Coordinates Analyses of Hydrated Interplanetary Dust Particles: Samples of Primitive Solar System Bodies

NASA Technical Reports Server (NTRS)

Keller, L. P.; Snead, C.; McKeegan, K. D.

2016-01-01

Interplanetary dust particles (IDPs) collected in the stratosphere fall into two major groups: an anhydrous group termed the "chondritic-porous (CP) IDPs and a hydrated group, the "chondritic-smooth (CS) IDPs, although rare IDPs with mineralogies intermediate between these two groups are known [1]. The CP-IDPs are widely believed to be derived from cometary sources [e.g. 2]. The hydrated CS-IDPs show mineralogical similarities to heavily aqueously altered carbonaceous chondrites (e.g. CI chondrites), but only a few have been directly linked to carbonaceous meteorite parent bodies [e.g. 3, 4]. Most CS-IDPs show distinct chemical [5] and oxygen isotopic composition differences [6-8] from primitive carbonaceous chondrites. Here, we report on our coordinated analyses of a suite of carbon-rich CS-IDPs focusing on their bulk compositions, mineralogy, mineral chemistry, and isotopic compositions.

Oxygen, Magnesium, and Aluminum Isotopes in the Ivuna CAI: Re-Examining High-Temperature Fractionations in CI Chondrites

NASA Technical Reports Server (NTRS)

Frank, D. R.; Huss, G. R.; Nagashima, K.; Zolensky, M. E.; Le, L.

2017-01-01

CI chondrites are thought to approximate the bulk solar system composition since they closely match the composition of the solar photosphere. Thus, chemical differences between a planetary object and the CI composition are interpreted to result from fractionations of a CI starting composition. This interpretation is often made despite the secondary mineralogy of CI chondrites, which resulted from low-T aqueous alteration on the parent asteroid(s). Prevalent alteration and the relatively large uncertainties in the photospheric abundances (approx. +/-5-10%) permit chemical fractionation of CI chondrites from the bulk solar system, if primary chondrules and/or CAIs have been altered beyond recognition. Isolated olivine and pyroxene grains that range from approx. 5 microns to several hundred microns have been reported in CI chondrites, and acid residues of Orgueil were found to contain refractory oxides with oxygen isotopic compositions matching CAIs. However, the only CAI found to be unambiguously preserved in a CI chondrite was identified in Ivuna. The Ivuna CAI's primary mineralogy, small size (approx.170 microns), and fine-grained igneous texture classify it as a compact type A. Aqueous alteration infiltrated large portions of the CAI, but other regions remain pristine. The major primary phases are melilite (Ak 14-36 ), grossmanite (up to 20.8 wt.% TiO 2 ), and spinel. Both melilite and grossmanite have igneous textures and zoning patterns. An accretionary rim consists primarily of olivine (Fa 2-17 ) and low-Ca pyroxene (Fs 2-10 ), which could be either surviving CI2 material or a third lithology.

The neodymium stable isotope composition of the silicate Earth and chondrites

NASA Astrophysics Data System (ADS)

McCoy-West, Alex J.; Millet, Marc-Alban; Burton, Kevin W.

2017-12-01

The non-chondritic neodymium (Nd) 142Nd/144Nd ratio of the silicate Earth potentially provides a key constraint on the accretion and early evolution of the Earth. Yet, it is debated whether this offset is due to the Earth being formed from material enriched in s-process Nd isotopes or results from an early differentiation process such as the segregation of a late sulfide matte during core formation, collisional erosion or a some combination of these processes. Neodymium stable isotopes are potentially sensitive to early sulfide segregation into Earth's core, a process that cannot be resolved using their radiogenic counterparts. This study presents the first comprehensive Nd stable isotope data for chondritic meteorites and terrestrial rocks. Stable Nd measurements were made using a double spike technique coupled with thermal ionisation mass spectrometry. All three of the major classes of chondritic meteorites, carbonaceous, enstatite and ordinary chondrites have broadly similar isotopic compositions allowing calculation of a chondritic mean of δ146/144Nd = -0.025 ± 0.025‰ (±2 s.d.; n = 39). Enstatite chondrites yield the most uniform stable isotope composition (Δ146/144Nd = 26 ppm), with considerably more variability observed within ordinary (Δ146/144Nd = 72 ppm) and carbonaceous meteorites (Δ146/144Nd = 143 ppm). Terrestrial weathering, nucleosynthetic variations and parent body thermal metamorphism appear to have little measurable effect on δ146/144Nd in chondrites. The small variations observed between ordinary chondrite groups most likely reflect inherited compositional differences between parent bodies, with the larger variations observed in carbonaceous chondrites being linked to varying modal proportions of calcium-aluminium rich inclusions. The terrestrial samples analysed here include rocks ranging from basaltic to rhyolitic in composition, MORB glasses and residual mantle lithologies. All of these terrestrial rocks possess a broadly similar Nd isotope composition giving an average composition for the bulk silicate Earth of δ146/144Nd = -0.022 ± 0.034‰ (n = 30). In the samples here magmatic differentiation appears to only have an effect on stable Nd in highly evolved magmas with heavier δ146/144Nd values observed in samples with >70 wt% SiO2. The average stable Nd isotope composition of chondrites and the bulk silicate Earth are indistinguishable at the 95% confidence level. However, mantle samples do possess variable stable Nd isotope compositions (Δ146/144Nd = 75 ppm) with an average δ 146 / 144Nd value of -0.008‰. If these heavier values represent the true composition of pristine mantle then it is not possible to completely rule out some role for core formation in accounting for some of the offset between the mantle and chondrites. Overall, these results indicate that the mismatch of 142Nd between the Earth and chondrites is best explained by a higher proportion of s-process Nd in the Earth, rather than partitioning into sulfide or S-rich metal in the core.

Trace element distributions in primitive achondrites

NASA Technical Reports Server (NTRS)

Davis, Andrew M.; Prinz, Martin; Weisberg, Michael K.

1993-01-01

The primitive achondrites have approximately chondritic bulk chemical composition but achondritic textures. Clayton et al. show that nine of these meteorites, the acapulcoites and the lodranites, have similar oxygen isotopic compositions. The acapulcoites appear to be highly metamorphosed, but undifferentiated meteorites of chondritic composition; whereas, the lodranites appear to have lost a feldspathic partial melt. In order to learn more about metamorphic processes and partial melt removal, we have measured the trace element compositions of constituent phases of a number of primitive achondrites by ion microprobe. We have analyzed two acapulcoites, Acapulco and ALH81261 (paired with ALH77081), and three londranites, Lodran, LEW88280, and MAC88177. In addition, we analyzed LEW88663, which has the bulk composition, mineral chemistry, and oxygen isotopic composition of L-chondrites, but is metal-free and has an achondrite texture; and Divnoe, a plagioclase-poor, olivine-rich primitive achondrite with an oxygen isotopic composition similar to that of the group IAB iron meteorites. These meteorites show a variety of REE patterns in their constituent phases, and there are consistent differences between acapulcoites and lodranites that are consistent with removal of a LREE- and Eu-enriched melt that is apparently responsible for the low plagioclase content of lodranites.

The origin of volatile element depletion in early solar system material: Clues from Zn isotopes in chondrules

NASA Astrophysics Data System (ADS)

Pringle, Emily A.; Moynier, Frédéric; Beck, Pierre; Paniello, Randal; Hezel, Dominik C.

2017-06-01

Volatile lithophile elements are depleted in the different planetary materials to various degrees, but the origin of these depletions is still debated. Stable isotopes of moderately volatile elements such as Zn can be used to understand the origin of volatile element depletions. Samples with significant volatile element depletions, including the Moon and terrestrial tektites, display heavy Zn isotope compositions (i.e. enrichment of 66Zn vs. 64Zn), consistent with kinetic Zn isotope fractionation during evaporation. However, Luck et al. (2005) found a negative correlation between δ66Zn and 1/[Zn] between CI, CM, CO, and CV chondrites, opposite to what would be expected if evaporation caused the Zn abundance variations among chondrite groups. We have analyzed the Zn isotope composition of multiple samples of the major carbonaceous chondrite classes: CI (1), CM (4), CV (2), CO (4), CB (2), CH (2), CK (4), and CK/CR (1). The bulk chondrites define a negative correlation in a plot of δ66Zn vs 1/[Zn], confirming earlier results that Zn abundance variations among carbonaceous chondrites cannot be explained by evaporation. Exceptions are CB and CH chondrites, which display Zn systematics consistent with a collisional formation mechanism that created enrichment in heavy Zn isotopes relative to the trend defined by CI-CK. We further report Zn isotope analyses of chondrite components, including chondrules from Allende (CV3) and Mokoia (CV3), as well as an aliquot of Allende matrix. All chondrules are enriched in light Zn isotopes (∼500 ppm on 66Zn/64Zn) relative to the bulk, contrary to what would be expected if Zn were depleted during evaporation, on the other hand the matrix has a complementary heavy isotope composition. We report sequential leaching experiments in un-equilibrated ordinary chondrites, which show sulfides are isotopically heavy compared to silicates and the bulk meteorite by ca. +0.65 per mil on 66Zn/64Zn. We suggest isotopically heavy sulfides were removed from either chondrules or their precursors, thereby producing the light Zn isotope enrichments in chondrules.

Osmium Stable Isotope Composition of Chondrites and Iron Meteorites: Implications for Planetary Core Formation

NASA Astrophysics Data System (ADS)

Nanne, J. A. M.; Millet, M. A.; Burton, K. W.; Dale, C. W.; Nowell, G. M.; Williams, H. M.

2016-12-01

Mass-dependent Os stable isotope fractionation is expected to occur during metal-silicate segregation as well as during crystallization of metal alloys due to the different bonding environment between silicate and metals. As such, Os stable isotopes have the potential to resolve questions pertaining to planetary accretion and differentiation. Here, we present stable Os isotope data for a set of chondrites and iron meteorites to examine the processes associated with core solidification. Carbonaceous, ordinary, and enstatite chondrites show no detectable stable isotope variation with a δ190Os weighted average of +0.12±0.04 (n=37). The uniform composition observed for chondrites implies Os stable isotope homogeneity of the bulk solar nebula. Contrary to chondrites, iron meteorites display a large range in Os stable isotope compositions from δ190Os of +0.05 up to +0.49‰. Variation is only observed in the IIAB and IIIAB irons. Type IVB irons display values similar to chondrites (+0.107±0.047 [n=3]) and IVA compositions are slightly different +0.187±0.004 (n=2). The type IIAB and IIIAB groups show values both within the chondritic range and up to heavier values extending up to +0.49‰. Since core formation in small planetary bodies is expected to quantitatively sequester Os in metal phases, bulk planetary cores are expected to display chondritic δ190Os values. Conversely, samples of the IIAB and IIIAB group display significant variation, possibly indicating that stable isotope fractionation occurred during solidification of the parent-body core. However, no covariation is observed between δ190Os and either Os abundance or radiogenic Os isotope ratios. Instead, liquid immiscibility during core crystallization, where the liquid metal splits into separate S- and P-rich liquids, may be a source of Os stable isotope fractionation.

Connections between the bulk composition, geodynamics and habitability of Earth

NASA Astrophysics Data System (ADS)

Jellinek, A. M.; Jackson, M. G.

2015-08-01

The bulk composition of the silicate part of Earth has long been linked to chondritic meteorites. Ordinary chondrites -- the most abundant meteorite class -- are thought to represent planetary building materials. However, a landmark discovery showed that the 142Nd/144Nd ratio of the accessible parts of the modern terrestrial mantle on Earth is greater than that of ordinary chondrites. If Earth was derived from these precursors, mass balance requires that a missing reservoir with 142Nd/144Nd lower than ordinary chondrites was isolated from the accessible mantle within 20 to 30 million years of accretion. This reservoir would host the equivalent of the modern continents' budget of radioactive heat-producing elements (uranium, thorium and potassium), yet has not been discovered. We argue that this reservoir could have been lost to space by ablation from early impactors. If so, Earth's radiogenic heat generation is between 18 and 45% lower than estimates based on a chondritic composition. Calculations of Earth's thermal history that incorporate such reduced radiogenic heating are consistent with a transition to the current plate tectonic mode in the past 2.5 billion years or so, a late onset of the dynamo and an evolving rate of volcanic outgassing consistent with Earth's long-term habitable climate. Reduced heat production compared with Venus and Mars could also explain aspects of the differences between the current climatic regimes of these planets and Earth.

Petrology and geochemistry of Patuxent Range 91501, a clast-poor impact-melt from the L chondrite parent body, and Lewis Cliff 88663, an L7 chondrite

NASA Astrophysics Data System (ADS)

Mittlefehldt, David W.; Lindstrom, Marilyn M.

2001-03-01

We have performed petrologic and geochemical studies of Patuxent Range 91501 and Lewis Cliff 88663. PAT 91501, originally classified as an L7 chondrite, is rather a unique, near total impact-melt from the L chondrite parent body. Lewis Cliff 88663 was originally classified as an "achondrite (?)," but we find that it is a very weakly shocked L7 chondrite. PAT 91501 is an unshocked, homogeneous, igneous-textured ultramafic rock composed of euhedral to subhedral olivine, low-Ca pyroxene, augite and chrome-rich spinels with interstitial albitic plagioclase and minor silica-alumina-alkali-rich glass. Only ~10% relict chondritic material is present. Olivine grains are homogeneous (Fa25.2-26.8). Low-Ca pyroxene (Wo1.9-7.2En71.9-78.2Fs19.9-20.9) and augite (Wo29.8-39.0En49.2-55.3Fs11.8-14.9) display a strong linear TiO2-Al2O3 correlations resulting from igneous fractionation. Plagioclase is variable in composition; Or3.0-7.7Ab79.8-84.1An8.2-17.2. Chrome-rich spinels are variable in composition and zoned from Cr-rich cores to Ti-Al-rich rims. Some have evolved compositions with up to 7.9 wt% TiO2. PAT 91501 bulk silicate has an L chondrite lithophile element composition except for depletions in Zn and Br. Siderophile and chalcophile elements are highly depleted due to sequestration in cm-size metal-troilite nodules. The minerals in LEW 88663 are more uniform in composition than those in PAT 91501. Olivine grains have low CaO and Cr2O3 contents similar to those in L5-6 chondrites. Pyroxenes have high TiO2 contents with only a diffuse TiO2-Al2O3 correlations. Low-Ca pyroxenes are less calcic (Wo1.6-3.1En76.5-77.0Fs20.4-21.4), while augites (Wo39.5-45.6En46.8-51.1Fs7.6-9.4) and plagioclases (Or2.6-5.7Ab74.1-83.1An11.2-23.3) are more calcic. Spinels are homogeneous and compositionally similar to those in L6 chondrites. LEW 88663 has an L chondrite bulk composition for lithophile elements, and only slight depletions in siderophile and chalcophile elements that are plausibly due to weathering and/or sample heterogeneity.

The Abundance and Isotopic Composition of Hg in Extraterrestrial Materials

NASA Technical Reports Server (NTRS)

Lauretta, D. S.

2004-01-01

During the past three year grant period we made excellent progress in our study of the abundances and isotopic compositions of Hg and other volatile trace elements in extraterrestrial materials. As part of my startup package I received funds to construct a state-of-the-art experimental facility to study gas-solid reaction kinetics. Much of our effort was spent developing the methodology to measure the abundance and isotopic composition of Hg at ultratrace levels in solid materials. In our first study, the abundance and isotopic composition of Hg was determined in bulk samples of the Murchison (CM) and Allende (CV) carbonaceous chondrites. We have continued our study of mercury in primitive meteorites and expanded the suite of meteorites to include other members of the CM and CV chondrite group as well as CI and CO chondrites. Samples of the CI chondrite Orgueil, the CM chondrites Murray, Nogoya, and Cold Bokkeveld, the CO chondrites Kainsaz, Omans, and Isna, and the CV chondrites Vigarano, Mokoia, and Grosnaja were tested. We have developed a thermal analysis ICP-MS technique and applied it to the study of a suite of thermally labile elements (Zn, As, Se, Cd, In, Sn, Sb, Te, Hg, Au, Tl, Pb, and Bi) in geologic materials as well.

The Butterflies of Principal Components: A Case of Ultrafine-Grained Polyphase Units

NASA Astrophysics Data System (ADS)

Rietmeijer, F. J. M.

1996-03-01

Dusts in the accretion regions of chondritic interplanetary dust particles [IDPs] consisted of three principal components: carbonaceous units [CUs], carbon-bearing chondritic units [GUs] and carbon-free silicate units [PUs]. Among others, differences among chondritic IDP morphologies and variable bulk C/Si ratios reflect variable mixtures of principal components. The spherical shapes of the initially amorphous principal components remain visible in many chondritic porous IDPs but fusion was documented for CUs, GUs and PUs. The PUs occur as coarse- and ultrafine-grained units that include so called GEMS. Spherical principal components preserved in an IDP as recognisable textural units have unique proporties with important implications for their petrological evolution from pre-accretion processing to protoplanet alteration and dynamic pyrometamorphism. Throughout their lifetime the units behaved as closed-systems without chemical exchange with other units. This behaviour is reflected in their mineralogies while the bulk compositions of principal components define the environments wherein they were formed.

Size scales over which ordinary chondrites and their parent asteroids are homogeneous in oxidation state and oxygen-isotopic composition

NASA Astrophysics Data System (ADS)

Rubin, Alan E.; Ziegler, Karen; Young, Edward D.

2008-02-01

Literature data demonstrate that on a global, asteroid-wide scale (plausibly on the order of 100 km), ordinary chondrites (OC) have heterogeneous oxidation states and O-isotopic compositions (represented, respectively, by the mean olivine Fa and bulk Δ 17O compositions of equilibrated samples). Samples analyzed here include: (a) two H5 chondrite Antarctic finds (ALHA79046 and TIL 82415) that have the same cosmic-ray exposure age (7.6 Ma) and were probably within ˜1 km of each other when they were excavated from the H-chondrite parent body, (b) different individual stones from the Holbrook L/LL6 fall that were probably within ˜1 m of each other when their parent meteoroid penetrated the Earth's atmosphere, and (c) drill cores from a large slab of the Estacado H6 find located within a few tens of centimeters of each other. Our results indicate that OC are heterogeneous in their bulk oxidation state and O-isotopic composition on 100-km-size scales, but homogeneous on meter-, decimeter- and centimeter-size scales. (On kilometer size scales, oxidation state is heterogeneous, but O isotopes appear to be homogeneous.) The asteroid-wide heterogeneity in oxidation state and O-isotopic composition was inherited from the solar nebula. The homogeneity on small size scales was probably caused in part by fluid-assisted metamorphism and mainly by impact-gardening processes (which are most effective at mixing target materials on scales of ⩽1 m).

Origin of magnetite and pyrrhotite in carbonaceous chondrites

USGS Publications Warehouse

Herndon, J.M.; Rowe, M.W.; Larson, E.E.; Watson, D.E.

1975-01-01

CARBONACEOUS chondrites, although comprising only about 2% of known meteorites, are extremely interesting for scientific investigation. Their mineral constitution, and the correspondence between their bulk chemical composition and the solar abundance of condensable elements, indicate that minimum chemical fractionation and thermal alteration have occurred. The mineral phases observed in these primitive chondrites are sufficiently unique, with respect to other meteorite classes, to have elicited considerable speculation about the physical environment in which they formed1-7. ?? 1975 Nature Publishing Group.

Mineralogy and composition of matrix and chondrule rims in carbonaceous chondrites

NASA Technical Reports Server (NTRS)

Zolensky, Michael; Barrett, Ruth; Browning, Lauren

1993-01-01

The degree of compositional variation of fine-grained minerals displayed by the members within any carbonaceous chondrite group (i.e., CI, CM, CV, CR) is a direct reflection of the range of aqueous alteration assemblages present. Matrix and fine-grained chondrule rims within any particular carbonaceous chondrite are mineralogically nearly identical to one another, but not necessarily similar in bulk elemental composition, even though they have subsequently experienced postaccretional secondary processing (aqueous alteration) under identical conditions. We propose that CO chondrites experienced parent body conditions of low f(O2), low water/rock ratios, and temperatures below 50 C. CR chondrites experienced higher water/rock ratios, potentially higher temperatures (not above 150 C), and a wide range of f(O2). The alteration mineralogy of CV chondrites indicates water/rock ratios at the high end (at least) of the range for CR chondrites, Essebi, and MAC 87300. CM chondrites experienced temperatures below 50 C, low f(O2) and low water/rock ratios, except EET 83334, which probably experienced relatively higher f(O2), and B-7904 and Y-86720, which experienced postalteration temperatures in the range 500-700 C. Most CI chondrites experienced temperatures between 50 and 150 C, relatively high water/rock ratios, and variable f(O2). Y-82162 witnessed postalteration heating, possibly as high as 400 C.

Selective Disparity of Ordinary Chondritic Precursors in Micrometeorite Flux

NASA Astrophysics Data System (ADS)

Rudraswami, N. G.; Fernandes, D.; Naik, A. K.; Shyam Prasad, M.; Carrillo-Sánchez, J. D.; Plane, J. M. C.; Feng, W.; Taylor, S.

2018-01-01

All known extraterrestrial dust (micrometeoroids) entering the Earth’s atmosphere is anticipated to have a significant contribution from ordinary chondritic precursors, as seen in meteorites, but this is an apparent contradiction that needs to be addressed. Ordinary chondrites represent a minor contribution to the overall meteor influx compared to carbonaceous chondrites, which are largely dominated by CI and/or CM chondrites. However, the near-Earth asteroid population presents a scenario with sufficient scope for generation of dust-sized debris from ordinary chondritic sources. The bulk chemical composition of 3255 micrometeorites (MMs) collected from Antarctica and deep-sea sediments has shown Mg/Si largely dominated by carbonaceous chondrites, and less than 10% having ordinary chondritic precursors. The chemical ablation model is combined with different initial chondritic compositions (CI, CV, L, LL, H), and the results clearly indicate that high-density (≥2.8 g cm‑3) precursors, such as CV and ordinary chondrites in the size range 100–700 μm and zenith angle 0°–70°, ablate at much faster rates and lose their identity even before reaching the Earth’s surface and hence are under-represented in our collections. Moreover, their ability to survive as MMs remains grim for high-velocity micrometeoroids (>16 km s‑1). The elemental ratio for CV and ordinary chondrites are also similar to each other irrespective of the difference in the initial chemical composition. In conclusion, MMs belonging to ordinary chondritic precursors’ concentrations may not be insignificant in thermosphere, as they are found on Earth’s surface.

Osmium isotope evidence for uniform distribution of s- and r-process components in the early solar system

NASA Astrophysics Data System (ADS)

Yokoyama, Tetsuya; Rai, Vinai K.; Alexander, Conel M. O'D.; Lewis, Roy S.; Carlson, Richard W.; Shirey, Steven B.; Thiemens, Mark H.; Walker, Richard J.

2007-07-01

We have precisely measured Os isotopic ratios in bulk samples of five carbonaceous, two enstatite and two ordinary chondrites, as well as the acid-resistant residues of three carbonaceous chondrites. All bulk meteorite samples have uniform 186Os/ 188Os, 188Os/ 189Os and 190Os/ 189Os ratios, when decomposed by an alkaline fusion total digestion technique. These ratios are also identical to estimates for Os in the bulk silicate Earth. Despite Os isotopic homogeneity at the bulk meteorite scale, acid insoluble residues of three carbonaceous chondrites are enriched in 186Os, 188Os and 190Os, isotopes with major contributions from stellar s-process nucleosynthesis. Conversely, these isotopes are depleted in acid soluble portions of the same meteorites. The complementary enriched and depleted fractions indicate the presence of at least two types of Os-rich components in these meteorites, one enriched in Os isotopes produced by s-process nucleosynthesis, the other enriched in isotopes produced by the r-process. Presolar silicon carbide is the most probable host for the s-process-enriched Os present in the acid insoluble residues. Because the enriched and depleted components present in these meteorites are combined in proportions resulting in a uniform chondritic/terrestrial composition, it requires that disparate components were thoroughly mixed within the solar nebula at the time of the initiation of planetesimal accretion. This conclusion contrasts with evidence from the isotopic compositions of some other elements (e.g., Sm, Nd, Ru, Mo) that suggests heterogeneous distribution of matter with disparate nucleosynthetic sources within the nebula.

