| 1. |
- Cámara, Fernando, 1967-, et al.
(författare)
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Zinkgruvanite, Ba4Mn2+4Fe3+2(Si2O7)2(SO4)2O2(OH)2, a new ericssonite-group mineral from the Zinkgruvan Zn-Pb-Ag-Cu deposit, Askersund, Örebro County, Sweden.
- 2021
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Ingår i: European journal of mineralogy. - : Nicolaus Copernicus University Press. - 0935-1221 .- 1617-4011. ; 33:6, s. 659-673
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Tidskriftsartikel (refereegranskat)abstract
- Zinkgruvanite, ideally Ba4Mn2+4Fe3+2(Si2O7)2(SO4)2O2(OH)2, is a new member of the ericssonite group, found in Ba-rich drill core samples from a sphalerite+galena- and diopside-rich metatuffite succession from the Zinkgruvan mine, Örebro county, Sweden. Zinkgruvanite is associated with massive baryte, barytocalcite, diopside and minor witherite, cerchiaraite-(Al) and sulfide minerals. It occurs as subhedral to euhedral flattened and elongated crystals up to 4 mm. It is almost black, semi-opaque with a dark brown streak. The luster is vitreous to sub-adamantine on crystal faces, resinous on fractures. The mineral is brittle with an uneven fracture. VHN100 = 539 and HMohs ~4½. In thin fragments, it is reddish-black, translucent and optically biaxial (+), 2Vz > 70°. Pleochroism is strong, deep brown-red (E ⊥ {001} cleavage) to olive-pale brown. Chemical point analyses by WDS-EPMA together with iron valencies determined from Mössbauer spectroscopy, yielded the empirical formula (based on 26 O+OH+F+Cl anions): (Ba4.02Na0.03)Σ4.05(Mn1.79Fe2+1.56Fe3+0.42Mg0.14Ca0.10Ni0.01Zn0.01)Σ4.03 (Fe3+1.74Ti0.20Al0.06)Σ2.00Si4(S1.61Si0.32P0.07)Σ1.99O24(OH1.63Cl0.29F0.08)Σ2.00. The mineral is triclinic, space group P–1, with unit-cell parameters a = 5.3982(1) Å, b = 7.0237(1) Å, c = 14.8108(4) Å, α = 98.256(2)º, β = 93.379(2)º, γ = 89.985(2)º and V = 554.75(2) Å3 for Z = 1. The eight strongest X-ray powder diffraction lines are [d Å (I%; hkl)]: 3.508 (70; 103), 2.980(70; 11–4), 2.814 (68; 1–22), 2.777 (70; 121), 2.699 (714; 200), 2.680 (68; 20–1), 2.125 (100; 124, 204), 2.107 (96; –221). The crystal structure (R1 = 0.0379 for 3204 reflections) is an array of TS (titanium silicate) blocks alternating with intermediate blocks. The TS blocks consist of HOH sheets (H = heteropolyhedral, O = octahedral) parallel to (001). In the O sheet, the Mn2+-dominant MO(1,2,3) sites give ideally Mn2+4 pfu. In the H sheet, the Fe3+-dominant MH sites and AP(1) sites give ideally Fe3+2Ba2 pfu. In the intermediate block, SO4 oxyanions and eleven coordinated Ba atoms give ideally 2 × SO4Ba pfu. Zinkgruvanite is related to ericssonite and ferro-ericssonite in having the same topology and type of linkage of layers in the TS block. Zinkgruvanite is also closely compositionally related to yoshimuraite, Ba4Mn4Ti2(Si2O7)2(PO4)2O2(OH)2, via the coupled heterovalent substitution 2 Ti4+ + 2 (PO4)3- →2 Fe3+ + 2 (SO4)2-, but presents a different type of linkage. The new mineral probably formed during a late stage of regional metamorphism of a Ba-enriched, syngenetic protolith, involving locally generated oxidized fluids of high salinity.
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| 2. |
- Sandgren, Fredrik, 1967-, et al.
(författare)
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Towns and rural industrialisation in Sweden 1850-1890: A spatial statistical approach
- 2009
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Ingår i: Scandinavian Economic History Review. - London : Routledge. - 0358-5522 .- 1750-2837. ; 57:3, s. 229-251
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Tidskriftsartikel (refereegranskat)abstract
- Using a spatial statistical analysis we study the relation between rural industrial employment and distance to towns and access to communications in nineteenth century Sweden. Our results show that rural parishes with access to communicationshad a higher proportion of rural industrial workers than parishes without. In a region with few towns, the south-east of Sweden, parishes close to large towns had a higher proportion of industrial employees than distant parishes in1850, while no significant correlation was observed in 1890. In a region with arelatively dense urban system, Mälardalen, only in 1890 did parishes close to large towns show a higher proportion of rural industrial workers than did more distant parishes. However, the mean positive effect was negligible beyond 10 km. Thus, in the second half of the nineteenth century the immediate urban hinterland was industrialising prior to large scale urbanisation and urban industrialisation.
