Complex zoning behavior in pyroxene in FeO-rich chondrules in the Semarkona ordinary chondrite

A detailed understanding of the properties of silicate minerals in chondrules is essential to the interpretation of chondrule formation conditions. This study is further work in a series of petrologic studies of chondrules in the least equilibrated LL chondrite, Semarkona (LL3.0). The objectives of this work are as follows: (1) to understand chondrule formation conditions and nebular processes; and (2) to use the data as a basis for understanding the effects of metamorphism in more equilibrated chondrites. FeO-rich pyroxene in the chondrules described shows complex zoning behavior. Low-Ca clinopyroxene, orthopyroxene, pigeonite, and augite are all observed, in various associations with one another. Coexisting olivine phenocrysts are also FeO-rich and strongly zoned. Compositional and zoning properties are similar to those observed in boninites and are interpreted as resulting from rapid cooling of individual chondrules

Oxygen Fugacity of the Upper Mantle of Mars. Evidence from the Partitioning Behavior of Vanadium in Y980459 (Y98) and other Olivine-Phyric Shergottites

Using partitioning behavior of V between olivine and basaltic liquid precisely calibrated for martian basalts, we determined the redox state of primitive (olivine-rich, high Mg#) martian basalts near their liquidus. The combination of oxidation state and incompatible element characteristics determined from early olivine indicates that correlations between fO2 and other geochemical characteristics observed in many martian basalts is also a fundamental characteristic of these primitive magmas. However, our data does not exhibit the range of fO2 observed in these previous studies.. We conclude that the fO2 for the martian upper mantle is approximately IW+1 and is incompatible-element depleted. It seems most likely (although clearly open to interpretation) that these mantle-derived magmas assimilated a more oxidizing (>IW+3), incompatible-element enriched, lower crustal component as they ponded at the base of the martian crust

Workshop on Evolution of Igneous Asteroids: Focus on Vesta and the HED Meteorites

This volume contains abstracts of papers that have been accepted for presentation at the Workshop on Evolution of Igneous Asteroids: Focus on Vesta and the HED Meteorites, October 16-18, 1996, in Houston, Texas

Valence State Partitioning of Cr and V Between Pyroxene - Melt: Estimates of Oxygen Fugacity for Martian Basalt QUE 94201

Several studies, using different oxybarometers, have suggested that the variation of fO2 in martian basalts spans about 3 log units from approx. IW-1 to IW+2. The relatively oxidized basalts (e.g., pyroxene-phyric Shergotty) are enriched in incompatible elements, while the relatively reduced basalts (e.g., olivine-phyric Y980459) are depleted in incompatible elements. A popular interpretation of the above observations is that the martian mantle contains two reservoirs; 1) oxidized and enriched, and 2) reduced and depleted. The basalts are thus thought to represent mixing between these two reservoirs. Recently, Shearer et al. determined the fO2 of primitive olivine-phyric basalt Y980459 to be IW+0.9 using the partitioning of V between olivine and melt. In applying this technique to other basalts, Shearer et al. concluded that the martian mantle shergottite source was depleted and varied only slightly in fO2 (IW to IW+1). Thus the more oxidized, enriched basalts had assimilated a crustal component on their path to the martian surface. In this study we attempt to address the above debate on martian mantle fO2 using the partitioning of Cr and V into pyroxene in pyroxene-phyric basalt QUE 94201

Geomagnetic paleointensity in historical pyroclastic density currents: Testing the effects of emplacement temperature and postemplacement alteration

