晶不一致,这表明$f_{rmS_2}$而不是温度是已知结晶顺序的主要原因。几个百分比的Rh的存在对OsS2的热稳定性有显著影响,并且与月桂石固溶体的熔点相比,降低了伊利石固溶物的熔点。
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引用次数: 0
Thermodynamics and crystal structures of krautite, Mn[AsO3(OH)]⋅H2O, koritnigite, Zn[AsO3(OH)]⋅H2O and cobaltkoritnigite, Co[AsO3(OH)]⋅H2O 镁云母Mn[AsO3(OH)]⋅H2O、钾褐铁矿、Zn[AsO3(OH)]⋅H2O和钴褐铁矿、Co[AsO3(OH)]⋅H2O的热力学和晶体结构
IF 2.7 3区 地球科学 Q2 MINERALOGY Pub Date : 2022-12-21 DOI: 10.1180/mgm.2022.140
J. Majzlan, J. Plášil, E. Dachs
Abstract Synthetic samples of krautite, Mn[AsO3(OH)]⋅H2O, koritnigite, Zn[AsO3(OH)]⋅H2O and cobaltkoritnigite, Co[AsO3(OH)]⋅H2O, were used for calorimetric experiments. For krautite and koritnigite, single-crystal X-ray diffraction was used to determine positions of all atoms, including the H atoms. These data allowed the hydrogen-bond network and the function of H2O molecules in these structures to be determined. The structural formulae are Mn4(H2[3]O)4[AsO3(OH)]4 and Zn4(H2[3]O)2[AsO3(OH)]4(H2[4]O)2, where [3]H2O and [4]H2O are the ‘transformer’ and ‘non-transformer’ H2O groups, respectively. Even though the principal features of these structures are identical, the details, especially those regarding the H2O groups, differ from one structure to another structure in this group. The solubility products (log Ksp) were determined from calorimetric data, that is, from the experimentally measured enthalpies of formation and entropies. They relate to the reaction M[AsO3(OH)]⋅H2O → M2+ + HAsO42– + H2O and are –6.10 for krautite, –6.88 for koritnigite and –6.83 for cobaltkoritnigite. We also estimated the log Ksp for magnesiokoritnigite as –2.0. Calculation of phase diagrams shows that all these phases originate under acidic conditions from solutions with high metal and arsenate concentration. They are restricted to local environments, to pockets that maintain such high concentrations over the time necessary for crystallisation of the krautite-group phases.
摘要:采用水铁矿、Mn[AsO3(OH)]∙H2O、钾镍矿、Zn[AsO3。对于钾铁矿和钾铁矿,使用单晶X射线衍射来确定包括H原子在内的所有原子的位置。这些数据使得氢键网络和H2O分子在这些结构中的功能得以确定。结构式为Mn4(H2[3]O)4[AsO3(OH)]4和Zn4(H2[3]O)2[AsO3。尽管这些结构的主要特征是相同的,但在该组中,细节,特别是关于H2O基团的细节,因结构不同而不同。溶解度产物(log Ksp)由量热数据确定,即由实验测量的形成焓和熵确定。它们与反应M[AsO3(OH)]-H2O有关→ M2++HAsO42–+H2O,对于钾铁矿为–6.10,对于钾镍矿为–6.88,对于钴钾镍矿则为–6.83。我们还估算了镁质辉长岩的log Ksp为–2.0。相图的计算表明,所有这些相都是在酸性条件下由高金属和砷酸盐浓度的溶液产生的。它们被限制在局部环境中,被限制在在克拉特群相结晶所需的时间内保持如此高浓度的区域中。
{"title":"Thermodynamics and crystal structures of krautite, Mn[AsO3(OH)]⋅H2O, koritnigite, Zn[AsO3(OH)]⋅H2O and cobaltkoritnigite, Co[AsO3(OH)]⋅H2O","authors":"J. Majzlan, J. Plášil, E. Dachs","doi":"10.1180/mgm.2022.140","DOIUrl":"https://doi.org/10.1180/mgm.2022.140","url":null,"abstract":"Abstract Synthetic samples of krautite, Mn[AsO3(OH)]⋅H2O, koritnigite, Zn[AsO3(OH)]⋅H2O and cobaltkoritnigite, Co[AsO3(OH)]⋅H2O, were used for calorimetric experiments. For krautite and koritnigite, single-crystal X-ray diffraction was used to determine positions of all atoms, including the H atoms. These data allowed the hydrogen-bond network and the function of H2O molecules in these structures to be determined. The structural formulae are Mn4(H2[3]O)4[AsO3(OH)]4 and Zn4(H2[3]O)2[AsO3(OH)]4(H2[4]O)2, where [3]H2O and [4]H2O are the ‘transformer’ and ‘non-transformer’ H2O groups, respectively. Even though the principal features of these structures are identical, the details, especially those regarding the H2O groups, differ from one structure to another structure in this group. The solubility products (log Ksp) were determined from calorimetric data, that is, from the experimentally measured enthalpies of formation and entropies. They relate to the reaction M[AsO3(OH)]⋅H2O → M2+ + HAsO42– + H2O and are –6.10 for