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| 3. |
- Andersson, Stefan, et al.
(författare)
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Metamorphism and deformation of a Palaeoproterozoic polymetallic sulphide-oxide mineralisation : Hornkullen, Bergslagen, Sweden
- 2016
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Ingår i: GFF. - : Informa UK Limited. - 1103-5897 .- 2000-0863. ; 138:3, s. 410-423
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Tidskriftsartikel (refereegranskat)abstract
- The Hornkullen mineralisation is situated in the westernmost part of the Bergslagen ore province, south-central Sweden. Here, polymetallic sulphides and oxides are hosted by an inlier of Svecofennian, c. 1.9Ga skarn-bearing metavolcanic units, enclosed in the c. 1.8Ga Filipstad granite belonging to the Transscandinavian Igneous Belt. The Ag- and Au-bearing mineralisation is dominated by veins and impregnations of magnetite, pyrrhotite, galena, chalcopyrite and arsenopyrite with subordinate pyrite, sphalerite, ilmenite, lollingite, Pb-Fe-Ag-Cu-Sb sulphosalts and rare gudmundite, pentlandite and molybdenite. Overall, a detailed textural and mineralogical study of the ore assemblages suggests significant deformation and remobilisation at high temperature, which is corroborated by sulphide geothermobarometry. The arsenopyrite geothermometer yields an average temperature of c. 525 degrees C, which is likely to be the result of metamorphic re-equilibration. Sphalerite geobarometry gives peak pressures of c. 300-400MPa, albeit with caveats. The combined observations suggest that the present mineralogical and textural nature of the ore assemblages at Hornkullen is primarily related to remobilisation during Svecokarelian regional metamorphism of a pre-existing, most likely syn-volcanic mineralisation. This scenario is likely to be applicable to many other Svecofennian metasupracrustal-hosted deposits in the Bergslagen ore province.
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| 4. |
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| 5. |
- Andersson, Stefan S., et al.
(författare)
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Apatite as a tracer of the source, chemistry and evolution of ore-forming fluids : The case of the Olserum-Djupedal REE-phosphate mineralisation, SE Sweden
- 2019
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Ingår i: Geochimica et Cosmochimica Acta. - : PERGAMON-ELSEVIER SCIENCE LTD. - 0016-7037 .- 1872-9533. ; 255, s. 163-187
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Tidskriftsartikel (refereegranskat)abstract
- This study explores the suitability of apatite as a tracer of the source(s), chemistry, and evolution of ore-forming hydrothermal fluids. This is tested by analysing the halogen (F, Cl, Br, and I), stable Cl isotopic, and trace element compositions of fluorapatite from the regional-scale Olserum-Djupedal rare earth element (REE) phosphate mineralisation in SE Sweden, which is dominated by monazite-(Ce), xenotime-(Y), and fluorapatite. The primary hydrothermal fluid flow system is recorded in a sequence from proximal granite-hosted to distal metasediment-hosted fluorapatite. Along this sequence, primary fluorapatite shows a gradual increase of Cl and Br concentrations and in (Gd/Yb)N, a decrease of F and I concentrations, a decrease in δ37Cl values, in (La/Sm)N, and partly in (La/Yb)N and (Y/Ho)N. Local compositional differences of halogen and trace element concentrations have developed along rims and in domains adjacent to fractures of fluorapatite due to late-stage partial reaction with fracture fluids. These differences are insignificant compared to the larger deposit-scale zoning. This suggests that apatite can retain the primary record of the original ore-forming fluid despite later overprinting fluid events. The agreement between Br/Cl and I/Cl ratios of apatite and those of co-existing fluid inclusions at lower temperatures indicates that only a minor fractionation of Br from I occurs during apatite precipitation. The halogen ratios of apatite can thus be used as a first-order estimate for the composition of the ore-forming fluid. Taking the small fractionation factors for Cl isotopes between apatite and co-existing fluid at high temperatures into account, we propose that the Cl isotopic composition of apatite and the halogen ratios derived from the apatite composition can be used jointly to trace the source(s) of ore-forming fluids. By contrast, most trace elements incorporated in apatite are affected by the host rock environment and by fluid-mineral partitioning due to growth competition between co-crystallising minerals. Collectively, apatite is sensitive to changing fluid compositions, yet it is also able to record the character of primary ore-forming fluids. Thus, apatite is suitable for tracing the origin, chemistry, and evolution of fluids in hydrothermal ore-forming settings.
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| 6. |
- Andersson, Stefan S., et al.
