Crystal fractionation and partial melting in the petrogenesis of a Proterozoic high-MgO volcanic suite,Ungava, Québec

There is little concensus on the relative importance of crystal fractionation and differential partial melting to the chemical diversity observed within most types of volcanic suites. A resolution to this controversy is best sought in suites containing high MgO lavas such as the Chukotat volcanics of the Proterozoic Cape Smith foldbelt, Ungava, Quebec. The succession of this volcanic suite consists of repetitive sequences, each beginning with olivine-phyric basalt (19-12 wt% MgO), grading upwards to pyroxene-phyric basalt (12-8 wt% MgO) and then, in later sequences, to plagioclase-phyric basalt (7-4 wt% MgO). Only the olivine-phyric basalts have compositions capable of equilibrating with the upper mantle and are believed to represent parental magmas for the suite. The pyroxene-phyric and plagioclase-phyric basalts represent magmas derived from these parents by the crystal fractionation of olivine, with minor chromite, clinopyroxene and plagioclase. The order of extrusion in each volcanic sequence is interpreted to reflect a density effect in which successively lighter, more evolved magmas are erupted as hydrostatic pressure wanes. The pyroxene-phyric basalts appear to have evolved at high levels in the active part of the conduit system as the eruption of their parents was in progress. The plagioclase-phyric basalts may represent residual liquids expelled from isolated reservoirs along the crust-mantle interface during the late stages of volcanic activity.A positive correlation between FeO and MgO in the early, most basic olivine-phyric basalts is interpreted to reflect progressive adiabatic partial melting in the upper mantle. Although this complicates the chemistry, it is not a significant factor in the compositional diversification of the volcanic suite. The preservation of such compositional melting effects, however, suggests that the most basic olivine-phyric basalts represent primitive magmas. The trace element characteristics of these magmas, and their derivatives, indicate that the mantle source for the Chukotat volcanics had experienced a previous melting event.     

Some trace element relationships among liquid and solid phases in the course of the fractional crystallization of magmas

The classical equations relating the trace element concentrations of the liquid and solid phases coexisting in the simple fractional crystallization of a parental magma have been put in a simple graphical form, which allows rapid analysis of the possible genetic relationships in a given rock suite. The effects of an incomplete separation between the two phases are taken into account. The approach does not require the use of otherwise estimated partition coefficients. Trace element data concerning the minerals of cumulates, where available, may provide an independent estimation of the effective mineral-liquid partition coefficients. With reasonable assumptions, this approach may even be applied to plutonic rocks. Interpretation of the published rare earth element data from the Southern California Batholith by this procedure suggests that a tonalitic parental magma could generate a granodioritic liquid by crystallizing 40–50 wt % of a solid residue of gabbroic composition, in agreement with Larsen's (Mem. Geol. Soc. Amer. 29, 1948) calculations. The calculated mineral-liquid partition coefficients for the REE fall in the range of published phenocryst-groundmass values for acidic volcanic rocks.     

(Trans)national Bodies, (Trans)national Languages and the Transformation of Local Urban Space

This paper discusses some of the ways that international students, particularly those from East Asia, are involved in the transformation of urban space in Auckland City. Using existing economic reports, local media accounts and the author's initial observations, the paper identifies how the embodied and linguistic practices of international students are involved in the changing landscapes of Auckland's inner city. This cursory reading serves to identify a research agenda and to reflect upon some key theoretical textxs. The insights of Arjun Appadurai, Michael Peter Smith and Ulrich Beck are used to suggest that the changes in Auckland, whilst certainly local, are also influenced fry factors that emerge from beyond the borders of international students' origin communities, cities and nations.     

Linking the Chassigny meteorite and the Martian surface rock Backstay: Insights into igneous crustal differentiation processes on Mars

Abstract— In order to use igneous surface lithologies to constrain Martian mantle characteristics, secondary processes that lead to compositional modification of primary mantle melts must be considered. Crystal fractionation of a mantle‐derived magma at the base of the crust followed by separation and ascent of residual liquids to the surface is common in continental hotspot regions on Earth. The possibility that this process also takes place on Mars was investigated by experimentally determining whether a surface rock, specifically the hawaiite Backstay analyzed by the MER Spirit could produce a known cumulate lithology with a deep origin (namely the assemblages of the Chassigny meteorite) if trapped at the base of the Martian crust. Both the major cumulus and melt inclusion mineral assemblages of the Chassigny meteorite were produced experimentally by a liquid of Backstay composition within the pressure range 9.3 to 6.8 kbar with bulk water contents between 1.5 and 2.6 wt%. Experiments at 4.3 and 2.8 kbar did not produce the requisite assemblages. This agreement suggests that just as on Earth, Martian mantle‐derived melts may rise to the surface or remain trapped at the base of the crust, fractionate, and lose their residual liquids. Efficient removal of these residual liquids at depth would yield a deep low‐silica cumulate layer for higher magmatic water content; at lower magmatic water content this cumulate layer would be basaltic with shergottitic affinity.     

