25 research outputs found

    Chondrules and Opaque Phases in Unequilibrated R Chondrites: A Comprehensive Assessment of Their Formation

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    Equilibrated Rumuruti (R) chondrites record an oxygen fugacity between 0 and 3.5 log units below the fayalite-magnetite-quartz buffer, and a sulfur fugacity (fS2) 2 log units above the iron-troilite buffer. They are more than an order of magnitude more oxidized than the ordinary chondrites [1], and orders of magnitude more sulfidized than solar values. Although the R chondrites have the highest (delta)O-17 value of any meteorites, analyses of unequilibrated R chondrites indicate chondrule formation in an oxygen isotope reservoir similar to that of the ordinary chondrite chondrules. We present the relationship of the R chondrite parent body to pre-accretionary volatiles O and S based on our analyses of unequilibrated R chondrite material in two thin sections from the meteorite Mount Prestrud (PRE) 95404

    Transient Cenozoic tectonic stages in the southern margin of the Caribbean plate : U-Th/He thermochronological constraints from Eocene plutonic rocks in the Santa Marta massif and Serranía de Jarara, northern Colombia

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    We use U-Th/(He) zircon and apatite thermochronology and Al in hornblende geobarometry from Eocene granitoids of the Sierra Nevada de Santa Marta and Guajira uplifted massifs in northern Colombia to elucidate the exhumation history of the northern South America continental margin and its bearing to Cenozoic Caribbean- South American plate interactions. Aluminium in hornblende geobarometry from the Eocene Santa Marta batholith yields pressures between 4.9±0.6kbar and 6.4±0.6kbar, which indicate that at least, 14.7-19.2km of unroofing took place since 56-50Ma in the northwestern Sierra Nevada de Santa Marta. In the Guajira Peninsula, calculated pressures for the Eocene Parashi stock are 2.3±0.6kbar and 3±0.6kbar. Stratigraphic considerations pertaining to Oligocene conglomerates from the Guajira area suggest that 6.9-9km of crust was lost between 50Ma and ca. 26Ma. U-Th/He zircon and apatite thermochronology from granitoids in the Sierra Nevada de Santa Marta shows the existence of major exhumation events in the Late Eocene (ca. 45-40Ma), Late Oligocene (ca. 25Ma) and Miocene (ca. 15Ma). The Guajira region records the Late Eocene to Early Oligocene (35-25Ma) event, but it lacks evidence for the Miocene exhumation phase. These differences reflect isolation of the Guajira region from the Sierra Nevada de Santa Marta and the Andean chain due to extensive block rotation and transtensional tectonics that affected the region during post-Eocene times. The post-Eocene events correlate in time with an increased convergence rate and the frontal approach of North and South America. It is suggested that the two major tectonic mechanisms that govern exhumation in these Caribbean massifs are: 1) subduction of the Caribbean plate, and 2) post Eocene changes in plate convergence obliquity and rates that caused the South American continental margin blocks to override the Caribbean plate. Temporal correlation with other Caribbean and Northern Andean events allows to resolve the regional Cenozoic plate tectonic reorganizations experienced by the South American, Caribbean and Pacific plates at a regional scale

    Ecosystem-bedrock interaction changes nutrient compartmentalization during early oxidative weathering

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    Ecosystem-bedrock interactions power the biogeochemical cycles of Earth's shallow crust, supporting life, stimulating substrate transformation, and spurring evolutionary innovation. While oxidative processes have dominated half of terrestrial history, the relative contribution of the biosphere and its chemical fingerprints on Earth's developing regolith are still poorly constrained. Here, we report results from a two-year incipient weathering experiment. We found that the mass release and compartmentalization of major elements during weathering of granite, rhyolite, schist and basalt was rock-specific and regulated by ecosystem components. A tight interplay between physiological needs of different biota, mineral dissolution rates, and substrate nutrient availability resulted in intricate elemental distribution patterns. Biota accelerated CO2 mineralization over abiotic controls as ecosystem complexity increased, and significantly modified stoichiometry of mobilized elements. Microbial and fungal components inhibited element leaching (23.4% and 7%), while plants increased leaching and biomass retention by 63.4%. All biota left comparable biosignatures in the dissolved weathering products. Nevertheless, the magnitude and allocation of weathered fractions under abiotic and biotic treatments provide quantitative evidence for the role of major biosphere components in the evolution of upper continental crust, presenting critical information for large-scale biogeochemical models and for the search for stable in situ biosignatures beyond Earth.Comment: 41 pages (MS, SI and Data), 16 figures (MS and SI), 6 tables (SI and Data). Journal article manuscrip

    Influence of Silicate Melt Composition on Metal/Silicate Partitioning of W, Ge, Ga and Ni

