Mineralium Deposita最新文献

Trace element concentrations in magnetite are dictated by the petrogenetic environment and by the physico-chemical conditions during magmatic, hydrothermal, or sedimentary processes. This makes magnetite chemistry a useful tool in the exploration of ore-forming processes. We describe magnetite compositions from Ni-Cu-(PGE)-sulfide mineralized rocks from seven mafic–ultramafic intrusions peripheral to the Mesoproterozoic AMCG (anorthosite-mangerite-charnockite-granite) suite of the Kunene Complex of Angola and Namibia to investigate metallogenic processes through the geochemical characterization of Fe-oxides, which were analyzed in-situ via Electron Probe Microanalysis (EPMA), and Laser Ablation-Inductively Coupled Plasma-Mass Spectrometry (LA-ICP-MS). We identified magmatic magnetite, segregated from both a silicate liquid and an immiscible sulfide liquid. Elements like Cr, Co and V suggest that the sulfide-related magnetite segregated from a relatively primitive Fe-rich monosulfide solid solution (MSS). Secondary Cr-rich magnetite appears in intrusions with abundant chromite or Cr-spinel. Two types of hydrothermal magnetite were identified, related to the pervasive replacement of sulfides and a late-stage, low-T fluid circulation event. Magnetite replacing sulfides is associated with serpentinized ultramafic rocks and is preferentially observed in the intrusions with the highest base and precious metal tenors. The high concentration of Ni, Co, Cu, Pd, As and Sb in these grains is corroborated by the identification of micron-size PGE mineral inclusions. We infer that serpentinization during hydrothermal fluid circulation was accompanied by desulphurization of sulfides with metal remobilization and reconcentration to generate magnetite carrying Pd microinclusions. We suggest that the highly serpentinized ultramafic rocks in the Kunene Complex region may become a possible target for economic Ni-Cu-(PGE) mineralization.

This study investigated the Boam mine area, a prominent Li-pegmatite deposits located in South Korea, using Li-bearing micas to determine the magmatic–aqueous transition involved in rare-element pegmatite formation. Muscovite–lepidolite series micas from the layered pegmatite exhibited six textures, classified into three stages (early, intermediate, and late) based on compositions of major and trace elements. The substitution mechanisms of muscovite–lepidolite series micas follow lithium fixation (Si ↔ Li + Al) and phengitic substitution (Al^iv + 2Al^vi ↔ Li + (Fe²⁺, Mg²⁺, Mn²⁺) + Si) vectors. Early-stage micas displayed a large grain size due to rapid crystal growth due from low undercooling. Diffusional zonation of these micas with the higher Nb–Ta and lower Li concentrations compared with later-stage lepidolite indicate a lower degree of fractionation. These features suggest a silicic melt origin for early-stage micas. Intermediate-stage micas are distinctly separated from the early-stage type and feature erratic boundaries with higher Li composition. B enrichment reduced the melt viscosity and increased the H₂O solubility, resulting in an increase in growth rate and retardation of mineralization. The inhibition of HFSE partitioning by B lead to a lower Nb–Ta concentration than the silicic melt, suggesting the existence of an aqueous melt. Fine-grained late-stage mica coexists with microcrystalline quartz, and is characterized by Cs enrichment and Nb–Ta depletion that exclusively occur in flux-rich aqueous fluids. Non-Rayleigh behavior of K-Rb-Cs indicates a deviation from fractional crystallization unlike melt phases, suggesting an aqueous fluid origin for late-stage micas. Consequently, the formation of Li-pegmatite in the deposit was predominantly controlled by the immiscibility of silicic melt–aqueous melt–aqueous fluid and fractional crystallization within each medium.

The ca. 3.0 Ga Ni sulfide mineralisation at Maniitsoq, SW Greenland, is hosted by a cluster of relatively small, irregularly shaped mafic-ultramafic intrusions, typically 10s of m to a few km across, that are lodged within broadly coeval gneiss. Many of the intrusions are fault bounded and fragmented so that their original sizes remain unknown. The sulfides form disseminations and sulfide matrix breccia veins displaying sharp contacts to the host intrusives. The mineralisation has relatively high Ni/Cu, with 4–10% Ni and 1–2% Cu. Correlations between Ni and Cu with sulfide content are strong, consistent with a magmatic origin of the mineralisation. PGE contents are mostly below 0.5 ppm, and Cu/Pd is typically above primitive mantle levels, interpreted to reflect equilibration of the parent magma with segregating sulfide melt prior to final magma emplacement. Sulfide segregation was likely triggered by assimilation of crustal sulfur, as suggested by whole rock S/Se ratios of 7000–9000. The sulfide melt underwent extensive fractionation after final emplacement, caused by downward percolation of Cu-rich sulfide melt through incompletely solidified cumulates. We suggest that the exposed Maniitsoq intrusions represent the Ni-rich upper portions of magma conduits implying that there is potential for Cu-rich sulfides in unexposed deeper portions of the belt.

