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At least 55 records · Page 3

Comparison of Synthetic and Natural Nakhlite Pyroxenes: Complexity of Minor Elements

Zoning in pyroxenes in martian meteorites contains a rich record of the petrogenesis of these samples. In the clinopyroxene cumulate nakhlite group, major element zoning is generally limited to the outer rims of the pyroxenes. However, minor element zoning, especially of Al, Ti, and Cr, is extensive, complex, and difficult to interpret [e.g., 1-3]. To help mine the rich information about petrogenetic processes from these samples, we have been comparing minor element zoning in synthetic pyroxenes grown under known conditions with zoning observed in natural nakhlite pyroxenes. We have focused on two nakhlites, MIL03346 (MIL), which is one of the most rapidly cooled nakhlites, and Y000593 (Y593), which cooled at a more moderate rate [e.g., 4].

McKay, G.↗

Characterization of crust formation on a parent body of achondrites and the moon by pyroxene crystallography and chemistry

Single crystal X-ray diffraction and electron microprobe techniques were used to study lunar crustal pyroxenes in a cataclastic norite, a pyroxene-rich clast, and anorthosite lunar samples, and also in meteorites including diogenites, eucrites, and the Yamoto (1) howardite. The crystallographic and chemical characteristics of pyroxenes in these materials are compared and are discussed in terms of the lower stability limit of pigeonite. A mechanical mixing model of howardite is proposed.

Takeda, H.↗

Pyroxenes in Serra de Mage - Cooling history in comparison with Moama and Moore County

Thin sections and single grains of pyroxenes from the Serra de Mage feldspar cumulate eucrites were studied by X-ray crystallography, electron microprobe and optical techniques. It was concluded that the pyroxene crystallized as pigeonite. On cooling augite was exsolved along (001) and inverted to hypersthene, with exsolution of (100) augite from hypersthene during continued slow cooling. The estimated original bulk composition of the pigeonite pyroxene is Wo10En51Fs39. The compositional data, textural relations, and existence of P2 sub 1 ca hypersthene suggest very low cooling (about 0.0004 deg C/year) below 800 deg. The Serra de Mage augite lamellae were found to be as thick or thicker than those of Moore County and Moama meteorites.

Harlow, G. E.↗

Effects of compositional variation on absorption spectra of lunar pyroxenes

Polarized absorption spectra of lunar pyroxenes with a range of iron, calcium, magnesium, titanium and chromium contents were measured on polished, oriented single crystals; spectral data on pure synthetic FeSiO3 were also recorded. The bands at 1 and 2 microns were found to vary significantly in position with composition within the pyroxene quadrilateral; wavelengths increased with increasing calcium and iron. In the visible region, a weak band at 640 nm correlates in intensity with Cr2O3, but not with titanium as had been previously suggested. The 505-nm ferrous iron peak is a sharp doublet in most low-calcium pyroxenes but a singlet in augites. A peak at 475 nm and an intense absorption edge below 700 nm correlated with titanium content.

Hazen, R. M.↗

Clouding of pyroxene and plagioclase in eucrites - Implications for post-crystallization processing

The clouding of pyroxene and plagioclase in the basaltic eucrites ALHA 77302, Juvinas, Pasamonte, and Stannern, is caused by finely disseminated inclusions. This clouding is interpreted to be the result of exsolution of minor components which became incompatible and crystallized on microfractures and other nucleation sites during postbrecciation metamorphism. The phases found in clouding require reduction of silicate FeO to metallic Fe in both pyroxene and plagioclase and possible redox of Cr(2+) to Cr(3+) in pyroxene. The assemblage of coexisting phases that make up clouding record conditions of T approximately equal to 900 C and f(O2) of 10 to the -16th to 10 to the -18th during slow cooling. Thus, clouding can be a useful indicator of postcrystallization conditions.

Harlow, G. E.↗

Charge balancing of trivalent trace elements in olivine and low-Ca pyroxene - A test using experimental partitioning data

Charge-balancing substitution mechanisms are determined for the incorporation of the trivalent cations Al and Sc in low-Ca pyroxene and Al, Sc, Yb, and Cr in olivine. In low-Ca pyroxene, the substitution mechanism is determined by evaluating covariations of trivalent trace cations with Si, Mg, Fe, and Ca. In olivine, substitution mechanisms are determined by comparing the observed compositional dependence of partitioning to the compositional dependence theoretically expected for each substitution reaction. A realistic equilibrium constant is formulated for trace element exchanges between olivines, low-Ca pyroxenes, and melt, making possible improved modeling of the variations of trace element partitioning with temperature and phase composition.