N-15-Rich Organic Globules in a Cluster IDP and the Bells CM2 Chondrite

NASA Technical Reports Server (NTRS)

Messenger, S.; Nakamura-Messenger, K.; Keller, Lindsay P.

2008-01-01

Organic matter in primitive meteorites and chondritic porous interplanetary dust particles (CP IDPs) is commonly enriched in D/H and 15N/14N relative to terrestrial values [1-3]. These anomalies are ascribed to the partial preservation of presolar cold molecular cloud material [1]. Some meteorites and IDPs contain m-size inclusions with extreme H and N isotopic anomalies [2-4], possibly due to preserved pristine primordial organic grains. We recently showed that the in the Tagish Lake meteorite, the principle carriers of these anomalies are sub- m, hollow organic globules [5]. The globules likely formed by photochemical processing of organic ices in a cold molecular cloud or the outermost regions of the protosolar disk [5]. We proposed that similar materials should be common among primitive meteorites, IDPs, and comets. Similar objects have been observed in organic extracts of carbonaceous chondrites [6-8], however their N and H isotopic compositions are generally unknown. Bulk H and N isotopic compositions may indicate which meteorites best preserve interstellar organic compounds. Thus, we selected the Bells CM2 carbonaceous chondrites for study based on its large bulk 15N (+335 %) and D (+990 %) [9].

An Amoeboid Olivine Aggregate in LEW 85300

NASA Technical Reports Server (NTRS)

Komatsu, M. D.; Yamaguchi, A.; Fagan, T. J.; Zolensky, M. E.; Shiran, N.; Mikouchi, T.

2016-01-01

Amoeboid Olivine aggregates (AOAs) are irregularly shaped objects commonly observed in carbonaceous chondrites. Because they are composed of fine-grained olivine and Ca-Al-rich minerals, they are sensitive indicators for nebular process and parent body alteration of their parent bodies. Recently an AOA was found in a carbonaceous clast in polymict eucrite LEW 85300. The bulk major element composition of the clast matrix in LEW 85300 suggests a relation to CM, CO and CV chondrites, whereas bulk clast trace and major element compositions do not match any carbonaceous chondrite, suggesting they have a unique origin. Here we characterize the mineralogy of AOA in LEW 85300 and discuss the origin of the carbonaceous clasts. Results and Discussion: The AOA is located in an impact melt vein. Half of the aggregate shows recrystallization textures (euhedral pyroxene and molten metal/FeS) due to impact melting, but the remaining part preserves the original texture. The AOA is composed of olivine, FeS and Mg,Al-phyllosilicate. Individual olivine grains measure 1-8 microns, with Fe-rich rims, probably due to impact heating. Olivines in the AOA are highly forsteritic (Fo95-99), indicating that the AOA escaped thermal metamorphism [4]. Although no LIME (Low-Fe, Mn-Enriched) olivine is observed, forsterite composition and the coexistence of Mg,Al-phyllosilicate suggest that the AOA is similar to those in the Bali-type oxidized CV (CVoxB) and CR chondrites. However, it should be noted that fayalitic olivine, which commonly occurs in CVoxB AOA, is not observed in this AOA. Also, the smaller grain size (<8 microns) of olivine suggests they may be related to CM or CO chondrites. Therefore, we cannot exclude the possibility that the AOA originated from a unique carbonaceous chondrite.

The Effect of Aqueous Alteration in Antarctic Carbonaceous Chondrites from Comparative ICP-MS Bulk Chemistry

NASA Technical Reports Server (NTRS)

Alonso-Azcarate, J.; Trigo-Rodriguez, J. M.; Moyano-Cambero, C. E.; Zolensky, M.

2014-01-01

Terrestrial ages of Antarctic carbonaceous chondrites (CC) indicate that these meteorites have been preserved in or on ice for, at least, tens of thousands of years. Due to the porous structure of these chondrites formed by the aggregation of silicate-rich chondrules, refractory inclusions, metal grains, and fine-grained matrix materials, the effect of pervasive terrestrial water is relevant. Our community defends that pristine CC matrices are representing samples of scarcely processed protoplanetary disk materials as they contain stellar grains, but they might also trace parent body processes. It is important to study the effects of terrestrial aqueous alteration in promoting bulk chemistry changes, and creating distinctive alteration minerals. Particularly because it is thought that aqueous alteration has particularly played a key role in some CC groups in modifying primordial bulk chemistry, and homogenizing the isotopic content of fine-grained matrix materials. Fortunately, the mineralogy produced by parent-body and terrestrial aqueous alteration processes is distinctive. With the goal to learn more about terrestrial alteration in Antarctica we are obtaining reflectance spectra of CCs, but also performing ICP-MS bulk chemistry of the different CC groups. A direct comparison with the mean bulk elemental composition of recovered falls might inform us on the effects of terrestrial alteration in finds. With such a goal, in the current work we have analyzed some members representative of CO and CM chondrite groups.

Properties of the Guin ungrouped iron meteorite - The origin of Guin and of group-IIE irons

NASA Astrophysics Data System (ADS)

Rubin, A. E.; Jerde, E. A.; Zong, P.; Wasson, J. T.; Westcott, J. W.; Mayeda, T. K.; Clayton, R. N.

1986-01-01

The composition and structure of the Guin ungrouped iron meteorite inclusions have been investigated experimentally. The structural characteristics of polished and etched slabs of the meteorite were studied microscopically in reflected light. Modal abundances of troilite nodules and silicate inclusions were determined by weighing paper traces. The bulk composition of the silicate inclusions was calculated by combining modal phase abundances and mineral compositions. It is found that the largest silicate inclusion (2 x 4 cm) consists mostly of a shock-melted plagioclase-rich matrix surrounding large, partly melted augite grains. The oxygen isotopic composition of the inclusion is near that of LL chondrites. The inclusion is found to be similar in composition to selected melt pocket glasses in ordinary chondrites produced in situ by preferential melting of plagioclase rock due to shock compression. It is suggested that the Guin assemblage was formed by impact melting on a chondritic parent body. Silicate inclusions in IIE irons share many of the compositional and petrological characteristics of the Guin inclusions, indicating that IIE irons also formed by impact-melting of chondritic materials. Black and white photomicrographs of the silicate inclusions are provided.

Petrology and thermal history of type IA chondrules in the Semarkona (LL3.0) chondrite

NASA Technical Reports Server (NTRS)

Jones, R. H.; Scott, E. R. D.

1989-01-01

Detailed petrologic studies have been made of 15 type IA, Fe-poor, porphyritic olivine chondrules in Semarkona (LL3.0). Major and minor element concentrations in olivines, pyroxenes, and mesostases, and bulk composition so the chondrules are measured along with zoning profiles in the olivine and pyroxene crystals. The mineral compositions and textures are best interpreted in terms of closed system crystallization in which the olivines and pyroxenes crystallized in situ from a melt corresponding to the bulk composition of the chondrule. Relict olivine grains are not found in the chondrules. Crystallization probably occurred at a cooling rate of the order of 1000 C/hr. Precursor materials of the chondrules were composed of two components, one refractory Ca-, Al-, and Ti-rich, and one less refractory Si-, Fe-, Cr-, and Mn-rich. The evidence is consistent with Semarkona being one of the least metamorphosed ordinary chondrites.

The Evolution of the EH4 Chondrite Indarch at High Pressure and Temperature: The First Experimental Results

NASA Technical Reports Server (NTRS)

Berthet, S.; Malavergne, V.; Righter, K.; Corgne, A.; Combes, R.

2006-01-01

Chondrite groups are characterized by variations in bulk composition and oxidation state, illustrating in part heterogeneity in the early solar nebula. Planetary accretion could be explained by at least two different scenarios: the homogeneous [1] and heterogeneous accretion models [2, 3]. In particular, for the formation of the Earth, some studies (e.g. [2, 3]) assume that one component is highly reduced material comparable to enstatite chondrites, devoid of volatile elements but containing all other elements in C1 abundance ratios. To derive constraints on the understanding of early differentiation processes, studies of the silicate phase relations and their interactions with metal, at relevant P-T-fO2, are required. Melting relations and equilibrium partitioning behaviour have been studied on peridotitic and chondritic starting compositions at pressures and temperatures corresponding to the transition zone and lower mantle [4, 5, 6]. However, enstatite chondrites, which are highly reduced primitive meteorites, have not yet been studied experimentally under such conditions. Thus, multianvil experiments have been performed at 20-25 GPa and 2000-2400 C on the EH4 chondrite Indarch.

Silicon in Mars' Core: A Prediction Based on Mars Model Using Nitrogen and Oxygen Isotopes in SNC Meteorites

NASA Technical Reports Server (NTRS)

Mohapatra, R. K.; Murty, S. V. S.

2002-01-01

Chemical and (oxygen) isotopic compositions of SNC meteorites have been used by a number of workers to infer the nature of precursor materials for the accretion of Mars. The idea that chondritic materials played a key role in the formation of Mars has been the central assumption in these works. Wanke and Dreibus have proposed a mixture of two types of chondritic materials, differing in oxygen fugacity but having CI type bulk chemical composition for the nonvolatile elements, for Mars' precursor. But a number of studies based on high pressure and temperature melting experiments do not favor a CI type bulk planet composition for Mars, as it predicts a bulk planet Fe/Si ratio much higher than that reported from the recent Pathfinder data. Oxygen forms the bulk of Mars (approximately 40% by wt.) and might provide clues to the type of materials that formed Mars. But models based on the oxygen isotopic compositions of SNC meteorites predict three different mixtures of precursor materials for Mars: 90% H + 10% CM, 85% H + 11% CV + 4% CI and 45% EH + 55% H. As each of these models has been shown to be consistent with the bulk geophysical properties (such as mean density, and moment of inertia factor) of Mars, the nature of the material that accreted to form Mars remains ambiguous.

Relationships Among Intrinsic Properties of Ordinary Chondrites: Oxidation State, Bulk Chemistry, Oxygen-isotopic Composition, Petrologic Type, and Chondrule Size

NASA Technical Reports Server (NTRS)

Rubin, Alan E.

2006-01-01

The properties of ordinary chondrites (OC) reflect both nebular and asteroidal processes. OC are modeled here as having acquired nebular water, probably contained within phyllosilicates, during agglomeration. This component had high Ai70 and acted like an oxidizing agent during thermal metamorphism. The nebular origin of this component is consistent with negative correlations in H, L, and LL chondrites between oxidation state (represented by olivine Fa) and bulk concentration ratios of elements involved in the metal-silicate fractionation (e.g., NdSi, Ir/Si, Ir/Mn, Ir/Cr, Ir/Mg, Ni/Mg, As/Mg, Ga/Mg). LL chondrites acquired the greatest abundance of phyllosilicates with high (delta)O-17 among OC (and thus became the most oxidized group and the one with the heaviest O isotopes); H chondrites acquired the lowest abundance, becoming the most reduced OC group with the lightest O isotopes. Chondrule precursors may have grown larger and more ferroan with time in each OC agglomeration zone. Nebular turbulence may have controlled the sizes of chondrule precursors. H-chondrite chondrules (which are the smallest among OC) formed from the smallest precursors. In each OC region, low-FeO chondrules formed before high-FeO chondrules during repeated episodes of chondrule formation. During thermal metamorphism, phyllosilicates were dehydrated; the liberated water oxidized metallic Fe-Ni. This caused correlated changes with petrologic type including decreases in the modal abundance of metal, increases in olivine Fa and low-Ca pyroxene Fs, increases in the olivine/pyroxene ratio, and increases in the kamacite Co and Ni contents. As water (with its heavy 0 isotopes) was lost during metamorphism, inverse correlations between bulk (delta)O-18 and bulk (delta)O-17 with petrologic type were produced. The H5 chondrites that were ejected from their parent body approx.7.5 Ma ago during a major impact event probably had been within a few kilometers of each other since they accreted approx.4.5 Ga ago. There are significant differences in the olivine compositional distributions among these rocks; these reflect stochastic nebular sampling of the oxidant (Le., phyllosilicates with high (delta)O-17) on a 0.1-1 km scale during agglomeration.

The provenances of asteroids, and their contributions to the volatile inventories of the terrestrial planets.

PubMed

Alexander, C M O'D; Bowden, R; Fogel, M L; Howard, K T; Herd, C D K; Nittler, L R

2012-08-10

Determining the source(s) of hydrogen, carbon, and nitrogen accreted by Earth is important for understanding the origins of water and life and for constraining dynamical processes that operated during planet formation. Chondritic meteorites are asteroidal fragments that retain records of the first few million years of solar system history. The deuterium/hydrogen (D/H) values of water in carbonaceous chondrites are distinct from those in comets and Saturn's moon Enceladus, implying that they formed in a different region of the solar system, contrary to predictions of recent dynamical models. The D/H values of water in carbonaceous chondrites also argue against an influx of water ice from the outer solar system, which has been invoked to explain the nonsolar oxygen isotopic composition of the inner solar system. The bulk hydrogen and nitrogen isotopic compositions of CI chondrites suggest that they were the principal source of Earth's volatiles.

Chemical compositions and classifica tion of five thermally altered carbonaceous chondrites

NASA Astrophysics Data System (ADS)

Noronha, Bianca A.; Friedrich, Jon M.

2014-08-01

To establish the chemical group provenance of the five thermally altered carbonaceous chondrites Asuka (A-) 881551, Asuka-882113, Elephant Moraine (EET) 96026, Mulga (west), and Northwest Africa (NWA) 3133, we quantified 44 trace elements in each of them. We also analyzed Larkman Nunatak (LAR) 04318 (CK4), Miller Range (MIL) 090001 (CR2), Roberts Massif (RBT) 03522 (CK5) as reference samples as their chemical group affinity is already recognized. We conclude that Asuka-881551, Asuka-882113, and Mulga (west) are thermally metamorphosed CK chondrites. Compositionally, Elephant Moraine 96026 most resembles the CV chondrites. NWA 3133 is the most significantly thermally altered carbonaceous chondrite in our suite of samples. It is completely recrystallized (no chondrules or matrix remain), but its bulk composition is consistent with a CV-CK clan provenance. The thermally labile element (e.g., Se, Te, Zn, and Bi) depletion in NWA 3133 indicates a chemically open system during the heating episode. It remains unclear if the heat necessary for its thermal alteration of NWA 3133 was due to the decay of 26Al or was impact related. Finally, we infer that MIL 090001, Mulga (west), and NWA 3133 show occasional compositional signatures indicative of terrestrial alteration. The alteration is especially evident within the elements Sr, Ba, La, Ce, Th, U, and possibly Sb. Despite the alteration, we can still confidently place each of the altered chondrites within an established chemical group or clan.

Evolution of Indarch (EH4 Chondrite) at 1 GPa and High Temperature

NASA Technical Reports Server (NTRS)

Berthet, S.; Malavergne, V.; Righter, K.

2008-01-01

The chondritic meteorites are materials that are as old as the solar system itself characterized by variations in bulk chemical and oxidation state, and have long been considered possible building blocks that accreted to form the terrestrial inner planets. Enstatite chondrites contain nearly FeO free enstatite, silicon-rich kamacite and various sulfides indicating formation under highly reducing conditions. These materials could have participated in the formation of the Earth. However, "fingerprinting" of meteoritic materials has shown that no known meteoritic class corresponds to a hypothetical bulk Earth composition in every aspect. To derive constraints on early accretion and differentiation processes and possibly resolve the debate on the formation of the Earth, it is required to study experimentally a variety of chondritic materials and investigate their melting relations and elemental partitioning behavior at variable pressure (P), temperature (T) and oxygen fugacities (fO2). Variations in fO2 can indeed change chemical features and phase equilibria dramatically. The P-T phase diagrams of peridotites and carbonaceous chondrites have been extensively studied experimentally up to pressures and temperatures corresponding to the transition zone and lower mantle. Even though partial melting experiments have been conducted at ambient pressure on the enstatite chondrite Indarch, enstatite meteorites have never been experimentally investigated at high PT. The following investigation focuses on the effect of the fO2 on the phase relations of Indarch, an EH4 chondrite.

Isotopic evidence for primordial molecular cloud material in metal-rich carbonaceous chondrites.

PubMed

Van Kooten, Elishevah M M E; Wielandt, Daniel; Schiller, Martin; Nagashima, Kazuhide; Thomen, Aurélien; Larsen, Kirsten K; Olsen, Mia B; Nordlund, Åke; Krot, Alexander N; Bizzarro, Martin

2016-02-23

The short-lived (26)Al radionuclide is thought to have been admixed into the initially (26)Al-poor protosolar molecular cloud before or contemporaneously with its collapse. Bulk inner Solar System reservoirs record positively correlated variability in mass-independent (54)Cr and (26)Mg*, the decay product of (26)Al. This correlation is interpreted as reflecting progressive thermal processing of in-falling (26)Al-rich molecular cloud material in the inner Solar System. The thermally unprocessed molecular cloud matter reflecting the nucleosynthetic makeup of the molecular cloud before the last addition of stellar-derived (26)Al has not been identified yet but may be preserved in planetesimals that accreted in the outer Solar System. We show that metal-rich carbonaceous chondrites and their components have a unique isotopic signature extending from an inner Solar System composition toward a (26)Mg*-depleted and (54)Cr-enriched component. This composition is consistent with that expected for thermally unprocessed primordial molecular cloud material before its pollution by stellar-derived (26)Al. The (26)Mg* and (54)Cr compositions of bulk metal-rich chondrites require significant amounts (25-50%) of primordial molecular cloud matter in their precursor material. Given that such high fractions of primordial molecular cloud material are expected to survive only in the outer Solar System, we infer that, similarly to cometary bodies, metal-rich carbonaceous chondrites are samples of planetesimals that accreted beyond the orbits of the gas giants. The lack of evidence for this material in other chondrite groups requires isolation from the outer Solar System, possibly by the opening of disk gaps from the early formation of gas giants.

Isotopic evidence for primordial molecular cloud material in metal-rich carbonaceous chondrites

PubMed Central

Van Kooten, Elishevah M. M. E.; Wielandt, Daniel; Schiller, Martin; Nagashima, Kazuhide; Thomen, Aurélien; Olsen, Mia B.; Nordlund, Åke; Krot, Alexander N.; Bizzarro, Martin

2016-01-01

The short-lived 26Al radionuclide is thought to have been admixed into the initially 26Al-poor protosolar molecular cloud before or contemporaneously with its collapse. Bulk inner Solar System reservoirs record positively correlated variability in mass-independent 54Cr and 26Mg*, the decay product of 26Al. This correlation is interpreted as reflecting progressive thermal processing of in-falling 26Al-rich molecular cloud material in the inner Solar System. The thermally unprocessed molecular cloud matter reflecting the nucleosynthetic makeup of the molecular cloud before the last addition of stellar-derived 26Al has not been identified yet but may be preserved in planetesimals that accreted in the outer Solar System. We show that metal-rich carbonaceous chondrites and their components have a unique isotopic signature extending from an inner Solar System composition toward a 26Mg*-depleted and 54Cr-enriched component. This composition is consistent with that expected for thermally unprocessed primordial molecular cloud material before its pollution by stellar-derived 26Al. The 26Mg* and 54Cr compositions of bulk metal-rich chondrites require significant amounts (25–50%) of primordial molecular cloud matter in their precursor material. Given that such high fractions of primordial molecular cloud material are expected to survive only in the outer Solar System, we infer that, similarly to cometary bodies, metal-rich carbonaceous chondrites are samples of planetesimals that accreted beyond the orbits of the gas giants. The lack of evidence for this material in other chondrite groups requires isolation from the outer Solar System, possibly by the opening of disk gaps from the early formation of gas giants. PMID:26858438

Ca-,Al-rich inclusions in the unique chondrite ALH85085 - Petrology, chemistry, and isotopic compositions

NASA Technical Reports Server (NTRS)

Kimura, Makoto; El-Goresy, Ahmed; Palme, Herbert; Zinner, Ernst

1993-01-01

A comprehensive study is performed for the Ca-,Al-rich inclusions (CAIs) in the unique chondrite ALH85085. The ALH85085 inclusions are smaller (5-80 microns) and more refractory than their counterparts in carbonaceous chondrites. The study includes 42 inclusions for petrography and mineralogy, 15 for bulk major and minor element chemical composition, six for Mg-Al isotopic systematics, 10 for Ca isotopes, nine for Ti isotopes, and six for trace element abundances. In addition, oxygen-isotopic compositions were determined in minerals from a single inclusion. No correlation is found between mineralogy, major element chemistry, and trace element abundances. It is further shown that the high-temperature geochemical behavior of ultrarefractory trace elements is decoupled from that of the major elements Ca and Ti (Ti is correlated with the relatively volatile elements Nb and Yb) implying that perovskite is of only minor importance as carrier of ultrarefractories.

147Sm-143Nd systematics of Earth are inconsistent with a superchondritic Sm/Nd ratio

PubMed Central

Huang, Shichun; Jacobsen, Stein B.; Mukhopadhyay, Sujoy

2013-01-01

The relationship between the compositions of the Earth and chondritic meteorites is at the center of many important debates. A basic assumption in most models for the Earth’s composition is that the refractory elements are present in chondritic proportions relative to each other. This assumption is now challenged by recent 142Nd/144Nd ratio studies suggesting that the bulk silicate Earth (BSE) might have an Sm/Nd ratio 6% higher than chondrites (i.e., the BSE is superchondritic). This has led to the proposal that the present-day 143Nd/144Nd ratio of BSE is similar to that of some deep mantle plumes rather than chondrites. Our reexamination of the long-lived 147Sm-143Nd isotope systematics of the depleted mantle and the continental crust shows that the BSE, reconstructed using the depleted mantle and continental crust, has 143Nd/144Nd and Sm/Nd ratios close to chondritic values. The small difference in the ratio of 142Nd/144Nd between ordinary chondrites and the Earth must be due to a process different from mantle-crust differentiation, such as incomplete mixing of distinct nucleosynthetic components in the solar nebula. PMID:23479630

High-precision Mg isotopic systematics of bulk chondrites

NASA Astrophysics Data System (ADS)

Schiller, Martin; Handler, Monica R.; Baker, Joel A.

