Sample records for allanite

  1. Allanite and epidote weathering at the Coweeta hydrologic laboratory, western North Carolina, U.S.A.

    Treesearch

    Jason R. Price; Michael L. Velbel; Lina C. Pantino

    2005-01-01

    Allanite and epidote occur in the parent rocks of weathered regolith at the Coweeta Hydrologic Laboratory in North Carolina and exhibit different responses to weathering. Petrographically, epidote and allanite are identical at Coweeta, and only with additional analytical techniques (e.g., EDS or LAICP- MS) can the two be distinguished. Allanite is more...

  2. The first allanite-bearing eclogite xenolith in kimberlite

    NASA Astrophysics Data System (ADS)

    Trojman-Nichols, S.; Heaman, L.

    2015-12-01

    Here we report the first allanite-bearing mantle eclogite xenolith, entrained in the 173 Ma Jericho kimberlite pipe, located in the Slave craton, northwestern Canada. This eclogite is unique among the other Jericho eclogites by an extreme LREE enrichment in all phases, and garnet alteration rims that are more calcic than the garnet cores. Allanite is an abundant accessory phase, present as dull orange, subhedral crystals. Other minerals in the paragenesis are garnet, clinopyroxene, apatite and sulfides; two compositionally and texturally distinct generations of phlogopite constitute a secondary paragenesis where allanite is no longer stable. Allanite in this sample is La-, Ce- and Th- rich, with concentrations at the weight % level, while Y is only present at the relatively low concentration of ~100 ppm. Electron backscatter imaging reveals complex zonation within the allanite crystals that is off-centre, non-symmetric, and patchy. It is often asserted that eclogite xenoliths represent subducted oceanic lithosphere, despite significant differences in the composition and mineralogy between mantle-derived eclogite xenoliths and eclogite massif material. Both types of eclogite occurrences can contain quartz/coesite; massif eclogites often have small, sparse allanite inclusions, but allanite has never been reported in eclogite xenoliths in kimberlite. Allanite in massif eclogite is thought to form during subduction by the break-down of lawsonite and the incorporation of LREE into zoisite. Lawsonite breaks down into grossular and H20 at high pressures, which may explain the anomalous high-Ca rims measured in some garnets in this sample. This allanite-bearing eclogite may provide an unprecedented window for exploring a crucial stage of eclogite metamorphism and fluid mobilization in subduction zones. In addition, the U-Pb systematics currently under investigation may constrain the age of eclogitization.

  3. Constraining metamorphic rates through allanite and monazite petrochronology: a case study from the Miyar Valley (High Himalayan Crystalline of Zanskar, NW India)

    NASA Astrophysics Data System (ADS)

    Robyr, Martin; Goswami-Banerjee, Sriparna

    2014-05-01

    Dating metamorphic rocks raises specific issues because metamorphism comprises a complex sequence of structural changes and chemical reactions that can be extended over millions or tens of millions of years so that metamorphic rocks cannot in general be said to have "an age". Therefore, an accurate interpretation of radiometric age data from metamorphic rocks requires first to establish the behavior of the isotopic system used for dating relative to the pressure and temperature (P-T) conditions that a metamorphic rock experienced. As the U-Th-Pb system in LREE-accessory phases like monazite and allanite is not easily reset during subsequent temperature increase, allanite and monazite U-Th-Pb ages are collectively interpreted as reflecting crystallization ages. As a consequence, to correctly interpret allanite and monazite crystallization ages, it is essential to accurately determine the physical conditions of their crystallization. A meticulous account of the chemical and textural evolution of monazite and allanite along a well constrained prograde pelitic sequence of the High Himalayan Crystalline of Zanskar (Miyar Valley; e.g. Robyr et al., 2002; 2006; 2014) reveals that: (1) the occurrence of the first metamorphic allanite coincides with the biotite-in isograd and (2) the formation of the first metamorphic monazite occurs at the staurolite-in isograd. The finding of both monazite and allanite as inclusion in staurolite porphyroblasts indicates that the breakdown of allanite and the formation of monazite occurred during staurolite crystallization. Thermobarometry results show that the metamorphic allanites are appeared in the 400-420 °C, while the signature of the first metamorphic monazite is found at ~ 600 °C with staurolite-in isograd. Allanite and monazite U-Th-Pb ages thus constrain the timing when the rocks reached the ~ 420 °C and ~ 600 °C isotherms respectively. In situ LA-ICPMS dating of coexisting allanite and monazite inclusions in garnet porphyroblasts yield respective ages of 33.6 ± 0.9 Ma and 29.5 ± 0.2 Ma, constraining the time elapsed between allanite crystallization (~ 420 °C) and monazite crystallization (~ 600°C). These data indicate that the rock needed ~ 4 Myr to be subducted from the 420 °C isotherm down to the 600°C isotherm, implying a heating rate of ca. 45°C/m.y. References Robyr, M., Epard, J.-L. & El Korh, A., 2014. Structural, metamorphic and geochronological relations between the Zanskar Shear Zone and the Miyar Shear Zone (NW Indian Himalaya): Evidence for two distinct tectonic structures and implications for the evolution of the High Himalayan Crystalline of Zanskar. Journal of Asian Earth Sciences, 79, 1-15. Robyr, M., Hacker, B. R. & Mattinson, J. M., 2006. Doming in compressional orogenic settings: New geochronological constraints from the NW Himalaya. Tectonics, 25. Robyr, M., Vannay, J. C., Epard, J. L. & Steck, A., 2002. Thrusting, extension, and doming during the polyphase tectonometamorphic evolution of the High Himalayan Crystalline Zone in NW India. Journal of Asian Earth Sciences, 21, 221-239.

  4. Allanite age-dating: Non-matrix-matched standardization in quadrupole LA-ICP-MS

    NASA Astrophysics Data System (ADS)

    Burn, M.; Lanari, P.; Pettke, T.; Engi, M.

    2014-12-01

    Allanite Th-U-Pb age-dating has recently been found to be powerful in unraveling the timing of geological processes such as the metamorphic dynamics in subduction zones and crystallization velocity of magmas. However, inconsistencies among analytical techniques have raised doubts about the accuracy of allanite age data. Spot analysis techniques such as LA-ICP-MS are claimed to be crucially dependent on matrix-matched standards, the quality of which is variable. We present a new approach in LA-ICP-MS data reduction that allows non-matrix-matched standardization via well constrained zircon reference materials as primary standards. Our data were obtained using a GeoLas Pro 193 nm ArF excimer laser ablation system coupled to an ELAN DRC-e quadrupole ICP-MS. We use 32 μm and 24 μm spot sizes; laser operating conditions of 9 Hz repetition rate and 2.5 J/cm2 fluence have proven advantageous. Matrix dependent downhole fractionation evolution is empirically determined by analyzing 208Pb/232Th and 206Pb/238U and applied prior to standardization. The new data reduction technique was tested on three magmatic allanite reference materials (SISSb, CAPb, TARA); within error these show the same downhole fractionation evolution for all allanite types and in different analytical sessions, provided measurement conditions remain the same. Although the downhole evolution of allanite and zircon differs significantly, a link between zircon and allanite matrix is established by assuming CAPb and TARA to be fixed at the corresponding reference ages. Our weighted mean 208Pb/232Th ages are 30.06 ± 0.22 (2σ) for SISSb, 275.4 ± 1.3 (2σ) for CAPb, and 409.9 ± 1.8 (2σ) for TARA. Precision of single spot age data varies between 1.5 and 8 % (2σ), dependent on spot size and common lead concentrations. Quadrupole LA-ICP-MS allanite age-dating has thus similar uncertainties as do other spot analysis techniques. The new data reduction technique is much less dependent on quality and homogeneity of allanite standard reference materials. This method of correcting for matrix-dependent downhole fractionation evolution opens new possibilities in the field of LA-ICP-MS data acquisition, e.g. the use of a NIST standard glass to date all material types given a set of well constrained reference materials.

  5. Resolving the age of Wilson Creek Formation tephras and the Mono Lake excursion using high-resolution SIMS dating of allanite and zircon rims

    NASA Astrophysics Data System (ADS)

    Vazquez, J. A.; Lidzbarski, M. I.

    2012-12-01

    Sediments of the Wilson Creek Formation surrounding Mono Lake preserve a high-resolution archive of glacial and pluvial responses along the eastern Sierra Nevada due to late Pleistocene climate change. An absolute chronology for the Wilson Creek stratigraphy is critical for correlating the paleoclimate record to other archives in the western U.S. and the North Atlantic region. However, multiple attempts to date the Wilson Creek stratigraphy using carbonates and interbedded rhyolitic tephras yield discordant 14C and 40Ar/39Ar results due to open-system effects, carbon reservoir uncertainties, as well as abundant xenocrysts entrained during eruption. Ion microprobe (SIMS) 238U-230Th dating of the final increments of crystallization recorded by allanite and zircon autocrysts from juvenile pyroclasts yields ages that effectively date eruption of key tephra beds and resolve age uncertainties about the Wilson Creek stratigraphy. To date the final several micrometers of crystal growth, individual allanite and zircon crystals were embedded in soft indium to allow sampling of unpolished rims. Isochron ages derived from rims on coexisting allanite and zircon (± glass) from hand-selected pumiceous pyroclasts delimit the timing of Wilson Creek sedimentation between Ashes 7 and 19 (numbering of Lajoie, 1968) to the interval between ca. 27 to ca. 62 ka. The interiors of individual allanite and zircon crystals sectioned in standard SIMS mounts yield model 238U-230Th ages that are mostly <10 k.y. older than their corresponding rim age, suggesting a relatively brief interval of allanite + zircon crystallization before eruption. A minority of allanite and zircon crystals yield rim and interior model ages of ca. 90-100 ka, and are likely to be antecrysts recycled from relatively early Mono Craters volcanism and/or intrusions. Tephra (Ash 15) erupted during the geomagnetic excursion originally designated the Mono Lake excursion yields a rim isochron age of ca. 41 ka indicating that the recorded event is instead the Laschamp excursion. The results are consistent with a depositional chronology from correlation of relative paleointensity (Zimmerman et al., 2006) that indicates quasi-synchronous glacial and hydrologic responses in the Sierra Nevada and Mono Basin to climate change, with intervals of lake filling and glacial-snowpack melting that are in phase with peaks in spring insolation. Moreover, the results demonstrate that high-spatial resolution SIMS dating of accessory mineral rims is an alternative and promising approach for resolving the depositional ages of silicic tephras containing minerals that crystallized over protracted intervals or that are plagued by incorporation of xenocrysts and/or antecrysts. References: Lajoie, K., 1968, PhD Dissertation, UC Berkeley; Zimmerman et al., 2006, EPSL 252: 94-106.

  6. Fractionation of rare-earth elements in allanite and monazite as related to geology of the Mt. Wheeler mine area, Nevada

    USGS Publications Warehouse

    Lee, D.E.; Bastron, H.

    1967-01-01

    Rare-earth contents of 20 allanites and 13 monazites, accessory minerals from a restricted outcrop area of intrusive granitic rocks, are reported. A quantity called sigma (??), which is the sum of the atomic percentages of La, Ce and Pr, is used as an index of composition with respect to the rare-earth elements. Values of sigma vary from 61.3 to 80.9 at.% for these allanites and monazites, representing an appreciable range of composition in terms of the rare-earth elements. Degree of fractionation of rare earths varies directly with CaO content of the granitic rocks, which in turn depends largely on proximity of limestone. Four xenoliths included in the study suggest that spotty mosaic equilibria are superimposed on the regional gradients and that locally the degree of fractionation of rare earths responds to whole rock composition over distances of a few yards or less. The chemistry of the granitic rocks under study appears to be similar in some respects to that of alkalio rocks and carbonatites. Allanites from the most calcium-rich rocks show a pronounced concentration of the most basic rare earths, and whole-rock concentrations of such rare constituents as total cerium earths, Zr, F, Ti, Ba and Sr increase sympathetically with whole-rock calcium. The explanation for the concentration gradients observed in this chemical system must involve assimilation more than magmatic differentiation. ?? 1967.

  7. Experimental constraints on the monazite-fluorapatite-allanite and xenotime-(Y,HREE)-rich fluorapatite-(Y,HREE)-rich epidote phase relations as a function of pressure, temperature, and Ca vs. Na activity in the fluid

    NASA Astrophysics Data System (ADS)

    Budzyń, Bartosz; Harlov, Daniel E.; Majka, Jarosław; Kozub, Gabriela A.

    2014-05-01

    Stability relations of monazite-fluorapatite-allanite and xenotime-(Y,HREE)-rich fluorapatite-(Y,HREE)-rich epidote are strongly dependent on pressure, temperature and fluid composition. The increased Ca bulk content expands stability field of allanite relative to monazite towards higher temperatures (Spear, 2010, Chem Geol 279, 55-62). It was also reported from amphibolite facies Alpine metapelites, that both temperature and bulk CaO/Na2O ratio control relative stabilities of allanite, monazite and xenotime (Janots et al., 2008, J Metam Geol 26, 5, 509-526). This study experimentally defines influence of pressure, temperature, high activity of Ca vs. Na in the fluid, and high vs. moderate bulk CaO/Na2O ratio on the relative stabilities of monazite-fluorapatite-allanite/REE-rich epidote and xenotime-(Y,HREE)-rich fluorapatite-(Y,HREE)-rich epidote. This work expands previous experimental study on monazite (Budzyń et al., 2011, Am Min 96, 1547-1567) to wide pressure-temperature range of 2-10 kbar and 450-750°C, utilizing most reactive fluids used in previous experiments. Experiments were performed using cold-seal autoclaves on a hydrothermal line (2-4 kbar runs) and piston-cylinder apparatus (6-10 kbar runs) over 4-16 days. Four sets of experiments, two for monazite and two for xenotime, were performed with 2M Ca(OH)2 and Na2Si2O5 + H2O fluids. The starting materials included inclusion-free crystals of monazite (pegmatite, Burnet County, TX, USA) or xenotime (pegmatite, Northwest Frontier Province, Pakistan) mixed with (1) labradorite (Ab37An60Kfs3) + K-feldspar + biotite + muscovite ± garnet + SiO2 + CaF2 + 2M Ca(OH)2 or (2) albite (Ab100) + K-feldspar + biotite + muscovite ± garnet + SiO2 + CaF2 + Na2Si2O5 + H2O. 20-35 mg of solids and 5 mg of fluid were loaded into 3x15 mm Au capsules and arc welded shut. The monazite alteration is observed in all runs. Newly formed REE-rich fluorapatite and/or britholite are stable in all experimental P-T range in the presence of both fluids. Alteration of monazite and subsequent formation of REE-rich epidote or allanite, REE-rich fluorapatite and britholite was promoted by high activity of Ca in the fluid, with high bulk CaO/Na2O ratio of ca. 11.5 in the system. In contrast, neither REE-rich epidote nor allanite does form in the presence of Na2Si2O5 + H2O fluid, with bulk CaO/Na2O ratio of ca. 1.0. Results indicating that stability field of allanite relative to monazite expands towards higher temperatures along with increased Ca bulk content are consistent with recent thermodynamic modeling of phase equilibria (Spear, 2010). Experiments also support natural observations from the amphibolite-facies Alpine metapelites regarding the influence of CaO/Na2O ratio in bulk content on the relative stabilities of monazite and REE-rich epidote (Janots et al., 2008). Alteration of xenotime is observed in all runs. (Y,HREE)-rich britholite or (Y,HREE)-rich fluorapatite always formed. In contrast to monazite experiments, (Y,HREE)-rich epidote formed only at 650°C and 8-10 kbar, in the presence of 2M Ca(OH)2. Results are partially consistent with natural observations showing that stability of (Y,HREE)-rich epidote is promoted by high Ca bulk content with high CaO/Na2O ratio (Janots et al., 2008). However, experimental results indicate that the relative stabilities of xenotime and (Y,HREE)-rich epidote are strongly controlled by pressure. Acknowledgements. The project was funded by the National Science Center of Poland, grant no. 2011/01/D/ST10/04588.

  8. The behaviour of monazite from greenschist facies phyllites to anatectic gneisses: An example from the Chugach Metamorphic Complex, southern Alaska

    PubMed Central

    Gasser, Deta; Bruand, Emilie; Rubatto, Daniela; Stüwe, Kurt

    2012-01-01

    Monazite is a common accessory mineral in various metamorphic and magmatic rocks, and is widely used for U–Pb geochronology. However, linking monazite U–Pb ages with the PT evolution of the rock is not always straightforward. We investigated the behaviour of monazite in a metasedimentary sequence ranging from greenschist facies phyllites into upper amphibolites facies anatectic gneisses, which is exposed in the Eocene Chugach Metamorphic Complex of southern Alaska. We investigated textures, chemical compositions and U–Pb dates of monazite grains in samples of differing bulk rock composition and metamorphic grade, with particular focus on the relationship between monazite and other REE-bearing minerals such as allanite and xenotime. In the greenschist facies phyllites, detrital and metamorphic allanite is present, whereas monazite is absent. In lower amphibolites facies schists (~ 550–650 °C and ≥ 3.4 kbar), small, medium-Y monazite is wide-spread (Mnz1), indicating monazite growth prior and/or simultaneous with growth of garnet and andalusite. In anatectic gneisses, new low-Y, high-Th monazite (Mnz2) crystallised from partial melts, and a third, high-Y, low-Th monazite generation (Mnz3) formed during initial cooling and garnet resorption. U–Pb SHRIMP analysis of the second and third monazite generations yields ages of ~ 55–50 Ma. Monazite became unstable and was overgrown by allanite and/or allanite/epidote/apatite coronas within retrograde muscovite- and/or chlorite-bearing shear zones. This study documents polyphase, complex monazite growth and dissolution during a single, relatively short-lived metamorphic cycle. PMID:26525358

  9. Post-magmatic solid solutions of CaCeAl2(Fe3+ 2/3□1/3)[Si2O7][SiO4]O(OH), allanite-(Ce) and REE-bearing epidote in miarolitic pegmatites of Permian Baveno granite (Verbania, central-southern alps, Italy)

    NASA Astrophysics Data System (ADS)

    Guastoni, Alessandro; Nestola, Fabrizio; Schiazza, Mariangela

    2017-06-01

    CaCeAl2(Fe3+ 2/3□1/3)[Si2O7][SiO4]O(OH), allanite-(Ce) and rare earth element (REE)-bearing epidote occur as globular aggregates and platy prismatic crystals in miarolitic cavities in a niobium, yttrium, fluorine (NYF) granitic pegmatite at Baveno, Verbania, Southern Alps, Italy. These samples were investigated by means of an electron probe micro-analyser (EPMA) and single-crystal X-ray diffraction. Our EPMA results show that the globular aggregates have the highest REE content in the core portion and decreases to REE-bearing epidote towards the rim whereas the prismatic crystals are characterized by marked oscillatory zoning that have the highest REE contents at the rim of the crystal. The unit-cell parameters of "allanites" have an intermediate unit-cell between CaCeAl2(Fe3+ 2/3□1/3)[Si2O7][SiO4]O(OH), allanite-(Ce) and REE-free epidote, because reflect the strong chemical heterogeneity of the samples which form complete solid solutions. Hydrothermal fluids control the activity and precipitation of incompatible elements like high field strength elements (HFSE), Sc and REE by hydrous F-rich fluids below the critical temperature which allow to deposit accessory minerals in the cavities with decreasing temperature. The source of REE and Y are the sheet and REE-silicates like siderophyllite-annite, and gadolinite-(Y) which underwent partial to complete decomposition by the activity of aggressive F-rich hydrothermal fluids.

  10. Petrology, chronology and sequence of vein systems: Systematic magmatic and hydrothermal history of a major intracontinental shear zone, Canadian Appalachians

    NASA Astrophysics Data System (ADS)

    Pe-Piper, Georgia; Piper, David J. W.; McFarlane, Chris R. M.; Sangster, Chris; Zhang, Yuanyuan; Boucher, Brandon

    2018-04-01

    Intra-continental shear zones developed during continental collision may experience prolonged magmatism and mineralization. The Cobequid Shear Zone formed part of a NE-SW-trending, orogen-parallel shear system in the late Devonian-early Carboniferous, where syn-tectonic granite-gabbro plutons and volcanic rocks 4 km thick were progressively deformed. In late Carboniferous to Permian, Alleghanian collision of Africa with Laurentia formed the E-W trending Minas Fault Zone, reactivating parts of the Cobequid Shear Zone. The 50 Ma history of hydrothermal mineralization following pluton emplacement is difficult to resolve from field relationships of veins, but SEM study of thin sections provides clear detail on the sequence of mineralization. The general paragenesis is: albite ± quartz ± chlorite ± monazite → biotite → calcite, allanite, pyrite → Fe-carbonates, Fe-oxides, minor sulfides, calcite and synchysite. Chronology was determined from literature reports and new U-Pb LA-ICPMS dating of monazite and allanite in veins. Vein mineralization was closely linked to magmatic events. Vein emplacement occurred preferentially during fault movement recognised from basin-margin inversion, as a result of fractures opening in the damage zone of master faults. The sequence of mineralization, from ca. 355 Ma riebeckite and albite veins to ca. 327 (-305?) Ma siderite-magnetite and sulfide mineralization, resembles Precambrian iron-oxide-copper-gold (IOCG) systems in the literature. The abundant magmatic Na, halogens and CO2 in veins and some magmatic bodies, characteristic of IOCG systems, were derived from the deeply subducted Rheic Ocean slab with little terrigenous sediment. Regional extension of the Magdalen Basin caused asthenospheric upwelling and melting of the previously metasomatized sub-continental lithospheric mantle. Crustal scale strike-slip faulting facilitated the rise of magmas, resulting in high heat flow driving an active hydrothermal system. Table S2 Location of all illustrated samples. Table S3 Monazite geochronology lab data. Table S4 Allanite geochronology lab data. Fig. S1 Monazite geochronology analytical spots. Fig. S2 Allanite geochronology analytical spots.

  11. 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 °C

    NASA Astrophysics Data System (ADS)

    Budzyń, Bartosz; Harlov, Daniel E.; Kozub-Budzyń, Gabriela A.; Majka, Jarosław

    2017-04-01

    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 °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 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 °C, 200-1000 MPa, and 550 °C, 200-600 MPa, and minor cheralite in runs at 650-750 °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 °C, 200-1000 MPa, and 550 °C, 200-600 MPa. A lack of compositional alteration in the Th, U, and Pb in monazite-(Ce) at 550 °C, 800-1000 MPa, and in experiments at 650-750 °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 °C, 800 MPa; 650 °C, 800 MPa; and 650 °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.

  12. Strata-bound Fe-Co-Cu-Au-Bi-Y-REE deposits of the Idaho Cobalt Belt: Multistage hydrothermal mineralization in a magmatic-related iron oxide copper-gold system

    USGS Publications Warehouse

    Slack, John F.

    2012-01-01

    Mineralogical and geochemical studies of strata-bound Fe-Co-Cu-Au-Bi-Y-rare-earth element (REE) deposits of the Idaho cobalt belt in east-central Idaho provide evidence of multistage epigenetic mineralization by magmatic-hydrothermal processes in an iron oxide copper-gold (IOCG) system. Deposits of the Idaho cobalt belt comprise three types: (1) strata-bound sulfide lenses in the Blackbird district, which are cobaltite and, less commonly, chalcopyrite rich with locally abundant gold, native bismuth, bismuthinite, xenotime, allanite, monazite, and the Be-rich silicate gadolinite-(Y), with sparse uraninite, stannite, and Bi tellurides, in a gangue of quartz, chlorite, biotite, muscovite, garnet, tourmaline, chloritoid, and/or siderite, with locally abundant fluorapatite or magnetite; (2) discordant tourmalinized breccias in the Blackbird district that in places have concentrations of cobaltite, chalcopyrite, gold, and xenotime; and (3) strata-bound magnetite-rich lenses in the Iron Creek area, which contain cobaltiferous pyrite and locally sparse chalcopyrite or xenotime. Most sulfide-rich deposits in the Blackbird district are enclosed by strata-bound lenses composed mainly of Cl-rich Fe biotite; some deposits have quartz-rich envelopes.Whole-rock analyses of 48 Co- and/or Cu-rich samples show high concentrations of Au (up to 26.8 ppm), Bi (up to 9.16 wt %), Y (up to 0.83 wt %), ∑REEs (up to 2.56 wt %), Ni (up to 6,780 ppm), and Be (up to 1,180 ppm), with locally elevated U (up to 124 ppm) and Sn (up to 133 ppm); Zn and Pb contents are uniformly low (≤821 and ≤61 ppm, respectively). Varimax factor analysis of bulk compositions of these samples reveals geochemically distinct element groupings that reflect statistical associations of monazite, allanite, and xenotime; biotite and gold; detrital minerals; chalcopyrite and sparse stannite; quartz; and cobaltite with sparse selenides and tellurides. Significantly, Cu is statistically separate from Co and As, consistent with the general lack of abundant chalcopyrite in cobaltite-rich samples.Paragenetic relations determined by scanning electron microscopy indicate that the earliest Y-REE-Be mineralization preceded deposition of Co, Cu, Au, and Bi. Allanite, xenotime, and gadolinite-(Y) commonly occur as intergrowths with and inclusions in cobaltite; the opposite texture is rare. Monazite, in contrast, forms a poikiloblastic matrix to cobaltite and thin rims on allanite and xenotime, reflecting a later metamorphic paragenesis. Allanite and xenotime also show evidence of late dissolution and reprecipitation, forming discordant rims on older anhedral allanite and xenotime and separate euhedral crystals of each mineral. Textural data suggest extensive deformation of the deposits by folding and shearing, and by pervasive recrystallization, all during Cretaceous metamorphism. Sensitive high resolution ion microprobe U-Pb geochronology by Aleinikoff et al. (2012) supports these paragenetic interpretations, documenting contemporaneous Mesoproterozoic growth of early xenotime and crystallization of megacrystic A-type granite on the northern border of the district. These ages are used together with mineralogical and geochemical data from the present study to support an epigenetic, IOCG model for Fe-Co-Cu-Au-Bi-Y-REE deposits of the Idaho cobalt belt. A sulfide facies variant of IOCG deposits is proposed for the Blackbird district, in which reducing hydrothermal conditions favored deposition of sulfide minerals over iron oxides. This new model includes Mesoproterozoic vein mineralization and related Fe-Cl metasomatism that formed the biotite-rich lenses, a predominantly felsic magmatic source for metals in the deposits, given their local abundance of Y, REEs, and Be, and a major sedimentary component in the hydrothermal fluids based on independent sulfur isotope and boron isotope data for sulfides and ore-related tourmaline, respectively.

  13. Genesis of the central zone of the Nolans Bore rare earth element deposit, Northern Territory, Australia

    NASA Astrophysics Data System (ADS)

    Schoneveld, Louise; Spandler, Carl; Hussey, Kelvin

    2015-08-01

    The Nolans Bore rare earth element (REE) deposit consists of a network of fluorapatite-bearing veins and breccias hosted within Proterozoic granulites of the Reynolds Range, Central Australia. Mineralisation is divided into three zones (north, central, and south-east), with the north and south-east zones consisting of massive REE-bearing fluorapatite veins, with minor brecciation and carbonate infill. The central zone is distinctively different in mineralogy and structure; it features extensive brecciation, a high allanite content, and a large, epidote-rich enveloping alteration zone. The central zone is a reworking of the original solid apatite veins that formed during the Chewings Orogeny at ca. 1525 Ma. These original apatite veins are thought to derive from phosphate-rich magmatic-hydrothermal fluid exsolved from as-yet unrecognised alkaline magmatic bodies at depth. We define four ore breccia types (BX1-4) in the central zone on the basis of detailed petrological and geochemical analysis of drillcore and thin sections. BX1 ore comprises fluorapatite with minor crackle brecciation with carbonate infill and resembles ore of the north and south-east zones. Breccia types BX2, BX3, and BX4 represent progressive stages of ore brecciation and development of calc-silicate mineral (amphibole, epidote, allanite, calcite) infill. Comparison of bulk ore sample geochemistry between breccia types indicates that REEs were not mobilised more than a few centimetres during hydrothermal alteration and brecciation. Instead, most of the REEs were partitioned from the original REE fluorapatite into newly formed allanite, REE-poor fluorapatite and minor REE carbonate in the breccias. Negative europium (Eu) anomalies in the breccia minerals are accounted for by a large positive Eu anomaly in epidote from the alteration zones surrounding the ore breccias. This observation provides a direct link between ore recrystallisation and brecciation, and the formation of the alteration halo in the surrounding host rocks. Where allanite and fluorapatite are texturally related, the fluorapatite is relatively depleted in the light rare earth elements (LREEs), whereas allanite is relatively LREE enriched, suggesting co-crystallisation. We tentatively date the BX1 ore stage to 1440 ± 80 Ma based on U-Pb dating of thorianite. Sm-Nd isotope isochrons derived from in situ isotope analysis of cognate apatite and allanite date the BX2 and BX3 events to ca. 400 Ma, while U-Pb dating of late-stage monazite from the BX4 ore stage returned an age of ca. 350 Ma. Therefore, formation of the central zone at Nolans Bore involved multiple alteration/brecciation events that collectively span over 1 billion years in duration. We suggest that the BX1-type veins and breccias were formed from REE-rich, saline (F- and Cl-bearing) fluids that infiltrated the granulite-grade host rocks in association with either shear activation events of the Redbank Shear Zone (1500-1400 Ma) or intrusion of late-stage pegmatites of the Mt Boothby area. BX2, BX3, and BX4 events record deformation and hydrothermal alteration associated with the Alice Springs Orogeny (400-350 Ma). These hydrothermal events occurred at temperatures of 450 to ~600 °C, due to inflow of highly acidic hydrous fluids derived from a magmatic source, or from mixing of meteoric and metamorphic fluids. Our data testify to the long and complex geological history of not only the Nolans Bore REE deposit, but also of the rocks of the eastern Reynolds Range, and demonstrate the great utility of using hydrothermally derived REE minerals to trace the timing of crustal deformation events and source of associated hydrothermal fluids.

  14. Hunting for eruption ages in accessory minerals

    NASA Astrophysics Data System (ADS)

    Vazquez, J. A.

    2012-12-01

    A primary goal in geochronology is to provide precise and accurate ages for tephras that serve as chronostratigraphic markers for constraining the timing and rates of volcanism, sedimentation, climate change, and catastrophic events in Earth history. Zircon remains the most versatile accessory mineral for dating silicic tephras due to its common preservation in distal pyroclastic deposits, as well as the robustness of its U-Pb and U-series systems even after host materials have been hydrothermally altered or weathered. Countless studies document that zircon may be complexly zoned in age due to inheritance, contamination, recycling of antecrysts, protracted crystallization in long-lived magma reservoirs, or any combination of these. Other accessory minerals such as allanite or chevkinite can retain similar records of protracted crystallization. If the goal is to date the durations of magmatic crystallization, differentiation, and/or magma residence, then these protracted chronologies within and between accessory minerals are a blessing. However, if the goal is to date the timing of eruption with high precision, i.e., absolute ages with millennial-scale uncertainties, then this age zoning is a curse. Observations from ion microprobe 238U-230Th dating of Pleistocene zircon and allanite provide insight into the record of near-eruption crystallization in accessory minerals and serve as a guide for high-precision whole-crystal dating. Although imprecise relative to conventional techniques, ion probe analysis allows high-spatial resolution 238U-230Th dating that can document multi-millennial age distributions at the crystal scale. Analysis of unpolished rims and continuous depth profiling of zircon from small and large volume eruptions (e.g., Coso, Mono Craters, Yellowstone) reveals that the final several micrometers of crystallization often yield ages that are indistinguishable from associated eruption ages from the 40Ar/39Ar or (U-Th)/He methods. Using this approach, we have derived relatively precise (± ~ 5%, 2σ) U-Th isochron ages from the unpolished rims of pumice-derived allanite and zircon from late Pleistocene Wilson Creek Formation tephras in eastern California, whose ages are controversial and have been difficult to resolve via 40Ar/39Ar and radiocarbon dating. Allanite and zircon rims from Ashes 7-19 in the lower portion of Wilson Creek sediments yield stratigraphically consistent ages of ca. 27 ka to ca. 62 ka, with a minority of crystals identifiable as xenocrysts from early Mono Craters rhyolites. Model ages for the interiors of allanite crystals are mostly < 10 k.y. older than their rims. Tephra deposited during the geomagnetic excursion debated to be either the Mono Lake or Laschamp event yields a rim isochron age of ca. 41 ka. This age is indistinguishable from an independent age of 41 ka derived at the latter excursion's type locality in France (Singer et al., 2009) as well as from age-models for deep-sea sediments. The results are in excellent agreement with a previously determined chronology derived from magnetostratigraphy (Zimmerman et al., 2006). Refs: Singer et al., 2009, EPSL 286: 80-88; Zimmerman et al., 2006, EPSL 252: 94-106

  15. The role of garnet in (Y+REE) mobility during fluid-initiated, localized, solid state dehydration of an amphibole-bearing migmatised granitic gneiss to charnockite

    NASA Astrophysics Data System (ADS)

    Harlov, D. E.; Anczkiewicz, R.; Johansson, L.

    2013-12-01

    On either side of 1 m wide granitic pegmatoid dyke, Söndrum stone quarry, Halmstad, SW Sweden, extends a 2.5-3 m wide Opx-bearing dehydration zone (DZ) (650-700 °C; 800 MPa; Opx-Cpx-Bt-Amph-Gt-allanite), which overprints the gneissic banding of the surrounding migmatised granitic gneiss (MGG) (Amph-Bt-Gt-allanite) (Harlov et al., 2006, J Petrol 47, 3). Whole-rock chemistry indicates that dehydration of the MGG was predominantly isochemical. Exceptions include (Y+HREE), Ba, Sr, and F, which are markedly depleted throughout the DZ while LREE-bearing allanite remains unaltered. Systematic trends in the Gt, Bt, Amph, and FAp mineral chemistry across the DZ include depletion in Fe, (Y+HREE), Na, K, F, and Cl, and enrichment in Mg, Mn, Ca, and Ti. Fluid inclusion data suggest that the solid state dehydration event was due to advective transport of a CO2-rich fluid with a minor Cl and F component originating from a tectonic fracture represented today by the pegmatoid dyke. LA-ICPMS analysis of (Y+REE) in Gt (NIST 612 Glass standard; for operating conditions cf. Anczkiewicz et al. 2012 Chem Geol 318-319, 16) across the traverse indicates at least two distinct populations of Gt from the DZ variably depleted in (Y+HREE) and LREE (Fig. 1) by an order of magnitude compared to Gt in the MGG (Fig. 2). Depletion most likely is the result of (Y+HREE) and LREE partitioning from the Gt into the dehydrating fluid to complex with F and Cl. Variable depletion suggests preferred inter-granular pathways for fluid flow through the DZ during the dehydration event allowing some Gt grains greater exposure to the fluid than other Gt grains.

