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  • Mineralogical Society of America  (8)
  • Chemie/Pharmazie  (8)
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Verlag/Herausgeber
  • Mineralogical Society of America  (8)
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  • Chemie/Pharmazie  (8)
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  • 1
    In: American Mineralogist, Mineralogical Society of America, Vol. 104, No. 1 ( 2019-01-1), p. 150-157
    Materialart: Online-Ressource
    ISSN: 0003-004X , 1945-3027
    RVK:
    Sprache: Englisch
    Verlag: Mineralogical Society of America
    Publikationsdatum: 2019
    ZDB Id: 3514-2
    ZDB Id: 2045960-9
    SSG: 13
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 2
    Online-Ressource
    Online-Ressource
    Mineralogical Society of America ; 2020
    In:  American Mineralogist Vol. 105, No. 5 ( 2020-05-1), p. 745-755
    In: American Mineralogist, Mineralogical Society of America, Vol. 105, No. 5 ( 2020-05-1), p. 745-755
    Kurzfassung: Lingbaoite, AgTe3, is a new silver telluride discovered in the S60 gold-bearing quartz vein, Xiaoqinling gold district, central China. The new mineral is named after Lingbao city, the municipality of which covers a major part of the Xiaoqinling gold district. Lingbaoite is only microscopically visible and occurs within pyrite as small composite inclusions ( & lt;50 μm) that commonly consist of lingbaoite, sylvanite, and chalcopyrite, and locally of bornite, galena, altaite, and stützite. The largest lingbaoite grain is about 30 × 12 μm in size. At least two stages of gold and telluride mineralization are recognized in the lingbaoite-bearing sample set. The first stage is characterized by the deposition of lingbaoite, native tellurium, and sylvanite, within the commonly observed mineral assemblages of lingbaoite + sylvanite + chalcopyrite and sylvanite + native tellurium + stützite. The second stage is characterized by the deposition of Bi-bearing minerals and native gold, within the commonly observed mineral assemblages of rucklidgeite + altaite + volynskite ± hessite ± petzite and rucklidgeite + gold ± altaite. Lingbaoite is opaque and exhibits no internal reflections. In plane-polarized reflected light, lingbaoite shows a creamy yellow reflection color. The calculated density is 7.06 g/cm3. Seventeen WDS spot analyses from 17 different lingbaoite grains gave an empirical formula of Ag0.946Fe0.134Cu0.008Pb0.003 Te2.841S0.067. When considering Ag and Te as the only two essential structural components, the empirical formula is Ag1.00Te3.00. The EBSD and SAED data confirm the structural identity of lingbaoite and synthetic AgTe3. Synthetic AgTe3 is trigonal, space group R3m, with a = 8.645 Å, c = 5.272 Å, V = 341.2 Å3, and Z = 3. The unit-cell parameters of lingbaoite are: a = 8.60 (5) Å, c = 5.40 (18) Å, V = 346 (9) Å3, and Z = 3. Synthetic AgTe3, and by analog lingbaoite, can be viewed as silver-stabilized cubic tellurium, which is an ordered (1:3 Ag:Te) analog of the α-polonium structure (i.e., simple cubic crystal structure). Synthetic AgTe3 becomes a stable phase at above 0.4 GPa, but can also occur in a metastable state at atmospheric pressure. Lingbaoite probably formed through the cooling of polymetallic melt droplets within the hydrothermal system. Lingbaoite and associated minerals (e.g., sylvanite, native tellurium) reveal a previously unrecognized but perhaps common magmatic-hydrothermal process in the Xiaoqinling gold district, which precedes the precipitation of native gold, suggesting that gold mineralization in the Xiaoqinling gold district involves multiple superimposed processes of gold enrichment.
