650 research outputs found

    Cosmological and communal wellbeing in the JSRP’s research on justice provision

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    In this blog, Tom Kirk and Holly Porter explore the JSRP’s work on how local understandings of justice are often embedded in notions of cosmological and communal wellbeing. Furthermore, they argue that practitioners that do not ground their interventions in these understandings risk creating a gap between their own normative assertions about what justice ought to achieve, and how justice is understood and practised by ordinary people

    Re-Os and Pb-Pb geochronology of the Archean Salobo iron oxide copper-gold deposit, Carajás mineral province, northern Brazil

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    Rhenium-osmium ages were determined for two molybdenite samples and a Pb-Pb age was derived from bornite-chalcopyrite-magnetite at the Salobo iron oxide copper-gold deposit to determine the timing of mineralization and its relation to the nearby Old Salobo Granite. Rhenium-osmium dating of molybdenite spatially associated with copper sulfide minerals yields ages with weighted means of 2576±8 and 2562±8Ma. Removing the error multiplier introduced by the decay constant uncertainty, appropriate for comparing ages from the same isotopic system, these data convincingly argue for two temporally separated pulses of molybdenite deposition at 2576.1±1.4Ma (n=2) and 2561.7±3.1Ma (n=3). The 2576±8Ma age coincides with a previously published U-Pb age of 2573±2Ma for the Old Salobo Granite, suggesting that main stage ore formation may have been contemporaneous with granite magmatism. The slightly younger 2562Ma age most likely represents new molybdenite precipitation associated with the development or reactivation of local shear zones. Lead-lead stepwise leaching of copper sulfide minerals yields a less precise isochron age of 2579±71Ma, and supports an Archean age for the Salobo ores. This is the first documentation of an Archean iron oxide copper-gold deposit, and the Re-Os and Pb-Pb geochronology herein support 2580-2550Ma estimates for basement reactivation and regional granite magmatism associated with the development of brittle-ductile shear zone

    Sr and Nd isotope data for arc-related (meta) volcanics (SW Iberia)

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    In the southern sector of the Ossa-Morena Zone (Iberian Variscan Chain), along its boundaries with the Beja-Acebuches Ophiolite and the South-Portuguese Zone, Upper Palaeozoic igneous mafic and intermediate rocks, both intrusive and extrusive, are widely represented. The so-called Odivelas Unit (Andrade,1983), include (meta-) basalts and (meta-) andesites, which, according with previous studies, display low-K tholeiitic to calc-alkaline signatures and, therefore, are interpreted as remnants of an active margin volcanic arc. Santos et al. (1990) subdivided those volcanics into two groups: in Alfundão-Peroguarda, the tholeiitic nature is dominant; in Odivelas-Penique, the calc-alkaline signature becomes more pronounced. Intercalation of limestone layers provided some age constraints, showing that the subduction-related volcanic activity in the studied area began in the Lower Devonian and continued, at least, through the Middle Devonian (Conde & Andrade, 1974; Machado et al., 2010). In this work, samples previously studied by Santos et al. (1990) and Silva et al. (2011) were analysed for Sm-Nd and Rb-Sr isotopes. Considering that the volcanics were systematically affected by hydrothermal metamorphism, it is expected that the Sr signatures show significant disturbance. In contrast, Nd isotope ratios probably reflect the primary features. Alfundão-Peroguarda samples show a very limited range of positive initial εNd, from +5.1 to +4.3 (assuming 400 Ma), showing no evidence for significant crustal assimilation and, therefore, allowing the attribution of negative Nb and Ta anomalies to arc-related processes On the other hand, 87Sr/86Sr varies from 0.7044 to 0.7060 (for 400Ma). These samples rocks define a horizontal trend on the initial εNd vs. initial 87Sr/86Sr plot, typical of co-genetic rocks that underwent interaction with seawater. On the other hand, Odivelas-Penique volcanics show wide spectra for both initial 87Sr/86Sr (from 0.7038 to 0.7066) and εNd (from +4.6 to -4.1). Significantly, the highest εNd values for this group are within the narrow range defined by Alfundão-Peroguarda tholeiitic basalts, suggesting a common mantle source (or very similar sources) for the most mafic magmas of both sectors. The whole set of Nd isotope ratios supports the distinction previously proposed between the two groups of volcanics. In addition, the variation from positive to negative initial εNd values in the Odivelas-Penique suite shows that its geochemical features were likely influenced by assimilation of continental crustal material