  16. Subduction / exhumation dynamics: Petrochronology in the Glacier-Rafray slice (Western Alps, Italy)

    NASA Astrophysics Data System (ADS)

    Burn, Marco; Lanari, Pierre; Engi, Martin

    2014-05-01

    Petrochronology is the combination of in situ age-dating, geothermobarometry and structural geology and aims to unravel Pressure-Temperature-deformation-time (P-T-ɛ-t) paths. To link P-T conditions to deformation stages is daily business for metamorphic petrologists, but recent micro-mapping techniques (XMapTools program) provide an additional tool to achieve this goal. Absolute age is often difficult to assess in metamorphic rocks, as it is challenging to link specific P-T conditions to most of the mineral chronometers. Allanite is a common accessory phase in high-P metamorphic rocks and is a potential target to determine Th(-U)/Pb ages. Allanite from a leucocratic gneiss of the Glacier-Rafray slice in the western Alps consists of several chemically different zones: one major zone can be linked to a first high-P phengite generation. To determine the age of this high-P growth zone we used La-ICP-MS in situ techniques, which allowed us to date an appropriate growth rim per grain. Even so particular care was required when evaluating the isotope signals laser ablation leads to the excavation of a volume, which potentially can be chemically and/or age-zoned. We have developed a new method to track changes in the plasma during the ablation. This method aims to identify discrete age zones. La-ICP-MS spectra have been modeled so as to reproduce the shape of the spectra measured. These results indicate that high-P allanite first grew in equilibrium with phengite at 84 ± 4 Ma, whereas a second growth event occurred at ~40 Ma. A final epidotic rim grew at greenschist facies conditions, but this stage could not be dated. These findings have implications for our interpretation of several units in the Western Alps: In the Sesia Zone (former Adriatic margin), the earliest high-P metamorphism occurred at 85 Ma (Regis et al., 2014), precisely as the first high-P peak we discovered in the Glacier-Rafray slice. Austroalpine klippen such as this are commonly seen as extensional allochthons; one would expect these to have entered the subduction zone together with the Piemonte oceanic units. Yet all high-P ages reported for the Piemonte oceanic units are around 40 Ma. We propose that the Glacier-Rafray slice experienced subduction together with Sesia units and may have been juxtaposed on the Piemont-Ligurian-Ocean units during Eocene exhumation. Strain associated with this juxtaposition may have triggered growth of the second allanite. Joint exhumation of the oceanic units and the Glacier-Rafray klippe followed at retrograde T.

  17. Formation conditions and REY enrichment of the 2060 Ma phosphorus mineralization at Schiel (South Africa): geochemical and geochronological constraints

    NASA Astrophysics Data System (ADS)

    Graupner, Torsten; Klemd, Reiner; Henjes-Kunst, Friedhelm; Goldmann, Simon; Behnsen, Helge; Gerdes, Axel; Dohrmann, Reiner; Barton, Jay M.; Opperman, Rehan

    2018-02-01

    Rocks of the rare-earth element (REY)-enriched apatite deposit in the eastern part of the Schiel Alkaline Complex (SAC; Southern Marginal Zone, Limpopo Belt) were studied for their whole-rock and mineral chemistry, REY mineral distribution and geochronology. Apart from phoscorite (sensu lato), pyroxenite and various syenitic rock types with quite variable apatite contents display P-REY enrichments. Field observations, mineralogical composition as well as major and trace element chemistry of soils make it possible to constrain the distribution of the hidden P-REY-rich rock types in the apatite deposit. Uranium-lead ages of zircon from phoscorite (sensu lato) and syenite are in the range of 2.06-2.05 Ga. Samarium-neodymium (ɛNd(t) -8.6 to -6.0) and in part Rb-Sr (87Sr/86Sr(t) 0.70819-0.70859) isotope data for whole-rock samples and mineral separates indicate an origin from an isotopically enriched and slightly variable source. Fluorapatite, early allanite and titanite are the main REY carriers at Schiel. Fluorapatite dominates the REY budget of pyroxenite and phoscorite, whereas early allanite hosts most of the REY in syenite. Three apatite types are distinguished based on their occurrence in the rocks, REYtotal contents and colouration in cathodoluminescence microscopy. Magmatic apatite in pyroxenite and in phoscorite (sensu lato) as well as early stage type I/II apatite in syenitic rocks have moderate to high REYtotal abundances (up to 3.2 wt%) with the mineral enriched in light REE. Early ferriallanite-(Ce) is strongly enriched in light REE and shows very high REYtotal values (13.7-26.4 wt%), while late allanite has lower REYtotal concentrations (6.9-14.9 wt%). Titanite is abundant in most syenitic rocks (REYtotal 1.7-6.4 wt%); chevkinite-(Ce) occurs locally and contributes to an REY enrichment in contact aureoles between syenite and different lithologies. Apatite-enriched rocks in the SAC in part contain significantly higher REYtotal concentrations in apatite grains compared to those in apatite-mineralized pyroxenite, phoscorite and carbonatite from Phalaborwa.

  18. Les minéraux accessoires des granitoïdes de la suite taourirt, Hoggar (Algérie): conséquences pétrogénétiques

    NASA Astrophysics Data System (ADS)

    Azzouni-Sekkal, Abla; Bonin, Bernard

    1998-01-01

    The post-Pan-African 'taourirt' suite of Hoggar (Algeria) is made up by themagmatic suite: G I monzogranite, G IIa monzogranite+syenogranite, G IIb subsolvus alkali feldspar granite (alaskite), GIII hypersolvus alkali feldspar syenite + granite. Silicates (zircon, thorite, allanite, chevkinite, titanite), oxides (magnetite, ilmenite, fergusonite) and phosphates (apatite, monazite), often abundant, constitute various accessory mineral associations. Crystal morphology, place in the sequence of crystallisation and mineral chemistry change as a function of parageneses. The constant titanite + magnetite + ilmenite assemblage in G I and G II rocks illustrates more oxidising conditions than in G III group, where hedenbergite + magnetite + ilmenite coexist. Two groups of accessory minerals are distinguished: (1) LREE rich (3×10 4 to 3×10 5 × chondrites) and Y rich (50 to 10 4 × chondrites), such as allanite, chevkinite and monazite, (2) LREE poor (100 to 10 4 × chondrites) and Y rich (1000 to 10 5 × chondrites), such as zircon, thorite, titanite and fergusonite. Shapes of chondrite-normalised patterns and evolutionary trends of REE, as well as of other HFSE, such as Nb, Zr, U and Th, in bulk rocks are dependent on relative abundances of the different accessory minerals.

  19. Accessory mineral U-Th-Pb ages and 40Ar/39Ar eruption chronology, and their bearing on rhyolitic magma evolution in the Pleistocene Coso volcanic field, California

    USGS Publications Warehouse

    Simon, J.I.; Vazquez, J.A.; Renne, P.R.; Schmitt, A.K.; Bacon, C.R.; Reid, M.R.

    2009-01-01

    We determined Ar/Ar eruption ages of eight extrusions from the Pleistocene Coso volcanic field, a long-lived series of small volume rhyolitic domes in eastern California. Combined with ion-microprobe dating of crystal ages of zircon and allanite from these lavas and from granophyre geothermal well cuttings, we were able to track the range of magma-production rates over the past 650 ka at Coso. In ??? 230 ka rhyolites we find no evidence of protracted magma residence or recycled zircon (or allanite) from Pleistocene predecessors. A significant subset of zircon in the ???85 ka rhyolites yielded ages between ???100 and 200 Ma, requiring that generation of at least some rhyolites involves material from Mesozoic basement. Similar zircon xenocrysts are found in an ???200 ka granophyre. The new age constraints imply that magma evolution at Coso can occur rapidly as demonstrated by significant changes in rhyolite composition over short time intervals (???10's to 100's ka). In conjunction with radioisotopic age constraints from other young silicic volcanic fields, dating of Coso rhyolites highlights the fact that at least some (and often the more voluminous) rhyolites are produced relatively rapidly, but that many small-volume rhyolites likely represent separation from long-lived mushy magma bodies. ?? The Author(s) 2009.

  20. New Gallium End-Member in Epidote Group

    NASA Astrophysics Data System (ADS)

    Soboleva, A. A.; Varlamov, D.; Mayorova, T.

    2011-12-01

    Unique ultrahigh-Ga (Ga up to 14.5 wt. %) mineral of epidote group is discovered in Tykatlova gold-sulfure ore occurrence in the eastern slope of the Subpolar Urals, Russia. It is the first find of the Ga silicate mineral in the world. Only five Ga minerals are presented in the IMA official list. Generally, two unique deposites in Africa contain Ga minerals - Tsumeb in Namibia and Kipushi in DR Congo. Tykatlova occurrence is situated in early Ordovician rhyolites and rhyodacites metamorphosed in greenschist facies, sulfide mineralization is located in fault zones. Ga-phases were found out in sphalerite-pyrite-galena assemblage with chalcopyrite and minor Ag-bearing bornite, tetrahedrite-tennantite, various Ag and Cu sulfides and sulfosalts. Secondary ore minerals are anglesite, cerussite, lead and zinc hydroxides. Vein minerals are quartz, calcite, Zn-Mn carbonates, anhydrite (or gypsum). Ga-minerals are usually inclusions (common in sphalerite, sometimes in pyrite and galena), they are rarely located between grains of sulfides or quartz. Ga-phases are assigned to epidote group due to morphology of grains, their chemical composition (EPMA using EDS and WDS), stoichiometry and Raman data. Their grains are elongated, roundish or well-shaped, they are 30-60 up to 100 μm in length, with complex zonality. The general sequence of zones from the core to rims: a) "epidote-(Ga)" with 6-20 wt.% Ga2O3, REE are almost absent; b) high Ga allanite-(Ce) with 3-11 wt.% Ga2O3, 3-20 wt.% REE (calculated as oxide); c) allanite-(Ce) with 0.0-2.0 wt.% Ga2O3, 4-19 wt.% REE; d) epidote-allanite rims without Ga, 0-6 wt.% REE. Empirical formula of phases mostly enriched in Ga: (Ca1.88Mg0.15Mn0.03)2.06(Al1.77Ga0.97Fe3+0.26)3.00(Si2.91Al0.09)3O12(OH) (Ca1.85Mg0.11Mn0.02)1.98(Al1.89Ga1.03Fe3+0.19)3.11(Si2.93Al0.07)3O12(OH). Crystal chemistry of Ga-epidote isn't clear yet, but we assume that Ga substitutes Fe3+ rather than Al. Correlation factor in Fe3+-Ga pair (core zones of grains) reaches -0.92. Decrease of Ga toward to grain rims "allows" occurrence of REE in the epidote structure, as Ga ceases to occupy a large octahedron where bivalent ions (Fe2+, Mg, Mn2+) can enter for compensation of trivalent REE cations. Raman spectra of the Ga-phases shows a high convergence with epidote spectra. Detectable Ga concentrations (0.048-0.058 wt.%, WDS) have been established only in sphalerite that includes grains of epidote-allanite enriched in Ga. So, the most probable source of Ga is Ga-enriched sphalerite. Growth of Ga phases might take place during greenschist facies metamorphism. However, we can't exclude vice versa variant - increase of Ga concentration in sphalerite in result of decomposition of primary high-Ga silicates. Conclusions: (1) A unique high-Ga mineral of the epidote group was discovered in the Subpolar Urals. (2) It is the first find of high-Ga silicate mineral in the world. Presumably it is new member of epidote group that could be named "epidote-(Ga)" (as it is recommended by the IMA Commission). Financial support by RFBR, grant 11-05-01087-a.

  1. Compositional and phase relations among rare earth element minerals

    NASA Technical Reports Server (NTRS)

    Burt, D. M.

    1990-01-01

    This paper discusses the compositional and phase relationships among minerals in which rare earth elements (REE) occur as essential constituents (e.g., bastnaesite, monazite, xenotime, aeschynite, allanite). Particular consideration is given to the vector representation of complex coupled substitutions in selected REE-bearing minerals and to the REE partitioning between minerals as related to the acid-base tendencies and mineral stabilities. It is shown that the treatment of coupled substitutions as vector quantities facilitates graphical representation of mineral composition spaces.

  2. How to build a mid-crustal intrusive suite: geologic mapping, U-Pb geo-/thermochronology, and thermal modeling of the Bergell Intrusion, Central Alps

    NASA Astrophysics Data System (ADS)

    Samperton, K. M.; Schoene, B.; Annen, C.

    2015-12-01

    Insights into the characteristic rates and processes of crustal magmatic systems can best be made through the integration of observational, analytical and modeling perspectives. We present such an approach in reconstructing the emplacement, differentiation and cooling history of the Bergell Intrusion (N Italy/SE Switzerland), a normally-zoned pluton preserving a ~10 km mid-crustal transect. U-Pb zircon, titanite and allanite geo-/thermochronology of Bergell granitoids provide key empirical constraints for informing numerical simulations of pulse-wise, incremental assembly. Protracted zircon crystallization histories, representing the time between magma zircon saturation and cooling to the solidus, provide a direct petrologic link to forward models of magma emplacement, both of which can be used to derive quantitative magmatic cooling rates for the middle crust. Titanite and allanite dates provide additional constraints on the timing of solidification. Geochronology and modeling are performed in the context of detailed field and structural observations, including those previously interpreted as evidence of upward, pluton-scale melt migration via floor convergence/roof ballooning. Combined Bergell data and modeling demonstrate that pulsed assembly can lead to the formation of substantial melt reservoirs in the middle crust: this finding is largely in contrast to similar models of shallow crustal plutons, highlighting the importance of factors such as ambient country rock temperature in affecting melt residence timescales. This work emphasizes the importance of implementing joint data/modeling studies to intrusive rocks across the full range of spatial scales, emplacement levels and tectonic settings observed on Earth.

  3. Compositional and phase relations among rare earth element minerals

    NASA Technical Reports Server (NTRS)

    Burt, D. M.

    1989-01-01

    A review is presented that mainly treats minerals in which the rare-earth elements are essential constituents, e.g., bastnaesite, monazite, xenotime, aeschynite, allanite. The chemical mechanisms and limits of REE substitution in some rock-forming minerals (zircon, apatite, titanite, garnet) are also derived. Vector representation of complex coupled substitutions in selected REE-bearing minerals is examined and some comments on REE-partitioning between minerals as related to acid-based tendencies and mineral stabilities are presented. As the same or analogous coupled substitutions involving the REE occur in a wide variety of mineral structures, they are discussed together.

  4. From Permo-Triassic lithospheric thinning to Jurassic rifting at the Adriatic margin: Petrological and geochronological record in Valtournenche (Western Italian Alps)

    NASA Astrophysics Data System (ADS)

    Manzotti, Paola; Rubatto, Daniela; Darling, James; Zucali, Michele; Cenki-Tok, Bénédicte; Engi, Martin

    2012-08-01

    Slices of polycyclic metasediments (marbles and meta-cherts) are tectonically amalgamated with the polydeformed basement of the Dent Blanche tectonic system along a major Alpine shear zone in the Western Alps (Becca di Salé area, Valtournenche Valley). A combination of techniques (structural analysis at various scales, metamorphic petrology, geochronology and trace element geochemistry) was applied to determine the age and composition of accessory phases (titanite, allanite and zircon) and their relation to major minerals. The results are used to reconstruct the polyphase structural and metamorphic histories, comprising both pre-Alpine and Alpine cycles. The pre-Alpine evolution is associated with low-pressure high-temperature metamorphism related to Permo-Triassic lithospheric thinning. In meta-cherts, microtextural relations indicate coeval growth of allanite and garnet during this stage, at ~ 300 Ma. Textures of zircon also indicate crystallisation at HT conditions; ages scatter from 263 to 294 Ma, with a major cluster of data at ~ 276 Ma. In impure marble, U-Pb analyses of titanite domains (with variable Al and F contents) yield apparent 206Pb/238U dates range from Permian to Jurassic. Chemical and isotopic data suggest that titanite formed at Permian times and was then affected by (extension-related?) fluid circulation during the Triassic and Jurassic, which redistributed major elements (Al and F) and partially opened the U-Pb system. The Alpine cycle lead to early blueschist facies assemblages, which were partly overprinted under greenschist facies conditions. The strong Alpine compressional overprint disrupted the pre-Alpine structural imprint and/or reactivated earlier structures. The pre-Alpine metamorphic record, preserved in these slices of metasediments, reflects the onset of the Permo-Triassic lithospheric extension to Jurassic rifting.

  5. Preliminary report on the geology and deposits of monazite, thorite and niobium-bearing rutile of the Mineral Hill district, Lemhi County, Idaho

    USGS Publications Warehouse

    Kaiser, Edward Peck

    1956-01-01

    Deposits of minerals containing niobium (columbium), thorium, and rare earths occur in the Mineral Hill district, 30 miles northwest of Salmon, Lemhi County, Idaho. Monazite, thorite, allanite, and niobium-bearing rutile form deposits in metamorphic limestone layers less than 8 feet thick. The known deposits are small, irregular, and typically located in or near small folds. Minor faults are common. Monazite generally is coarsely crystalline and contains less than one percent thorium. Rutile forms massive lumps up to 3 inches across; it contains between 5 and 10 percent niobium. Rutile occurs in the northwestern half of the district, thorite in the central and southeastern parts. Monazite occurs in all deposits. Allanite is locally abundant and contains several percent thorium. Magnetite and ilmenite are also locally abundant. A major thrust fault trending northwest across the map-area separates moderately folded quartzite and phyllitic rocks of Belt age, on the northeast, from more intensely metamorphosed and folded rocks on the southwest. The more metamorphosed rocks include amphibolite, porphyroblastic feldspar gneiss, quartzite, and limestone, all probably of sedimentary origin, and probably also of Belt (late Precambrian) age. The only rocks of definite igneous origin are rhyolite dikes of probable Tertiary age. The more metamorphosed rocks were formed by metasomatic metamorphism acting on clastic sediments, probably of Belt age, although they may be older than Belt. Metamorphism doubtless was part of the episode of emplacement of the Idaho batholith, but the history of that episode is not well understood. The rare-element deposits show no evidence of fracture-controlled hydrothermal introduction, such as special fracture systems, veining, and gangue material. They may, however, be of hydrothermal type. More likely they are metamorphic segregations or secretions, deposited in favorable stratigraphic and structural positions during regional metamorphism.

  6. Mid Carboniferous lamprophyres, Cobequid Fault Zone, eastern Canada, linked to sodic granites, voluminous gabbro, and albitization

    NASA Astrophysics Data System (ADS)

    Pe-Piper, Georgia; Piper, David J. W.; Papoutsa, Angeliki

    2018-01-01

    Major intra-continental shear zones developed during the later stages of continental collision in a back-arc setting are sites of prolonged magmatism. Mantle metasomatism results from both melting of subducted sediments and oceanic crust. In the Cobequid Fault Zone of the northern Appalachians, back-arc A-type granites and gabbros dated ca. 360 Ma are locally intruded by lamprophyric dykes dated ca. 335 Ma. All the lamprophyres are kersantites with biotite and albite, lesser ilmenite, titanite and fluorapatite, and minor magmatic calcite, allanite, pyrite, magnetite, quartz and K-feldspar in some samples. The lamprophyres show enrichment in Rb, Ba, K, Th and REE and classify as calc-alkaline lamprophyre on the basis of biotite and whole rock chemistry. Pb isotopes lie on a mixing line between normal mantle-derived gabbro and OIB magma. Nd isotopes range from 1.3-3.5 εNdt, a little lower than in local gabbro. Most lamprophyres have δ18O = 3.8-4.4‰. Country rock is cut by pyrite-(Mg)-chlorite veins with euhedral allanite crystals that resemble the lamprophyres mineralogically, with the Mg-chlorite representing chloritized glass. Early Carboniferous unenriched mafic dykes and minor volcanic rocks are widespread along the major active strike-slip fault zones. The lamprophyres are geographically restricted to within 10 km of a small granitoid pluton with some sodic amphibole and widespread albitization. This was displaced by early Carboniferous strike-slip faulting from its original position close to the large Wentworth Pluton, the site of mantle-derived sodic amphibole granite, a major late gabbro pluton, and a volcanic carapace several kilometres thick, previously demonstrated to be the site of mantle upwelling and metasomatism. The age of the lamprophyres implies that enriched source material in upper lithospheric mantle or lower crust was displaced 50 km by crustal scale strike-slip faulting after enrichment by the mantle upwelling before lamprophyre emplacement. This indicates a multi-stage process to emplace lamprophyric magma.

  7. Enrichment of trace elements in garnet amphibolites from a paleo-subduction zone: Catalina Schist, southern California

    USGS Publications Warehouse

    Sorensen, Sorena S.; Grossman, J.N.

    1989-01-01

    The abundance, P-T stability, solubility, and element-partitioning behavior of minerals such as rutile, garnet, sphene, apatite, zircon, zoisite, and allanite are critical variables in models for mass transfer from the slab to the mantle wedge in deep regions of subduction zones. The influence of these minerals on the composition of subduction-related magmas has been inferred (and disputed) from inverse modelling of the geochemistry of island-arc basalt, or by experiment. Although direct samples of the dehydration + partial-melting region of a mature subduction zone have not been reported from subduction complexes, garnet amphibolites from melanges of circumpacific and Caribbean blueschist terranes reflect high T (>600??C) conditions in shallower regions. Such rocks record geochemical processes that affected deep-seated, high-T portions of paleo-subduction zones. In the Catalina Schist, a subduction-zone metamorphic terrane of southern California, metasomatized and migmatitic garnet amphibolites occur as blocks in a matrix of meta-ultramafic rocks. This mafic and ultramafic complex may represent either slab-derived material accreted to the mantle wedge of a nascent subduction zone or a portion of a shear zone closely related to the slab-mantle wedge contact, or both. The trace-element geochemistry of the complex and the distribution of trace elements among the minerals of garnet amphibolites were studied by INAA, XRF, electron microprobe, and SEM. In order of increasing alteration from a probable metabasalt protolith, three common types of garnet amphibolite blocks in the Catalina Schist are: (1) non-migmatitic, clinopyroxene-bearing blocks, which are compositionally similar to MORB that has lost an albite component; (2) garnet-amphibolite blocks, which have rinds that reflect local interaction between metabasite, metaperidotite, and fluid; and (3) migmatites that are extremely enriched in Th, HFSE, LREE, and other trace elements. These trace-element enrichments are mineralogically controlled by rutile, garnet, sphene, apatite, zircon, zoisite, and allanite. Alkali and alkaline earth elements are much less enriched in the solid assemblage, and thus appear to be decoupled from the other elements in the inferred metasomatic process(es). The compositions of migmatitic garnet amphibolite blocks seem to complement that of "average" island-arc tholeiite. Trace-element metasomatism reflects fluid-solid, rather than melt-solid, interaction. The metasomatic effects indicate that H2O-rich fluid, perhaps with a significant component of Na-Al silicate and alkalis, carried Th, U, Sr, REE, and HFSE. Fractionations of LREE in migmatites resemble those of migmatitic metasedimentary rocks underlying the mafic and ultramafic complex. "Exotic" LREE deposited in allanite in migmatites could have been derived from fluids in equilibrium with subducted sediment. If the paleo-subduction zone represented by the mafic and ultramafic complex of the Catalina Schist had continued its thermal and fluid evolution, a selvage of similarly enriched rocks might have been generated along the slab-mantle wedge contact between ~30 and 85 km depth. Rocks affected by "subduction-zone metasomatism," although rarely recognized at the surface, could be volumetrically significant products of the initiation of subduction and may prove to be geochemical probes of convergent margins that approach the significance of xenoliths in the study of other magmatic environments. ?? 1989.

  8. The Nolans Bore rare-earth element-phosphorus-uranium mineral system: geology, origin and post-depositional modifications

    NASA Astrophysics Data System (ADS)

    Huston, David L.; Maas, Roland; Cross, Andrew; Hussey, Kelvin J.; Mernagh, Terrence P.; Fraser, Geoff; Champion, David C.

    2016-08-01

    Nolans Bore is a rare-earth element (REE)-U-P fluorapatite vein deposit hosted mostly by the ~1805 Ma Boothby Orthogneiss in the Aileron Province, Northern Territory, Australia. The fluorapatite veins are complex, with two stages: (1) massive to granular fluorapatite with inclusions of REE silicates, phosphates and (fluoro)carbonates, and (2) calcite-allanite with accessory REE-bearing phosphate and (fluoro)carbonate minerals that vein and brecciate the earlier stage. The veins are locally accompanied by narrow skarn-like (garnet-diopside-amphibole) wall rock alteration zones. SHRIMP Th-Pb analyses of allanite yielded an age of 1525 ± 18 Ma, interpreted as the minimum age of mineralisation. The maximum age is provided by a ~1550 Ma SHRIMP U-Pb age for a pegmatite that predates the fluorapatite veins. Other isotopic systems yielded ages from ~1443 to ~345 Ma, implying significant post-depositional isotopic disturbance. Calculation of initial ɛNd and 87Sr/86Sr at 1525 Ma and stable isotope data are consistent with an enriched mantle or lower crust source, although post-depositional disturbance is likely. Processes leading to formation of Nolans Bore began with north-dipping subduction along the south margin of the Aileron Province at 1820-1750 Ma, producing a metasomatised, volatile-rich, lithospheric mantle wedge. About 200 million years later, near the end of the Chewings Orogeny, this reservoir and/or the lower crust sourced alkaline low-degree partial melts which passed into the mid- and upper-crust. Fluids derived from these melts, which may have included phosphatic melts, eventually deposited the Nolans Bore fluorapatite veins due to fluid-rock interaction, cooling, depressurisation and/or fluid mixing. Owing to its size and high concentration of Th (2500 ppm), in situ radiogenic heating caused significant recrystallisation and isotopic resetting. The system finally cooled below 300 °C at ~370 Ma, possibly in response to unroofing during the Alice Springs Orogeny. Surface exposure and weathering of fluorapatite produced acidic fluids and intense, near-surface kaolinitised zones that include high-grade, supergene-enriched cheralite-rich ores.

  9. Exhumation rates in the Gran Paradiso Massif (Western Alps) constrained by in situ U-Th-Pb dating of accessory phases (monazite, allanite and xenotime)

    NASA Astrophysics Data System (ADS)

    Manzotti, Paola; Bosse, Valérie; Pitra, Pavel; Robyr, Martin; Schiavi, Federica; Ballèvre, Michel

    2018-03-01

    Exhumation rates for high-pressure metamorphic rocks need to be carefully estimated to decipher tectonic processes in subduction/collision belts. In the Gran Paradiso Massif (Western Alps), the Money Unit crops out as a tectonic window below the Gran Paradiso Unit. According to previous studies, the Gran Paradiso and Money Units reached peak pressure conditions at 18 to 20 kbar, 480-520 °C and 17 to 18 kbar, 500-550 °C, respectively. This yields a maximum difference of 9 to 10 km in the subduction depth reached by these two units during the Alpine history. Thrusting of the Gran Paradiso Unit over the Money Unit led to the simultaneous development of the main foliation under the same metamorphic conditions ( 12.5 to 14.5 kbar and 530-560 °C) in both units. The thrust contact was subsequently folded and then both units were exhumed together. The relative timing of the growth and dissolution of the accessory phases was assessed by combining thermodynamic modelling with inclusion, textural and chemical (major and trace element) data from both major and accessory phases. The age of monazite constrained the high-pressure metamorphism in both the Gran Paradiso Unit and the Money Unit at 41.5 ± 0.3 and 42.0 ± 0.6 Ma, respectively. Allanite replacing monazite in the matrix has been dated at 32.7 ± 4.2 Ma. The late growth of xenotime associated with the crystallization of biotite pseudomorphs at the expense of garnet (at about 10 kbar) was dated at 32.3 ± 1.0 Ma. Our petrochronological data indicate about 10 m.y. between the peak pressure conditions and the crystallization of xenotime leading to an exhumation rate of the order of 2.2-5 mm/year. The new ages allow to better constrain the timing of the displacement of the thrust defining the lower boundary of the extruding wedge of eclogite-facies rocks.

  10. Late Pleistocene eruptive history of the Mono Craters rhyolites, eastern California, from U-Th dating of explosive and effusive products

    NASA Astrophysics Data System (ADS)

    Marcaida, M.; Vazquez, J. A.; Calvert, A. T.; Miller, J. S.

    2016-12-01

    During late Pleistocene-Holocene time, repeated explosive and effusive eruptions of high-silica rhyolite magma south of Mono Lake, California, have produced a chain of massive domes known as the Mono Craters and a time-series of tephra deposits preserved in sediments of the Wilson Creek formation of ancestral Mono Lake. The record of late Holocene volcanism at Mono Craters is relatively well constrained by tephrostratigraphy and 14C dating, and the timing of late Pleistocene eruptions is similarly well constrained by tephrochronology and magnetostratigraphy of the Wilson Creek formation. However, the chronology of eruptions for the Mono Craters chain, comprising at least 28 individual domes, has thus far been based on age estimates from hydration rind dating of obsidian that is highly dependent on local calibration. We constrain the timing of late Pleistocene dome emplacement by linking independently dated Wilson Creek tephras to their dome equivalents in the Mono Craters using combined titanomagnetite geochemistry and U-Th geochronology. Ion microprobe 238U-230Th dating of unpolished allanite and zircon rims gives isochron dates of ca. 42 ka, ca. 38 ka, ca. 26 ka, and ca. 20 ka for domes 19, 24, 31 (newly recognized), and 11 of the Mono Craters, respectively. These domes are biotite-bearing rhyolites with titanomagnetites that are compositionally identical to those from several Wilson Creek tephras. Specifically, we correlate Ash 15, Ash 7, and Ash 3 of the Wilson Creek formation to domes 19, 31, and 11 of the Mono Craters, respectively, based on matching titanomagnetite compositions and indistinguishable U-Th ages. 40Ar/39Ar dating of single sanidines from domes 19 and 31 yield mean dates that are 10 k.y. older than their corresponding U-Th dates, likely due to excess argon from melt inclusions and/or incompletely re-equilibrated antecrysts. Based on our new U-Th isochron date of ca. 34 ka for allanite-zircon from Ash 8 pumice and the ca. 26-27 ka age of Ash 7 and its extrusive equivalent dome 31, we infer that the stratigraphic position of the ca. 32 ka Auckland/Mono Lake geomagnetic excursion, if recorded in beds of the Wilson Creek formation, is between Ashes 7 and 8. Accordingly, the prominent geomagnetic excursion bisected by Ash 15 lower in the section is the ca. 41 ka global Laschamp event.

  11. Petrography, geochemistry, and U-Pb geochronology of pegmatites and aplites associated with the Alvand intrusive complex in the Hamedan region, Sanandaj-Sirjan zone, Zagros orogen (Iran)

    NASA Astrophysics Data System (ADS)

    Sepahi, Ali Asghar; Salami, Sedigheh; Lentz, David; McFarlane, Christopher; Maanijou, Mohammad

    2018-04-01

    The Alvand intrusive complex in the Hamedan area in Iran is in the Sanandaj-Sirjan zone of the Zagros orogen. It consists of a wide range of plutonic rocks, mainly gabbro, diorite, granodiorite, granite, and leucogranites that were intruded by aplitic and pegmatitic dykes. At least three successive magmatic episodes generated an older gabbro-diorite-tonalite assemblage, followed by a voluminous granodiorite-granite association, which was then followed by minor leucocratic granitoids. Aplitic and pegmatitic dykes and bodies have truncated both plutonic rocks of the Alvand intrusive complex and its metamorphic aureole. Chemically they belong to peraluminous LCT (Li-, Cs-, and Ta-bearing) family of pegmatites. Mineralogically, they resemble Muscovite (MS) and Muscovite Rare Element (MSREL) classes of pegmatites. High amounts of some elements, such as Sn (up to 10,000 ppm), Rb (up to 936 ppm), Ba (up to 706 ppm), and LREE (up to 404 ppm) indicate the highly fractionated nature of some of these aplites and pegmatites. U-Pb dating of monazite, zircon, and allanite by LA-ICPMS indicate the following ages: monazite-bearing aplites of Heydareh-e-Poshteshahr and Barfejin areas, southwest of Hamedan, give an age range of 162-172 Ma; zircon in Heydareh-e-Poshteshar gives an average age of 165 Ma and for allanite-bearing pegmatites of Artiman area, north of Tuyserkan, an age of 154.1 ± 3.7 Ma was determined. These overlap with previously reported ages (ca. 167-153 Ma) for the plutonic rocks of the Alvand complex. Therefore, these data reveal that the Jurassic was a period of magmatism in the Hamedan region and adjacent areas in the Sanandaj-Sirjan zone, which was situated at the southern edge of the central Iranian micro-plate (southern Eurasian plate) at this time. Our results also suggest that advective heating in a continental arc setting has caused melting of fertile supracrustal lithologies, such as meta-pelites. These partial melts were then emplaced at much higher crustal levels, but within a thermally anomalous environment, which, therefore, leads to formation of evolved felsic rocks, such as the studied LCT aplite-pegmatite suite and their parental granitic rocks. This is a new result that indicates the role of syn-subduction crustal partial melting in the region as part of Zagros orogeny.

  12. High REE and Y concentrations in Co-Cu-Au ores of the Blackbird district, Idaho

    USGS Publications Warehouse

    Slack, J.F.

    2006-01-01

    Analysis of 11 samples of strata-bound Co-Cu-Au ore from the Blackbird district in Idaho shows previously unknown high concentrations of rare earth elements (REE) and Y, averaging 0.53 wt percent ???REE + Y oxides. Scanning electron microscopy indicates REE and Y residence in monazite, xenotime, and allanite that form complex intergrowths with cobaltite, suggesting coeval Co and REE + Y mineralization during the Mesoproterozoic. Occurrence of high REE and Y concentrations in the Blackbird ores, together with previously documented saline-rich fluid inclusions and Cl-rich biotite, suggest that these are not volcanogenic massive sulfide or sedimentary exhalative deposits but instead are iron oxide-copper-gold (IOCG) deposits. Other strata-bound Co deposits of Proterozoic age in the North American Cordillera and elsewhere in the world may have potential for REE and Y resources. IOCG deposits with abundant light REE should also be evaluated for possible unrecognized heavy REE and Y mineralization. ?? 2006 by Economic Geology.