    Materialart: Online-Ressource
    ISSN: 0003-004X , 1945-3027
    RVK:
    Sprache: Englisch
    Verlag: Mineralogical Society of America
    Publikationsdatum: 2020
    ZDB Id: 3514-2
    ZDB Id: 2045960-9
    SSG: 13
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 3
    Online-Ressource
    Online-Ressource
    Mineralogical Society of America ; 2016
    In:  American Mineralogist Vol. 101, No. 1 ( 2016-01), p. 134-145
    In: American Mineralogist, Mineralogical Society of America, Vol. 101, No. 1 ( 2016-01), p. 134-145
    Materialart: Online-Ressource
    ISSN: 0003-004X
    RVK:
    Sprache: Englisch
    Verlag: Mineralogical Society of America
    Publikationsdatum: 2016
    ZDB Id: 3514-2
    ZDB Id: 2045960-9
    SSG: 13
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 4
    Online-Ressource
    Online-Ressource
    Mineralogical Society of America ; 2022
    In:  American Mineralogist Vol. 107, No. 2 ( 2022-02-1), p. 206-220
    In: American Mineralogist, Mineralogical Society of America, Vol. 107, No. 2 ( 2022-02-1), p. 206-220
    Kurzfassung: The Au mineralization in the giant Jiaodong Au province is enigmatic and difficult to fit current classic mineralization models, primarily because of uncertainties as to the sources of ore-forming fluids and metals. The ca. 120 Ma Au mineralization has been previously proposed to have occurred during a magmatic lull, which would negate a magmatic-hydrothermal genetic model. However, recent drilling has revealed a buried mineralized monzonite equivalent in age to the Au mineralization in the Linglong goldfield. Here, we present comprehensive textural, geochemical [LA-(MC)-ICP-MS trace element, Nd and S isotopes] and geochronological (LA-ICP-MS U-Pb dating) analyses of titanite and pyrite from this previously unrecognized monzonite. Three types of titanite were distinguished, including magmatic Ttn1 and hydrothermal Ttn2 and Ttn3, which show indistinguishable U-Pb ages (120.7 ± 3.1 and 120.9 ± 2.6 Ma), REE patterns and Nd isotopes [εNd(t) = –14.7 to –12.9] , implying that hydrothermal fluids were directly exsolved from the monzonitic magma, contemporaneous with the large-scale Au mineralization at ca. 120 Ma. The Nd isotopes of titanite potentially indicate a lower crustal source mixed with mantle materials for the monzonite. Four types of pyrite were analyzed, including magmatic Py1 from fresh biotite monzonite, hydrothermal Py2 from altered biotite monzonite, hydrothermal Py3 from quartz-pyrite veins with a monazite U-Pb age of 118.2 ± 4.6 Ma, and magmatic Py4 from mafic enclaves of the Gushan granite at ca.120 Ma. The δ34S values of magmatic Py1 and Py4 (+1.9 to +6.3‰, and +5.0 to +6.4‰, respectively) and hydrothermal Py2 and Py3 (+6.4 to +9.5‰ and +6.5 to +7.6‰, respectively) are consistent with sulfur isotopic fractionation between melt and fluid. Hydrothermal Py2 and Py3 also have higher Co, As, Ag, Sb, and Bi contents and submicrometer gold inclusions, implying that the magmatic-hydrothermal fluids were fertile for mineralization. This study highlights the importance of monzonite magmatism and exsolved fertile fluids in regional Au mineralization. Hydrous magmas at ca.120 Ma probably extracted Au efficiently from the lower crustal-mantle sources and released auriferous fluids at the late magmatic stage, leading to the formation of Au deposits in the Jiaodong province.