krautite, –6.88 for koritnigite and –6.83 for cobaltkoritnigite. We also estimated the log Ksp for magnesiokoritnigite as –2.0. Calculation of phase diagrams shows that all these phases originate under acidic conditions from solutions with high metal and arsenate concentration. They are restricted to local environments, to pockets that maintain such high concentrations over the time necessary for crystallisation of the krautite-group phases.","PeriodicalId":18618,"journal":{"name":"Mineralogical Magazine","volume":"87 1","pages":"194 - 203"},"PeriodicalIF":2.7,"publicationDate":"2022-12-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46470088","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Argentotetrahedrite-(Cd), Ag6(Cu4Cd2)Sb4S13, a new member of the tetrahedrite group from Rudno nad Hronom, Slovakia. 银四面体-(Cd), Ag6(Cu4Cd2)Sb4S13,四面体基团的新成员,来自斯洛伐克Rudno nad ronom。
IF 2.7 3区 地球科学 Q2 MINERALOGY Pub Date : 2022-12-19 DOI: 10.1180/mgm.2022.138
T. Mikuš, Jozef Vlasáč, J. Majzlan, J. Sejkora, G. Steciuk, J. Plášil, C. Rößler, Christian Matthes
Abstract Argentotetrahedrite-(Cd), Ag6(Cu4Cd2)Sb4S13, has been approved as a new mineral species by the Commission on New Minerals, Nomenclature and Classification of the International Mineralogical Association using samples from Rudno nad Hronom, Slovak Republic. It occurs as anhedral grains up to 30 μm in size, steel-grey to black in colour, with a metallic lustre, in association with greenockite and other tetrahedrite-group minerals [argentotetrahedrite-(Zn) and tetrahedrite-(Zn)], earlier base-metal minerals, Ag sulfides and sulfosalts (acanthite, pyrargyrite and polybasite) and later galena. Argentotetrahedrite-(Cd) is isotropic, grey in colour, with a creamy tint and rapidly (tens of minutes) tarnishes to orange–brown. Reflectance data for Commission on Ore Mineralogy (COM) wavelengths in air are [λ (nm), R (%)]: 470, 30.4; 546, 30.3; 589, 30.3; and 650, 28.7. The chemical formula of the samples studied, recalculated on the basis of ΣMe = 16 atoms per formula unit, is: (Ag3.28Cu2.72)Ʃ6.00[Cu4(Cd1.68Fe0.27Zn0.16)]Ʃ6.11(Sb3.71As0.15)Ʃ3.86S12.79. Argentotetrahedrite-(Cd) is cubic, I$bar{4}$3m, with a = 10.65(2) Å, V = 1208(4) Å3 and Z = 2. Argentotetrahedrite-(Cd) is isotypic with other members of the tetrahedrite group. The structural relationship between argentotetrahedrite-(Cd) and other members of the freibergite series are discussed and previous findings of this species are briefly reviewed.
摘要银四面体-(Cd),Ag6(Cu4Cd2)Sb4S13,已被国际矿物学协会新矿物、命名和分类委员会批准为一种新矿物,使用了斯洛伐克共和国Rudno nad Hronom的样品。它以大小达30μm的二面体颗粒出现,颜色从钢灰色到黑色,具有金属光泽,与绿柱石和其他四面体族矿物[银四面体-(Zn)和四面体-(Zn。银四面体-(Cd)是各向同性的,颜色为灰色,呈乳白色,并迅速(数十分钟)变色为橙色-棕色。矿石矿物学委员会(COM)波长在空气中的反射率数据为[λ(nm),R(%)]:470,30.4;54630.3;58930.3;以及650、28.7。所研究样品的化学式,根据∑Me=每个化学式单位16个原子重新计算,为:(Ag3.28Cu2.72)Ʃ6.00[Cu4(Cd1.68Fe0.27Zn0.16)]4256.11(Sb3.71As0.15)4253.86S12.79。银四面体-(Cd)为立方,I$bar{4}$3m,a=10.65(2)Å,V=1208(4)Å3,Z=2。银四面体-(Cd)与四面体群的其他成员是同型的。本文讨论了银四面体-(Cd)与氟绿柱石系列其他成员的结构关系,并简要评述了该物种的研究进展。
{"title":"Argentotetrahedrite-(Cd), Ag6(Cu4Cd2)Sb4S13, a new member of the tetrahedrite group from Rudno nad Hronom, Slovakia.","authors":"T. Mikuš, Jozef Vlasáč, J. Majzlan, J. Sejkora, G. Steciuk, J. Plášil, C. Rößler, Christian Matthes","doi":"10.1180/mgm.2022.138","DOIUrl":"https://doi.org/10.1180/mgm.2022.138","url":null,"abstract":"Abstract Argentotetrahedrite-(Cd), Ag6(Cu4Cd2)Sb4S13, has been approved as a new mineral species by the Commission on New Minerals, Nomenclature and Classification of the International Mineralogical Association using samples from Rudno nad Hronom, Slovak Republic. It occurs as anhedral grains up to 30 μm in size, steel-grey to black in colour, with a metallic