1. |
- Melcher, Frank, et al.
(författare)
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The Haidbach deposit in the Central Tauern Window, Eastern Alps, Austria : a metamorphosed orthomagmatic Ni-Cu-Co-PGE mineralization in the Polymetallic Ore District Venediger Nappe System – Hollersbach Complex
- 2021
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Ingår i: Austrian Journal of Earth Sciences. - : Walter de Gruyter. - 0251-7493 .- 2072-7151. ; 114:1, s. 1-26
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Tidskriftsartikel (refereegranskat)abstract
- Cu-Ni-Co-PGE mineralization occurs at Haidbachgraben in the Early Palaeozoic, Subpenninic Hollersbach Complex of the Central Tauern Window, Austria. Massive sulfide ore formed from sulfide melt segregated from silicate melt during intrusion of pyroxenite into magmatic rocks formed in an MORB-type environment. Relics of magmatic minerals include chromian spinel and polyphase sulfide droplets composed of pyrrhotite, chalcopyrite and pentlandite preserved in recrystallized pyrite. Both ore and host rocks were multiply deformed and metamorphosed, leading to hornblendite carrying the ore, enveloped by chlorite-epidote schist. Conditions of – likely Variscan – amphibolite facies metamorphism are documented by relict pargasitic cores in hornblende and actinolite-tremolite, and by ternary sulfarsenide compositions in the Co-Ni-Fe solid solution series that are the most common accessory minerals found in the sulfide ore. Pyrrhotite, pentlandite, chalcopyrite and pyrite are the major sulfide minerals. Chalcopyrite is Cd-rich and retains a high-temperature magmatic signature. High Co/Sb and moderate Se/As ratios in pyrite also point to a magmatic environment of mineralization. The accessory mineral assemblage of small grain size (mostly <10 µm) comprises native Au-Ag alloy and petzite as Au-Ag minerals, sperrylite, a variety of Pd tellurides and bismuthotellurides with elevated Sb, irarsite, and Re sulfides such as tarkianite and a Pb-Re sulfide. In addition, minor molybdenite, bournonite, scheelite and selenides have been identified. Two precious metal assemblages are present in individual samples: (1) hessite associated with Pd tellurides, often accompanied by sphalerite and chalcopyrite; (2) tarkianite forming euhedral inclusions in pyrite. Sperrylite and Au-Ag native alloys are present throughout and were also detected in silicate matrix. Most of the precious metal-bearing phases must have formed during recrystallization of base metal sulfides after the magmatic, and probably during later metamorphic events terminating in the Neoalpine Tauern crystallization.
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4. |
- Aiglsperger, Thomas, et al.
(författare)
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Geochemistry of REE-rich karst bauxite ore deposits from the Sierra de Bahoruco, Dominican Republic
- 2019
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Ingår i: Proceedings of the 15th SGA Biennial Meeting, 27-30 August. - : University of Glasgow Publicity Services. ; , s. 1834-1836
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Konferensbidrag (refereegranskat)abstract
- In this work the geochemistry of REE-rich karst bauxite ore from several deposits of the Sierra de Bahoruco (Dominican Republic) has been investigated. The bauxite ores are geochemically heterogenous and show differences with respect to major, minor and trace elements. According to their major element geochemistry, the studied ores classify mostly as Fe-rich bauxites. The minor elements Cr and Ni are in general relatively high (up to 1250 and 2370 ppm, respectively), hence pointing towards a (ultra-)mafic source for the bauxite formation. The sum of REE contents range from similar to 400 to similar to 5400 ppm (average similar to 1200 ppm) at varying LREE/HREE between similar to 1 and similar to 25 (average similar to 8). In general, REE chondrite-normalized patterns for studied bauxites show negative Ce and Eu anomalies with rather flat segments for HREE. However, three samples from different bauxite ore deposits with the highest REE contents show significant enrichment trends for heavier REE, particularly for Pr, Nd, Sm, Gd as well as for Tb and Dy (one sample). Mineralogical studies reveal that formation of secondary REE-bearing minerals (i.e. phosphates, carbonates and oxides) occurred. Karst bauxite ores hosted in the Sierra de Bahoruco represent an excellent natural laboratory to study the geochemical behaviour of REE in weathering systems.
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5. |
- Aiglsperger, Thomas, et al.
(författare)
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Open system Re-Os isotope behavior in platinum-group minerals during laterization?