    2,6-Dimethyl-4-m-tolyl­cyclo­hex-3-enecarboxylic acid

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    The title compound, C16H20O2, was synthesized to study the hydrogen-bonding inter­action of the two enanti­omers in the solid state. The racemate is made up of carboxylic acid RS dimers. Inter­molecular O—H⋯O hydrogen bonds produce centrosymmetric R 2 2(8) rings which dimerize the two chiral enanti­omers through their carboxyl groups. The chirality of this compound is generated by the presence of the double bond in the cyclo­hexene ring and a chiral axis due to the meta-methyl substituent on the aromatic ring

    A hidden alkaline and carbonatite province of early carboniferous age in northeast Poland: Zircon U-Pb and pyrrhotite Re-Os geochronology

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    Extensive geophysical investigations in NE Poland in the 1950s and 1960s led to the discovery of an alkaline and carbonatite magmatic province buried under thick (600-800 m) Meso-Cenozoic cover north of the Trans-European Suture Zone, or Tornquist Line. Drilling focused on geophysical anomalies identified three intrusions in the Paleoproterozoic metasedimentary and metavolcanic rocks of the Mazowsze Domain: the Pisz gabbro-syenite massif, the Ełk syenite massif, and the small, differentiated Tajno body consisting of clinopyroxenite cumulates and syenites crosscut by carbonatite veins. Emplacement ages for these intrusions have been obtained by (1) zircon U-Pb geochronology on a gabbro from Pisz, a syenite from Ełk, and an albitite from Tajno and (2) a Re-Os model age for pyrrhotite from a Tajno carbonatite. The ages measured by both methods fall in the narrow range 354-345 Ma (Early Carboniferous: Tournaisian). This is slightly younger than the Late Devonian (380-360 Ma) Kola Peninsula alkaline and carbonatite province (20 intrusions) of NW Russia and Karelia but is of comparable age to the first manifestations of the long-lasting (~100 m.yr.) Carboniferous to Permian magmatic event (360-250 Ma) manifest in northern Europe (from the British Isles to southern Scandinavia, the North Sea, and northern Germany) in the foreland of the Variscan orogeny (in the so-called West European Carboniferous Basin) and the East European Craton

    U-Pb, Re-Os, and 40Ar/39Ar geochronology of the Nambija Au-skarn and Pangui porphyry Cu deposits, Ecuador: implications for the Jurassic metallogenic belt of the Northern Andes

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    New U-Pb, Re-Os, and 40Ar/39Ar dates are presented for magmatic and hydrothermal mineral phases in skarn- and porphyry-related ores from the Nambija and Pangui districts of the Subandean zone, southeastern Ecuador. Nambija has been one of the main gold-producing centers of Ecuador since the 1980s due to exceptionally high-grade ores (average 15g/t, but frequently up to 300g/t Au). Pangui is a recently discovered porphyry Cu-Mo district. The geology of the Subandean zone in southeastern Ecuador is dominated by the I-type, subduction-related, Jurassic Zamora batholith, which intrudes Triassic volcanosedimentary rocks. The Zamora batholith is in turn cut by porphyritic stocks, which are commonly associated with skarn formation and/or porphyry-style mineralization. High precision U-Pb and Re-Os ages for porphyritic stocks (U-Pb, zircon), associated prograde skarn (U-Pb, hydrothermal titanite), and retrograde stage skarn (Re-Os, molybdenite from veins postdating gold deposition) of the Nambija district are all indistinguishable from each other within error (145Ma) and indicate a Late Jurassic age for the gold mineralization. Previously, gold mineralization at Nambija was considered to be Early Tertiary based on K-Ar ages obtained on various hydrothermal minerals. The new Jurassic age for the Nambija district is slightly younger than the 40Ar/39Ar and Re-Os ages for magmatic-hydrothermal minerals from the Pangui district, which range between 157 and 152Ma. Mineralization at Nambija and Pangui is associated with porphyritic stocks that represent the last known episodes of a long-lived Jurassic arc magmatism (∼190 to 145Ma). A Jurassic age for mineralization at Nambija and Pangui suggests that the Northern Andean Jurassic metallogenic belt, which starts in Colombia at 3° N, extends down to 5° S in Ecuador. It also adds a new mineralization style (Au-skarn) to the metal endowment of this bel