lustre, in association with greenockite and other tetrahedrite-group minerals [argentotetrahedrite-(Zn) and tetrahedrite-(Zn)], earlier base-metal minerals, Ag sulfides and sulfosalts (acanthite, pyrargyrite and polybasite) and later galena. Argentotetrahedrite-(Cd) is isotropic, grey in colour, with a creamy tint and rapidly (tens of minutes) tarnishes to orange–brown. Reflectance data for Commission on Ore Mineralogy (COM) wavelengths in air are [λ (nm), R (%)]: 470, 30.4; 546, 30.3; 589, 30.3; and 650, 28.7. The chemical formula of the samples studied, recalculated on the basis of ΣMe = 16 atoms per formula unit, is: (Ag3.28Cu2.72)Ʃ6.00[Cu4(Cd1.68Fe0.27Zn0.16)]Ʃ6.11(Sb3.71As0.15)Ʃ3.86S12.79. Argentotetrahedrite-(Cd) is cubic, I$bar{4}$3m, with a = 10.65(2) Å, V = 1208(4) Å3 and Z = 2. Argentotetrahedrite-(Cd) is isotypic with other members of the tetrahedrite group. The structural relationship between argentotetrahedrite-(Cd) and other members of the freibergite series are discussed and previous findings of this species are briefly reviewed.","PeriodicalId":18618,"journal":{"name":"Mineralogical Magazine","volume":"87 1","pages":"262 - 270"},"PeriodicalIF":2.7,"publicationDate":"2022-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46398837","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Auroselenide, AuSe, a new mineral from Maletoyvayam deposit, Kamchatka peninsula, Russia 俄罗斯堪察加半岛Maletoyvayam矿床的一种新矿物
IF 2.7 3区 地球科学 Q2 MINERALOGY Pub Date : 2022-12-19 DOI: 10.1180/mgm.2022.137
N. Tolstykh, A. Kasatkin, F. Nestola, A. Vymazalová, A. Agakhanov, G. Palyanova, V. Korolyuk
Abstract Auroselenide, ideally AuSe, is a new mineral from the Gaching ore occurrence of the Maletoyvayam deposit, Kamchatka peninsula, Russia. It occurs as anhedral grains up to 0.05 × 0.02 mm and as intergrowths up to 0.06 mm with maletoyvayamite–tolstykhite-series minerals, enclosed in native gold. Other associated minerals include pyrite, calaverite, fischesserite, gachingite, tetrahedrite-group minerals [stibiogoldfieldite, its As-analogue, tennantite-(Cu) and tetrahedrite-(Zn)], tripuhyite, minerals of the famatinite–luzonite and selenium–tellurium series, paraguanajuatite, petrovskaite, součekite and tiemannite. Auroselenide is bluish-grey, opaque with metallic lustre and grey streak. It is brittle and has an uneven fracture. Dcalc = 9.750 g/cm3. In reflected light, auroselenide is grey with a bluish shade. Bireflectance is very weak. No pleochroism and internal reflections are observed. In crossed polars, it is strongly anisotropic with bluish to brownish rotation tints. The reflectance values for wavelengths recommended by the Commission on Ore Mineralogy of the International Mineralogical Association are (Rmin/Rmax, %): 28.4/31.5 (470 nm), 30.2/33.3 (546 nm), 31.9/34.9 (589 nm) and 34.3/37.3 (650 nm). The principal bands in the Raman spectrum of auroselenide are at 93, 171, 200, 210 and 325 cm–1. The empirical formula calculated on the basis of 2 atoms per formula unit is (Au0.98Ag0.01)Σ0.99(Se0.79S0.17Te0.05)Σ1.01. Auroselenide is monoclinic, space group C2/m, a = 8.319(1), b = 3.616(1), c = 6.276(2) Å, β = 104.54(2)°, V = 182.74(5) Å3 and Z = 4. The strongest lines of the powder X-ray diffraction pattern [d, Å (I, %) (hkl)] are: 4.015 (54) (200); 3.033 (25) (${bar 1}$11, 002); 2.780 (100) (${bar 2}$02, 111); 2.172 (20) (${bar 3}$11, 310); and 1.811 (25) (${bar 1}$13). Auroselenide is the natural analogue of synthetic β-AuSe. The structural identity between them is confirmed by powder X-ray diffraction and Raman spectroscopy. The mineral is named according to its composition, as a combination of the main elements Au (aurum) and Se (selenium).