- 2021
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Ingår i: Minerals. - : MDPI. - 2075-163X. ; 11:10
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Tidskriftsartikel (refereegranskat)abstract
- In this short communication, we present preliminary data on the Re-Os isotopic systematics of platinum-group minerals (PGM) recovered from different horizons in the Falcondo Ni-laterite in the Dominican Republic. The results show differences in the Os-isotope composition in different populations of PGM: (i) pre-lateritic PGM yield 187 Os/188 Os varying from 0.11973 ± 0.00134 to 0.12215 ± 0.00005 (2σ uncertainty) whereas (ii) lateritic PGM are more radiogenic in terms of 187 Os/188 Os (from 0.12390 ± 0.00001 to 0.12645 ± 0.00005; 2σ uncertainty). We suggest that these differences reflect the opening of the Re-Os system in individual grains of PGM during lateritic weathering. The implications of these results are twofold as they will help to (1) elucidate the small-scale mobility of noble metals in the supergene setting and therefore the possible formation of PGM at these very low temperatures, (2) better refine the Os-isotopic datasets of PGM that are currently being used for defining dynamic models of core–mantle separation, crustal generation, and fundamental plate-tectonic processes such as the opening of oceans.
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8. |
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9. |
- Aydin, Faruk, et al.
(författare)
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Temporal, geochemical and geodynamic evolution of the Late Cretaceous subduction zone volcanism in the eastern Sakarya Zone, NE Turkey : Implications for mantle-crust interaction in an arc setting
- 2020
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Ingår i: Journal of Asian Earth Sciences. - : Elsevier. - 1367-9120 .- 1878-5786. ; 192
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Tidskriftsartikel (refereegranskat)abstract
- The Late Cretaceous Artvin volcanic rocks (LCAVs) from the eastern Sakarya zone (ESZ) of NE Turkey are composed of mafic/basaltic (S1-Çatak and S2-Çağlayan) and felsic/acidic (S1-Kızılkaya and S2-Tirebolu) rock types that occurred in two successive stages: (i) first stage (S1: Turonian–Early Santonian) and (ii) second stage (S2: Late Santonian–Campanian). Clinopyroxene thermobarometric results point that the S2-Çağlayan basaltic rocks have crystallised at higher temperatures and under deeper crustal conditions than those of the S1-Çatak basaltic rocks.The LCAVs show a wide compositional spectrum, ranging from tholeiite to calc-alkaline/shoshonite and are typically represented by a geochemical composition resembling subduction-related arc rocks although the 87Sr/86Sr(i) (0.7044–0.7071) and ɛNd(i) values (−0.63 to + 3.47) as well as 206Pb/204Pb(i) (18.07–18.56), 207Pb/204Pb(i) (15.57–15.62) and 208Pb/204Pb(i) (37.12–38.55) ratios show very limited variation. The parent magmas of the S1-Çatak and S2-Çağlayan mafic volcanic rocks were derived from underplated basaltic melts that originated by partial melting of metasomatised spinel lherzolite and spinel-garnet lherzolite, respectively. It is proposed that the compositions of the S1-Kızılkaya (mainly dacitic) and S2-Tirebolu (rhyolitic to trachytic) felsic rocks were particularly controlled by metasomatised mantle–crust interaction and MASH zone + shallow crustal fractionation processes. Our data, together with data from previous studies, suggest that the S1- and S2-mafic and felsic rocks of the LCAVs (~95–75 Ma) are the products of two-stage volcanic event that took place during the northward subduction of the northern Neotethys Ocean (NNO).
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11. |
- Cabri, Louis J., et al.
(författare)
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A review of hexaferrum based on new mineralogical data
- 2018
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Ingår i: Mineralogical magazine. - : Mineralogical Society of Great Britain and Ireland. - 0026-461X .- 1471-8022. ; 82:3, s. 531-538
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Tidskriftsartikel (refereegranskat)abstract
- Hexaferrum, defined as an hcp Fe mineral containing varying amounts of Ru, Os, or Ir(Mochalov et al. 1998) was re-examined in the light of new analyses of similar alloys from the Loma Peguera and Loma Larga chromitites, in the central part of Loma Caribe peridotite, Cordillera Central of the Dominican Republic, together with a review of the phase chemistry inthe Fe-Ni-Ir and Fe-Ru-Ir systems. We conclude that the hcp (Fe,Ir) mineral corresponds to theε-phase of Raub et al. (1964) and should be differentiated from hexaferrum [(Fe,Os) and(Fe,Ru)] because it is separated by one to two miscibility gaps and therefore is not a continuous solid solution with Fe.
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12. |
- Domínguez-Carretero, Diego, et al.
