| 1. |
- Budzyn, Bartosz, et al.
(author)
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Experimental constraints on the relative stabilities of the two systems monazite-(Ce) - allanite-(Ce) - fluorapatite and xenotime-(Y) - (Y,HREE)-rich epidote - (Y,HREE)-rich fluorapatite, in high Ca and Na-Ca environments under P-T conditions of 200-1000 MPa and 450-750 A degrees C
- 2017
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In: Mineralogy and Petrology. - : SPRINGER WIEN. - 0930-0708 .- 1438-1168. ; 111:2, s. 183-217
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Journal article (peer-reviewed)abstract
- The relative stabilities of phases within the two systems monazite-(Ce) - fluorapatite - allanite-(Ce) and xenotime-(Y) - (Y,HREE)-rich fluorapatite - (Y,HREE)-rich epidote have been tested experimentally as a function of pressure and temperature in systems roughly replicating granitic to pelitic composition with high and moderate bulk CaO/Na2O ratios over a wide range of P-T conditions from 200 to 1000 MPa and 450 to 750 A degrees C via four sets of experiments. These included (1) monazite-(Ce), labradorite, sanidine, biotite, muscovite, SiO2, CaF2, and 2 M Ca(OH)(2); (2) monazite-(Ce), albite, sanidine, biotite, muscovite, SiO2, CaF2, Na2Si2O5, and H2O; (3) xenotime-(Y), labradorite, sanidine, biotite, muscovite, garnet, SiO2, CaF2, and 2 M Ca(OH)(2); and (4) xenotime-(Y), albite, sanidine, biotite, muscovite, garnet, SiO2, CaF2, Na2Si2O5, and H2O. Monazite-(Ce) breakdown was documented in experimental sets (1) and (2). In experimental set (1), the Ca high activity (estimated bulk CaO/Na2O ratio of 13.3) promoted the formation of REE-rich epidote, allanite-(Ce), REE-rich fluorapatite, and fluorcalciobritholite at the expense of monazite-(Ce). In contrast, a bulk CaO/Na2O ratio of similar to 1.0 in runs in set (2) prevented the formation of REE-rich epidote and allanite-(Ce). The reacted monazite-(Ce) was partially replaced by REE-rich fluorapatite-fluorcalciobritholite in all runs, REE-rich steacyite in experiments at 450 A degrees C, 200-1000 MPa, and 550 A degrees C, 200-600 MPa, and minor cheralite in runs at 650-750 A degrees C, 200-1000 MPa. The experimental results support previous natural observations and thermodynamic modeling of phase equilibria, which demonstrate that an increased CaO bulk content expands the stability field of allanite-(Ce) relative to monazite-(Ce) at higher temperatures indicating that the relative stabilities of monazite-(Ce) and allanite-(Ce) depend on the bulk CaO/Na2O ratio. The experiments also provide new insights into the re-equilibration of monazite-(Ce) via fluid-aided coupled dissolution-reprecipitation, which affects the Th-U-Pb system in runs at 450 A degrees C, 200-1000 MPa, and 550 A degrees C, 200-600 MPa. A lack of compositional alteration in the Th, U, and Pb in monazite-(Ce) at 550 A degrees C, 800-1000 MPa, and in experiments at 650-750 A degrees C, 200-1000 MPa indicates the limited influence of fluid-mediated alteration on volume diffusion under high P-T conditions. Experimental sets (3) and (4) resulted in xenotime-(Y) breakdown and partial replacement by (Y,REE)-rich fluorapatite to Y-rich fluorcalciobritholite. Additionally, (Y,HREE)-rich epidote formed at the expense of xenotime-(Y) in three runs with 2 M Ca(OH)(2) fluid, at 550 A degrees C, 800 MPa; 650 A degrees C, 800 MPa; and 650 A degrees C, 1000 MPa similar to the experiments involving monazite-(Ce). These results confirm that replacement of xenotime-(Y) by (Y,HREE)-rich epidote is induced by a high Ca bulk content with a high CaO/Na2O ratio. These experiments demonstrate also that the relative stabilities of xenotime-(Y) and (Y,HREE)-rich epidote are strongly controlled by pressure.