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    The depletion of the siderophile elements in the Earth's upper mantle relative to the chondritic meteorites is a geochemical imprint of core segregation. Therefore, metal/silicate partition coefficients (Dm/s) for siderophile elements are essential to investigations of core formation when used in conjunction with the pattern of elemental abundances in the Earth's mantle. The partitioning of siderophile elements is controlled by temperature, pressure, oxygen fugacity, and by the compositions of the metal and silicate phases. Several recent studies have shown the importance of silicate melt composition on the partitioning of siderophile elements between silicate and metallic liquids. It has been demonstrated that many elements display increased solubility in less polymerized (mafic) melts. However, the importance of silicate melt composition was believed to be minor compared to the influence of oxygen fugacity until studies showed that melt composition is an important factor at high pressures and temperatures. It was found that melt composition is also important for partitioning of high valency siderophile elements. Atmospheric experiments were conducted, varying only silicate melt composition, to assess the importance of silicate melt composition for the partitioning of W, Co and Ga and found that the valence of the dissolving species plays an important role in determining the effect of composition on solubility. In this study, we extend the data set to higher pressures and investigate the role of silicate melt composition on the partitioning of the siderophile elements W, Ge, Ga and Ni between metallic and silicate liquid

    Olivine and Ca-Phosphate in the Diogenites Manegaon and Roda

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    The textural relationships between the different primary minerals in igneous rocks provide one of the most fundamental pieces of evidence available for inferring the crystallization history of their parent magmas. Unfortunately, the high degree of brecciation that characterizes most diogenites, along with the low modal abundance and small grain sizes of minerals other than orthopyroxene, combine to make identifying and interpreting such textural relationships extremely difficult in this class of meteorites. A few descriptions of primary igneous contacts between orthopyroxene and chromite, troilite, and to a lesser extent, olivine in diogenites have been provided in the literature. In addition to these, in previous work, our research group has characterized several types of igneous contacts between Ca-pyroxene, plagioclase and orthopyroxene in the Bilanga diogenite. We have also described primary igneous inclusions of troilite + kamacite + chromite + Ca-pyroxene +/- Ca-phosphate in orthopyroxene (i.e. Metal/Troilite- Ball inclusions) in the diogenites Bilanga, Manegaon, Johnstown, Roda, Shalka, and Tatahouine. However, for the most part, detailed data on igneous textural relations between minerals other than orthopyroxene in diogenites are still sparse. Of the diogenite samples that we have examined

    New data on hemihedrite from Arizona

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    Hemihedrite from the Florence Lead-Silver mine in Pinal County, Arizona, USA was first described and assigned the ideal chemical formula Pb10Zn(CrO4)(6)(SiO4)(2)F-2, based upon a variety of chemical and crystal-structure analyses. The primary methods used to determine the fluorine content for hemihedrite were colorimetry, which resulted in values of F that were too high and inconsistent with the structural data, and infrared (IR) spectroscopic analysis that failed to detect OH or H2O. Our reinvestigation using electron microprobe analysis of the type material, and additional samples from the type locality, the Rat Tail claim, Arizona, and Nevada, reveals the absence of fluorine, while the presence of OH is confirmed by Raman spectroscopy. These findings suggest that the colorimetric determination of fluorine in the original description of hemihedrite probably misidentified F due to the interferences from PO4 and SO4, both found in our chemical analyses. As a consequence of these results, the study presented here proposes a redefinition of the chemical composition of hemihedrite to the ideal chemical formula Pb10Zn(CrO4)(6)(SiO4)(2)(OH)(2). Hemihedrite is isotypic with iranite with substitution of Zn for Cu, and raygrantite with substitution of Cr for S. Structural data from a sample from the Rat Tail claim, Arizona, indicate that hemihedrite is triclinic in space group P (1) over bar, a = 9.4891(7), b = 11.4242(8), c = 10.8155(7) angstrom, alpha = 120.368(2)degrees, ss = 92.017(3)degrees, gamma = 55.857(2)degrees, V = 784.88(9) angstrom(3), Z = 1, consistent with previous investigations. The structure was refined from single-crystal X-ray diffraction data to R-1 = 0.022 for 5705 unique observed reflections, and the ideal chemical formula Pb10Zn(CrO4)(6)(SiO4)(2)(OH)(2) was assumed during the refinement. Electron microprobe analyses of this sample yielded the empirical chemical formula Pb-10.05(Zn0.91Mg0.02)(Sigma) (= 0.93) (Cr5.98S0.01P0.01)(Sigma = 6.00) Si1.97O34 H-2.16 based on 34 O atoms and six (Cr + S + P) per unit cell.NASA, Mars Science Laboratory Investigations [NNX11AP82A]12 month embargo; published online: 01 August 2017.This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at [email protected]

    NWA 2736: An Unusual New Graphite-bearing Aubrite

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    Aubrites are enstatite-rich achondrites that are probably related to enstatite chondrite parent bodies. The exact link, if any, is not understood. They may have formed from melting within one or more enstatite chondrite parent bodies. Description of NWA 2736: One complete stone weighing 171.51 grams was recovered from the Sahara Desert by nomads sometime before September 2004. It was completely covered with fusion crust and desert varnish. This stone is severely weathered, with caramel brown coloration throughout and calcite veins that extend into the interior of the sample. Mineral analyses were performed and elemental x-ray maps were obtained with a CAMECA SX-50 electron microprobe at the Lunar and Planetary Laboratory at the University of Arizona. The relatively high modal abundance of albitic plagioclase, presence of euhedral graphite, depletion of troilite, and occurrence of pervasive kamacite veins (some with daubreelite) all indicate that NWA 2736 has a complex history and may sample a new region of the aubrite parent body. A discussion and analysis on the overall texture of NWA 2736 is presented
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