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Le, L.

Publications and source records attributed to Le, L..

At least 73 records · Page 4

Calibration of the EU Oxybarometer for Nakhlites

Martian meteorites have various characteristics, which are direct clues to understanding the petrogenesis of Mars rocks. The variation in oxidation state among the Martian meteorites must have important implications for redox conditions of the Martian crust/mantle and overall differentiation on Mars. Wadhwa [1] and Herd et al. [2] reported that Martian basalts were formed under a range of oxidation states, suggesting complex petrogenesis processes. The nakhlites, which have rather different characteristics from basaltic shergottites, may give us additional clues to Martian petrogenesis. The oxidation states of meteorites are usually described by the oxygen fugacity (fO2) under which the meteorites crystallized. One of the methods to estimate the oxygen fugacity is the depth of Eu anomaly. Eu(2+)/Eu(3+) is determined by the oxygen fugacity and partitioning is different for Eu(2+) and Eu(3+). Therefore, the depth of Eu anomaly in a mineral is a function of the oxygen fugacity and the Eu2+/Eu3+ in the melt from which the mineral crystallized. This method has some advantages over another major method, the two-oxide oxybarometer [3], which can more easily be affected by subsolidus processes. The Eu oxybarometer can analyze the cores of the earliest formed crystals in Martian meteorites, which means it can give us a better indication of the oxygen fugacity of the parent melt. The calibration of the Eu oxybarometer has been done with the basaltic shergottites before [4]. However, it has never been applied to nakhlites (Oe et al. [5] measured the depth of Eu anomaly in the synthetic pyroxene only at QFM). Partition coefficients are strongly affected by phase compositions, especially pyroxene Ca content and melt Al content [e.g., 5,6]. The composition of nakhlite pyroxene is rather different from basaltic shergottite pyroxene. Thus, there may be problems in applying the Eu oxybarometer calibration for the basaltic shergottites [7] to nakhlites. Thus, we report in this abstract preliminary results of our experimental calibration of the depth of Eu anomaly in pyroxene vs. oxygen fugacity for nakhlites.

Makishima, J.↗

Pyroxenes in Martian meteorites as petrogenetic indicators

Pyroxenes in Martian meteorites are important recorders of petrogenetic processes. Understanding the details of pyroxene major and minor element compositional variations can provide important insights into those processes. A combination of careful petrographic analysis of natural samples and experimental crystallization studies can lead to better understanding of the processes that gave rise to these samples on Mars. In addition, experimentally determined major, minor and trace element partition coefficients are important for using natural pyroxenes to estimate the compositions of the melts from which they crystallized and the oxidation conditions that prevailed during crystallization. We will report on minor element (Al, Ti, Cr) zoning in nakhlite pyroxenes and in synthetic pyroxenes that we have grown for the purposes of determining pyroxene/melt partition coefficients for Sr and REE. The natural pyroxenes have patchy Al zoning that, by analogy with our experimental pyroxenes, we interpret as sector zoning. The irregular patchy nature of the zoning is probably the result of the vagaries of growth kinetics and local environment during crystal growth. More slowly cooled nakhlites have the most distinct bimodal zoning, with one mode having Al2O3 around 0.5-0.6 wt%, and the other around 0.9 %. Average Al content increases with increasing cooling rate. This feature is puzzling, since the cumulus pyroxenes were almost certainly present at the time of eruption. Al and Ti are strongly correlated, but Cr is completely decoupled from those elements. The synthetic pyroxenes are distinctly sector zoned in Al and Ti, and the sector-to-sector variation in Al within a single crystal has important effects on trace element partition coefficients. Trivalent REE are strongly correlated with Al, while divalent elements (Sr, Eu+2) show a significantly weaker correlation. For example, as the Al2O3 content varies from 0.3 to 0.6 wt % from one sector to another, D(Gd) increases by approx.80% while D(Sr) and D(Eu) only increase by 20-30% at oxygen fugacities near IW. The different Al dependency of D for trivalent REE vs. divalent Eu and Sr considerably complicates the calibration of the Eu oxybarometer.