(författare)
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Mineral paragenesis and sulphide trace element distribution in the metamorphosed Lovisa Zn-Pb deposit, Bergslagen (Sweden), as revealed by 3D X-ray tomography, ore petrography and LA-ICP-MS analysis
- 2022
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Ingår i: Ore Geology Reviews. - : Elsevier BV. - 0169-1368 .- 1872-7360. ; 140
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Tidskriftsartikel (refereegranskat)abstract
- This study encompasses the ore mineralogy, textures and sulphide trace element chemistry of the Palaeoproterozoic Lovisa stratiform Zn-Pb deposit and the stratigraphically underlying Lovisa Fe Formation in the Bergslagen ore province (Sweden). We investigate the relative timing of formation and subsequent modifications of its ores in relation to the c. 1.87-1.80 Ga Svecokarelian orogeny. The Lovisa Zn-Pb deposit consists of several different ore types. The massive sphalerite-galena ore is distinctly deformed, exhibiting a multiple-scale "ball ore" texture with rounded silicate clasts within a deformed, fine-grained sulphide matrix. Underlying the massive ore is a locally folded, sphalerite-rich laminated ore, interpreted to represent a metamorphosed relict primary lamination. Several generations of sphalerite-galena fracture fillings and veins occur adjacent to the main ore zones and they cross-cut early ductile structures and metamorphic features. The trace element signatures of the sphalerite-galena infillings generally mimic those of the two main ore zones, thus supporting an origin by localised remobilisation of the primary sulphide ore and demonstrating limited trace element redistribution during this process. In contrast, discrete sulphosalt-rich fracture fillings cross-cutting earlier galena-chalcopyriterich fracture fillings and veinlets in the Lovisa Fe Formation suggest a significant but still relatively localised redistribution of metals. Trace element mapping of sulphides from the Lovisa Zn-Pb deposit reveals that inclusion-free overgrowths on pyrite crystals are locally Co-enriched compared to the cores, which resulted from the redistribution of Co during late metamorphic processes. Combined textural and geochemical evidence suggest that the originally syngenetic exhalative sulphide ore at Lovisa was locally strongly affected by polyphase deformation and remobilisation. This was initiated during the first stage of amphibolite facies grade regional metamorphism and deformation (D1, c. 1.87-1.85 Ga) but is mostly evident from the later stages (D2) and the evolution to retrograde and brittle conditions (c. 1.83-1.80 Ga and later).
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| 7. |
- Andersson, Stefan S., et al.
(författare)
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Mineralogy, paragenesis, and mineral chemistry of REEs in the Olserum-Djupedal REE-phosphate mineralization, SE Sweden
- 2018
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Ingår i: American Mineralogist. - : MINERALOGICAL SOC AMER. - 0003-004X .- 1945-3027. ; 103:1, s. 125-142
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Tidskriftsartikel (refereegranskat)abstract
- The rapidly growing use of rare earth elements and yttrium (REE) in modern-day technologies, not least within the fields of green and carbon-free energy applications, requires exploitation of new REE deposits and deposit types. In this perspective, it is vital to develop a fundamental understanding of the behavior of REE in natural hydrothermal systems and the formation of hydrothermal REE deposits. In this study, we establish a mineralogical, textural, and mineral-chemical framework for a new type of deposit, the hydrothermal Olserum-Djupedal REE-phosphate mineralization in SE Sweden. An early, high-temperature REE stage is characterized by abundant monazite-(Ce) and xenotime-(Y) coexisting with fluorapatite and subordinate amounts of (Y,REE,U,Fe)-(Nb,Ta) oxides. During a subsequent stage, allanite-(Ce) and ferriallanite-(Ce) formed locally, partly resulting from the breakdown of primary monazite-(Ce). Alteration of allanite-(Ce) or ferriallanite-(Ce) to bastnasite-(Ce) and minor synchysite-(Ce) at lower temperatures represents the latest stage of REE mineral formation. The paragenetic sequence and mineral chemistry of the allanites record an increase in Ca content in the fluid. We suggest that this local increase in Ca, in conjunction with changes in oxidation state, were the key factors controlling the stability of monazite-(Ce) in the assemblages of the Olserum-Djupedal deposit. We interpret the alteration and replacement of primary monazite-(Ce), xenotime-(Y), fluorapatite, and minor (Y,REE,U,Fe)-(Nb, Ta) oxide phase(s), to be the consequence of coupled dissolution-reprecipitation processes. These processes mobilized REE,Th,U, and Nb-Ta, which caused the formation of secondary monazite-(Ce), xenotime-(Y), fluorapatite, and minor amounts of allanite-(Ce) and ferriallanite-(Ce). In addition, these alteration processes produced uraninite, thorite, columbite-(Fe), and uncharacterized (Th,U,Y,Ca)-silicates. Textural relations show that the dissolution-reprecipitation processes affecting fluorapatite preceded those affecting monazite-(Ce), xenotime-(Y), and the (Y, REE, U, Fe)-(Nb, Ta) oxide phase(s). The mineralogy of the primary ore mineralization and the subsequently formed alteration assemblages demonstrate the combined mobility of REE and HFSE in a natural F-bearing high-temperature hydrothermal system. The observed coprecipitation of monazite-(Ce), xenotime-(Y), and fluorapatite during the primary REE mineralization stage highlights the need for further research on the potentially important role of the phosphate ligand in hydrothermal REE transporting systems.