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| 2. |
- Galas, Andrzej, et al.
(author)
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Origin of andradite in the Quaternary volcanic Andahua Group, Central Volcanic Zone, Peruvian Andes
- 2021
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In: Mineralogy and Petrology. - : Springer Nature. - 0930-0708 .- 1438-1168. ; 115:3, s. 257-269
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Journal article (peer-reviewed)abstract
- Euhedral andradite crystals were found in trachyandesitic (latitic) lavas of the volcanic Andahua Group (AG) in the Central Andes. The AG comprises around 150 volcanic centers, most of wich are monogenetic. The studied andradite is complexly zoned (enriched in Ca and Al in its core and mantle, and in Fe in this compositionally homogenous rim). The core-mantle regions contain inclusions of anhydrite, halite, S- and Cl-bearing silicate glass, quartz, anorthite, wollastonite magnetite and clinopyroxene. The chemical compositions of the garnet and its inclusions suggest their contact metamorphic to pyrometamorphic origin. The observed zoning pattern and changes in the type and abundance of inclusions are indicative of an abrupt change in temperature and subsequent devolatilization of sulfates and halides during the garnet growth. This process is interpreted to have taken place entirely within a captured xenolith of evaporite-bearing wall rock in the host trachyandesitic magma. The devolitilization of sediments, especially sulfur-bearing phases, may have resulted in occasional but voluminous emissions of gases and may be regarded as a potential hazard associated with the AG volcanism.
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| 3. |
- Goluchowska, Karolina, et al.
(author)
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Magma storage of an alkali ultramafic igneous suite from Chamberlindalen, SW Svalbard
- 2016
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In: Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0930-0708 .- 1438-1168. ; 110:5, s. 623-638
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Journal article (peer-reviewed)abstract
- An alkali mafic-ultramafic igneous suite of composite intrusions, lenses and associated greenstones are hosted by Neoproterozoic metasedimentary sequences in Chamberlindalen, Southwest Svalbard. This study focuses on the alkali igneous suite of Chamberlindalen with a view to determining the conditions of magma storage. The rocks from Chamberlindalen display cumulate textures, are highly magnesian and are classified as alkaline by the occurrence of kaersutite. They have textures that indicate cocrystallization of primary magmatic minerals such as diopside, kaersutite-ferrokaersutite and biotite-phlogopite in different proportions. The historic magma plumbing system for the alkaline cumulates has been reconstructed by thermobarometry. Diopside and kaersutite crystallization in the alkaline cumulates show a dominant level of magma storage between 30 and 50 km in the subcontinental lithospheric mantle.
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| 4. |
- Holtstam, Dan, et al.