  13. Direct dating and characterization of the Pope's Hill REE Deposit, Labrador

    NASA Astrophysics Data System (ADS)

    Chafe, A. N.; Hanchar, J. M.; Fisher, C.; Piccoli, P. M.; Crowley, J. L.; Dimmell, P. M.

    2012-12-01

    The Pope's Hill rare earth element (REE) trend (PHT) is located approximately 100 km southwest of Happy Valley-Goose Bay, along the Trans Labrador Highway, in central Labrador. Whole-rock geochemical analyses of the main REE-bearing unit indicate total rare earth element contents ranging from 1 to 22 weight percent (wt%) REE3+. The REE-enriched unit is hosted within a hydrothermally altered syenite, trending northeast and traceable for approximately 2.8km. Samples of ore, host rock, and country rock, were collected from throughout the trend in order to: 1) quantify which phases concentrate the REE and their abundances and distribution in the ore; and 2) use in situ LA-ICPMS and ID-TIMS U-Pb geochronology and in situ Sm-Nd isotopes using LA-MC-ICPMS in monazite from the ore and host rock to constrain the timing of mineralization and determine the source of the REE. These data will help develop predictive models for this type of mineral deposit elsewhere. The PHT is defined as the host syenite and REE-enriched segregations; two contrasting lithologies. The rare earth element minerals (REE) occur in millimeter- to centimeter-scale pods that are locally discontinuous. The REE are hosted in a variety of silicate, phosphate, carbonate, and niobate phases; with a majority hosted in allanite(-Ce), titanite(-Ce), monazite(-Ce), britholite(-Ce); and a minor percentage in REE-carbonates and fergusonite(-Nd). Both apatite and titanite occur in two different compositional forms that range in chemistry from end-member stoichiometric apatite and titanite to highly REE-enriched - apatite-britholite and titanite(-Ce), where chemical substitutions, such as Si4+ + REE3+ substitute for Ca2+ + P5+ in apatite and REE3+ + Fe3+ substitute for Ca2+ + Ti4+ in titanite in order to incorporate up to ~40 wt% REE2O3 in both minerals. The U-Pb geochronology indicate that allanite, titanite(-Ce), monazite and fergusonite crystallized from ~1060 to ~940 Ma, a period spanning ~120 Ma. Sm-Nd tracer isotope data from the same minerals indicate that the syenite and ore have initial Nd within a single ɛNd unit. This combined with their field relationship to the foliation and the microtextures observed in thin section suggests that the REE minerals experienced syndeformational growth from a hydrothermal fluid, acting on both host and ore, where REEs in aqueous hard ligand complexes became saturated in silicate, phosphate, carbonate, and niobate minerals through the changing T, P and chemical conditions brought on by deformation.

  14. The post-collisional late Variscan ferroan granites of southern Sardinia (Italy): Inferences for inhomogeneity of lower crust

    NASA Astrophysics Data System (ADS)

    Conte, Aida Maria; Cuccuru, Stefano; D'Antonio, Massimo; Naitza, Stefano; Oggiano, Giacomo; Secchi, Francesco; Casini, Leonardo; Cifelli, Francesca

    2017-12-01

    The post-collisional late Variscan magmatism of Sardinia-Corsica batholith attained a peak at about 290 Ma. In southern Sardinia, in the frontal part of the Variscan orogenic wedge, this magmatism is represented by three suites of granitoids, here defined as GS1, GS2 and GS3. GS1, GS2 and GS3 are slightly peraluminous and F-bearing granitoids; GS1 and GS3 granites show in addition a ferroan character, whereas GS2 rocks range from magnesian to ferroan, from granodiorites to leucogranites. From magnetic susceptibility data, GS1 and GS2 belong to the ilmenite series, whereas GS3 is a slightly oxidized rock-suite plotting on the ilmenite/magnetite series boundary. Each rock-suite shows distinctive characters, in terms of petrography, petrochemistry, rock associations, as well as metallogenic signature of the related fluids. The distinction among rock-suite types is made on the basis of both mafic and characteristic accessory minerals. Siderophyllitic dark mica as the only mafic phase, and accessory xenotime (Y) characterize the GS1 rocks; GS2 mineral associations include biotite ± hornblende + allanite + magnetite; GS3 rocks show an association of hastingsite + annite + allanite + magnetite. Chemical variations in the studied samples suggest different magmatic evolution of independent magmas. Pb, Sr and Nd isotopic data constrain the origin of magmas to lower crustal sources. Chemical composition of rocks and dark micas meet those of liquids experimentally obtained by low degrees of partial melting of different meta-igneous deep crustal sources, felsic for GS1 rock-types and more mafic for GS3 rock-types. GS1 intrusions show granophile-type (Sn-W-Mo) metallogenic signatures, very low magnetic susceptibility, and Nd model ages (referred to the Depleted Mantle - TDM) of 2.3 Ga, coherent with a possible derivation from an old (early Proterozoic-Neoarchean), reduced and weathered basement, tectonically buried under Variscan covers. A definite deep crustal inhomogeneity is mirrored by GS3 granites, whose compositional and isotopic features indicate a younger (Nd model age: 1.6 Ga) tonalitic amphibolite source. Overall, the peculiarities of the studied granitoids suggest further compositional differences in the deep crust between southern and northern portion of the Sardinia-Corsica Variscan transect. Late Variscan lithospheric delamination appears as the most reliable mechanism that may have determined the high thermal regime that triggered partial melting of the crust. The close field association, at 290 Ma, of tholeiitic dike swarms and ferroan granitoids, supports this inference.

  15. Uranium-lead dating of hydrothermal zircon and monazite from the Sin Quyen Fe-Cu-REE-Au-(U) deposit, northwestern Vietnam

    NASA Astrophysics Data System (ADS)

    Li, Xiao-Chun; Zhou, Mei-Fu; Chen, Wei Terry; Zhao, Xin-Fu; Tran, MyDung

    2018-03-01

    The Sin Quyen deposit in northwestern Vietnam contains economic concentrations of Cu, Au and LREE, and sub-economic concentration of U. In this deposit, massive and banded replacement ores are hosted in Neoproterozoic metapelite. The paragenetic sequence includes sodic alteration (stage I), calcic-potassic alteration and associated Fe-REE-(U) mineralization (stage II), Cu-Au mineralization (stage III), and sulfide-(quartz-carbonate) veins (stage IV). The Sin Quyen deposit experienced an extensive post-ore metamorphic overprint, which makes it difficult to precisely determine the mineralization age. In this study, zircon and monazite U-Pb geochronometers and the Rb-Sr isochron method are used to constrain the timing of mineralization. Zircon grains in the ore are closely intergrown or texturally associated with hydrothermal minerals of stage II (e.g., garnet, allanite, and hedenbergite). They may contain primary fluid inclusions and display irregular zoning in cathodoluminescence (CL) images. Zircon grains are rich in U (688 to 2902 ppm) and poor in Th (0.2 to 2.9 ppm). Their δ18OV-SMOW values range from 11.9 to 14.0‰, higher than those of typical magmatic zircon. These textural and compositional features imply that zircon precipitated from 18O- and U-rich hydrothermal fluids, coeval with the minerals of stage II. Monazite occurs in close association with stage II magnetite and allanite and has low contents of Th (<2700 ppm), indicative of a hydrothermal origin. Hydrothermal zircon and monazite have indistinguishable U-Pb ages of 841 ± 12 and 836 ± 18 Ma, respectively, representing the timing of Fe-REE mineralization. There is no direct isotopic constraint on the timing of the Cu-Au mineralization, but geological observations suggest that the Cu-Au and Fe-REE ores most likely formed within a single evolved hydrothermal process. In the plot of 87Rb/86Sr vs. 87Sr/86Sr, the composition of bulk-ore and biotite separates from ore lie along a reference line for 30 Ma, which is consistent with the timing of metamorphism in the region. The mineralization age of the Sin Quyen deposit falls within the overall age range (740 to 860 Ma) of the regional Neoproterozoic igneous rocks. This temporal linkage, in combination with the magmatic-like sulfur isotopes of sulfide minerals (δ34SV-CDT = -0.8 to 3.1), indicates that the mineralization may have a close genetic association with the Neoproterozoic igneous activity.

  16. RADIOACTIVITY DOSAGE OF ORNAMENTAL GRANITIC ROCKS BASED ON CHEMICAL, MINERALOGICAL AND LITHOLOGICAL DATA

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Salas, H.T.; Nalini, H.A. Jr.; Mendes, J.C.

    2004-10-03

    One hundred samples of granitic rock were collected from granite traders in Belo Horizonte. Autoradiography, optical microscopy, diffractometry, and chemical analysis (X-ray spectrometry, X-ray fluorescence, neutron activation, gravimetry and electron probe microanalysis) were used to determine the mineral assemblages and lithotypes. Autoradiographic results for several samples showed the presence of monazite, allanite and zircon. Chemical analysis revealed concentrations of uranium of {le} 30ppm, and thorium {le} 130ppm. Higher concentrations generally correlated with high concentrations of light rare earths in silica-rich rocks of granitic composition. Calculations were made of radioactive doses for floor tiles in a standard room for samples withmore » total concentration of uranium and thorium greater than 60ppm. On the basis of calculations of {sup 232}Th, {sup 40}K and {sup 226}Ra from Th, K and U analysis, the doses calculated were between 0.11 and 0.34 mSv/year, which are much lower than the acceptable international exposure standard of 1.0 mSv/year.« less

  17. The rare earth element compositions of the Changjiang (Yangtze) and Huanghe (Yellow) river sediments

    NASA Astrophysics Data System (ADS)

    Yang, Shou Ye; Jung, Hoi Soo; Choi, Man Sik; Li, Cong Xian

    2002-07-01

    Thirty-four samples from the Changjiang and Huanghe were analyzed to characterize their rare earth element (REE) compositions. Although REE concentrations in the Changjiang sediments are higher than those of the Huanghe sediments, the former are less variable. Bulk samples and acid-leachable fractions have convex REE patterns and middle REE enrichments relative to upper continental crust, whereas flat patterns are present in the residual fractions. Source rock composition is the primary control on REE composition, and weathering processes play a minor role. Grain size exerts some influence on REE composition, as demonstrated by the higher REE contents of clay minerals in sediments from both rivers. Heavy minerals contribute about 10-20% of the total REE in the sediments. Apatite is rare in the river sediments, and contributes less than 2% of the REE content, but other heavy minerals such as sphene, allanite and zircon are important reservoirs of residual REE fractions. The Fe-Mn oxides phase accounts for about 14% of bulk REE content in the Changjiang sediments, which could be one of the more important factors controlling REE fractionation in the leachable fraction.

  18. Reconnaissance for radioactive deposits in the vicinity of Teller and Cape Nome, Seward Peninsula, Alaska, 1946-47

    USGS Publications Warehouse

    White, Max Gregg; West, W.S.; Matzko, J.J.

    1953-01-01

    Placer-mining areas and bedrock exposures near Teller on the Seward Peninsula, Alaska, were investigated in June and July, 1946, for possible sources of radioactive materials. The areas that were investigated are: Dese Creek, southeast of Teller; Bluestone River basin, south and southeast of Teller; Sunset Creek and other small streams flowing south into Grantley Harbor, northeast of Teller; and, also northeast of Teller, Swanson Creek and its tributaries, which flow north into the Agiapuk River basin. No significant amount of radioactive material was found, either in the stream gravels or in the bedrock of any of the areas. A heavy-mineral fraction obtained from a granite boulder probably derived from a bench gravel on Gold Run contains 0. 017 percent equivalent uranium, but the radioactivity is due to allanite and zircon. The types of bedrock tested include schist, slate, and greenstone. Readings on fresh surfaces of rock were the same as, or only slightly above the background count. The maximum radioactivity in stream concentrates is 0. 004 percent equivalent uranium in a sluice concentrate from Sunset Creek.

  19. Th-REE- and Nb-Ta-accessory minerals in post-collisional Ediacaran felsic rocks from the Katerina Ring Complex (S. Sinai, Egypt): An assessment for the fractionation of Y/Nb, Th/Nb, La/Nb and Ce/Pb in highly evolved A-type granites

    NASA Astrophysics Data System (ADS)

    Moreno, J. A.; Molina, J. F.; Bea, F.; Abu Anbar, M.; Montero, P.

    2016-08-01

    The relationships of Y/Nb, Th/Nb, La/Nb and Ce/Pb ratios in A-type felsic rocks from the Ediacaran Katerina Ring Complex, northernmost Arabian-Nubian Shield (ANS; S. Sinai, Egypt), are investigated in this work to understand their behavior during generation of highly evolved granitic magmas and to explore the nature of magma sources. Textural and compositional relationships of cognate Th-REE- and Nb-Ta-accessory minerals in Katerina felsic rocks show that chevkinite-group minerals (CGM), monazite, thorite, allanite and xenotime formed from residual liquids in quartz syenite porphyries, quartz monzonites and peralkaline granites, whereas in aluminous granites, allanite and monazite crystallized early, and thorite and columbite formed from residual liquids. Relationships of Y/Nb, Th/Nb, La/Nb and Ce/Pb ratios with Zr/Hf ratios in the aluminous granites and with Be abundances in the peralkaline granites suggest a decrease in La/Nb and Ce/Pb ratios in the former, and in Y/Nb and La/Nb ratios in the latter with crystallization progress. This contrasts with absence of systematic variations of Th/Nb and Ce/Pb ratios in the peralkaline compositions and of Y/Nb ratio in the aluminous ones. In this latter, Th/Nb ratio can present a significant decrease only in highly evolved compositions. An analysis of Y/Nb, Th/Nb, La/Nb and Ce/Pb relationships in worldwide OIB and subduction-related magmatic suites reveals that A-type felsic rocks with (Th/Nb)N < 1.3, (La/Nb)N < 1.3, and (Ce/Pb)N > 1 may have A1-type affinity, and those with (Th/Nb)N > 2, (La/Nb)N > 2, and (Ce/Pb)N < 1 tend to present A2-type affinity. The crystal fractionation of Th-LREE- and Nb-Ta-accessory minerals and mixing of components derived from the two granite groups may cause deviations from these compositional limits that can be evaluated using constraints imposed by Th/Nb-La/Nb, Ce/Pb-Th/Nb and Ce/Pb-La/Nb relationships in OIB and subduction-related magmatic suites. Three mantle sources might have been involved in the Ediacaran alkaline magmatism from northernmost ANS that are chemically similar to those of (1) OIB suites, (2) subduction-related magmatic suites, and (3) carbonatite-metasomatized peridotites. In addition, compositions characterized by (Y/Nb)N > 0.18, (Th/Nb)N > 2, (La/Nb)N > 2, (Ce/Pb)N < 1, and crustal-like Nb/Ta ratios may point to a significant contribution of crustal sources.

  20. Fluid inclusion studies of the Rodeo de Los Molles REE and Th deposit, Las Chacras Batholith, Central Argentina

    NASA Astrophysics Data System (ADS)

    Lira, Raul; Ripley, Edward M.

    1990-03-01

    The Rodeo de Los Molles rare earth element (REE) and thorium deposit is located in granitic rocks of the Las Chacras-Piedras Coloradas Batholith, in the southern block of the Eastern Pampean Ranges, Central Argentina. Mineralization occurs within an elongate (2 km × 0.6 km) body of alkalifeldspar granite (alaskite) localized along the northeastern edge of a composite batholith. The surrounding lithology is predominantly a biotite monzogranite. Both the alaskite and localized areas of quartz alkalifeldspar syenite within the alaskite have been produced by hydrothermal alteration of a late-crystallizing phase of the monzogranite. REE minerals are primarily of the cerium group and include britholite and allanite, both partially replaced by bastnaesite or thorbastnaesite. These minerals occur as nodules with quartz, fluorite, aegirine-augite, sphene, and Fe-Ti oxides within aplitic to pegmatoidal quartz alkalifeldspar syenite. Uranothorite, along with a second generation of fluorite and minor amounts of MnBa oxides, occurs in the alaskite as nodules, or within quartz-lined miarolitic cavities, but is not found with the Ce-mineralization. Studies of fluid inclusions contained in quartz and fluorite indicate a complex history of open-system fluid migration and interaction with monzogranite host rocks. Fluids responsible for REE mineralization and quartz deposition, along with initial alteration of the monzogranite to alaskite and quartz alkalifeldspar syenite, were of relatively high temperature (T h of fluid inclusions in quartz = 356-535°C) and moderate salinity (15-25 eq. wt% NaCl). Mixed CO 2H 2O fluids (XCO 2 = .13-.07) found as both primary and secondary inclusions within fluorite are representative of fluids involved in the replacement of britholite-allanite by bastnaesite and sphene, aegirine-augite, and plagioclase by calcite. Minimum pressures of mineral deposition estimated from H 2OCO 2NaCl phase relations range from 1 to 2 kbars. Secondary aqueous fluid inclusions in quartz define a trend of low salinity-high temperature to high salinity-low temperature, thought to be a result of hydration reactions occurring in alaskite and quartz alkali-feldspar syenite. The highest salinity fluids (35-37 eq. wt% NaCl) detected in the area are associated with the formation of uranothorite and late fluorite. Multiple periods of hydrothermal fluid introduction are consistent with recent geological data that indicate that the batholith is composed of several stock-like bodies. The location of the mineralized area near the top of the magma chamber, the presence of numerous miarolitic cavities, and the bulk composition of inclusion fluids (Na ≥ K > Ca) suggest that the fluids responsible for REE and Th mineralization were of magmatic origin.

  1. Single and multiphase inclusions in metapelitic garnets of the Rhodope Metamorphic Province, NE Greece.

    PubMed

    Mposkos, Evripidis; Perraki, Maria; Palikari, Sarra

    2009-08-01

    Single and multiphase inclusions in garnet porphyroblasts from the diamond-bearing pelitic gneisses were studied by means of combined Raman Spectroscopy and Electron Scanning Microscopy (SEM/EDX). They are either randomly distributed or with preferred orientation within the garnet host and their dimensions vary from less than 5 up to 60 microm. In the single-phase inclusions quartz, rutile, kyanite and graphite dominate. Biotite, zircon, apatite, monazite and allanite are also common. Two types of multiphase inclusions were recognized, hydrous silicate (Type I) and silicate-carbonate (Type II) ones. The carbon-bearing multiphase inclusions predominantly consist of Mg-siderite+graphite+CO(2)+muscovite+quartz formed by a high density carboniferous fluid rich in Fe, Mg, Si and less Ca, Mn, Al and K trapped in the growing garnet in a prograde stage of metamorphism at high-pressure (HP) conditions. The carbon-free multiphase inclusions predominantly consist of biotite+quartz+rutile+/-kyanite+muscovite formed through decompression-dehydration/melting reactions of pre-existing phengite. Single and multiphase inclusions are characterized by polygonal to negative crystal shape formed by dissolution-reprecipitation mechanism between the garnet host and the inclusions during the long lasting cooling period (>100 Ma) of the Kimi Complex.

  2. Progress toward accurate high spatial resolution actinide analysis by EPMA

    NASA Astrophysics Data System (ADS)

    Jercinovic, M. J.; Allaz, J. M.; Williams, M. L.

    2010-12-01

    High precision, high spatial resolution EPMA of actinides is a significant issue for geochronology, resource geochemistry, and studies involving the nuclear fuel cycle. Particular interest focuses on understanding of the behavior of Th and U in the growth and breakdown reactions relevant to actinide-bearing phases (monazite, zircon, thorite, allanite, etc.), and geochemical fractionation processes involving Th and U in fluid interactions. Unfortunately, the measurement of minor and trace concentrations of U in the presence of major concentrations of Th and/or REEs is particularly problematic, especially in complexly zoned phases with large compositional variation on the micro or nanoscale - spatial resolutions now accessible with modern instruments. Sub-micron, high precision compositional analysis of minor components is feasible in very high Z phases where scattering is limited at lower kV (15kV or less) and where the beam diameter can be kept below 400nm at high current (e.g. 200-500nA). High collection efficiency spectrometers and high performance electron optics in EPMA now allow the use of lower overvoltage through an exceptional range in beam current, facilitating higher spatial resolution quantitative analysis. The U LIII edge at 17.2 kV precludes L-series analysis at low kV (high spatial resolution), requiring careful measurements of the actinide M series. Also, U-La detection (wavelength = 0.9A) requires the use of LiF (220) or (420), not generally available on most instruments. Strong peak overlaps of Th on U make highly accurate interference correction mandatory, with problems compounded by the ThMIV and ThMV absorption edges affecting peak, background, and interference calibration measurements (especially the interference of the Th M line family on UMb). Complex REE bearing phases such as monazite, zircon, and allanite have particularly complex interference issues due to multiple peak and background overlaps from elements present in the activation volume, as well as interferences from fluorescence at a distance from adjacent phases or distinct compositional domains in the same phase. Interference corrections for elements detected during boundary fluorescence are further complicated by X-ray focusing geometry considerations. Additional complications arise from the high current densities required for high spatial resolution and high count precision, such as fluctuations in internal charge distribution and peak shape changes as satellite production efficiency varies from calibration to analysis. No flawless method has yet emerged. Extreme care in interference corrections, especially where multiple and sometime mutual overlaps are present, and maximum care (and precision) in background characterization to account for interferences and curvature (e.g., WDS scan or multipoint regression), are crucial developments. Calibration curves from multiple peak and interference calibration measurements at different concentrations, and iterative software methodologies for incorporating absorption edge effects, and non-linearities in interference corrections due to peak shape changes and off-axis X-ray defocussing during boundary fluorescence at a distance, are directions with significant potential.

  3. Linking microstructures, petrology and in situ U-(Th)-Pb geochronology to constrain P-T-t-D evolution of the Greather Himalyan Sequences in Western Nepal (Central Himalaya)

    NASA Astrophysics Data System (ADS)

    Iaccarino, Salvatore; Montomoli, Chiara; Carosi, Rodolfo; Langone, Antonio

    2013-04-01

    Last advances in forward modelling of metamorphic rocks and into the understanding of accessories minerals behaviour, suitable for geochronology (e.g. zircon and monazite), during metamorphism, bring new insights for understanding the evolution of metamorphic tectonites during orogenic cycles (Williams and Jercinovic, 2012 and reference therein). One of the best exposure of high- to medium grade- metamorphic rocks, is represented by the Greater Himalayan Sequence (GHS) in the Himalayan Belt, one of the most classic example of collisional orogen. Recent field work in Mugu Karnali valley, Western Nepal (Central Himalaya), identified a compressional top to the South ductile shear zone within the core of the GHS, named Magri Shear Zone (MSZ), developed in a high temperature regime as testified by quartz microstructures and syn-kinematic growth of sillimanite. In order to infer the tectono-metamorphic meaning of MSZ, a microstructural study coupled with pseudosection modelling and in situ U-(Th)-Pb monazite geochronology was performed on selected samples from different structural positions. Footwall sample constituted by (Grt + St ± Ky) micaschist shows a prograde garnet growth (cores to inner rims zoning), from ~500°C, ~0.60GPa (close to garnet-in curve) to ~580°C, ~1.2 GPa temporal constrained between 21-18 Ma, by medium Y cores to very low Y mantles monazite micro-chemical/ages domain . In this sample garnet was still growing during decompression and heating at ~640°C, ~0.75 GPa (rims), and later starts to be consumed, in conjunction with staurolite growth at 15-13 Ma, as revealed by high Y rims monazite micro-chemical/ages domain. Hanging-wall mylonitic samples have a porphyroclastic texture, with garnet preserve little memory of prograde path. Garnet near rim isoplets and matrix minerals intersect at ~700°C and ~0.70 GPa. A previous higher P stage, at ~1.10 GPa ~600°C, is testified by cores of larger white mica porhyroclasts. Prograde zoned allanite (Janots et al., 2008) is rarely found within garnet crystal, while monazite found only along mylonitic foliation helps to constrain the age of shearing and hanging-wall rocks exhumation, between 25 Ma (low Y cores interpretd as Aln out product, close to P peak) and 18 Ma (high Y rims interpreted as Grt breakdown/melt crystallization product during decompression). The present results point out the occurence of a high-temperature shear zone, in the core of the GHS, active before the onset of the Main Central Thrust, responsible of at least a part of the exhumation of the metamorphic rocks. References Janots, E., Engi, M., Berger, J., Allaz, J., Schwarz, O., Spandler, C., (2008): Prograde metamorphic sequence of REE minerals in pelitic rocks of the Central Alps: implications for allanite monazite-xenotime phase relations from 250 to 610°C. Journal of Metamorphic Geology 26, 509-526. Williams, M.L., Jercinovic, M.J., (2012): Tectonic interpretation of metamorphic tectonites: integrating compositional mapping, microstructrual analyses and in situ monazite dating. Journal of Metamorphic Geology 30, 739-752.

  4. Application of Scanning Electron Microscopy/Energy-Dispersive X-Ray Spectroscopy for Characterization of Detrital Minerals in Karst Cave Speleothems.

    PubMed

    Zupančič, Nina; Miler, Miloš; Šebela, Stanka; Jarc, Simona

    2016-02-01

    Micro-scale observations in karst caves help to identify different processes that shaped local morphology. Scanning electron microscopy/energy-dispersive X-ray spectroscopy inspection of speleothems from two karst caves in Slovenia, Predjama and Črna Jama, confirmed the presence of sub-angular to sub-rounded detrital fragments of clay minerals, feldspars, quartz, Fe-oxides/hydroxides, rutile and Nb-rutile, xenotime, kassite, allanite, fluorapatite, epidote, ilmenite, monazite, sphene, and zircon, between 2 and 50 μm across. These occur in porous layers separating calcite laminae in the clayey coating on the layer below the surface of the speleothems, and are also incorporated within actual crystals. It is likely that they are derived from the weathered rocks of the Eocene flysch. Probably they were first transported into the caves by floodwaters forming cave sediments. Later, depending upon the climate conditions, they were moved by air currents or by water to the surface of active speleothems. They might also be redeposited from overlying soils enriched with wind-transported minerals from the flysch, or from higher passages filled with weathered flysch sediment, by drip water percolating through the fissured limestone. As some of the identified minerals are carriers of rare earth elements, Ti and Zr, their presence could affect any palaeoclimatic interpretations that are based upon the geochemical composition of the speleothems.

  5. The Statherian itabirite-bearing sequence from the Morro Escuro Ridge, Santa Maria de Itabira, Minas Gerais, Brazil

    NASA Astrophysics Data System (ADS)

    Silveira Braga, Flávia Cristina; Rosière, Carlos Alberto; Queiroga, Gláucia Nascimento; Rolim, Vassily Khoury; Santos, João Orestes Schneider; McNaughton, Neal Jesse

    2015-03-01

    The itabirite-bearing metasedimentary sequence from Morro Escuro Ridge comprises the basal units of the Espinhaço Supergroup and makes up a small tectonic inlier developed during one of the Brasiliano orogenic events (800-500 Ma), amongst horses of the Archean TTG gneisses, including sheared granites of the anorogenic Borrachudos Suite (˜1700 Ma). The metasedimentary rocks are comprised of low-to intermediate-amphibolite facies schists, quartzites, conglomerates and banded iron formation (itabirite) correlatable with the sequences of the Serro Group, which underlies the metasedimentary rocks of the Espinhaço Supergroup in the Serra da Serpentina Ridge. A maximum Statherian deposition age (1668 Ma) was established using SHRIMP U-Pb isotopic constraints on zircon grains from conglomerate and quartzite units overlying the itabirite. The itabirite is predominantly hematitic and its geochemical characteristics are typical of a Lake Superior-type BIF deposited in a platformal, suboxic to anoxic environment distant from Fe-bearing hydrothermal vents. Close to the contact zone with amphibolites of the Early Neoproterozoic Pedro Lessa mafic suite, an increase of the magnetite content and crystallization of metasomatic Mg-hornblende and Ce-allanite can be observed. These mineralogical changes developed preferentially along the igneous contact zone but are probably co-genetic with the formation of alteration haloes in zircon grains during the Neoproterozoic Brasiliano orogeny (506 ± 6 Ma).

  6. Spectroscopic study of inclusions in gem corundum from Mercaderes, Cauca, Colombia

    NASA Astrophysics Data System (ADS)

    Zeug, Manuela; Rodríguez Vargas, Andrés Ignacio; Nasdala, Lutz

    2017-03-01

    Mineral inclusions in gem corundum from Mercaderes, Cauca, Colombia, were investigated non-destructively using Raman and photoluminescence spectroscopy, with special focus lying on phases containing radioactive elements. Besides abundant rutile, the minerals zircon, apatite, feldspar, and an epidote-group species, most probably allanite-(Ce), were found. The latter is detected easily from its characteristic Nd3+ emission pattern, which may prove useful in future provenance studies. Zircon inclusions range from well crystalline to moderately radiation damaged [FWHM (full width at half band maximum) of the ν 3(SiO4) Raman band 1.8-10.9 cm-1]. Both the zircon inclusions and their neighbouring host corundum are affected by compressive stress, which is assigned to (1) heterogeneous volume expansion of the host-inclusion couple upon pressure release during the uplift following primary growth and (2) volume expansion of the zircon inclusion due to the accumulation of self-irradiation damage. Internal stress of zircon inclusions averages 1.1 GPa. Heat treatment of corundum leads to structural reconstitution of zircon (narrowed zircon Raman bands with FWHMs in the range 1.8-2.7 cm-1) and accompanying stress release in the adjacent corundum (indicated by downshifts of the R 1 emission of Cr3+). The observation of broadened Raman band of zircon inclusions therefore allows one to exclude high-temperature enhancement of the host corundum.

  7. Natural and anthropogenic radionuclides in rocks and beach sands from Ezine region (Canakkale), Western Anatolia, Turkey.

    PubMed

    Orgün, Y; Altinsoy, N; Sahin, S Y; Güngör, Y; Gültekin, A H; Karahan, G; Karacik, Z

    2007-06-01

    This paper represents the first reports on the natural and anthropogenic radionuclides in Kestanbol granitic pluton and surrounding rocks, and coastal region of the Ezine town. To assess the radiological hazard of the natural radioactivity, the radium equivalent activity, the absorbed dose rate and the external hazard index were calculated, and in situ gamma dose rates were measured. The high-activity concentrations were measured in the pluton and sands, which was originated mainly from the pluton, due to the presence of zircon, allanite, monazite, thorite, uranothorite and apatite. The average activity concentrations of (238)U, (232)Th and (40)K are 174.78, 204.69 and 1171.95 Bq kg(-1) for pluton, and 290.36, 532.04 and 1160.75 Bq kg(-1) for sands, respectively. (137)Cs in Ezine region ranged from 0-6.57 Bq kg(-1). The average absorbed dose rate for the granitic and sand samples were calculated to be 251.6 and 527.92 nGy h(-1), respectively. The maximum contribution to the total absorbed gamma dose rate in air was due to the (232)Th (52.3% for pluton and 67.1% for sands). The Raeq activities of the pluton and sands are higher than the recommended maximum value of 370 Bq kg(-1) criterion limit of Raeq activity for building materials.

  8. Airborne and ground reconnaissance of part of the syenite complex near Wausau, Marathon county, Wisconsin

    USGS Publications Warehouse

    Vickers, R.C.

    1955-01-01

    Airborne and ground reconnaissance for radioactive minerals in part of the syenite complex near Wausau, Marathon county, Wis., found 12 radioactive mineral localities. The rocks in the area are of Precambrian age and consist of syenite and nepheline syenite, which have intruded older granite, greenstone, quartzite, and argillite. There are very few outcrops, and much of the bedrock is deeply weathered and covered by residual soil. Thorium-bearing zircon pegatite float was found within the area of syenite and nepheline syenite at four localities. Reddish-brown euhedral to subeuhedral crystals of well-zoned zircon (variety cyrtolite) comprise more than 40 percent of some of the specimens. The radioactive mineral at four localities outside the area of syneites was identified as thorogummite, which occurred in nodular masses in residual soil. Alinement of the thorogummite float and associated radioactivity suggests that the thorogummite has resulted from weathering of narrow veins or pegmatites containing thorium-bearing minerals. Unidentified thorium-bearing minerals were found at three localities, and a specimen of allanite weighing about 2 pounds was found at one locality. Shallow trenches at two of the largest radioactivity anomalies showed that the radioactive material extended down into weathered bedrock. The occurrences might warrant additional physical exploration should there be sufficient demand for thorium. Further reconnaissance in the area would probably result in the discovery of additional occurrences.

  9. Towards the challenging REE exploration in Indonesia

    NASA Astrophysics Data System (ADS)

    Setiawan, Iwan

    2018-02-01

    Rare earth elements (REE) are the seventeen elements, including fifteen from 57La to 71Lu, in addition to 21Sc and 39Y. In rock-forming minerals, rare earth elements typically occur in compounds as trivalent cations in carbonates, oxides, phosphates, and silicates. The REE occur in a wide range of rock types: igneous, sedimentary and metamorphic rocks. REE are one of the critical metals in the world. Their occurrences are important to supply the world needs on high technology materials. Indonesia has a lot of potential sources of REE that are mainly from residual tin mining processes in Bangka islands, which are associated with radioactive minerals e.g. monazite and xenotime. However, the REE from monazite and xenotime are difficult to extract and contain high radioactivity. Granitoids are widely distributed in Sumatra, Sulawesi, Kalimantan and Papua. They also have a very thick weathering crusts. Important REE-bearing minerals are allanite and titanite. Their low susceptibilities during weathering result an economically potential REE concentration. I-/A- type granitoids and their weathered crusts are important REE sources in Indonesia. Unfortunately, their distribution and genesis have not been deeply studied. Future REE explorations challenge are mainly of the granitoids their weathered crusts. Geochemical and mineralogical characterization of type of granitoids and their weathered crusts, the hydrothermally altered rocks, and clear REE regulation will help discover REE deposits in Indonesia.