2010-08-01

Variations of the mass-independent abundance of 26Mg ( δ26Mg*) and stable Mg ( δ25Mg) isotope composition of chondrites are important because they constrain the homogeneity of 26Al and Mg isotopes in the proto-planetary disc and the validity of the short-lived 26Al-to- 26Mg chronometer applied to meteorites. We present high-precision Mg isotope data and Al/Mg ratios of chondrites representing nearly all major chondrite classes, including a step-leaching experiment on the CM2 chondrite Murchison. δ26Mg* variations in leachates of Murchison representing acid soluble material are ≤ 30 times smaller than reported for neutron-rich isotopes of Ti and Cr and do not reveal resolvable deficits in δ26Mg* (-0.002 to + 0.118‰). Very small variations in δ26Mg* anomalies in bulk chondrites (-0.006 to + 0.019‰) correlate with increasing 27Al/ 24Mg ratios and δ50Ti, reflecting the variable presence of calcium-aluminium-rich inclusions (CAIs) in some types of carbonaceous chondrites. Similarly, release of radiogenic 26Mg produced by 26Al decay from CAI material in the step-leaching of Murchison best explains the high δ26Mg* observed in the last, aggressive, leaching steps of this experiment. Overall, the observed variations in δ26Mg* are small and potential differences beyond that which result from the presence of CAI-like material cannot be detected within the analytical uncertainties of this study (± 0.004‰). The results do not allow radical heterogeneity of 26Al (≥±30%) or measurable Mg nucleosynthetic heterogeneity (≥±0.005‰) to have existed on a planetesimal scale in the proto-planetary disc. Combined with published δ26Mg* data for CAIs, the bulk chondrite data yield a precise initial ( 26Al/ 27Al) 0 = (5.21 ± 0.06) × 10 -5 and δ26Mg* = -0.0340 ± 0.0016‰ for the Solar System. However, it is not possible with the currently available data to determine with certainty whether CAIs and the material from which planetesimals accreted including chondrite parent bodies had precisely the same initial levels of 26Al, although planetesimals and planets appear to have accreted from material with a mean initial ( 26Al/ 27Al) 0 in the range of 2.1 to 6.7 × 10 - 5 . The average stable Mg isotope composition of all analysed chondrites, with the exception of a chondrule from the CBa chondrite Gujba ( δ25Mg DSM-3 = -0.032 ± 0.035‰), is δ25Mg DSM-3 = -0.152 ± 0.079‰ (2 sd) and is indistinguishable from that of the Earth's mantle.

Chemical and mineralogical size segregation in the impact disruption of inhomogeneous, anhydrous meteorites

NASA Astrophysics Data System (ADS)

Flynn, George J.; Durda, Daniel D.

2004-10-01

We performed impact disruption experiments on pieces from eight different anhydrous chondritic meteorites - four weathered ordinary chondrite finds from North Africa (NWA791, NWA620, NWA869 and MOR001), three almost unweathered ordinary chondrite falls (Mbale, Gao, and Saratov), and an almost unweathered carbonaceous chondrite fall (Allende). In each case the impactor was a small (1/8 or 1/4 in) aluminum sphere fired at the meteorite target at ˜5km/s, comparable to the mean collision speed in the main-belt. Some of the ˜5 to ˜150μm debris from each disruption was collected in aerogel capture cells, and the captured particles were analyzed by in situ synchrotron-based X-ray fluorescence. For each meteorite, many of the smallest particles ( <10μm up to 35μm in size, depending on the meteorite) exhibit very high Ni/Fe ratios compared to the Ni/Fe ratios measured in the larger particles (>45μm), a composition consistent with the smallest debris being dominated by matrix material while the larger debris is dominated by fragments from olivine chondrules. These results may explain why the ˜10μm interplanetary dust particles (IDPs) collected from the Earth's stratosphere are C-rich and volatile-rich compared to the presumed solar nebula composition. The ˜10μm IDPs may simply sample the matrix of an inhomogeneous parent body, structurally and mineralogically similar to the chondritic meteorites, which are inhomogeneous assemblages of compact, strong, C- and volatile-poor chondrules that are distributed in a more porous, C- and volatile-rich matrix. In addition, these results may explain why the micrometeorites, which are ˜50μm to millimeters in size, recovered from the polar ices are Ni- and S-poor compared to chondritic meteorites, since these polar micrometeorites may preferentially sample fragments from the Ni- and S-poor olivine chondrules. These results indicate that the average composition of the IDPs may be biased towards the composition of the matrix of the parent body while the average composition of the polar micrometeorites may be more heavily weighted towards the composition of the chondrules and clasts. Thus, neither the IDPs nor the polar micrometeorites may sample the bulk composition of their respective parent bodies. We determined the threshold collisional specific energy (QD*) for these chondritic meteorites to be 1419 J/kg, about twice the value for terrestrial basalt. Comparison of the mass of the largest fragment produced in the disruption of an ˜100g sample of the porous ordinary chondrite Saratov with the largest fragment produced in the disruption of an ˜100g sample of the compact ordinary chondrite MOR001 when each was struck by an impactor having approximately the same kinetic energy confirms that it requires significantly more energy to disrupt a porous target than a non-porous target. These results may also have important implications for the design of spacecraft missions intended to sample the composition and mineralogy of the chondritic asteroids and other inhomogeneous bodies. A Stardust-like spacecraft intended to sample asteroids by collecting only the small debris from a man-made impact onto the asteroid may collect particles that over-sample the matrix of the target and do not provide a representative sample of the bulk composition. The impact collection technique to be employed by the Japanese HAYABUSA (formerly MUSES-C) spacecraft to sample the asteroid Itokawa may result in similar mineral segregation.

Meteorite zircon constraints on the bulk Lu-Hf isotope composition and early differentiation of the Earth.

PubMed

Iizuka, Tsuyoshi; Yamaguchi, Takao; Hibiya, Yuki; Amelin, Yuri

2015-04-28

Knowledge of planetary differentiation is crucial for understanding the chemical and thermal evolution of terrestrial planets. The (176)Lu-(176)Hf radioactive decay system has been widely used to constrain the timescales and mechanisms of silicate differentiation on Earth, but the data interpretation requires accurate estimation of Hf isotope evolution of the bulk Earth. Because both Lu and Hf are refractory lithophile elements, the isotope evolution can be potentially extrapolated from the present-day (176)Hf/(177)Hf and (176)Lu/(177)Hf in undifferentiated chondrite meteorites. However, these ratios in chondrites are highly variable due to the metamorphic redistribution of Lu and Hf, making it difficult to ascertain the correct reference values for the bulk Earth. In addition, it has been proposed that chondrites contain excess (176)Hf due to the accelerated decay of (176)Lu resulting from photoexcitation to a short-lived isomer. If so, the paradigm of a chondritic Earth would be invalid for the Lu-Hf system. Herein we report the first, to our knowledge, high-precision Lu-Hf isotope analysis of meteorite crystalline zircon, a mineral that is resistant to metamorphism and has low Lu/Hf. We use the meteorite zircon data to define the Solar System initial (176)Hf/(177)Hf (0.279781 ± 0.000018) and further to identify pristine chondrites that contain no excess (176)Hf and accurately represent the Lu-Hf system of the bulk Earth ((176)Hf/(177)Hf = 0.282793 ± 0.000011; (176)Lu/(177)Hf = 0.0338 ± 0.0001). Our results provide firm evidence that the most primitive Hf in terrestrial zircon reflects the development of a chemically enriched silicate reservoir on Earth as far back as 4.5 billion years ago.

Meteorite zircon constraints on the bulk Lu−Hf isotope composition and early differentiation of the Earth

PubMed Central

Iizuka, Tsuyoshi; Yamaguchi, Takao; Hibiya, Yuki; Amelin, Yuri

2015-01-01

Knowledge of planetary differentiation is crucial for understanding the chemical and thermal evolution of terrestrial planets. The 176Lu−176Hf radioactive decay system has been widely used to constrain the timescales and mechanisms of silicate differentiation on Earth, but the data interpretation requires accurate estimation of Hf isotope evolution of the bulk Earth. Because both Lu and Hf are refractory lithophile elements, the isotope evolution can be potentially extrapolated from the present-day 176Hf/177Hf and 176Lu/177Hf in undifferentiated chondrite meteorites. However, these ratios in chondrites are highly variable due to the metamorphic redistribution of Lu and Hf, making it difficult to ascertain the correct reference values for the bulk Earth. In addition, it has been proposed that chondrites contain excess 176Hf due to the accelerated decay of 176Lu resulting from photoexcitation to a short-lived isomer. If so, the paradigm of a chondritic Earth would be invalid for the Lu−Hf system. Herein we report the first, to our knowledge, high-precision Lu−Hf isotope analysis of meteorite crystalline zircon, a mineral that is resistant to metamorphism and has low Lu/Hf. We use the meteorite zircon data to define the Solar System initial 176Hf/177Hf (0.279781 ± 0.000018) and further to identify pristine chondrites that contain no excess 176Hf and accurately represent the Lu−Hf system of the bulk Earth (176Hf/177Hf = 0.282793 ± 0.000011; 176Lu/177Hf = 0.0338 ± 0.0001). Our results provide firm evidence that the most primitive Hf in terrestrial zircon reflects the development of a chemically enriched silicate reservoir on Earth as far back as 4.5 billion years ago. PMID:25870298

In search of the Earth-forming reservoir: Mineralogical, chemical, and isotopic characterizations of the ungrouped achondrite NWA 5363/NWA 5400 and selected chondrites

NASA Astrophysics Data System (ADS)

Burkhardt, Christoph; Dauphas, Nicolas; Tang, Haolan; Fischer-GöDde, Mario; Qin, Liping; Chen, James H.; Rout, Surya S.; Pack, Andreas; Heck, Philipp R.; Papanastassiou, Dimitri A.

2017-05-01

High-precision isotope data of meteorites show that the long-standing notion of a "chondritic uniform reservoir" is not always applicable for describing the isotopic composition of the bulk Earth and other planetary bodies. To mitigate the effects of this "isotopic crisis" and to better understand the genetic relations of meteorites and the Earth-forming reservoir, we performed a comprehensive petrographic, elemental, and multi-isotopic (O, Ca, Ti, Cr, Ni, Mo, Ru, and W) study of the ungrouped achondrites NWA 5363 and NWA 5400, for both of which terrestrial O isotope signatures were previously reported. Also, we obtained isotope data for the chondrites Pillistfer (EL6), Allegan (H6), and Allende (CV3), and compiled available anomaly data for undifferentiated and differentiated meteorites. The chemical compositions of NWA 5363 and NWA 5400 are strikingly similar, except for fluid mobile elements tracing desert weathering. We show that NWA 5363 and NWA 5400 are paired samples from a primitive achondrite parent-body and interpret these rocks as restite assemblages after silicate melt extraction and siderophile element addition. Hafnium-tungsten chronology yields a model age of 2.2 ± 0.8 Myr after CAI, which probably dates both of these events within uncertainty. We confirm the terrestrial O isotope signature of NWA 5363/NWA 5400; however, the discovery of nucleosynthetic anomalies in Ca, Ti, Cr, Mo, and Ru reveals that the NWA5363/NWA 5400 parent-body is not the "missing link" that could explain the composition of the Earth by the mixing of known meteorites. Until this "missing link" or a direct sample of the terrestrial reservoir is identified, guidelines are provided of how to use chondrites for estimating the isotopic composition of the bulk Earth.

Aqueous alteration and brecciation in Bells, an unusual, saponite-bearing, CM chondrite

NASA Astrophysics Data System (ADS)

Brearley, Adrian J.

1995-06-01

The petrological and mineralogical characteristics of the unusual CM2 chondrite, Bells, have been investigated in detail by scanning electron microscopy (SEM), electron microprobe analysis (EPMA), and transmission electron microscopy (TEM). Bells is a highly brecciated chondrite which contains few intact chondrules, a very low abundance of refractory inclusions, and is notable in having an unusually high abundance of magnetite, which is disseminated throughout the fine-grained matrix. Fragmental olivines and pyroxenes are common and, based on compositional data, appear to have been derived from chondrules as a result of extensive brecciation. The fine-grained mineralogy of matrix in Bells differs considerably from other CM chondrites and has closer affinities to matrix in CI chondrites. The dominant phases are fine-grained saponite interlayered with serpentine, and phases such as tochilinite and cronstedtite, which are typical of CM chondrite matrices, are entirely absent. Pentlandite, pyrrhotite, magnetite, anhydrite, calcite, and rare Ti-oxides also occur as accessory phases. Based on its oxygen and noble gas isotopic compositions (Zadnik, 1985; Rowe et al., 1994), Bells can be considered to be a CM2 chondrite, although its bulk composition shows some departures from the typical range exhibited by this group. However, these variations in bulk chemistry are entirely consistent with the observed mineralogy of Bells. The unusual fine-grained mineralogy of Bells matrix can be reasonably attributed to the combined effects of aqueous alteration and advanced brecciation in a parent body environment. Extensive brecciation has assisted aqueous alteration by reducing chondrules and mineral grains into progressively smaller grains with high surface areas, which are more susceptible to dissolution reactions involving aqueous fluids. This has resulted in the preferential dissolution of Fe-rich chondrule olivines, which are now completely absent in Bells although present in other CM chondrites. The formation of saponite in Bells probably resulted from the dissolution of relatively silica-rich phases, such as pyroxene and olivine, that were derived from chondrules. The result of such dissolution reactions would be to increase the activity of silica in the fluid phase, at least on a localized scale, stabilizing saponite in preference to serpentine. An increase in aSiO 2 would also have destabilized preexisting cronstedtite which may have reacted to form magnetite and MgFe serpentine under conditions of constant ƒO 2 .

Principal components - Petrology and chemistry of polyphase units in chondritic porous interplanetary dust particles

NASA Astrophysics Data System (ADS)

Rietmeijer, Frans J. M.

1997-03-01

Chondritic porous (CP) interplanetary dust particles (IDPs) can be described as 'cosmic sediments'. It should be possible to recognize in these IDPs the 4500 Myrs old solar nebula dusts. The studies of unaltered chondritic IDPs show that their matrices are a mixture of three different principal components (PCs) that also describe variable C/Si ratios of chondritic IDPs. Among others, PCs include polyphase units (PUs) that are amorphous to holocrystalline, both ultrafine- and coarse-grained, ferromagnesiosilica(te) materials with minor Al and Ca. The properties of PCs and their alteration products define the physical and chemical processes that produced and altered these components. PCs are also cornerstones of IDP classification. For example, the bulk composition of ultrafine-grained PCs can be reconstructed using the 'butterfly method' and also allows an evaluation of the metamorphic signatures, (e.g., dynamic pyrometamorphism), in chondritic IDPs.

Mineralogy, petrology and geochemistry of carbonaceous chondritic clasts in the LEW 85300 polymict eucrite

NASA Technical Reports Server (NTRS)

Zolensky, M. E.; Hewins, R. H.; Mittlefehldt, D. W.; Lindstrom, M. M.; Xiao, X.; Lipschutz, M. E.

1992-01-01

We have performed a detailed petrologic and mineralogic study of two chondritic clasts from the polymict eucrite Lewis Cliff (LEW) 85300, and performed chemical analyses by INAA and RNAA on one of these. Petrologically, the clasts are identified and are composed of dispersed aggregates, chondrules, and chondrule fragments supported by matrix. The aggregates and chondrules are composed of olivine, orthopyroxene, plus some diopside. The matrix consists of fine-grained olivine, and lesser orthopyroxene and augite. Fine-grained saponite is common in the matrix. The bulk major composition of the clast studied by INAA and RNAA shows unusual abundance patterns for lithophile, siderophile and chalcophile elements but is basically chondritic. The INAA/RNAA data preclude assignment of the LEW 85300,15 clast to any commonly accepted group of carbonaceous chondrite.

Textural variability of ordinary chondrite chondrules: Implications of their formation

NASA Technical Reports Server (NTRS)

Zinovieva, N. G.; Mitreikina, O. B.; Granovsky, L. B.

1994-01-01

Scanning electron microscopy (SEM) and microprobe examination of the Raguli H3-4, Saratov L3, and Fucbin L5-6 ordinary chondrites and the analysis of preexisted data on other meteorites have shown that the variety of textural types of chondrules depends on the chemical composition of the chondrules. The comparison of bulk-rock chemistries of the chondrules by major components demonstrates that they apparently fall, like basic-ultrabasic rock, into groups of dunitic and pyroxenitic composition. This separation is further validated by the character of zoning in chondrules of the intermediate, peridotitic type. The effect is vividly demonstrated by the 'chondrule-in-chondrule' structure.

Super-chondritic Sm/Nd ratios in Mars, the Earth and the Moon.

PubMed

Caro, Guillaume; Bourdon, Bernard; Halliday, Alex N; Quitté, Ghylaine

2008-03-20

Small isotopic differences in the atomic abundance of neodymium-142 (142Nd) in silicate rocks represent the time-averaged effect of decay of formerly live samarium-146 (146Sm) and provide constraints on the timescales and mechanisms by which planetary mantles first differentiated. This chronology, however, assumes that the composition of the total planet is identical to that of primitive undifferentiated meteorites called chondrites. The difference in the 142Nd/144Nd ratio between chondrites and terrestrial samples may therefore indicate very early isolation (<30 Myr from the formation of the Solar System) of the upper mantle or a slightly non-chondritic bulk Earth composition. Here we present high-precision 142Nd data for 16 martian meteorites and show that Mars also has a non-chondritic composition. Meteorites belonging to the shergottite subgroup define a planetary isochron yielding an age of differentiation of 40 +/- 18 Myr for the martian mantle. This isochron does not pass through the chondritic reference value (100 x epsilon(142)Nd = -21 +/- 3; 147Sm/144Nd = 0.1966). The Earth, Moon and Mars all seem to have accreted in a portion of the inner Solar System with approximately 5 per cent higher Sm/Nd ratios than material accreted in the asteroid belt. Such chemical heterogeneities may have arisen from sorting of nebular solids or from impact erosion of crustal reservoirs in planetary precursors. The 143Nd composition of the primitive mantle so defined by 142Nd is strikingly similar to the putative endmember component 'FOZO' characterized by high 3He/4He ratios.

Hydrogen and major element concentrations on 433 Eros: Evidence for an L- or LL-chondrite-like surface composition.

PubMed

Peplowski, Patrick N; Bazell, David; Evans, Larry G; Goldsten, John O; Lawrence, David J; Nittler, Larry R

2015-03-01

A reanalysis of NEAR X-ray/gamma-ray spectrometer (XGRS) data provides robust evidence that the elemental composition of the near-Earth asteroid 433 Eros is consistent with the L and LL ordinary chondrites. These results facilitated the use of the gamma-ray measurements to produce the first in situ measurement of hydrogen concentrations on an asteroid. The measured value, 1100-700+1600 ppm, is consistent with hydrogen concentrations measured in L and LL chondrite meteorite falls. Gamma-ray derived abundances of hydrogen and potassium show no evidence for depletion of volatiles relative to ordinary chondrites, suggesting that the sulfur depletion observed in X-ray data is a surficial effect, consistent with a space-weathering origin. The newfound agreement between the X-ray, gamma-ray, and spectral data suggests that the NEAR landing site, a ponded regolith deposit, has an elemental composition that is indistinguishable from the mean surface. This observation argues against a pond formation process that segregates metals from silicates, and instead suggests that the differences observed in reflectance spectra between the ponds and bulk Eros are due to grain size differences resulting from granular sorting of ponded material.

A nondestructive analytical method for stone meteorites and a controversial discrepancy

NASA Astrophysics Data System (ADS)

Fredriksson, K.; Brenner, P. R.; Fredriksson, B. J.; Olsen, E.

1997-01-01

A method is described for whole rock analyses of major elements in stone meteorites using the electron microprobe and requiring only powdering of the sample, most of which can be retrieved after analysis for additional analytical studies, such as INAA, RNAA and oxygen isotope analysis. Whole individual chondrules of _ 1 milligram can be analyzed. The method is especially attractive for meteorites in short supply, or of great rarity. A total of 398 meteorites were analyzed by this method. The results compare favorably with wet chemical analyses. A study was made of seventeen ordinary chondrites to compare their whole rock (metal free) compositions with the averaged compositions of eleven to thirty-eight of their respective individual chondrules (a total of 374 chondrules). The oxide ratio Al2O3/CaO is generally lower in chondrules than in their respective chondrites, the disparity being larger for petrographic grade 5 than for grade 3. Ordinary chondrites are not simply the sum of their respective chondrules. Furthermore, correlations between CaO, Al2O3 and TiO2 are strong for chondrules in unequilibrated chondrites and nonexistent in equilibrated chondrites. Also H, L and LL chondrite groups have similar bulk compositions within their respective groups, in spite of the different proportions of chondrules, kinds of chondrules, chondrule debris and matrix. All this brings into question the metamorphic classification in which high petrographic grades are the metamorphosed equivalents of low petrographic grades.

Formation of Apollo 16 impactites and the composition of late accreted material: Constraints from Os isotopes, highly siderophile elements and sulfur abundances

NASA Astrophysics Data System (ADS)

Gleißner, Philipp; Becker, Harry

2017-03-01

Fe-Ni metal-schreibersite-troilite intergrowths in Apollo 16 impact melt rocks and new highly siderophile element (HSE) and S abundance data indicate that millimeter-scale closed-system fractional crystallization processes during cooling of impactor-derived metal melt droplets in impact-melts are the main reason for compositional variations and strong differences in abundances and ratios of HSE in multiple aliquots from Apollo 16 impact melt rocks. Element ratios obtained from linear regression of such data are therefore prone to error, but weighted averages take into account full element budgets in the samples and thus represent a more accurate estimate of their impactor contributions. Modeling of solid metal-liquid metal partitioning in the Fe-Ni-S-P system and HSE patterns in impactites from different landing sites suggest that bulk compositions of ancient lunar impactites should be representative of impact melt compositions and that large-scale fractionation of the HSE by in situ segregation of solid metal or sulfide liquid in impact melt sheets most likely did not occur. The compositional record of lunar impactites indicates accretion of variable amounts of chondritic and non-chondritic impactor material and the mixing of these components during remelting of earlier ejecta deposits. The non-chondritic composition appears most prominently in some Apollo 16 impactites and is characterized by suprachondritic HSE/Ir ratios which increase from refractory to moderately volatile HSE and exhibit a characteristic enrichment of Ru relative to Pt. Large-scale fractional crystallization of solid metal from sulfur and phosphorous rich metallic melt with high P/S in planetesimal or embryo cores is currently the most likely process that may have produced these compositions. Similar materials or processes may have contributed to the HSE signature of the bulk silicate Earth (BSE).

Early inner solar system origin for anomalous sulfur isotopes in differentiated protoplanets.

PubMed

Antonelli, Michael A; Kim, Sang-Tae; Peters, Marc; Labidi, Jabrane; Cartigny, Pierre; Walker, Richard J; Lyons, James R; Hoek, Joost; Farquhar, James

2014-12-16

Achondrite meteorites have anomalous enrichments in (33)S, relative to chondrites, which have been attributed to photochemistry in the solar nebula. However, the putative photochemical reactions remain elusive, and predicted accompanying (33)S depletions have not previously been found, which could indicate an erroneous assumption regarding the origins of the (33)S anomalies, or of the bulk solar system S-isotope composition. Here, we report well-resolved anomalous (33)S depletions in IIIF iron meteorites (<-0.02 per mil), and (33)S enrichments in other magmatic iron meteorite groups. The (33)S depletions support the idea that differentiated planetesimals inherited sulfur that was photochemically derived from gases in the early inner solar system (<∼2 AU), and that bulk inner solar system S-isotope composition was chondritic (consistent with IAB iron meteorites, Earth, Moon, and Mars). The range of mass-independent sulfur isotope compositions may reflect spatial or temporal changes influenced by photochemical processes. A tentative correlation between S isotopes and Hf-W core segregation ages suggests that the two systems may be influenced by common factors, such as nebular location and volatile content.