(författare)
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Ultramafic-hosted volcanogenic massive sulfide deposits from Cuban ophiolites
- 2022
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Ingår i: Journal of South American Earth Sciences. - : Elsevier. - 0895-9811 .- 1873-0647. ; 119
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Tidskriftsartikel (refereegranskat)abstract
- Ultramafic-hosted volcanogenic massive sulfide deposits (UM-VMS) located in the Havana-Matanzas ophiolite (Cuba) are the only known example of this type of mineralization in the Caribbean realm. UM-VMS from Havana-Matanzas are enriched in Cu, Ni, Co, Au, and Ag. The mineralization consists of massive sulfide bodies mostly composed of pyrrhotite and hosted by serpentinized upper mantle peridotites. Chemical composition of unaltered cores in Cr-spinel grains found within the massive sulfide mineralization and in the peridotite host indicates formation in the fore-arc region of the Greater Antilles volcanic arc. A first stage of serpentinization probably took place prior to the sulfide mineralization event. The UM-VMS mineralization formed by the near-complete replacement of the silicate assemblage of partially serpentinized peridotites underneath the seafloor. The sequence of sulfide mineralization has been divided into two stages. The first stage is characterized by a very reduced hydrothermal mineral assemblage consisting of pyrrhotite, Co–Ni–Fe diarsenides, chalcopyrite, Co-rich pentlandite, and electrum. In the second stage, pyrite and Co–Ni–Fe sulfarsenides partially replaced pyrrhotite and diarsenides, respectively, under a more oxidizing regime during the advanced stages of ongoing serpentinization. The proposed conceptual genetic model presented here can be useful for future exploration targeting this type of deposit in the Caribbean region and elsewhere.
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13. |
- Farre-de-Pablo, Julia, et al.
(författare)
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Low-temperature hydrothermal Pt mineralization in uvarovite-bearing ophiolitic chromitites from the Dominican Republic
- 2022
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Ingår i: Mineralium Deposita. - : Springer. - 0026-4598 .- 1432-1866. ; 57:6, s. 955-976
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Tidskriftsartikel (refereegranskat)abstract
- Platinum-group elements (PGEs) occur in ophiolitic chromitite in the Dominican Republic as platinum-group minerals (PGMs) in spatial association with hydrothermal uvarovite and chromian clinochlore. Bulk-rock total PGE content in a single analyzed chromitite sample is of 6.54 g/t. Three main PGM types are distinguished: euhedral magmatic laurite completely encased in chromite, subhedral to euhedral Ru-Os-Fe-(Ir) compounds partially encased in chromite, and anhedral Pt-Fe-Ni-rich grains exclusively embedded in uvarovite or chromian clinochlore. The Ru-Os-Fe-(Ir) compounds are interpreted as magmatic Ru-Os sulfides that experienced desulfurization during hydrothermal alteration of the chromitites, whereas the Pt-Fe-Ni-rich grains are hydrothermal in origin. We propose a model in which the Pt-Fe-Ni-rich PGMs formed via the accumulation of nanoparticles directly precipitated from the hydrothermal fluids. An estimation of the temperature of crystallization of uvarovite and chromian clinochlore suggests hydrothermal alteration of the chromitite within the thermal range of 150-350 degrees C. Thermodynamic modeling shows that, within this range of temperature, Pt could be mobilized as aqueous bisulfide complexes (HS-) by S-poor, highly reducing hydrothermal fluids originated during serpentinization of the host chromitite rock. The crystallization of Ni sulfides in the chromitite would drop the S concentration of the fluid, causing the precipitation of Pt as native element. Ultimately, this process contributes to constrain the conditions for the genesis of hydrothermal PGE mineralizations in ophiolitic chromitites.
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14. |
- Farré-de-Pablo, Júlia, et al.