  10. Preliminary summary review of thorium-bearing mineral occurrences in Alaska

    USGS Publications Warehouse

    Bates, Robert G.; Wedow, Helmuth

    1952-01-01

    Thorium-bearing minerals are known at 47 localities in Alaska. At these localities the thorium occurs as a major constituent or in minor amounts as an impurity in one or more of the following 12 minerals: allanite, columbite, ellsworthite, eschynite, gummite, monazite, orangite, parisite, thorianite, thorite, xenotime, and zircon. In addition other minerals, such as biotite and sphene, are radioactive and may contain thorium. Several unidentified columbate minerals with uranium or thorium and uranium as major constituents have been recognized at some localities. The distribution, by type of deposit, of the 57 thorium occurrences is as follows: lode - 3, lode and placer - 1, granitic rock - 3, granitic rock and related placer - 14, and placer - 26. Of the four lode occurrences only the radioactive veins at Salmon Bay in southeastern Alaska and the contact metamorphic deposit in the Nixon Fork area of central Alaska warrant further consideration, although insufficient data are available to determine whether these two deposits have commercial possibilities. The remaining occurrences of thorium-bearing minerals in Alaska are limited to placer deposits and disseminations of accessory minerals in granitic rocks. In most of these occurrences the thorium-bearing minerals occur in only trace amounts and consequently warrent little further consideration. More data are needed to determine the possibilities of byproduct recovery of thorium-bearing minerals from several of the gold and tin placers.

  11. Garnet cannibalism provides clues to extensive hydration of lower crustal fragments in a subduction channel (Sesia Zone, Northwestern Alps)

    NASA Astrophysics Data System (ADS)

    Giuntoli, Francesco; Lanari, Pierre; Engi, Martin

    2015-04-01

    The extent to which granulites are transformed to eclogites is thought to impose critical limits on the subduction of continental lower crust. Although it is seldom possible to document such densification processes in detail, the transformation is believed to depend on fluid access and deformation. Remarkably complex garnet porphyroblasts are widespread in eclogite facies micaschists in central parts of the Sesia Zone (Western Italian Alps). They occur in polydeformed samples in assemblages involving phengite+quartz+rutile ±paragonite, Na-amphibole, Na-pyroxene, chloritoid. Detailed study of textural and compositional types reveals a rich inventory of growth and partial resorption zones in garnet. These reflect several stages of the polycyclic metamorphic evolution. A most critical observation is that the relict garnet cores indicate growth at 900 °C and 0.9 GPa. This part of the Eclogitic Micaschist Complex thus derived from granulite facies metapelites of Permian age. These dry rocks must have been extensively hydrated during Cretaceous subduction, and garnet records the conditions of these processes. Garnet from micaschist containing rutile, epidote, paragonite and phengite were investigated in detail. Two types of garnet crystals are found in many thin sections: mm-size porphyroclasts and smaller atoll garnets, some 100 µm in diameter. X-ray maps of the porphyroclasts show complex zoning in garnet: a late Paleozoic HT-LP porphyroclastic core is overgrown by several layers of HP-LT Alpine garnet, these show evidence of growth at the expense of earlier garnet generations. Textures indicate 1-2 stages of resorption, with garnet cores that were fractured and then sealed by garnet veins, rimmed by multiple Alpine overgrowth rims with lobate edges. Garnet rim 1 forms peninsula and embayment structures at the expense of the core. Rim 2 surrounds rim 1, both internally and externally, and seems to have grown mainly at the expense of the core. Rim 3 grew mainly at the expense of earlier Alpine rims. In the same samples that show porphyroclastic garnet, atoll garnet occurs, filled with quartz, and the same Alpine overgrowth zones are observed in both types of garnet. Similar features of garnet zoning are present in various lithotypes, allowing the evolution of this continental domain during subduction to be traced. Modeling the different garnet growth zones is challenging, each growth step demanding an estimate the effective bulk composition. According to the XRF analyses of the bulk sample, the core is found to have formed at 900°C, 0.9 GPa. Based on effective bulk compositions, the successive Alpine rims are found to reflect an increase from 600°C, 1.55-1.60 GPa for rim 1 to 630-640°C, 1.9-2.0 GPa for rim 2. Allanite crystals contain inclusions of Alpine garnet; in situ geochronology (U-Th-Pb by LA-ICP-MS) on allanite yields a (minimum) age of ~69 Ma for the main growth of garnet. In summary, the textures and mineral compositions clearly reflect reactive interaction of major amounts of hydrous fluids with dry protoliths. The source of these fluids responsible for converting granulites back to micaschists at eclogite facies conditions within the Sesia subduction channel is being investigated.

  12. High-resolution tephrochronology of the Wilson Creek Formation (Mono Lake, California) and Laschamp event using 238U-230Th SIMS dating of accessory mineral rims

    NASA Astrophysics Data System (ADS)

    Vazquez, Jorge A.; Lidzbarski, Marsha I.

    2012-12-01

    Sediments of the Wilson Creek Formation surrounding Mono Lake preserve a high-resolution archive of glacial and pluvial responses along the eastern Sierra Nevada due to late Pleistocene climate change. An absolute chronology for the Wilson Creek stratigraphy is critical for correlating the paleoclimate record to other archives in the western U.S. and the North Atlantic region. However, multiple attempts to date the Wilson Creek stratigraphy using carbonates and tephras yield discordant results due to open-system effects and radiocarbon reservoir uncertainties as well as abundant xenocrysts. New ion microprobe 238U-230Th dating of the final increments of crystallization recorded by allanite and zircon autocrysts from juvenile pyroclasts yield ages that effectively date eruption of key tephra beds and delimit the timing of basal Wilson Creek sedimentation to the interval between 26.8±2.1 and 61.7±1.9 ka. Tephra (Ash 15) erupted during the geomagnetic excursion originally designated the Mono Lake excursion yields an age of 40.8±1.9 ka, indicating that the event is instead the Laschamp excursion. The new ages support a depositional chronology from magnetostratigraphy that indicates quasi-synchronous glacial and hydrologic responses in the Sierra Nevada and Mono Basin to regional climate change, with intervals of lake filling and glacial-snowpack melting that are in phase with peaks in spring insolation.

  13. Accessory mineral records of tectonic environments? (Invited)

    NASA Astrophysics Data System (ADS)

    Storey, C.; Marschall, H. R.; Enea, F.; Taylor, J.; Jennings, E. S.

    2010-12-01

    Accessory mineral research continues to gather momentum as we seek to unleash their full potential. It is now widely recognised that robust accessory minerals, such as zircon, rutile, titanite, allanite and monazite, are archives of important trace elements that can help deduce metamorphic reaction history in metapelites, metabasites and other rock types. Moreover, they are important carriers of certain trace elements and govern or influence the products of partial melting and of fluid-rock interaction (e.g. magmas and mineralisation) in settings like subduction zones and hydrothermal systems. Perhaps most importantly, they can often be dated using the U-Th-Pb system. More recently, radiogenic (Lu-Hf, Sm-Nd, Rb-Sr) and stable (O) isotope systems have been applied and have further pushed the utility of accessory mineral research. In this talk I will discuss some of these advances towards one particular aim: the use of detrital accessory minerals for fingerprinting tectonic environments. This is a particularly laudable aim in Precambrian rocks, for which the preservation potential of orogenic belts and fossil subduction zones and their diagnostic metamorphic rocks is low. The implication is that our understanding of plate tectonics, particularly in the Archaean, is biased by the preserved in-tact rock record. An analogy is that Jack Hills zircons record evidence of Earth’s crust some 400 Ma before the preserved rock record begins. I will focus on some recent advances and new data from rutile and also the mineral inclusion record within zircon, which shows great promise for petrologic interpretation.

  14. New data on carbonatites of the Il'mensky-Vishnevogorsky alkaline complex, the southern Urals, Russia

    NASA Astrophysics Data System (ADS)

    Nedosekova, I. L.

    2007-04-01

    Carbonatites that are hosted in metamorphosed ultramafic massifs in the roof of miaskite intrusions of the Il’mensky-Vishnevogorsky alkaline complex are considered. Carbonatites have been revealed in the Buldym, Khaldikha, Spirikha, and Kagan massifs. The geological setting, structure of carbonatite bodies, distribution of accessory rare-metal mineralization, typomorphism of rock-forming minerals, geochemistry, and Sr and Nd isotopic compositions are discussed. Dolomite-calcite carbonatites hosted in ultramafic rocks contain tetraferriphlogopite, richterite, accessory zircon, apatite, magnetite, ilmenite, pyrrhotite, pyrite, and pyrochlore. According to geothermometric data and the composition of rock-forming minerals, the dolomite-calcite carbonatites were formed under K-feldspar-calcite, albite-calcite, and amphibole-dolomite-calcite facies conditions at 575-300°C. The Buldym pyrochlore deposit is related to carbonatites of these facies. In addition, dolomite carbonatites with accessory Nb and REE mineralization (monazite, aeschynite, allanite, REE-pyrochlore, and columbite) are hosted in ultramafic massifs. The dolomite carbonatites were formed under chlorite-sericite-ankerite facies conditions at 300-200°C. The Spirikha REE deposit is related to dolomite carbonatite and alkaline metasomatic rocks. It has been established that carbonatites hosted in ultramafic rocks are characterized by high Sr, Ba, and LREE contents and variable Nb, Zr, Ti, V, and Th contents similar to the geochemical attributes of calcio-and magnesiocarbonatites. The low initial 87Sr/86Sr = 0.7044-0.7045 and ɛNd ranging from 0.65 to -3.3 testify to their derivation from a deep mantle source of EM1 type.

  15. High-resolution tephrochronology of the Wilson Creek Formation (Mono Lake, California) and Laschamp event using 238U-230Th SIMS dating of accessory mineral rims

    USGS Publications Warehouse

    Vazquez, Jorge A.; Lidzbarski, Marsha I.

    2012-01-01

    Sediments of the Wilson Creek Formation surrounding Mono Lake preserve a high-resolution archive of glacial and pluvial responses along the eastern Sierra Nevada due to late Pleistocene climate change. An absolute chronology for the Wilson Creek stratigraphy is critical for correlating the paleoclimate record to other archives in the western U.S. and the North Atlantic region. However, multiple attempts to date the Wilson Creek stratigraphy using carbonates and tephras yield discordant results due to open-system effects and radiocarbon reservoir uncertainties as well as abundant xenocrysts. New ion microprobe 238U-230Th dating of the final increments of crystallization recorded by allanite and zircon autocrysts from juvenile pyroclasts yield ages that effectively date eruption of key tephra beds and delimit the timing of basal Wilson Creek sedimentation to the interval between 26.8±2.1 and 61.7±1.9 ka. Tephra (Ash 15) erupted during the geomagnetic excursion originally designated the Mono Lake excursion yields an age of 40.8±1.9 ka, indicating that the event is instead the Laschamp excursion. The new ages support a depositional chronology from magnetostratigraphy that indicates quasi-synchronous glacial and hydrologic responses in the Sierra Nevada and Mono Basin to regional climate change, with intervals of lake filling and glacial-snowpack melting that are in phase with peaks in spring insolation.

  16. Evidence for polymetamorphic garnet growth in the Çine (southern Menderes) Massif, Western Turkey

    NASA Astrophysics Data System (ADS)

    Baker, C. B.; Catlos, E. J.; Sorensen, S. S.; Çemen, I.; Hancer, M.

    2008-07-01

    Garnet-based thermobarometry is often used to develop models for the evolution of the Menderes Massif, a key Aegean metamorphic core complex. Here we present X-ray element maps and high-contrast backscattered electron (BSE) and cathodoluminescence (CL) images from a garnet-bearing rock from the Çine (southern Menderes) Massif. The images document a polymetamorphic history as plagioclase and garnet grains show distinct cores and rims. The sample contains matrix monazite in reaction with allanite. The garnet in the sample is likely not in equilibrium with its matrix minerals. This is evidenced by BSE images that document compositional variability in both core and rim zoning and tracks of bright streaks extending from rim to core. We propose that some garnet that is now present in the Menderes Massif formed due to collision during Cambro-Ordovician and may have recrystallized during subsequent collisional and extensional events. These processes led to non-equilibrium compositions and can result in spurious pressure-temperature (P-T) calculations. To establish the feasibility of the P-T estimates of rocks from the Çine Massif for input into tectonic models for the region, more than one sample from single outcrops should be analyzed. Rocks within the Çine Massif have been suggested to display inverted metamorphism, an increase in T towards structurally higher levels. Based on the garnet documented here, we propose that the inverted metamorphism may be a consequence of apparent P-T rather than a real phenomenon.

  17. Natural radionuclide concentrations in granite rocks in Aswan and Central-Southern Eastern Desert, Egypt and their radiological implications.

    PubMed

    Issa, Shams A M; Uosif, M A M; Abd el-Salam, L M

    2012-07-01

    Different types of granites, used extensively in local construction, were collected from five localities in Egypt, namely: Abu Ziran (Central Eastern Desert), Gabal El Maesala (Aswan) and three areas from Wadi Allaqi, (Gabal Abu Marw, Gabal Haumor and Gabal um Shalman), in the South Eastern Desert. Granite samples were studied radiologically, petrographically and geochemically. The contents of natural radionuclides ((226)Ra, (232)Th and (40)K) were measured in investigated samples by using gamma spectrometry [NaI (Tl) 3'×3']. The activity concentrations of (226)Ra, (232)Th and (40)K in the selected granite samples ranged from 9±0.5 to 111±7, 8±1 to 75±4 and 100±6 to 790±40 Bq kg(-1), respectively. The external hazard index (H(ex)), absorbed dose and annual effective dose rate were evaluated to assess the radiation hazard for people living in dwellings made of the materials studied. The calculated radium equivalents were lower than the values recommended for construction materials (370 Bq kg(-1)). The excess lifetime cancer risks were also calculated. Petrographically, the granites studied are varied in the form of potash-feldspar, quartz, plagioclase, mica and hornblende. The accessory minerals are zircon, apatite and allanite. Geochemically, the chemical composition of the granite is studied especially for major oxides. They are characterized to have SiO(2), K(2)O, Na(2)O and Al(2)O(3) with depletion in CaO, MgO, TiO(2) and P(2)O(5).

  18. Petrology and geobarometry of Admiralty-Revillagigedo belt granitoids near Petersburg, southeastern Alaska

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Hammarstrom, J.M.; Brew, D.A.

    1993-04-01

    The Admiralty-Revillagigedo belt (ARB) of southeastern Alaska is an approximately 400 mile long northwest-trending belt of Late Cretaceous ([approximately]95 Ma) calcalkalic plutons that extends from Juneau to Ketchikan. The ARB is bounded on the east by the younger Coast plutonic complex sill and on the west by the mid-Cretaceous Muir-Chichagof plutonic belt. Near Petersburg, the ARB consists of a variety of plutons that include equigranular and porphyritic quartz diorite, tonalite, quartz monzodiorite, and granodiorite. Minerals in these plutons are: hornblende, biotite, plagioclase, potassium feldspar, quartz, apatite, zircon, titanite, and ilmenite [+-] epidote, minor allanite, magnetite, grossular-almandine garnet, clinopyroxene, and locallymore » trace amounts of sulfide minerals. New geochemical data for six samples from three plutons near Petersburg overlap data for the rest of the ARB, which is metaluminous to slightly peraluminous. The central ARB granitoids are moderately LREE-enriched with slightly negative to slightly positive europium anomalies. High strontium (700 to 800 ppm) and low rubidium contents in central ARB plutons overlap compositions of ARB plutons to the north and south, and magmatic epidote-bearing plutons elsewhere. Pressure estimates for pluton emplacement based on hornblende geobarometry (6 to 9 kbars) are compatible with pressure estimates for plutons to the south and for metamorphic aureole assemblages around ARB plutons elsewhere in the western metamorphic belt of southeastern Alaska. These data support the chemical consanguinity of plutons along the length of the magmatic arc now preserved as the ARB and suggest that the whole ARB has been uplifted and eroded to expose plutons emplaced at relatively deep crustal levels.« less

  19. Fitful and protracted magma assembly leading to a giant eruption, Youngest Toba Tuff, Indonesia

    USGS Publications Warehouse

    Reid, Mary R; Vazquez, Jorge A.

    2017-01-01

    The paroxysmal eruption of the 74 ka Youngest Toba Tuff (YTT) of northern Sumatra produced an extraordinary 2800 km3 of non-welded to densely welded ignimbrite and co-ignimbrite ash-fall. We report insights into the duration of YTT magma assembly obtained from ion microprobe U-Th and U-Pb dates, including continuous age spectra over >50% of final zircon growth, for pumices and a welded tuff spanning the compositional range of the YTT. A relatively large subpopulation of zircon crystals nucleated before the penultimate caldera-related eruption at 501 ka, but most zircons yielded interior dates 100-300 ka thereafter. Zircon nucleation and growth was likely episodic and from diverse conditions over protracted time intervals of >100 to >500 ka. Final zircon growth is evident as thin rim plateaus that are in Th/U chemical equilibrium with hosts, and that give crystallization ages within tens of ka of eruption. The longevity and chemical characteristics of the YTT zircons, as well as evidence for intermittent zircon isolation and remobilization associated with magma recharge, is especially favored at the cool and wet eutectoid conditions that characterize at least half of the YTT, wherein heat fluxes could dissolve major phases but have only a minor effect on larger zircon crystals. Repeated magma recharge may have contributed to the development of compositional zoning in the YTT but, considered together with limited allanite, quartz, and other mineral dating and geospeedometry, regular perturbations to the magma reservoir over >400 ka did not lead to eruption until 74 ka ago.

  20. Sm-Nd isotopic compositions of LREE minerals for use as reference materials for in situ analysis by LA-MC-ICPMS

    NASA Astrophysics Data System (ADS)

    Fisher, C. M.; McFarlane, C. R.; Sylvester, P.; Hanchar, J. M.; Lam, R.; Schmitz, M. D.

    2009-12-01

    Recent work has demonstrated the possibility of obtaining both accurate and precise in situ Sm-Nd isotopic data in light rare earth enriched (LREE) accessory minerals including apatite, titanite, and monazite, using laser ablation-multicollector-inductively coupled plasma mass spectrometry (LA-MC-ICPMS). A distinct advantage of using LA-MC-ICPMS is that Sm-Nd isotopic data from these minerals can be determined in sub-grain domains potentially avoiding problems of isotopic mixing from inherited or xenocrystic components and allowing both valuable tracer isotope and geochronologic data to be obtained. However, a number of analytical obstacles complicate accurate Sm-Nd determination by LA-MC-ICPMS including mass bias corrections, the 144Sm isobaric interference on 144Nd, and potential offset (ca. 20-40 ppm) from thermal ionization mass spectrometry (TIMS) determination of similar materials. Thus, in order to verify Sm-Nd isotopic determination from unknowns, matrix-matched quality control standards (i.e., reference materials) must be developed to test the data handling protocol. This talk will present new Sm-Nd isotopic data determined by both TIMS as well as LA-MC-ICPMS of a number of natural potential reference minerals including Durango apatite, Fish Canyon titanite, Daibosatsu allanite, Trebilcock monazite, as well as a monazite from the Doi Inthanon core complex in northern Thailand. Our preliminary LA-MC-ICPMS results demonstrate that Durango apatite, Fish Canyon titanite, and Thailand monazite show both inter- and intra-grain homogeneity at current levels of precision (ca. 0.3-0.5 ɛNd) and close agreement with our TIMS data.

  1. The Life and Times of Supervolcanoes: Inferences from Long Valley Caldera

    NASA Technical Reports Server (NTRS)

    Simon, Justin

    2014-01-01

    Cataclysmic eruptions of silicic magma from "supervolcanoes" are among the most awe-inspiring natural phenomena found in the geologic record, in terms of size, power, and potential hazard. Based on the repose intervals between eruptions of this magnitude, the magmas responsible for them could accumulate gradually in the shallow crust over time scales that may be in excess of a million years (Smith, 1979; Spera and Crisp, 1981; Shaw, 1985). Pre-eruption magma residence time scales can also be inferred from the age difference between eruption (i.e., using 40Ar/39Ar dating to determine the time when hot erupted material cools to below its Ar closure temperature, 200 to 600 degC) and early pre-eruption crystallization (i.e., zircon saturation temperatures; Reid et al., 1997). I will discuss observations from Long Valley a Quaternary volcanic center in California. Long Valley is a voluminous, dominantly silicic caldera system. Based on extensive dating of accessory minerals (e.g., U-Th-Pb dating of zircon and allanite) along with geochemical and isotopic data we find that silicic magmas begin to crystallize 10's to 100's of thousands of years prior to their eruption and that rhyolites record episodes of punctuated and independent evolution rather than the periodic tapping of a long-lived magma. The more punctuated versus more gradual magma accumulation rates required by the absolute and model ages, respectively, imply important differences in the mass and heat fluxes associated with the generation, differentiation, and storage of voluminous rhyolites and emphasize the need to reconcile the magmatic age differences.

  2. Pervasive Eclogitization Due to Brittle Deformation and Rehydration of Subducted Basement: Effects on Continental Recycling?

    NASA Astrophysics Data System (ADS)

    Engi, Martin; Giuntoli, Francesco; Lanari, Pierre; Burn, Marco; Kunz, Barbara; Bouvier, Anne-Sophie

    2018-03-01

    The buoyancy of continental crust opposes its subduction to mantle depths, except where mineral reactions substantially increase rock density. Sluggish kinetics limit such densification, especially in dry rocks, unless deformation and hydrous fluids intervene. Here we document how hydrous fluids in the subduction channel invaded lower crustal granulites at 50-60 km depth through a dense network of probably seismically induced fractures. We combine analyses of textures and mineral composition with thermodynamic modeling to reconstruct repeated stages of interaction, with pulses of high-pressure (HP) fluid at 650-670°C, rehydrating the initially dry rocks to micaschists. SIMS oxygen isotopic data of quartz indicate fluids of crustal composition. HP growth rims in allanite and zircon show uniform U-Th-Pb ages of ˜65 Ma and indicate that hydration occurred during subduction, at eclogite facies conditions. Based on this case study in the Sesia Zone (Western Italian Alps), we conclude that continental crust, and in particular deep basement fragments, during subduction can behave as substantial fluid sinks, not sources. Density modeling indicates a bifurcation in continental recycling: Chiefly mafic crust, once it is eclogitized to >60%, are prone to end up in a subduction graveyard, such as is tomographically evident beneath the Alps at ˜550 km depth. By contrast, dominantly felsic HP fragments and mafic granulites remain positively buoyant and tend be incorporated into an orogen and be exhumed with it. Felsic and intermediate lithotypes remain positively buoyant even where deformation and fluid percolation allowed them to equilibrate at HP.

  3. The El Horror uranium anomaly in northeastern Sonora, Mexico: Constraints from geochemical and mineralogical approaches

    NASA Astrophysics Data System (ADS)

    Grijalva-Rodríguez, T.; Valencia-Moreno, M.; Calmus, T.; Del Rio-Salas, R.; Balcázar-García, M.

    2017-12-01

    This work reviews the characteristics of the El Horror uranium prospect in northeastern Sonora, Mexico. It was formerly detected by a radiometric anomaly after airborne gamma ray exploration carried out in the 70's by the Mexican government. As a promising site to contain important uranium resources, the El Horror was re-evaluated by CFE (Federal Electricity Commission) by in situ gamma ray surveys. The study also incorporates rock and stream sediment ICP-MS geochemistry, X-ray diffraction, X-ray fluorescence, Raman spectrometry and Scanning Electron Microscopy (SEM) to provide a better understanding of the radiometric anomaly. The results show that, instead of a single anomaly, it comprises at least five individual anomalies hosted in hydrothermally altered Laramide (80-40 Ma) andesitic volcanic rocks of the Tarahumara Formation. Concentrations for elemental uranium and uranium calculated from gamma ray surveys (i.e., equivalent uranium) are not spatially coincident within the anomaly, but, at least at some degree, they do so in specific sites. X-ray diffraction and Raman spectrometry revealed the presence of rutile/anatase, uvite, bukouvskyte and allanite as the more likely mineral phases to contain uranium. SEM studies revealed a process of iron-rich concretion formation, suggesting that uranium was initially incorporated to the system by adsorption, but was largely removed later during incorporation of Fe+3 ions. Stream sediment geochemistry reveals that the highest uranium concentrations are derived from the southern part of the Sierra La Madera batholith (∼63 Ma), and decrease toward the El Horror anomaly.

  4. Origin of Miocene andesite and dacite in the Goldfield-Superstition volcanic province, central Arizona: Hybrids of mafic and silicic magma mixing

    NASA Astrophysics Data System (ADS)

    Fodor, R. V.; Johnson, Kelly G.

    2016-07-01

    The Miocene Goldfield-Superstition volcanic province (G-SVP), ∼8000 km2 in central Arizona, is composed largely of silicic pyroclastic rocks and lavas, and smaller volumes of alkalic basalt and intermediate-composition lavas. Volcanism began ∼20.5 Ma as sparse rhyolitic and mainly basaltic lavas followed by intermediate lavas, lasting until ∼19 Ma. At that time, ∼1 m.y. of silicic eruptions began, creating most of the G-SVP. Petrologic studies are available for basalts and some for silicic rocks, but petrologic/geochemical information is sparse for intermediate-composition lavas. These latter, andesites and dacites, are the focus of this study, in which we present the processes and sources responsible for their origins. Goldfield-Superstition andesites and dacites have SiO2 ∼56-70 wt.% and Na2O + K2O that qualifies some as trachy-andesite and -dacite. A prominent petrographic feature is plagioclase-phyric texture (∼11-30 vol% plagioclase), where oligoclase-andesine phenocrysts have cores surrounded by corroded, or reacted, zones, mantled by higher An% plagioclase. Where corroded zones are absent, margins are etched, curved, or embayed. Groundmass plagioclase is labradorite, also more calcic than the phenocrysts. Other minerals are quartz (subrounded; embayed), clinopyroxene, amphibole, biotite, and rare titanite and zircon. A salient compositional characteristic that provides insight to andesite-dacite origins with respect to other G-SVP rocks is revealed when using SiO2 as an index. Namely, abundances of many incompatible elements, mainly HFSE and REE, decrease over the low to high SiO2 range (i.e., abundances are lower in dacites than in co-eruptive andesites and underlying alkalic basalts). As examples: G-SVP basalts have ∼50-70 ppm La, and andesites-dacites have ∼59-22 ppm La; for Zr, basalts have ∼225-170 ppm, but most andesites-dacites have ∼180-50; for Y, basalts >20 ppm, andesites-dacites ∼18-9 ppm. To understand these trends of lower HFSE and REE with increasing SiO2, we modeled fractional crystallization of G-SVP alkalic basalt (∼50 wt.% SiO2; ∼9 wt.% MgO), dehydration melting (10-25%) of granodiorite and high-K amphibolite, and basalt-rhyolite magma mixing. Fractionation and melting each require specific modal percentages of titanite, zircon, and allanite (e.g., ⩽1%), the high ends of ranges for accessory-mineral/liquid partitioning coefficients, continual crystallization of accessory minerals from basalt to dacite (for fractionation), and specific source-melting percentages and low titanite, zircon, and allanite melting proportions (∼0.02; dehydration melting). These requirements are too stringent to be realistic. Moreover, accessory minerals are rare in these lavas, and neither fractionation nor melting accounts for the plagioclase textures observed. On the other hand, low-HFSE, -REE rhyolites (e.g., La 9-31 ppm; Zr 31-93; Nb 9-17; Y 4-10) containing Na-plagioclase are in the G-SVP and were temporally and spatially available to have mixed with G-SVP basalts. Mixing proportions of 20:80 to 90:10 for different rhyolite:basalt combinations yield hybrid compositions that overlap the G-SVP andesite-dacite compositional fields. Also, basalt invading rhyolite reservoirs containing mush zones can account for Na-plagioclase concentrations of ∼11-30 vol% formed after mush disruption and dispersal, plagioclase corroded-cores and higher-An% mantles and groundmass, and subrounded-embayed quartz. The straightforward explanation for G-SVP intermediate lavas, then, is repeated hybridization of basaltic and low-HFSE, -REE rhyolitic magmas during the early stages of G-SVP magmatism.

  5. Uranium potential of precambrian rocks in the Raft River area of northwestern Utah and south-central Idaho. Final report

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Black, B.A.

    1980-09-01

    A total of 1214 geochemical samples were collected and analyzed. The sampling media included 334 waters, 616 stream sediments, and 264 rocks. In addition, some stratigraphic sections of Elba and Yost Quartzites and Archean metasedimentary rock were measured and sampled and numerous radiation determinations made of the various target units. Statistical evaluation of the geochemical data permitted recognition of 156 uranium anomalies, 52 in water, 79 in stream sediment, and 25 in rock. Geographically, 68 are located in the Grouse Creek Mountains, 43 in the Raft River Mountains, and 41 in the Albion Range. Interpretation of the various data leadsmore » to the conclusion that uranium anomalies relate to sparingly and moderately soluble uraniferous heavy minerals, which occur as sparse but widely distributed magmatic, detrital, and/or metamorphically segregated components in the target lithostratigraphic units. The uraniferous minerals known to occur and believed to account for the geochemical anomalies include allanite, monazite, zircon, and apatite. In some instances samarskite may be important. These heavy minerals contain uranium and geochemically related elements, such as Th, Ce, Y, and Zr, in sufficient quantities to account for both the conspicuous lithologic preference and the generally observed low amplitude of the anomalies. The various data generated in connection with this study, as well as those available in the published literature, collectively support the conclusion that the various Precambrian W and X lithostratigraphic units pre-selected for evaluation probably lack potential to host important Precambrian quartz-pebble conglomerate uranium deposits. Moreover it is also doubted that they possess any potential to host Proterozoic unconformity-type uranium deposits.« less

  6. "Gris Quintana": a Spanish granite from the Past into the Future.

    NASA Astrophysics Data System (ADS)

    José Tejado, Juan; Mota, M. Isabel; Pereira, Dolores

    2014-05-01

    "Gris Quintana" is a medium-grained, biotite and amphibole granodiorite extracted in the Pluton of Quintana de la Serena (Extremadura, Spain). It is a constant light grey granite from the Hercynian geologic with excellent physicomechanical and physicochemical properties. The granodiorite is composed of plagioclase, biotite, quartz and alkali feldspar, with accessory allanite, titanite, apatite, zircon and ilmenite, mostly as inclusions within the biotite crystals. This commercial variety is extracted from many quarries in the late Hercynian plutons located in the Iberian Massif in Spain period (transition between Central Iberian and Ossa-Moren Zones), having large reserves of granite. Many of the quarries have their own transformation factory (high production zone), with which the sector is offered an endless variety of finishes and constructive rock typologies. A wide range of solutions to architects and designers are offered. Gris Quintana granite is one of the materials with highest technological benefits that are used in arquitecture. "Gris Quintana" granite has been used since ancient times, not only at a regional, but also at national and international level: paving, building (structural, exterior façadas, interior uses), urban decoration and funeral art. It can be found in monuments and more recently, in buildings of different styles and uses, that stand out in beauty and splendor, lasting in time. Some singular works in "Gris Quintana" granite all over the world: extension to the "Congreso de Diputados" (Parliament) in Madrid, "Puerta de San Vicente" in Madrid, Andalucia Parliament columns in Sevilla, New Senate Buiding in Madird, "Gran Vía" pavement in Madrid, "Teatro Real façade" in Madrid… "Gris Quintana" granite accomplishes all the requirements for its nomination as Global Heritage Stone Resource, for both its use in construction and for artistic purposes.

  7. Mineralogy and Geochemistry of Granitic rocks within Lichen Hills, Outback Nunatak, Northern Victoria Land, Antarctica

    NASA Astrophysics Data System (ADS)

    KIM, T.; KIM, Y.; Lee, I.; Lee, J.; Woo, J.

    2015-12-01

    The study areas, Lichen Hills and Outback Nunatak are located in the Northern Victoria Land which is close to Pacific Ocean side of Transantarctic Mountain (TAM), Antarctica. According to the study of Zeller and Dreschoff (1990), the radioactivity values of Lichen hills and Frontier Mt. area in the Victoria Land were very high. To identify the geochemical characteristics of granitic rocks in these areas, 13 samples of Lichen Hills rocks and 4 samples of Outback Nunatak rocks are analyzed. For mineralogical study, samples were observed in macroscale as well as microscale including microscope electron probe analysis. Rock samples of Lichen Hills, Outback Nunatak are mainly leucogranite and granitic pegmatite. These rock samples are composed of quartz, k-feldspar, plagioclase, muscovite, garnet, tourmaline like granite. In SEM-EDS analysis, the observed light colored minerals show relatively high Th, U, Dy, Ce, Nb concentration. This suggests that rock samples may contain minerals such as fergusonite, monazite, thorite, allanite, karnasurtite which are considered to be REE-bearing minerals. Samples of related rocks have been analyzed in terms of major, trace and rare earth element (REE) concentrations using X-ray fluorescence (XRF) spectrometer and Inductively Coupled Plasma Mass Spectrometer (ICP-MS). As concentration of SiO2 increase, Al2O3, TiO2, Fe2O3, MgO, P2O5 concentration decrease and Na2O, K2O, MnO concentration increase. Analyzed trace elements and REE are normalized using CI Chondrite, Primitive mantle. The normalized data show that LREE are enriched compared to HREE. The distinct negative anomalies of Eu, Sr are observed, indicating that rock-forming melts are fairly processed state of fractional crystallization. It means that Th, U, Nb, Ta are much enriched in the melts.

  8. Foliation development and reaction softening by dissolution and precipitation in the transformation of granodiorite to orthogneiss, Glastonbury Complex, Connecticut, U.S.A

    USGS Publications Warehouse

    Wintsch, R.P.; Aleinikoff, J.N.; Yi, K.