Fractionation of highly siderophile and chalcogen elements in components of EH3 chondrites

NASA Astrophysics Data System (ADS)

Kadlag, Yogita; Becker, Harry

2015-07-01

Abundances of highly siderophile elements (HSE: Re, platinum group elements and Au), chalcogens (Te, Se and S), 187Os/188Os and the major and minor elements Mg, Ca, Mn, Fe, Ni and Co were determined in the components of Sahara 97072 (EH3, find) and Kota Kota (EH3, find) in order to understand the element fractionation processes. In a 187Re-187Os isochron diagram, most magnetic components lie close to the 4.56 Ga IIIA iron meteorite isochron, whereas most other components show deviations from the isochron caused by late redistribution of Re, presumably during terrestrial weathering. Metal- and sulfide rich magnetic fractions and metal-sulfide nodules are responsible for the higher 187Os/188Os in bulk rocks of EH chondrites compared to CI chondrites. The HSE and chalcogens are enriched in magnetic fractions relative to slightly magnetic and nonmagnetic fractions and bulk compositions, indicating that Fe-Ni metal is the main host phase of the HSE in enstatite chondrites. HSE abundance patterns indicate mixing of two components, a CI chondrite like end member and an Au-enriched end member. Because of the decoupled variations of Au from those of Pd or the chalcogens, the enrichment of Au in EH metal cannot be due to metal-sulfide-silicate partitioning processes. Metal and sulfide rich nodules may have formed by melting and reaction of pre-existing refractory element rich material with volatile rich gas. A complex condensation and evaporation history is required to account for the depletion of elements having very different volatility than Au in EH chondrites. The depletions of Te relative to HSE, Se and S in bulk EH chondrites are mainly caused by the depletion of Te in metal. S/Se and S/Mn are lower than in CI chondrites in almost all components and predominantly reflect volatility-controlled loss of sulfur. The latter most likely occurred during thermal processing of dust in the solar nebula (e.g., during chondrule formation), followed by the non-systematic loss of S during terrestrial weathering.

On the origin and composition of Theia: Constraints from new models of the Giant Impact

NASA Astrophysics Data System (ADS)

Meier, M. M. M.; Reufer, A.; Wieler, R.

2014-11-01

Knowing the isotopic composition of Theia, the proto-planet which collided with the Earth in the Giant Impact that formed the Moon, could provide interesting insights on the state of homogenization of the inner Solar System at the late stages of terrestrial planet formation. We use the known isotopic and modeled chemical compositions of the bulk silicate mantles of Earth and Moon and combine them with different Giant Impact models, to calculate the possible ranges of isotopic composition of Theia in O, Si, Ti, Cr, Zr and W in each model. We compare these ranges to the isotopic composition of carbonaceous chondrites, Mars, and other Solar System materials. In the absence of post-impact isotopic re-equilibration, the recently proposed high angular momentum models of the Giant Impact ("impact-fission", Cúk, M., Stewart, S.T. [2012]. Science 338, 1047; and "merger", Canup, R.M. [2012]. Science 338, 1052) allow - by a narrow margin - for a Theia similar to CI-chondrites, and Mars. The "hit-and-run" model (Reufer, A., Meier, M.M.M., Benz, W., Wieler, R. [2012]. Icarus 221, 296-299) allows for a Theia similar to enstatite-chondrites and other Earth-like materials. If the Earth and Moon inherited their different mantle FeO contents from the bulk mantles of the proto-Earth and Theia, the high angular momentum models cannot explain the observed difference. However, both the hit-and-run as well as the classical or "canonical" Giant Impact model naturally explain this difference as the consequence of a simple mixture of two mantles with different FeO. Therefore, the simplest way to reconcile the isotopic similarity, and FeO dissimilarity, of Earth and Moon is a Theia with an Earth-like isotopic composition and a higher (∼20%) mantle FeO content.

Evidence for extreme Ti-50 enrichments in primitive meteorites

NASA Technical Reports Server (NTRS)

Fahey, A.; Mckeegan, K. D.; Zinner, E.; Goswami, J. N.

1985-01-01

The results of the first high mass resolution ion microprobe study of Ti isotopic compositions in individual refractory grains from primitive carbonaceous meteorites are reported. One hibonite from the Murray carbonaceous chondrite has a 10 percent excess of Ti-50, 25 times higher than the maximum value previously reported for bulk samples of refractory inclusions from carbonaceous chondrites. The variation of the Ti compositions between different hibonite grains, and among pyroxenes from a single Allende refractory inclusion, indicates isotopic inhomogeneities over small scale lengths in the solar nebula and emphasizes the importance of the analysis of small individual phases. This heterogeneity makes it unlikely that the isotopic anomalies were carried into the solar system in the gas phase.

Spinel-Bearing, Al-Rich Chrondrules in the Unequilibrated Ordinary Chondrite NWA7402

NASA Technical Reports Server (NTRS)

Ross, D. K.; Simon, J. I.; Cato, M. J.

2017-01-01

Several Al-rich chondrules (ARCs) have been discovered in the unequilibrated ordinary chondrite NWA7402. Two of these three ARCs are spinel-bearing. Here we have characterized these unusual chondrules with respect to their mineralogy and bulk compositions. These objects will be targets for future O and Mg isotope analysis. NWA7402 is clearly unequilibrated, with wide ranges of olivine compositions in chondrules (Fo99-Fo70, excluding rims). Chromium-oxide contents in olivine, and Raman organic spectral parameters support the classification of this meteorite as petrologic type 3.1 [1]. NWA7402 is similar to, and could be paired with NWA5717, in that they both possess light and dark lithologies.

Non-CI refractory lithophile abundances in bulk planetary materials

NASA Astrophysics Data System (ADS)

Dauphas, N.

2015-12-01

Refractory inclusions in meteorites show evidence for fractionation of refractory lithophile elements relative to one another. For bulk planetary materials, it is most often assumed that refractory lithophile elements (e.g., Ca, Al, Ti, REEs) are in proportions similar to CI carbonaceous chondrites, which is taken to be a proxy for solar composition. A diagnostic feature of REE patterns in refractory inclusions in meteorites is the presence of thulium anomalies, arising from the fact that this heavy REE is more volatile than the highly refractory HREEs surrounding it (Tm/Tm* is defined relative to either Er-Yb or Er-Lu). Tm anomalies thus represent an excellent diagnostic tool to test the assumption that refractory lithophile elements have uniform relative abundances at a bulk planetary scale. Prior to this work, high precision Tm measurements were lacking because it is mono-isotopic and as such is not amenable to high-precision single spike measurements. We have developed a multi-collector REE abundance measurement technique to measure all REEs at high precision, including the mono-isotopic ones. This technique was used to revise the abundance of CI and PAAS REE abundances (Pourmand et al. 2012) and the CI composition agrees well with an independent study (Barrat et al. 2012). The same technique was applied to measure REE patterns in 41 chondrites as well as terrestrial rocks (Dauphas and Pourmand, 2015). Our results reveal the presence of Tm anomalies of about -4.5 % in terrestrial rocks, enstatite and ordinary chondrites, relative to carbonaceous chondrites including CIs. This demonstrates that the assumption that refractory lithophile elements are in constant proportions among planetary bodies is unwarranted. It also shows that carbonaceous chondrites cannot be a major constituent of the Earth. The presence of Tm anomalies in meteorites and terrestrial rocks suggests that either (i) the material in the inner part of the solar system was formed from a gas reservoir that had been depleted in refractory dust or (ii) CI are enriched in refractory dust and are not representative of solar composition for refractory elements. Barrat J.A. et al. (2012) GCA 83, 79-92. Dauphas N., Pourmand A. (2015) GCA 163, 234-261. Pourmand et al. (2012) Chem. Geol. 291, 38-54.

Evaporation in the young solar nebula as the origin of 'just-right' melting of chondrules

PubMed

Cohen; Hewins; Yu

2000-08-10

Chondrules are millimetre-sized, solidified melt spherules formed in the solar nebula by an early widespread heating event of uncertain nature. They were accreted into chondritic asteroids, which formed about 4.56 billion years ago and have not experienced melting or differentiation since that time. Chondrules have diverse chemical compositions, corresponding to liquidus temperatures in the range 1,350-1,800 degrees C. Most chondrules, however, show porphyritic textures (consisting of large crystals in a distinctly finer grained or glassy matrix), indicative of melting within the narrow range 0-50 degrees C below the liquidus. This suggests an unusual heating mechanism for chondrule precursors, which would raise each individual chondrule to just the right temperature (particular to individual bulk composition) in order to form porphyritic textures. Here we report the results of isothermal melting of a chondritic composition at nebular pressures. Our results suggest that evaporation stabilizes porphyritic textures over a wider range of temperatures below the liquidus (about 200 degrees C) than previously believed, thus removing the need for individual chondrule temperature buffering. In addition, we show that evaporation explains many chondrule bulk and mineral compositions that have hitherto been difficult to understand.

Experimental Investigation of Chromium Behavior During Mercury's Differentiation

NASA Astrophysics Data System (ADS)

Boujibar, A.; Nittler, L. R.; Chabot, N.; McCubbin, F. M.; Righter, K.; Vander Kaaden, K. E.; McCoy, T. J.

2018-05-01

We use experimental data on Cr partitioning and its concentration on Mercury's surface to constrain on Mercury's oxidation state. We found that Mercury's bulk Cr composition can be chondritic and its core segregated at an fO2 of IW- 4.5 to IW-3.

The formation and alteration of the Renazzo-like carbonaceous chondrites I: Implications of bulk-oxygen isotopic composition

NASA Astrophysics Data System (ADS)

Schrader, Devin L.; Franchi, Ian A.; Connolly, Harold C., Jr.; Greenwood, Richard C.; Lauretta, Dante S.; Gibson, Jenny M.

2011-01-01

To better understand the role of aqueous alteration on the CR chondrite parent asteroid, a whole-rock oxygen isotopic study of 20 meteorites classified as Renazzo-like carbonaceous chondrites (CR) was conducted. The CR chondrites analyzed for their oxygen isotopes were Dhofar 1432, Elephant Moraine (EET) 87770, EET 92042, EET 96259, Gao-Guenie (b), Graves Nunataks (GRA) 95229, GRA 06100, Grosvenor Mountains (GRO) 95577, GRO 03116, LaPaz Ice Field (LAP) 02342, LAP 04720, Meteorite Hills (MET) 00426, North West Africa (NWA) 801, Pecora Escarpment (PCA) 91082, Queen Alexandra Range (QUE) 94603, QUE 99177, and Yamato-793495 (Y-793495). Three of the meteorites, Asuka-881595 (A-881595), GRA 98025, and MET 01017, were found not to be CR chondrites. The remaining samples concur petrographically and with the well-established oxygen-isotope mixing line for the CR chondrites. Their position along this mixing line is controlled both by the primary oxygen-isotopic composition of their individual components and their relative degree of aqueous alteration. Combined with literature data and that of this study, we recommend the slope for the CR-mixing line to be 0.70 ± 0.04 (2σ), with a δ 17O-intercept of -2.23 ± 0.14 (2σ). Thin sections of Al Rais, Shişr 033, Renazzo, and all but 3 samples analyzed for oxygen isotopes were studied petrographically. The abundance of individual components is heterogeneous among the CR chondrites, but FeO-poor chondrules and matrix are the most abundant constituents and therefore, dominate the whole-rock isotopic composition. The potential accreted ice abundance, physico-chemical conditions of aqueous alteration (e.g. temperature and composition of the fluid) and its duration control the degree of alteration of individual CR chondrites. Combined with literature data, we suggest that LAP 02342 was exposed to lower temperature fluid during alteration than GRA 95229. With only two falls, terrestrial alteration of the CR chondrites complicates the interpretation of their whole rock isotopic composition, particularly in the most aqueously altered samples, and those with relatively higher matrix abundances. We report that QUE 99177 is the isotopically lightest whole rock CR chondrite known (δ 18O = -2.29‰, δ 17O = -4.08‰), possibly due to isotopically light unaltered matrix; which shows that the anhydrous component of the CR chondrites is isotopically lighter than previously thought. Although it experienced aqueous alteration, QUE 99177 provides the best approximation of the pristine CR-chondrite parent body's oxygen-isotopic composition, before aqueous alteration took place. Using this value as a new upper limit on the anhydrous component of the CR chondrites, water/rock ratios were recalculated and found to be higher than previously thought; ratios now range from 0.281 to 1.157. We also find that, according to their oxygen isotopes, a large number of CR chondrites appear to be minimally aqueously altered; although sample heterogeneity complicates this interpretation.

Theoretical predictions of volatile bearing phases and volatile resources in some carbonaceous chondrites

NASA Technical Reports Server (NTRS)

Ganguly, Jibamitra; Saxena, Surendra K.

1989-01-01

Carbonaceous chondrites are usually believed to be the primary constituents of near-Earth asteroids and Phobos and Diemos, and are potential resources of fuels which may be exploited for future planetary missions. The nature and abundances are calculated of the major volatile bearing and other phases, including the vapor phase that should form in C1 and C2 type carbonaceous chondrites as functions of pressure and temperature. The results suggest that talc, antigorite plus or minus magnesite are the major volatile bearing phases and are stable below 400 C at 1 bar in these chondritic compositions. Simulated heating of a kilogram of C2 chondrite at fixed bulk composition between 400 and 800 C at 1 bar yields about 135 gm of volatile, which is made primarily of H2O, H2, CH4, CO2 and CO. The relative abundances of these volatile species change as functions of temperature, and on a molar basis, H2 becomes the most dominant species above 500 C. In contrast, Cl chondrites yield about 306 gm of volatile under the same condition, which consist almost completely of 60 wt percent H2O and 40 wt percent CO2. Preliminary kinetic considerations suggest that equilibrium dehydration of hydrous phyllosilicates should be attainable within a few hours at 600 C. These results provide the framework for further analyses of the volatile and economic resource potentials of carbonaceous chondrites.

Magmatic evolution of lunar highland rocks estimated from trace elements in plagioclase: A new bulk silicate Moon model with sub-chondritic Ti/Ba, Sr/Ba, and Sr/Al ratios

NASA Astrophysics Data System (ADS)

Togashi, Shigeko; Kita, Noriko T.; Tomiya, Akihiko; Morishita, Yuichi

2017-08-01

The compositions of host magmas of ferroan anorthosites (FAN-host magmas) were estimated from secondary ion mass spectrometry analyses of plagioclase in lunar highland rocks. The evolution of the magmas was investigated by considering phase relations based on the MELTS algorithm and by re-examining partition coefficients for trace elements between plagioclase and melts. Data little affected by post-magmatic processes were selected by using plagioclase with relatively primitive Sc and Co contents. The FAN-host magma contained 90-174 ppm Sr, 40-119 ppm Ba and 0.5-1.3% TiO2, and had sub-chondritic Sr/Ba and Ti/Ba ratios. It is difficult to account for the formation of FAN-host magma on the basis of magma evolution processes of previously proposed bulk silicate Moon models with chondritic ratios for refractory elements at global scale. Therefore, the source of the FAN-host magma must have had primordial sub-chondritic Sr/Ba and Ti/Ba ratios. The FAN-host magmas were consistent in refractory elements with the estimated host mafic magma for feldspathic crust based on lunar meteorites, and some very-low-Ti mare rocks from lunar meteorites. Here, we propose an alternative bulk silicate Moon model (the cBSM model), which is enriched in crustal components of proto-bodies relative to the present whole Earth-Moon system.

Oxygen Isotope Ratios of Magnetite in CI-Like Clasts from a Polymict Ureilite

NASA Technical Reports Server (NTRS)

Kita, N. T.; Defouilloy, C.; Goodrich, C. A.; Zolensky, M. E.

2017-01-01

Polymict ureilites contain a variety of Less than or equal to mm to cm sized non-ureilitic clasts, many of which can be identifed as chondritic and achondritic meteorite types. Among them, dark clasts have been observed in polymict ureilites that are similar to CI chondrites in mineralogy, containing phyllosilicates, magnetite, sulfide and carbonates. Bulk oxygen isotope analyses of a dark clast in Nilpena plot along the CCAM line and above the terrestrial fractionation line, on the O-poor extension of the main group ureilite trend and clearly different from bulk CI chondrites. One possible origins of such dark clast is that they represent aqueously altered precursors of ureilite parent body (UPB) that were preserved on the cold surface of the UPB. Oxygen isotope analyses of dark clasts are key to better understanding their origins. Oxygen isotope ratios of magnetite are of special interest because they reflect the compositions of the fluids in asteroidal bodies. In primitive chondrites, Delta O (= Delta O - 0.52× Delta O) values of magnetites are always higher than those of the bulk meteorites and represent minimum Delta O values of the initial O-poor aqueous fluids in the parent body. Previous SIMS analyses on magnetite and fayalite in dark clasts from the DaG 319 polymict ureilite were analytically difficult due to small grain sizes, though data indicated positive Delta O values of 3-4 per mille, higher than that of the dark clast in Nilpena (1.49per mille).

FIB-TEM Investigations of Fe-NI-Sulfides in the CI Chondrites Alais and Orgueil

NASA Technical Reports Server (NTRS)

Berger, Eve L.; Lauretta, D. S.; Zega, T. J.; Keller, L. P.

2013-01-01

The CI chondrites are primitive meteorites with bulk compositions matching the solar photosphere for all but the lightest elements. They have been extensively aqueously altered, and are composed primarily of fine-grained phyllosilicate matrix material which is host to carbonates, sulfates, sulfides, and minor amounts of olivine and pyroxene. The alteration, while extensive, is heterogeneous. For example, CI-chondrite cubanite and carbonate grains differ on mm to sub-mm scales, demonstrating multiple aqueous episodes. CI-chondrite variability is also evidenced by degree of brecciation, abundance and size of coarse-grained phyllosilicates, olivine and pyroxene abundance, as well as Ni-content and size of sulfide grains. Our previous work revealed Orgueil sulfide grains with variable Ni-contents, metal:S ratios, crystal structures and textures. We continue to explore the variability of CI-chondrite pyrrhotite (Po, (FeNi)1-xS) and pentlandite (Pn, (Fe,Ni)9S8) grains. We investigate the microstructure of sulfides within and among CI-chondrite meteorites in order to place constraints on the conditions under which they formed.

Comparing Amino Acid Abundances and Distributions Across Carbonaceous Chondrite Groups

NASA Technical Reports Server (NTRS)

Burton, Aaron S.; Callahan, Michael P.; Glavin, Daniel P.; Elsila, Jamie E.; Dworkin, Jason P.

2012-01-01

Meteorites are grouped according to bulk properties such as chemical composition and mineralogy. These parameters can vary significantly among the different carbonaceous chondrite groups (CI, CM, CO, CR, CH, CB, CV and CK). We have determined the amino acid abundances of more than 30 primary amino acids in meteorites from each of the eight groups, revealing several interesting trends. There are noticeable differences in the structural diversity and overall abundances of amino acids between meteorites from the different chondrite groups. Because meteorites may have been an important source of amino acids to the prebiotic Earth and these organic compounds are essential for life as we know it, the observed variations of these molecules may have been important for the origins of life.

Partial melting of the St. Severin (LL) and Lost City (H) ordinary chondrites: One step backwards and two steps forward

NASA Technical Reports Server (NTRS)

Jurewicz, A. J. G.; Jones, J. H.; Mittlefehldt, D. W.

1994-01-01

This study looks at partial melting in H and LL chondrites at nearly one atmosphere of total pressure as part of a continuing study of the origins of basaltic achondrites. Previously, melting experiments on anhydrous CM and CV chondrites showed that, near its solidus, the CM chondrite produced melts having major element chemistries similar to the Sioux County eucrite; but, the pyroxenes in the residuum were too iron-rich to form diogenites. Our preliminary results from melting experiments on ordinary (H, LL) chondrites suggested that, although the melts did not look like any known eucrites, pyroxenes from these charges bracketed the compositional range of pyroxenes found in diogenites. We had used the Fe/Mg exchange coefficients calculated for olivine, pyroxene, and melt in these charges to evaluate the approach to equilibrium, which appeared to be excellent. Unfortunately, mass balance calculations later indicated to us that, unlike our CM and CV charges, the LL and H experimental charges had lost significant amounts of iron to their (Pt or PtRh) supports. Apparently, pyroxene stability in chondritic systems is quite sensitive to the amount of FeO, and it was this unrecognized change in the bulk iron content which had stabilized the high temperature, highly magnesian pyroxenes. Accordingly, this work reinvestigates the phase equilibria of ordinary chondrites, eliminating iron and nickel loss, and reports significant differences. It also looks closely at how the iron and sodium in the bulk charge affect the stability of pyroxene, and it comments on how these new results apply to the problems of diogenite and eucrite petrogenesis.

Contributors to chromium isotope variation of meteorites

NASA Astrophysics Data System (ADS)

Qin, Liping; Alexander, Conel M. O.'D.; Carlson, Richard W.; Horan, Mary F.; Yokoyama, Tetsuya

2010-02-01

We report the results of a comprehensive, high precision survey of the Cr isotopic compositions of primitive chondrites, along with some differentiated meteorites. To ensure complete dissolution of our samples, they were first fused with lithium borate-tetraborate at 1050-1000 °C. Relative to the NIST Cr standard SRM 3112a, carbonaceous chondrites exhibit excesses in 54Cr/ 52Cr from 0.4 to 1.6 ɛ (1 ɛ = 1 part in 10,000), and ordinary chondrites display a common 54Cr/ 52Cr deficit of ˜0.4 ɛ. Analyses of acid-digestion residues of chondrites show that carbonaceous and ordinary chondrites share a common 54Cr-enriched carrier, which is characterized by a large excess in 54Cr/ 52Cr (up to 200 ɛ) associated with a very small deficit in 53Cr/ 52Cr (<2 ɛ). We did not find 54Cr anomalies in either bulk enstatite chondrites or in leachates of their acid-digestion residues. This either requires that the enstatite chondrite parent bodies did not incorporate the 54Cr anomaly carrier phase during their accretion, or the phase was destroyed by parent body metamorphism. Chromium in the terrestrial rocks and lunar samples analyzed here show no deviation from the NIST SRM 3112a Cr standard. The eucrite and Martian meteorites studied exhibit small deficits in 54Cr/ 52Cr. The 54Cr/ 52Cr variations among different meteorite classes suggest that there was a spatial and/or temporal heterogeneity in the distribution of a 54Cr-rich component in the inner Solar System. We confirm the correlated excesses in 54Cr/ 52Cr and 53Cr/ 52Cr for bulk carbonaceous chondrites, but the new data yield a steeper slope (˜6.6) than that reported in Shukolyukov and Lugmair (2006). The correlated excesses may affect the use of the Mn-Cr chronometer in carbonaceous chondrites. We could not confirm the bulk carbonaceous chondrite Mn-Cr isochron reported by Shukolyukov and Lugmair (2006) and Moynier et al. (2007), mostly because we find much smaller total variations in ɛ53Cr (˜0.2). All bulk chondrites have small ɛ53Cr excesses (up to 0.3) relative to the Earth, most likely reflecting the sub-chondritic Mn/Cr ratio of the Earth. The ɛ53Cr variations in chondrites do seem to grossly correlate with Mn/Cr and yield an initial Solar System 53Mn/ 55Mn value of 5.4(±2.4) × 10 -6, corresponding to an absolute age of 4566.4 (±2.2) Ma. Nuclear interactions with cosmic rays result in coupled excesses in ɛ54Cr and ɛ53Cr with a ˜4:1 ratio in phases with high Fe/Cr. These are most dramatically demonstrated in the iron meteorite Carbo, showing excesses in ɛ54Cr of up to 140 ɛ. These new results show that the Mn-Cr chronometer should be used with caution in samples/minerals with high Fe/Cr and long cosmic ray exposure ages.

Melting of the Primitive Mercurian Mantle, Insights into the Origin of Its Surface Composition

NASA Technical Reports Server (NTRS)

Boujibar, A.; Righter, K.; Rapp, J. F.; Ross, D. K.; Pando, K. M.; Danielson, L. R.; Fontaine, E.