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| 8. |
- Andersson, Stefan S., et al.
(författare)
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Origin of the high-temperature Olserum-Djupedal REE-phosphate mineralisation, SE Sweden : A unique contact metamorphic-hydrothermal system
- 2018
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Ingår i: Ore Geology Reviews. - : Elsevier BV. - 0169-1368 .- 1872-7360. ; 101, s. 740-764
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Tidskriftsartikel (refereegranskat)abstract
- The Swedish part of the Fennoscandian Shield hosts a variety of rare earth element (REE) deposits, including magmatic to magmatic-hydrothermal types. This paper focuses on the origin of the Olserum-Djupedal REEphosphate mineralisation located in the sparsely studied Vastervik region, SE Sweden. Here, mineralisation occurs in three main areas, Olserum, Djupedal and Bersummen. Primary hydrothermal REE mineralisation formed at high temperatures (about 600 degrees C), leading to precipitation of monazite-(Ce), xenotime-(Y), fluor apatite and minor (Y,REE,U,Fe)-(Nb,Ta)-oxides in veins and vein zones dominated by biotite, amphibole, magnetite and quartz. The veins are hosted primarily by metasedimentary rocks present close to, or within, the contact aureole of a local 1.8 Ga ferroan alkali feldspar granite pluton, but also occur within in the chemically most primitive granite in the outermost part of that pluton. In the Djupedal area, REE-mineralised metasedimentary bodies are extensively migmatised, with migmatisation post-dating the main stage of mineralisation. In the Olserum and Bersummen areas, the REE-bearing veins are cross-cut by abundant pegmatitic to granitic dykes. The field-relationships demonstrate a-protracted magmatic evolution of the granitic,pluton and a clear spatial and temporal relationship of the REE mineralisation to the granite. The major and trace element chemistry of ore-associated biotite and magnetite support genetic links between all mineralised areas. Biotite mineral chemistry data further demonstrate a distinct chemical trend from meta sediment-hosted ore-associated biotite distal to the major contact of the granite to the biotite in the granite hosted veins. This trend is characterised by a systematic decrease in Mg and Na and a coupled increase in Fe and Ti with proximity to the granite-hosted veins. The halogen compositions of ore-associated biotite indicate elevated contents of HCl and HF in the primary REE mineralising fluid. Calculated log(f(HF)/f(HCL)) values in the Olserum area suggest a constant ratio of about -1 at temperatures of 650-550 degrees C during the evolution of the primary hydrothermal system. In the Djupedal and Bersummen areas, the fluid locally equilibrated at lower log (f(HF)/f(HCl)) values down to -2. High Na contents in ore-associated biotite and amphibole, and the abundance of primary ore-associated biotite indicate a K- and Na-rich character of the primary REE mineralising fluid and suggest initial high-temperature K-Na metasomatism. With subsequent cooling of the system, the fluid evolved locally to more Ca-rich compositions as indicated by the presence of the Ca-rich minerals allanite-(Ce) and uvitic tourmaline and by the significant calcic alteration of monazite-(Ce). The later Ca-rich stages were probably coeval with low to medium-high temperature (200-500 degrees C) Na-Ca metasomatism variably affecting the granite and the wall rocks, producing distinct white quartz-plagioclase rocks. All observations and data lead us to discard the prevailing model that the REE mineralisation in the Olserum-Djupedal district represents assimilated and remobilised former heavy mineral-rich beds. Instead, we propose that the primary REE mineralisation formed by granite-derived fluids enriched in REE and P that were expelled early during the evolution of a local granitic pluton. The REE mineralisation developed primarily in the contact aureole of this granite and represents the product of a high temperature contact metamorphic-hydrothermal mineralising system. The REE mineralisation probably formed synchronously with K-Na and subsequent Na-Ca metasomatism affecting the granite and the wall rocks. The later Na-Ca metasomatic stage is probably related to a regional Na +/- Ca metasomatic and associated U +/- REE mineralising system operating concurrently with granitic magmatism at c. 1.8 Ga in the Vastervik region. This highlights the potential for discovering hitherto unknown REE deposits and for the reappraisal of already known deposits in this part of the Fennoscandian Shield.
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