| 1. |
- Hålenius, Ulf, et al.
(författare)
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Mangani-pargasite, NaCa2(Mg4Mn3+)(Si6Al2)O22(OH)2, a new mineral species of the amphibole supergroup
- 2020
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Ingår i: Periodico di Mineralogia. - : EDIZIONI NUOVA CULTURA. - 0369-8963 .- 2239-1002. ; 89:2, s. 125-131
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Tidskriftsartikel (refereegranskat)abstract
- Mangani-pargasite, ideally NaCa2(Mg4Mn3+)(Si6Al2)O-22(OH)(2), is a new mineral species of the calcium amphibole subgroup of the amphibole supergroup. The type specimen was found on the mine dump of the Langban Fe-Mn-(Ba-As-Pb-Sb) deposit in Varmland, Sweden. Crystal chemical analyses resulted in the empirical chemical formula: (A)(Na0.90Pb0.07K0.03)(Sigma 1.00)(B)(Ca1.93Mn0.072+)(Sigma 2.00)(C)(Mg4.25Mn0.393+Al0.26Fe0.103+)Sigma(T)(5.00)(Si6.35Al1.65)Sigma 8.00O22W(OH)(2). In order to complete the description of this newly approved (IMA 2018-151) mineral we report here additional data to those published in papers by Jonsson and Halenius (2010) and Halenius and Bosi (2012). Mangani-pargasite is biaxial positive, with alpha=1.635(5), beta=1.645(5), gamma=1.660(5) and the measured optic angle 2V is 85(5)degrees. The dispersion is weak (r>v), and the optic orientation is: Y parallel to b; Z<^>c=25(3)degrees. Mangani-pargasite is red to brownish red with weak pleochroism; X=pale reddish brown, Y=pale reddish brown and Z=pale brownish red; X approximate to Y>Z. The unit-cell parameters are a=9.9448(5), b=18.0171(9), c=5.2829(3) angstrom, beta=105.445(3)degrees, V=912.39(9) angstrom(3), Z=2, space group C2/m. The ten strongest reflections in the X-ray powder diffraction pattern [d-values in angstrom, I, (h k l)] are: 8.420, 29, (110); 3.368, 17, (131), 3.279, 49, (240); 3.141, 100, (310); 2.817, 44, (33 0); 2.698, 21, (151); 2.389, 18, (350); 1.904, 29, (510); 1.650, 22, (461) and 1.448, 46, (661).
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| 2. |
- Deegan, Frances M., et al.
(författare)
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Pyroxene standards for SIMS oxygen isotope analysis and their application to Merapi volcano, Sunda arc, Indonesia
- 2016
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Ingår i: Chemical Geology. - : Elsevier BV. - 0009-2541 .- 1872-6836. ; 447, s. 1-10
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Tidskriftsartikel (refereegranskat)abstract
- Measurement of oxygen isotope ratios in common silicate minerals such as olivine, pyroxene, feldspar, garnet, and quartz is increasingly performed by Secondary Ion Mass Spectrometry (SIMS). However, certain mineral groups exhibit solid solution series, and the large compositional spectrum of these mineral phases will result in matrix effects during SIMS analysis. These matrix effects must be corrected through repeated analysis of compositionally similar standards to ensure accurate results. In order to widen the current applicability of SIMS to solid solution mineral groups in common igneous rocks, we performed SIMS homogeneity tests on new augite (NRM-AG-1) and enstatite (NRM-EN-2) reference materials sourced from Stromboli, Italy and Webster, North Carolina, respectively. Aliquots of the standard minerals were analysed by laser fluorination (LF) to establish their δ18O values. Repeated SIMS measurements were then performed on randomly oriented fragments of the same pyroxene crystals, which yielded a range in δ18O less than ± 0.42 and ± 0.58‰ (2σ) for NRM-AG-1 and NRM-EN-2, respectively. Homogeneity tests verified that NRM-AG-1 and NRM-EN-2 do not show any crystallographic orientation bias and that they are sufficiently homogeneous on the 20 μm scale to be used as routine mineral standards for SIMS δ18O analysis. We subsequently tested our new standard materials on recently erupted pyroxene crystals from Merapi volcano, Indonesia. The δ18O values for Merapi pyroxene obtained by SIMS (n = 204) agree within error with the LF-derived δ18O values for Merapi pyroxene but differ from bulk mineral and whole-rock data obtained by conventional fluorination. The bulk samples are offset to higher δ18O values as a result of incorporation of mineral and glass inclusions that in part reflects crustal contamination processes. The Merapi pyroxene SIMS data, in turn, display a frequency peak at 5.8‰, which allows us to estimate the δ18O value of the primary mafic magma at Merapi to ~ 6.1‰ when assuming closed system differentiation.
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| 3. |
- Johansson, Åke, et al.
(författare)
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Petrogenesis and geotectonic setting of early Svecofennian arc cumulates in the Roslagen area, east-central Sweden
- 2012
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Ingår i: Geological Journal. - : Wiley. - 0072-1050 .- 1099-1034. ; 47:6, s. 557-593
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Tidskriftsartikel (refereegranskat)abstract
- Several intrusions of ultrabasic to basic composition occur in the Roslagen area of east-central Sweden in close spatial and temporal association with the surrounding 1.90-1.87Ga old early orogenic Svecofennian granitoids. An imprecise Sm-Nd WR errorchron yields an age of 1895±71Ma. In spite of the penetrative deformation in the granitoids, the basic-ultrabasic rocks mostly appear undeformed and largely preserve magmatic textures with plagioclase, olivine (in some rock types), orthopyroxene and clinopyroxene, and amphibole as major constituents. The plagioclase is typically very anorthitic (ca. An 90). The Roslagen intrusions range in composition from primitive to evolved (Mg# 80 to 49) but contain only 40-50wt% SiO 2. Many samples are highly elevated in Al 2O 3 (up to 30wt%), CaO (up to 16wt%) and Sr (up to 800ppm), with strongly positive Eu and Sr anomalies, in line with being plagioclase cumulates. Although masked by cumulus effects, the relative trace element contents indicate a volcanic arc signature. The initial Nd isotope composition is homogeneously 'mildly depleted', with ε Nd of +0.3 to +1.1, and the initial Sr isotope composition 'mildly enriched', with ε Sr of +8 to +15. Non-cumulus rocks with small Eu and Sr anomalies can be used to deduce the composition of the parental magma. This LILE- and LREE-enriched and HFSE-depleted high-alumina basalt magma, with Mg# of ca. 50-60 and Ca# of ca. 80, most likely formed by partial melting of mantle material, enriched by fluids in a subduction environment, at 1.9Ga. The cumulate rocks apparently crystallized from a somewhat more evolved water-rich magma with Mg# of ca. 40. Crystallization was followed by the development of late-magmatic to post-magmatic coronas between olivine and plagioclase in the presence of H 2O-rich fluids. The subduction-related setting would make these intrusions Palaeoproterozoic counterparts of Alaskan-type ultramafic intrusions, but they differ from those in being plagioclase enriched, possibly reflecting different levels of exposure.
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