To evaluate the fertility of porphyry mineralization in the Delamerian Orogen (South Australia), zircon and apatite from four prospects, including Anabama Hill, Netley Hill, Bendigo, and Colebatch, have been analyzed by LA-ICP-MS and electron microprobe. The zircon is characterized by heavy REEs enrichment relative to light REEs, high (Ce/Nd)_N (1.3–45), and weak to moderate negative Eu/Eu* (0.2–0.78). The apatite has right-sloped REE patterns with variably negative to positive Eu anomalies. Low Mg (< 670 ppm) and Sr/Y ratios (< 5) in apatite likely illustrate fractional crystallization trends for the granitic melts in shallow crust. The Yb/Gb and Eu/Eu* in zircon reveal that intrusions at Anabama Hill, Netley Hill, and Bendigo underwent fractional crystallization controlled by amphibole (< 50–60%), garnet (< 15%), apatite (< 0.6%), and/or titanite (< 0.3%). These stocks have average fO₂ values reported relative to fayalite-magnetite-quartz buffer (ΔFMQ), from 0.7 ± 0.9 to 2.1 ± 0.4, ascribed to prolonged magmatic evolution or sulfur degassing during post-subduction processes. Our data imply that both Anabama and Bendigo complexes experienced prevalent (garnet-) amphibole crystallization from hydrous melts that have moderately high oxidation (ΔFMQ + 1 to + 3) and elevated sulfur-chlorine components (Anabama, 37 ± 9 to 134 ± 83 ppm S and 0.30 ± 0.24 to 0.64 ± 0.89 wt% Cl; Bendigo, 281 ± 178 to 909 ± 474 ppm S and 0.45 ± 0.47 to 3.01 ± 1.54 wt% Cl). These are crucial ingredients to form porphyry Cu–Mo ± Au ores with economic significance, which provides encouragement for mineral exploration in this orogen.

The Felbertal tungsten deposit is the only economic scheelite mine in Europe, yet its genesis is not fully understood. It has been argued recently that the formation of the deposit is most likely related to granitic intrusions of Variscan age, contrasting a previously suggested syn-depositional stratabound origin of Early Cambrian age. Solving this controversy remains challenging due to the polymetamorphic evolution of the deposit, which experienced both Variscan and Alpine metamorphism. In this contribution we present a comprehensive new data set of scheelite major, minor, and trace element concentrations from multiple scheelite generations of the Felbertal deposit along with microstructural observations. Our results show that Mo, Mo/Mn, REE, Y/Ho, Nb, and Nb/Ta in scheelite are variable within the different scheelite generations and are predominantly controlled by the host-rock lithologies on the local scale, whereas in general the data show a strong response to the shift of P, T, and pH upon changing magmatic-hydrothermal to metamorphic conditions. For the first time, we identify remnants of primary scheelite in the Western Ore Zone. The presented data support a magmatic-hydrothermal origin of the first scheelite mineralization during the Variscan orogeny with primary scheelite being characterized by wing-shaped REE patterns with a negative Eu-anomaly, high trace element concentrations, non-chondritic Y/Ho, and high Nb/Ta. Primary scheelite underwent metamorphic/hydrothermal alteration (recrystallization and dissolution-reprecipitation processes) during the Variscan and Alpine orogeny. This case study highlights that indicative mineralization-controlling geochemical ratios like Sr/Mn cannot be applied for polymetamorphic tungsten deposits like Felbertal.