(author)
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Brattforsite, Mn19(AsO3)12Cl2, a new arsenite mineral relatedto magnussonite, from Brattforsgruvan, Nordmark,Värmland, Sweden
- 2021
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In: Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0930-0708 .- 1438-1168. ; 115:5, s. 595-609
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Journal article (peer-reviewed)abstract
- Brattforsite is an approved mineral (IMA2019-127), with ideal formula Mn19(AsO3)12Cl2. Associated minerals in the type specimen from the Brattfors mine, Nordmark (Värmland, Sweden) include jacobsite, alleghanyite, phlogopite, calcite anddolomite. Brattforsite, forming subhedral, mostly equant crystals up to 0.5 mm across, is orange to reddish-brown with a white streak, and translucent with a resinous to vitreous lustre. The fracture is uneven to subconchoidal, and no cleavage is observed. It is very weakly pleochroic in yellow, optically biaxial (–) with 2V = 44(5)° and has calculated mean refractive index of 1.981. Measured and calculated density values are 4.49(1) and 4.54(1) g·cm−3, respectively. Chemical analyses yields (in wt%): MgO 0.62, CaO 1.26, MnO 48.66, FeO 0.13, As2O3 46.72, Cl 2.61, H2Ocalc 0.07, O ≡ Cl –0.59, sum 99.49, corresponding to the empirical formula (Mn17.67Ca0.58Mg0.40Fe0.05)Σ18.70As12.17O35.90Cl1.90(OH)0.20, based on 38 (O + Cl + OH) atoms per formula unit. The five strongest Bragg peaks in the powder X-ray diffraction pattern are [d (Å), I (%), (hkl)]: 2.843,100, (-444)); 2.828, 99,(444); 1.731, 32, (880); 2.448, 28, (800); 1.739, 25, (088). Brattforsite is monoclinic and pseudotetragonal, space group I2/a, with unit-cell parameters a = 19.5806(7), b = 19.5763(7), c = 19.7595(7) Å, β = 90.393(3)°, V = 7573.9(5) Å3 and Z = 8. The crystal structure was solved and refined to an R1 index of 3.4% for 7445 reflections [Fo > 4σ(Fo)]. Brattforsite has the same overall structural topology as magnussonite (i.e., the species can be considered as homeotypic), but with 12 independent tetrahedrally coordinated As sites and 21 Mn sites with varying (4–8) coordination. The Mn-centered polyhedra, bonded through edge- and face-sharing, give rise to a three-dimensional framework. The (AsO3)3− groups are bonded to this framework through corner- and edge-sharing. Spectroscopic measurements (optical absorption, Raman, FTIR) carried out support the interpretation of the compositional and structural data.
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| 5. |
- Holtstam, Dan, 1963-, et al.
(author)
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Recognition and approval of potassic-richerite, an amphibole supergroup mineral, from the Pajsberg mines, Filipstad, Sweden.
- 2019
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In: Mineralogy and Petrology. - : Springer. - 0930-0708 .- 1438-1168. ; 113, s. 7-16
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Journal article (peer-reviewed)abstract
- Potassic-richterite, ideally AKB(NaCa)CMg5TSi8O22W(OH)2, is recognized as a valid member of the amphibole supergroup (IMA CNMNC 2017–102). Type material is from the Pajsberg Mn-Fe ore field, Filipstad, Värmland, Sweden, where the mineral occurs in a Mn-rich skarn, closely associated with mainly phlogopite, jacobsite and tephroite. The megascopic colour is straw yellow to grayish brown and the luster vitreous. The nearly anhedral crystals, up to 4 mm in length, are pale yellow (non-pleochroic) in thin section andoptically biaxial (−), with α = 1.615(5), β = 1.625(5), γ = 1.635(5). The calculated density is 3.07 g·cm−1. VHN100 is in the range 610–946. Cleavage is perfect along {110}. EPMA analysis in combination with Mössbauer and infrared spectroscopy yields the empirical formula (K0.61Na0.30Pb0.02)Σ0.93(Na1.14Ca0.79Mn0.07)Σ2(Mg4.31Mn0.47Fe3+0.20)Σ5(Si7.95Al0.04Fe3+0.01)Σ8O22(OH1.82F0.18)Σ2 for a fragmentused for collection of single-crystal X-ray diffraction data. The infra-red spectra show absorption bands at 3672 cm−1 and 3736 cm−1 for the α direction. The crystal structure was refined in space group C2/m to R1=3.6% [I >2σ(I)], with resulting cellparameters a = 9.9977(3) Å, b = 18.0409(4) Å, c = 5.2794(2) Å, γ = 104.465(4)°, V = 922.05(5) Å3 and Z=2. The A and M(4) sites split into A(m) (K+), A(2/m) (Na+), A(2) (Pb2+), and M(4′) (Mn2+) subsites, respectively. The remaining Mn2+ is strongly ordered at theoctahedrally coordinated M(2) site, possibly together with most of Fe3+. The skarn bearing potassic-richterite formed at peak metamorphism, under conditions of low SiO2 and Al2O3 activities and relatively high oxygen fugacities.