摘要Auoselenide,最好是AuSe,是俄罗斯堪察加半岛Maletoyvayam矿床Gaching矿点的一种新矿物。它以高达0.05×0.02 mm的二面体颗粒和高达0.06 mm的共生体的形式与包裹在天然金中的马来托瓦亚姆岩-托尔斯提克岩系列矿物共生。其他伴生矿物包括黄铁矿、calaverite、Fishesserite、gachinite、四面体组矿物[锑金矿石、其As类似物、tennantite-(Cu)和四面体-(Zn)]、三辉橄榄岩、法马汀岩-绿宗岩和硒-碲系矿物、副瓜华岩、彼得罗夫斯凯特、苏切克岩和铁镁石。Auroselenide呈蓝灰色,不透明,具有金属光泽和灰色条纹。它很脆,断裂不均匀。Dcalc=9.750 g/cm3。在反射光中,极光是带蓝色阴影的灰色。观鸟能力很弱。未观察到多色性和内部反射。在交叉极坐标中,它具有强烈的各向异性,带有蓝色到棕色的旋转色调。国际矿物学协会矿石矿物学委员会建议的波长反射率值为(Rmin/Rmax,%):28.4/31.5(470 nm)、30.2/33.3(546 nm)、31.9/34.9(589 nm)和34.3/37.3(650 nm)。auroselenide拉曼光谱中的主要波段分别为9317120210和325cm-1。以每个化学式单位2个原子为基础计算的经验公式为(Au0.98Ag0.01)∑0.99(Se0.79S1017Te0.05)∑1.01。Auroselenide是单斜晶系,空间群C2/m,a=8.319(1),b=3.616(1)、c=6.276(2)Å、β=104.54(2)°、V=182.74(5)Å3和Z=4。粉末X射线衍射图的最强谱线[d,Å(I,%)(hkl)]为:4.015(54)(200);3.033(25)(110002美元);2.780(100)(02111美元);2.172(20)(11310美元);和1.811(25)(13美元)。Auoselenide是合成β-AuSe的天然类似物。通过粉末X射线衍射和拉曼光谱证实了它们之间的结构一致性。该矿物根据其成分命名,由主要元素Au(Au)和Se(Se)组成。
{"title":"Auroselenide, AuSe, a new mineral from Maletoyvayam deposit, Kamchatka peninsula, Russia","authors":"N. Tolstykh, A. Kasatkin, F. Nestola, A. Vymazalová, A. Agakhanov, G. Palyanova, V. Korolyuk","doi":"10.1180/mgm.2022.137","DOIUrl":"https://doi.org/10.1180/mgm.2022.137","url":null,"abstract":"Abstract Auroselenide, ideally AuSe, is a new mineral from the Gaching ore occurrence of the Maletoyvayam deposit, Kamchatka peninsula, Russia. It occurs as anhedral grains up to 0.05 × 0.02 mm and as intergrowths up to 0.06 mm with maletoyvayamite–tolstykhite-series minerals, enclosed in native gold. Other associated minerals include pyrite, calaverite, fischesserite, gachingite, tetrahedrite-group minerals [stibiogoldfieldite, its As-analogue, tennantite-(Cu) and tetrahedrite-(Zn)], tripuhyite, minerals of the famatinite–luzonite and selenium–tellurium series, paraguanajuatite, petrovskaite, součekite and tiemannite. Auroselenide is bluish-grey, opaque with metallic lustre and grey streak. It is brittle and has an uneven fracture. Dcalc = 9.750 g/cm3. In reflected light, auroselenide is grey with a bluish shade. Bireflectance is very weak. No pleochroism and internal reflections are observed. In crossed polars, it is strongly anisotropic with bluish to brownish rotation tints. The reflectance values for wavelengths recommended by the Commission on Ore Mineralogy of the International Mineralogical Association are (Rmin/Rmax, %): 28.4/31.5 (470 nm), 30.2/33.3 (546 nm), 31.9/34.9 (589 nm) and 34.3/37.3 (650 nm). The principal bands in the Raman spectrum of auroselenide are at 93, 171, 200, 210 and 325 cm–1. The empirical formula calculated on the basis of 2 atoms per formula unit is (Au0.98Ag0.01)Σ0.99(Se0.79S0.17Te0.05)Σ1.01. Auroselenide is monoclinic, space group C2/m, a = 8.319(1), b = 3.616(1), c = 6.276(2) Å, β = 104.54(2)°, V = 182.74(5) Å3 and Z = 4. The strongest lines of the powder X-ray diffraction pattern [d, Å (I, %) (hkl)] are: 4.015 (54) (200); 3.033 (25) (${bar 1}$11, 002); 2.780 (100) (${bar 2}$02, 111); 2.172 (20) (${bar 3}$11, 310); and 1.811 (25) (${bar 1}$13). Auroselenide is the natural analogue of synthetic β-AuSe. The structural identity between them is confirmed by powder X-ray diffraction and Raman spectroscopy. The mineral is named according to its composition, as a combination of the main elements Au (aurum) and Se (selenium).","PeriodicalId":18618,"journal":{"name":"Mineralogical Magazine","volume":"87 1","pages":"284 - 291"},"PeriodicalIF":2.7,"publicationDate":"2022-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41535948","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Bounahasite, Cu+Cu2+2(OH)3Cl2, a new mineral from the Bou Nahas Mine, Morocco Bounahasite,Cu+Cu2+2(OH)3Cl2,摩洛哥Bou Nahas矿的一种新矿物
