Across-arc geochemical variations in the Southern Volcanic Zone, Chile (34.5- 38.0°S): Constraints on Mantle Wedge and Input Compositions

Crustal assimilation (e.g. Hildreth and Moorbath, 1988) and/or subduction erosion (e.g. Stern, 1991; Kay et al., 2005) are believed to control the geochemical variations along the northern portion of the Chilean Southern Volcanic Zone. In order to evaluate these hypotheses, we present a comprehensive geochemical data set (major and trace elements and O-Sr-Nd-Hf-Pb isotopes) from Holocene primarily olivine-bearing volcanic rocks across the arc between 34.5-38.0°S, including volcanic front centers from Tinguiririca to Callaqui, the rear arc centers of Infernillo Volcanic Field, Laguna del Maule and Copahue, and extending 300 km into the backarc. We also present an equivalent data set for Chile Trench sediments outboard of this profile. The volcanic arc (including volcanic front and rear arc) samples primarily range from basalt to andesite/trachyandesite, whereas the backarc rocks are low-silica alkali basalts and trachybasalts. All samples show some characteristic subduction zone trace element enrichments and depletions, but the backarc samples show the least. Backarc basalts have higher Ce/Pb, Nb/U, Nb/Zr, and Ta/Hf, and lower Ba/Nb and Ba/La, consistent with less of a slab-derived component in the backarc and, consequently, lower degrees of mantle melting. The mantle-like δ18O in olivine and plagioclase phenocrysts (volcanic arc = 4.9-5.6 and backarc = 5.0-5.4 per mil) and lack of correlation between δ18O and indices of differentiation and other isotope ratios, argue against significant crustal assimilation. Volcanic arc and backarc samples almost completely overlap in Sr and Nd isotopic composition. High precision (double-spike) Pb isotope ratios are tightly correlated, precluding significant assimilation of older sialic crust but indicating mixing between a South Atlantic Mid Ocean-Ridge Basalt (MORB) source and a slab component derived from subducted sediments and altered oceanic crust. Hf-Nd isotope ratios define separate linear arrays for the volcanic arc and backarc, neither of which trend toward subducting sediment, possibly reflecting a primarily asthenospheric mantle array for the volcanic arc and involvement of enriched Proterozoic lithospheric mantle in the backarc. We propose a quantitative mixing model between a mixed-source, slab-derived melt and a heterogeneous mantle beneath the volcanic arc. The model is consistent with local geodynamic parameters, assuming water-saturated conditions within the slab

Renewed Search for FUN (Fractionated and Unidentified Nuclear Effects) in Primitive Chondrites

Ca-Al-rich inclusions (CAIs) found in primitive chondrites record processes and conditions of the earliest solar system as they are the oldest known solid objects formed in the solar system [1,2]. CAIs with fractionation and unidentified nuclear anomalies (FUN CAIs; [3]) are very rare and thusfar found exclusively in CV carbonaceous chondrites (e.g., Allende and Vigarano)[4]. FUN CAIs are characterized by large nucleosynthetic anomalies in several elements (Ca, Ti, Si, Sr, Ba, Nd, and Sm), large mass-dependant isotope fractionation (Mg, Si, and O), and very little initial {sup 26}Al [4,5 and reference therein]. Formation of FUN CAIs by thermal processing of presolar dust aggregates prior to the injection of {sup 26}Al into the protoplanetary disk has been proposed. More recently [5] proposed that FUN CAIs formed from a protosolar molecular cloud after injection of {sup 26}Al but before {sup 26}Al and {sup 27}Al were completely homogenized. Therefore discovering more FUN CAIs to perform U-Pb and other short-lived chronometric dating will provide key constraints on the age of the solar system, the isotopic composition of the protosolar molecular cloud, the earliest stages of the thermal processing in the solar system and the timing of {sup 26}Al and other short-lived radionuclide injection into the nascent solar system. Most known FUN CAIs were discovered and studied > 30 yr ago, and their isotope ratios determined using thermal ionization mass spectrometry (TIMS). Most of these FUN CAIs were almost or entirely consumed during their respective analyses. [5] recently identified a new FUN CAI (NWA 779 KS-1) based on O and Mg isotope ratios determined by SIMS and MCICPMS, respectively. We have initiated a systematic search for FUN CAIs in primitive chondrites, taking advantage of the large mass-dependant Mg isotope effects known for FUN inclusions with little or no inferred {sup 26}Al. Our strategy is to use newly developed sample cells capable of holding very large slabs of meteorites for laser ablation interfaced with a multicollector inductively coupled plasma mass spectrometry (LA-MC-ICPMS) at UC Davis. Here report the initial findings of our search and describe the instrument setup we use that provides rapid throughput and accurate results

An inter-laboratory assessment of the thorium isotopic composition of synthetic and rock reference materials

We present a concerted international effort to cross-calibrate five synthetic Th isotope reference materials (UCSC Th "A", OU Th "U", WUN, IRMM-35 and IRMM-36), and six rock reference materials (UCSC TML, Icelandic ATHO, USGS BCR-2, USGS W-2, USGS BHVO-2, LV18) using multi-collector inductively coupled plasma-mass spectrometry (MC-ICP-MS). We then compare our new values with a compilation of literature mass spectrometric data for these reference materials and derive recommended "consensus" 230Th/232 Th values for each. We also present isotope dilution U and Th concentration data for four rock reference materials (UCSC TML, Icelandic ATHO, USGS BCR-2, USGS W-2). © 2008 International Association of Geoanalysts

The May 2003 eruption of Anatahan volcano, Mariana Islands: Geochemical evolution of a silicic island-arc volcano

The first historical eruption of Anatahan volcano began on May 10, 2003. Samples of tephra from early in the eruption were analyzed for major and trace elements, and Sr, Nd, Pb, Hf, and O isotopic compositions. The compositions of these tephras are compared with those of prehistoric samples of basalt and andesite, also newly reported here. The May 2003 eruptives are medium-K andesites with 59–63 wt.% SiO_2, and are otherwise homogeneous (varying less than 3% 2σ about the mean for 45 elements). Small, but systematic, chemical differences exist between dark (scoria) and light (pumice) fragments, which indicate fewer mafic and oxide phenocrysts in, and less degassing for, the pumice than scoria. The May 2003 magmas are nearly identical to other prehistoric eruptives from Anatahan. Nonetheless, Anatahan has erupted a wide range of compositions in the past, from basalt to dacite (49–66 wt.% SiO_2). The large proportion of lavas with silicic compositions at Anatahan (> 59 wt.% SiO_2) is unique within the active Mariana Islands, which otherwise erupt a narrow range of basalts and basaltic andesites. The silicic compositions raise the question of whether they formed via crystal fractionation or crustal assimilation. The lack of ^(87)Sr/^(86)Sr variation with silica content, the MORB-like δ^(18)O, and the incompatible behavior of Zr rule out assimilation of old crust, altered crust, or zircon-saturated crustal melts, respectively. Instead, the constancy of isotopic and trace element ratios, and the systematic variations in REE patterns are consistent with evolution by crystal fractionation of similar parental magmas. Thus, Anatahan is a type example of an island-arc volcano that erupts comagmatic basalts to dacites, with no evidence for crustal assimilation. The parental magmas to Anatahan lie at the low ^(143)Nd/^(144)Nd, Ba/La, and Sm/La end of the spectrum of magmas erupted in the Marianas arc, consistent with 1–3 wt.% addition of subducted sediment to the mantle source, or roughly one third of the sedimentary column. The high Th/La in Anatahan magmas is consistent with shallow loss of the top ∼ 50 m of the sedimentary column during subduction