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| 6. |
- Jansson, Nils, et al.
(author)
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The origin of skarn beds, Ryllshyttan Zn–Pb–Ag + magnetite deposit, Bergslagen, Sweden
- 2011
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In: Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0930-0708 .- 1438-1168. ; 103:1-4, s. 49-78
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Journal article (peer-reviewed)abstract
- Thin- to medium-bedded, stratiform calc-silicate deposits (banded skarns) are a peculiar, but important, component of the supracrustal successions in the Palaeoproterozoic Bergslagen mining district of central Sweden. They are referred to as “skarn-banded leptites” in the literature and are common in areas and at stratigraphic levels that contain iron oxide and base metal sulphide deposits. The stratigraphic hanging wall of the stratabound Ryllshyttan Zn–Pb–Ag + magnetite deposit at Garpenberg, contains approximately 100–150 m of interbedded aluminous skarn beds and rhyolitic ash-siltstones. The skarn beds are mineralogically variable and dominantly composed of grandite, spessartine, epidote, actinolite, quartz, clinopyroxene, and locally magnetite. Integrated field-mapping, and whole-rock lithogeochemical, microscopic and mineral chemical analyses suggest that the stratiform skarn beds are the products of at least two discrete hydrothermal events and subsequent metamorphism. The first event comprised accumulation in a quiescent subaqueous environment, below wave base, of calcareous and ferruginous sediments rich in Fe, Mn, Ca, and Mg. These chemical sediments were deposited concurrently with rhyolitic ash-silt sedimentation, thus forming a (now metamorphosed) laminated calcareous Fe formation with both a detrital rhyolitic component and rhyolitic siltstone interbeds. Positive Eu-anomalies and negative Ce-anomalies for normalized rare earth element analyses of skarn beds suggest that the iron may have been derived from exhalation of hot and reduced hydrothermal fluids, which upon mixing with more oxidized seawater, precipitated Fe oxides and/or carbonates that settled from suspension to the seafloor. The size of the positive Eu-anomalies of the chemical sediments are modified by the content of rhyolitic volcaniclastic material, which has a negative Eu anomaly, such that positive Eu-anomalies are only observed in skarn beds that possess a minor volcaniclastic component. Subsequently, the calcareous Fe formations were subjected to post-depositional alteration by hydrothermal fluids, locally yielding more manganoan and magnesian assemblages. The Mn-alteration is manifested by lateral gradations from epidote-grandite-clinopyroxene±magnetite rocks into significantly more Mn-rich quartz-spessartine rocks and massive andradite rocks over distances of less than 10 cm within individual skarn beds. Magnesian alteration is manifested by the development of discordant zones of pargasite para-amphibolites and formation of stratiform pargasite rocks texturally similar to the interlaminated grandite-epidote-ferroan diopside rocks. The latter increase in abundance towards the Ryllshyttan deposit and are associated with pre-metamorphic/pre-tectonic K–Mg–Fe±Si alteration (now biotite-phlogopite-garnet-cordierite-pargasite rocks) that is related to base metal mineralization. The zone of Mn- and Mg-altered skarn beds extends beyond the zone of pervasive K–Mg–Fe±Si alteration around Ryllshyttan. This suggests that the skarn bed progenitors, or their sedimentary contacts against rhyolitic ash-siltstones, acted as conduits to outflowing hydrothermal fluids. The chemical and mineralogical imprint, imposed on affected beds by alteration, may serve as indicators of proximity to intense K–Mg–Fe±Si alteration envelopes around other base metal sulphide deposits in Bergslagen. The last recorded event comprised syn-tectonic veining of competent massive andradite skarn beds. The veins contain quartz-albite-epidote-ferroan diopside-actinolite assemblages.
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| 7. |
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| 8. |
- Ooteman, A, et al.