McKay, Gordon↗

Minor Elements in Nakhlite Pyroxenes: Cr in MIL00346

Nakhlites are olivine-bearing clinopyroxene cumulates. Based on petrographic characteristics, they may be divided into groups that cooled at different rates and may have been formed at different depths in a single flow. The order of cooling rate from slowest to fastest is NWA998<Lafayette < Governador Valadares ~ Nakhla < Yamato000593 < NWA817 ~ MIL03346. Nakhlite cumulus pyroxene grains consist of large cores that are nearly homogeneous in major element composition surrounded by thin rims that are zoned to Fe-rich compositions. Detailed study of these pyroxenes is important because they retain a record of the crystallization history of the nakhlite magma. Moreover, because the composition of the nakhlite parent melt cannot be directly determined, inversion of the major and minor element composition of the cumulate pyroxene cores can be used to estimate the composition of that melt. Thus it is important to understand the major and minor element zoning in the cumulus pyroxenes. While major elements are nearly homogeneous, minor elements exhibit distinctive zoning patterns that vary from one nakhlite to another. This paper reports unusual Cr zoning patterns in pyroxenes from MIL03346 (MIL) and contrast these with pyroxenes from Y593.

McKay, G. A.↗

Aluminum Effect on the Calibration of the Eu Oxybarometer for Nakhlites

Recent studies of Martian meteorites have shown that Martian magma had wide range of oxygen fugacity. In order to estimate the redox state of the Martian crust and mantle, the partitioning coefficient of Eu in the shergottite pyroxene has been extensively studied. Nakhlite, a cumulate clinopyroxenite, is another important group of Martian meteorites. We have studied synthetic compositions (NT, NL, NJ, NJ2 and NJ4) in order to estimate the Nakhla parent melt composition. In our previous work, we calibrated the Eu oxybarometer for nakhlite using the NJ4 composition which we believe is the closest to the Nakhla parent melt. Consequently, we concluded that Nakhla may have crystallized under fairly reducing condition. However, we also found that the partition coefficient is strongly affected by Al contents in melt and in pyroxene. In this abstract we report the correlation between the D values and Al contents in melt and in pyroxene from our Nakhla experimental studies. Also we check the reliability of our previous calibration of Eu oxybarometer, because Rare Earth Elements (REEs) are easily affected by Al content in melt and in pyroxene and Nakhla pyroxene shows unusual patchy Al zoning.

Makishima, J.↗

Yamato 980459: The Most Primitive Shergottite?

The Antarctic Research Center of the Japanese National Institute of Polar Research (NIPR) recently announced the discovery of a new Martian shergottite, Y98(0459). This sample is a member of the subgroup of basaltic shergottites that contain abundant olivine phenocrysts, and are thus olivine- phyric. Y98 may have special significance among the basaltic shergottites because (1) it appears to have been the most magnesian Martian magma yet found, and thus can provide valuable clues to magma petrogenesis on Mars; (2) it contains no late-crystallizing phases, but instead contains approx. 30% interstitial glass, which can provide unambiguous incompatible element patterns of the parent melt; and (3) it carries an LREE-depleted signature similar to QUE 94201, whose isotopic characteristics are the most primitive of all basaltic shergottites.

McKay, G.↗

The Vaguries of Pyroxene Nucleation and the Resulting Chondrule Textures

Pyroxene is a major phase in chondrules, but often follows olivine in the crystallization sequence and depending on the melting temperature and time may not nucleate readily upon cooling. Dynamic crystallization experiments based on total or near total melting were used to study PO (porphyritic olivine) and PP (Porphyritic pyroxene) compositions as defined by. The experiments showed that pyroxene nucleated only at subliquidus temperatures in the PP melts and rarely in the PO melts. Porphyritic chondrules with phenocrysts of both olivine and pyroxene (POP chondrules) were not easily produced in the experiments. POP chondrules are common and it is important for deciphering their formation that we understand pyroxene nucleation properties of chondrule melts.

Lofgren, G. E.↗

Aqueous Alteration Mineralogy in CM Carbonaceous Chondrites

Iron-nickel sulfides are found in most or all solar system environments, and are probably the only minerals found in all extraterrestrial materials on hand. Despite the ubiquity, they have not received the attention they deserve. The most common Fe-Ni sulfides in chondrites are troilite (FeS), pyrrhotite (Fe1- XS) and pentlandite (Fe,Ni)9S8. Troilite is believed to have resulted from sulfidation of metal (Fe-Ni) grains in an H2Scontaining environment. Pyrrhotite is produced when friable troilite grains, which are exfoliated from the metal nucleus, are submitted to continued sulfidation [1]. Some asteroids are known to have experienced aqueous alteration, forming products including new generations of sulfides (pyrrhotite and pentlandite). Pentlandite in particular is known to form during such alteration [1]. However, experimental work by Lauretta has indicated that pentlandite may also have been formed during the initial sulfidation process [2], due to the faster diffusion rate of nickel into the forming sulfide, as compared to iron. Finally, there is considerable evidence [1,3&4] for a family of phases intermediate between pyrrhotite and pentlandite, following the trend of the high temperature monosulfide solid solution [5], something not encountered in terrestrial rocks.