    2005-01-01

    Textures, microstructures, and patterns of chemical zoning in minerals in a granodioritic orthogneiss in the Glastonbury Complex, Connecticut, lead to the interpretation that foliation development was facilitated by retrograde hydration reactions in the presence of an aqueous fluid. Incomplete replacement of the metastable magmatic minerals K-feldspar + hastingsite + magnetite produced foliation-defining biotite + epidote + quartz. These reaction products did not replace K-feldspar - hastingsite interfaces; rather, either biotite or epidote replaced the amphibole, and plagioclase replaced K-feldspar. Biotite and epidote precipitated syntectonically in discrete layers that define the foliation in the orthogneiss, whereas quartz precipitated primarily in ribbons, further enhancing the fabric. Metastable REE-rich igneous titanite also dissolved, and was incompletely replaced by REE-poor, Al-bearing metamorphic titanite. The similar concentrations of the REE in epidote and titanite show that the REE released by titanite dissolution were precipitated locally as the allanite component in adjacent grains of epidote. The entire process was syntectonic, with most grains showing multiple overgrowths in the direction of extension as defined by stretched xenoliths. Sufficient U was present in the titanite overgrowths to allow SHRIMP dating of cores, mantles, and rims. These results suggest at least three retrograde Alleghanian events of growth in a span of ???30 m.y. Thus the dissolution - transportation - precipitation process not only describes the reaction mechanism but also leads to the redistribution of reaction products into nearly monomineralic layers, thus contributing to metamorphic differentiation and to the development of the foliation. The resulting orthogneiss was much weaker that the granodiorite protolith, owing to this reaction and textural softening.

  9. Crystallization conditions of porphyritic high-K calc-alkaline granitoids in the extreme northeastern Borborema Province, NE Brazil, and geodynamic implications

    NASA Astrophysics Data System (ADS)

    Campos, Benedita Cleide Souza; Vilalva, Frederico Castro Jobim; Nascimento, Marcos Antônio Leite do; Galindo, Antônio Carlos

    2016-10-01

    An integrated textural and chemical study on amphibole, biotite, plagioclase, titanite, epidote, and magnetite was conducted in order to estimate crystallization conditions, along with possible geodynamic implications, for six Ediacaran porphyritic high-K calc-alkaline granite plutons (Monte das Gameleiras, Barcelona, Acari, Caraúbas, Tourão, and Catolé do Rocha) intrusive into Archean to Paleoproterozoic rocks of the São José do Campestre (SJCD) and Rio Piranhas-Seridó (RPSD) domains, northern Borborema Province. The studied rocks include mainly porphyritic leucocratic monzogranites, as well as quartz-monzonites and granodiorites. Textures are marked by K-feldspar megacrysts (5-15 cm long) in a fine-to medium-grained matrix composed of quartz, plagioclase, amphibole, biotite, as well as titanite, epidote, Fesbnd Ti oxides, allanite, apatite, and zircon as accessory minerals. Amphibole, biotite and titanite share similar compositional variations defined by increasing Al and Fe, and decreasing Mg contents from the plutons emplaced into the SJCP (Monte das Gameleiras and Barcelona) towards those in the RPSD (Acari, Caraúbas, Tourão, and Catolé do Rocha). Estimated intensive crystallization parameters reveal a weak westward range of increasing depth of emplacement, pressure and temperature in the study area. The SJCD plutons (to the east) crystallized at shallower crustal depths (14-21 km), under slightly lower pressure (3.8-5.5 kbar) and temperature (701-718 °C) intervals, and high to moderate oxygen fugacity conditions (+0.8 < ΔFQM < +2.0). On the other hand, the RPSD plutons (to the west) were emplaced at slightly deeper depths (18-23 km), under higher, yet variable pressures (4.8-6.2 kbar), temperatures (723-776 °C), and moderate to low oxygen fugacity conditions (-1.0 < ΔFQM < +1.8). These results reinforce the contrasts between the tectono-strutuctural domains of São José do Campestre and Rio Piranhas-Seridó in the northern Borborema Province.

  10. The origin of secondary heavy rare earth element enrichment in carbonatites: Constraints from the evolution of the Huanglongpu district, China

    NASA Astrophysics Data System (ADS)

    Smith, M.; Kynicky, J.; Xu, Cheng; Song, Wenlei; Spratt, J.; Jeffries, T.; Brtnicky, M.; Kopriva, A.; Cangelosi, D.

    2018-05-01

    The silico‑carbonatite dykes of the Huanglongpu area, Lesser Qinling, China, are unusual in that they are quartz-bearing, Mo-mineralised and enriched in the heavy rare earth elements (HREE) relative to typical carbonatites. The textures of REE minerals indicate crystallisation of monazite-(Ce), bastnäsite-(Ce), parisite-(Ce) and aeschynite-(Ce) as magmatic phases. Burbankite was also potentially an early crystallising phase. Monazite-(Ce) was subsequently altered to produce a second generation of apatite, which was in turn replaced and overgrown by britholite-(Ce), accompanied by the formation of allanite-(Ce). Bastnäsite and parisite where replaced by synchysite-(Ce) and röntgenite-(Ce). Aeschynite-(Ce) was altered to uranopyrochlore and then pyrochlore with uraninite inclusions. The mineralogical evolution reflects the evolution from magmatic carbonatite, to more silica-rich conditions during early hydrothermal processes, to fully hydrothermal conditions accompanied by the formation of sulphate minerals. Each alteration stage resulted in the preferential leaching of the LREE and enrichment in the HREE. Mass balance considerations indicate hydrothermal fluids must have contributed HREE to the mineralisation. The evolution of the fluorcarbonate mineral assemblage requires an increase in aCa2+ and aCO32- in the metasomatic fluid (where a is activity), and breakdown of HREE-enriched calcite may have been the HREE source. Leaching in the presence of strong, LREE-selective ligands (Cl-) may account for the depletion in late stage minerals in the LREE, but cannot account for subsequent preferential HREE addition. Fluid inclusion data indicate the presence of sulphate-rich brines during alteration, and hence sulphate complexation may have been important for preferential HREE transport. Alongside HREE-enriched magmatic sources, and enrichment during magmatic processes, late stage alteration with non-LREE-selective ligands may be critical in forming HREE-enriched carbonatites.

  11. Ion-adsorption REEs in regolith of the Liberty Hill pluton, South Carolina, USA: An effect of hydrothermal alteration

    USGS Publications Warehouse

    Bern, Carleton R.; Yesavage, Tiffany; Foley, Nora K.

    2017-01-01

    Ion-adsorbed rare earth element (REE) deposits supply the majority of world heavy REE production and substantial light REE production, but relatively little is known of their occurrence outside Southeast Asia. We examined the distribution and forms of REEs on a North American pluton located in the highly weathered and slowly eroding South Carolina Piedmont. The Hercynian Liberty Hill pluton experiences a modern climate that includes ~ 1500 mm annual rainfall and a mean annual temperature of 17 °C. The pluton is medium- to coarse-grained biotite-amphibole granite with minor biotite granite facies. REE-bearing phases are diverse and include monazite, zircon, titanite, allanite, apatite and bastnäsite. Weathered profiles were sampled up to 7 m-deep across the ~ 400 km2 pluton. In one profile, ion-adsorbed REEs plus yttrium (REE + Y) ranged up to 581 mg/kg and accounted for up to 77% of total REE + Y in saprolite. In other profiles, ion-adsorbed REE + Y ranged 12–194 mg/kg and only accounted for 3–37% of totals. The profile most enriched in ion-adsorbed REEs was located along the mapped boundary of two granite facies and contained trioctahedral smectite in the saprolite, evidence suggestive of hydrothermal alteration of biotite at that location. Post-emplacement deuteric alteration can generate easily weathered REE phases, particularly fluorocarbonates. In the case of Liberty Hill, hydrothermal alteration may have converted less soluble to more soluble REE minerals. Additionally, regolith P content was inversely correlated with the fraction ion-adsorbed REEs, and weathering related secondary REE-phosphates were found in some regolith profiles. Both patterns illustrate how low P content aids in the accumulation of ion-adsorbed REEs. The localized occurrence at Liberty Hill sheds light on conditions and processes that generate ion-adsorbed REEs.

  12. Co-Cu-Au deposits in metasedimentary rocks-A preliminary report

    USGS Publications Warehouse

    Slack, J.F.; Causey, J.D.; Eppinger, R.G.; Gray, J.E.; Johnson, C.A.; Lund, K.I.; Schulz, K.J.

    2010-01-01

    A compilation of data on global Co-Cu-Au deposits in metasedimentary rocks refines previous descriptive models for their occurrence and provides important information for mineral resource assessments and exploration programs. This compilation forms the basis for a new classification of such deposits, which is speculative at this early stage of research. As defined herein, the Co-Cu-Au deposits contain 0.1 percent or more by weight of Co in ore or mineralized rock, comprising disseminated to semi-massive Co-bearing sulfide minerals with associated Fe- and Cu-bearing sulfides, and local gold, concentrated predominantly within rift-related, siliciclastic metasedimentary rocks of Proterozoic age. Some deposits have appreciable Ag ? Bi ? W ? Ni ? Y ? rare earth elements ? U. Deposit geometry includes stratabound and stratiform layers, lenses, and veins, and (or) discordant veins and breccias. The geometry of most deposits is controlled by stratigraphic layering, folds, axial-plane cleavage, shear zones, breccias, or faults. Ore minerals are mainly cobaltite, skutterudite, glaucodot, and chalcopyrite, with minor gold, arsenopyrite, pyrite, pyrrhotite, bismuthinite, and bismuth; some deposits have appreciable tetrahedrite, uraninite, monazite, allanite, xenotime, apatite, scheelite, or molybdenite. Magnetite can be abundant in breccias, veins, or stratabound lenses within ore or surrounding country rocks. Common gangue minerals include quartz, biotite, muscovite, K-feldspar, albite, chlorite, and scapolite; many deposits contain minor to major amounts of tourmaline. Altered wall rocks generally have abundant biotite or albite. Mesoproterozoic metasedimentary successions constitute the predominant geologic setting. Felsic and (or) mafic plutons are spatially associated with many deposits and at some localities may be contemporaneous with, and involved in, ore formation. Geoenvironmental data for the Blackbird mining district in central Idaho indicate that weathering of abundant Fe, S, As, Co, and Cu in sulfide minerals of the deposits produces acidic waters, especially in pyrite-rich deposits; mine runoff has high concentrations of Fe, Cu, and Mn that exceed U.S. drinking water or aquatic life standards.

  13. Critical Zone Weathering and Your Smartphone: Understanding How Mineral Decomposition and Colloid Redistribution Can Generate Rare Earth Element Deposits

    NASA Astrophysics Data System (ADS)

    Bern, C.; Foley, N.

    2014-12-01

    Rare earth elements (REE's) are crucial in the manufacture of smartphones and many other high tech devices. Increasing global demand and relatively narrow geographic sourcing have promoted interest in understanding REE deposit genesis and distribution. Highly weathered, clay-hosted, ion-exchange type deposits in southern China are the source of much of the world's production of the more valuable heavy REEs. Such deposits form as REE-bearing minerals weather and REEs released to solution in ionic form are retained by negatively charged exchange sites on clay minerals. We are investigating the potential for ion-exchange REE deposits in the Piedmont of the southeastern United States, where slow erosion rates have preserved thick (up to 20 m) regolith, as required for such deposits. The Liberty Hill pluton outcrops as coarse-grained biotite-amphibole granite and quartz monzonite over nearly 400 km2 in South Carolina, and has an age of 305 Ma (new SHRIMP ion microprobe zircon age). In weathered profiles over the pluton, ion-exchangeable REE content ranges from 8 to 580 ppm and accounts for 2 to 80% of bulk REE content. Elemental and heavy mineral distributions suggest the wide ranging differences in leachability may be attributable to the amount and distribution of resistant REE-bearing phases (e.g., monazite) relative to more easily weathered phases (e.g., allanite) in the parent granite. The REEs show little mobility within the regolith, indicating the effectiveness of the ion-exchange retention mechanism. In contrast, vertical redistribution of colloidal material shows maximum accumulations at ~1 m depth, as traced by the newly developed dual-phase (colloids vs. solution) mass balance model. The contrast suggests redistributed colloidal material has minimal influence on REE mobilization or retention. Conditions and processes necessary for ion-exchange REE deposit development exist in the Piedmont, but their presence will depend upon favorable parent rock mineralogy.

  14. Signal or noise? Separating grain size-dependent Nd isotope variability from provenance shifts in Indus delta sediments, Pakistan

    NASA Astrophysics Data System (ADS)

    Jonell, T. N.; Li, Y.; Blusztajn, J.; Giosan, L.; Clift, P. D.

    2017-12-01

    Rare earth element (REE) radioisotope systems, such as neodymium (Nd), have been traditionally used as powerful tracers of source provenance, chemical weathering intensity, and sedimentary processes over geologic timescales. More recently, the effects of physical fractionation (hydraulic sorting) of sediments during transport have called into question the utility of Nd isotopes as a provenance tool. Is source terrane Nd provenance resolvable if sediment transport strongly induces noise? Can grain-size sorting effects be quantified? This study works to address such questions by utilizing grain size analysis, trace element geochemistry, and Nd isotope geochemistry of bulk and grain-size fractions (<63μm, 63-125 μm, 125-250 μm) from the Indus delta of Pakistan. Here we evaluate how grain size effects drive Nd isotope variability and further resolve the total uncertainties associated with Nd isotope compositions of bulk sediments. Results from the Indus delta indicate bulk sediment ɛNd compositions are most similar to the <63 µm fraction as a result of strong mineralogical control on bulk compositions by silt- to clay-sized monazite and/or allanite. Replicate analyses determine that the best reproducibility (± 0.15 ɛNd points) is observed in the 125-250 µm fraction. The bulk and finest fractions display the worst reproducibility (±0.3 ɛNd points). Standard deviations (2σ) indicate that bulk sediment uncertainties are no more than ±1.0 ɛNd points. This argues that excursions of ≥1.0 ɛNd points in any bulk Indus delta sediments must in part reflect an external shift in provenance irrespective of sample composition, grain size, and grain size distribution. Sample standard deviations (2s) estimate that any terrigenous bulk sediment composition should vary no greater than ±1.1 ɛNd points if provenance remains constant. Findings from this study indicate that although there are grain-size dependent Nd isotope effects, they are minimal in the Indus delta such that resolvable provenance-driven trends can be identified in bulk sediment ɛNd compositions over the last 20 k.y., and that overall provenance trends remain consistent with previous findings.

  15. Geochemistry of the Serifos calc-alkaline granodiorite pluton, Greece: constraining the crust and mantle contributions to I-type granitoids

    NASA Astrophysics Data System (ADS)

    Stouraiti, C.; Baziotis, I.; Asimow, P. D.; Downes, H.

    2017-11-01

    The Late Miocene (11.6-9.5 Ma) granitoid intrusion on the island of Serifos (Western Cyclades, Aegean Sea) is composed of syn- to post-tectonic granodiorite with quartz monzodiorite enclaves, cut by dacitic and aplitic dikes. The granitoid, a typical I-type metaluminous calcic amphibole-bearing calc-alkaline pluton, intruded the Cycladic Blueschists during thinning of the Aegean plate. Combining field, textural, geochemical and new Sr-Nd-O isotope data presented in this paper, we postulate that the Serifos intrusion is a single-zoned pluton. The central facies has initial 87Sr/86Sr = 0.70906 to 0.7106, ɛNd(t) = - 5.9 to - 7.5 and δ18Οqtz = + 10 to + 10.6‰, whereas the marginal zone (or border facies) has higher initial 87Sr/86Sr = 0.711 to 0.7112, lower ɛ Nd(t) = - 7.3 to - 8.3, and higher δ18Οqtz = + 10.6 to + 11.9‰. The small range in initial Sr and Nd isotopic values throughout the pluton is paired with a remarkable uniformity in trace element patterns, despite a large range in silica contents (58.8 to 72 wt% SiO2). Assimilation of a crustally derived partial melt into the mafic parental magma would progressively add incompatible trace elements and SiO2 to the evolving mafic starting liquid, but the opposite trend, of trace element depletion during magma evolution, is observed in the Serifos granodiorites. Thermodynamic modeling of whole-rock compositions during simple fractional crystallization (FC) or assimilation-fractional crystallization (AFC) processes of major rock-forming minerals—at a variety of pressure, oxidation state, and water activity conditions—fails to reproduce simultaneously the major element and trace element variations among the Serifos granitoids, implying a critical role for minor phases in controlling trace element fractionation. Both saturation of accessory phases such as allanite and titanite (at SiO2 ≥ 71 wt%)(to satisfy trace element constraints) and assimilation of partial melts from a metasedimentary component (to match isotopic data) must have accompanied fractional crystallization of the major phases.

  16. Re-thinking the Laramide: Investigating the role of fluids in producing surface uplift using xenolith mineralogy and geochronology

    NASA Astrophysics Data System (ADS)

    Butcher, Lesley Ann

    High-temperature, high-pressure mineral assemblages preserved in much of the North American lithosphere owe their origins to Archean and Proterozoic tectonic processes. Whether subsequent mechanical, thermal, or chemical modification of ancient lithosphere affects overlying crust and the extent to which such processes contribute to anomalous deformation and topography is the interior of continents is poorly understood. This study addresses the occurrence and effects of hydration on continental crust in producing regionally elevated topography in the Colorado Plateau since the Late Cretaceous. Mineralogical characteristics of two deep crustal xenoliths (GR-11 and RM-21) from the Four Corners Volcanic field record varying degrees of hydrous alteration including extensive replacement of garnet by hornblende, secondary albite and phengite growth at the expense of primary plagioclase, and secondary monazite growth in association with fluid-related allanite and plagioclase breakdown. Results from forward petrological modeling for both deep crustal xenoliths are consistent with hydration at greater than 20 km depth prior to exhumation in the ~20 Ma volcanic host. In situ Th/Pb dating provides evidence for a finite period of fluid-related monazite crystallization in xenolith RM-21 from 91 +/- 2.8 Ma to 58 +/- 4 Ma, concurrent with timing estimates of low-angle subduction of the Farallon slab. Hydration-related reactions at depth lead to a net density decrease as low-density hydrous phases (hbl+/-ab+/-phg) grow at the expense of high-density, anhydrous minerals (gt+/-pl) abundant in unaltered Proterozoic crust. If these reactions are sufficiently pervasive and widespread, reductions in lower crustal density would provide a significant and quantifiable source of lithospheric buoyancy. Calculations for density decreases associated with extensive hydration recorded in xenolith GR-11 for an ~25 km thick crustal layer yield uplift estimates on the order of hundreds of meters associated with phase changes at depth. The results of this study substantiate the hypothesis that chemical alteration of lower continental crust by slab-derived fluids played a role in producing Laramide-related surface uplift of the Colorado Plateau and establishes chemical modification of continental lithosphere as a credible possibility for producing elevated regional topography in continental interiors.

  17. The role of superheating in the formation of Glass Mountain obsidians (Long Valley, CA) inferred through crystallization of sanidine

    NASA Astrophysics Data System (ADS)

    Waters, Laura E.; Andrews, Benjamin J.

    2016-10-01

    The Glass Mountain obsidians (Long Valley, CA) are crystal poor (<8 vol%) and highly evolved (high SiO2, low Sr), and therefore, their formation required extremely efficient separation of melts from a crystal-rich source. A petrologic and experimental investigation of the mineral phases in Glass Mountain lavas identifies conditions under which phenocrysts grew and the driving mechanism for crystallization, which places constraints on the possible processes that generated the obsidians. The obsidian in this study (GM-11) is saturated in nine phases (sanidine + quartz + plagioclase + titanomagnetite + ilmenite + zircon + apatite + allanite + biotite), and results of high-resolution SEM compositional mapping and electron microprobe analysis reveal that individual sanidine crystals are normally zoned and span a range of compositions (Or40-78). Sanidines have a "granophyric" texture, characterized by intergrowths of quartz and sanidine. Mineral phases in the natural sample are compared to H2O-saturated phase equilibrium experiments conducted in cold-seal pressure vessels, over a range of conditions (700-850 °C; 75-225 MPa), and all are found to be plausible phenocrysts. Comparison of sanidine compositions from the natural sample with those grown in phase equilibrium experiments demonstrates that sanidine in the natural sample occurs in a reduced abundance. Further comparison with phase equilibrium experiments suggests that sanidine compositions track progressive loss of dissolved melt water (±cooling), suggesting that crystallization in the natural obsidian was driven predominantly by degassing resulting from decompression. It is paradoxical that an effusively (slowly) erupted lava should contain multiple phenocryst phases, including sanidine crystals that span a range of compositions with granophyric textures, and yet remain so crystal poor. To resolve this paradox, it is necessary that the solidification mechanism (degassing or cooling) that produced the sanidine crystals (and other mineral phases) must have an associated kinetic effect(s) that efficiently hinders crystal nucleation and growth. Decompression experiments conducted in this study and from the literature collectively demonstrate that the simplest way to inhibit nucleation during degassing-induced crystallization is to initiate degassing ± cooling from superliquidus conditions, and therefore, the Glass Mountain obsidians were superheated prior to crystallization.

  18. Textures and compositions of cobalt pentlandite and cobaltian mackinawite from the Madan-Kudan copper deposit, Khetri Copper Belt, Rajasthan, India

    NASA Astrophysics Data System (ADS)

    Baidya, Abu Saeed; Sen, Atlanta; Pal, Dipak C.

    2018-06-01

    The Khetri Copper Belt (KCB), a part of the Proterozoic Delhi-Aravalli fold belt in western India, hosts several Cu deposits, which are known to contain considerable Au, Ag, Co and Ni. Although many Co-bearing phases have been reported from the KCB and adjacent areas, detailed textural and geochemical data are either unavailable or scant except for mackinawite. In this study, we describe the textures and compositions (determined by EPMA) of two very rare Co-rich phases, namely cobaltian mackinawite (containing up to 12.68 wt.% Co, 1.90 wt.% Ni and 2.52 wt.% Cu) and cobalt-pentlandite (containing up to 49.30 wt.% Co and 10.19 wt.% Ni), identified based on composition, from the Madan-Kudan deposit. To the best of our knowledge, neither cobalt-pentlandite nor such highly Co-rich mackinawite have previously been reported from this area. The common sulphide minerals viz. chalcopyrite, pyrrhotite and rare pyrite occur in chalcopyrite-pyrrhotite ± pyrite-magnetite-chlorite-blue amphibole (Cl-rich hastingsite-pargasite-sadanagaite) ± marialitic scapolite ± allanite ± uraninite veins in amphibole-bearing feldspathic quartzite and garnetiferous chlorite schist. Cobaltian mackinawite is invariably associated with chalcopyrite and occurs as exsolution and inclusion within chalcopyrite or outside, but at the contact of chalcopyrite. On the other hand, cobalt-pentlandite is invariably associated with pyrrhotite and shows similar textural relation with pyrrhotite as that of mackinawite with chalcopyrite. Mineralogically diverse undeformed sulphide veins comprising Cl-rich amphibole and locally Cl-rich marialitic scapolite suggests epigenetic hydrothermal mineralization involving Cl-rich saline fluid in the Madan-Kudan deposit. Transport of metals, derived from a mafic source rock with high intrinsic Ni:Co ratio, by Cl-rich fluid can suitably explain the high Co:Ni ratio of the studied ore minerals. Presence of such highly Co-rich phases and other circumstantial evidences, enumerated in this work, are consistent with variants of Fe oxide (-Cu-Au) (IOCG) style mineralization, at least for some stages of mineralization in the Madan-Kudan deposit.

  19. Thermometers and thermobarometers in granitic systems

    USGS Publications Warehouse

    Anderson, J.L.; Barth, A.P.; Wooden, J.L.; Mazdab, F.; ,

    2008-01-01

    The ability to determine the thermal and barometric history during crystallization and emplacement of granitic plutons has been enhanced by several new calibrations applicable to granitic mineral assemblages. Other existing calibrations for granitic plutons have continued to be popular and fairly robust. Recent advances include the trace element thermometers Ti-in-quartz, Ti-in-zircon, and Zr-in-sphene (titanite), which need to be further evaluated on the roles of reduced activities due to lack of a saturating phase, the effect of pressure dependence (particularly for the Ti-in-zircon thermometer), and how resistive these thermometers are to subsolidus reequilibration. As zircon and sphene are also hosts to radiogenic isotopes, these minerals potentially also provide new insights into the temperature - time history of magmas. When used in conjunction with pressure-sensitive mineral equilibria in the same rocks, a complete assessment of the P-T-t (pressure-temperature-time) path is possible given that the mineralogy of plutons can reflect crystallization over a range of pressure and temperature during ascent and emplacement and that many intrusions are now seen as forming over several millions of years during the protracted history of batholith construction. Accessory mineral saturation thermometers, such as those for zircon, apatite, and allanite, provide a different and powerful perspective, specifically that of the temperature of the onset of crystallization of these minerals, which can allow an estimate of the range of temperature between the liquidus and solidus of a given pluton. In assessment of the depth of crystallization and emplacement of granitic plutons, the Al-in-hornblende remains popular for metaluminous granites when appropriately corrected for temperature. For peraluminous granites, potential new calibrations exist for the assemblages bearing garnet, biotite, plagioclase, muscovite, and quartz. Other thermometers, based on oxygen abundance, and including Fe-Ti oxides, pyroxene, fayalitic olivine, quartz, sphene, and/or biotite, some of which have been recently revised, can provide additional information on temperature and oxygen fugacity. Oxygen fugacity can range over several orders of magnitude in different magmatic systems and can have profound influence on the mineralogy and mineral compositions in granitic magmas. It also forms the foundation of the popular magnetite- versus ilmenite-series granite classification. Copyright ?? Mineralogical Society of America.

  20. REE enrichment due to fenitization of Devonian granites, Rodeo de Los Molles, Central Argentina

    NASA Astrophysics Data System (ADS)

    Lorenz, M.; Altenberger, U.; Trumbull, R. B.; Lira, R.; Lopez De Luchi, M. G.; Viñas, N.

    2017-12-01

    The Rodeo de Los Molles rare earth element (REE) mineralization is characterized by an uncommon REE-bearing assemblage located within a fenitized biotite-monzogranite. The fenitization is found in a NNE-SSW trending, possibly fault related elliptical body in the northern margin of the Devonian Las Chacras-Piedras Coloradas Batholith, San Luis province, Central Argentina. The fenite was produced by the metasomatic addition of K and Na, as well as the loss of Ca and Sr, leading to the transformation of monzogranite to (quartz) alkali-feldspar syenite composition. Whole-rock geochemistry revealed a local enrichment in light rare earth elements within the fenitized zone. Drill-core samples from a mineral exploration campaign (Lira et al., 1999) and new surface samples are the basis for the present investigation, which aims to decipher the fluid evolution and REE-mineralization. REE-bearing minerals are located in irregularly patches and nodules ranging from a few millimeters to more than one meter in diameter. The REE-rich assemblage comprises an intergrowth of primary britholite (Ce,Ca)5(SiO4, PO4)3(OH,F), allanite and apatite with aegirine-augite, titanite, fluorite, bastnaesite and, quartz as well as complex thorium-rich accessory minerals. In more intensely altered areas clinochlore, spherolitic quartz, calcite, kaolinite, hematite and phlogopite also occur. Britholite is an extraordinary mineral belonging to the apatite group, usually described as an accessory mineral. Aside from being one of only three localites in the world where it occurs in ore quantities, Rodeo de Los Molles further contains atypical huge aggregates of the rare mineral. In general, britholite is thought to form by late-magmatic crystallization or alteration of primary minerals in alkali-rich granites (Uher et al., 2015). Its origin as an abundant phase in the Rodeo de Los Molles mineralization is one focus of this study. Lira, R., Barbieri, M., Ripley, E.M., Viñas, N.A. (1999) Actas II South American Symposium on Isotope Geology, p.219-222. Uher, P., Ondrejka, M., Bačík, P., Broska, I., & Konečný, P. (2015) Lithos, 236, p.212-225.

  1. Postorogenic carbonatites at Eden Lake, Trans-Hudson Orogen (northern Manitoba, Canada): Geological setting, mineralogy and geochemistry

    NASA Astrophysics Data System (ADS)

    Chakhmouradian, A. R.; Mumin, A. H.; Demény, A.; Elliott, B.

    2008-07-01

    The Eden Lake pluton in the Trans-Hudson Orogen is the first known occurrence of carbonatites in Manitoba. The pluton is largely made up of modally and geochemically diverse syenitic rocks derived from postorogenic magma(s) of shoshonitic affinity. Their diversity can be accounted for by a combination of crystal fractionation and fluid release in the final evolutionary stage (crystallization of quartz alkali-feldspar syenite). At Eden Lake, carbonatites, represented predominantly by coarse-grained massive to foliated sövite, occur as branching veins and lenticular bodies up to 4 m in thickness showing crosscutting relations with respect to all of the syenitic units. The host rocks are intensely fenitized at the contact, and there is also abundant mineralogical and textural evidence for assimilation of silicate material by carbonatitic magma through wallrock reaction and xenolith fragmentation and digestion. The bulk of the carbonatites are composed of (in order of crystallization): Sr-REE-rich fluorapatite, aegirine-augite, and coarse calcite crystals surrounded by fine-grained calcite (on average, ˜ 90 vol.% of the rock). Noteworthy accessory constituents are celestine, bastnäsite-(Ce) (both as primary inclusions in calcite), Nb-Zr-rich titanite, low-Hf zircon, allanite-(Ce) and andradite. The calcite is chemically uniform (Sr-rich, Mg-Mn-Fe-poor and low in 13C), but shows clear evidence of ductile deformation and syndeformational cataclasis. Geochemically, the carbonatites are enriched in Sr, Ba, light rare-earth elements, Th and U, but depleted in high-field-strength elements (particularly, Ti, Nb and Ta). The stable-isotope composition of coarse- and fine-grained calcite from the carbonatites and interstitial calcite from syenites is remarkably uniform: ca. - 8.16 ± 0.27‰ δ13C (PDB) and + 8.04 ± 0.19‰ δ18O (SMOW). The available textural and geochemical evidence indicates that the Eden Lake carbonatites are not consanguineous with the associated syenites and may have been derived from a Nb-Ti-retentive and 13C-depleted source such as the subducted crustal material underlying the Eden Lake deformation corridor.

  2. Nd Isotope and U-Th-Pb Age Mapping of Single Monazite Grains by Laser Ablation Split Stream Analysis

    NASA Astrophysics Data System (ADS)

    Fisher, C. M.; Hanchar, J. M.; Miller, C. F.; Phillips, S.; Vervoort, J. D.; Martin, W.

    2015-12-01

    Monazite is a common accessory mineral that occurs in medium to high grade metamorphic and Ca-poor felsic igneous rocks, and often controls the LREE budget (including Sm and Nd) of the host rock in which it crystallizes. Moreover, it contains appreciable U and Th, making it an ideal mineral for determining U-Th-Pb ages and Sm-Nd isotopic compositions, both of which are readily determined using in situ techniques with very high spatial resolution like LA-MC-ICPMS. Here, we present the results of laser ablation split stream analyses (LASS), which allows for simultaneous determination of the age and initial Nd isotopic composition in a single analysis. Analyses were done using a 20mm laser spot that allowed for detailed Nd isotope mapping of monazite grains (~30 analyses per ~250mm sized grain). Combined with LREE ratios (e.g., Sm/Nd, Ce/Gd, and Eu anomalies) these results yield important petrogenetic constraints on the evolution of peraluminous granites from the Old Woman-Piute batholith in southeastern California. Our findings also allow an improved understanding of the causes of isotope heterogeneity in granitic rocks. U-Th-Pb age mapping across the crystals reveals a single Cretaceous age for all grains with precision and accuracy typical of laser ablation analyses (~2%). In contrast, the concurrent Nd isotope mapping yields homogeneous initial Nd isotope compositions for some grains and large initial intra-grain variations of up to 8 epsilon units in others. The grains that yield homogeneous Nd isotope compositions have REE ratios suggesting that they crystallized in a fractionally crystallizing magma. Conversely, other grains, which also record fractional crystallization of both feldspar and LREE rich minerals, demonstrate a change in the Nd isotope composition of the magma during crystallization of monazite. Comparison of inter- and intra-grain Nd isotope compositions reveals further details on the potential mechanisms responsible for isotope heterogeneity present in single rock samples. This method highlights the potential of single grain isotope mapping of LREE phases such as monazite, allanite, and titanite for understanding both igneous and metamorphic petrogenesis.

  3. Microstructural observation and chemical dating on monazite from the Shilu Group, Hainan Province of South China: Implications for origin and evolution of the Shilu Fe-Co-Cu ore district

    NASA Astrophysics Data System (ADS)

    Xu, Deru; Kusiak, Monika A.; Wang, Zhilin; Chen, Huayong; Bakun-Czubarow, Nonna; Wu, Chuanjun; Konečný, Patrik; Hollings, Peter

    2015-02-01

    New monazite chemical U-Th-total-Pb (CHIME) ages, combined with microstructural observations, mineral compositions, and whole-rock geochemistry, indicate that the large-scale, banded iron formation (BIF)-type Shilu Fe-Co-Cu ore district in Hainan Province, South China is a multistage product of sedimentation, metamorphism, and hydrothermal-metasomatic alteration associated with multiple orogenies. Two types of monazite, i.e. "polygenetic" and "metamorphic", were identified. The "polygenetic monazite" comprises a magmatic and/or metamorphic core surrounded by a metamorphic rim, and shows complex zoning. Breakdown corona structure, with a core of monazite surrounded by a mantle of fluorapatite, allanite, and/or epidote as concentric growth rings, is commonly observed. This type of monazite yielded three main CHIME-age peaks at ca. 980 Ma, ca. 880 Ma and ca. 450 Ma. The ages which range up to ca. 880 Ma for detrital cores, record a pre-deformational magmatic and/or metamorphic event(s), and is considered to be the depositional time-interval of the Shilu Group and interbedded BIFs in a marine, back-arc foreland basin likely due to the Grenvillian or South China Sibao orogeny. After deposition, the Shilu district was subjected to an orogenic event, which is recorded by the syndeformational metamorphic monazite with ca. 560-450 Ma population. Probably this event not only caused amphibolite facies metamorphism and associated regional foliation S1 but also enriched the original BIFs, and most likely corresponds to the "Pan-African" and/or the South China Caledonian orogeny. The post-deformational "metamorphic" monazite occurs mostly as inclusions in garnet and shows ca. 260 Ma age. It likely represents the Late Permian post-magmatic hydrothermal and related retrograde event(s) initiated by the Indosinian orogeny due to the closure of the Paleo-Tethys. The breakdown of monazite to secondary coronal mineral phases as well as the Fe-remobilization and associated skarnization of the Shilu BIF ore source rocks might also be induced during this retrograde greenschist-facies metamorphism.

  4. REE Mineralization in Kiruna-type Magnetite-Apatite Ore Deposits: Magmatism and Metasomatism

    NASA Astrophysics Data System (ADS)

    Harlov, D. E.