(author)
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An electron microscopy study of deformation microstructures in granitic mylonites from southwestern Sweden, with special emphasis on the micas
- 2003
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In: Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0930-0708 .- 1438-1168. ; 78:3-4, s. 255-268
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Journal article (peer-reviewed)abstract
- The lithology, age, geological setting, structural and metamorphic history of the granitic mylonites from the Mylonite Zone (MZ) in southwestern Sweden have been studied extensively. The deformation history, growth of microstructures, intensity of deformation, changes in mineral compositions, and pressure-temperature conditions of deformation have, however, not been addressed. In this study, powder X-ray diffraction, optical microscopy, electron microprobe analysis and transmission electron microscopy of micas, chlorite, and plagioclase are combined to understand the physical and textural changes experienced by the rocks during mylonitization. It is shown that the occurrence of foliated micas in shear bands, recrystallization of quartz and biotite, and undulatory extinction in quartz grains were not uniform throughout the samples studied. Occurrence of dislocations and low-angle grain boundaries confirm that deformation occurred largely by glide dislocations. The low-angle grain boundaries observed are formed by the re-arrangement of these dislocations during grain size reduction processes. The micas show a high degree of spatial stacking order, but spatial stacking disorder in micas and chlorites has also been found. Ordered stacking faults are formed during low strain while disordered stacking faults are formed under high strain conditions. Occurrence of both ordered and disordered stacking faults indicates that the intensity of deformation was not uniform through the entire MZ. Moreover, the chemical composition of plagioclase shows that the exsolution lamellae observed with optical and electron microscopy are due to Ca-subsolidus reactions during low temperature deformation. Several substitution reactions occurring in the micas indicate that deformation took place between 0.3 and 0.4 GPa, at a temperature higher than 500degreesC.
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| 9. |
- Romer, Rolf L.
(author)
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Caledonian upgrading of Proterozoic low-grade base-metal deposits in northern Sweden
- 1994
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In: Mineralogy and Petrology. - 0930-0708 .- 1438-1168. ; 50:4, s. 271-285
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Journal article (peer-reviewed)abstract
- Proterozoic sulfide deposits within the basement of northern Sweden have lead isotopic compositions that fall on a mixing line in the206Pb/204Pb-207Pb/204Pb diagram. These deposits contain a highly radiogenic Phanerozoic lead component that was leached from the Proterozoic basement at around 0.4 Ga during the Caledonian orogeny. Within the Proterozoic deposits, the less radiogenic lead isotopic compositions occur in undeformed and little deformed sections, while the more radiogenic lead isotopic compositions are observed along fault, fracture, and shear zones. These zones with radiogenic Phanerozoic lead also have higher contents of lead, zinc, and gold, respectively, than the other parts of the deposits, which suggests that these metals were introduced together with the radiogenic lead at a much later event than the metals in the unaltered Proterozoic deposit. The Proterozoic deposits acted as traps for metal additions along Caledonian reactivated fault and shear zones in the Proterozoic basement.
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| 10. |
- Romer, Rolf L., et al.
(author)
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Crystal-chemical and genetic controls of U-Pb systematics of columbite-tantalite
- 1996
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In: Mineralogy and Petrology. - 0930-0708 .- 1438-1168. ; 57:3-4, s. 243-260
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Journal article (peer-reviewed)abstract
- Columbite-tantalite can accommodate considerable amounts of uranium and excludes lead almost completely. It is thus potentially suited for U-Pb dating. Discordias generally yield closely constrained upper intercept ages. Yet, in a few cases, the U-Pb system of columbite-tantalite gives poorly constrained ages due to excess scatter or inverse discordance. These anomalous features do not show any relation with gross mineral chemistry or pegmatite fractionation. Recrystallization or the presence of exsolutions and inclusions generally do not result in anomalous and scattered U-Pb systematics, unless the inclusions are uraninite or secondary Nb, Ta-bearing phases. Open-system behavior of uraninite, whose occurrence seems to be related to the local host-rock-influenced redox conditions during pegmatite crystallization, often results in inverse discordance. Secondary Nb, Ta-bearing phases that accept Pb and U derived from uraninite inclusions into their structure may inherit this inverse discordance.
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