2016-01-01

Recent findings of the MESSENGER mission on Mercury have brought new evidence for its reducing nature, widespread volcanism and surface compositional heteregeneity. MESSENGER also provided major elemental ratios of its surface that can be used to infer large-scale differentiation processes and the thermal history of the planet. Mercury is known as being very reduced, with very low Fe-content and high S and alkali contents on its surface. Its bulk composition is therefore likely close to EH enstatite chondrites. In order to elucidate the origin of the chemical diversity of Mercury's surface, we determined the melting properties of EH enstatite chondrites, at pressures between 1 bar and 3 GPa and oxygen fugacity of IW-3 to IW-5, using piston-cylinder experiments, combined with a previous study on EH4 melting at 1 bar. We found that the presence of Ca-rich sulfide melts induces significant decrease of Ca-content in silicate melts at low pressure and low degree of melting (F). Also at pressures lower than 3 GPa, the SiO2-content decreases with F, while it increases at 3 GPa. This is likely due to the chemical composition of the bulk silicate which has a (Mg+Fe+Ca)/Si ratio very close to 1 and to the change from incongruent to congruent melting of enstatite. We then tested whether the various chemical compositions of Mercury's surface can result from mixing between two melting products of EH chondrites. We found that the majority of the geochemical provinces of Mercury's surface can be explained by mixing of two melts, with the exception of the High-Al plains that require an Al-rich source. Our findings indicate that Mercury's surface could have been produced by polybaric melting of a relatively primitive mantle.

The Fall and Recovery of the Tagish Lake Meteorite

DOE Office of Scientific and Technical Information (OSTI.GOV)

Hildebrand, Alan R.; McCausland, Phil J.; Brown, Peter G.

2006-03-01

The Tagish Lake C2 (ungrouped) carbonaceous chondrite fall of January 18, 2000 delivered >10 kg of one of the most primitive and physically weak meteorites yet studied. In this paper we report the detailed circumstances of the fall and the recovery of all documented Tagish Lake fragments. We also provide measurements of bulk physical properties (mass, grain and bulk density), bulk triple oxygen-isotope ratios, and short-lived cosmogenic radionuclides counts for several fragments. Ground eyewitnesses and recorded observations of the Tagish Lake fireball event provide a refined estimate of the fireball trajectory, and hence, its pre-atmospheric orbit. From its calculated orbitmore » and its similarity to the remotely-sensed properties of the D and P-class asteroids, the Tagish Lake carbonaceous chondrite represents these outer belt asteroids, and is not of cometary origin. The bulk oxygen-isotope compositions reported here are among the highest known for meteorites. These data plot just below the Terrestrial Fractionation Line, following a trend similar to the CM meteorite mixing line. The bulk density of the Tagish Lake material (1.66 ±0.02 g/cm3) is the same, within error, as the total bulk densities of many C-class and especially D- and P-class asteroids. The high microporosity of Tagish Lake samples (~40%) provides an obvious candidate material for the composition of low bulk density primitive asteroids such as Phobos, Deimos and the P-class binary 87 Sylvia, without requiring a substantial contribution from macroporosity in the form of ice, thick regolith or “rubble pile” assemblages with large interior voids.« less

Cadmium Isotope Variations in Bulk Chondrites: The Effect of Thermal Neutron Capture

NASA Astrophysics Data System (ADS)

Toth, E. R.; Schönbächler, M.; Friebel, M.; Fehr, M. A.

2017-07-01

Cadmium isotope data will be presented for bulk carbonaceous and enstatite chondrites, and acid leachates of Jbilet Winselwan (CM). Results of bulk samples show Cd isotope variations that are in good agreement with models of thermal neutron capture.

Rhenium-osmium isotope and highly-siderophile-element abundance systematics of angrite meteorites

NASA Astrophysics Data System (ADS)

Riches, Amy J. V.; Day, James M. D.; Walker, Richard J.; Simonetti, Antonio; Liu, Yang; Neal, Clive R.; Taylor, Lawrence A.

2012-11-01

Coupled 187Os/188Os compositions and highly-siderophile-element (HSE: Os, Ir, Ru, Pt, Pd, and Re) abundance data are reported for eight angrite achondrite meteorites that include quenched- and slowly-cooled textural types. These data are combined with new major- and trace-element concentrations determined for bulk-rock powder fractions and constituent mineral phases, to assess angrite petrogenesis. Angrite meteorites span a wide-range of HSE abundances from <0.005 ppb Os (e.g., Northwest Africa [NWA] 1296; Angra dos Reis) to >100 ppb Os (NWA 4931). Chondritic to supra-chondritic 187Os/188Os (0.1201-0.2127) measured for Angra dos Reis and quenched-angrites correspond to inter- and intra-sample heterogeneities in Re/Os and HSE abundances. Quenched-angrites have chondritic-relative rare-earth-element (REE) abundances at 10-15×CI-chondrite, and their Os-isotope and HSE abundance variations represent mixtures of pristine uncontaminated crustal materials that experienced addition (<0.8%) of exogenous chondritic materials during or after crystallization. Slowly-cooled angrites (NWA 4590 and NWA 4801) have fractionated REE-patterns, chondritic to sub-chondritic 187Os/188Os (0.1056-0.1195), as well as low-Re/Os (0.03-0.13), Pd/Os (0.071-0.946), and relatively low-Pt/Os (0.792-2.640). Sub-chondritic 187Os/188Os compositions in NWA 4590 and NWA 4801 are unusual amongst planetary basalts, and their HSE and REE characteristics may be linked to melting of mantle sources that witnessed prior basaltic melt depletion. Angrite HSE-Yb systematics suggest that the HSE behaved moderately-incompatibly during angrite magma crystallization, implying the presence of metal in the crystallizing assemblage. The new HSE abundance and 187Os/188Os compositions indicate that the silicate mantle of the angrite parent body(ies) (APB) had HSE abundances in chondritic-relative proportions but at variable abundances at the time of angrite crystallization. The HSE systematics of angrites are consistent with protracted post-core formation accretion of materials with chondritic-relative abundances of HSE to the APB, and these accreted materials were rapidly, yet inefficiently, mixed into angrite magma source regions early in Solar System history.

Origin and abundance of water in carbonaceous asteroids

NASA Astrophysics Data System (ADS)

Marrocchi, Yves; Bekaert, David V.; Piani, Laurette

2018-01-01

The origin and abundance of water accreted by carbonaceous asteroids remains underconstrained, but would provide important information on the dynamic of the protoplanetary disk. Here we report the in situ oxygen isotopic compositions of aqueously formed fayalite grains in the Kaba and Mokoia CV chondrites. CV chondrite bulk, matrix and fayalite O-isotopic compositions define the mass-independent continuous trend (δ17O = 0.84 ± 0.03 × δ18O - 4.25 ± 0.1), which shows that the main process controlling the O-isotopic composition of the CV chondrite parent body is related to isotopic exchange between 16O-rich anhydrous silicates and 17O- and 18O-rich fluid. Similar isotopic behaviors observed in CM, CR and CO chondrites demonstrate the ubiquitous nature of O-isotopic exchange as the main physical process in establishing the O-isotopic features of carbonaceous chondrites, regardless of their alteration degree. Based on these results, we developed a new approach to estimate the abundance of water accreted by carbonaceous chondrites (quantified by the water/rock ratio) with CM (0.3-0.4) ≥ CR (0.1-0.4) ≥ CV (0.1-0.2) > CO (0.01-0.10). The low water/rock ratios and the O-isotopic characteristics of secondary minerals in carbonaceous chondrites indicate they (i) formed in the main asteroid belt and (ii) accreted a locally derived (inner Solar System) water formed near the snowline by condensation from the gas phase. Such results imply low influx of D- and 17O- and 18O-rich water ice grains from the outer part of the Solar System. The latter is likely due to the presence of a Jupiter-induced gap in the protoplanetary disk that limited the inward drift of outer Solar System material at the exception of particles with size lower than 150 μm such as presolar grains. Among carbonaceous chondrites, CV chondrites show O-isotopic features suggesting potential contribution of 17-18O-rich water that may be related to their older accretion relative to other hydrated carbonaceous chondrites.

Collisional erosion and the non-chondritic composition of the terrestrial planets.

PubMed

O'Neill, Hugh St C; Palme, Herbert

2008-11-28

The compositional variations among the chondrites inform us about cosmochemical fractionation processes during condensation and aggregation of solid matter from the solar nebula. These fractionations include: (i) variable Mg-Si-RLE ratios (RLE: refractory lithophile element), (ii) depletions in elements more volatile than Mg, (iii) a cosmochemical metal-silicate fractionation, and (iv) variations in oxidation state. Moon- to Mars-sized planetary bodies, formed by rapid accretion of chondrite-like planetesimals in local feeding zones within 106 years, may exhibit some of these chemical variations. However, the next stage of planetary accretion is the growth of the terrestrial planets from approximately 102 embryos sourced across wide heliocentric distances, involving energetic collisions, in which material may be lost from a growing planet as well as gained. While this may result in averaging out of the 'chondritic' fractionations, it introduces two non-chondritic chemical fractionation processes: post-nebular volatilization and preferential collisional erosion. In the latter, geochemically enriched crust formed previously is preferentially lost. That post-nebular volatilization was widespread is demonstrated by the non-chondritic Mn/Na ratio in all the small, differentiated, rocky bodies for which we have basaltic samples, including the Moon and Mars. The bulk silicate Earth (BSE) has chondritic Mn/Na, but shows several other compositional features in its pattern of depletion of volatile elements suggestive of non-chondritic fractionation. The whole-Earth Fe/Mg ratio is 2.1+/-0.1, significantly greater than the solar ratio of 1.9+/-0.1, implying net collisional erosion of approximately 10 per cent silicate relative to metal during the Earth's accretion. If this collisional erosion preferentially removed differentiated crust, the assumption of chondritic ratios among all RLEs in the BSE would not be valid, with the BSE depleted in elements according to their geochemical incompatibility. In the extreme case, the Earth would only have half the chondritic abundances of the highly incompatible, heat-producing elements Th, U and K. Such an Earth model resolves several geochemical paradoxes: the depleted mantle occupies the whole mantle, is completely outgassed in (40)Ar and produces the observed (4)He flux through the ocean basins. But the lower radiogenic heat production exacerbates the discrepancy with heat loss.

Clay minerals in primitive meteorites and interplanetary dust 1

NASA Technical Reports Server (NTRS)

Zolensky, M. E.; Keller, L. P.

1991-01-01

Many meteorites and interplanetary dust particles (IDPs) with primitive compositions contain significant amounts of phyllosilicate minerals, which are generally interpreted as evidence of protoplanetary aqueous alteration at an early period of the solar system. These meteorites are chondrites (near solar composition) of the carbonaceous and ordinary varieties. The former are subdivided (according to bulk composition and petrology) into CI, CM, CV, CO, CR, and ungrouped classes. IDPs are extraterrestrial particulates, collected in stratosphere, which have chemical compositions indicative of a primitive origin; they are typically distinct from the primitive meteorites. Characterization of phyllosilicates in these materials is a high priority because of the important physico-chemical information they hold. The most common phyllosilicates present in chondritic extraterrestrial materials are serpentine-group minerals, smectites, and micas. We discuss these phyllosilicates and describe the interpretation of their occurrence in meteorites and IDPs and what this indicates about history of their parent bodies, which are probably the hydrous asteroids.

Neodymium isotope heterogeneity of ordinary and carbonaceous chondrites and the origin of non-chondritic 142Nd compositions in the Earth

NASA Astrophysics Data System (ADS)

Fukai, Ryota; Yokoyama, Tetsuya

2017-09-01

We present high-precision Nd isotope compositions for ordinary and carbonaceous chondrites determined using thermal ionization mass spectrometry with dynamic and multistatic methods. The ordinary chondrites had uniform and non-terrestrial μ142 Nd , μ148 Nd , and μ150 Nd values, with data that plot along the mixing line between s-process and terrestrial components in μ150 Nd versus μ148 Nd and μ142 Nd versus μ148,150Nd diagrams. In contrast, the carbonaceous chondrites were characterized by larger anomalies in their μ142 Nd , μ148 Nd , and μ150 Nd values compared to ordinary chondrites. Importantly, the data for carbonaceous chondrites plot along the s-process and terrestrial mixing line in a μ150 Nd versus μ148 Nd diagram, whereas they have systematically lower μ142 Nd values than the s-process and terrestrial mixing line in μ142 Nd versus μ148,150Nd diagrams. This shift likely results from the incorporation of calcium- and aluminum-rich inclusions (CAIs), indicating that the Nd isotopic variability in the ordinary chondrites and CAI-free carbonaceous chondrites was caused solely by the heterogeneous distribution of s-process nuclides. The isotopic variation most likely results from nebular thermal processing that caused selective destruction of s-process-depleted (or r-process-enriched) dust grains in the inner Solar System where the parent bodies of ordinary chondrites formed, whereas such grains were preserved in the region of carbonaceous chondrite parent body formation. The Nd isotope dichotomy between ordinary and bulk aliquots of carbonaceous chondrites can be related to the presence of Jupiter, which may have separated two isotopically distinct reservoirs that were present in the solar nebula. After correcting for s-process anomalies and CAI contributions to the Nd isotopes observed in the chondrites, we obtained a μ142 Nd value (- 2.4 ± 4.8 ppm) that was indistinguishable from the terrestrial value. Our results corroborate the interpretation that a missing reservoir (e.g., a hidden enriched reservoir, erosional loss of crust) is not required to explain the observed differences in 142Nd/144Nd ratios between chondrites and terrestrial materials.

Hydrogen isotopes in lunar volcanic glasses and melt inclusions reveal a carbonaceous chondrite heritage.

PubMed

Saal, Alberto E; Hauri, Erik H; Van Orman, James A; Rutherford, Malcolm J

2013-06-14

Water is perhaps the most important molecule in the solar system, and determining its origin and distribution in planetary interiors has important implications for understanding the evolution of planetary bodies. Here we report in situ measurements of the isotopic composition of hydrogen dissolved in primitive volcanic glass and olivine-hosted melt inclusions recovered from the Moon by the Apollo 15 and 17 missions. After consideration of cosmic-ray spallation and degassing processes, our results demonstrate that lunar magmatic water has an isotopic composition that is indistinguishable from that of the bulk water in carbonaceous chondrites and similar to that of terrestrial water, implying a common origin for the water contained in the interiors of Earth and the Moon.

Structure and Bonding of Carbon in Clays from CI Carbonaceous Chondrites

NASA Technical Reports Server (NTRS)

Garview, Laurence a. J.; Buseck, Peter R.

2005-01-01

Carbonaceous chondrites (CC) contain a diverse suite of C-rich materials. Acid dissolution of these meteorites leaves a C-rich residue with chemical and structural affinities to kerogen. This material has primarily been analyzed in bulk, and much information has been provided regarding functional groups and elemental and isotopic compositions. However, comparatively little work has been done on C in unprocessed meteorites. Studies of CCs suggest a spatial relationship of some C-rich materials with products of aqueous alteration. Recent studies revealed discrete submicronsized, C-rich particles in Tagish Lake and a range of CM2 meteorites. A challenge is to correlate the findings from the bulk acid-residue studies with those of high-spatial resolution-mineralogical and spectroscopic observations of unprocessed meteorites. Hence, the relationship between the C-rich materials in the acid residues and its form and locations in the unprocessed meteorite remains unclear. Here we provide information on the structure and bonding of C associated with clays in CI carbonaceous chondrites. Additional information is included in the original extended abstract.

Possible impact-induced refractory-lithophile fractionations in EL chondrites

NASA Astrophysics Data System (ADS)

Rubin, Alan E.; Huber, Heinz; Wasson, John T.

2009-03-01

Literature data show that refractory-lithophile elements in most chondrite groups are unfractionated relative to CI chondrites; the principal exception is the EL-chondrite group whose observed falls (all of which are type 6) are depleted in Ca and light REE. In contrast, literature data and our new INAA data on EL3 PCA 91020, EL3 MAC 88136 and EL4 Grein 002 show that some replicates of these samples have nearly flat REE patterns (unlike those of EL6 chondrites); other replicates exhibit fractionated REE patterns similar to those of EL6 chondrites. Petrographic examination shows that many EL6 (and some EL3 and EL4) chondrites are impact-melt breccias or contain impact-melted portions. We suggest that the same impact processes that formed these breccias and produced melt are responsible for the observed bulk compositional fractionations in refractory-lithophile elements, i.e., EL6 chondrites were produced from initially unequilibrated EL3 material. When large amounts of impact heat were deposited, plagioclase and/or oldhamite (CaS) (the major REE carriers in enstatite chondrites) may have been melted and then transported appreciable (>10 cm) distances. EL6 chondrites represent the residuum that is depleted in REE (particularly in LREE) and Ca. Unlike the case for EL chondrites, our new INAA data on ALH 84170, EET 87746 and SAH 97096 (all EH3) show some scatter but are consistent with the EH group having uniform refractory-lithophile abundances.

Deformation of Ordinary Chondrite Under Very Reducing Conditons: Implications for Liquid Metal Compositions, HSE Partitioning and Enstatite Chondrites

NASA Astrophysics Data System (ADS)

Rushmer, T.; Corgne, A.

2008-12-01

One important method in which to gain insight into metallic liquid compositions and their ability to control HSE (highly siderophile element) distribution is through experimentation. Deformation experiments can additionally provide information into mechanisms and chemical consequences of dynamic liquid metal segregation under a variety of conditions. We report results on metallic liquid HSE compositions and their distribution from a set of deformation experiments on a natural H6 ordinary chondrite, performed under very reducing conditions and a series of phase equilibria experiments focused on HSE partitioning between Si-rich and S-rich Fe molten alloys. The deformation experiments were conducted at temperatures between 925°C and 950°C, at 1.3 GPa confining pressure with a strain rate of 10-4/s. Major element analyses of both silicate and metal phases show that they are considerably reduced and the typically lithophile elements are behaving like siderophiles. Fe-Ni-Si compositions are found in the shear zones produced during the deformation experiment. Metallic compositions also include (Mg,Fe,Ca)S, Fe-Ni-Si, FeP, and Fe-Ni-S quench metal. Silicate phases include forsterite (Fo92-96) and enstatite (En98). Highly siderophile element (HSE) concentrations have been measured in the sulphide ((Fe,Mg,Ca)S) and metal (Fe- Ni-Si) phases by LA-ICPMS and compared with results from an earlier set of experiments on the same material but which were not performed under reducing conditions. The partitioning of the PGE is modified by the changing conditions with elements such as Ir and Os having higher DMetal/Sulphide values under reducing conditions. Partitioning experiments between molten FeS and Ni-, Si-bearing molten Fe were performed at 1.5-5.0 GPa and 1500-1750° to further investigate this observation. The starting material is synthetic, doped with a range of trace and HSE elements. The results confirm the preference of the HSE for the metallic phase with DMetal/Sulphide > 100 in most cases, in contrast to Cu and Ag, which have D values near or below 1, respectively. Our results also suggest the possibility of significant PGE fractionation since D values are larger for Ir and Os and smaller for Pd and Au, with Pt, Ru, Rh having intermediate values. It is not clear with the present data set whether T and P variations can affect significantly HSE partitioning. These results have been applied to the most naturally reduced material we know, the Enstatite chondrites. Several E chondrites have bulk HSE data available, but no HSE data available on sulphide and metallic phases themselves. We have now a set of HSE data for individual metallic phases in several enstatite chondrites, both EH and ELs. The bulk data show that for elements such as Os and Pd, the abundances are positively correlated and overall Pd is much higher in abundance. We find in the experiments that DPd ranges between 10-100, but do not fully explain the bulk trends. Additional phases, such as FeP have therefore been analyzed and we find that Pd is concentrated in FeP and the presence of schreibersite may help explain the high Pd ratios (e.g. Pd/Ir) observed in the Enstatite chondrites.

Barium isotope abundances in meteorites and their implications for early Solar System evolution

NASA Astrophysics Data System (ADS)

Bermingham, K. R.; Mezger, K.; Scherer, E. E.; Horan, M. F.; Carlson, R. W.; Upadhyay, D.; Magna, T.; Pack, A.

2016-02-01

Several nucleosynthetic processes contributed material to the Solar System, but the relative contributions of each process, the timing of their input into the solar nebula, and how well these components were homogenized in the solar nebula remain only partially constrained. The Ba isotope system is particularly useful in addressing these issues because Ba isotopes are synthesized via three nucleosynthetic processes (s-, r-, p-process). In this study, high precision Ba isotope analyses of 22 different whole rock chondrites and achondrites (carbonaceous chondrites, ordinary chondrites, enstatite chondrites, Martian meteorites, and eucrites) were performed to constrain the distribution of Ba isotopes on the regional scale in the Solar System. A melting method using aerodynamic levitation and CO2-laser heating was used to oxidize SiC, a primary carrier of Ba among presolar grains in carbonaceous chondrites. Destruction of these grains during the fusion process enabled the complete digestion of these samples. The Ba isotope data presented here are thus the first for which complete dissolution of the bulk meteorite samples was certain. Enstatite chondrites, ordinary chondrites, and all achondrites measured here possess Ba isotope compositions that are not resolved from the terrestrial composition. Barium isotope anomalies are evident in most of the carbonaceous chondrites analyzed, but the 135Ba anomalies are generally smaller than previously reported for similarly sized splits of CM2 meteorites. Variation in the size of the 135Ba anomaly is also apparent in fused samples from the same parent body (e.g., CM2 meteorites) and in different pieces from the same meteorite (e.g., Orgueil, CI). Here, we investigate the potential causes of variability in 135Ba, including the contribution of radiogenic 135Ba from the decay of 135Cs and incomplete homogenization of the presolar components on the <0.8 g sample scale.

Reassessing the Formation of CK7 Northwest Africa (NWA) 8186

NASA Technical Reports Server (NTRS)

Srinivasan, P.; McCubbin, F. M.; Lapen, T. J.; Righter, M.; Agee, C. B.

2017-01-01

The classification of meteorites is commonly determined using isotopes, modal mineralogy, and bulk compositions [1]. Bulk rare earth elements (REEs) in meteorites are additionally utilized to understand parent body processes. Numerous authors have shown that chondritic groups exhibit REE patterns that may be attributable to their parent bodies [e.g. 2-4], and variations in abundances and concentrations of REEs may reflect early nebular processes, thermal metamorphism, and aqueous alteration on the parent body [5-6].

The isotope composition of selenium in chondrites constrains the depletion mechanism of volatile elements in solar system materials

NASA Astrophysics Data System (ADS)

Vollstaedt, Hauke; Mezger, Klaus; Leya, Ingo

2016-09-01

Solar nebula processes led to a depletion of volatile elements in different chondrite groups when compared to the bulk chemical composition of the solar system deduced from the Sun's photosphere. For moderately-volatile elements, this depletion primarily correlates with the element condensation temperature and is possibly caused by incomplete condensation from a hot solar nebula, evaporative loss from the precursor dust, and/or inherited from the interstellar medium. Element concentrations and interelement ratios of volatile elements do not provide a clear picture about responsible mechanisms. Here, the abundance and stable isotope composition of the moderately- to highly-volatile element Se are investigated in carbonaceous, ordinary, and enstatite chondrites to constrain the mechanism responsible for the depletion of volatile elements in planetary bodies of the inner solar system and to define a δ 82 / 78 Se value for the bulk solar system. The δ 82 / 78 Se of the studied chondrite falls are identical within their measurement uncertainties with a mean of - 0.20 ± 0.26 ‰ (2 s.d., n = 14, relative to NIST SRM 3149) despite Se abundance depletions of up to a factor of 2.5 with respect to the CI group. The absence of resolvable Se isotope fractionation rules out a kinetic Rayleigh-type incomplete condensation of Se from the hot solar nebula or partial kinetic evaporative loss on the precursor material and/or the parent bodies. The Se depletion, if acquired during partial condensation or evaporative loss, therefore must have occurred under near equilibrium conditions to prevent measurable isotope fractionation. Alternatively, the depletion and cooling of the nebula could have occurred simultaneously due to the continuous removal of gas and fine particles by the solar wind accompanied by the quantitative condensation of elements from the pre-depleted gas. In this scenario the condensation of elements does not require equilibrium conditions to avoid isotope fractionation. The results further suggest that the processes causing the high variability of Se concentrations and depletions in ordinary and enstatite chondrites did not involve any measurable isotope fractionation. Different degrees of element depletions and isotope fractionations of the moderately-volatile elements Zn, S, and Se in ordinary and enstatite chondrites indicate that their volatility is controlled by the thermal stabilities of their host phases and not by the condensation temperature under canonical nebular conditions.