Chokai, J.↗

Palagonitic Mars: A Basalt Centric View of Surface Composition and Aqueous Alteration

Palagonitic tephra from certain areas on Mauna Kea Volcano (Hawaii) are well-established spectral and magnetic analogues of high-albedo regions on Mars. By definition, palagonite is "a yellow or orange isotropic mineraloid formed by hydration and devitrification of basaltic glass." The yellow to orange pigment is nanometer-sized ferric oxide particles (np-Ox) dispersed throughout the hydrated basaltic glass matrix. The hydration state of the np-Ox particles and the matrix is not known, but the best Martian spectral analogues contain allophane-like materials and not crystalline phyllosilicates. Martian low-albedo regions are also characterized by a palagonite-like ferric absorption edge, but, unlike the highalbedo regions, they also show evidence for absorption by ferrous iron. Thermal emission spectra (TES) obtained by the Mars Global Surveyor Thermal Emission Spectrometer suggest that basaltic (surface Type 1) and andesitic (surface Type 2) volcanic compositions preferentially occur in southern (Syrtis Major) and northern (Acidalia) hemispheres, respectively. The absence of a ferric-bearing component in the modeling of TES spectra is in apparent conflict with VNIR spectra of Martian dark regions, as discussed above. However, the andesitic spectra have also been interpreted as oxidized basalt using phyllosilicates instead of high-SiO2 glass as endmembers in the spectral deconvolution of surface Type 2 TES spectra. We show here that laboratory VNIR and TES spectra of rinds on basaltic rocks are spectral endmembers that provide a consistent explanation for both VNIR and TES data of Martian dark regions.

Morris, R. V.↗

Samples of Asteroid Surface Ponded Deposits in Chondritic Meteorites

One of the many unexpected observations of asteroid 433 Eros by the Near Earth Asteroid Rendezvous (NEAR) mission was the many ponds of fine-grained materials [1-3]. The ponds have smooth surfaces, and define equipotential surfaces up to 10's of meters in diameter [4]. The ponds have a uniformly sub-cm grain size and appear to be cohesive or indurated to some degree, as revealed by slumping. The ponds appear to be concentrated within 30 degrees of the equator of Eros, where gravity is lowest. There is some insight into the mineralogy and composition of the ponds surfaces from NEAR spectroscopy [2,4,5,6]. Compared to the bulk asteroid, ponds: (1) are distinctly bluer (high 550/760 nm ratio), (2) have a deeper 1um mafic band, (3) have reflectance elevated by 5%.

Zolensky, M. E.↗

Dynamic Crystallization Experiments on LEW97008: Experimental Reproduction of Chondroid Textures

Dynamic crystallization experiments were conducted using LEW97008 (L3.4) as starting material. Experiments were melted at temperatures well below its liquidus (1250-1450 C) in order to document the textural and compositional changes that occur in UOC material with modest amounts of partial melting and subsequent crystallization. The textures of the experimental products compare very well to natural chondroids (partially melted nebular particles that would become chondrules if more completely melted). Thus it is possible to use the textures in these experiments as a guide to unraveling the melting and cooling histories of natural chondroids. The Antarctic meteorite LEW97008 was chosen as the starting material for our experiments. As an L3.4 it is slightly more metamorphosed than would ordinarily be preferred, but this meteorite is unusually fresh for an Antarctic meteorite, which made it attractive.