IF 2.7 3区 地球科学 Q2 MINERALOGY Pub Date : 2022-12-09 DOI: 10.1180/mgm.2022.133
I. Lykova, R. Rowe, G. Poirier, H. Friis, K. Helwig
Abstract The new mineral bounahasite, Cu+Cu2+2(OH)3Cl2, was found in the oxidation zone of the Bou Nahas Mine, Morocco. It forms pseudo-hexagonal plates up to 3 × 30 × 40 μm in size combined in loose clusters with native copper and paratacamite. The mineral is green with vitreous lustre. The cleavage is parallel to {110}, perfect. Dcalc is 3.90 g/cm3. The infrared spectrum is reported. The composition (wt.%) is Cu2O 23.26, CuO 51.72, Cl 23.36, H2O 8.71, O = Cl2 –5.27, total 101.78. The empirical formula calculated on the basis of 3 Cu atoms per formula unit is: Cu+Cu2+2(OH)2.97Cl2.03. The mineral is monoclinic, P21/n, a = 8.5925(1), b = 6.4189(1), c = 10.4118(2) Å, β = 111.804(2)°, V = 533.17(2) Å3 and Z = 4. The strongest reflections of the powder X-ray diffraction pattern [d,Å(I)(hkl)] are: 7.71(70)($bar{1}$01), 5.34(22)(011), 3.856(100)(012, $bar{2}$02), 2.673(36)(022), 2.665 (30)(103) and 2.350 (71)($bar{1}$23, 301, $bar{2}$14). The crystal structure, refined from single-crystal X-ray diffraction data (R1 = 0.028), is based on two alternating sheets coplanar to (110): one consists of alternating edge-sharing Cu2+(OH)6 octahedra and two Cu2+(OH)4Cl2 octahedra, whereas the other one is based on Cu+Cl4 tetrahedra forming edge-sharing Cu+2Cl6 dimers.
摘要在摩洛哥Bou Nahas矿的氧化带中发现了一种新的界面矿,即Cu+Cu2+2(OH)3Cl2。它形成了尺寸高达3×30×40μm的假六边形板,与天然铜和副金云母松散成团。这种矿物是绿色的,有玻璃光泽。解理平行于{110},完全。Dcalc为3.90 g/cm3。报道了红外光谱。成分(wt.%)为Cu2O 23.26,CuO 51.72,Cl 23.36,H2O 8.71,O=Cl2–5.27,总计101.78。基于每个化学式单元3个Cu原子计算的经验公式为:Cu+Cu2+2(OH)2.97Cl2.03。该矿物为单斜晶系,P21/n,a=8.5925(1),b=6.4189(1)、c=10.4118(2)Å、β=11.804(2)°、V=553.17(2)å3和Z=4。粉末X射线衍射图[d,Å(I)(hkl)]的最强反射为:7.71(70)($bar{1}$01)、5.34(22)(011)、3.856(100)(012,$bar{2}$02)、2.673(36)(022)、2.665(30)(103)和2.350(71)($par{2}$23301,$bar{2}$14)。从单晶X射线衍射数据(R1=0.028)中提炼出的晶体结构基于与(110)共面的两个交替片:一个由交替的共边Cu2+(OH)6八面体和两个Cu2+(OH4Cl2八面体组成,而另一个基于形成共边Cu+2Cl6二聚体的Cu+Cl4四面体。
{"title":"Bounahasite, Cu+Cu2+2(OH)3Cl2, a new mineral from the Bou Nahas Mine, Morocco","authors":"I. Lykova, R. Rowe, G. Poirier, H. Friis, K. Helwig","doi":"10.1180/mgm.2022.133","DOIUrl":"https://doi.org/10.1180/mgm.2022.133","url":null,"abstract":"Abstract The new mineral bounahasite, Cu+Cu2+2(OH)3Cl2, was found in the oxidation zone of the Bou Nahas Mine, Morocco. It forms pseudo-hexagonal plates up to 3 × 30 × 40 μm in size combined in loose clusters with native copper and paratacamite. The mineral is green with vitreous lustre. The cleavage is parallel to {110}, perfect. Dcalc is 3.90 g/cm3. The infrared spectrum is reported. The composition (wt.