Search for Nucleosynthetic Cadmium Isotope Variations in Bulk Carbonaceous Chondrites

NASA Astrophysics Data System (ADS)

Toth, E. R.; Schönbächler, M.; Friebel, M.; Fehr, M. A.

2016-08-01

New high-precision Cd isotope data will be presented for bulk carbonaceous chondrites, such as Allende and Murchison. Volatile element isotope anomalies and their potential nucleosynthetic sources will be discussed.

Highly Siderophile Elements, 187Re-187 Os and 182Hf-182W Isotopic Systematics of Early Solar System Materials: Constraining the Early Evolution of Chondritic and Achondritic Parent Bodies

NASA Astrophysics Data System (ADS)

Archer, Gregory J.

Highly siderophile element (HSE) abundances and 187Re- 187Os isotopic systematics for H chondrites and ungrouped achondrites, as well as 182Hf-182W isotopic systematics of H and CR chondrites are reported. Achondrite fractions with higher HSE abundances show little disturbance of 187Re-187Os isotopic systematics. By contrast, isotopic systematics for lower abundance fractions are consistent with minor Re mobilization. For magnetically separated H chondrite fractions, the magnitudes of disturbance for the 187Re-187Os isotopic system follow the trend coarse-metal isotopic system follow the trend coarse-metal

Minor and trace element concentrations in adjacent kamacite and taenite in the Krymka chondrite

NASA Astrophysics Data System (ADS)

Meftah, N.; Mostefaoui, S.; Jambon, A.; Guedda, E. H.; Pont, S.

2016-04-01

We report in situ NanoSIMS siderophile minor and trace element abundances in individual Fe-Ni metal grains in the unequilibrated chondrite Krymka (LL3.2). Associated kamacite and taenite of 10 metal grains in four chondrules and one matrix metal were analyzed for elemental concentrations of Fe, Ni, Co, Cu, Rh, Ir, and Pt. The results show large elemental variations among the metal grains. However, complementary and correlative variations exist between adjacent kamacite-taenite. This is consistent with the unequilibrated character of the chondrite and corroborates an attainment of chemical equilibrium between the metal phases. The calculated equilibrium temperature is 446 ± 9 °C. This is concordant with the range given by Kimura et al. (2008) for the Krymka postaccretion thermal metamorphism. Based on Ni diffusivity in taenite, a slow cooling rate is estimated of the Krymka parent body that does not exceed ~1K Myr-1, which is consistent with cooling rates inferred by other workers for unequilibrated ordinary chondrites. Elemental ionic radii might have played a role in controlling elemental partitioning between kamacite and taenite. The bulk compositions of the Krymka metal grains have nonsolar (mostly subsolar) element/Ni ratios suggesting the Fe-Ni grains could have formed from distinct precursors of nonsolar compositions or had their compositions modified subsequent to chondrule formation events.

Assessing the Formation of Ungrouped Achondrite Northwest Africa 8186: Residue, Crystallization Product, or Recrystallized Chondrite?

NASA Technical Reports Server (NTRS)

Srinivasan, P.; McCubbin, F. M.; Agee, C. B.

2016-01-01

The recent discoveries of primitive achondrites, metachondrites, and type 7 chondrites challenge the long held idea that all chondrites and achondrites form on separate parent bodies. These meteorites have experienced metamorphic temperatures above petrologic type 6 and have partially melted to various degrees. However, because of their isotopic and compositional similarities to both undifferentiated and differentiated groups, the provenance of these 'type 6+' meteorites remains largely unknown. CK and CV chondrites have recently been linked to a few achondrites due to their strong compositional, mineralogical, and isotopic similarities], suggesting a common origin between these meteorites. Although CVs have generally undergone low degrees of alteration near petrologic type 3, CKs have experienced a wide range of thermal alteration from petrologic type 3 to 6. Thermal evolution models on early accreting bodies predict that an early forming body can partially differentiate due to radiogenic heating, and, as a result, form radial layers of material increasing in thermal grade (types 3 to 6+) from the unmelted chondritic surface towards the differentiated core.Northwest Africa (NWA) 8186 is an ungrouped achondrite that provides compelling evidence for higher degrees of thermal processing and/or melting and differentiation on some CK/CV parent bodies. NWA 8186 plots on the CCAM line on a 3-oxygen isotope diagram directly with CK and CV chondrites and also plots with the CKs in regards to Cr isotopes. This meteorite is dominated by Nickel(II)Oxygen-rich olivine (less than 80%), lacks iron metal, and contains four oxide phases, indicating a high fOxygen (above FMQ) similar to the CKs. Additionally, NWA 8186 does not contain chondrules. We have further investigated the origins of NWA 8186 by examining and comparing the bulk composition of this CK-like achondrite with CK and CV chondrites, allowing us to assess the various scenarios in which NWA 8186 may have formed from CK/CV precursor material.

Petrologic and oxygen isotopic study of ALH 85085-like chondrites

NASA Astrophysics Data System (ADS)

Prinz, M.; Weisberg, M. K.; Clayton, R. N.; Mayeda, T. K.; Ebihara, M.

1994-07-01

Four meteorites (PAT 91546, PCA 91328, PCA 91452, PCA 91467) petrologically similar to ALH 85085 chondrite have now been found. Previous studies of ALH 85085 showed it be a new kind of CR-related microchondrule-bearing chondrite, although one called it a sub-chondrite. The purpose of this study is to learn more about ALH 85085-like meteorites and their relationship to CR and CR-related (LEW 85332, Acfer 182, Bencubbin) chondrites. The methods used included petrology, INA bulk chemical analysis (PAT 91546, PCA 91467), and O isotopic analyses of the whole rocks and separated chondrules and dark inclusions (DIs) from PAT 91546. Since microchondrules and fragments are approximately 20 microns it was necessary to analyze composite samples for O; one was of approximately 100 chondrules, and another was of 5 DIs. Petrologically, the four meteorites are similar to ALH 85085, and there is no basis for determining if all of them, or any combinations, are paired. Mineralogically, olivine and pyroxene are highly magnesian FeNi metal generally has 3-10% Ni, and has a positive Ni-Co correlation similar to that in CR and CR-related chondrites. Refractory inclusions are similar in size to the chondrules and have the following assemblages: (1) hibonite-perovskite, (2) melilite-fassaite-forsterite, (3) grossite (Ca-dialuminate)-melilite-perovskite, (4) spinel-melilite, and (5) spinel-pyroxene aggregates. Chemically, INA analyses indicate that PAT 91546 and PCA 91467 are generally similar to ALH 85085. Oxygen isotopic analyses of the four whole-rock compositions fall along the CR mixing line as does ALH 85085; they are also close to LEW 85332, Acfer 182, and Bencubbin. This supports the concept that these are all CR-related chondrites. Even stronger support is found in the compositions of the chondrules and DIs in PAT 91546, which also plot on or near the CR line.

The origin of inner Solar System water

NASA Astrophysics Data System (ADS)

Alexander, Conel M. O'D.

2017-04-01

Of the potential volatile sources for the terrestrial planets, the CI and CM carbonaceous chondrites are closest to the planets' bulk H and N isotopic compositions. For the Earth, the addition of approximately 2-4 wt% of CI/CM material to a volatile-depleted proto-Earth can explain the abundances of many of the most volatile elements, although some solar-like material is also required. Two dynamical models of terrestrial planet formation predict that the carbonaceous chondrites formed either in the asteroid belt (`classical' model) or in the outer Solar System (5-15 AU in the Grand Tack model). To test these models, at present the H isotopes of water are the most promising indicators of formation location because they should have become increasingly D-rich with distance from the Sun. The estimated initial H isotopic compositions of water accreted by the CI, CM, CR and Tagish Lake carbonaceous chondrites were much more D-poor than measured outer Solar System objects. A similar pattern is seen for N isotopes. The D-poor compositions reflect incomplete re-equilibration with H2 in the inner Solar System, which is also consistent with the O isotopes of chondritic water. On balance, it seems that the carbonaceous chondrites and their water did not form very far out in the disc, almost certainly not beyond the orbit of Saturn when its moons formed (approx. 3-7 AU in the Grand Tack model) and possibly close to where they are found today. This article is part of the themed issue 'The origin, history and role of water in the evolution of the inner Solar System'.

Reclassification of Villalbeto de la Peña—Occurrence of a winonaite-related fragment in a hydrothermally metamorphosed polymict L-chondritic breccia

NASA Astrophysics Data System (ADS)

Bischoff, Addi; Dyl, Kathryn A.; Horstmann, Marian; Ziegler, Karen; Wimmer, Karl; Young, Edward D.

2013-04-01

The Villalbeto de la Peña meteorite that fell in 2004 in Spain was originally classified as a moderately shocked L6 ordinary chondrite. The recognition of fragments within the Villalbeto de la Peña meteorite clearly bears consequences for the previous classification of the rock. The oxygen isotope data clearly show that an exotic eye-catching, black, and plagioclase-(maskelynite)-rich clast is not of L chondrite heritage. Villalbeto de la Peña is, consequently, reclassified as a polymict chondritic breccia. The oxygen isotope data of the clast are more closely related to data for the winonaite Tierra Blanca and the anomalous silicate-bearing iron meteorite LEW 86211 than to the ordinary chondrite groups. The REE-pattern of the bulk inclusion indicates genetic similarities to those of differentiated rocks and their minerals (e.g., lunar anorthosites, eucritic, and winonaitic plagioclases) and points to an igneous origin. The An-content of the plagioclase within the inclusion is increasing from the fragment/host meteorite boundary (approximately An10) toward the interior of the clast (approximately An52). This is accompanied by a successive compositionally controlled transformation of plagioclase into maskelynite by shock. As found for plagioclase, compositions of individual spinels enclosed in plagioclase (maskelynite) also vary from the border toward the interior of the inclusion. In addition, huge variations in oxygen isotope composition were found correlating with distance into the object. The chemical and isotopical profiles observed in the fragment indicate postaccretionary metamorphism under the presence of a volatile phase.

Hf-W chronology of CR chondrites: Implications for the timescales of chondrule formation and the distribution of 26Al in the solar nebula

DOE Office of Scientific and Technical Information (OSTI.GOV)

Budde, Gerrit; Kruijer, Thomas S.; Kleine, Thorsten

The CR chondrites are distinct from most other chondrites in having younger chondrule 26Al- 26Mg ages, but the significance of these ages and whether they reflect true formation times or a heterogeneous distribution of 26Al are not well understood. To better determine the timescales of CR chondrule formation and CR chondrite parent body accretion, we obtained Hf-W isotopic data for metal, silicate, and chondrule separates from four CR chondrites. We also obtained Mo isotopic data for the same samples, to assess potential genetic links among the components of CR chondrites, and between these components and bulk chondrites. The isotopic datamore » demonstrate that metal and silicate in CR chondrites exhibit distinct nucleosynthetic W and Mo isotope anomalies, caused by the heterogeneous distribution of a single presolar s-process carrier. These isotope signatures are akin to the complementary anomalies found previously for chondrules and matrix in CV chondrites and indicate that the major components of CR chondrites are genetically linked and formed from a common reservoir of solar nebula dust. The obtained Hf-W age of 3.6±0.6 million years (Ma) after the formation of Ca-Al-rich inclusions (CAIs) most likely dates metal-silicate separation during chondrule formation and is consistent with Al-Mg and Pb-Pb ages for CR chondrules, indicating that CR chondrules formed ~1–2 Ma later than chondrules from most other chondrite groups. Moreover, chemical, isotopic, and chronological data imply close temporal link between chondrule formation and chondrite accretion, making the CR chondrite parent body one of the youngest meteorite parent bodies. Such a late accretion at ~3.6 Ma after CAIs is consistent with isotopic composition of CR chondrites (e.g., 15N/ 14N) that is indicative of a formation at a larger heliocentric distance, probably beyond the orbit of Jupiter. As such, the accretion age of the CR parent body provides the earliest possible time at which Jupiter could have migrated inwards, leading to scattering of carbonaceous meteorite parent bodies into the inner solar system. Finally, the concordant Hf-W and Al- Mg ages for CR chondrules, combined with Hf-W and Al-Mg data for bulk CAIs, angrites, and CV chondrules, provide strong evidence for a disk-wide, homogeneous distribution of 26Al in the early solar system.« less

Hf-W chronology of CR chondrites: Implications for the timescales of chondrule formation and the distribution of 26Al in the solar nebula

DOE PAGES

Budde, Gerrit; Kruijer, Thomas S.; Kleine, Thorsten

2017-10-24

The CR chondrites are distinct from most other chondrites in having younger chondrule 26Al- 26Mg ages, but the significance of these ages and whether they reflect true formation times or a heterogeneous distribution of 26Al are not well understood. To better determine the timescales of CR chondrule formation and CR chondrite parent body accretion, we obtained Hf-W isotopic data for metal, silicate, and chondrule separates from four CR chondrites. We also obtained Mo isotopic data for the same samples, to assess potential genetic links among the components of CR chondrites, and between these components and bulk chondrites. The isotopic datamore » demonstrate that metal and silicate in CR chondrites exhibit distinct nucleosynthetic W and Mo isotope anomalies, caused by the heterogeneous distribution of a single presolar s-process carrier. These isotope signatures are akin to the complementary anomalies found previously for chondrules and matrix in CV chondrites and indicate that the major components of CR chondrites are genetically linked and formed from a common reservoir of solar nebula dust. The obtained Hf-W age of 3.6±0.6 million years (Ma) after the formation of Ca-Al-rich inclusions (CAIs) most likely dates metal-silicate separation during chondrule formation and is consistent with Al-Mg and Pb-Pb ages for CR chondrules, indicating that CR chondrules formed ~1–2 Ma later than chondrules from most other chondrite groups. Moreover, chemical, isotopic, and chronological data imply close temporal link between chondrule formation and chondrite accretion, making the CR chondrite parent body one of the youngest meteorite parent bodies. Such a late accretion at ~3.6 Ma after CAIs is consistent with isotopic composition of CR chondrites (e.g., 15N/ 14N) that is indicative of a formation at a larger heliocentric distance, probably beyond the orbit of Jupiter. As such, the accretion age of the CR parent body provides the earliest possible time at which Jupiter could have migrated inwards, leading to scattering of carbonaceous meteorite parent bodies into the inner solar system. Finally, the concordant Hf-W and Al- Mg ages for CR chondrules, combined with Hf-W and Al-Mg data for bulk CAIs, angrites, and CV chondrules, provide strong evidence for a disk-wide, homogeneous distribution of 26Al in the early solar system.« less

Experimental evidence for the absence of iron isotope fractionation between metal and silicate liquids at 1 GPa and 1250-1300 °C and its cosmochemical consequences

NASA Astrophysics Data System (ADS)

Hin, Remco C.; Schmidt, Max W.; Bourdon, Bernard

2012-09-01

Iron isotope fractionation during metal-silicate differentiation has been proposed as a cause for differences in iron isotope compositions of chondrites, iron meteorites and the bulk silicate Earth. Stable isotope fractionation, however, rapidly decreases with increasing temperature. We have thus performed liquid metal-liquid silicate equilibration experiments at 1250-1300 °C and 1 GPa to address whether Fe isotope fractionation is resolvable at the lowest possible temperatures for magmatic metal-silicate differentiation. A centrifuging piston cylinder apparatus enabled quantitative metal-silicate segregation. Elemental tin or sulphur was used in the synthetic metal-oxide mixtures to lower the melting temperature of the metal. The analyses demonstrate that eight of the 10 experimental systems equilibrated in a closed isotopic system, as was assessed by varying run durations and starting Fe isotope compositions. Statistically significant iron isotope fractionation between quenched metals and silicates was absent in nine of the 10 experiments and all 10 experiments yield an average metal-silicate fractionation factor of 0.01 ± 0.04‰, independent of whether graphite or silica glass capsules were used. This implies that Fe isotopes do not fractionate during low pressure metal-silicate segregation under magmatic conditions. In large bodies such as the Earth, fractionation between metal and high pressure (>20 GPa) silicate phases may still be a possible process for equilibrium fractionation during metal-silicate differentiation. However, the 0.07 ± 0.02‰ heavier composition of bulk magmatic iron meteorites relative to the average of bulk ordinary/carbonaceous chondrites cannot result from equilibrium Fe isotope fractionation during core segregation. The up to 0.5‰ lighter sulphide than metal fraction in iron meteorites and in one ordinary chondrite can only be explained by fractionation during subsolidus processes.

Porosity and Permeability of Chondritic Materials

NASA Technical Reports Server (NTRS)

Zolensky, Michael E.; Corrigan, Catherine M.; Dahl, Jason; Long, Michael

1996-01-01

We have investigated the porosity of a large number of chondritic interplanetary dust particles and meteorites by three techniques: standard liquid/gas flow techniques, a new, non-invasive ultrasonic technique, and image processing of backscattered images . The latter technique is obviously best suited to sub-kg sized samples. We have also measured the gas and liquid permeabilities of some chondrites by two techniques: standard liquid/gas flow techniques, and a new, non-destructive pressure release technique. We find that chondritic IDP's have a somewhat bimodal porosity distribution. Peaks are present at 0 and 4% porosity; a tail then extends to 53%. These values suggest IDP bulk densities of 1.1 to 3.3 g/cc. Type 1-3 chondrite matrix porosities range up to 30%, with a peak at 2%. The bulk porosities for type 1-3 chondrites have the same approximate range as exhibited by matrix, indicating that other components of the bulk meteorites (including chondrules and aggregates) have the same average porosity as matrix. These results reveal that the porosity of primitive materials at scales ranging from nanogram to kilogram are similar, implying similar accretion dynamics operated through 12 orders of size magnitude. Permeabilities of the investigated chondrites vary by several orders of magnitude, and there appears to be no simple dependence of permeability with degree of aqueous alteration, or chondrite type.

Titanium stable isotopic variations in chondrites, achondrites and lunar rocks

NASA Astrophysics Data System (ADS)

Greber, Nicolas D.; Dauphas, Nicolas; Puchtel, Igor S.; Hofmann, Beda A.; Arndt, Nicholas T.

2017-09-01

Titanium isotopes are potential tracers of processes of evaporation/condensation in the solar nebula and magmatic differentiation in planetary bodies. To gain new insights into the processes that control Ti isotopic variations in planetary materials, 25 komatiites, 15 chondrites, 11 HED-clan meteorites, 5 angrites, 6 aubrites, a martian shergottite, and a KREEP-rich impact melt breccia have been analyzed for their mass-dependent Ti isotopic compositions, presented using the δ49Ti notation (deviation in permil of the 49Ti/47Ti ratio relative to the OL-Ti standard). No significant variation in δ49Ti is found among ordinary, enstatite, and carbonaceous chondrites, and the average chondritic δ49Ti value of +0.004 ± 0.010‰ is in excellent agreement with the published estimate for the bulk silicate Earth, the Moon, Mars, and the HED and angrite parent-bodies. The average δ49Ti value of komatiites of -0.001 ± 0.019‰ is also identical to that of the bulk silicate Earth and chondrites. OL-Ti has a Ti isotopic composition that is indistinguishable from chondrites and is therefore a suitable material for reporting δ49Ti values. Previously published isotope data on another highly refractory element, Ca, show measurable variations among chondrites. The decoupling between Ca and Ti isotope systematics most likely occurred during condensation in the solar nebula. Aubrites exhibit significant variations in δ49Ti, from -0.07 to +0.24‰. This is likely due to the uniquely reducing conditions under which the aubrite parent-body differentiated, allowing chalcophile Ti3+ and lithophile Ti4+ to co-exist. Consequently, the observed negative correlation between δ49Ti values and MgO concentrations among aubrites is interpreted to be the result of isotope fractionation driven by the different oxidation states of Ti in this environment, such that isotopically heavy Ti4+ was concentrated in the residual liquid during magmatic differentiation. Finally, KREEPy impact melt breccia SaU 169 exhibits a heavy δ49Ti value of +0.330 ± 0.034‰ which is interpreted to result from Ti isotopic fractionation during ilmenite precipitation in the late stages of lunar magma ocean crystallization. A Rayleigh distillation calculation predicts that a δ49Ti value of +0.330‰ is achieved after removal of 94% of Ti in ilmenite.

Causes of 142Nd Variation in Earth

NASA Astrophysics Data System (ADS)

Boyet, M.; Bouvier, A.; Gannoun, A.; Carlson, R.

2015-12-01

Variability of the 142Nd/144Nd ratio can reflect Sm/Nd fractionation during the lifetime of 146Sm, i.e. the first 500 Ma of Solar System history1 and nucleosynthetic heterogeneity inherited from the solar nebula. Deciphering the message carried by 142Nd variability requires a detailed examination of the data for Earth and meteorites. The elevated 142Nd/144Nd in terrestrial samples relative to average chondrites suggests that all terrestrial rocks sampled by volcanism over the Earth's history come from a geochemical reservoir characterized by a superchondritic Sm/Nd ratio. The chemical compliment to this reservoir, however, has never been seen, so it either was lost during Earth's accretion2,3, or is preserved in a deep hidden reservoir 1,4. These models are based on a comparison of Earth rocks and O-chondrites because they do not show any variation in stable Sm and Nd isotopic composition compared to Earth6-8. The first analyzed E-chondrites with terrestrial 142Nd/144Nd showed 144Sm excesses that reflect an excess p-process contribution. Although 142Nd is mainly produced by s-process, there is a direct p-process component estimated to be lower than 4 %. We will present new Sm and Nd isotopic data on meteoritic materials. CAIs show deficits in both r- and p-process isotopes that would lead to elevated 142Nd, yet the bulk C-chondrites in which they are contained show excesses in r-process isotopes and hence 142Nd/144Nd lower than terrestrial. The new E-chondrites data do not confirm the 142Nd-144Sm correlation observed in bulk chondrites In light of these results and using 146Sm-142Nd isochrons for constraining the bulk 142Nd/144Nd ratio of planetary bodies, we will discuss the 142Nd signature of terrestrial samples (from Hadean to present). 1Boyet & Carlson, Science 2005; 2O'Neill & Palme, Phil. Trans. R. Soc 2008; 3Caro et al. Nature 2008; 4Andreasen et al. EPSL 2008; 6Andreasen & Sharma, Science 2006; 7Carlson et al., Science 2007; 8Gannoun et al. PNAS 2011.

Elemental depletions in Antarctic micrometeorites and Arctic cosmic spherules: Comparison and relationships

NASA Technical Reports Server (NTRS)

Presper, T.; Kurat, G.; Koeberl, C.; Palme, H.; Maurette, Michel

1993-01-01

Antarctic micrometeorites (MM's) and Arctic cosmic spherules (CS's) have bulk compositions comparable to those of chondritic meteorites. However, abundance of Na, Ca, Mn, Ni, Co, and S are commonly lower in MM's and CS's as compared to chondrites. Our SEM, EMP, and INAA studies suggest that these elemental depletions in unmelted MM's are likely to be due to leaching of soluble components from the MM's in the upper atmosphere and the melt ice water. Depletions in CS's appear to be mainly due to volatilization during melting in the atmosphere or to sampling bias during aggregate formation or parent rock break-up.