High-grade (> 10 g/t) gold mineralization in orogenic gold deposits is of significant economic importance. Understanding the formation of such enriched ore zones is critical for gold exploration success. The world-class Jundee-Bogada gold camp in the Yilgarn Craton of Western Australia comprises both high-grade (avg. > 10 g/t, Jundee deposit) and low-grade (avg. < 3 g/t, Bogada prospect) lodes, despite shared host stratigraphy. The paragenetic framework established for the Jundee gold deposit suggests that the overall gold endowment developed over three deformation events. An early episode of low-grade gold mineralization is associated with colloform-crustiform veins that formed during extensional deformation (D_JB2A). A switch to transtensional deformation (D_JB2B) resulted in brecciation of the colloform-crustiform veins and coeval deposition of native gold. Late reverse faults record evidence for a third mineralization stage resulting from a NE-SW-directed shortening (D_JB3). Mineralization during this late stage was dominantly low-grade, with local occurrences of ultra-high-grade ore zones (> 100 g/t). Each event records transient changes in fluid chemistry during continued hydrothermal activity that spanned local deformation histories. We argue that at the Jundee gold deposit, protracted gold enrichment during three polyphased mineralization episodes resulted in the formation of high-grade gold ores. Whereas the complete metallogenic history is recorded at the Jundee deposit, gold within the Bogada prospect was introduced solely during the late contractional stage (D_JB3), resulting in a bulk low-grade endowment. We hypothesize that gold enrichment in high-grade orogenic gold deposits is a direct consequence of the spatial superimposition of protracted ore-forming events.

Phanerozoic orogenic gold deposits worldwide are commonly considered to be formed from metamorphic devolatilization of marine carbonaceous sedimentary rocks. Here we show that the Yindongpo gold deposit from the Qinling orogen (central China) is genetically associated with the metamorphism of volcanic rocks during the late Paleozoic orogeny, which involved the closure of the Shangdan ocean. Gold mineralization at Yindongpo is hosted in lower Paleozoic metavolcanic-sedimentary sequences and occurs mainly as lenticular to stratiform ore bodies that formed in three paragenetic stages represented by quartz-ankerite-pyrite (stage I), quartz-carbonate-sulfide (stage II) and quartz-calcite assemblages (stage III), respectively. Rutile grains coexisting with auriferous pyrite from stage II yield U–Pb ages of 395 ± 9 to 400 ± 13 Ma (2σ). Fluid inclusions in quartz of stages I and II are dominated by CO₂-rich (~ 10 mol%) aqueous fluids with low salinities (< 4.9 wt% NaCl equivalent) and total homogenization temperatures ranging from 241 to 352 ºC, whereas the values for H₂O-rich inclusions of stage III are 0.2 to 2.6 wt% NaCl equivalent and 151 to 164 °C. Based on secondary ion mass spectrometry analysis of oxygen isotopes of quartz (Qz-1 to Qz-4), the calculated δ¹⁸O_fluid values for the quartz-forming fluids are 1.3 to 7.0‰ in stage I, –3.1 to 6.6‰ in stage II, and –9.6 to –3.7‰ in stage III. These data indicate a metamorphic origin of ore fluids that underwent Rayleigh fractionation and incursion of meteoric water. The large variation in ⁴⁰Ar^*/⁴He ratios (1.7–30.0), caused by accumulation of radiogenic Ar^* and He loss within some pyrite samples, can be ascribed to regional metamorphism and deformation. Ore sulfides have sulfur (δ³⁴S_V-CDT = –2.1 to 3.3‰) and lead (²⁰⁶Pb/²⁰⁴Pb = 17.008–17.152, ²⁰⁷Pb/²⁰⁴Pb = 15.402–15.493, and ²⁰⁸Pb/²⁰⁴Pb = 38.254–38.564) isotopic compositions that are consistent with those of pyrite in the metavolcanic host rocks. Results presented here suggest that the ore fluids and, by inference, gold of the Yindongpo deposit were derived primarily from the volcanic sequences during regional metamorphism and deformation in response to the Early Devonian Qinling collisional orogeny. The Yindongpo deposit represents the first recognized Paleozoic orogenic gold deposit in the Qinling orogen, and thus has important implications for regional metallogeny and gold exploration.