%) is Cu2O 23.26, CuO 51.72, Cl 23.36, H2O 8.71, O = Cl2 –5.27, total 101.78. The empirical formula calculated on the basis of 3 Cu atoms per formula unit is: Cu+Cu2+2(OH)2.97Cl2.03. The mineral is monoclinic, P21/n, a = 8.5925(1), b = 6.4189(1), c = 10.4118(2) Å, β = 111.804(2)°, V = 533.17(2) Å3 and Z = 4. The strongest reflections of the powder X-ray diffraction pattern [d,Å(I)(hkl)] are: 7.71(70)($bar{1}$01), 5.34(22)(011), 3.856(100)(012, $bar{2}$02), 2.673(36)(022), 2.665 (30)(103) and 2.350 (71)($bar{1}$23, 301, $bar{2}$14). The crystal structure, refined from single-crystal X-ray diffraction data (R1 = 0.028), is based on two alternating sheets coplanar to (110): one consists of alternating edge-sharing Cu2+(OH)6 octahedra and two Cu2+(OH)4Cl2 octahedra, whereas the other one is based on Cu+Cl4 tetrahedra forming edge-sharing Cu+2Cl6 dimers.","PeriodicalId":18618,"journal":{"name":"Mineralogical Magazine","volume":"87 1","pages":"218 - 224"},"PeriodicalIF":2.7,"publicationDate":"2022-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46652149","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Selsurtite, (H3O)12Na3(Ca3Mn3)(Na2Fe)Zr3□Si[Si24O69(OH)3](OH)Cl⋅H2O, a new eudialyte-group mineral from the Lovozero alkaline massif, Kola Peninsula, Russia
IF 2.7 3区 地球科学 Q2 MINERALOGY Pub Date : 2022-12-09 DOI: 10.1180/mgm.2022.136
N. Chukanov, S. Aksenov, O. Kazheva, I. Pekov, D. Varlamov, M. Vigasina, D. I. Belakovskiy, S. A. Vozchikova, S. Britvin
Abstract The new eudialyte-group mineral selsurtite, ideally (H3O)12Na3(Ca3Mn3)(Na2Fe)Zr3□Si[Si24O69(OH)3](OH)Cl⋅H2O, was discovered in metasomatic peralkaline rock from the Flora mountain, northern spur of the Selsurt mountain, Lovozero alkaline massif, Kola Peninsula, Russia. The associated minerals are aegirine, albite and orthoclase, as well as accessory lorenzenite, calciomurmanite, natrolite, lamprophyllite and sergevanite. Selsurtite occurs as brownish-red to reddish-orange, equant or flattened on (0001) crystals up to 2 mm across and elongate crystals up to 3 cm long. The main crystal forms are {0001}, {11$bar{2}$0}, and {10$bar{1}$1}. Selsurtite is brittle, with the Mohs’ hardness of 5. No cleavage is observed. Parting is distinct on (001). D(meas) = 2.73(2) and D(calc) = 2.722 g⋅cm–3. Selsurtite is optically uniaxial (–), with ω = 1.598(2) and ɛ = 1.595(2). The chemical composition is (wt.%, electron microprobe): Na2O 6.48, K2O 0.27, MgO 0.10, CaO 6.83, MnO 4.73, FeO 1.18, SrO 1.88, La2O3 0.57, Ce2O3 1.07, Pr2O3 0.20, Nd2O3 0.44, Al2O3 0.29, SiO2 50.81, ZrO2 13.50, HfO2 0.45, TiO2 0.61, Nb2О5 1.10, Cl 1.01, SO3 0.29, H2O 8.10, –O≡Cl –0.23, total 99.68. The empirical formula is H25.94Na6.03K0.16Mg0.07Ca3.51Sr0.52Ce0.19La0.10Nd0.08Pr0.03Mn1.91Fe0.47Ti0.22Zr3.16Hf0.06Nb0.24Si24.40Al0.16S0.10Cl0.82O79.13. The crystal structure was determined using single-crystal X-ray diffraction data and refined to R = 0.0484. Selsurtite is trigonal, space group R3, with a = 14.1475(7) Å, c = 30.3609(12) Å, V = 5262.65(7) Å3 and Z = 3. Infrared and Raman spectra show that hydronium cations are involved in very strong hydrogen bonds and form Zundel- and Eigen-like complexes. The strongest lines of the powder X-ray diffraction pattern [d, Å (I, %)(hkl)] are: 11.38 (56)(101), 7.08 (59)(110), 5.69 (36)(202), 4.318 (72)(205), 3.793 (36)(303), 3.544 (72)(027, 220, 009), 2.970 (100)(315) and 2.844 (100)(404). The mineral is named after the discovery locality.