    2015-12-01

    Magnetite-apatite ore bodies of the Kiruna type occur worldwide and are generally associated with volcanic rocks or volcanism. They also show strong evidence of extensive metasomatism over a wide P-T range. Notable examples include the Kiirunavaara ore body, northern Sweden (Harlov et al., 2002, Chem. Geol., 191, 47-72); the Grängesberg ore body, central Sweden (Jonsson et al., 2010, NGF abstracts, vol 1, 88-89); the Mineville ore body, Adirondacks, New York, USA (McKeown and Klemc, 1956, U.S. Geol Sur Bull (1956), pp. 9-23); the Pea Ridge ore body, SE Missouri, USA (Kerr, 1998, MS Thesis, Univ. Windsor, Windsor, Ontario, Canada 113 pp); the Jurassic Marcona ore body in south-central Peru (Chen et al., 2010, Econ Geol, 105, 1441-1456); and a collection of ore bodies from the Bafq Region, central Iran (Daliran et al., 2010, Geol. Assoc. Canada, Short Course Notes, v. 20, p.147-159). In these ore bodies, low Th and U monazite, xenotime, allanite, REE carbonates, and/or REE fluorides are commonly associated with the apatite as inclusions, rim grains, or as independent grains in the surrounding mineral matrix. High contrast BSE imaging, coupled with EMPA and LA-ICPMS, indicates that the apatite has experienced fluid-induced alteration in the form of (Y+REE) + Na + Si + Cl depletion implying that it served as the source for the (Y+REE) (e.g. Kiirunavaara, northern Sweden; Harlov et al., 2002). Formation of monazite and xenotime associated with fluorapatite, as inclusions or rim grains, has experimentally been demonstrated to originate from the fluorapatite as the result of fluid-aided, coupled dissolution-reprecipitation processes (Harlov et al., 2005, Contrib. Mineral. Petrol. 150, 268-286). This is explains the low Th and U content of the monazite and xenotime. Fluid sources could range from 700-900 °C, residual, acidic (HCl, H2HSO4) grain boundary fluids, remaining after the last stages of ore body crystallization, to later stage, cooler (< 600 °C) (H2O-CO2-(Na,K)Cl) fluids originating in the surrounding country rock or as fluids associated with metamorphic events such as regional albitization or actinolization. The abundance of (Y+REE)-bearing minerals in these deposits suggests that in addition to being mined for their Fe ore, they could also be economically mined for (Y+REE) as well.

  5. Petrogenetic evolution of the Mesoproterozoic garnet-bearing granitoids of Dumka, Eastern India: Implication of garnet and biotite composition

    NASA Astrophysics Data System (ADS)

    Roy, P.; Goswami, B.; Ghosal, A.; Nanda, J.; Basak, A.; Bhattacharyya, C.

    2017-12-01

    Garnet is a petrologically significant accessory mineral of igneous rocks. Granite, tonalite, charnoenderbite and enderbite are prominent facies of 1450 Ma old Dumka Granitoids, Jharkhand district, India. Interestingly all the facies of Dumka granitoids contain good amount of garnet and biotite. Sphene, magnetite, ilmenite, zircon, monazite, allanite and rare hornblende present as accessory minerals. The garnets are mainly solid solutions between almandine, pyrope and grossular. Garnets contain 70.5-75.8 mol% of the almandine, 12.8-17.5 mol% of pyrope, 8-11 mol% of grossular and 0.6-2.9 mol% of spessartine. Composition of garnets fit well in the compositional range of igneous garnets suggested by Miller and Stoddard (1981). High MgO and CaO contents together with very low MnO of these garnets suggest that these have been crystallized from granitoid magma under high pressure in the lower crust. No compositional zoning is found in the analyzed garnets. Biotites of the granitoids are rich in Mg [Mg/(Fe+Mg) ratio > 0.4]. Biotites plot in Abdel-Rahman's (1994) field for biotites of calc-alkaline granites. The matrix biotites in these granitoids have higher Ti content than biotites coexist with garnets. Biotites coexisting with garnet are richer in Mg/Fe ratio than matrix biotites. Mg/Fe distribution coefficients between garnet core and matrix biotite (KD= (Mg/Fe)grt/(Mg/Fe)bt) for the Dumka enderbite and tonalite are 0.275 to 0.280 while for the granites the KD varies from 0.189 to 0.264. These KD values are higher than the values obtained from high-grade metamorphic rocks and are consistent with the values of igneous granitoids as shown by Lyons and Morse (1970). Absence of zoning in magmatic garnets in Dumka Granitoids indicate that these have crystallized above 700 °C, whereas absence of "spessartine bell-shaped profile" of the garnets of present study refute their metamorphic origin or that these crystallized below 700 °C (Dahlquist et al., 2007). Geothermobaric calculations reveal an initial crystallization temperature of 850°C and a pressure of 7.0-8.0 kbar, indicating that the parental magma was emplaced at lower crustal depths ( 25 km). Our studies reveal that garnets of Dumka Granitoids formed by direct crystallization from calc-alkaline magma in equilibrium with solid phases such as biotite.

  6. Isotopic and geothermometric constraints on the structural and metamorphic evolution of Homestake gold deposit, Black Hills, South Dakota (USA)

    NASA Astrophysics Data System (ADS)

    Terry, M.; Dahl, P.; Frei, R.

    2003-04-01

    The Homestake Deposit, located in the northern Black Hills and host for 40 million ounces of gold, shows evidence for extensive remobilization of gold related to regional metamorphism deformation associated with the Early Proterozoic assembly of supercontinent Laurentia. Field and petrographic evidence for gold remobilization includes the occurrence of abundant quartz veins associated with selvages of chlorite-siderite-ankerite-pyrrhotite-arsenopyrite-gold in the Homestake Fm. The deposit is located on the western limb of a major anticlinorium that coincides with a vertical N-S-striking garnet isograd, and garnet-biotite geothermometry of metapelites sampled across the anticlinorium indicates a steep metamorphic field gradient of 150^oC/km (east side warmer). This gradient is mirrored by a pronounced fractionation of oxygen isotopes observed in the vein quartz, with δ18O ranging from 10 to 18 ppm. The isograd is parallel with a major N-S-striking shear zone, and kinematic indicators predominantly indicate oblique sinistral motion with east-side up. Garnet was separated from a subsurface sample of the Homestake Fm. collected from the nose of the so-called "main ledge" synform and subjected to Pb stepwise leaching (PbSL) to determine the age of garnet growth and thus metamorphism. PbSL analysis revealed a 207Pb/206Pb age of 1746 ± 10 Ma (± 2σ). Recent work in the southern Black Hills indicates that almandine does not contain sufficient Pb to be dated directly by this method; instead, the PbSL result represents the bulk age of abundant allanite inclusions observed in the garnet. Thus, 1746 Ma is interpreted as a maximum age of prograde garnet growth during regional thermotectonism. Mineral assemblages from selvages in Main Ledge indicate that mineralization occurred at or after peak metamorph, which indicates that 1746 Ma also represents a maximum age for gold remobilization. A minimum 1715 Ma age of these events is indicated by published ages of post-tectonic leucogranite in the Black Hills. Regionally, the N-S orientation, 1746--1715 Ma timing, and sinistral-transpressive motion combine to suggest that this major shear zone in the northern Black Hills represents a northerly extension of the Hartville fault, which is exposed in SE Wyoming, ˜200 km SSW. Correlation of these shear zones would have important implications for Proterozoic terrane assembly in this part of Laurentia.

  7. Synkinematic emplacement of the magmatic epidote bearing Major Isidoro tonalite-granite batholith: Relicts of an Ediacaran continental arc in the Pernambuco-Alagoas domain, Borborema Province, NE Brazil

    NASA Astrophysics Data System (ADS)

    Silva, Thyego R. da; Ferreira, Valderez P.; Lima, Mariucha M. Correia de; Sial, Alcides N.; Silva, José Mauricio R. da

    2015-12-01

    The Neoproterozoic Major Isidoro batholith (˜100 km2), composed of metaluminous to slightly peraluminous magmatic epidote-bearing tonalite to granite, is part of the Águas Belas-Canindé composite batholith, which intruded the Pernambuco-Alagoas Domain of the Borborema Province, northeastern Brazil. These rocks contain biotite, amphibole, titanite and epidote that often shows an allanite core as key mafic mineral phases. K-diorite mafic enclaves are abundant in this pluton as well as are amphibole-rich clots. The plutonic rocks are medium-to high-K calc-alkaline, with SiO2 varying from 59.1 to 71.6%, Fe# from 0.6 to 0.9 and total alkalis from 6.1 to 8.5%. Chondrite-normalized REE patterns are moderately fractionated, show (La/Lu)N ratios from 13.6 to 31.8 and discrete negative Eu anomalies (0.48-0.85). Incompatible-element spidergrams exhibit negative Nb-Ta and Ti anomalies. This batholith was emplaced around 627 Ma (U-Pb SHRIMP zircon age) coevally with an amphibolite-facies metamorphic event in the region. It shows Nd-model age varying from 1.1 to 1.4 Ga, average ɛNd(627Ma) of -1.60 and back-calculated (627 Ma) initial 87Sr/86Sr ratios from 0.7069 to 0.7086. Inherited zircon cores that yielded 206Pb/238U ages from 800 to 1000 Ma are likely derived from rocks formed during the Cariris Velhos (1.1-0.9 Ga) orogenic event. These isotopic data coupled with calculated δ18O(w.r.) value of +8.75‰ VSMOW indicate an I-type source and suggest a reworked lower continental crust as source rock. A granodioritic orthogneiss next to the Major Isidoro pluton, emplaced along the Jacaré dos Homens transpressional shear zone, yielded a U-Pb SHRIMP zircon age of 642 Ma, recording early tectonic movements along this shear zone that separates the Pernambuco-Alagoas Domain to the north, from the Sergipano Domain to the south. The emplacement of the Major Isidoro pluton was synkinematic, coeval with the development of a regional flat-lying foliation, probably during the peak of metamorphism related to the convergence/contractional deformation of the São Francisco craton and Pernambuco-Alagoas block during the Brasiliano Orogeny.

  8. Geochemistry of the Spor Mountain rhyolite, western Utah, as revealed by laser ablation ICP-MS, cathodoluminescence, and electron microprobe analysis

    NASA Astrophysics Data System (ADS)

    Dailey, S. R.; Christiansen, E. H.; Dorais, M.; Fernandez, D. P.

    2015-12-01

    The Miocene topaz rhyolite at Spor Mountain in western Utah hosts one of the largest beryllium deposits in the world and was responsible for producing 85% of the beryllium mined worldwide in 2010 (Boland, 2012). The Spor Mountain rhyolite is composed primarily of Ca-poor plagioclase (An8), sodic sanidine (Or40), Fe-rich biotite (Fe/(Fe+Mg)>0.95; Al 1.2-1.4 apfu), and Ti-poor quartz, along with several trace-element rich accessory phases including zircon, monazite, thorite, columbite, and allanite. Cathodoluminescence (CL) studies of quartz show oscillatory zoning, with 80% of the examined crystals displaying euhedral edges and slightly darker rims. CL images were used to guide laser ablation (LA) ICP-MS analysis of quartz, along with analyses of plagioclase, sanidine, biotite, and glass. Ti concentrations in quartz are 20±6 ppm; there is no quantifiable variation of Ti from core to rim within the diameter of the laser spot (53 microns). Temperatures, calculated using Ti in quartz (at 2 kb, aTiO2=0.34), vary between 529±10 C (Thomas et al., 2011), 669±13 C (Huang and Audetat, 2012), and 691±13 C (Wark and Watson, 2006). Two feldspar thermometry yield temperatures of 686±33 C (Elkins and Grove, 1990) and 670±41 C (Benisek et al., 2010). Zr saturation temperatures (Watson and Harrison, 1983) average 711±28 C. Analysis of the glass reveal the Spor Mountain rhyolite is greatly enriched in rare elements (i.e. Li, Be, F, Ga, Rb, Nb, Mo, Sn, and Ta) compared to average continental crust (Rudnick and Gao, 2003). Be in the glass can have as much as 100 ppm, nearly 50 times the concentration in continental crust. REE partition coefficients for sanidine are 2 to 3 times higher in the Spor Mountain rhyolite when compared to other silicic magmas (Nash and Crecraft, 1985; Mahood and Hildreth, 1983), although plagioclase tends to have lower partition coefficients; biotite has lower partition coefficients for LREE and higher partition coefficients for HREE. The patterns of trace element enrichment and depletion are similar to those of the measured partition coefficients, consistent with a major role for extensive fractional crystallization in the origin of the Be enriched magma.

  9. The petrogenesis of the Early Permian Variscan granites of the Cornubian Batholith: Lower plate post-collisional peraluminous magmatism in the Rhenohercynian Zone of SW England

    NASA Astrophysics Data System (ADS)

    Simons, B.; Shail, Robin K.; Andersen, Jens C. Ø.

    2016-09-01

    The Early Permian Cornubian Batholith was generated during an extensional regime following Variscan convergence within the Rhenohercynian Zone of SW England. Its component granites can be classified, using mineralogical, textural and geochemical criteria, into five main types, all of which are peraluminous (A/CNK > 1.1): G1 (two-mica), G2 (muscovite), G3 (biotite), G4 (tourmaline) and G5 (topaz). G1 granites formed through up to 20% muscovite and minor biotite dehydration melting of a metagreywacke source at moderate temperatures and pressures (731-806 °C, > 5 kbar). Younger G3 granites formed through higher temperature, lower pressure (768-847 °C, < 4 kbar) biotite-dominated melting of a similar source. Partial melting was strongly influenced by the progressive lower-mid crustal emplacement of mafic igneous rocks during post-Variscan extension and a minor (< 5%-10%) mantle-derived component in the granites is possible. Two distinct fractionation series, G1-G2 and G3-G4, are defined using whole-rock geochemical and mineral chemical data. Variations in the major elements, Ba, Sr and Rb indicate that G1 and G3 granites underwent 15%-30% fractionation of an assemblage dominated by plagioclase, alkali feldspar and biotite to form more evolved G2 and G4 granites, respectively. Decreasing whole-rock abundances of Zr, Th and REE support the fractionation of zircon, monazite, apatite and allanite. Subsolidus alteration in G2 and G4 granites is indicated by non-primary muscovite and tourmaline and modification of major and trace element trends for G3-G4 granites, particularly for P2O5 and Rb. Topaz (G5) granites show low Zr, REE and extreme enrichment in Rb (up to 1530 ppm) and Nb (79 ppm) that cannot be related in a straightforward manner to continued differentiation of the G1-G2 or G3-G4 series. Instead, they are considered to represent partial melting, mediated by granulite facies fluids, of a biotite-rich restite following extraction of G1 and/or G3 magmas; they do not exhibit the typical geochemical characteristics of intraplate A-type granites.

  10. Constraints on the timing of multiple thermal events and re-equilibration recorded by high-U zircon and xenotime: Case study of pegmatite from Piława Górna (Góry Sowie Block, SW Poland)

    NASA Astrophysics Data System (ADS)

    Budzyń, Bartosz; Sláma, Jiří; Kozub-Budzyń, Gabriela A.; Konečný, Patrik; Holický, Ivan; Rzepa, Grzegorz; Jastrzębski, Mirosław

    2018-06-01

    The application of zircon and xenotime geochronometers requires knowledge of their potential and limitations related to possible disturbance of the age record. The alteration of the intergrown zircon and xenotime in pegmatite from the Góry Sowie Block (SW Poland) was studied using the electron microprobe analysis, X-ray WDS compositional mapping, micro-Raman analysis, and LA-ICP-MS U-Pb dating of zircon and xenotime, as well as the U-Th-total Pb dating of uraninite. These microanalytical techniques were applied to understand the formation mechanisms of the secondary textures related to post-magmatic processes in the zircon and xenotime intergrowth, and to constrain their timing. Textural and compositional features combined with U-Pb data indicate that the pegmatite-related crystallization of the zircon and xenotime intergrowth occurred ca. 2.09 Ga (2086 ± 35 Ma for zircon and 2093 ± 52 Ma for xenotime), followed by the re-equilibration of zircon and xenotime ca. 370 Ma (373 ± 18 Ma and 368 ± 6 Ma, respectively) during the formation of the younger pegmatite. The zircon and xenotime were most likely derived from Precambrian basement rocks and emplaced in the pegmatite as a restite. The zircon preserved textures related to diffusion-reaction processes that affected its high-U core (up to ca. 9.6 wt% UO2), which underwent further metamictization and amorphization due to self-radiation damage. The zircon rim and xenotime were affected by coupled dissolution-reprecipitation processes that resulted in patchy zoning, age disturbance and sponge-like textures. Xenotime was also partially replaced by fluorapatite or hingganite-(Y) and Y-enriched allanite-(Ce). The termination of the low-temperature alteration was constrained by the U-Th-total Pb age of the uraninite inclusions that crystallized in zircon at 281 ± 2 Ma, which is consistent with the age of 278 ± 15 Ma obtained from the youngest cluster of U-Pb ages in the re-equilibrated high-U zircon domains. This study demonstrates the importance of the careful examination of compositional, microtextural and geochronological data obtained using microanalytical techniques to reconstruct the complex thermal histories recorded by accessory minerals.

  11. High-K granites of the Rum Jungle Complex, N-Australia: Insights into the Late Archean crustal evolution of the North Australian Craton

    NASA Astrophysics Data System (ADS)

    Drüppel, K.; McCready, A. J.; Stumpfl, E. F.

    2009-08-01

    The Late Archean (c. 2.54-2.52 Ga) high-K granitoids of the Rum Jungle Complex, Northern Australia, display the igneous mineral assemblage of K-feldspar, quartz, plagioclase, biotite, and magnetite, and accessories such as zircon, monazite, titanite, allanite, apatite, and ilmenite. The granites underwent a variably severe greenschist facies alteration and associated deformation during the Barramundi Orogeny (1.88-1.85 Ga). The K-rich granitoids have variable compositions, mainly comprising syenogranite and quartz-monzonite. They can be subdivided into two major groups, (1) felsic granites and (2) intermediate to felsic granites, quartz-monzonites, and diorite. The felsic group (69-76 wt.% SiO 2) shares many features with typical Late Archean potassic granites. They are K- and LILE-rich and show marked depletion in Sr and Eu and the high field strength elements (HFSE), particularly Nb and Ti, relative to LILE and LREE. Compared to the average upper crust they have anomalously high Th (up to 123 ppm) and U (up to 40 ppm). The intermediate to felsic group (56-69 wt.% SiO 2) differs from the felsic group in having weakly lower Th and U but higher Mg#, Ti, Ba, Sr, Ni, Cr and REE, with a less pronounced negative Eu anomaly. This group displays well-defined trends in Harker diagrams, involving a negative correlation of Si with Sr, Ca, Na, and P whereas K, Rb, and Ba increase in the same direction, suggesting fractional crystallization of feldspar was more prominent than in the felsic suite. The mineralogical and geochemical characteristics of the felsic group are consistent with granite formation by intracrustal melting of plagioclase-rich igneous protoliths, probably of tonaltic to granodioritic composition, at moderate crustal levels. The intermediate to felsic granites, on the other hand, appear to be the products of mantle-crust interaction, possibly by melting of or mixing with more mafic igneous rocks. As evidenced by the presence of older inherited zircons crustal recycling of a pre-greenstone crust of the North Australian Craton of > 3.5 Ga played an important role in the formation of the Late Archean granites of the Rum Jungle Complex.

  12. Y,REE,Nb,Ta,Ti-oxide (AB 2O 6) minerals from REL-REE euxenite-subtype pegmatites of the Třebíč Pluton, Czech Republic; substitutions and fractionation trends

    NASA Astrophysics Data System (ADS)

    Škoda, Radek; Novák, Milan

    2007-04-01

    Aeschynite-group minerals (AGM) and euxenite-group minerals (EGM) occur in REL-REE euxenite-subtype pegmatites from the Třebíč Pluton, Czech Republic. They form strongly metamictized, light brown to black, equigranular to needle-like, subhedral to anhedral grains enclosed in blocky K-feldspar and less commonly in albite, and blocky quartz, and in the graphic unit (quartz and K-feldspar). Both AGM and EGM are homogeneous to slightly heterogeneous in BSE images. They are not commonly associated with the other primary Y,REE,Ti,Nb-bearing minerals, i.e. allanite-(Ce), monazite-(Ce), titanite, and ilmenite, which occur within the same textural-paragenetic unit. Aeschynite-(Y), aeschynite-(Ce), aeschynite-(Nd), nioboaeschynite-(Ce), tantalaeschynite-(Ce), vigezzite and polycrase-(Y) were identified using EMP and canonical discrimination analysis [Ercit, T.S., 2005a. Identification and alteration trends of granitic-pegmatite-hosted (Y,REE,U,Th)-(Nb,Ta,Ti) oxide minerals: a statistical approach. Can. Mineral. 43, 4 1291-1303.]. The exchange vector ACa B(Nb,Ta) A(Y,REE) - 1 BTi - 1 or its combination with the exchange vector ACa 2B(Nb,Ta) 3A(U,Th) - 1 A(Y,REE) - 1 BTi - 3 have been elucidated for the AGM. The exchange vector ACa A(U,Th) A(Y,REE) - 2 is predominant in the EGM. The AGM are enriched in HREE, whereas LREE are concentrated in the EGM. Weak to none-existent geochemical fractionations, as expressed by the U/(U + Th), Y/(Y + REE), Ta/(Ta + Nb) and (Nb + Ta)/(Ti + Nb + Ta) ratios, were noted for single grains from both the AGM and EGM, as well as in grains of polycrase-(Y) from four different textural-paragenetic units located in the Vladislav pegmatite. Simultaneous increase of U/(U + Th) and Y/(Y + REE) in the AGM during fractionation is typical. The Ta/(Ta + Nb) fractionation is usually weak and contradicts the Y/(Y + REE) and U/(U + Th) fractionation trends. This unusual behavior of Nb and Ta may be controlled by associated Ti-rich minerals (titanite, ilmenite, rutile), the composition of parental melt and/or by elevated F activity. The AGM and EGM from pegmatites of the Třebíč Pluton are quite similar in composition to those from REL-REE euxenite-subtype pegmatites in the Trout Creek Pass, Chaffee County, Colorado, USA, which are generally Ca,U,Th-depleted, show lower Ta/(Ta+Nb), and lower variation in HREE/LREE.

  13. Eruptive history, petrology, and petrogenesis of the Joe Lott Tuff Member of the Mount Belknap Volcanics, Marysvale volcanic field, west-central Utah

    USGS Publications Warehouse

    Budding, Karin E.

    1982-01-01

    The Joe Lott Tuff Member of the Mount Belknap Volcanics is the largest rhyolitic ash-flow tuff sheet in the Marysvale volcanic field. It was erupted 19 m.y. ago, shortly after the changeover from intermediate-composition calc-alkalic volcanism to bimodal basalt-rhyolite volcanism. Eruption of the tuff resulted in the formation of the Mount Belknap Caldera whose pyroclastic intracaldera stratigraphy parallels that in the outflow facies. The Joe Loft Tuff Member is a composite ash-flow sheet that changes laterally from a simple cooling unit near the source to four distinct cooling units toward the distal end. The lowest of these units is the largest and most widespread; it is 64 m thick and contains a basal vitrophyre. Eruption of the lower unit led to the initial collapse of the caldera. The lower unit is followed upward by a 43 m middle unit, a 26 m pink-colored unit which is separated by a prominent air- fall layer, and a 31 m upper unit. The Joe Loft Tuff Member is an alkali rhyolite with 75.85-77.31 wt. % silica and 8.06-9.32 wt. % K2O+Na2O; the agpaitic index (Na2O+ K2O/Al2O3) is .77-.98. The tuff contains about I% phenocrysts of quartz, sanidine, oligoclase, augite, apatite, zircon, sphene, biotite, and oxidized Fe-Ti oxides. The basal vitrophyre contains accessory allanite, chevkinite, and magnesiohastingsite. The main cooling units are chemically and mineralogically zoned indicating that the magma chamber restratified prior to each major eruption. Within each of the two thickest cooling units, the mineralogy changes systematically upwards; the Or content and relative volume of sanidine decreases and An content of plagioclase increases. The basal vitrophyre of the lower unit has a bulk composition that lies in the thermal trough near the minima of Or-Ab-Q at 1 kb PH2O. Microprobe analyses of feldspar and chemical modeling on experimental systems indicate that pre-eruption temperatures were near 750?C and that the temperature increased during the eruption of the cooling units. The chemical gradients in the apatite and whole-rock data in the Joe Loft Tuff Member and the consistent mineral assemblages throughout the ash-flow cannot be explained by crystal settling. The fractionation of the Joe Lott Tuff Member appears to closer fit the model of convection-driven thermogravitational diffusion.

  14. 2.9-1.9 Ga paleoalterations of Archean granitic basement of the Franceville basin (Gabon)

    NASA Astrophysics Data System (ADS)

    Mouélé, Idalina Moubiya; Dudoignon, Patrick; El Albani, Abderrazak; Meunier, Alain; Boulvais, Philippe; Gauthier-Lafaye, François; Paquette, Jean-Louis; Martin, Hervé; Cuney, Michel

    2014-09-01

    The Archean granitoids in the Kiéné area, Gabon, are overlained by the Paleoproterozoic sediments of the Franceville basin (2.1 Ga). The basin is known for its high-grade uranium deposits among which some have been forming natural nuclear fission reactors. Most of the studies were dedicated to the FA-FB Paleoproterozoic sediments hosting these uranium deposits. Little is known on the Archean basement itself and specifically on the hydrous alteration events it experienced before and after the sediment deposition. The present work is focused on their petrographical, mineralogical and geochemical characterization. Dating the successive alteration events has been attempted on altered monazite crystals. Rocks in different alteration states have been sampled from eight drill cores crosscutting the Archean - Paleoproterozoic unconformity. The Archean granitoids observed in the deepest levels exhibit typical petrographical features of a propylitic alteration while they are intensely illitized up to the unconformity. The propylitic alteration is mainly pervasive but the original texture of the granitoïds is conserved in spite of the formation of new minerals: Mg-chlorite, allanite and epidote forming a typical paragenesis. The illitic alteration is much more invasive near the unconformity. The illitization process leads to the replacement of feldspars and the corrosion of quartz crysals by an illitic matrix while the ferromagnesian minerals are pseudomorphosed by a Fe-chlorite + phengite + hematite assemblage. The final fluid-rock interaction step is marked by fissural deposits of calcite and anhydrite. The δ13C isotopic data show that the fissural carbonates precipitated from diagenetic fluids enriched carbon products deriving from the maturation of organic matter. The U-Pb isotopic analyzes performed on monazite crystals have dated three distinct events: 3.0-2.9 Ga (magmatic), 2.6 Ga (propylitic alteration) and 1.9 Ga (diagenetic illitization). The calculation of geochemical mass balances suggests that the water-rock ratio during the propylitic alteration event was weak. On the contrary, it was much higher during the overprinted illitization which is characterized by an intense leaching of Na, Ca, Mg, Sr, REE and an enrichment in K, Rb,Cs. Neither the petrographic features nor the geochemical data militate for an Archean weathering event (paleosol). In the present case, diagenetic fluids have percolated from the unconformity into the basement where they overprinted the illitization processes upon the previously propylitized rocks. These fluids were probably oxidant as they are also responsible of the U mobilization which led to the formation of the ore deposits close to the FA-FB interface.

  15. Pliocene to late Pleistocene magmatism in the Aurora Volcanic Field, Nevada and California, USA

    NASA Astrophysics Data System (ADS)

    Kingdon, S.; Cousens, B.; John, D. A.; du Bray, E. A.

    2013-12-01

    The 3.9- 0.1 Ma Aurora Volcanic Field (AVF) covers 325 km2 east and southeast of the Bodie Hills, north of Mono Lake, California, USA. The AVF is located immediately northwest of the Long Valley magmatic system and adjacent and overlapping the Miocene Bodie Hills Volcanic Field (BHVF). Rock types range from trachybasalt to trachydacite, and high-silica rhyolite. The trachybasalts to trachydacites are weakly to moderately porphyritic (1-30%) with variable phenocryst assemblages that are some combination of plagioclase, hornblende, clinopyroxene, and lesser orthopyroxene, olivine, and/or biotite. Microphenocrysts are dominated by plagioclase, and include opaque oxides, clinopyroxene, and apatite. These rocks are weakly to strongly devitrified. The high-silica rhyolites are sparsely porphyritic with trace to 10% phenocrysts of quartz, sanidine, plagioclase, biotite, (+/- hornblende), accessory opaque oxide minerals, titanite, allanite, (+/-apatite, zircon), and have glassy groundmasses. Rocks in the AVF are less strongly porphyritic than those of BHVF. Plagioclase phenocrysts are often oscillatory zoned and many have sieve texture. Amphiboles have distinct black opaque rims. Xenocrystic quartz and plagioclase are rare. AVF lavas have bimodal SiO2 compositions, ranging from 49 to 78 wt%, with a gap between 65 and 75 wt%. They are high-K calc-alkaline to shoshonitic in composition, and are metaluminous to weakly peraluminous. They are enriched in rare earth elements (REE), especially light REEs, compared to the Miocene BHVF rocks. Primordial mantle-normalized incompatible element patterns show arc- or subduction-related signatures, with enrichment in Ba and Pb, and depletion in Nb and Ta. Enrichment in K and Sr and depletion in Ti are less pronounced than in the BHVF rocks. There is no correlation between lead isotope ratios and silica (initial 206Pb/204Pb ratios range from 18.974 to 19.151). Neodymium isotope ratios show a moderate negative correlation with silica within the range of 50 to 75 wt% SiO2 (initial 143Nd/144Nd ratios range from 0.51238 to 0.51258, and ɛNdt ranges from -1.09 to -4.01). Strontium ratios show a strong positive correlation with silica for SiO2 above 50 wt% (initial 87Sr/86Sr ratios range from 0.70513 to 0.70691). Pb, Nd, and Sr isotope compositions do not systematically change with time. The Aurora volcanic rocks are interpreted to be postsubduction erupted from an extensional tectonic setting. Compared with the BHVF rocks, the AVF rocks are more radiogenic and crustal assimilation is a more influential process.

  16. Archaeological jade mystery solved using a 119-year-old rock collection specimen

    NASA Astrophysics Data System (ADS)

    Harlow, G. E.; Davies, H. L.; Summerhayes, G. R.; Matisoo-Smith, E.

    2012-12-01

    In a recent publication (Harlow et al. 2012), a ~3200-year old small stone artefact from an archaeological excavation on Emirau Island, Bismarck Archipelago, Papua New Guinea was described and determined to be a piece of jadeite jade (jadeitite). True jadeitite from any part of New Guinea was not previously known, either in an archaeological or geological context, so this object was of considerable interest with respect to its geological source and what that would mean about trade between this source and Emirau Island. Fortuitously, the artefact, presumably a wood-carving gouge, is very unusual with respect to both pyroxene composition and minor mineral constituents. Pyroxene compositions lie essentially along the jadeite-aegirine join: Jd94Ae6 to Jd63Ae36, and without any coexisting omphacite. This contrasts with Jd-Di or Jd-Aug compositional trends commonly observed in jadeitites worldwide. Paragonite and albite occur in veins and cavities with minor titanite, epidote-allanite, and zircon, an assemblage seen in a few jadeitites. Surprisingly, some titanite contains up to 6 wt% Nb2O5 with only trace Ta and a single grain of a Y-Nb phase (interpreted as fergusonite) is present; these are unique for jadeitite. In a historical tribute to C.E.A. Wichmann, a German geologist who taught at Utrecht University, the Netherlands, a previously unpublished description of chlormelanite from the Torare River in extreme northeast Papua, Indonesia was given. The bulk composition essentially matches the pyroxene composition of the jade, so this sample was hypothesized as coming from the source. We were able to arrange a loan from the petrology collection at Utrecht University of the specimen acquired by Wichmann in 1893. In addition we borrowed stone axes from the Natural History Museum - Naturalis in Leiden obtained from natives near what is now Jayapura in eastern-most Papua. Petrography and microprobe analysis of sections of these samples clearly show that (1) Wichmann's 1893 Torare River "chloromelanite" is an extremely close match texturally and mineralogically with the jadeitite jade gouge, including Nb-rich titanite—thus a match, but that (2) the axes are omphacitites that have a geologically similar origin (high pressure/low-temperature subduction channel) but do not share the jadeite+aegerine-rich pyroxene or Nb-Y rich accessory phases. This research clearly shows that natural history collections are important archives that contain samples of potentially important value for science and cultural research. Moreover, research like this that connects geology, archaeology, history and preserved collections can yield a story that makes science and collections tangible and interesting to a popular audience. References: Harlow et al. 2012, Eur. J. Mineral. 24, 391-399.

  17. Advances and limitations on interpreting the erosional record from isotopic analysis of single detrital mineral grains

    NASA Astrophysics Data System (ADS)

    Parrish, Randall

    2010-05-01

    The analysis of provenance of clastic sediments is useful for reconstructing the characteristics and rates of exhumation of source areas, and sometimes placing minimum age constraints on depositional age. Due largely to increased availability and ease of access to LA-ICP-MS instrumentation, the analysis of provenance using single detrital accessory minerals has grown very rapidly over recent years. With this however is a culture of casual users who may not fully appreciate subtleties of measurement and isotope interpretation. The isotopic provenance literature is dominated by zircon-centric studies that use U-Pb dating and Hf isotope measurements of single zircons, but unfortunately an increasing number of these studies appear to lack sufficient understanding of U-Pb and Hf systematics; misleading interpretations are increasingly common. The inherent information contained in detrital accessory minerals is potentially immense, scientifically, but comprehensive interpretations attempting to reconstruct the geological make-up and evolution of sources require dating of multiple types of accessory minerals (i.e. zircon, titanite, monazite, garnet inclusions, micas, allanite, rutile, apatite) by various methods (U-Pb, fission track, Ar-Ar…) at times accompanied by isotope geochemical data (Lu-Hf, Sm-Nd, Rb-Sr) of phases where Sr, Hf, or REE comprise a major element (≥0.5%). Many approaches have been demonstrated but the mix of methodologies needs to be tailored to the problem, in view of the variable effort and expense needed to acquire good datasets. To date there are few comprehensive multi-mineral, multi-isotope system applications, and too many studies that follow a prescriptive cookbook that lacks innovation and fails to address a problem. The field needs to focus effort on the approaches that can solve a problem well rather than doing either just the easy methods or too many methods only moderately well. Zircon studies require strategies that reduce or eliminate discordance, collect sufficient data on each grain to make a robust age interpretation, improve accuracy of data by more attention to standards and uncertainties, can analyze thin overgrowths that reveal the magmatic or metamorphic age, and minimize sample consumption, not an easy task for the vast majority of laboratories doing provenance applications. Detrital monazite, monazite-in garnet, titanite and rutile can reveal much of the higher temperature metamorphic time-temperature path, and coupled U-Pb and fission track studies of single zircon and apatite grains can be useful for determining lower temperature exhumation rates. Isotope geochemistry (Hf-Nd-Sr-O) is more time consuming but can be pivotal to distinguish subtle differences in sources and to test specific hypotheses. Examples of improved methods and applications will be presented to illustrate the presentation.

