Ferric Iron in CaTiO3 Perovskite as an Oxygen Barometer for Kimberlitic Magmas I: Experimental Calibration

A method to estimate the oxygen fugacity (fO₂) during the crystallizationof kimberlites is developed using the Fe content of CaTiO₃ perovskite(Pv), a common groundmass phase in these rocks. With increasingfO₂, more Fe exists in the kimberlitic liquid as Fe³⁺, and thuspartitions into Pv. Experiments to study the partitioning ofFe between Pv and kimberlite liquid were conducted at 100 kPaon simple and complex anhydrous kimberlite bulk compositionsfrom 1130 to 1300°C over a range of fO₂ from NNO –5 to NNO + 4 (where NNO is the nickel–nickel oxide buffer),and at Nb and rare earth element (REE) contents in the startingmaterials of 0–5 wt % and 1500 ppm, respectively. Thepartitioning of Fe between Pv and kimberlite liquid is influencedmostly by fO₂, although the presence of Nb increases the partitionof Fe³⁺ into perovskite at a given T and fO₂. Multiple linearregression (MLR) of all the experimental data produces a relationshipthat describes the variation of Fe and Nb in Pv with fO₂ relativeto the NNO buffer:

(uncertaintiesat 2, and Nb and Fe as cations per three oxygens). Over therange of conditions of our experiments, this relationship showsno temperature (T) dependence, is not affected by the bulk Fecontent of the kimberlite starting material and reproduces experimentaldata to within 1 log fO₂ unit. KEY WORDS: kimberlites; oxygen fugacity; perovskite; ferric iron; magma     

Mildly incompatible elements in peridotites and the origins of mantle lithosphere

The abundances of the mildly incompatible elements Al, Cr, V, Sc and Yb in more than 1700 mantle peridotite bulk rock analyses are interpreted in the light of a fractional melting model based on experimentally measured partition coefficients (D) and melting reaction stoichiometries. All peridotites examined, irrespective of sample type (abyssal peridotites, orogenic massifs, ophiolites, on/off craton xenoliths), tectonic environment (divergent/convergent/passive margin, intraplate) or the pressure (P) they last equilibrated at in the mantle (plagioclase-, spinel- , or garnet facies), originated as residues at less than 3 GPa, mainly within the spinel-facies. Mantle rocks currently in the garnet facies likely were originally spinel-facies lithosphere underthrust or subducted to greater depths in convergent margins. This view is inescapable even within the widest range of D values employed in the calculations, and is furthermore strengthened when metasomatic effects on the abundances of the mildly incompatible elements in residues are considered. A pressure of origin of below 3 GPa for most mantle lithosphere creates difficulties for any model ascribing a significant volume of deep, cratonic mantle roots to plume sub-cretion or any other vertical tectonic mechanism.     

Aqueous alteration of kamacite in CM chondrites

Abstract– The study of aqueous alteration of kamacite in CM chondrites provides insight on the conditions, products, and relative timing of aqueous alteration. We studied unaltered, partially altered, and fully altered kamacite grains from Murray, Murchison, Cold Bokkeveld, and Nogoya using optical microscopy, electron microprobe analysis, scanning electron microscopy, and Raman spectroscopy. From textual evidence and chemical analysis, we established three separate microchemical environments. 1) In a microchemical environment with a high S activity, kamacite alters to form tochilinite, P‐bearing sulfides, eskolaite, and schreibersite. Mass balance calculations show that 81% of the Fe in kamacite is removed from the alteration region, making it available for the formation of other minerals or Fe‐rich aureoles. The release of Fe can alter the mesostasis of type‐I chondrules forming cronstedtite. 2) In a microchemical environment with a high Si activity and a low S activity, kamacite alters to form cronstedtite with small accessory sulfide inclusions. 3) A microchemical environment with limited S and Si activity results in kamacite alteration forming magnetite. The resulting magnetite retains associated Ni that can distinguish it from precipitated magnetite. In addition, the accessory phases of pentlandite and apatite can be formed if S or Ca are present. Finally, we note that small tochilinite grains in the matrix lack typical Ni, P, and Co levels, suggesting that they did not form from kamacite but possibly by sulfidization of magnetite.     

Can the Intermediate Western Boundary Current recirculation trigger the Vitória Eddy formation?

Ocean Dynamics - South of the Vitória-Trindade Ridge, a seamount chain off East Brazil, the Brazil Current (BC) meanders cyclonically within Tubarão Bight, occasionally forming the...     