(författare)
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Ophiolite hosted chromitite formed by supra-subduction zone peridotite –plume interaction
- 2020
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Ingår i: Geoscience Frontiers. - : Elsevier. - 1674-9871. ; 11:6, s. 2083-2102
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Tidskriftsartikel (refereegranskat)abstract
- Chromitite bodies hosted in peridotites typical of suboceanic mantle (s.l. ophiolitic) are found in the northern and central part of the Loma Caribe Peridotite in the Cordillera Central of the Dominican Republic. These chromitites are massive pods of small size (less than a few meters across) and veins that intrude both dunite and harzburgite. Compositionally, they are high-Cr chromitites [Cr# = Cr/(Cr+Al) atomic ratio = 0.71–0.83] singularly enriched in TiO2 (up to 1.25 wt.%), Fe2O3 (2.77–9.16 wt.%) as well as some trace elements (Ga, V, Co, Mn, and Zn) and PGE (up to 4548 ppb in whole-rock). This geochemical signature is unknown for chromitites hosted in oceanic upper mantle but akin to those chromites crystallized from mantle plume derived melts. Noteworthy, the melt estimated to be in equilibrium with such chromite from the Loma Caribe chromitites is similar to basalts derived from different source regions of a heterogeneous Caribbean mantle plume. This mantle plume is responsible for the formation of the Caribbean Large Igneous Province (CLIP). Dolerite dykes with back-arc basin basalt (BABB) and enriched mid-ocean ridge basalt (E-MORB) affinities commonly intrude the Loma Caribe Peridotite, and are interpreted as evidence of the impact that the Caribbean plume had in the off-axis magmatism of the back-arc basin, developed after the Caribbean island-arc extension in the Late Cretaceous. We propose a model in which chromitites were formed in the shallow portion of the back-arc mantle as a result of the metasomatic reaction between the supra-subduction zone (SSZ) peridotites and upwelling plume-related melts.
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15. |
- Farré-de-Pablo, Júlia, et al.
(författare)
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Orthopyroxenite hosted chromitite veins anomalously enriched in platinum-group minerals from the Havana-Matanzas Ophiolite, Cuba
- 2020
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Ingår i: Boletín de la Sociedad Geológica Mexicana. - : Universidad Nacional Autónoma de México. - 1405-3322 .- 1405-3322. ; 72:3
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Tidskriftsartikel (refereegranskat)abstract
- The Havana–Matanzas Ophiolite contains one of the few examples of ophiolitic platinum group minerals (PGM)-rich chromitites associated with orthopyroxenites in the mantle section of ophiolitic complexes. The chromitites occur as veins hosted by orthopyroxenite bands within mantle peridotites. The peridotites are mostly harzburgites and their accessory chromite shows high-Al compositions (Cr# [Cr/(Cr+Al), atomic ratio] = 0.39–0.50), which are typical of spinels in abyssal peridotites. Conversely, chromite from the chromitite veins and their host orthopyroxenite are high-Cr (Cr# = 0.72–0.73 and 0.62–0.69, respectively), with lower Mg# [Mg/(Mg+Fe2+), atomic ratio]. This suggests that both the chromitite and the orthopyroxenite formed from melts with boninitic affinity. The abundant PGM inclusions found in the chromitites are mainly Os-rich laurite grains, which is also characteristic of chromitites formed from magmas with boninitic affinity. Therefore, we propose that the chromitite veins and the orthopyroxenite bands probably formed contemporaneously in the fore-arc setting of an intra-oceanic arc during subduction. The chromitite-orthopyroxenite pair of the Havana-Matanzas Ophiolite could form after the reaction of a Si-rich melt with boninitic affinity and mantle harzburgite, with the orthopyroxenite bands preserving fingerprints of the infiltration of boninitic-affinity melts within the mantle. The small volume of forming chromitite could maximize the efficiency for the mechanical collection of the PGM forming in the parental melt of these rocks, resulting in the anomalous enrichment of primary PGM in the chromitites.
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18. |
- García-Tudela, Matías, et al.