    Materialart: Online-Ressource
    ISSN: 0003-004X , 1945-3027
    RVK:
    Sprache: Englisch
    Verlag: Mineralogical Society of America
    Publikationsdatum: 2022
    ZDB Id: 3514-2
    ZDB Id: 2045960-9
    SSG: 13
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 5
    Online-Ressource
    Online-Ressource
    Mineralogical Society of America ; 2022
    In:  American Mineralogist Vol. 107, No. 2 ( 2022-02-1), p. 282-293
    In: American Mineralogist, Mineralogical Society of America, Vol. 107, No. 2 ( 2022-02-1), p. 282-293
    Kurzfassung: The time and processes of hydrothermal mineralization are long-standing problems in geology. This work addresses these questions with reference to the Maoniuping giant rare earth elements (REE) deposit (southwest China), which has rare earth oxides (REO) reserves of 3.17 million tons with an average grade of 2.95 wt%. Bastnäsite is the dominant economic mineral, occurring as four distinct paragenetic types in the Maoniuping syenite–carbonatite complex: (1) primary euhedral bastnäsite (type-A) in syenite, with isolated melt inclusions; (2) macro-crystalline tabular euhedral bastnäsite (type-B) in pegmatitic dikes, with a diverse variety of fluid inclusions; (3) fine-grained, anhedral veinlet-disseminated bastnäsite (type-C) in syenite; and (4) coarse-grained anhedral bastnäsite (type-D) in carbonatite dikes, occurring as veinlets or interstitial to calcite, fluorite, and barite. From the paragenetic and compositional variations, it is inferred that type-A bastnäsite is of primary magmatic origin, whereas the other three types have characteristics of hydrothermal origins. In situ LA-ICP-MS U-Pb geochronology of the four types of bastnäsite results in lower intercept ages of 28.2 ± 0.5 Ma (n = 95, MSWD = 5.10), 27.8 ± 0.4 Ma (n = 43, MSWD = 0.73), 26.8 ± 0.7 Ma (n = 50, MSWD = 0.83), and 25.8 ± 0.7 Ma (n = 55, MSWD = 1.70), respectively, which are consistent with the weighted average 206Pb/238U and 208Pb/232Th ages by 207Pb-correction method. Compositional variations of clinopyroxene and apatite from the associated syenite, pegmatitic and carbonatitic dikes indicate a genetic relationship of the Maoniuping alkaline complex. The compositions of clinopyroxene range from Ae44–67Di14–18Hd17–41 in pegmatitic dikes, Ae43–66Di6–20Hd21–38 in carbonatitic dikes to Ae68–90Di0–3Hd10–30 in syenite. Apatites in the pegmatitic and carbonatitic dikes have similar compositions with higher F, total REE, and Sr, and lower CaO contents than those in the syenite, which suggests a cogenetic origin for the associated pegmatite and carbonatite. Clinopyroxene and apatite compositions suggest that the pegmatitic melt might differentiate directly from the initial carbonatitic melt rather than the syenitic magma. The bastnäsite U-Pb geochronology and minerals data indicate continuous magmatic-hydrothermal evolution for the REE mineralization in the Maoniuping alkaline complex.
    Materialart: Online-Ressource
    ISSN: 0003-004X , 1945-3027
    RVK:
    Sprache: Englisch
    Verlag: Mineralogical Society of America
    Publikationsdatum: 2022
    ZDB Id: 3514-2
    ZDB Id: 2045960-9
    SSG: 13
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 6
    Online-Ressource
    Online-Ressource
    Mineralogical Society of America ; 2021
    In:  American Mineralogist Vol. 106, No. 2 ( 2021-02-1), p. 265-281
    In: American Mineralogist, Mineralogical Society of America, Vol. 106, No. 2 ( 2021-02-1), p. 265-281
    Kurzfassung: Two generations of garnet are recognized in a granite and a pegmatite from the Gangdese orogen in southeastern Tibet on the basis of a combined study of petrography, major and trace element profiles, and garnet O isotopes. Zircon U-Pb dating and Hf-O isotope compositions also help constrain the origin of both granite and pegmatite. The first generation of garnet (Grt-I) occurs as residues in the center of garnet grains, and it represents an early stage of nucleation related to magmatic-hydrothermal fluids. Grt-I is dark in backscattered electron (BSE) images, rich in spessartine, and poor in almandine and grossular. Its chondrite-normalized rare earth element (REE) patterns show obvious negative Eu anomalies and depletion in heavy REE (HREE) relative to middle REE (MREE). The second generation of pegmatite garnet (Grt-II) occurs as rims of euhedral garnets or as patches in Grt-I domains of the pegmatite, and it crystallized after dissolution of the preexisting pegmatite garnet (Grt-I domains) in the presence of the granitic magma. Compared with Grt-I, Grt-II is bright in BSE images, poor in spessartine, and rich in almandine and grossular contents. Its chondrite-normalized REE patterns exhibit obvious negative Eu anomalies but enrichment in HREE relative to MREE. The elevation of grossular and HREE contents for Grt-II relative to Grt-I domains indicate that the granitic magma had higher contents of Ca than the magmatic-hydrothermal fluids. The garnets in the granite, from core to rim, display homogenous profiles in their spessartine, almandine, and pyrope contents but increasing grossular and decreasing REE contents. They are typical of magmatic garnets that crystallized from the granitic magma. Ti-in-zircon temperatures demonstrate that the granite and pegmatite may share the similar temperatures for their crystallization. Grt-II domains in the pegmatite garnet have the same major and trace element compositions as the granite garnet, suggesting that the pegmatite Grt-II domains crystallized from the same granitic magma. Therefore, the pegmatite crystallized at first from early magmatic-hydrothermal fluids, producing small amounts of Grt-I, and the fluids then mixed with the surrounding granitic magma. The U-Pb dating and Hf-O isotope analyses of zircons from the granite and pegmatite yield almost the same U-Pb ages of 77–79 Ma, positive eHf(t) values of 5.6 to 11.9, and d18O values of 5.2 to 7.1‰. These data indicate that the granite and pegmatite were both derived from reworking of the juvenile crust in the newly accreted continental margin prior to the continental collision in the Cenozoic.