Colson, R. O.↗

Near-Earth and near-Mars asteroids: Prognosis of pyroxene types

The diagnostic signs of ferrous absorption band at 505nm and color index (u-x) found at main-belt asteroids and 6-parametric classification of light stone meteorites have been the basis of the work. The colorimetric data of light near-Earth and near-Mars asteroids from TRIAD and ECAS were analyzed. Composition fields of pyroxenes were obtained for these asteroids by the value of (u-x) and 505-nm ferrous absorption band position within the pyroxenes quadrilateral. Pyroxenes of the S-asteroids from Apollo-Amor which have spectral parameters similar to achondrites may be presented by the diopside series.

Shestopalov, D. I.↗

Petrogenesis of the Zagami meteorite - Inferences from synchrotron X-ray (SXRF) microprobe and electron microprobe analyses of pyroxenes

Major and minor element abundances in pyroxene, principally pigeonite, from Zagami meteorite samples were determined by electron microprobe; abundances of trace elements Ni, Cu, Zn, and Ga were obtained by synchrotron X-ray (SXRF) microprobe. Abundances of Ni and Cr in the magnesian zones and cores are partially decoupled from abundances of other compatible (Mg) and incompatible (Fe,Ti) elements. The textures, chemical zoning, and element decouplings in the pigeonites are consistent with igneous crystal growth at moderate cooling rates, not isothermally or near equilibrium. From element partitioning and mass balance, Zagami is estimated to contain 20 +/- 5 percent or less cumulus pyroxene (half augite and half pigeonite), half the proportion suggested by equilibrium distribution of Fe/Mg between pigeonite and melt. This inconsistency may be resolved if all pigeonite/melt element partitioning was affected by the rapid growth of the pigeonites. The inference that the pyroxene zoning patterns reflect only magmatic events is consistent with an igneous age of 180 m.y. for Zagami.

Treiman, A. H.↗

Synthetic and natural Nakhla pyroxenes: Parent melt composition and REE partition coefficients

Nakhla is one of the SNC meteorites, generally believed to be of martian origin. It is composed mainly of cumulus augite, in which primary igneous zoning is apparently preserved, and which serves as a recorder of the composition of Nakhla's parent melt and the conditions under which it crystallized. Knowledge of the composition and petrogenesis of this parent melt may help unravel Nakhla's relationship to the other SNC's, and provide clues to martian petrogenesis in general. This abstract reports new results of an ongoing study in which we are (1) comparing the major and minor element compositions of synthetic pyroxenes crystallized from various proposed parent melt compositions with those in Nakhla pyroxene to constrain the composition of the parent melt, and (2) measuring minor and trace element partition coefficients, particularly those of the REE, in order to obtain the most applicable D values with which to invert the natural pyroxene compositions to obtain the trace element composition of the parent melt. Results suggest that recent estimates of Nakhla's parent melt composition are too aluminous, and that mafic or ultramafic melts are more likely candidates.

Mckay, G.↗

Trace Elements in High-Ca Pyroxene and Plagioclase in the Bilanga Diogenite: Implications for the Magmatic Evolution of Diogenites

High-Ca pyroxene and plagioclase are typically present as minor phases in diogenites. However, although the trace element content of diogenite orthopyroxene has been measured in a number of studies; almost no trace element data is available for the high-Ca pyroxene and plagioclase with which it routinely coexists in these meteorites. These data could provide insights into the nature and evolution of the melts from which diogenites crystallized in the HED parent body. In this study we have obtained initial measurements of several REEs in high-Ca pyroxene, plagioclase, and orthopyroxene in the Bilanga. Measurement of additional incompatible trace element concentrations in these phases is currently in progress.

Domanik, K. J.↗

Comparative Planetary Mineralogy: Valence State Partitioning of Cr, Fe, Ti, and V Among Crystallographic Sites in Olivine, Pyroxene, and Spinel from Planetary Basalts

We have considered the valence-state partitioning of Cr, Fe, Ti, and V over crystallographic sites in olivine, pyroxene, and spinel from planetary basalts. The sites that accommodate these cations are the M2 site (6-8 coordinated) and M1 site (6 coordinated) in pyroxene, the M2 site (6-8 coordinated) and M1 site (6 coordinated) in olivine, and the tetrahedral and octahedral sites in spinel. The samples we studied are basalts from Earth, Moon, and Mars, which have fO2 conditions that range from IW-2 (Moon) to IW+6 (Earth) with Mars somewhere between at IW to IW+2. In this range of fO2 the significant elemental valences are (from low to high fO2) Ti4+, V3+, Fe2+, Cr2+, Cr3+, V3+, V4+, and Fe3+. V2+ and Ti3+ play a minor role in the phases considered for the Moon, and are probably in very low concentrations. V5+ plays a minor role in these phases in terrestrial basalts because it is probably in lower abundance than V4+ and it has an ionic radii that is so small (0.054 nm, 6- coordinated,[1]) that it is almost at the lower limit for octahedral coordination. The role of Cr2+ in the Moon is significant, as Sutton et al. [2] found that lunar olivine contains mostly Cr2+ while coexisting pyroxene contains mostly Cr3+. Hanson one vacancy only accommodates one V4+. Thus more vacancies are required in V4+ substitutions into olivine. In the Moon V3+ is much more abundant than V4+ [7, 8]. Thus in lunar chromite V3+ follows Cr3+, whereas in Earth V4+ (which is much greater in abundance than V3+) follows Ti4+ (eg in ulv spinel). We could go on in this vein for some time but space limitations do not permit us to do so.