(författare)
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The chromitites of the Herbeira massif (Cabo Ortegal Complex, Spain) revisited
- 2024
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Ingår i: Ore Geology Reviews. - : Elsevier. - 0169-1368 .- 1872-7360. ; 170
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Tidskriftsartikel (refereegranskat)abstract
- The ultramafic rocks of the Herbeira Massif in the Cabo Ortegal Complex (NW Iberia) host chromitite bodies. The textural and compositional study of the host rocks and the chromitites classified them into: (1) Type-I chromitites, forming massive pods of intermediate-Cr chromite (Cr# = 0.60–0.66) within dunites; and (2) Type-II chromitites forming semi-massive horizons of high-Cr chromite (Cr# = 0.75–0.82) interlayered with dunites and pyroxenites. Minor and trace elements (Ga, Ti, Ni, Zn, Co, Mn, V and Sc) contents in the unaltered chromite cores from both types show patterns very similar to fore-arc chromitites, mimicked by the host dunites and pyroxenites. Calculated parental melt compositions suggest that Type-I chromitites crystallized from a melt akin to fore-arc basalt (FAB), while Type-II chromitites originated from a boninite-like parental melt. Both melts are characteristic of a fore-arc setting affected by extension during rollback subduction and have been related to the development of a Cambrian-Ordovician arc. These chromitites are extremely enriched in platinum-group elements (PGE), with bulk-rock PGE contents between 2,460 and 3,600 ppb. Also, the host dunites and pyroxenites exhibit high PGE contents (167 and 324 ppb, respectively), which are higher than those from the primitive mantle and global ophiolitic mantle peridotites. The PGE enrichment is expressed in positively-sloped chondrite-normalized PGE patterns, characterized by an enrichment in Pd-group PGE (PPGE: Rh, Pt and Pd) over the Ir-group PGE (IPGE: Os, Ir and Ru) and abundant platinum-group minerals (PGM) dominated by Rh-Pt-Pd phases (i.e. Rh-Ir-Pt-bearing arsenides and sulfarsenides, Pt-Ir-Pd-base-metal-bearing alloys, and Pt-Pd-bearing sulfides). The PGM assemblage is associated with base-metal sulfides (mostly pentlandite and chalcopyrite) and occurs at the edges of chromite or embedded within the interstitial (serpentinized) silicate groundmass. Their origin has been linked to direct crystallization from a S-As-rich melt(s), segregated by immiscibility from evolved volatile-rich small volume melts during subduction. At c. 380 Ma, retrograde amphibolite-facies metamorphism occurred during the exhumation of the HP-HT rocks of the Capelada Unit, which affected chromitites and their host rocks but preserved the primary composition of chromite cores of the chromitites. This event contributed to local remobilization of PGE as suggested by the negative slope between Pt and Pd and high Pt/Pd ratios in the studied chromitites, and host dunites and pyroxenites. In addition, it promoted the alteration of primary PGM assemblage and the formation of secondary PGM. Nanoscale observations made by focused ion beam high-resolution transmission electron microscopy (FIB/HRTEM) analysis of a composite grain of Rh-bearing arsenide with PGE-base-metal bearing alloys suggest the mobilization and accumulation of small nanoparticles of PGE and base-metals that precipitated from metamorphic fluids forming PGE-alloys. Finally, we offer a comparison of the Cabo Ortegal chromitites with other ophiolitic chromitites involved in the Variscan orogeny, from the Iberian Peninsula to the Polish Sudetes. The studied Cabo Ortegal chromitites are similar to the Variscan chromitites documented in the Bragança (northern Portugal) and Kraubath (Styria, Austria) ophiolitic massifs.
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19. |
- González-Jiménez, José M., et al.
(författare)
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Precious metals in magmatic Fe-Ni-Cu sulfides from the Potosí chromitite deposit, eastern Cuba
- 2020
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Ingår i: Ore Geology Reviews. - : Elsevier. - 0169-1368 .- 1872-7360. ; 118
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Tidskriftsartikel (refereegranskat)abstract
- The Moa-Baracoa ophiolite in eastern Cuba is one of the few known ophiolites that display sulfide mineralization attributable to a magmatic origin in association with podiform-chromite ores hosted in the mantle-crust transition. These sulfide ores chiefly consist of Fe-Ni-Cu sulfides, namely pyrrhotite, pentlandite, chalcopyrite and cubanite partly altered to valleriite. The sulfide mineralization is located along the contact between the podiform-like chromite ores and intruding pegmatitic gabroic dykes. The detailed mineralogical study of the sulfide mineralization coupled with the first ever laser ablation ICP-MS analysis reveals that this sulfide mineralization show contents of the precious metals (Os, Ir, Ru, Pt, Re, Au, Ag) and other (semi)-metals (Co, Ni, Cu, Se, Te, Bi, Pb, As Sb) comparable to those sulfides from the magmatic sulfide deposits associated with mafic complexes hosted in the continental crust. The results obtained from this study confirm that Fe-Ni-Cu sulfides at Potosí are magmatic in origin, and very likely derived from the solidification of droplets of sulfide melt segregated by immiscibility from the intruding mafic melts once they interacted with the pre-existing chromitite at the mantle-crust transition zone of the ophiolite. The immiscibility of sulfide melt was achieved as a result of a progressive increase of fS2, very likely triggered by a set of circumstances, including the progressive fractionation of the intruding mafic melt leading to increase of aSiO2 and accumulation of volatiles as well as the crystallization of oxides. Two main generations of pentlandite were observed. One generation is primary in origin and it was locally exsolved along with pyrrhotite from monosulfide solid solution (MSS) during low-temperature cooling. The second type of pentlandite resulted from the reaction of MSS with coexisting droplets of Cu-and Ni-rich sulfide melt. LA-ICP-MS analysis reveals that most precious metals (Ru, Os, Ir, Re, Au, Ag) were concentrated along with the base-metal sulfides (BMS), although their distribution among the different BMS (pyrrhotite, pentlandite, chalcopyrite and cubanite) does not strictly follow the expected distribution according to the known melt-solid and solid-solid partition coefficients. Unlike the other analyzed PGEs, Pt was not preferentially concentrated in BMS but as discrete micrometer-sized sperrylite grains. The crystallization of sperrylite took place before and contemporaneous to sulfide segregation, and Pt-As nanoparticles probably played an important role in the Pt uptake as nucleation seeds for the formation of micron-sized sperrylite grains. These observations highlight the open-system nature of the ore forming system as well as the important role of arsenic in concentrating PGE in high-temperature silicate and sulfide melts.