    Materialart: Online-Ressource
    ISSN: 0003-004X , 1945-3027
    RVK:
    Sprache: Englisch
    Verlag: Mineralogical Society of America
    Publikationsdatum: 2021
    ZDB Id: 3514-2
    ZDB Id: 2045960-9
    SSG: 13
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 7
    Online-Ressource
    Online-Ressource
    Mineralogical Society of America ; 2019
    In:  American Mineralogist Vol. 104, No. 8 ( 2019-08-1), p. 1173-1179
    In: American Mineralogist, Mineralogical Society of America, Vol. 104, No. 8 ( 2019-08-1), p. 1173-1179
    Kurzfassung: In this study, we have measured the compressional and shear wave velocities of (Mg1.77Fe0.22Ca0.01)Si2O6 natural orthopyroxene up to 13.5 GPa and 873 K using ultrasonic interferometry in conjunction with in situ synchrotron X-ray diffraction and imaging techniques. Previous acoustic experiments on orthoenstatite (OEn) MgSiO3 indicated that both compressional and shear velocities (VP and VS) of OEn undergo continuous velocity softening above 9 GPa at room temperature, which has been attributed to the phase transition from OEn to the metastable, high-pressure clinoenstatite HPCEn2. For the first time, our results suggest that pressure-induced velocity softening can occur in natural orthopyroxene at high-temperature conditions relevant to the Earth's cold subduction zones. Estimates of the impedance and velocity contrasts between orthopyroxene (Opx) and high-pressure clinopyroxene (HPCpx) have been calculated, and the possibility of this phase transformation being a plausible candidate for seismic X-discontinuities at depth around 250–350 km is re-evaluated.
    Materialart: Online-Ressource
    ISSN: 0003-004X , 1945-3027
    RVK:
    Sprache: Englisch
    Verlag: Mineralogical Society of America
    Publikationsdatum: 2019
    ZDB Id: 3514-2
    ZDB Id: 2045960-9
    SSG: 13
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 8
    Online-Ressource
    Online-Ressource
    Mineralogical Society of America ; 2021
    In:  American Mineralogist Vol. 106, No. 11 ( 2021-11-1), p. 1744-1750
    In: American Mineralogist, Mineralogical Society of America, Vol. 106, No. 11 ( 2021-11-1), p. 1744-1750
    Kurzfassung: Sound velocities of iron and iron-based alloys at high pressure and high temperature are crucial for understanding the composition and structure of Earth’s and other telluric planetary cores. In this study, we performed ultrasonic interferometric measurements of both compressional (νP) and shear (νS) velocities on a polycrystalline body-centered-cubic (bcc)-Fe90Ni10 up to 8 GPa and 773 K. The elastic moduli and their pressure and temperature derivatives are derived from least-square fits to third-order finite strain equations, yielding KS0 = 154.2(8) GPa, G0 = 73.2(2) GPa, KS0′ = 4.6(2), G0′ = 1.5(1), ∂KS/∂T = –0.028(1) GPa/K, and ∂G/∂T = –0.023(1) GPa/K. A comparison with literature data on bcc-Fe suggests that nickel not only decreases both P and S wave velocities but also weakens the temperature effects on the elastic moduli of Fe-Ni alloys.
    Materialart: Online-Ressource
    ISSN: 0003-004X , 1945-3027
    RVK:
    Sprache: Englisch
    Verlag: Mineralogical Society of America
    Publikationsdatum: 2021
    ZDB Id: 3514-2
    ZDB Id: 2045960-9
    SSG: 13
    Standort Signatur Einschränkungen Verfügbarkeit
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