Papike, J. J.↗

Silica and Pyroxene in IVA Irons; Possible Formation of the IVA Magma by Impact Melting and Reduction of L-LL-Chondrite Materials Followed by Crystallization and Cooling

Group IVA is a large magmatic group of iron meteorites. The mean DELTA O-17 (= delta O-17 - 0.52(raised dot) delta O-18) of the silicates is approx. plus or minus 1.2%o, similar to the highest values in L chondrites and the lowest values in LL chondrites; delta O-18 values are also in the L/LL range. This strongly suggests that IVA irons formed by melting L-LL parental material, but the mean Ni content of IVA irons (83 mg/g) is much lower than that of a presumed L-LL parent (approx. 170 mg/g) and the low-Ca pyroxene present in two IVA meteorites is Fs13, much lower than the Fs20-29 values in L and LL chondrites. Thus, formation from L-LL precursors requires extensive addition of metallic Fe, probably produced by reduction of FeS and FeO. Group IVA also has S/Ni, Ga/Ni, and Ge/Ni ratios that are much lower than those in L-LL chondrites or any chondrite group that preserves nebular compositions, implying loss of these volatile elements during asteroidal processing. We suggest that these reduction and loss processes occurred near the surface of the asteroid during impact heating, and resulted partly from reduction by C, and partly from the thermal dissociation of FeS and FeO with loss of O and S. The hot (approx. 1770 K) low-viscosity melt quickly moved through channels in the porous asteroid to form a core. Two members of the IVA group, Sao Joao Nepomuceno (hereafter, SJN) and Steinbach, contain moderate amounts of orthopyroxene and silica, and minor amounts of low-Ca clinopyroxene. Even though SJN formed after approx. 26% crystallization and Steinbach formed after approx. 77% Crystallization of the IVA core, both could have originated within several tens of meters of the core-mantle interface if 99% of the crystallization occurred from the center outwards. Two other members of the group (Gibeon and Bishop Canyon) contain tabular tridymite, which we infer to have initially formed as veins deposited from a cooling SiO-rich vapor. The silicates were clearly introduced into IVA irons after the initial magma crystallized. Because the y-iron crystals in SJN are typically about 5 cm across, an order of magnitude smaller than in IVA irons that do not contain massive silicates, we infer that the metal was in the gamma-iron field when the silicates were injected. The SJN and Steinbach silicate compositions are near the low-Ca-pyroxene/silica eutectic compositions. We suggest that a tectonic event produced a eutectic-like liquid and injected it together with unmelted pyroxene grains into fissures in the solid metal core. Published estimates of IVA metallographic cooling rates range from 20 to 3000 K/Ma, leading to a hypothesized breakup of the core during a major impact followed by scrambling of the core and mantle debris [Haack, H., Scott, E.R.D., Love, S.G., Brearley, A. 1996. Thermal histories of IVA stony-iron and iron meteorites: evidence for asteroid fragmentation and reaccretion. Geochim. Cosmochim. Acta 60, 3103-3113]. This scrambling model is physically implausible and cannot explain the strong correlation of estimated cooling rates with metal composition. Previous workers concluded that the low-Ca clinopyroxene in SJN and Steinbach formed from protopyroxene by quenching at a cooling rate of 10(sup 12) K/Ma, and suggested that this also supported an impact-scrambling model. This implausible spike in cooling rate by a factor of 10(sup 10) can be avoided if the low-Ca clinopyroxene were formed by a late shock event that converted orthopyroxene to clinopyroxene followed by minimal growth in the clinopyroxene field, probably because melt was also produced. We suggest that metallographic cooling-rate estimates (e.g., based on island taenite) giving similar values throughout the metal compositional range are more plausible, and that the IVA parent asteroid can be modeled by monotonic cooling followed by a high-temperature impact event that introduced silicates into the metal and a low-temperature impact event that partially converted thopyroxene into low-Ca clinopyroxene.

Wasson, John T.↗

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.