A simple pore water hydrogen diffusion syringe sampler

Molecular hydrogen (H(2)) is an important intermediate product and electron donor in microbial metabolism. Concentrations of dissolved H(2) are often diagnostic of the predominant terminal electron-accepting processes in ground water systems or aquatic sediments. H(2) concentrations are routinely measured in ground water monitoring wells but are rarely measured in saturated aquatic sediments due to a lack of simple and practical sampling methods. This report describes the design and development (including laboratory and field testing) of a simple, syringe-based H(2) sampler in (1) saturated, riparian sediments, (2) surface water bed sediments, and (3) packed intervals of a fractured bedrock borehole that are inaccessible by standard pumped methods.     

Characterization of uranium-contaminated sediments from beneath a nuclear waste storage tank from Hanford, Washington: Implications for contaminant transport and fate

The concentration and distribution of uranium (U) in sediment samples from three boreholes recovered near radioactive waste storage tanks at Hanford, Washington, USA, were determined in detail using bulk and micro-analytical techniques. The source of contamination was a plume that contained an estimated 7000 kg of dissolved U that seeped into the subsurface as a result of an accident that occurred during filling of tank BX-102. The desorption character and kinetics of U were also determined by experiment in order to assess the mobility of U in the vadose zone. Most samples contained too little moisture to obtain quantitative information on pore water compositions. Concentrations of U (and contaminant phosphate—P) in pore waters were therefore estimated by performing 1:1 sediment-to-water extractions and the data indicated concentrations of these elements were above that of uncontaminated “background” sediments. Further extraction of U by 8 N nitric acid indicated that a significant fraction of the total U is relatively immobile and may be sequestered in mobilization-resistant phases. Fine- and coarse-grained samples in sharp contact with one another were sub-sampled for further scrutiny and identification of U reservoirs. Segregation of the samples into their constituent size fractions coupled with microwave-assisted digestion of bulk samples showed that most of the U contamination was sequestered within the fine-grained fraction. Isotope exchange (²³³U) tests revealed that ∼51% to 63% of the U is labile, indicating that the remaining fund of U is locked up in mobilization-resistant phases. Analysis by Micro-X-ray Fluorescence and Micro-X-ray Absorption Near-Edge Spectroscopy (μ-XRF and μ-XANES) showed that U is primarily associated with Ca and is predominately U(VI). The spectra obtained on U-enriched “hot spots” using Time-Resolved Laser-Induced Fluorescence Spectroscopy (TRLIFS) provide strong evidence for uranophane-type [Ca(UO₂)₂(SiO₃OH)₂(H₂O)₅] and uranyl phosphate [Ca(UO₂)₂(PO₄)₂(H₂O)_10-12] phases. These data show that disseminated micro-precipitates can form in narrow pore spaces within the finer-grained matrix and that these objects are likely not restricted to lithic fragment environments. Uranium mobility may therefore be curtailed by precipitation of uranyl silicate and phosphate phases, with additional possible influence exerted by capillary barriers. Consequently, equilibrium-based desorption models that predict the concentrations and mobility of U in the subsurface matrix at Hanford are unnecessarily conservative.     

The Meteoritical Bulletin,No. 111

Meteoritical Bulletin 111 contains the 3094 meteorites approved by the Nomenclature Committee of the Meteoritical Society in 2022. It includes 11 falls (Antonin, Botohilitano, Cranfield, Golden, Great Salt Lake, Longde, Msied, Ponggo, Qiquanhu, Tiglit, Traspena), with 2533 ordinary chondrites, 165 HED, 123 carbonaceous chondrites (including 4 ungrouped), 82 lunar meteorites, 28 Rumuruti chondrites, 27 iron meteorites, 23 ureilites, 22 mesosiderites, 22 Martian meteorites, 21 primitive achondrites (one ungrouped), 17 ungrouped achondrites, 13 pallasites, 7 enstatite achondrites, 6 enstatite chondrites, and 5 angrites. Of the meteorites classified in 2022, 1787 were from Antarctica, 1078 from Africa, 180 from South America, 34 from Asia, 6 from North America, 4 from Europe, and 1 from Oceania.