  18. Tracing Nile sediment sources by Sr and Nd isotope signatures (Uganda, Ethiopia, Sudan)

    NASA Astrophysics Data System (ADS)

    Padoan, Marta; Garzanti, Eduardo; Harlavan, Yehudit; Villa, Igor Maria

    2011-06-01

    Strontium and neodymium isotopes, measured on diverse mud and sand fractions of sediment in transit along all major Nile branches, identify detritus sourced from Precambrian basements, Mesozoic strata, and Tertiary volcanic rocks exposed along the shoulders of the East African rift and in Ethiopian highlands. Sr and Nd isotopic ratios reflect the weighted average of detrital components generated in different catchments, allowing us to discriminate provenance, calculate sediment budgets, and investigate grain-size and hydraulic-sorting effects. 87Sr/ 86Sr and 143Nd/ 144Nd range, respectively, from as high as 0.722 and as low as 0.5108 for sediment derived from Archean gneisses in northern Uganda, to 0.705 and 0.5127 for sediment derived from Neoproterozoic Ethiopian and Eritrean basements. 87Sr/ 86Sr and 143Nd/ 144Nd, ranging 0.705-0.709 and 0.5124-0.5130 for Blue Nile tributaries, are 0.704-0.705 and 0.5127-0.5128 for largely volcaniclastic sediments of River Tekeze-Atbara, and 0.705-0.706 and 0.5126-0.5127 for main Nile sediments upstream Lake Nasser. Model mantle derivation ages ( tDM), oldest in Uganda where sediment is principally derived from the Congo Craton (3.4-3.0 Ga for Victoria and Albert Nile), progressively decrease northward across the Saharan Metacraton, from 2.6 Ga (Bahr el Jebel in South Sudan), to 2.4-2.2 Ga (Bahr ez Zeraf across the Sudd), and finally 1.6-1.3 Ga (White Nile upstream Khartoum). Instead, tDM ages of Sobat mud increase from 0.9 to 1.5 Ga across the Machar marshes. TDM ages are younger for sediments shed by Ethiopian (1.2-0.7 Ga) and Eritrean basements (1.5-1.2 Ga), and youngest for sediments shed from Ethiopian flood basalts (0.3-0.2 Ga). Integrated geochemical, mineralogical, and settling-equivalence analyses suggest influence on the Nd isotopic signal by volcanic lithic grains and titanite rather than by LREE-rich monazite or allanite. Because contributions by ultradense minerals is subordinate, intrasample variability of Sr and Nd ratios is minor. In Blue Nile, Atbara and main Nile sediments of mixed provenance, however, the Nd ratio tends to be higher and tDM ages lower in largely volcaniclastic mud than in mixed volcaniclastic/metamorphiclastic sand. The complete geochemical database presented here, coupled with high-resolution bulk-petrography and heavy-mineral data, provides a key to reconstructing erosion patterns and detrital fluxes across the whole Nile basin, and to investigate and understand how sources of sediment have changed in the historical and pre-historical past in relation to shifting climatic zones across arid northern Africa.

  19. Reconnaissance for radioactive materials in northeastern United States during 1952

    USGS Publications Warehouse

    McKeown, Francis A.; Klemic, Harry

    1953-01-01

    Reconnaissance for radioactive materials was made in parts of Maine, New York, New Jersey, and Pennsylvania. The primary objective was to examine the iron ore deposits and associated rocks in the Adirondack Mountains of New York and the Highlands of New Jersey. In addition, several deposits known or reported to contain radioactive minerals were examined to delimit their extent. Most of the deposits examined are not significant as possible sources of radioactive elements and the data pertaining to them are summarized in table form. Deposits that do warrant more description than can be given in table form are: Benson Mines, St. Lawrence County, N. Y.; Rutgers mine, Clinton County, N. Y.; Mineville Mines, Essex County, N. Y.l Canfield phosphate mine, Morris County, N. J.; Mullgan quarry, Hunterdon County, N. J.; and the Chestnut Hill-Marble Mountain area, Pennsylvania and New Jersey. The Old Bed in the Mineville district is the only deposit that may be economically significant. Apatite from Old Bed ore contains as much as 4.9 percent total rare earth. 0.04 percent thorium, and 0.018 percent uranium. Magnetite ore at the Rutgers mine contains radioactive zircon and apatite. Radioactivity measurements of outcrops and dump material show that the ore contains from 0.005 to 0.010 percent equivalent uranium. One sample of lean magnetite ore contains 0.006 percent equivalent uranium. Garnet-rich zones in the Benson Mines magnetite deposit contain as much as 0.017 equivalent uranium. Most of the rock and ore, however, contains about 0.005 percent equivalent uranium. Available data indicate that the garnet-rich zones are enriched in radioactive allanite. A shear zone in the Kittatinny limestone of Cambrian age at the Mulligan quarry contains uraniferous material. Radioactivity anomalies elsewhere in the quarry and in adjacent fields indicate that there may be other uraniferous shear zones. Assays of samples and measurements of outcrop radioactivity indicate that the uranium content of these zones is low; samples contain from 0.008 to 0.068 percent equivalent uranium. The anomalies, however, may indicate greater concentrations of uranium below surficial leached zones. The Chestnut Hill-Marble Mountain area contains radioactivity anomalies for about 2 miles along the strike of the contact of pre-Cambrian Pickering gneiss and Franklin limestone formations. In places this contact is injected with pegmatite, which probably was the source of the radioelements. The most favorable area for further study is at Marble Mountain, where a nearly continuous anomaly extends for about 1500 feet. Samples from part of this area contain as much as 0.044 percent equivalent uranium and 0.005 percent uranium. Radioactive hematite and florencite, in which thorium may have substituted for cerium, are the only radioactive minerals observed in the Marble Mountain area.

  20. Mineral chemistry and shrimp U-Pb Geochronology of mesoproterozoic polycrase-titanite veins in the sullivan Pb-Zn-Ag Deposit, British Columbia

    USGS Publications Warehouse

    Slack, J.F.; Aleinikoff, J.N.; Belkin, H.E.; Fanning, C.M.; Ransom, P.W.

    2008-01-01

    Small polycrase-titanite veins 0.1-2 mm thick cut the tourmalinite feeder zone in the deep footwall of the Sullivan Pb-Zn-Ag deposit, southeastern British Columbia. Unaltered, euhedral crystals of polycrase and titanite 50-100 ??m in diameter are variably replaced by a finer-grained alteration-induced assemblage composed of anhedral polycrase and titanite with local calcite, albite, epidote, allanite, and thorite or uranothorite (or both). Average compositions of the unaltered and altered polycrase, as determined by electron-microprobe analysis, are (Y0.38 REE0.49 Th0.10 Ca0.04 Pb0.03 Fe0.01U0.01) (Ti1.48 Nb0.54 W0.04 Ta0.02)O6 and (Y0.42 REE0.32 Th0.15 U0.06 Ca0.04 Pb0.01 Fe0.01) (Ti1.57 Nb0.44 W0.04 Ta0.02)O6, respectively. The unaltered titanite has, in some areas, appreciable F (to 0.15 apfu), Y (to 0.40 apfu), and Nb (to 0.13 apfu). SHRIMP U-Pb geochronology of eight grains of unaltered polycrase yields a weighted 207Pb/206Pb age of 1413 ?? 4 Ma (2??) that is interpreted to be the age of vein formation. This age is 50-60 m.y. younger than the ca. 1470 Ma age of synsedimentary Pb-Zn-Ag mineralization in the Sullivan deposit, which is based on combined geological and geochronological data. SHRIMP ages for altered polycrase and titanite suggest later growth of minerals during the ???1370-1320 Ma East Kootenay and ???1150-1050 Ma Grenvillian orogenies. The 1413 ?? 4 Ma age for the unaltered polycrase in the veins records a previously unrecognized post-ore (1370 Ma) mineralizing event in the Sullivan deposit and vicinity. The SHRIMP U-Pb age of the polycrase and high concentrations of REE, Y, Ti, Nb, and Th in the veins, together with elevated F in titanite and the absence of associated sulfides, suggest transport of these high-field-strength elements (HFSE) by F-rich and S-poor hydrothermal fluids unrelated to the fluids that formed the older Fe-Pb-Zn-Ag sulfide ores of the Sullivan deposit. Fluids containing abundant REE, HFSE, and F may have been derived from a geochemically specialized magma such as those that form alkaline granites, pegmatites, or carbonatites. In an alternative model. preferred here, these fluids were associated with a rift-related, crustal metasomatic event in the region. Determination of a Mesoproterozoic age for the polycrase-titanite veins establishes the first known occurrence of pre-Grenvillian REE-rich mineralization in the Belt-Purcell basin.

  1. Geochemistry and Temperatures Recorded by Zircon During the Final Stages of the Youngest Toba Tuff Magma Chamber, Sumatra, Indonesia

    NASA Astrophysics Data System (ADS)

    Gaither, T.; Reid, M. R.; Vazquez, J. A.

    2009-12-01

    The ~74 ka eruption of the Youngest Toba Tuff (YTT) in Sumatra, Indonesia, was one of the largest single volcanic eruptions in geologic history, on par with other voluminous silicic eruptions such as the Huckleberry Ridge Tuff of Yellowstone and the Bishop Tuff of Long Valley, California. We are exploring how zircon and other accessory mineral phases record compositional and thermal changes that occurred in the YTT magma, and the important clues these crystal scale records hold for magma chamber dynamics and processes that lead up to supervolcano eruptions. In this study, we report trace element (REE, U, Th, Ti, and Hf) characteristics, Ti-in-zircon crystallization temperatures, and apparent REE partition coefficients obtained for YTT zircon rims. Twenty-nine zircons from pumices with a compositional range of 70-76 wt% SiO2 were analyzed on the UCLA Cameca ims 1270 ion microprobe. The grains were mounted so that only the outermost ~1.5 microns of the crystals were analyzed. Median Zr/Hf ratios of 34 to 38 characterize zircons from the pumices; the high silica rhyolite grains have lower Zr/Hf. Chondrite-normalized REE patterns are strongly LREE-depleted. Positive Ce anomalies are large (Ce/Ce* ranges up to 88) and Eu/Eu* varies by a factor of four (0.05 to 0.21). Eu/Eu*, Nd/Yb, and Th/U decrease with decreasing Zr/Hf, showing that the variation in zircon rim compositions may be related by co-precipitation of feldspar and allanite along with zircon. Titanium contents also decrease with decreasing Zr/Hf, suggesting that the chemical differences could be related to temperature changes. REE partition coefficients calculated from zircon rim compositions and pumice glass compositions give a good fit to a lattice strain model. They are also quite similar to the partition coefficients of Sano et al. (2002) which have been shown to be successful at reproducing melt compositions in other settings. Temperatures of crystallization calculated using the Ti-in-zircon geothermometer (Watson et al., 1996), assuming a melt aTiO2 of 0.5, yield very low median values (even without a possible pressure correction of -40 to -80°C), ranging from 640-667°C. Virtually all of the zircon rims record temperatures lower than eruption temperatures of 700-780°C estimated for the YTT by Chesner (1998) using FeTi oxide equilibria. It is possible that the low zircon temperatures reflect uncertainties in the Ti-in-zircon geothermometer but they are nonetheless permissive of re-entrainment of zircon from a near-solidus mush close to the time of eruption. The analytically significant chemical variations within the individual zircon populations, especially those of Zr/Hf, Eu/Eu*, and Nd/Yb, suggest that crystals from distinct compositional domains were brought together during a final merging/coalescence of magma that catalyzed the eruption.

  2. Geologic history of the Blackbird Co-Cu district in the Lemhi subbasin of the Belt-Purcell Basin

    USGS Publications Warehouse

    Bookstrom, Arthur A.; Box, Stephen E.; Cossette, Pamela M.; Frost, Thomas P.; Gillerman, Virginia; King, George; Zirakparvar, N. Alex

    2016-01-01

    The Blackbird cobalt-copper (Co-Cu) district in the Salmon River Mountains of east-central Idaho occupies the central part of the Idaho cobalt belt—a northwest-elongate, 55-km-long belt of Co-Cu occurrences, hosted in grayish siliciclastic metasedimentary strata of the Lemhi subbasin (of the Mesoproterozoic Belt-Purcell Basin). The Blackbird district contains at least eight stratabound ore zones and many discordant lodes, mostly in the upper part of the banded siltite unit of the Apple Creek Formation of Yellow Lake, which generally consists of interbedded siltite and argillite. In the Blackbird mine area, argillite beds in six stratigraphic intervals are altered to biotitite containing over 75 vol% of greenish hydrothermal biotite, which is preferentially mineralized.Past production and currently estimated resources of the Blackbird district total ~17 Mt of ore, averaging 0.74% Co, 1.4% Cu, and 1.0 ppm Au (not including downdip projections of ore zones that are open downward). A compilation of relative-age relationships and isotopic age determinations indicates that most cobalt mineralization occurred in Mesoproterozoic time, whereas most copper mineralization occurred in Cretaceous time.Mesoproterozoic cobaltite mineralization accompanied and followed dynamothermal metamorphism and bimodal plutonism during the Middle Mesoproterozoic East Kootenay orogeny (ca. 1379–1325 Ma), and also accompanied Grenvilleage (Late Mesoproterozoic) thermal metamorphism (ca. 1200–1000 Ma). Stratabound cobaltite-biotite ore zones typically contain cobaltite1 in a matrix of biotitite ± tourmaline ± minor xenotime (ca. 1370–1320 Ma) ± minor chalcopyrite ± sparse allanite ± sparse microscopic native gold in cobaltite. Such cobaltite-biotite lodes are locally folded into tight F2 folds with axial-planar S2 cleavage and schistosity. Discordant replacement-style lodes of cobaltite2-biotite ore ± xenotime2 (ca. 1320–1270 Ma) commonly follow S2fractures and fabrics. Discordant quartz-biotite and quartz-tourmaline breccias, and veins contain cobaltite3 ± xenotime3 (ca. 1058–990 Ma).Mesoproterozoic cobaltite deposition was followed by: (1) within-plate plutonism (530–485 Ma) and emplacement of mafic dikes (which cut cobaltite lodes but are cut by quartz-Fe-Cu-sulfide veins); (2) garnet-grade metamorphism (ca. 151–93 Ma); (3) Fe-Cu-sulfide mineralization (ca. 110–92 Ma); and (4) minor quartz ± Au-Ag ± Bi mineralization (ca. 92–83 Ma).Cretaceous Fe-Cu-sulfide vein, breccia, and replacement-style deposits contain various combinations of chalcopyrite ± pyrrhotite ± pyrite ± cobaltian arsenopyrite (not cobaltite) ± arsenopyrite ± quartz ± siderite ± monazite (ca. 144–88 Ma but mostly 110–92 Ma) ± xenotime (104–93 Ma). Highly radiogenic Pb (in these sulfides) and Sr (in siderite) indicate that these elements resided in Mesoproterozoic source rocks until they were mobilized after ca. 100 Ma. Fe-Cu-sulfide veins, breccias, and replacement deposits appear relatively undeformed and generally lack metamorphic fabrics.Composite Co-Cu-Au ore contains early cobaltite-biotite lodes, cut by Fe-Cu-sulfide veins and breccias, or overprinted by Fe-Cu-sulfide replacement-style deposits, and locally cut by quartz veinlets ± Au-Ag ± Bi minerals.

  3. Origin of heavy REE mineralisation in carbonatites: Constraints form the Huanglongpu Mo-HREE deposit, Qinling, China.

    NASA Astrophysics Data System (ADS)

    Smith, Martin; Cheng, Xu; Kynicky, Jindrich; Cangelosi, Delia; Wenlei, Song

    2017-04-01

    The carbonatite dykes of the Huanglongpu area, Lesser Qinling, China, are unusual in that they are quartz-bearing, Mo-mineralised and enriched in the heavy rare earth elements (HREE) relative to typical carbonatites. Carbonatite monazite (208.9±4.6 Ma to 213.6±4.0; Song et al., 2016) gives a comparable U-Pb radiometric age to molybdenite (220Ma; Stein et al., 1997), confirming interpretations that Mo is derived from the carbonatite, and not a subsequent overprint from regional porphyry-style mineralisation ( 141Ma). The sulphides in the carbonatites have mantle-like 34S ( 1‰) and low δ26Mg values (-1.89 to -1.07‰), similar to sedimentary carbonates, suggesting a recycled sediment contribution in their mantle sources that may be responsible for the Mo and HREE enrichment (Song et al., 2016). The textures of REE minerals indicate crystallisation of monazite-(Ce), bastnäsite-(Ce), parisite-(Ce) and aeschynite-(Ce) as magmatic phases. Monazite-(Ce) was subsequently altered to produce apatite, which was in turn replaced by britholite-(Ce), accompanied by the formation of allanite-(Ce). The REE-fluorcarbonates where replaced by synchysite-(Ce) and röntgenite-(Ce). Aeschynite-(Ce) was altered initially to uranopyrochlore and then pyrochlore with uraninite inclusions. The mineralogical evolution reflects the evolution from magmatic carbonatite, through to more silica-rich conditions during the magmatic-hydrothermal transition, to fully hydrothermal conditions accompanied by the formation of sulphate minerals. Each alteration stage resulted in the preferential leaching of the LREE and enrichment in the HREE. Mass balance considerations indicate that the HREE enrichment could not be a passive process, and that hydrothermal fluids must have contributed HREE to the system. The evolution of the fluorcarbonate mineral assemblage requires an increase in aCa2+ and aCO32- in the metasomatic fluid, and so breakdown of HREE-enriched calcite may have been the HREE source. Solubility products are lower for LREE minerals compared to HREE minerals, so leaching in the presence of strong, LREE-selective ligands (Cl-, CO32-) may account for the depletion in late stage minerals in the LREE, but cannot account for subsequent preferential HREE addition. Fluid inclusion data indicate the presence of sulphate-rich brines during late stage alteration, and hence sulphate complexation may have been important for preferential HREE transport, as sulphate has been shown to be non-LREE selective during the formation of complex ions. The combination of mantle source with a recycled oceanic sediment component, and REE enrichment during magmatic processes, and late stage alteration with non-LREE selective ligands such as sulphate may be critical in forming HREE-enriched carbonatites. Song et al., (2016) Origin of unusual HREE-Mo-rich carbonatites in the Qinling orogen, China. Scientific Reports, 6:37377 | DOI: 10.1038/srep37377. Stein et al. (1997) Highly precise and accurate Re-Os ages for molybdenite from the East Qinling-Dabie molybdenum belt, Shaanxi province, China. Econ. Geol. 92, 827-835 (1997)

  4. Geologic setting of the Mountain Pass rare earth deposits, San Bernardino County, California

    USGS Publications Warehouse

    Olson, Jerry Chipman

    1952-01-01

    The Mountain Pass district is in a block of pre-Cambrian metamorphic rocks bounded on the east and south by the alluvium of Ivanpah Valley. This block is separated from Paleozoic and Mesozoic sedimentary and volcanic rocks on the west by the Clark Mountain normal fault, and the northern boundary of the district is a prominent transverse fault. The pre-Cambrian metamorphic complex comprises a great variety of lithologic types including garnetiferous mica gneisses and schists; biotite-garnet-sillimenite gneiss; hornblende gneiss, schist, and amphibolite; biotite gneiss and schist; granitic gneisses and migmatites; pegmatites; and minor amounts of foliated mafic rocks. The rare earth-bearing carbonate rocks are related to potash-rich igneous rocks, of uncertain age, that cut the metamorphic complex. The larger potash-rich intrusive masses, 300 or more feet wide, comprise one granite, two syenite, and four composite shonkinite-syenite bodies. One of the shonkinite-syenite stocks is more than a mile long. Several hundred relatively thin dikes of these potash-rich rocks range in composition, and generally decreasing age, from biotite shonkinite through syenite to granite. A few thin fine-grained shonkinite dikes cut the granite. These potash-rich rocks are cut by east-trending andesitic dikes and by faults. Veins of carbonate rock are most abundant in and near the southwest side of the largest shonkinite-syenite body. Although most veins are less than 6 feet thick, one mass of carbonate rock near the Sulphide Queen min4e is 600 feet in maximum width and 2,400 feet long. About 200 veins have been mapped in the district; their aggregate surface area is probably less than one-tenth that of the large carbonate mass. The carbonate materials, which make up about 60 percent of the veins and the large carbonite body, are chiefly calcite, dolomite, ankerite, and siderite. The other constituents are barite, bastnaesite and perisite, quartz, and variable small quantities of crocidolite, biotite, phlogopite, chlorite, muscovite, apatite, iron oxides, fluorite, monazite, galena, allanite, sphene, pyrite, chalcopyrite, tetrahedrite, malachite, azurite, corussite, wulfenite, aragonite, and thorite. The rare earth oxide content in most of the carbonate rock is less than 13 percent, but in some local concentrations of bastnaesite the content is as high as 40 percent. The origin of the carbonate rocks and related potash-rich igneous rocks is considered in the light of similar associations of carbonate and alkalinic rocks in Sweden, Norway, Russia, South Africa, and the United States. The carbonate rock may have originated (1) as a pre-Cambrian limestone or evaporate sequence in the gneisses; (2) by reaction between magma and the Paleozoic dolomite and limestone overlying the pre-Cambrian complex; (3) by alteration of pre-Cambrian gneisses by emanations from an unknown deep-seated source; or (4) by differentiation of an alkaline magma from shonkinite to syenite to granite, leading to a final carbonate-rich fraction, containing the rare elements, which was emplaced either as a concentrated or a dilute solution. The fourth hypothesis is considered the most plausible.

  5. Menzerite-(Y) a New Species {(Y REE)(Ca Fe2plus)2}[(Mg Fe2plus)(Fe3plus Al)](Si3)O12 from a Felsic Granulite Parry Sound Ontario and a New Garnet End-member (Y2Ca)Mg2(SiO4)3

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    E Grew; J Marsh; M Yates

    2011-12-31

    Menzerite-(Y), a new mineral species, forms reddish brown cores, n = 1.844 (20), up to 70 {micro}m across, rimmed successively by euhedral almandine containing up to 2.7 wt% Y{sub 2}O{sub 3} and by K-feldspar in a felsic granulite on Bonnet Island in the interior Parry Sound domain, Grenville Orogenic Province, Canada. It is named after Georg Menzer (1897-1989), the German crystallographer who solved the crystal structure of garnet. Single-crystal X-ray-diffraction results yielded space group Ia3d, a = 11.9947(6) {angstrom}. An electron-microprobe analysis of the grain richest in Y (16.93 wt% Y{sub 2}O{sub 3}) gave the following formula, normalized to eightmore » cations and 12 oxygen atoms: {l_brace}Y{sub 0.83}Gd{sub 0.01}Dy{sub 0.05}Ho{sub 0.02}Er{sub 0.07}Tm{sub 0.01}Yb{sub 0.06}Lu{sub 0.02}Ca{sub 1.37}Fe{sub 0.49}{sup 2+}Mn{sub 0.07}{r_brace} [Mg{sub 0.55}Fe{sub 0.42}{sup 2+}Fe{sub 0.58}{sup 3+}Al{sub 0.35} V{sub 0.01}Sc{sub 0.01}Ti{sub 0.08}](Si{sub 2.82}Al{sub 0.18})O{sub 12}, or {l_brace}(Y,REE)(Ca,Fe{sup 2+}){sub 2}{r_brace}[(Mg,Fe{sup 2+})(Fe{sup 3+},Al)](Si{sub 3})O{sub 12}. Synchrotron micro-XANES data gave Fe{sup 3+}/{Sigma}Fe = 0.56(10) versus 0.39(2) calculated from stoichiometry. The scattering power refined at the octahedral Y site, 17.68 epfu, indicates that a relatively light element contributes to its occupancy. Magnesium, as determined by electron-microprobe analyses, would be a proper candidate. In addition, considering the complex occupancy of this site, the average Y-O bond length of 2.0244(16) {angstrom} is in accord with a partial occupancy by Mg. The dominance of divalent cations with Mg > Fe{sup 2+} and the absence of Si at the octahedral Y site (in square brackets) are the primary criteria for distinguishing menzerite-(Y) from other silicate garnet species; the menzerite-(Y) end-member is {l_brace}Y{sub 2}Ca{r_brace}[Mg{sub 2}](Si{sub 3})O{sub 12}. The contacts of menzerite-(Y) with almandine are generally sharp and, in places, cuspate. It is interpreted to have equilibrated with ferrosilite, augite, quartz, oligoclase, allanite-(Ce), magnetite, ilmenite and fluorapatite, in the absence of almandine, on the prograde path at 7-8.5 kbar and T {approx} 700-800 C, and subsequently dissolved incongruently in an anatectic melt to form almandine, most likely, at P {approx} 8.5-9.5 kbar and T {approx} 800-850 C.« less

  6. Petrologic evolution of the Caetano magmatic system: What can we learn from a dissected, 34 Ma caldera in the northern Great Basin, western U.S.A.?

    NASA Astrophysics Data System (ADS)

    Watts, K. E.; Colgan, J. P.; John, D. A.; Henry, C. D.

    2012-12-01

    Eruption of the >1,100 km3 Caetano Tuff and formation of the Caetano caldera occurred during the mid-Tertiary ignimbrite flare-up in the Great Basin. Post-collapse extension and faulting created a series of tilted fault blocks that expose >4 km thick intracaldera tuff, two generations of resurgent granitic plutons, silicic ring-fracture intrusions, a tuff dike that fed the early eruption, and pre- and post-caldera andesites. We integrate new petrologic data for extrusive and intrusive Caetano units with geologic mapping and geochronology to provide an exceptional view into the inner workings of a large caldera center. The Caetano Tuff is a phenocryst-rich (~30-50%) ignimbrite with a mineralogy of plagioclase + sanidine + quartz + biotite + orthopyroxene + Fe-Ti oxides ± hornblende + accessory zircon and allanite. Plagioclase crystals in the Caetano Tuff and cogenetic intrusive units span a wide compositional range (>30 mol% An) and have diverse petrographic textures ranging from euhedral phenocrysts to anhedral, sieved crystals with melt-rich cores. Plagioclase compositions measured by electron microprobe for whole rock thin sections are consistent with compositional zoning of the intracaldera tuff shown by XRF whole rock analyses, oligoclase (~10-30 mol% An) and andesine (~30-50 mol% An) in the most evolved (75-77% SiO2) and least evolved (72-74% SiO2) tuff units, respectively. However, orthopyroxene compositions are apparently decoupled from the host tuff composition, with the highest Mg#s (~60-70%) occurring in the most evolved tuff samples. In the Caetano Tuff, equilibrium pairs of Fe-Ti oxides yield an average eruption temperature of 745°C, which is consistent with the average Ti-in-zircon temperature of 750±70°C (1 stdev, n=90 spots) obtained from Ti concentrations measured by SHRIMP for single zircons. Application of Al-in-hornblende geobarometry indicates an average equilibration pressure of 4.5±0.1 kbar, corresponding to mid-crustal magma storage depths of ~14-15 km. In light of our new petrologic data, we highlight the following key points: (1) Diverse crystal cargoes, disequilibrium textures, and wide compositional oscillations in single phenocrysts and among discrete mineral populations indicate prolonged and complex episodes of magma assembly and growth. Based on zircon U-Pb SHRIMP ages that range from ~34-37 Ma, assembly and growth may have spanned ~2-3 Ma, or a 34 Ma Caetano magma chamber may have assimilated older igneous rocks in and around the caldera. (2) Mineral chemistry, U-Pb and Ar-Ar geochronology, O isotope geochemistry, and whole rock major and trace element geochemistry indicate a genetic connection between the Caetano Tuff and resurgent granitic plutons, supporting the role of linked volcanic-plutonic components in caldera settings. (3) Generation and eruption of crystal-rich "monotonous" rhyolite calls into question the prevailing paradigms of crystal-poor rhyolites derived from crystal mushes, or crystal-rich "monotonous intermediates" derived from homogeneous dacitic magma reservoirs. The Caetano Tuff may be a representative end member of caldera-forming eruptions that is important for understanding large-volume rhyolite genesis in the shallow-middle crust.

  7. Pan-Africa/Pan-Brazilian detrital zircons in Lower Palaeozoic schists of SW Norway - enigmatic detrital zircon U-Pb ages

    NASA Astrophysics Data System (ADS)

    Zimmermann, Udo; Bjørheim, Maren; Clark, Chris

    2013-04-01

    We present Sensitive High Resolution Ion Microprobe (SHRIMP) U-Pb zircon age data from metasedimentary rocks (schists and quartzites) located in the town of Stavanger (SW Norway). The metasedimentary sequence is composed of schists, medium grained quartz-rich metawackes and quartzites. Quartzites and meta-quartz-wackes exhibit a mylonitic fabric with newly grown fine-grained muscovite defining the fabric. Accessory minerals are zircon, allanite, detrital apatite, monazite, ilmenite, rutile and zircon. The schists are dark and dominated by quartz and feldspar in a fine chloritic and silica-rich matrix and represent the dominant lithology of the region. While quartzites and metawackes show typical geochemical characteristics for strongly reworked rocks, the schists have very low Zr/Sc and Th/Sc ratios below 0.9 and point together with other trace element ratios (La/Sc, Ti/Zr) to the strong influence of less fractionated, mafic, sources in the detritus, possibly arc derived. U-Pb ages of detrital zircon from quartzites range between 740 to 1800 Ma. There is a defined population at 1135 and 1010 Ma tentatively correlated with the Sveconorwegian orogeny. A second population at ~1450 Ma that can be related to a tectono-magmatic event during the Earliest Mesoproterozoic, also recorded in Oslo, southern Sweden and Bornholm, mapped along the proposed southern margin of Baltica. Other detrital zircons record ages between 1586 - 1664 Ma that are not related to the latter event. The oldest U-Pb detrital zircon grain age was 1796 Ma and is potentially associated with the terminal phase of the Svecofennian orogeny. Detrital zircons from the associated schists do show a similar abundance of main age clusters but the oldest found zircons dates to 2013 Ma while the maximum depositional age could be determined by grains of Cambrian to even Ordovician ages with a large 1 sigma error, as such that we rather propose a Cambrian maximum depositional age. It is possible to speculate that the black schists are an equivalent of the Alum shale successions, which is exposed in the Oslo region, southern Sweden and Bornholm (Denmark) and would be then belong to the margin of Baltica. However, detrital zircons with Ediacaran to Lower Palaeozoic ages are exotic to Baltica, and especially unexpected for the proposed passive margin. Magmatic events in SW Baltica of such an age are yet unknown, besides the intrusion of mafic dykes which cannot account for this large number of detrital zircons in the schists. Hence, there are several possibilities to explain this population: 1. The source area was not in Baltica and this sliver of schists is exotic to Baltica and was accreted during the Caledonian orogeny as the rocks show Caledonian deformation and metamorphism. 2. The depositional area had been in Baltica but the source area has drifted away and the schists are younger than Middle Cambrian, possibly Caledonian. 3. The schists are one of the few relicts which reflect magmatic events of Ediacaran and Lower Paleozoic ages (pre-Caledonian) in Baltica, which we have not been aware of so far and for which we have no geodynamic explanation (as the current opinion interprets a passive margin at the western boundary of Baltica) and might indicate unexpectedly young rift magmatism. If possibility (1) is taken into account then the candidates for the origin are somewhat restricted to Gondwana as on the eastern margin of Laurentia massive magmatism of Ediacaran to Lower Paleozoic ages is as well not well constrained.

  8. Gneiss wastes as secondary raw material for the ceramic industry: an example from the Verbano Cusio Ossola district (Piedmont, north-western Alps, Italy)

    NASA Astrophysics Data System (ADS)

    Cavallo, Alessandro

    2015-04-01

    The Verbano Cusio Ossola province (VCO, Piedmont, north-western Italy) is one of the most important Italian quarrying districts, due to the peculiarity and variety of its exploited rock types, mainly orthogneisses such as Serizzo and Beola, and subordinately granites, marbles and other rocks. The most important and extensively exploited ornamental stone from the VCO province is surely the Serizzo, commercialized in four main varieties, and representing about 70% of all the stone production from the VCO area. The protholith of the Serizzo is a Permian granite - granodiorite metamorphosed during the alpine events, and the rock-forming minerals are mainly quartz, K-feldspar, plagioclase (andesine), biotite, with variable amounts of muscovite and epidote (allanite). The other important ornamental stone of the VCO province is the Beola, a series of heterogeneous materials (mainly orthogneisses) with marked (mylonitic) foliation and strong mineralogical lineation, occurring in the median Ossola Valley; its production (15% of the whole stones of the VCO) is subordinated with respect to that of Serizzo. The mineralogical composition of the Beola varieties is similar to Serizzo, consisting of quite homogeneous quartz, K-feldspar (orthoclase or microcline), plagioclase, biotite and muscovite. The main differences relate to the grain size, the rock fabric (generally mylonitic) and to the presence of accessory/secondary minerals. Recent regulatory developments and the growing environmental awareness, require an increasing reuse of wastes deriving from the extraction and processing of dimension stones (up to 50 % of the extracted gross volume). Granite wastes from the VCO (Baveno pink granite and Montorfano white granite), after specific industrial treatments (crushing, sieving, drying, magnetic separation of biotite and hornblende), are used successfully as quartz-feldspars mix in the ceramic industry, with very low FeOtot content. On the other hand, other quartzose-feldspathic rocks (i.e. Serizzo and Beola), are potential sources of secondary raw materials for the ceramic industry. To assess the feasibility of a reuse of these waste materials, an extensive sampling was performed on the main quarry dumps. The waste rocks were characterized by polarized light optical microscopy (OM) on thin sections, scanning electron microscopy (SEM), quantitative X-ray powder diffraction (XRD-QPA with the Rietveld method), electron microprobe (WDS and EDS) and whole-rock geochemistry (ICP-AES, ICP-MS and LECO®). The performed analyzes show a marked mineralogical and chemical heterogeneity (e.g. highly variable content of phyllosilicates, FeOtot content between 0.39 and 6.99 wt.%), as well as important textural and granulometric differences. On the other hand, the composition of feldspars is quite homogeneous, with the plagioclase ranging from almost pure albite to oligoclase (An 25 - 30%). Some varieties of Serizzo and Beola (Serizzo Sempione, Serizzo Formazza and Beola Bianca) are preferable because of their relatively low FeOtot content, but granulometric and textural factors should never be overlooked, as they have an important feedback in the efficiency and feasibility of the industrial treatments (e.g. magnetic separation). Specifically, some Beola varieties with particularly fine grain size and mylonitic texture, are poorly-suited to industrial ore treatments. On the contrary, the Serizzo varieties, although with a generally higher FeOtot content, have a coarser and homogeneous (and therefore preferable) grain size. Waste materials with different composition could be mixed properly until reaching the desired "ideal" compositions for the following industrial treatments. In any case, an accurate characterization of the waste materials from each of quarry dump is of fundamental importance.