Investigation of magnesium isotope fractionation during basalt differentiation: Implications for a chondritic composition of the terrestrial mantle

USGS Publications Warehouse

Teng, F.-Z.; Wadhwa, M.; Helz, R.T.

2007-01-01

To investigate whether magnesium isotopes are fractionated during basalt differentiation, we have performed high-precision Mg isotopic analyses by multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) on a set of well-characterized samples from Kilauea Iki lava lake, Hawaii, USA. Samples from the Kilauea Iki lava lake, produced by closed-system crystal-melt fractionation, range from olivine-rich cumulates to highly differentiated basalts with MgO content ranging from 2.37 to 26.87??wt.%. Our results demonstrate that although these basalts have diverse chemical compositions, mineralogies, crystallization temperatures and degrees of differentiation, their Mg isotopic compositions display no measurable variation within the limits of our external precision (average ??26Mg = - 0.36 ?? 0.10 and ??25Mg = - 0.20 ?? 0.07; uncertainties are 2SD). This indicates that Mg isotopic fractionation during crystal-melt fractionation at temperatures of ??? 1055????C is undetectable at the level of precision of the current investigation. Calculations based on our data suggest that at near-magmatic temperatures the maximum fractionation in the 26Mg/24Mg ratio between olivine and melt is 0.07???. Two additional oceanic basalts, two continental basalts (BCR-1 and BCR-2), and two primitive carbonaceous chondrites (Allende and Murchison) analyzed in this study have Mg isotopic compositions similar to the Kilauea Iki lava lake samples. In contrast to a recent report [U. Wiechert, A.N. Halliday, Non-chondritic magnesium and the origins of the inner terrestrial planets, Earth and Planetary Science Letters 256 (2007) 360-371], the results presented here suggest that the Bulk Silicate Earth has a chondritic Mg isotopic composition. ?? 2007.

Nucleosynthetic Heterogeneity Controls Vanadium Isotope Variations in Bulk Chondrites

NASA Technical Reports Server (NTRS)

Nielsen, S. G.; Righter, K.; Wu, F.; Owens, J. D.; Prytulak, J.; Burton, K.; Parkinson, I.; Davis, D.

2018-01-01

The vanadium (V) isotope composition of early solar system materials have been hypothesized to be sensitive to high energy irradiation that originated from the young Sun. Vanadium has two isotopes with masses 50 and 51 that have (51)V/(50)V ratio of approximately 410. High energy irradiation produces (50)V from various target isotopes of Ti, Cr and Fe, which would result in light V isotope compositions (expressed as delta (51)V in per mille = 1000 x (((51)V/(50)V(sub sample)/(51)V/(50)V(sub AlfaAesar)) - 1)) relative to a presumably chondritic starting composition. Recently published V isotope data for calcium aluminium inclusions (CAIs) has revealed some very negative values relative to chondrites (by almost -4 per mille) that were indeed interpreted to reflect irradiation processes despite the fact that the studied CAIs all exhibited significant initial abundances of (10)Be, while only a few CAIs displayed light V isotope compositions. It is difficult to relate V isotope variations directly to a singular process because V only possesses two isotopes. Therefore, V isotope variations can principally be produced both mass dependent and independent processes. Mass dependent kinetic stable isotope fractionation is common in CAIs for refractory elements due to partial condensation/evaporation processes. The element strontium (Sr) has an almost identical condensation temperature to V and studies of stable Sr isotope compositions in CAIs reveal both heavy and light values relative to chondrites of several permil. These variations are similar in magnitude to those reported for V isotopes in CAIs, which suggests it is possible that some of the V isotope variation in CAIs could be due to kinetic stable isotope fractionation during condensation/evaporation processes.

Effects of Microsecond Pulse Laser Irradiation on Vis-NIR Reflectance Spectrum of Carbonaceous Chondrite Simulant: Implications for Martian Moons and Primitive Asteroids

NASA Technical Reports Server (NTRS)

Hiroi, T.; Moroz, L. V.; Shingareva, T. V.; Basilevsky, A. T.; Pieters, M.

2003-01-01

Goal of this study is to make a progress in understanding the optical effects of space weathering on small bodies believed to be similar in composition to carbonaceous chondrites: C, G, B, F, T, D, and P asteroids and possibly Martian satellites Phobos and Deimos. The companion work focuses on petrological and mineralogical aspects of this process. One of the main factors of space weathering is meteorite and micrometeorite bombardment leading, in particular, to impact melting of components of the regolith. Studies of lunar regolith and laboratory experiments simulating impact melting show that the melting products differ from the unmelted material in mineralogy and distribution of chemical components among different phases that results in spectral changes. We simulate impact melting of CM chondrite by pulse laser irradiation of an artificial analog of such a meteorite. The analog is a mixture of 46 wt.% non-magnetic fraction of L5 ordinary chondrite Tsarev, 47 wt.% serpentine, 5 wt.% kerite, and 2 wt.% calcite. It simulates rather well bulk chemistry, including volatiles such as H2O and CO2, and only approximately the CM chondrite mineralogy. Thus, we do not expect the mixture to be spectrally similar to CM chondrites, but expect the laser melting products to be similar to those formed by impact melting of natural CM chondrites.

Calcium and titanium isotopes in refractory inclusions from CM, CO, and CR chondrites

NASA Astrophysics Data System (ADS)

Kööp, Levke; Davis, Andrew M.; Krot, Alexander N.; Nagashima, Kazuhide; Simon, Steven B.

2018-05-01

Previous studies have shown that CV and CM chondrites incorporated Ca, Al-rich inclusions (CAIs) with different isotopic characteristics, which may represent different snapshots in the isotopic evolution of the early Solar System. To better understand how the isotopic characteristics of CAIs vary between different chondrite groups, we have studied calcium and titanium isotopes in CAIs from CM, CO, and CR chondrites. We show that all three chondrite groups contain CAIs with large anomalies in 48Ca and/or 50Ti (10s of ‰ or 100s of ε-units) as well as CAIs with no anomalies resolved beyond measurement uncertainties. Isotopically, the anomalous CO and CR chondrite CAIs resemble the platy hibonite crystals (PLACs) from CM chondrites, but they are more mineralogically complex. The new data are consistent with the well-established mutual exclusivity relationship between incorporation of 26Al and the presence of large anomalies in 48Ca and 50Ti. The two highly anomalous CO chondrite CAIs have correlated anomalies in 46Ti and 50Ti, while most other highly anomalous CAIs do not. This result could indicate that the reservoir with coupled 46Ti and 50Ti that was sampled by bulk meteorites and CV chondrite CAIs already existed before arrival and/or homogeneous distribution of 26Al in the protoplanetary disk. Among the studied CM chondrite CAIs are ten spinel-hibonite inclusions (SHIBs) with known oxygen isotopic compositions. Our results show that these objects sampled a reservoir that was well-mixed in oxygen, calcium, and titanium isotopes. We further show that SHIBs tend to be slightly enriched in the heavy calcium isotopes, suggesting that their formation history was different from CV chondrite CAIs.

The origin of inner Solar System water.

PubMed

Alexander, Conel M O'D

2017-05-28

Of the potential volatile sources for the terrestrial planets, the CI and CM carbonaceous chondrites are closest to the planets' bulk H and N isotopic compositions. For the Earth, the addition of approximately 2-4 wt% of CI/CM material to a volatile-depleted proto-Earth can explain the abundances of many of the most volatile elements, although some solar-like material is also required. Two dynamical models of terrestrial planet formation predict that the carbonaceous chondrites formed either in the asteroid belt ('classical' model) or in the outer Solar System (5-15 AU in the Grand Tack model). To test these models, at present the H isotopes of water are the most promising indicators of formation location because they should have become increasingly D-rich with distance from the Sun. The estimated initial H isotopic compositions of water accreted by the CI, CM, CR and Tagish Lake carbonaceous chondrites were much more D-poor than measured outer Solar System objects. A similar pattern is seen for N isotopes. The D-poor compositions reflect incomplete re-equilibration with H 2 in the inner Solar System, which is also consistent with the O isotopes of chondritic water. On balance, it seems that the carbonaceous chondrites and their water did not form very far out in the disc, almost certainly not beyond the orbit of Saturn when its moons formed (approx. 3-7 AU in the Grand Tack model) and possibly close to where they are found today.This article is part of the themed issue 'The origin, history and role of water in the evolution of the inner Solar System'. © 2017 The Author(s).

Synchrotron-based Infrared Microspectroscopy as a Useful Tool to Study Hydration States of Meteorite Constituents

NASA Technical Reports Server (NTRS)

Moroz, L. V.; Schmidt, M.; Schade, U.; Hiroi, T.; Ivanova, M. A.

2005-01-01

The meteorites Dho 225 and Dho 735 were recently found in Oman. Studies of their mineralogical and chemical composition suggest that these unusual meteorites are thermally metamorphosed CM2 chondrites [1,2,3]. Similar to Antarctic metamorphosed carbonaceous chondrites, the Dho 225 and Dho 735 are enriched in heavy oxygen compared to normal CMs [1,2]. However, IR studies indicating dehydration of matrix phyllosilicates are needed to confirm that the two new meteorites from Oman are thermally metamorphosed [4]. Synchrotron-based IR microspectroscopy is a new promising technique which allows the acquisition of IR spectra from extremely small samples. Here we demonstrate that this non-destructive technique is a useful tool to study hydration states of carbonaceous chondrites in situ. In addition, we acquired reflectance spectra of bulk powders of the Dho 225 and Dho 735 in the range of 0.3-50 microns.

Surviving High-temperature Components in CI Chondrites

NASA Technical Reports Server (NTRS)

Zolensky, M.; Frank, D.

2014-01-01

The CI1 chondrites, while having the most solar-like compo-sition of any astromaterial available for laboratory analysis, have also been considerably altered by asteroidal processes including aqueous alteration. It is of fundamental importance to determine their pre-alteration mineralogy, so that the state of matter in the early Solar System can be better determined. In the course of a re-examination of the compositional range of olivine and low-Ca pyroxene in CI chondrites Orgueil, Ivuna and Alais [1] we found the first reported complete CAI, as already reported [2], with at-tached rock consisting mainly of olivine and low-Ca pyroxene. The range of residual olivine major element compositions we have determined in the CIs (Fig. 1) may now be directly com-pared with those of other astromaterials, including Wild 2 grains. The abundance of olivine and low-Ca pyroxene in CIs is higher than is generally appreciated, and in fact much higher than for some CMs [1]. We also noted numerous rounded objects varying in shape from spheres to oblate spheroids, and ranging up to 100µm in size (Fig. 2), which have been previously noted [3] but have not been well documented or appreciated. We characterized the mineralogy by transmission electron microscopy and found that they consist mainly of rather fine-grained, flaky single phase to intergrown serpentine and saponite. These two materials in fact dominate the bulk of the host CI1 chondrites. With the exception of sparse spinels, the rounded phyllosilicate objects are remarka-bly free of other minerals, suggesting that the precursor from which the phyllosilicates were derived was a homogeneous mate-rial. We suggest that these round phyllosilicates aggregates in CI1 chondrites were cryptocrystalline to glassy microchondrules. If so then CI chondrites cannot be considered chondrule-free. Small though they are, the abundance of these putative microchondrules is the same as that of chondrules in the Tagish Lake meteorite.

A geochemical study of the winonaites: Evidence for limited partial melting and constraints on the precursor composition

NASA Astrophysics Data System (ADS)

Hunt, Alison C.; Benedix, Gretchen K.; Hammond, Samantha J.; Bland, Philip A.; Rehkämper, Mark; Kreissig, Katharina; Strekopytov, Stanislav

2017-02-01

The winonaites are primitive achondrites which are associated with the IAB iron meteorites. Textural evidence implies heating to at least the Fe, Ni-FeS cotectic, but previous geochemical studies are ambiguous about the extent of silicate melting in these samples. Oxygen isotope evidence indicates that the precursor material may be related to the carbonaceous chondrites. Here we analysed a suite of winonaites for modal mineralogy and bulk major- and trace-element chemistry in order to assess the extent of thermal processing as well as constrain the precursor composition of the winonaite-IAB parent asteroid. Modal mineralogy and geochemical data are presented for eight winonaites. Textural analysis reveals that, for our sub-set of samples, all except the most primitive winonaite (Northwest Africa 1463) reached the Fe, Ni-FeS cotectic. However, only one (Tierra Blanca) shows geochemical evidence for silicate melting processes. Tierra Blanca is interpreted as a residue of small-degree silicate melting. Our sample of Winona shows geochemical evidence for extensive terrestrial weathering. All other winonaites studied here (Fortuna, Queen Alexander Range 94535, Hammadah al Hamra 193, Pontlyfni and NWA 1463) have chondritic major-element ratios and flat CI-normalised bulk rare-earth element patterns, suggesting that most of the winonaites did not reach the silicate melting temperature. The majority of winonaites were therefore heated to a narrow temperature range of between ∼1220 (the Fe, Ni-FeS cotectic temperature) and ∼1370 K (the basaltic partial melting temperature). Silicate inclusions in the IAB irons demonstrate partial melting did occur in some parts of the parent body (Ruzicka and Hutson, 2010), thereby implying heterogeneous heat distribution within this asteroid. Together, this indicates that melting was the result of internal heating by short-lived radionuclides. The brecciated nature of the winonaites suggests that the parent body was later disrupted by a catastrophic impact, which allowed the preservation of the largely unmelted winonaites. Despite major-element similarities to both ordinary and enstatite chondrites, trace-element analysis suggests the winonaite parent body had a carbonaceous chondrite-like precursor composition. The parent body of the winonaites was volatile-depleted relative to CI, but enriched compared to the other carbonaceous classes. The closest match are the CM chondrites; however, the specific precursor is not sampled in current meteorite collections.

Early Earth evolution: new insight from Sm and Nd isotopes in meteoritic inclusions

NASA Astrophysics Data System (ADS)

Bouvier, A.; Boyet, M.

2014-12-01

The interpretation of Sm-Nd systematics for the early Earth relies on knowing the composition of the silicate Earth and the 146Sm decay constant. We have measured both 146Sm-142Nd and 147Sm-143Nd internal systematics of four individual Calcium, Aluminum-rich Inclusions (CAIs), the first solids formed in the Solar System [1], from 3 different carbonaceous chondrites from the CV3 group: Allende, Northwest Africa (NWA) 2364 and NWA 6991. Results obtained on NWA 6991 plot on a well-defined mineral and bulk isochron with a Solar System initial 146Sm/144Sm ratio of 0.0070 ±0.0024. This ratio is more consistent with the ratio defined from internal isochrons of differentiated meteorites using the half-life of 103 Ma for 146Sm [2], instead of the value obtained considering the half-life of 68 Ma [3]. On the basis of nucleosynthethic anomalies in Sm and Nd isotopes [4], the ordinary (O) and enstatite (E) chondrites remain potential candidates for the Earth's building blocks. OC have an average deficit of -18±3 ppm relative to modern terrestrial 142Nd/144Nd, whereas EC range from the OC to the terrestrial values [4-6]. Sm stable isotope compositions of the analyzed CAIs indicate that galactic cosmic rays did not affect the 142Nd/144Nd compositions, but deficits are found in the pure p-process 144Sm nuclide (-240 to -290 ppm/ standard). These deficits may translate to 142Nd deficits of a few ppm. NWA 6991 CAI 146Sm-142Nd internal isochron passes through a 142Nd/144Nd ratio of -6 ±6 ppm relative to the terrestrial standard at a chondritic 147Sm/144Nd of 0.1960. We note that this value is identical to the enstatite chondrite average and the 142Nd/144Nd ratio of the lunar mantle, as defined recently by [7] using a chondritic Sm/Nd and Lu/Hf for the bulk Moon. While the determination of the Sm-Nd reference parameters for the bulk Earth is still contentious, the difference in 142Nd/144Nd between modern terrestrial rocks and meteorites analyzed so far is <10ppm. [1] Bouvier and Wadhwa (2010) Nat. Geosc. 3, 637. [2] Boyet et al. (2010) Earth Planet. Sci. Lett. 291, 172. [3] Kinoshita et al. (2012) Science 335, 1614. [4] Carlson et al. (2007) Science 316, 1175. [5] Boyet and Carlson (2005) Science 309, 576. [6] Gannoun et al. (2011) Proc. Nat. Acad. Sc. 108, 7693. [7] Sprung et al. (2013) Earth Planet. Sci. Lett. 380, 77.

DOE Office of Scientific and Technical Information (OSTI.GOV)

Jura, M.; Xu, S.; Klein, B.

Using ultraviolet spectra obtained with the Cosmic Origins Spectrograph on the Hubble Space Telescope, we extend our previous ground-based optical determinations of the composition of the extrasolar asteroids accreted onto two white dwarfs, GD 40 and G241-6. Combining optical and ultraviolet spectra of these stars with He-dominated atmospheres, 13 and 12 polluting elements are confidently detected in GD 40 and G241-6, respectively. For the material accreted onto GD 40, the volatile elements C and S are deficient by more than a factor of 10 and N by at least a factor of 5 compared to their mass fractions in primitivemore » CI chondrites and approach what is inferred for bulk Earth. A similar pattern is found for G241-6 except that S is undepleted. We have also newly detected or placed meaningful upper limits for the amount of Cl, Al, P, Ni, and Cu in the accreted matter. Extending results from optical studies, the mass fractions of refractory elements in the accreted parent bodies are similar to what is measured for bulk Earth and chondrites. Thermal processing, perhaps interior to a snow line, appears to be of central importance in determining the elemental compositions of these particular extrasolar asteroids.« less

High abundances of presolar grains and 15N-rich organic matter in CO3.0 chondrite Dominion Range 08006

NASA Astrophysics Data System (ADS)

Nittler, Larry R.; Alexander, Conel M. O'D.; Davidson, Jemma; Riebe, My E. I.; Stroud, Rhonda M.; Wang, Jianhua

2018-04-01

NanoSIMS C-, N-, and O-isotopic mapping of matrix in CO3.0 chondrite Dominion Range (DOM) 08006 revealed it to have in its matrix the highest abundance of presolar O-rich grains (257 +76/-96 ppm, 2σ) of any meteorite. It also has a matrix abundance of presolar SiC of 35 (+25/-17, 2σ) ppm, similar to that seen across primitive chondrite classes. This provides additional support to bulk isotopic and petrologic evidence that DOM 08006 is the most primitive known CO meteorite. Transmission electron microscopy of five presolar silicate grains revealed one to have a composite mineralogy similar to larger amoeboid olivine aggregates and consistent with equilibrium condensation, two non-stoichiometric amorphous grains, and two olivine grains, though one is identified as such solely based on its composition. We also found insoluble organic matter (IOM) to be present primarily as sub-micron inclusions with ranges of C- and N-isotopic anomalies similar to those seen in primitive CR chondrites and interplanetary dust particles. In contrast to other primitive extraterrestrial materials, H isotopic imaging showed normal and homogeneous D/H. Most likely, DOM 08006 and other CO chondrites accreted a similar complement of primitive and isotopically anomalous organic matter to that found in other chondrite classes and IDPs, but the very limited amount of thermal metamorphism experienced by DOM 08006 has caused loss of D-rich organic moieties, while not substantially affecting either the molecular carriers of C and N anomalies or most inorganic phases in the meteorite. One C-rich grain that was highly depleted in 13C and 15N was identified; we propose it originated in the Sun's parental molecular cloud.

Bulk density of asteroid 243 Ida from the orbit of its satellite Dactyl

USGS Publications Warehouse

Belton, M.J.S.; Chapmant, C.R.; Thomas, P.C.; Davies, M.E.; Greenberg, R.; Klaasen, K.; Byrnes, D.; D'Amario, L.; Synnott, S.; Johnson, T.V.; McEwen, A.; Merline, W.J.; Davis, D.R.; Petit, J.-M.; Storrs, A.; Veverka, J.; Zellner, B.

1995-01-01

DURING its reconnaissance of the asteroid 243 Ida, the Galileo spacecraft returned images of a second object, 1993(243)1 Dactyl1 - the first confirmed satellite of an asteroid. Sufficient data were obtained on the motion of Dactyl to determine its orbit as a function of Ida's mass. Here we apply statistical and dynamical arguments to constrain the range of possible orbits, and hence the mass of Ida. Combined with the volume of Ida2, this yields a bulk density of 2.6??0.5 g cm-3. Allowing for the uncertainty in the porosity of Ida, this density range is consistent with a bulk chondritic composition, and argues against some (but not all) classes of meteoritic igneous rock types that have been suggested as compositionally representative of S-type asteroids like Ida.

Bulk density of asteroid 243 Ida from the orbit of its satellite Dactyl

USGS Publications Warehouse

Belton, M.J.S.; Chapman, C.R.; Thomas, P.C.; Davies, M.E.; Greenberg, R.; Klaasen, K.; Byrnes, D.; D'Amario, L.; Synnott, S.; Johnson, T.V.; McEwen, A.; Merline, W.J.; Davis, D.R.; Petit, J.-M.; Storrs, A.; Veverka, J.; Zellner, B.

1995-01-01

DURING its reconnaissance of the asteroid 243 Ida, the Galileo spacecraft returned images of a second object, 1993(243)1 Dactyl1 - the first confirmed satellite of an asteroid. Sufficient data were obtained on the motion of Dactyl to determine its orbit as a function of Ida's mass. Here we apply statistical and dynamical arguments to constrain the range of possible orbits, and hence the mass of Ida. Combined with the volume of Ida2, this yields a bulk density of 2.6 ?? 0.5 g cm-3. Allowing for the uncertainty in the porosity of Ida, this density range is consistent with a bulk chon-dritic composition, and argues against some (but not all) classes of meteoritic igneous rock types that have been suggested as compositionally representative of S-type asteroids like Ida. ?? 2002 Nature Publishing Group.

Volatile-bearing phases in carbonaceous chondrites: Compositions, modal abundance, and reaction kinetics

NASA Technical Reports Server (NTRS)

Ganguly, Jibamitra

1990-01-01

The spectral and density characteristics of Phobos and Deimos (the two small natural satellites of Mars) strongly suggest that a significant fraction of the near-earth asteroids are made of carbonaceous chondrites, which are rich in volatile components and, thus, could serve as potential resources for propellants and life supporting systems in future planetary missions. However, in order to develop energy efficient engineering designs for the extraction of volatiles, knowledge of the nature and modal abundance of the minerals in which the volatiles are structurally bound and appropriate kinetic data on the rates of the devolatilization reactions is required. Theoretical calculations to predict the modal abundances and compositions of the major volatile-bearing and other mineral phases that could develop in the bulk compositions of C1 and C2 classes (the most volatile rich classes among the carbonaceous chondrites) were performed as functions of pressure and temperature. The rates of dehydration of talc at 585, 600, 637, and 670 C at P(total) = 1 bar were determine for the reaction: Talc = 3 enstatite + quartz + water. A scanning electron microscopic study was conducted to see if the relative abundance of phases can be determined on the basis of the spectral identification and x ray mapping. The results of this study and the other studies within the project are discussed.

Determining Possible Building Blocks of the Earth and Mars

NASA Technical Reports Server (NTRS)

Burbine, T. H.; OBrien, K. M.

2004-01-01

One of the fundamental questions concerning planetary formation is exactly what material did the planets form from? All the planets in our solar system are believed to have formed out of material from the solar nebula. Chondritic meteorites appear to sample this primitive material. Chondritic meteorites are generally classified into 13 major groups, which have a variety of compositions. Detailed studies of possible building blocks of the terrestrial planets require samples that can be used to estimate the bulk chemistry of these bodies. This study will focus on trying to determine possible building blocks of Earth and Mars since samples of these two planets can be studied in detail in the laboratory.