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20. |
- Gonzalez-Jimenez, José Maria, et al.
(författare)
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Titanian clinohumite and chondrodite in antigorite serpentinites from Central Chile : evidence for deep and cold subduction
- 2017
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Ingår i: European journal of mineralogy. - : E. Schweizerbart'sche Verlagsbuchhandlung. - 0935-1221 .- 1617-4011. ; 29:6, s. 959-970
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Tidskriftsartikel (refereegranskat)abstract
- Humite minerals, including Ti-rich, hydroxyl-dominant chondrodite and clinohumite, occur in Paleozoic antigorite serpentinite in the La Cabaña area, in the Chilean Coastal Cordillera (~38° 30 ′ S–73° 15 ′ W). This may be the first report from South America. Humite minerals are intergrown with Mn-rich olivine hosting antigorite blades in textural equilibrium, indicating a metamorphic origin. A comparison with previous results from piston-cylinder experiments and petrological studies of other high-P serpentinites constrains the formation conditions of the humite + olivine + antigorite assemblage to ca. 2.0–2.5 GPa and <600°C. Thus, the assemblage is interpreted as having formed during cold subduction of a segment of oceanic lithosphere to a depth >60 km, suggesting that the Paleozoic serpentinites were entrained into the mantle at higher P– T conditions than those experienced by the spatially associated olivine–lizardite metadunites and enclosing metasedimentary rocks (subducted to < 30 km). During exhumation along the subduction channel, high- P serpentinites together with metadunites underwent tectonic mingling with metasediments of the accretionary prism, preserving their signature of distinct metamorphic trajectories. This could be similar to the tectonic evolution of blueschists and high-P amphibolites found as isolated blocks in the metasediments of the Chilean Coastal Cordillera.
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21. |
- Hernández-González, Juan S., et al.
(författare)
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Petrology and geochemistry of high-Al chromitites from the Medellín Metaharzburgitic Unit (MMU), Colombia
- 2020
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Ingår i: Boletín de la Sociedad Geológica Mexicana. - : Universidad Nacional Autónoma de México. - 1405-3322 .- 1405-3322. ; 72:3
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Tidskriftsartikel (refereegranskat)abstract
- The Medellin Metaharzburgitic Unit (MMU), emplaced onto the western continental margin of Pangea during Triassic time, is located in the Central Cordillera of Colombia and consists of metaharzburgites, minor metadunites and chromitite bodies (Patio Bonito and San Pedro ore deposits). The ultramafic rocks contain relicts of mantle-derived olivine, chromian spinel and minor orthopyroxene, and a later metamorphic mineral assemblage composed by tremolite, chlorite, talc, fine-grained recrystallized olivine, serpentine-group minerals, magnetite, and secondary chromian spinel, formed during the thermal evolution of the unit. The Cr# [Cr/(Cr+Al) atomic ratio] of the accessory primary chromian spinel in the metaperidotites ranges from 0.58 to 0.62 and overlaps those of supra-subduction peridotites from ophiolites. According to textural and compositional variations, the accessory chromian spinel in the metaperidotites can be classified into three groups: i) partially altered chromian spinel with an Al-rich core, ii) porous, Cr-Fe2+-enriched and Al-Mg-depleted chromian spinel, and iii) homogeneous Fe3+-rich chromian spinel. These variations can be related to superimposed medium-T metamorphism that reached amphibolite facies (ca. 600 ºC). Chromitite bodies associated with the metaperidotites have massive and semi-massive textures, and mainly consist of chromian spinel crystals, which show large unaltered cores surrounded by thin alteration rims of ferrian chromian spinel and chlorite. Chromitites are Al-rich (#Cr <0.6) and strongly depleted in platinum group elements (ΣPGE <41 ppb). The primary petrological and geochemical characteristics preserved in the metaperidotites and chromitites indicate that the MMU formed at shallow levels of a suboceanic lithospheric mantle related to a supra-subduction zone (back-arc basin/incipient arc scenario), and that the chromitites crystallized from a tholeiitic magma (back-arc basin basalt type).