Nettles, J. W.↗

Experimental Replication of Relict "Dusty" Olivine in Type 1B Chondrules

Introduction: Relict "dusty" olivine is considered to be a remnants of previous chondrule forming events based on petrographic and chemical evidence. Dynamic crystallization experiments confirm that dusty olivine can be produced by reduction of FeO-rich olivine in Unequilibrated Ordinary Chondrite (UOC) material. The results of these experiments compliment those of who also produced dusty olivine, but from synthetic starting materials. Techniques: Dynamic crystallization experiments were conducted in which UOC material was reduced in presence of graphite. Starting material was coarsely ground GR095554 or WSG95300 that contained olivine of Fo 65-98. Approximately 75 mg. of UOC material was placed in a graphite crucible and sealed in an evacuated silica tube. The tube was suspended in a gas-mixing furnace operated at 1 log unit below the IW buffer. The experiments were as brief as 1.5 hrs up to 121 hrs. Results: Dusty olivine was produced readily in experiments melted at 1400 C for I hr. and cooled between 5 and 100 C/hr or melted at 1300-1400 C for 24 hours. Fe-rich olivine (dusty olivine precursors) that have been partially reduced were common in the experiments melted at 1400 C and cooled at 1000 C/hr or melted at 1200 C for 24 hrs. Relict olivine is absent in experiments melted at 1400 for 24 hrs, melted above 1400 C, or cooled more slowly than 10 C/hr. Relict olivine in the experiments has minimum Fo value of 83 . Thus even in the shortest experiments the most Fe-rich olivine has been altered significantly. The precursor olivine disappears in a few to many hours depending on temperature. The experiments show Fe-rich olivine in all stages of transition to the new dusty form. The olivine is reduced to form dusty olivine in a matter of a few hours at temperatures less than 1400 C and in minutes at higher temperatures. The reduction appears to proceed from the rim of the crystal inward with time. The reduction appears initially rectilinear as if controlled by crystallography, but with time Fe-metal blebs are randomly distributed throughout the olivine. In a given experiment, dusty olivine can be found in varying stages of development, but in the longest experiments, the Fe-metal blebs are dominant and they appear to be migrating out of the olivine. The composition of the dusty olivine ranges from Fo 94-99. The Cr, Mn, and Ca content of the newly formed, dusty olivine is slightly less on average that the precursor olivine, but is till with the range of type 1 olivine. Chadacrysts in the low Ca pyroxene are most common in the higher temperature, more slowly cooled experiments and range in composition from Fo 90-99. Application to chondrule formation: These experiments place time-temperature limits on the preservation of Fe-rich olivine and the production of dusty olivine during chondrule forming events. The reduction process proceeds in a few hours at temperatures above 1400 C and in 10's of hours at temperature between 1200 and 1300 C. This result further confirms th at chondrules form in a few hours to days as suggested earlier. The experiments also confirm that dusty olivine can form from typical Fe-rich olivine in UOC material during the recycling of such olivine in the chondrule forming process.

Lofgren, Gary E.↗

Experimental Reproduction of Type 1B Chondrules

We have replicated type 1B chondrule textures and compositions with crystallization experiments in which UOC material was melted at 1400 deg.C and cooled at 5-1000 deg.C/hr using graphite crucibles in evacuated silica tubes to provide a reducing environment. Additional information is contained in the original extended abstract.

Lofgren, G. E.↗

REE and Strontium Partition Coefficients for Nakhla Pyroxenes

We present new partition coefficients for REE and Sr determined using a synthetic melt that crystallizes pyroxenes very similar in composition to Nakhla pyroxene cores. We believe these are the most appropriate partition coefficients to use in studying Nakhla Additional information is contained in the original extended abstract..

Oe, K.↗

Preliminary Examination of Sahara 99555: Mineralogy and Experimental Studies of a New Angrite

A 2710 g meteorite, Sahara 99555 (Sah99), was recently recovered from the Sahara and reported to be the 5th angrite. It is the largest angrite ever found and may offer useful information to better understand the unusual petrogeneses of this rare achondrite group. It may also allow us to examine the chronological record of igneous activity in the very early solar system. We obtained a 2.6 g chip of Sah99 and here present a preliminary report of its petrology and mineralogy in conjunction with a crystallization experiment on an analogue composition.

Mikouchi, T.↗

Experimentally Produced Spinel Rims on Ca-Al-Rich Inclusion Bulk Compositions

Most Ca-Al-rich inclusions (CAls) from Allende are surrounded by a series of mineralogically distinct rim layers. Proposed modes of formation for these layers include flash heating, evaporation, and condensation. The innermost of these rim layers is generally spinel (SP), in some cases intergrown with perovskite (PV), and commonly containing varying amounts of secondary iron increasing towards the edge of the CAI. The SP or SP+PV rim is not always contiguous with the other rim layers, indicating that it is probably the result of a separate event. We have produced continuous SP rims on synthetic analogs representing Type A/B1, average Type B, and Type B2 bulk compositions by reheating a solid glass experimental charge to subliquidus crystallization temperatures. This experimental result is consistent with the formation of chondrules; and CAIs by more than one sequence of heating and cooling. Previous work indicated that prior crystallization events produced observable effects in the texture and chemistry of the final run product. Information on the nature of the heating/cooling cycles experienced by CAls and chondrules is important in modeling the environment of their formation. Additional information is contained in the original extended abstract.

Paque, Julie M.↗

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.↗