Karner, J. M.↗

Metasomatic Control of Water in Garnet and Pyroxene from Kaapvaal Craton Mantle Xenoliths

Fourier transform infrared spectrometry (FTIR) and laser ablation inductively coupled plasma mass spectrometry (LA-ICPMS) were used to determine water, rare earth (REE), lithophile (LILE), and high field strength (HFSE) element contents in garnet and pyroxene from mantle xenoliths, Kaapvaal craton, southern Africa. Water enters these nominally anhydrous minerals as protons bonded to structural oxygen in lattice defects. Pyroxene water contents (150-400 ppm in clinopyroxene; 40-250 ppm in orthopyroxene) correlate with their Al, Fe, Ca and Na and are homogeneous within a mineral grains and a xenolith. Garnets from Jagersfontein are chemically zoned for Cr, Ca, Ti and water contents. Garnets contain 0 to 20 ppm H2 Despite the fast diffusion rate of H in mantle m inerals, the observations above indicate that the water contents of mantle xenolith minerals were not disturbed during kimberlite entrainment and that the measured water data represent mantle values. Trace elements in all minerals show various degrees of light REE and LILE enrichments indicative of minimal to strong metasomatism. Water contents of peridotite minerals from the Kaapvaal lithosphere are not related to the degree of depletion of the peridotites. Instead, metasomatism exerts a clear control on the amount of water of mantle minerals. Xenoliths from each location record specific types of metasomatism with different outcomes for the water contents of mantle minerals. At pressures . 5.5 GPa, highly alkaline melts metasomatized Liqhobong and Kimberley peridotites, and increased the water contents of their olivine, pyroxenes and garnet. At higher pressures, the circulation of ultramafic melts reacting with peridotite resulted in co-variation of Ca, Ti and water at the edge of garnets at Jagersfontein, overall decreasing their water content, and lowered the water content of olivines at Finsch Mine. The calculated water content of these melts varies depending on whether the water content of the peridotite (2 wt% HO. 2O) or individual m inerals (<0.5-13 wt% H2O) are used, and also depend on the mineral-melt water partition coefficients. These metasomatic events are thought to have occurred during the Archean and Proterozoic, meaning that the water contents measured here have been preserved since that time and can be used to investigate viscocity and longevity of cratonic mantle roots.

Peslier, Anne H.↗

Pristine Pyroxene-Bearing Boulders Analyzed By Supercam in the Jezero Western Fan, Mars

During its exploration of the upper surface of the Jezero western fan, the Mars 2020 Perseverance rover encountered a population of boulders that likely represents a late-stage deposit from high-energy floods. These boulders can be divided into two groups based on their inferred mineralogy: olivine-rich and pyroxene-bearing. The first group, the most abundant one, is described in ref.[2]. Here, we present the analyses performed by the SuperCam instrument on the pyroxene-bearing boulders and show that they are among the most pristine rocks encountered so far in the mission. We also draw a comparison with the Boston Knob outcrop, located on the fan front, which may be a buried and stratigraphically lower equivalent of the pyroxene-bearing boulders of the upper fan.

Mars 2020↗

Minor and trace element distribution in melilite and pyroxene from the Allende meteorite

Melilite and pyroxene were separated from a coarsely crystalline chondrule in the Allende meteorite and analyzed by microprobe and spark source mass spectrometer techniques. Elemental abundances in the bulk chondrule are consistent with a mixture of equal amounts of the two minerals, as observed microscopically. The lanthanide distributions are markedly different in the two minerals; relative to chondrite abundances, melilite shows progressive depletion of the lanthanides La-Sm, a positive Eu anomaly, and relatively constant abundances of the heavier lanthanides (Gd-Yb, and Y) whereas pyroxene shows progressive enrichment towards the heavier lanthanides, on which is superimposed a negative Eu anomaly. Both minerals, and the bulk chondrule, show unusual concentrations of the platinum metals, but the crystallographic site or sites of these metals remains to be determined.

Mason, B.↗

Pyroxenes in the Patwar mesosiderite

Major and minor elements were determined with an electron microprobe in pyroxene from Patwar, one of the least metamorphosed mesosiderites. All but two orthopyroxene crystal fragments fall in the range Wo(2.3)En(73) to Wo(3.9)En(59), while pigeonite from a basalt clast clusters around Wo(13)En(38). Absolute and relative amounts of Ti, Cr, and Al are distinct from those in pyroxenes in irons-with-silicate inclusions. Zoning within orthopyroxene grains suggests crystallization from an igneous melt in the presence of plagioclase and chromite, followed at some later time by brecciation and subsequent minor thermal metamorphism. Compositional data support petrographic evidence that the silicates in Patwar were derived from a heterogeneous source.

Weigand, P. W.↗