摘要新的真透析物族矿物selsurtite,理想的是(H3O)12Na3(Ca3Mn3)(Na2Fe)Zr3□Si[Si24O69(OH)3](OH)Cl·H2O是在俄罗斯科拉半岛Lovozero碱性地块Selsurt山北端Flora山交代过碱性岩石中发现的。伴生矿物有赤铁矿、钠长石和正长石,以及副洛伦岑岩、钙硅钙石、钠长石、煌斑岩和蛇绿岩。Selsurtite呈棕红色至红橙色,在(0001)晶体上均匀或扁平,直径可达2毫米,细长晶体长可达3厘米。主要晶型为{0001}、{11$bar{2}$0}和{10$bar{1}$1}。Selsurtite是脆性的,莫氏硬度为5。未观察到解理。(001)上的分隔不同。D(meas)=2.73(2),D(calc)=2.722 g·cm–3。Selsurtite为光学单轴(–),ω=1.598(2)和y=1.595(2)。化学成分为(wt.%,电子探针):Na2O 6.48,K2O 0.27,MgO 0.10,CaO 6.83,MnO 4.73,FeO 1.18,SrO 1.88,La2O3 0.57,Ce2O3 1.07,Pr2O3 0.20,Nd2O3 0.44,Al2O3 0.29,SiO2 50.81,ZrO2 13.50,HfO2 0.45,TiO2 0.61,Nb2О5 1.10,Cl 1.01,SO3 0.29,H2O 8.10,–O Select Cl–0.23,总计99.68。经验公式为H25.94Na6.03K0.16Mg0.07Ca3.51Sr0.52Ce0.19La0.10Nd0.08Pr0.03Mn1.91Fe0.47Ti0.22Zr3.16Hf0.06Nb0.24Si24.40Al0.16S0.10Cl0.82O79.13。使用单晶X射线衍射数据测定晶体结构,并将其细化至R=0.0484。Selsurtite是三角的,空间群R3,a=11.4475(7)Å,c=30.3609(12)Å、V=552.65(7)å3和Z=3。红外光谱和拉曼光谱表明,水合氢阳离子与非常强的氢键有关,并形成类Zundel和类Eigen络合物。粉末X射线衍射图的最强谱线[d,Å(I,%)(hkl)]为:11.38(56)(101)、7.08(59)(110)、5.69(36)(202)、4.318(72)(205)、3.793(36)、3.544(72)、2.970(100)和2.844(100)(404)。该矿物以发现地命名。
{"title":"Selsurtite, (H3O)12Na3(Ca3Mn3)(Na2Fe)Zr3□Si[Si24O69(OH)3](OH)Cl⋅H2O, a new eudialyte-group mineral from the Lovozero alkaline massif, Kola Peninsula, Russia","authors":"N. Chukanov, S. Aksenov, O. Kazheva, I. Pekov, D. Varlamov, M. Vigasina, D. I. Belakovskiy, S. A. Vozchikova, S. Britvin","doi":"10.1180/mgm.2022.136","DOIUrl":"https://doi.org/10.1180/mgm.2022.136","url":null,"abstract":"Abstract The new eudialyte-group mineral selsurtite, ideally (H3O)12Na3(Ca3Mn3)(Na2Fe)Zr3□Si[Si24O69(OH)3](OH)Cl⋅H2O, was discovered in metasomatic peralkaline rock from the Flora mountain, northern spur of the Selsurt mountain, Lovozero alkaline massif, Kola Peninsula, Russia. The associated minerals are aegirine, albite and orthoclase, as well as accessory lorenzenite, calciomurmanite, natrolite, lamprophyllite and sergevanite. Selsurtite occurs as brownish-red to reddish-orange, equant or flattened on (0001) crystals up to 2 mm across and elongate crystals up to 3 cm long. The main crystal forms are {0001}, {11$bar{2}$0}, and {10$bar{1}$1}. Selsurtite is brittle, with the Mohs’ hardness of 5. No cleavage is observed. Parting is distinct on (001). D(meas) = 2.73(2) and D(calc) = 2.722 g⋅cm–3. Selsurtite is optically uniaxial (–), with ω = 1.598(2) and ɛ = 1.595(2). The chemical composition is (wt.%, electron microprobe): Na2O 6.48, K2O 0.27, MgO 0.10, CaO 6.83, MnO 4.73, FeO 1.18, SrO 1.88, La2O3 0.57, Ce2O3 1.07, Pr2O3 0.20, Nd2O3 0.44, Al2O3 0.29, SiO2 50.81, ZrO2 13.50, HfO2 0.45, TiO2 0.61, Nb2О5 1.10, Cl 1.01, SO3 0.29, H2O 8.10, –O≡Cl –0.23, total 99.68. The empirical formula is H25.94Na6.03K0.16Mg0.07Ca3.51Sr0.52Ce0.19La0.10Nd0.08Pr0.03Mn1.91Fe0.47Ti0.22Zr3.16Hf0.06Nb0.24Si24.40Al0.16S0.10Cl0.82O79.13. The crystal structure was determined using single-crystal X-ray diffraction data and refined to R = 0.0484. Selsurtite is trigonal, space group R3, with a = 14.1475(7) Å, c = 30.3609(12) Å, V = 5262.65(7) Å3 and Z = 3. Infrared and Raman spectra show that hydronium cations are involved in very strong hydrogen bonds and form Zundel- and Eigen-like complexes. The strongest lines of the powder X-ray diffraction pattern [d, Å (I, %)(hkl)] are: 11.38 (56)(101), 7.08 (59)(110), 5.69 (36)(202), 4.318 (72)(205), 3.793 (36)(303), 3.544 (72)(027, 220, 009), 2.970 (100)(315) and 2.844 (100)(404). The mineral is named after the discovery locality.","PeriodicalId":18618,"journal":{"name":"Mineralogical Magazine","volume":"87 1","pages":"241 - 251"},"PeriodicalIF":2.7,"publicationDate":"2022-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43251829","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