Giant mafic-ultramafic layered intrusions of Archaean-Proterozoic age are the fossilised remnants of huge injections of silicate magma in the Earth’s crust and are our most important repositories of platinum-group elements. Magmatic PGE-rich ore deposits, such as the Merensky Reef, are typically hosted in stratiform reefs at the contacts between ultramafic and feldspathic cumulates. The Merensky Reef is commonly characterised by coarse-grained and pegmatoidal textures that may provide important clues to its origin. We present textural and in situ geochemical data for Merensky pegmatoids at Styldrift Mine (Impala Bafokeng) in the Western Bushveld Complex of South Africa. This region is adjacent to an inferred magmatic feeder zone to the Bushveld. The Merensky pegmatoids are characterised by (i) amoeboid olivine inclusions in zoned orthopyroxene megacrysts with increasing molar Mg# of orthopyroxene towards olivine, (ii) fine-grained chains of orthopyroxene in compositional equilibrium with adjacent orthopyroxene megacrysts, (iii) increasing molar Mg# of orthopyroxene megacrysts and increasing molar An with decreasing ⁸⁷Sr/⁸⁶Sr_i (at 2.06 Ga) of plagioclase oikocrysts in pegmatoids laterally across a 10-km section distal to the feeder, and (iv) highly variable molar An and initial ⁸⁷Sr/⁸⁶Sr_i of interstitial plagioclase proximal to the feeder. We interpret the coarse-grained and pegmatoidal textures, their dissolution-reprecipitation features, and lateral chemical variations as the product of lateral melt infiltration and mixing in a crystal mush. We suggest that the platiniferous Merensky Reef was not formed at the base of a large melt-filled magma chamber but was instead the product of non-sequential magma emplacement that rejuvenated the crystal mush.

New inorganic and organic geochemical data from thucholite in the Upper Permian (Wuchiapingian) Kupferschiefer (T1) shale collected at the Polkowice-Sieroszowice Cu-Ag mine in Poland are presented. Thucholite, which forms spherical or granular clusters, appears scattered in the T1 dolomitic shale at the oxic-anoxic boundary occurring within the same shale member. The composition of thucholite concretions and the T1 shale differs by a higher content of U- and REE-enriched mineral phases within the thucholite concretions compared to the T1 shale, suggesting a different mineralising history. The differences also comprise higher N_tot, C_tot, H_tot, S_tot contents and higher C/N, C/S ratios in thucholite than in the T1 shale. The hydrocarbon composition of the thucholite and the surrounding T1 shale also varies. Both are dominated by polycyclic aromatic compounds and their phenyl derivatives. However, higher abundances of unsubstituted polycyclic aromatic hydrocarbons in the thucholite are indicative of its pyrogenic origin. Pyrolytic compounds such as benz[a]anthracene or benzo[a]pyrene are more typical of the thucholite than the T1 shale. Microscopic observations of the thucholite and its molecular composition suggest that it represents well-rounded small charcoal fragments. These charcoals were formed during low-temperature combustion, as confirmed by semifusinite reflectance values, indicating surface fire temperatures of about 400 °C, and the absence of the high-temperature pyrogenic polycyclic aromatic hydrocarbons. Charred detrital particles, likely the main source of insoluble organic matter in the thucholite, migrated to the sedimentary basin in the form of spherical carbonaceous particulates, which adsorbed uranium and REE in particular, which would further explain their different contents and sorption properties in the depositional environment. Finally, the difference in mineral content between thucholite and the T1 shale could also have been caused by microbes, which might have formed biofilms on mineral particles, and caused a change in the original mineral composition.

The Xianghualing large tin-polymetallic skarn deposit is located in the Nanling W-Sn metallogenic belt, South China, showing distinct spatial zoning of mineralization. From the contact between granite and carbonate rocks, the mineralization transitions from proximal skarn Sn ore to cassiterite-sulfide ore and more distal Pb–Zn-sulfide ore. This study reveals the fluid evolution and genetic links among these different ore types. The physical and chemical characteristics of fluid inclusions from each ore types indicate that the skarn Sn ore, cassiterite-sulfide ore, and Pb–Zn-sulfide ore all originated from the identical magmatic fluid exsolved from the Laiziling granite. Their formation, however, is controlled by diverse fluid evolutionary processes and host rock characteristics. The Sn–Pb-Zn-rich fluids were primarily derived from cooled and diluted magmatic brine, which is generated by boiling of initial single phase magmatic fluid. Mixing of magmatic brine with meteoric water is crucial to form skarn Sn ore. Redox reactions of aqueous Sn (II) complexes with As (III) species and/or minor CO₂ during short cooling period of ore-forming fluid is likely an effective mechanism to form high-grade cassiterite-sulfide ores, accompanied by favorable pH conditions maintained through interaction with carbonate host rocks. The later stage addition of meteoric water prompts the formation of Pb–Zn-sulfide ore. Comparing these findings with the characteristics of initial or pre-ore magmatic fluids in both mineralized and barren granitic systems indicates that high Sn content in the pre-ore fluids and the suitable fractional crystallization degree of the parent magma may determine high Sn mineralization potential in granitic magmatic-hydrothermal systems.