Thellier-type paleointensity experiments were conducted on welded ash matrix or pumice from the 1912 Novarupta (NV) and 1980 Mt. St. Helens (MSH) pyroclastic density currents (PDCs) with the intention of evaluating their suitability for geomagnetic paleointensity studies. PDCs are common worldwide, but can have complicated thermal and alteration histories. We attempt to address the role that emplacement temperature and postemplacement hydrothermal alteration may play in nonideal paleointensity behavior of PDCs. Results demonstrate two types of nonideal behavior: unstable remanence in multidomain (MD) titanomagnetite, and nonideal behavior linked to fumarolic and vapor phase alteration. Emplacement temperature indirectly influences MSH results by controlling the fraction of homogenous MD versus oxyexsolved pseudo-single domain titanomagnetite. NV samples are more directly influenced by vapor phase alteration. The majority of NV samples show distinct two-slope behavior in the natural remanent magnetization—partial thermal remanent magnetization plots. We interpret this to arise from a (thermo)chemical remanent magnetization associated with vapor phase alteration, and samples with high water content (\u3e0.75% loss on ignition) generate paleointensities that deviate most strongly from the true value. We find that PDCs can be productively used for paleointensity, but that—as with all paleointensity studies—care should be taken in identifying potential postemplacement alteration below the Curie temperature, and that large, welded flows may be more alteration-prone. One advantage in using PDCs is that they typically have greater areal (spatial) exposure than a basalt flow, allowing for more extensive sampling and better assessment of errors and uncertainty

A New Spinel-Olivine Oxybarometer: Near-Liquidus Partitioning of V between Olivine-Melt, Spinel-Melt, and Spinel-Olivine in Martian Basalt Composition Y980459 as a Function of Oxygen Fugacity

Our research on valence state partitioning began in 2005 with a review of Cr, Fe, Ti, and V partitioning among crystallographic sites in olivine, pyroxene, and spinel [1]. That paper was followed by several on QUE94201 melt composition and specifically on Cr, V, and Eu partitioning between pyroxene and melt [2-5]. This paper represents the continuation of our examination of the partitioning of multivalent V between olivine, spinel, and melt in martian olivine-phyric basalts of Y980459 composition [6, 7]. Here we introduce a new, potentially powerful oxybarometer, V partitioning between spinel and olivine, which can be used when no melt is preserved in the meteorite. The bulk composition of QUE94201 was ideal for our study of martian pyroxene-phyric basalts and specifically the partitioning between pyroxene-melt for Cr, V, and Eu. Likewise, bulk composition Y980459 is ideal for the study of martian olivine-phyric basalts and specifically for olivine-melt, spinel-melt, and spinel-olivine partitioning of V as a function of oxygen fugacity

An unusual clast in lunar meteorite MacAlpine Hills 88105: a unique lunar sample or projectile debris?

Lunar meteorite MacAlpine Hills (MAC) 88105 is a well-studied feldspathic regolith breccia dominated by rock and mineral fragments from the lunar highlands. Thin section MAC 88105,159 contains a small rock fragment, 400 × 350 μm in size, which is compositionally anomalous compared with other MAC 88105 lithic components. The clast is composed of olivine and plagioclase with minor pyroxene and interstitial devitrified glass component. It is magnesian, akin to samples in the lunar High Mg-Suite, and also alkali-rich, akin to samples in the lunar High Alkali Suite. It could represent a small fragment of late-stage interstitial melt from an Mg-Suite parent lithology. However, olivine and pyroxene in the clast have Fe/Mn ratios and minor element concentrations that are different from known types of lunar lithologies. As Fe/Mn ratios are notably indicative of planetary origin, the clast could either (1) have a unique lunar magmatic source, or (2) have a nonlunar origin (i.e., consist of achondritic meteorite debris that survived delivery to the lunar surface). Both hypotheses are considered and discussed

Chromium Oxidation State in Planetary Basalts: Oxygen Fugacity Indicator and Critical Variable for Cr-Spinel Stability

Cr is a ubiquitous and relatively abundant minor element in basaltic, planetary magmas. At the reduced oxidation states (<FMQ) of many planetary basalts Cr is present in melts as both divalent and trivalent forms. The ratio of trivalent to divalent Cr present in the melt has many consequences for the stability and Cr concentration of magmatic phases such as spinel, clinopyroxene, and olivine. However, understanding the Cr valence in quenched melts has historically been plagued with analytical issues, and only recently has reliable methodology for quantifying Cr valence in quenched melts been developed. Despite this substantial difficulty, the pioneering works of Hanson and Jones and Berry and O'Neill provided important insights into the oxidation state of Cr in in silicate melts. Here we present a series of 1-bar gas mixing experiments performed with a Fe-rich basaltic melt in which have determined the Cr redox ratio of the melt at over a range of fO2 values by measuring this quantity in olivine with X-ray Absorption Near Edge Spectroscopy (XANES). The measured Cr redox ratio of the olivine phenocrysts can be readily converted to the ratio present in the conjugate melt via the ratio of crystal-liquid partition coefficients for Cr3+ and Cr2+. We have applied these results to modeling Cr spinel stability and Cr redox ratios in a primitive, iron-rich martian basalt