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22. |
- Jansson, Nils, et al.
(författare)
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Cobalt and REE distribution at the Zinkgruvan Zn-Pb-Ag and Cu deposit, Bergslagen, Sweden
- 2022
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Ingår i: EGU General Assembly 2022. - : Copernicus GmbH.
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Konferensbidrag (refereegranskat)abstract
- The metamorphosed, stratiform, c. 1.9 Ga Zinkgruvan Zn-Pb-Ag deposit is one of Europe’s largest producers of Zn. Since 2010, disseminated Cu mineralization is also mined from dolomite marble in a hydrothermal vent-proximal position in the stratigraphic footwall. Local enrichments of Co and REE exist in the vent-proximal mineralization types, albeit their distribution is poorly known. This contribution provides new data on the distribution of Co and REE within the Zinkgruvan deposit.LA-ICP-MS analysis suggest that lattice-bound cobalt in sphalerite range between 44 ppm and 1372 ppm, with the lowest and highest values occurring in distal and proximal mineralization, respectively. Proximal Co-rich sphalerite is always Fe-rich. Lattice-bound Co also occur in pyrrhotite; ranging from 52 ppm in distal ore to 1608 ppm in proximal ore. There is a concurrent increase in lattice-bound Ni from 3 ppm to 529 ppm. In proximal ore, Co is also hosted by cobalt minerals such as costibite (27.37 wt.% Co), safflorite (16.21 wt.% Co), nickeline (7.54 wt.% Co), cobaltite (32.74 wt.% Co) and cobaltpentlandite (25.49 wt.% Co). Automated quantitative mineralogy suggest that these minerals are highly subordinate to sphalerite (<70.11%) and pyrrhotite (<14.69%), amounting to <2.88% cobalt minerals with safflorite being most common (up to 2.67%). Cobalt deportment calculations suggest that the proportion of whole-rock Co that is lattice-bound to sphalerite and pyrrhotite ranges from 7.80% to 100%, with sphalerite being the main host. Whole-rock As and Ni contents pose a strong control on whether Co occurs lattice-bound or as Co minerals.LA-ICP-MS analysis show that accessory apatite in proximal, marble-hosted Cu mineralization carries a few thousand ppm ∑REE, but locally up to c. 1.6 wt.% ∑REE. The apatite can be subdivided into two types. Type 1 apatite is characterized by dumbbell-shaped chondrite-normalized REE profiles with relative enrichment of in particular Sm-Tb, depletion of Yb-Lu relative to La-Pr, local positive Gd anomalies, and weak positive to negative Eu anomalies. Type 2 apatite is characterized by flat to negatively sloping REE profiles from La to Gd and relative HREE depletion. Additional REE is hosted by monazite. Type 1 apatite was only found as a gangue to Cu mineralization. The Type 1 apatite REE signature is characteristic of hydrothermal apatite, and a direct genetic association with vent-proximal Cu mineralization can be inferred.Comparison with published REE contents in apatite suggest that vent-proximal Zinkgruvan apatite is locally as REE-rich as apatite from Kiruna-type apatite iron oxide deposits, and more REE-rich than apatite in other metamorphosed sediment-hosted sulphide deposits in the world, such as the Gamsberg deposit (RSA).
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23. |
- Kaasalainen, Hanna, et al.
(författare)
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Impact of declining oxygen conditions on metal(loid) release from partially oxidized waste rock
- 2019
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Ingår i: Environmental Science and Pollution Research. - : Springer. - 0944-1344 .- 1614-7499. ; 26:20, s. 20712-20730
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Tidskriftsartikel (refereegranskat)abstract
- The best available technology for preventing the formation of acid drainage water from the sulfidic waste rock at mine closure aims to limit the oxygen access to the waste. There is, however, a concern that contaminants associated with secondary minerals become remobilized due to changing environmental conditions. Metal(loid) mobility from partially oxidized sulfidic waste rock under declining and limited oxygen conditions was studied in unsaturated column experiments. The concentrations of sulfate and metal(loid)s peaked coincidently with declining oxygen conditions from 100 to < 5 sat-% and to a lesser extent following a further decrease in the oxygen level during the experiment. However, the peak concentrations only lasted for a short time and were lower or in the similar concentration range as in the leachate from a reference column leached under atmospheric conditions. Despite the acid pH (~ 3), the overall quality of the leachate formed under limited oxygen conditions clearly improved compared with atmospheric conditions. In particular, the release of As was two orders of magnitude lower, while cationic metals such as Fe, Cu, Mn, and Zn also decreased, although to a lesser extent. Decreased sulfide oxidation is considered the primary reason for the improved water quality under limited oxygen conditions. Another reason may be the immobility of Fe with the incorporation of metal(loid)s in Fe(III) minerals, in contrast to the expected mobilization of Fe. The peaking metal(loid) concentrations are probably due to remobilization from solid Fe(III)-sulfate phases, while the relatively high concentrations of Al, Mn, and Zn under limited oxygen conditions were due to release from the adsorbed/exchangeable fraction. Despite the peaking metal(loid) concentrations during declining oxygen conditions, it is clear that the primary remediation goal is to prevent further sulfide oxidation.