A comparison of the fenites at the Chilwa Island and Kangankunde carbonatite complexes, Malawi 马拉维Chilwa岛和Kangankunde碳酸岩杂岩中的fenite的比较
IF 2.7 3区 地球科学 Q2 MINERALOGY Pub Date : 2022-12-09 DOI: 10.1180/mgm.2022.134
E. Dowman, F. Wall, P. Treloar
Abstract Carbonatites are igneous carbonate rocks. They are the main source of the rare earth elements (REE) that are essential in low carbon and high technology applications. Exploration targeting and mine planning would both benefit from a better understanding of the processes that create the almost ubiquitous alkaline and REE-bearing metasomatic aureoles in the surrounding country rocks. Using scanning electron microscopy and whole-rock geochemistry, we investigated the composition and mineralogy of the fenite aureoles developed around the REE-poor Chilwa Island carbonatite and the REE-rich Kangankunde carbonatite, which intrude similar country rocks in the Chilwa Alkaline Province of Southern Malawi. Although common characteristics and trends in their mineralogy and composition may be typical of fenites in general, there are significant differences in their petrography and petrogenesis. For example, the mineralogically diverse breccia at Kangankunde contrasts with the intensely altered potassic breccia of Chilwa Island. This might be caused by differing sequences of fluids expelled from the carbonatites into the aureoles. The main REE-bearing mineral in fenite is different at each complex, and reflects the characteristic REE-bearing mineral of the main carbonatite: fluorapatite at Chilwa Island; and monazite at Kangankunde. Each fenite has distinctive mineral assemblages, in which the relative abundance of the REE-bearing minerals appears to be determined by the mineralogy of their respective host carbonatites. At both localities, the REE minerals in fenite are less enriched in lanthanum and cerium than their equivalents in carbonatite, a characteristic that we attribute to REE fractionation within fluids in the aureole. Identifying the mineral assemblages present in fenite and understanding the sequence of alkaline and mineralising fluid events could therefore be useful in predicting whether a fenite is associated with a REE-rich carbonatite. Detailed studies of other aureoles would be required to assess the reliability of these characteristics.
摘要碳酸盐岩是火成碳酸盐岩。它们是稀土元素的主要来源,稀土元素在低碳和高科技应用中至关重要。勘探目标和矿山规划都将受益于更好地了解在周围围岩中形成几乎普遍存在的碱性和含REE交代金矿的过程。利用扫描电子显微镜和全岩地球化学,我们研究了在马拉维南部奇尔瓦碱性省侵入类似围岩的贫稀土奇尔瓦岛碳酸盐岩和富稀土Kangankunde碳酸盐岩周围发育的fenite金矿的组成和矿物学。尽管它们的矿物学和成分的共同特征和趋势可能是一般fenite的典型特征,但它们的岩石学和岩石成因存在显著差异。例如,Kangankunde的矿物多样角砾岩与Chilwa岛的强烈蚀变钾质角砾岩形成对比。这可能是由于从碳酸盐岩排出到金矿的流体顺序不同造成的。各杂岩中的主要含REE矿物不同,反映了主要碳酸盐岩的特征含REE矿石:奇尔瓦岛的氟磷灰石;康甘昆德的独居石。每一种fenite都有独特的矿物组合,其中含REE矿物的相对丰度似乎由其各自宿主碳酸盐岩的矿物学决定。在这两个地方,fenite中的REE矿物的镧和铈富集程度低于碳酸盐岩中的稀土矿物,我们将这一特征归因于Aurele中流体中REE的分馏。因此,识别fenite中存在的矿物组合并了解碱性和矿化流体事件的顺序,对于预测fenite是否与富含REE的碳酸岩有关可能是有用的。需要对其他光环进行详细研究,以评估这些特征的可靠性。
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引用次数: 0
MGM volume 86 issue 6 Cover and Back matter 米高梅第86卷第6期封面和封底
IF 2.7 3区 地球科学 Q2 MINERALOGY Pub Date : 2022-12-01 DOI: 10.1180/mgm.2022.131
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引用次数: 0
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Mineralogical Magazine
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