  9. Metallogeny of Mesoproterozoic Sedimentary Rocks in Idaho and Montana - Studies by the Mineral Resources Program, U.S. Geological Survey, 2004-2007

    USGS Publications Warehouse

    O'Neill, J. Michael

    2007-01-01

    Preface By J.Michael O'Neill The major emphasis of this project was to extend and refine the known Mesoproterozoic geologic and metallogenic framework of the region along and adjacent to the Idaho-Montana boundary north of the Snake River Plain. The Mesoproterozoic metasedimentary rocks in this part of east-central Idaho host important Cu-Co-Au stratabound mineral resources as well as younger, epigenetic hydrothermal, sulfide base-metal mineral deposits. Two tasks of this study were to more accurately understand and portray the character and origin of cobalt-copper-gold deposits that compose the Idaho cobalt belt and specifically to analyze ore mineralogy and metallogenesis within the Blackbird mining district in the central part of the belt. Inasmuch as the cobalt belt is confined to the Mesoproterozoic Lemhi Group strata of east-central Idaho, geologic investigations were also undertaken to determine the relationship between strata of the Lemhi Group and the more extensive, noncobalt-bearing, Belt-Purcell Supergroup strata to the north and northwest. Abrupt lateral differences in the character and thickness of stratigraphic units in the Mesoproterozoic Lemhi Basin may indicate differential sedimentation in contemporaneous fault-bounded subbasins. It is suggested that northeast-trending basement faults of the Great Falls tectonic zone controlled development of the subbasins. O'Neill and others (chapter A, this volume) document a second major basement fault in this area, the newly recognized northwest-striking Great Divide megashear, a zone 1-2 km wide of left-lateral strike-slip faults active during Mesoproterozoic sedimentation and bounding the Cu-Co belt on the northwest. The megashear is a crustal-scale tectonic feature that separates Lemhi Group strata from roughly coeval Belt-Purcell strata to the north and northwest in Montana and northern Idaho. The results of numerous geologic investigations of the Cu- and Co-bearing Mesoproterozoic rocks of east-central Idaho are integrated and summarized by Bookstrom and others (chapter B, this volume). In particular, their field investigations and analysis of evidence and previous arguments for synsedimentary versus epigenetic mineral deposit types, both of which have been postulated by earlier workers, led them to conclude that both processes were likely instrumental in forming the ore deposits of the Blackbird district. Finally, this report supplies new data on isotopic ratios of sulfur, oxygen, carbon, and helium in minerals associated with cobalt-bearing ores of the cobalt belt. Slack (chapter C, this volume) identified several previously unrecognized rare-earth-element minerals in Blackbird ores: monazite (Ce,La,Y,Th)PO4, xenotime (YPO4), allanite (CaCe)2(Al,Fe)3Si3O12(OH), and gadolinite (Be2FeY2Si2O10). Light rare-earth elements reside mostly in monazite, whereas yttrium and heavy rare-earth minerals reside mostly in xenotime. Dated monazite, which in the Blackbird district is interstitial to cobaltite, is Cretaceous. This date brings into question the otherwise geologically convincing interpretation of Blackbird ores as being of Mesoproterozoic age and synsedimentary origin. This volume consists of three summary articles: A. Great Divide megashear, Montana, Idaho, and Washington: An intraplate crustal-scale shear zone recurrently active since the Mesoproterozoic by J. Michael O'Neill, Edward T. Ruppel, and David A. Lopez B. Blackbird Fe-Cu-Co-Au-REE deposits by Arthur A. Bookstrom, Craig A. Johnson, Gary P. Landis, and Thomas P. Frost C. Geochemical and mineralogical studies of sulfide and iron oxide deposits in the Idaho cobalt belt by John F. Slack

  10. Geochemistry of biotite granites from the Lamas de Olo Pluton, northern Portugal

    NASA Astrophysics Data System (ADS)

    Fernandes, Susana; Gomes, Maria; Teixeira, Rui; Corfu, Fernando

    2013-04-01

    In the Central Iberian Zone (CIZ) extensive crustal recycling occurred during the post-thickening extension stage of the Variscan orogeny (~330-290 Ma). After the ductile deformation phase D3 (~320-300 Ma), characterized by the intrusion of large volumes of highly peraluminous granitic magmas, rapid and drastic tectonic changes at about 300 Ma gave rise to the brittle phase of deformation D4 that controlled the emplacement of Fe-K subalkaline granites (296-290 Ma; Dias et al. 1998). The Lamas de Olo Pluton (LOP) is controlled by NE-SW and NW-SE fracture systems, probably related to the Régua-Verin fault zone (Pereira, 1989). The LOP is a medium to coarse-grained, porphyritic biotite granite, accompanied by medium- to fine grained, porphyritic biotite granite (Alto dos Cabeços- AC) and a more leucocratic, fine-grained, slightly porphyritic biotite-muscovite granite (Barragens- BA). The contacts between LO and AC are generally diffuse, whereas those to BA are sharp. In fact, the BA granite can occur in dykes and sills cutting LO and AC. Microgranular enclaves and xenoliths are very rare. The LOP intrudes the Douro Group, presumably of Precambrian to Cambrian age, and two-mica granites from the Vila Real composite massif. The LOP granites consist of quartz, microcline, plagioclase, biotite, zircon, titanite, tourmaline apatite, fluorite, ilmenite, magnetite, and rutile, with muscovite in BA granite and rare allanite in the LO and AC granites. The plagioclase composition is of oligoclase (An12) - andesine (An35) for LO granite, albite (An9) - andesine (An30) for CA granite and albite (An5) - oligoclase (An20) for BA granite. There are decreases in: a) anorthite content from phenocryst to matrix plagioclase; b) Ba content from phenocryst to matrix microcline in all granites. The Fe2+ biotite has a composition similar to that of biotite from calc-alkaline to sub-alkaline rock series. The LO and AC granites are meta- to peraluminous with ASI variable between 1.05 and 1.21, and display isotopic signatures of (87Sr/86Sr)i = 0.7044-0.7077 and Nd = -2.2 to -1.1. Six samples of LO define a whole rock isochron age of 285±15 Ma with (87Sr/86Sr)i = 0.7051±0.001 (MSWD = 0.11). Two monazite analyses for the LO granite yield an weighted average 207Pb/235U age of 297.19±0.73 Ma, consistent with the preliminary ID-TIMS U-Pb analyses of two transparent and euhedral prisms of zircon that define a concordia age of 296.37 ±0.52 Ma (MSWD = 0.66). The linear trends of major and trace elements variation diagrams of LO and AC granites and their similar mean values of (87Sr/86Sr)i point, at this stage, to an involvement of mid-crustal sources, probably mixed with asthenospheric material. Therefore, LOP consists of post-D3 biotite granites installed in higher structural crustal levels, testifying the occurrence of a crustal growth episode after the major recycling processes that occurred during the deformation phase D3. We thank Prof. J.F. Santos and Dr. S. Ribeiro and Petrochron project (PTDC/CTE-GIX/112561/2009) for the Rb-Sr isotopic data obtained at LGI of University of Aveiro, Portugal. Dias, G. et al. 1998. Lithos, 45, 349-369. Pereira, E., 1989. Serviços Geológicos de Portugal.

  11. Summary of reconnaissance for radioactive deposits in Alaska, 1945-1954, and an appraisal of Alaskan uranium possibilities

    USGS Publications Warehouse

    Wedow, Helmuth

    1956-01-01

    In the period 1945-1954 over 100 investigations for radioactive source materials were made in Alaska. The nature of these investigations ranged from field examinations of individual prospects or the laboratory analysis of significantly radioactive samples submitted by prospectors to reconnaissance studies of large districts. In this period no deposits of uranium or thorium that would warrant commercial exploitation were discovered. The investigations, however, disclosed that radioactive materials occur in widely scattered areas of Alaska and in widely diverse environments. Many igneous rocks throughout Alaska are weakly radioactive because of uranium- and thorium-bearing accessory minerals, such as allanite, apatite, monazite, sphene, xenotime, and zircon; more rarely the radioactivity of these rocks is due to thorianite or thorite and their uranoan varieties. The felsic rocks, for example, granites and syenites, are generally more radioactive than the mafic igneous rocks. Pegmatites, locally, have also proved to be radioactive, but they have little commercial significance. No primary uranium oxide minerals have been found yet in Alaskan vein deposits, except, perhaps, for a mineral tentatively identified as pitchblende in the Hyder district of southeastern Alaska. However, certain occurrences of secondary uranium minerals, chiefly those of the uranite group, on the Seward Peninsula, in the Russian Mountains, and in the vicinity of Kodiak suggest that pitchblende-type ores may occur at depth beneath zones of alteration. Thorite-bearing veins have been discovered on Prince of Wales Island in southeastern Alaska. Although no deposits or carnotite-type minerals have been found in Alaska, several samples containing such minerals have been submitted by Alaskan prospectors. Efforts to locate the deposits from which these minerals were obtained have been unsuccessful, but review of available geologic data suggests that several Alaskan areas are potentially favorable for carnotite-type deposits. The chief of these areas is the Alaska Peninsula-Cook Inlet area which encompasses most of the reported occurrences of the prospectors' carnotite-type samples. Alaska is also potentially favorable for the occurrence of large bodies of the very low-grade uraniferous sedimentary rocks, such as phosphorites and black shales. This type of deposit, however, has not received much study because of the emphasis on the search for bonanza-type high-grade ores. Uraniferous phosphorites similar to those of Idaho, Montana, and Wyoming occur in northern Alaska on the north flank of the Brooks Range; black shales comparable to the uraniferous shales of the Chattanooga formation of southeastern United States have been noted along the Yukon River near the international boundary. Placer deposits in Alaska have some small potential for the production of the radioactive elements as byproducts of gold- and tin-placer mining. the placer area believed to have the relatively greatest potential in Alaska lies in the Kahiltna River valley where concentrates are known to contain such commercial minerals as ilmenite, cassiterite, platinum, and gold in addition to uranothorianite and monazite. The possibilities of the natural fluids--water and petroleum--have not yet been tested in Alaska to any great extent. Studies of fluids are in progress to determine whether they may be used to discover and define areas potentially favorable for the occurrence of uraniferous lodes.

  12. U-Pb, Re-Os, and Ar/Ar geochronology of rare earth element (REE)-rich breccia pipes and associated host rocks from the Mesoproterozoic Pea Ridge Fe-REE-Au deposit, St. Francois Mountains, Missouri

    USGS Publications Warehouse

    Aleinikoff, John N.; Selby, David; Slack, John F.; Day, Warren C.; Pillers, Renee M.; Cosca, Michael A.; Seeger, Cheryl; Fanning, C. Mark; Samson, Iain

    2016-01-01

    Rare earth element (REE)-rich breccia pipes (600,000 t @ 12% rare earth oxides) are preserved along the margins of the 136-million metric ton (Mt) Pea Ridge magnetite-apatite deposit, within Mesoproterozoic (~1.47 Ga) volcanic-plutonic rocks of the St. Francois Mountains terrane in southeastern Missouri, United States. The breccia pipes cut the rhyolite-hosted magnetite deposit and contain clasts of nearly all local bedrock and mineralized lithologies.Grains of monazite and xenotime were extracted from breccia pipe samples for SHRIMP U-Pb geochronology; both minerals were also dated in one polished thin section. Monazite forms two morphologies: (1) matrix granular grains composed of numerous small (<50 μm) crystallites intergrown with rare xenotime, thorite, apatite, and magnetite; and (2) coarse euhedral, glassy, bright-yellow grains similar to typical igneous or metamorphic monazite. Trace element abundances (including REE patterns) were determined on selected grains of monazite (both morphologies) and xenotime. Zircon grains from two samples of host rhyolite and two late felsic dikes collected underground at Pea Ridge were also dated. Additional geochronology done on breccia pipe minerals includes Re-Os on fine-grained molybdenite and 40Ar/39Ar on muscovite, biotite, and K-feldspar.Ages (±2σ errors) obtained by SHRIMP U-Pb analysis are as follows: (1) zircon from the two host rhyolite samples have ages of 1473.6 ± 8.0 and 1472.7 ± 5.6 Ma; most zircon in late felsic dikes is interpreted as xenocrystic (age range ca. 1522–1455 Ma); a population of rare spongy zircon is likely of igneous origin and yields an age of 1441 ± 9 Ma; (2) pale-yellow granular monazite—1464.9 ± 3.3 Ma (no dated xenotime); (3) reddish matrix granular monazite—1462.0 ± 3.5 Ma and associated xenotime—1453 ± 11 Ma; (4) coarse glassy-yellow monazite—1464.8 ± 2.1, 1461.7 ± 3.7 Ma, with rims at 1447.2 ± 4.7 Ma; and (5) matrix monazite (in situ)—1464.1 ± 3.6 and 1454.6 ± 9.6 Ma, and matrix xenotime (in situ)—1468.0 ± 8.0 Ma. Two slightly older ages of cores are about 1478 Ma. The young age of rims on the coarse glassy monazite coincides with an Re-Os age of 1440.6 ± 9.2 Ma determined in this study for molybdenite intergrown with quartz and allanite, and with the age of monazite inclusions in apatite from the magnetite ore (Neymark et al., 2016). A 40Ar/39Ar age of 1473 ± 1 Ma was obtained for muscovite from a breccia pipe sample.Geochronology and trace element geochemical data suggest that the granular matrix monazite and xenotime (in polygonal texture), and cores of coarse glassy monazite precipitated from hydrothermal fluids during breccia pipes formation at about 1465 Ma. The second episode of mineral growth at ca. 1443 Ma may be related to faulting and fluid flow that rebrecciated the pipes. The ca. 10-m.y. gap between the ages of host volcanic rocks and breccia pipe monazite and xenotime suggests that breccia pipe mineral formation cannot be related to the felsic magmatism represented by the rhyolitic volcanic rocks, and hence is linked to a different magmatic-hydrothermal system.

  13. Zircon Trace Element Contents and Refined U-Pb Crystallization Ages for the Tatoosh Pluton, Mount Rainier National Park, Washington Cascades

    NASA Astrophysics Data System (ADS)

    Bacon, C. R.; Du Bray, E. A.; John, D. A.; Mazdab, F. K.; Wooden, J. L.

    2008-12-01

    The 7x12 km Tatoosh pluton south of Mount Rainier consists of 4 petrographic/compositional phases, here termed Nisqually, Reflection, Pyramid, and Stevens, that intrude Tertiary volcanic and sedimentary wall and roof rocks; contacts between the 4 intrusive units are rarely exposed. We used the USGS-Stanford SHRIMP- RG to analyze, in a continuous session, zircons from each of 6 quartz monzodiorite (qmd), quartz monzonite (qm), or granodiorite (grd) samples for 206Pb/238U ages and, concurrently, U, Th, Hf, and REE concentrations. A round-robin procedure yielded statistically robust geochronological results. Ages that we reported previously (FM07) were compromised by instrument instability and by calibration differences between analytical sessions. Between 11 and 31 new analyses of zircons from each sample were evaluated using the TuffZirc and Umix Ages routines of Isoplot 3.41 (Ludwig, 2003). TuffZirc solidification ages for the intrusions are: Nisqually grd (Paradise Valley; 65.4% SiO2) 17.29 +0.37/-0.24 Ma, Nisqually grd (Christine Falls; 66.4%) 17.70 +0.30/-0.16 Ma, Reflection qm (Pinnacle Peak trail; 66.6%) 18.38 +0.45/-0.28 Ma, Pyramid qmd (58.5%) 18.58 +0.20/-0.15 Ma, Stevens grd (Stevens Canyon; 67.8%) 19.15 +0.15/-0.12 Ma, and Stevens grd (south of Louise Lake; 69.3%) 19.20 +0.31/-0.26 Ma (U-Th initial-disequilibrium corrected, ±2σ). Precision of the U-Pb data limits rigorous identification of antecrysts to those with ages ~1 Myr > solidification ages. Antecryst ages that produce subsidiary modes in relative probability diagrams for the two Stevens samples give weighted mean values of 20.18 ±0.26 Ma and 20.07 ±0.18 Ma. Wide ranges in trace element concentrations and ratios indicate that many analyzed zircons grew in highly fractionated residual liquids in high-crystallinity environments. Concentrations of Th and U in Tatoosh zircons vary by two orders of magnitude, cores tend to have higher Th, U, and Th/U than rims, and overgrowths that fill reentrants have high U contents and low Th/U ratios. Chondrite-normalized REE patterns have familiar convex-up shapes with positive Ce and negative Eu anomalies: LaN = 0.03-6 (10 values >6 may reflect inclusions), YbN = 380-33,900, Ce/Ce* = 0.7-505, and Eu/Eu* = 0.06-1.25. Slopes of REE patterns increase subtly in the order Reflection < Pyramid ≤ Nisqually < Stevens. Fractionation of plagioclase + pyroxene and(or) amphibole + Fe-Ti oxide + apatite + zircon should produce relative-LREE- enriched successive liquids. Observed marginally steeper REE patterns (greater positive slopes) for rims, lower REE concentrations, and lower Th/U ratios may reflect co-precipitation of allanite ± thorite. Two parallel arrays in Eu/Eu* versus Hf, in which Eu/Eu* decreases as Hf increases, are consistent with growth of higher-Hf, lower-Eu/Eu* zircon from more evolved melts; separate arrays imply Nisqually and Pyramid + Reflection intrusions. Zircon Eu/Eu* and Hf in the Stevens granodiorite define one high-Eu/Eu* field and another similar to that for Pyramid and Reflection samples that imply more than one parental magma. The zircon ages indicate solidification in three episodes: Stevens ~19.2 Ma, Pyramid + Reflection ~18.5 Ma, and Nisqually ~17.5 Ma. An ~20.1 Ma stage is represented by antecrysts in Stevens samples. The source(s) of the pluton were active for at least ~2.7 Myr and major crystallization episodes were separated by intervals of 0.7-1.0 Myr.

  14. Cataclastic rocks of the San Gabriel fault—an expression of deformation at deeper crustal levels in the San Andreas fault zone

    NASA Astrophysics Data System (ADS)

    Anderson, J. Lawford; Osborne, Robert H.; Palmer, Donald F.

    1983-10-01

    The San Gabriel fault, a deeply eroded late Oligocene to middle Pliocene precursor to the San Andreas, was chosen for petrologic study to provide information regarding intrafault material representative of deeper crustal levels. Cataclastic rocks exposed along the present trace of the San Andreas in this area are exclusively a variety of fault gouge that is essentially a rock flour with a quartz, feldspar, biotite, chlorite, amphibole, epidote, and Fe-Ti oxide mineralogy representing the milled-down equivalent of the original rock (Anderson and Osborne, 1979; Anderson et al., 1980). Likewise, fault gouge and associated breccia are common along the San Gabriel fault, but only where the zone of cataclasis is several tens of meters wide. At several localities, the zone is extremely narrow (several centimeters), and the cataclastic rock type is cataclasite, a dark, aphanitic, and highly comminuted and indurated rock. The cataclastic rocks along the San Gabriel fault exhibit more comminution than that observed for gouge along the San Andreas. The average grain diameter for the San Andreas gouge ranges from 0.01 to 0.06 mm. For the San Gabriel cataclastic rocks, it ranges from 0.0001 to 0.007 mm. Whereas the San Andreas gouge remains particulate to the smallest grain-size, the ultra-fine grain matrix of the San Gabriel cataclasite is composed of a mosaic of equidimensional, interlocking grains. The cataclastic rocks along the San Gabriel fault also show more mineralogiec changes compared to gouge from the San Andreas fault. At the expense of biotite, amphibole, and feldspar, there is some growth of new albite, chlorite, sericite, laumontite, analcime, mordenite (?), and calcite. The highest grade of metamorphism is laumontite-chlorite zone (zeolite facies). Mineral assemblages and constrained uplift rates allow temperature and depth estimates of 200 ± 30° C and 2-5 km, thus suggesting an approximate geothermal gradient of ~50°C/km. Such elevated temperatures imply a moderate to high stress regime for the San Andreas, which is consistent with experimental rock failure studies. Moreover, these results suggest that the previously observed lack of heat flow coaxial with the fault zone may be the result of dissipation rather than low stress. Much of the mineralogy of the cataclastic rocks is still relict from the earlier igneous or metamorphic history of the protolith; porphyroclasts, even in the most deformed rocks, consist of relict plagioclase (oligoclase to andesine), alkali feldspar, quartz, biotite, amphibole, epidote, allanite, and Fe-Ti oxides (ilmenite and magnetite). We have found no significant development of any clay minerals (illite, kaolinite, or montmorillonite). For many sites, the compositions of these minerals directly correspond to the mineral compositions in rock types on one or both sides of the fault. Whole rock major and trace element chemistry coupled with mineral compositions show that mixing within the zone of cataclasis is not uniform, and that originally micaceous foliated, or physically more heterogeneous rock units may contribute a disproportionally large amount to the resultant intrafault material. As previously found for the gouge along the San Andreas, chemical mobility is not a major factor in the formation of cataclastic rocks of the San Gabriel fault. We see only minor changes for Si and alkalies; however, there is a marked mobility of Li, which is a probable result of the alteration and formation of new mica minerals. The gouge of the San Andreas and San Gabriel faults probably formed by cataclastic flow. There is some indication, presently not well constrained, that the fine-grained matrix of the cataclasite of from the San Gabriel fault formed in response to superplastic flow.

  15. Genesis of a zoned granite stock, Seward Peninsula, Alaska

    USGS Publications Warehouse

    Hudson, Travis

    1977-01-01

    A composite epizonal stock of biotite granite has intruded a diverse assemblage of metamorphic rocks in the Serpentine Hot Springs area of north-central Seward Peninsula, Alaska. The metamorphic rocks include amphibolite-facies orthogneiss and paragneiss, greenschist-facies fine-grained siliceous and graphitic metasediments, and a variety of carbonate rocks. Lithologic units within the metamorphic terrane trend generally north-northeast and dip moderately toward the southeast. Thrust faults locally juxtapose lithologic units in the metamorphic assemblage, and normal faults displace both the metamorphic rocks and some parts of the granite stock. The gneisses and graphitic metasediments are believed to be late Precambrian in age, but the carbonate rocks are in part Paleozoic. Dating by the potassium-argon method indicates that the granite stock is Late Cretaceous. The stock has sharp discordant contacts, beyond which is a well-developed thermal aureole with rocks of hornblende hornfels facies. The average mode of the granite is 29 percent plagioclase, 31 percent quartz, 36 percent K-feldspar, and 4 percent biotite. Accessory minerals include apatite, magnetite, sphene, allanite, and zircon. Late-stage or deuteric minerals include muscovite, fluorite, tourmaline, quartz, and albite. The stock is a zoned complex containing rocks with several textural facies that are present in four partly concentric zones. Zone 1 is a discontinuous border unit, containing fine- to coarse-grained biotite granite, that grades inward into zone 2. Zone 2 consists of porphyritic biotite granite with oriented phenocrysts of pinkish-gray microcline in a coarse-grained equigranular groundmass of plagioclase, quartz, and biotite. It is in sharp, concordant to discordant contact with rocks of zone 3. Zone 3 consists of seriate-textured biotite granite that has been intruded by bodies of porphyritic biotite granite containing phenocrysts of plagioclase, K-feldspar, quartz, and biotite in an aplitic groundmass. Flow structures, pegmatite and aplite segregations, and miarolitic cavities are common in the seriate-textured granite. Zone 4, which forms the central part of the complex, consists of fine- to medium-grained biotite granite and locally developed leucogranite. Small miarolitic cavities are common within it. Eight textural facies have been defined within the complex, and mineralogic, petrographic, modal, and chemical variations are broadly systematic within the facies sequence. Study of these variations shows that the gradational facies of zones l and 2 systematically shift toward more mafic compositions inward within the complex. Seriate-textured rocks of zone 3 are similar in composition to those of zone 2, but porphyritic rocks of zone 3 and rocks of zone 4 mark shifts to more felsic compositions. These late-crystallizing felsic rocks are products of an interior residual magma system. This system was enriched in water and certain trace elements including tin, lithium, niobium, lead, and zinc. The complex as a whole has higher concentrations of these elements than many other granites. The nature of this geochemical specialization is particularly well demonstrated by the trace-element composition of biotite. The crystallization history of the pluton was complex. The available data suggest that this history could have included: (1) chilling and metasomatic alteration adjacent to the contact, (2) in-situ crystallization in several marginal facies accompanied by some transfer of residual constituents toward interior parts of the pluton, (3) slight upward displacement of magma that was subjacent to the crystallized walls, accompanied by disequilibrium crystallization and local vapor saturation, (4) upward displacement of part of the residual water-rich interior magma, accompanied by rapid loss of a separated vapor phase, and (5) displacement of the margins of the pluton by normal faults, accompanied by loss of an exsolved vapor phase from th

  16. Black and red granites in the Egyptian Antiquity Museum of Turin. A minero-petrographic and provenance study.

    NASA Astrophysics Data System (ADS)

    Serra, M.; Borghi, A.; Vaggelli, G.; D'Amicone, E.; Vigna, L.

    2009-04-01

    The University of Turin, in cooperation with the Egyptian Antiquity Museum, has recently undertaken several projects aimed at developing a scientific approach to the analysis of ancient Egyptian finds. In particular, a straightforward project to investigate the stony handcrafts preserved in the statuary rooms started in 2006 to obtain their systematic petrographic classification and their possible geological sources. The main intent of the project was to understand the provenance of the materials used in Pharaonic period, setting the base for the identification of the ancient quarry sites and for a correct interpretation of the extraction and working techniques, in order to provide fundamental information about economical and social development of Egyptian civilization through historical times. The choice to focus attention on black and red granites came from the statement of the percentage relevance (40 of the 54 sculptures actually exposed) of these materials in the statuary rooms. Moreover, especially for black granites, the need of detailed minero-petrographic analysis arose from the difficulty in making a macroscopic classification of the fine-grained dark-coloured rock varieties. Therefore, five black granite statues, belonging to the Drovetti collection were sampled in a micro-invasive way: three sculptures of goddess Sekhmet (cat. 260, 251, 247), the statue of Ramses II (cat. 1380) and the statue of goddess Hathor (cat. 694). The choice to analyse even three of the twenty-one statues of goddess Sekhmet (cat. 247, cat. 251, cat. 260), originally located in the same Egyptian temple but ichnographically different, derived from the need of answering the archaeological questions about their provenance. On the other hand, the opportunity of studying the fine-grained black rocks used for the sculptures of goddess Hathor (cat. 694) and of Ramses II in Majesty (cat. 1380), symbol of the Egyptian museum of Turin, provided the opportunity to analyse and classify the materials used for two of the best known masterpieces of Egyptian art. As regards to red granites, it has been observed that most of the exposed sculptures were made of rocks closely akin to Aswan granite. Just in one case, the Ram headed sphinx (cat. 836), macroscopic differences in colour index, grain size and isoorientation of feldspar phenocrysts, suggested a different provenance of the source material and determined the choice of picking up a small fragment for minero-petrographic analysis. The sample collected from the sarcophagus of Nefertari (suppl. 5153) during the recent restoration of the sculpture, was analysed in order to test the accuracy of the results, as the provenance of the material used for its realization was already certain. Petrographic observations and chemical analysis were undertaken by a scanning electron microscope equipped with an energy-dispersive spectrometer. Minero-petrographic data primarily showed that all samples vary in composition from granite (red granites) to granodiorite and tonalite (black granites). The main sialic phases are represented by plagioclase (albite to oligoclase), alkali-feldspar (microcline) and quartz, while femic phases are amphibole (green horneblende) and biotite (Fe- to Mg-biotite), always coexisting in variable relative percentages. Minor amount of apatite (≈ 1 wt.%), magnetite, ilmenite, often associated to sphene, zircon, pyrite and allanite also occur. The identification of some compositional markers in all samples suggested a common provenance for all the rocks used for the sculptures. Thus, it was supposed that they could all have been quarried in the famous district of Aswan, well known at least since Dynastic period. This provenance hypothesis was confirmed by geological literature and archeological evidences, considering the relative proximity of Aswan quarries to Nile river and to the key centres of power in the New Kingdom. Therefore, several geological samples were collected in Aswan area, in order to perform a minero - petrographical and geochemical comparison with the rocks of the statues. According to the petrographic and minero-chemical results, it was possible to define the provenance of the granitoids used for the realization of the sculptures and finally to highlight the importance of an archaeometric approach to historical and archaeological problems.

  17. Beryl-bearing pegmatites in the Ruby Mountains and other areas in Nevada and northwestern Arizona

    USGS Publications Warehouse

    Olson, Jerry C.; Hinrichs, E. Neal

    1960-01-01

    Pegmatite occurs widely in Nevada and northwestern Arizona, but little mining has been done for such pegmatite minerals as mica, feldspar, beryl, and lepidolite. Reconnaissance for beryl-bearing pegmatite in Nevada and in part of Mohave County, Ariz., and detailed studies in the Dawley Canyon area, Elko County, Nev., have shown that beryl occurs in at least 11 districts in the region. Muscovite has been prospected or mined in the Ruby and Virgin Mountains, Nev., and in Mohave County, Ariz. Feldspar has been mined in the southern part of the region near Kingman, Ariz., and in Clark County, Nev. The pegmatites in the region range in age from Precambrian to late Mesozoic or Tertiary. Among the pegmatite minerals found or reported in the districts studied are beryl, chrysoberyl, scheelite, wolframite, garnet, tourmaline, fluorite, apatite, sphene, allanite, samarskite, euxenite, gadolinite, monazite, autunite, columbite-tantalite, lepidolite, molybdenite, and pyrite and other sulflde minerals. The principal beryl-bearing pegmatites examined are in the Oreana and Lakeview (Humboldt Canyon) areas, Pershing County; the Dawley Canyon area in the Ruby Mountains, Elko County, Nev.; and on the Hummingbird claims in the Virgin Mountains, Mohave County, Ariz. Beryl has also been reported in the Marietta district, Mineral County; the Sylvania district, Esmeralda County; near Crescent Peak and near Searchlight, Clark County, Nev.; and in the Painted Desert near Hoover Dam, Mohave County, Ariz. Pegmatites are abundant in the Ruby Mountains, chiefly north of the granite stock at Harrison Pass. In the Dawley Canyon area of 2.6 square miles at least 350 pegmatite dikes more than 1 foot thick were mapped, and beryl was found in small quantities in at least 100 of these dikes. Four of these dikes exceed 20 feet in thickness, and 1 is 55 feet thick. A few pegmatites were also examined in the Corral Creek, Gilbert Canyon, and Hankins Canyon areas in the Ruby Mountains.The pegmatite dikes in the Dawley Canyon area intrude granite and metamorphic rocks which consist chiefly of quartzite and schist of probable Early Cambrian age. The granite is of two types: a biotite-muscovite granite that forms the main mass of the stock and albite granite that occurs in the metamorphic rocks near the borders of the stock. The pegmatites were emplaced chiefly along fractures in the granite and along schistosity or bedding planes in the metamorphic rocks.Many of the Dawley Canyon pegmatite dikes are zoned, having several rock units of contrasting mineralogy or grain size formed successively from the walls inward. Aplitic units occur either as zones or in irregular positions in the pegmatite dikes and are a distinctive feature of the Dawley Canyon pegmatites. Some of the aplitic and fine-grained pegmatite units are characterized by thin layers of garnet crystals, forming many parallel bands on outcrop surfaces. The occurrence of aplitic and pegmatitic textures in the same dike presumably indicates abrupt changes in physical-chemical conditions during crystallization, such as changes in viscosity and in content of volatile constituents. Concentrations of 0.1 percent or more beryl, locally more than 1 percent, occur in certain zones in the Dawley Canyon pegmatites. Spectrographic analyses of 23 samples indicate that the BeO content ranges from 0.0017 to 0.003 percent in the albite granite, from ,0.0013 to 0.039 percent in aplitic units in pegmatite, from 0.0005 to 0.10 percent in coarse-grained pegmatite, and from less than 0.0001 to 0.0004 percent in massive quartz veins. The scheelite-beryl deposits at Oreana and in Humboldt Canyon, Pershing County, are rich in beryllium. Twelve samples from the Lakeview (Humboldt Canyon) deposit range from 0.018 to 0.11 percent BeO, but underground crosscuts have failed to intersect similar rock at depth. Beryl locally constitutes as much as 10 percent of the pegmatitic ore at Oreana. The beryl was not recovered during tungsten mining at Oreana and is now in the tailings of the mill at Toulon, Nev. The percentage of beryl is lower than the Oreana ore because of dilution by tailings from other ores milled at Toulon. Beryl has been found in many pegmatite dikes in the Virgin Mountains. Both beryl and chrysoberyl occur in dikes on the Hummingbird claims, north of Virgin Peak, in Mohave County, Ariz. Spectrographic analyses of 5 representative samples of the principal dike on the Hummingbird claims range from 0.055 to 0.11 percent BeO.

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