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24. |
- López-Males, Gladys G., et al.
(författare)
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New mineralogical data on platinum-group minerals from the Río Santiago alluvial placer, Esmeraldas province, Ecuador
- 2020
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Ingår i: Boletín de la Sociedad Geológica Mexicana. - : Universidad Nacional Autónoma de México. - 1405-3322. ; 72:3
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Tidskriftsartikel (refereegranskat)abstract
- Mineralogical studies on platinum-group minerals found in placer deposits from the Río Santiago (Ecuador) are scarce. In this investigation, one sample collected from the Río Santiago alluvial placer was studied via a multi-disciplinary approach, including optical microscopy, scanning electron microscopy, electron microprobe, and Raman spectroscopy. Whole-rock geochemistry data of the sample confirms elevated Au and platinum-group elements contents and the chondrite-normalized pattern reveals pronounced positive Ir and Pt anomalies. Free grains of platinum-group minerals were separated via hydroseparation techniques and identified as: i) Pt-Fe alloy (Pt3Fe), ii) tulameenite (Pt2FeCu) and iii) hongshiite (PtCu). The most abundant platinum-group mineral is Pt-Fe alloy (85%) that occasionally hosts cuprorhodsite (CuRh2S4) inclusions. Although the primary source remains unknown, the geochemical and mineralogical data suggests that the source of platinum-group minerals in the Río Santiago alluvial placer is a mafic-ultramafic Ural-Alaska type complex. Possible primary sources are the mafic and ultramafic rocks found in the mafic basement of the coastal region and the Western Cordillera (Piñón, San Juan and Pallatanga units), which derive from the Late Cretaceous Caribbean Colombia Oceanic Plateau (CCOP).
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25. |
- Navidad, Marina, et al.
(författare)
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Ordovician magmatism in the Eastern Pyrenees : Implications for the geodynamic evolution of northern Gondwana
- 2018
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Ingår i: Lithos. - : Elsevier. - 0024-4937 .- 1872-6143. ; 314-315, s. 479-496
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Tidskriftsartikel (refereegranskat)abstract
- New data on the geochemistry and geochronology of different felsic gneisses and metabasites from the Variscan massifs of Eastern Pyrenees have allowed us to shed some light on the Ordovician magmatic evolution in northern Gondwana during the opening of the Rheic Ocean. According to these data, the Ordovician magmatism represents a continuous event of anatectic melting, with limited mantle influence, that lasted 20 m.y., from Early to Late Ordovician. In the Canigó massif, peraluminous monzogranitic and granodioritic metaigneous rocks intruded a late Ediacaran-early Cambrian sequence at 464.3 ± 1.6 Ma and 461.6 ± 1.5 Ma, respectively, and leucogranitic gneisses intruded at 457.4 ± 1.6 Ma. Whole-rock geochemistry of the felsic rocks (plutonic and subvolcanic) points to a volcanic arc setting. However, the geological context and the geochemistry of the coeval metabasites are incompatible with this tectonic setting and point out to the inception of an extensional margin. Sm-Nd isotopic data suggest that the felsic rocks are derived from the anatexis of juvenile igneous rocks (probably Cadomian), mixed with older crustal components present in a late Neoproterozoic crust. We interpret that the Ordovician magmas inherited the geochemical signature of the rocks formed at the former Cadomian convergent margin. The variation of the εNd values from −2 to −4 in the Lower Ordovician rocks, to −5 in the Upper Ordovician rocks suggests a greater implication of the older component in a within-plate geodynamic context, coeval with the evolution of an extensional marginal basin linked to the opening of the Rheic Ocean. A similar isotopic evolution, more depleted first and with a greater implication of the crust in the younger sample, is shown by the studied metabasites.
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