Valence State Partitioning of V between Pyroxene and Melt for Martian Melt Compositions Y 980459 and QUE 94201: The Effect of Pyroxene Composition and Crystal Structure

A spiked (with REE, V, Sc) martian basalt Y980459 composition was used to synthesize olivine, spinel, and pyroxene at 1200 C at 5 oxygen fugacities: IW-1, IW, IW+1, IW+2, and QFM. The high spike levels for REE were used for two specific reasons. First, we wanted to be able to analyze REE by both electron microprobe and ion probe. Second, we wanted the most important "Others" components, (i.e., those outside the pyroxene quadrilateral such as Al, Cr3+, Fe3+, REE3+, V3+, V4+, etc.) to be REE3+Mg (Si,Al)2O6. At the doped levels we used, the most important "Others" component is REE3+ in the M2 site coupled with Al in the tetrahedral site. The goal of this paper is to explain the significant increase in the value of D(sub V)(sup pyroxene/melt) with increased Wo content of the pyroxene. We compare augite (Wo approx. 33), pigeonite (Wo approx. 13) and orthopyroxene (Wo approx 3.8). We also show olivine for comparison. The crystal chemical factors which account for this remarkable increase of DV with Wo are twofold. First, with Ca in the M2 site (as in diopside, CaMgSi2O6) the site is large and 8-coordinated while Mg in the M2 site (as in enstatite, Mg2Si2O6) the site is smaller and 6- coordinated. Second, tetrahedral Al in the pyroxene chains provides charge balance and makes the M2 site larger and more compliant for the introduction of REE

The Mineralogy, Geochemistry, and Redox State of Multivalent Cations During the Crystallization of Primitive Shergottitic Liquids at Various (f)O2. Insights into the (f)O2 Fugacity of the Martian Mantle and Crustal Influences on Redox Conditions of Martian Magmas.

The (f)O2 [oxygen fugacity] of crystallization for martian basalts has been estimated in various studies to range from IW-1 to QFM+4 [1-3]. A striking geochemical feature of the shergottites is the large range in initial Sr isotopic ratios and initial epsilon(sup Nd) values. Studies by observed that within the shergottite group the (f)O2 [oxygen fugacity] of crystallization is highly correlated with these chemical and isotopic characteristics with depleted shergottites generally crystallizing at reduced conditions and enriched shergottites crystallizing under more oxidizing conditions. More recent work has shown that (f)O2 [oxygen fugacity] changed during the crystallization of these magmas from one order of magnitude in Y980459 (Y98) to several orders of magnitude in Larkman Nunatak 06319. These real or apparent variations within single shergottitic magmas have been attributed to mixing of a xenocrystic olivine component, volatile loss-water disassociation, auto-oxidation during crystallization of mafic phases, and assimilation of an oxidizing crustal component (e.g. sulfate). In contrast to the shergottites, augite basalts such as NWA 8159 are highly depleted yet appear to be highly oxidized (e.g. QFM+4). As a first step in attempting to unravel petrologic complexities that influence (f)O2 [oxygen fugacity] in martian magmas, this study explores the effect of (f)O2 [oxygen fugacity] on the liquid line of descent (LLD) for a primitive shergottite liquid composition (Y98). The results of this study will provide a fundamental basis for reconstructing the record of (f)O2 [oxygen fugacity] in shergottites and other martian basalts, its effect on both mineral chemistries and valence state partitioning, and a means for examining the role of crystallization (and other more complex processes) on the petrologic linkages between olivine-phyric and pyroxene-plagioclase shergottites