Iron in monticellite as an oxygen barometer for kimberlite magmas

Monticellite is a common magmatic mineral in the groundmass of kimberlites. A new oxygen barometer for kimberlite magmas is calibrated based on the Fe content of monticellite, CaMgSiO₄, in equilibrium with kimberlite liquids in experiments at 100 kPa from 1,230 to 1,350°C and at logfO₂ from NNO-4.1 to NNO+5.3 (where NNO is the nickel–nickel oxide buffer). The XFe_Mtc/XFe_liq was found to decrease with increasing fO₂, consistent with only Fe²⁺ entering the monticellite structure. Although the XFe-in-monticellite varies with temperature and composition, these dependencies are small compared to that with fO₂. The experimental data were fitted by weighted least square regression to the following relationship: \Updelta \textNNO = \frac{ log[ 0.858( ±0.021)\fracX_\textFe^\textLiq X_\textFe^\textMtc ] - 0.139( ±0.022) }0.193( ±0.004) \Updelta {\text{NNO}} = \frac{{\left\{ {\log \left[ {0.858( \pm 0.021)\frac{{X_{\text{Fe}}^{\text{Liq}} }}{{X_{\text{Fe}}^{\text{Mtc}} }}} \right] - 0.139( \pm 0.022)} \right\}}}{0.193( \pm 0.004)} where ΔNNO is the fO₂ relative to that of the Nickel-bunsenite (NNO) buffer and XFe_liq/XFe_Mtc is the ratio of mole fraction of Fe in liquid and Fe-in-monticellite (uncertainties at 2σ). The application of this oxygen barometer to natural kimberlites from both the literature and our own investigations, assuming the bulk rock FeO is that of their liquid FeO, revealed a range in fO₂ from NNO-3.5 to NNO+1.7. A range of Mg/(Mg + Fe²⁺) (Mg#) for kimberlite melts of 0.46–0.88 was derived from the application of the experimentally determined monticellite-liquid Kd Fe²⁺–Mg to natural monticellites. The range in Mg# is broader and less ultramafic than previous estimates of kimberlites, suggesting an evolution under a wide range of petrologic conditions.     

Constraints on the merger models of elliptical galaxies from their globular cluster systems

The discovery of protoglobular cluster candidates in many present-day mergers allows us to understand better the possible effects of a merger event on the globular cluster system of a galaxy, and to foresee the properties of the end-product. By comparing these expectations with the properties of globular cluster systems of elliptical galaxies at the present time we can constrain merger models. The observational data indicate that (i) every gaseous merger induces the formation of new star clusters, and (ii) the number of new clusters formed in such a merger increases with the gas content of the progenitor galaxies. Low-luminosity (about M _V  > −21), discy ellipticals are generally thought to be the result of a gaseous merger. As such, new globular clusters are expected to form but have not been detected to date. We investigate various reasons for the non-detection of subpopulations in low-luminosity ellipticals, i.e. absence of an old population, absence of a new population, destruction of one of the populations and, finally, an age–metallicity conspiracy that allows old and new globular clusters to appear indistinguishable at the present epoch. All of these possibilities lead us to a similar conclusion, namely that low-luminosity ellipticals did not form recently ( z  < 1) in a gas-rich merger, and might not have formed in a major merger of stellar systems at all. High-luminosity ellipticals do reveal globular cluster subpopulations. However, it is difficult to account for the two populations in terms of mergers alone and, in particular, we can rule out scenarios in which the second subpopulation is the product of a recent, gas-poor merger.     

Wave-Based Techniques for Evaluating Elastic Modulus and Poisson’s Ratio of Laboratory Compacted Lateritic Soils

A rapid, low-cost evaluation methodology using the wave-based techniques is proposed in this study in order to determine the design parameters e.g., elastic modulus and Poisson’s ratio of the laboratory compacted lateritic soils. Knowing the elastic wave velocities as measured with the wave propagation technique (i.e., a small-strain non-destructive test) and total mass density of the specimens, the elastic moduli and Poisson’s ratio of the soil specimens can be determined. In addition, the unconfined compression test (i.e., a large-strain destructive test) is also performed on the same specimens under the same unconfined testing condition in order to compare the moduli corresponding to different strain levels. The experimental results showed the potentials and limitations of using impulse signal for the determination of the elastic moduli and Poisson’s ratio for laboratory compacted soil specimens from elastic wave propagation techniques.