    Temporal record of osmium concentrations and 187Os/188Os in organic-rich mudrocks: Implications for the osmium geochemical cycle and the use of osmium as a paleoceanographic tracer

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    The final publication is available at Elsevier via https://doi.org/10.1016/j.gca.2017.06.046 © 2017. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/We present a compilation of 192Os concentrations (representing non-radiogenic Os) and initial 187Os/188Os isotope ratios from organic-rich mudrocks (ORM) to explore the evolution of the Os geochemical cycle during the past three billion years. The initial 187Os/188Os isotope ratio of a Re-Os isochron regression for ORM constrains the local paleo-seawater 187Os/188Os, which is governed by the relative magnitudes of radiogenic Os (old continental crust) and unradiogenic Os (mantle, extraterrestrial, and juvenile/mafic/ultramafic crust) fluxes to seawater. A first-order increase in seawater 187Os/188Os ratios occurs from the Archean to the Phanerozoic, and may reflect a combination of increasing atmosphere-ocean oxygenation and weathering of progressively more radiogenic continental crust due to in-growth of 187Os from radioactive decay of 187Re. Superimposed on this long-term trend are shorter-term fluctuations in seawater 187Os/188Os ratios as a result of climate change, emplacement of large igneous provinces, bolide impacts, tectonic events, changes in seafloor spreading rates, and lithological changes in crustal terranes proximal to sites of ORM deposition. Ediacaran-Phanerozoic ORM have mildly higher 192Os concentrations overall compared with pre-Ediacaran Proterozoic ORM based on the mean and 95% confidence interval of 10,000 median values derived using a bootstrap analysis for each time bin (insufficient Archean data exist for robust statistical comparisons). However, there are two groups with anomalously high 192Os concentrations that are distinguished by their initial 187Os/188Os isotope ratios. Ediacaran-Cambrian ORM from South China have radiogenic initial 187Os/188Os, suggesting their high 192Os concentrations reflect proximal Os-rich crustal source(s), ultraslow sedimentation rates, and/or other unusual depositional conditions. In contrast, the unradiogenic initial 187Os/188Os and high 192Os concentrations of some Mesozoic ORM can be tied to emplacement of large igneous provinces. Excluding these two anomalous groups and repeating the bootstrap analysis, we find that, overall, the 192Os concentrations for the Ediacaran-Phanerozoic and pre-Ediacaran Proterozoic time bins are not significantly different. An improved understanding of Os geochemical behavior in modern environments is required before our compilation can be fully used to constrain the temporal evolution of the seawater Os reservoir.NSERC Discovery Grant || (RGPIN-435930

    4-(3-Methoxy­phen­yl)-2,6-dimethyl­cyclo­hex-3-enecarboxylic acid

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    The racemic title compound, C16H20O3, was synthesized to study the hydrogen-bonding inter­action of the two enanti­o­mers in the solid state. In the crystal structure, R and S pairs of the racemate are linked by pairs of inter­molecular O—H⋯O hydrogen bonds, producing centrosymmetric R 2 2(8) rings
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