Oxygen isotope constraints on the alteration temperatures of CM chondrites

NASA Astrophysics Data System (ADS)

Verdier-Paoletti, Maximilien J.; Marrocchi, Yves; Avice, Guillaume; Roskosz, Mathieu; Gurenko, Andrey; Gounelle, Matthieu

2017-01-01

We report a systematic oxygen isotopic survey of Ca-carbonates in nine different CM chondrites characterized by different degrees of alteration, from the least altered known to date (Paris, 2.7-2.8) to the most altered (ALH 88045, CM1). Our data define a continuous trend that crosses the Terrestrial Fractionation Line (TFL), with a general relationship that is indistinguishable within errors from the trend defined by both matrix phyllosilicates and bulk O-isotopic compositions of CM chondrites. This bulk-matrix-carbonate (BMC) trend does not correspond to a mass-dependent fractionation (i.e., slope 0.52) as it would be expected during fluid circulation along a temperature gradient. It is instead a direct proxy of the degree of O-isotopic equilibration between 17,18O-rich fluids and 16O-rich anhydrous minerals. Our O-isotopic survey revealed that, for a given CM, no carbonate is in O-isotopic equilibrium with its respective surrounding matrix. This precludes direct calculation of the temperature of carbonate precipitation. However, the O-isotopic compositions of alteration water in different CMs (inferred from isotopic mass-balance calculation and direct measurements) define another trend (CMW for CM Water), parallel to BMC but with a different intercept. The distance between the BMC and CMW trends is directly related to the temperature of CM alteration and corresponds to average carbonates and serpentine formation temperatures of 110 °C and 75 °C, respectively. However, carbonate O-isotopic variations around the BMC trend indicate that they formed at various temperatures ranging between 50 and 300 °C, with 50% of the carbonates studied here showing precipitation temperature higher than 100 °C. The average Δ17O and the average carbonate precipitation temperature per chondrite are correlated, revealing that all CMs underwent similar maximum temperature peaks, but that altered CMs experienced protracted carbonate precipitation event(s) at lower temperatures than the least altered CMs. Our data suggest that the Δ17O value of Ca-carbonates could be a reliable proxy of the degree of alteration experienced by CM chondrites.

A collection of diverse micrometeorites recovered from 100 tonnes of Antarctic blue ice

NASA Technical Reports Server (NTRS)

Maurette, M.; Olinger, C.; Michel-Levy, M. C.; Kurat, G.; Pourchet, M.

1991-01-01

A new type of meteoritic material, intermediate in size between meteorites and interplanetary dust particles (IDPs), is described. Melting and filtering of about 100 tons of blue ice near Cap Prudhomme, Antarctica, yielded 7500 or more irregular, friable particles and about 1500 melted spherules, about 100 microns in size, both showing a 'chondritic' composition suggestive of an extraterrestrial origin. Analyzed irregular particles appear to be unmelted and have similarities with the fine-grained matrix of primitive carbonaceous chondrites, but are extremely diverse in composition. Isotopic analysis of trapped neon confirms an extraterrestrial origin for 16 of 47 irregular particles and 2 of 19 spherules studied and strongly suggests that they were exposed in space as micrometeoroids. These large Antarctic micrometeorites constitute a new family, or at least a new population, of solar system objects, in a mass range corresponding to the bulk of extraterrestrial material accreted by the earth today.

A divergent heritage for complex organics in Isheyevo lithic clasts

NASA Astrophysics Data System (ADS)

van Kooten, Elishevah M. M. E.; Nagashima, Kazuhide; Kasama, Takeshi; Wampfler, Susanne F.; Ramsey, Jon P.; Frimann, Søren; Balogh, Zoltan I.; Schiller, Martin; Wielandt, Daniel P.; Franchi, Ian A.; Jørgensen, Jes K.; Krot, Alexander N.; Bizzarro, Martin

2017-05-01

Primitive meteorites are samples of asteroidal bodies that contain a high proportion of chemically complex organic matter (COM) including prebiotic molecules such as amino acids, which are thought to have been delivered to Earth via impacts during the early history of the Solar System. Thus, understanding the origin of COM, including their formation pathway(s) and environment(s), is critical to elucidate the origin of life on Earth as well as assessing the potential habitability of exoplanetary systems. The Isheyevo CH/CBb carbonaceous chondrite contains chondritic lithic clasts with variable enrichments in 15N believed to be of outer Solar System origin. Using transmission electron microscopy (TEM-EELS) and in situ isotope analyses (SIMS and NanoSIMS), we report on the structure of the organic matter as well as the bulk H and N isotope composition of Isheyevo lithic clasts. These data are complemented by electron microprobe analyses of the clast mineral chemistry and bulk Mg and Cr isotopes obtained by inductively coupled plasma and thermal ionization mass spectrometry, respectively (MC-ICPMS and TIMS). Weakly hydrated (A) clasts largely consist of Mg-rich anhydrous silicates with local hydrated veins composed of phyllosilicates, magnetite and globular and diffuse organic matter. Extensively hydrated clasts (H) are thoroughly hydrated and contain Fe-sulfides, sometimes clustered with organic matter, as well as magnetite and carbonates embedded in a phyllosilicate matrix. The A-clasts are characterized by a more 15N-rich bulk nitrogen isotope composition (δ15N = 200-650‰) relative to H-clasts (δ15N = 50-180‰) and contain extremely 15N-rich domains with δ15N < 5000‰. The D/H ratios of the clasts are correlated with the degree of clast hydration and define two distinct populations, which we interpret as reflecting mixing between D-poor fluid(s) and distinct organic endmember components that are variably D-rich. High-resolution N isotope data of 15N-rich domains show that the lithic clast diffuse organic matter is typically more 15N-rich than globular organic matter. The correlated δ15N values and C/N ratios of nanoglobules require the existence of multiple organic components, in agreement with the H isotope data. The combined H and N isotope data suggest that the organic precursors of the lithic clasts are defined by an extremely 15N-poor (similar to solar) and D-rich component for H-clasts, and a moderately 15N-rich and D-rich component for A-clasts. In contrast, the composition of the putative fluids is inferred to include D-poor but moderately to extremely 15N-rich H- and N-bearing components. The variable 15N enrichments in H- and A-clasts are associated with structural differences in the N bonding environments of their diffuse organic matter, which are dominated by amine groups in H-clasts and nitrile functional groups in A-clasts. We suggest that the isotopically divergent organic precursors in Isheyevo clasts may be similar to organic moieties in carbonaceous chondrites (CI, CM, CR) and thermally recalcitrant organic compounds in ordinary chondrites, respectively. The altering fluids, which are inferred to cause the 15N enrichments observed in the clasts, may be the result of accretion of variable abundances of NH3 and HCN ices. Finally, using bulk Mg and Cr isotope composition of clasts, we speculate on the accretion regions of the various primitive chondrites and components and the origin of the Solar System's N and H isotope variability.

Correlated Amino Acid and Mineralogical Analyses of Milligram and Submilligram Samples of Carbonaceous Chondrite Lonewolf Nunataks 94101

NASA Technical Reports Server (NTRS)

Burton, S.; Berger, E. L.; Locke, D. R.; Lewis, E. K.

2018-01-01

Amino acids, the building blocks of proteins, have been found to be indigenous in the eight carbonaceous chondrite groups. The abundances, structural, enantiomeric and isotopic compositions of amino acids differ significantly among meteorites of different groups and petrologic types. These results suggest parent-body conditions (thermal or aqueous alteration), mineralogy, and the preservation of amino acids are linked. Previously, elucidating specific relationships between amino acids and mineralogy was not possible because the samples analyzed for amino acids were much larger than the scale at which petrologic heterogeneity is observed (sub mm-scale differences corresponding to sub-mg samples); for example, Pizzarello and coworkers measured amino acid abundances and performed X-ray diffraction (XRD) on several samples of the Murchison meteorite, but these analyses were performed on bulk samples that were 500 mg or larger. Advances in the sensitivity of amino acid measurements by liquid chromatography with fluorescence detection/time-of-flight mass spectrometry (LC-FD/TOF-MS), and application of techniques such as high resolution X-ray diffraction (HR-XRD) and scanning electron microscopy (SEM) with energy dispersive spectroscopy (EDS) for mineralogical characterizations have now enabled coordinated analyses on the scale at which mineral heterogeneity is observed. In this work, we have analyzed samples of the Lonewolf Nunataks (LON) 94101 CM2 carbonaceous chondrite. We are investigating the link(s) between parent body processes, mineralogical context, and amino acid compositions in meteorites on bulk samples (approx. 20mg) and mineral separates (< or = 3mg) from several of spatial locations within our allocated samples. Preliminary results of these analyses are presented here.

The Mukundpura meteorite, a new fall of CM chondrite

NASA Astrophysics Data System (ADS)

Ray, Dwijesh; Shukla, Anil D.

2018-02-01

Mukundpura is a new CM chondrite fell near Jaipur, Rajasthan, India on June 6, 2017 at 5:15 IST. The fall was observed by local villager. According to eyewitness, the meteorite was fragmented into several pieces once the object hit the ground. Based on petrography, mineralogy and bulk composition, Mukundpura is classified as CM2 chondrite. The chondrules are mainly similar to type I (Olivine: Fo99). Olivines are often found associated with pyroxene (Wo10-35En62-87Fs2-7) phenocryst. However, occurrences of forsteritic and fayalitic olivine (Fa58-71) as isolated mineral clast in matrix are not uncommon. Other types of chondrules include porphyritic pyroxene (En86Fs14) and barred olivine (Fa32.7±0.3) clast. Chondrules are commonly rimmed by fine-grained accretionary dust mantles. Phyllosilicates are the most dominant secondary mineral in matrix and largely associated with poorly characterised phases (PCP). FeO/SiO2 and S/SiO2 of PCP are 2.7 and 0.4 respectively. Other phases in matrix generally include calcite (pure CaCO3), Fe-Ni metal and sulphides. Spinel and perovskite occur occasionally as inclusions. The spherical or elliptical shaped metals (within chondrule or in isolated grains) are low-Ni type (kamacite <7.5 wt%) and resembles the solar Ni/Co ratio. However, Ni content in metal rarely exceeds 8.5 wt% (up to 23 wt%, taenite). Pyrrhotite (Fe ∼62 wt%; S ∼38 wt%) and pentlandite (Fe ∼31-33 wt%, Ni ∼28-32 wt%, S ∼33 wt%)) are the common sulphides occur as isolated grains within the matrix, however, the former is the most dominant. The bulk chemical composition of Mukundpura is largely similar to other CM type chondrite (e.g. Paris CM). Based on petrography, we infer a modest aqueous alteration stage for Mukundpura while the effect of thermal metamorphism was negligible.

Silica-rich orthopyroxenite in the Bovedy chondrite

NASA Technical Reports Server (NTRS)

Ruzicka, Alex; Kring, David A.; Hill, Dolores H.; Boynton, William V.; Clayton, Robert N.; Mayeda, Toshiko K.

1995-01-01

A large (greater than 4.5 x 7 x 4 mm), igneous-textured clast in the Bovedy (L3) chondrite is notable for its high bulk SiO2 content (is approximately equal to 57.5 wt%). The clast consists of normally zoned orthopyroxene (83.8 vol%), tridymite (6.2%), an intergrowth of feldspar (5.8%) and sodic glass (3.1%), pigeonite (1.0%), and small amounts of chromite (0.2%), augite, and Fe,Ni-metal; it is best described as a silica-rich orthopyroxenite. The oxygen-isotopic composition of the clast is similar, but not identical, to Bovedy and other ordinary chondrites. The clast has a superchondritic Si/Mg ratio, but has Mg/(Mg + Fe) and Fe/Mn ratios that are similar to ordinary chondrite silicate. The closest chemical analogues to the clast are radial-pyroxene chondrules, diogenites, pyroxene-silica objects in ordinary chondrites, and silicates in the IIE iron meteorite Weekeroo Station. The clast crystallized from a siliceous melt that cooled fast enough to prevent complete attainment of equilibrium but slow enough to allow nearly complete crystallization. The texture, form, size and composition of the clast suggestion that it is an igneous differentiate from an asteroid or planetesimal that formed in the vicinity of ordinary chondrites. The melt probably cooled in the near-surface region of the parent object. It appears that in the source region of the clast, metallic and silicate partial melt were largely-to-completely lost during a relatively low degree of melting, and that during a higher degree of melting, olivine and low-Ca pyroxene separated from the remaining liquid, which ultimately solidified to form the clast. While these fractionation steps could not have all occurred at the same temperature, they could have been accomplished in a single melting episode, possibly as a result of heating by radionuclides or by electromagnetic induction. Fractionated magmas can also account for other Si-rich objects in chondrites.

16O enrichments in aluminum-rich chondrules from ordinary chondrites

NASA Astrophysics Data System (ADS)

Russell, Sara S.; MacPherson, Glenn J.; Leshin, Laurie A.; McKeegan, Kevin D.

2000-12-01

The oxygen isotopic compositions of seven Al-rich chondrules from four unequilibrated ordinary chondrites were measured in situ using an ion microprobe. On an oxygen three isotope plot, the data are continuous with the ordinary chondrite ferromagnesian chondrule field but extend it to more 16O-enriched values along a mixing line of slope=0.83±0.09, with the lightest value recorded at δ18O=-15.7±1.8‰ and δ17O=-13.5±2.6‰. If Al-rich chondrules were mixtures of ferromagnesian chondrules and CAI material, their bulk chemical compositions would require them to exhibit larger 16O enrichments than we observe. Therefore, Al-rich chondrules are not simple mixtures of these two components. Three chondrules exhibit significant internal isotopic heterogeneity indicative of partial exchange with a gaseous reservoir. Porphyritic Al-rich chondrules are consistently 16O-rich relative to nonporphyritic ones, suggesting that degree of melting is a key factor and pointing to a nebular setting for the isotopic exchange process. Because Al-rich chondrules are closely related to ferromagnesian chondrules, their radiogenic Mg isotopic abundances can plausibly be applied to help constrain the timing or location of chondrule formation.

A New Type of Foreign Clast in A Polymict Ureilite: A CAI or AL-Rich Chondrule

NASA Technical Reports Server (NTRS)

Goodrich, C. A.; Ross, D. K.; Treiman, A. H.

2017-01-01

Introduction: Polymict ureilites are breccias interpreted to represent regolith formed on a ureilitic asteroid [1-3]. They consist of approximately 90-95% clasts of various ureilite types (olivine-pyroxene rocks with Fo 75-95), a few % indigenous feldspathic clasts, and a few % foreign clasts [4-20]. The foreign clasts are diverse, including fragments of H, L, LL and R chondrites, angrites, other achondrites, and dark clasts similar to CC [6,7,9-19]. We report a new type of foreign clast in polymict ureilite DaG 999. Methods: Clast 8 in Dar al Gani (DaG) 999/1 (Museum fur Naturkunde) was discovered during a survey of feldspathic clasts in polymict ureilites [19,20]. It was studied by BEI, EMPA, and X-ray mapping on the JEOL 8530F electron microprobe at ARES, JSC. Petrography and Mineral Compositions: Clast 8 is sub-rounded to irregular in shape, approximately 85 micrometers in diameter, and consists of approximately 68% pyroxene and 32% mesostasis (by area). Part of the pyroxene (top half of clast in Fig. 1a and 2) shows a coarse dendritic morphology; the rest appears massive. Mesostasis may be glassy and contains fine needles/grains of pyroxene. The pyroxene has very high CaO (23.5 wt.%) and Al2O3 (19.7 wt.%), with the formula: (Ca(0.91)Mg(0.63)Fe(0.01)Al(sup VI) (0.38)Cr(0.01)Ti(0.05)1.99 Si2O6. The bulk mesostasis also has very high Al2O3 (approximately 26 wt.%). A bulk composition for the clast was obtained by combining modal abundances with phase compositions (Table 1, Fig. 3). Discussion: The pyroxene in clast 8 has a Ca-Al-(Ti)- rich (fassaitic) composition that is clearly distinct from compositions of pyroxenes in main group ureilites [22] or indigenous feldspathic clasts in polymict ureilites [4-8]. It also has significantly higher Al than fassaite in angrites (up to approximately 12 wt.% [23]), which occur as xenoliths in polymict ureilites. Ca-Al-Ti rich pyroxenes are most commonly found in CAIs, Al-rich chondrules and other types of refractory inclusions in chondrites [21,24-31]. However, the clast 8 pyroxene matches only the most Al-Ca-rich of these, e.g., pyroxenes in type B CAIs in CV3 chondrites [25,30,31], a pyroxene-hibonite spherule and a pyroxene-anorthitespinel fragment from unique CC Acfer 094 [29], and one Al-rich chondrule from Chainpur (LL3.4) [21]. The mineralogy of clast 8 is not consistent with the mineral assemblages of any of these objects (since it lacks hibonite, spinel and/or anorthite), which suggests that it is unrepresentatively sectioned or is a fragment of a more mineralogically diverse object. Its bulk composition (Table 1; Fig. 3) is similar to bulk compositions of some Al-rich chondrules, as well as those of Type C CAIs (which plot in the sp+An+L field in Fig. 3), although it is enriched in silica relative to type C CAIs [e.g., 31]. This suggests a more likely affinity to Al-rich chondrules, although most Al-rich chondrules have less Al-Ca-rich pyroxene [21,26,27]. These bulk compositional comparisons may not be definitive, however, if the clast is unrepresentatively sampled. One of eleven Al-rich chondrules from UOCs described by [21] has textural and compositional characteristics that make it a possible progenitor type for clast 8. This chondrule (Chainpur 1251-14-2) is anorthiteporphyritic, with an interstitial dendritic intergrowth of pyroxene (similar in composition to that in clast 8) and plagioclase [21]. Clast 8 is conceivably a fragment from the interstitial area of such an object. The occurrence of glassy mesostasis (in clast 8) rather than plagioclase may not be a significant difference; it could result from a difference only in cooling rate. Al-rich chondrules with glassy mesostasis are rare, and known occurrences are Ca-poor [26], unlike clast 8. Polymict ureilites are known to contain xenoliths of various chondrites (including OC, R and CC) as well as individual ferromagnesian and silica-pyroxene chondrules probably derived from OC or RC [6,9,15,16,18]. This is the first report of an individual chondritic refractory inclusion as a xenolith in a polymict ureilite. An RC-like sample from anomalous polymict ureilite Almahata Sitta contains CAIs, but they are spinel-rich and not similar to clast 8 [13,14]. Further studies of this clast (which, unfortunately, may not be possible), or the discovery of additional (more representative?) materials of this type would be needed to determine the exact nature of this xenolith and the type of chondrite from which it is derived.

Dark inclusions in CO3 chondrites: new indicators of parent-body processes

NASA Astrophysics Data System (ADS)

Itoh, Daisuke; Tomeoka, Kazushige

2003-01-01

A petrographic and scanning electron microscopic study of the four CO3 chondrites Kainsaz, Ornans, Lancé, and Warrenton reveals for the first time that dark inclusions (DIs) occur in all the meteorites. DIs are mostly smaller in size than those reported from CV3 chondrites. They show evidence suggesting that they were formed by aqueous alteration and subsequent dehydration of a chondritic precursor and so probably have a formation history similar to that of DIs in CV3 chondrites. DIs in the CO3 chondrites consist mostly of fine-grained, Fe-rich olivine and can be divided into two types on the basis of texture. Type I DIs contain rounded, porous aggregates of fine grains in a fine-grained matrix and have textures suggesting that they are fragments of chondrule pseudomorphs. Veins filled with Fe-rich olivine are common in type I DIs, providing evidence that they experienced aqueous alteration on the parent body. Type II DIs lack rounded porous aggregates and have a matrix-like, featureless texture. Bulk chemical compositions of DIs and mineralogical characteristics of olivine grains in DIs suggest that these two types of DIs have a close genetic relationship. The DIs are probably clasts that have undergone aqueous alteration and subsequent dehydration at a location different from the present location in the meteorites. The major element compositions, the mineralogy of metallic phases, and the widely dispersed nature of the DIs suggest that their precursor was CO chondrite material. The CO parent body has been commonly regarded to have been dry, homogeneous, and unprocessed. However, the DIs suggest that the CO parent body was a heterogeneous conglomerate consisting of water-bearing regions and water-free regions and that during asteroidal heating, the water-bearing regions were aqueously altered and subsequently dehydrated. Brecciation may also have been active in the parent body. The DIs and the matrices are similarly affected by thermal metamorphism in their own host CO3 chondrites (petrologic subtypes 3.1 to 3.6), but the degree of the secondary processing (aqueous alteration and subsequent dehydration) of the DIs has no apparent correlation with the petrologic grades of the host chondrites. These observations suggest that the DIs had been incorporated into the host chondrites before the thermal metamorphism took place and that the secondary processes that affected the DIs largely occurred before the thermal metamorphism.

Bright Stuff on Ceres = Sulfates and Carbonates on CI Chondrites

NASA Technical Reports Server (NTRS)

Zolensky, Michael; Chan, Queenie H. S.; Gounelle, Matthieu; Fries, Marc

2016-01-01

Recent reports of the DAWN spacecraft's observations of the surface of Ceres indicate that there are bright areas, which can be explained by large amounts of the Mg sulfate hexahydrate (MgSO4•6(H2O)), although the identification appears tenuous. There are preliminary indications that water is being evolved from these bright areas, and some have inferred that these might be sites of contemporary hydro-volcanism. A heat source for such modern activity is not obvious, given the small size of Ceres, lack of any tidal forces from nearby giant planets, probable age and presumed bulk composition. We contend that observations of chondritic materials in the lab shed light on the nature of the bright spots on Ceres

Bulk Composition of Vesta as Constrained by the Dawn Mission and the HED Meteorites

NASA Technical Reports Server (NTRS)

Toplis, M. J.; Mizzon, H.; Forni, O.; Monnereau, H.; Prettyman, T. H.; McSween, H. Y.; McCoy, T. J.; Mittlefehldt, D. W.; DeSactis, M. C.; Raymond, C. T.;

Mn-Cr isotopic systematics of Chainpur chondrules and bulk ordinary chondrites

NASA Technical Reports Server (NTRS)

Nyquist, L.; Lindstrom, D.; Wiesmann, H.; Bansal, B.; Shih, C.-Y.; Mittlefehldt, D.; Martinez, R.; Wentworth, S.

1994-01-01

We report on ongoing study of the Mn-Cr systematics of individual Chainpur (LL3.4) chondrules and compare the results to those for bulk ordinary chondrites. Twenty-eight chondrules were surveyed for abundances of Mn, Cr, Na, Fe, Sc, Hf, Ir, and Zn by INAA. Twelve were chosen for SEM/EDX and high-precision Cr-isotopic studies on the basis of LL-chondrite-normalized Mn(LL), Sc(LL), (Mn/Fe)(LL), and (Sc/Fe)(LL) as well as their Mn/Cr ratios. Classification into textural types follows from SEM/EDX examination of interior surfaces.

Genetic Relationships Between Chondrules, Rims and Matrix

NASA Technical Reports Server (NTRS)

Huss, G. R.; Alexander, C. M. OD.; Palme, H.; Bland, P. A.; Wasson, J. T.

2004-01-01

The most primitive chondrites are composed of chondrules and chondrule fragments, various types of inclusions, discrete mineral grains, metal, sulfides, and fine-grained materials that occur as interchondrule matrix and as chondrule/inclusion rims. Understanding how these components are related is essential for understanding how chondrites and their constituents formed and were processed in the solar nebula. For example, were the first generations of chondrules formed by melting of matrix or matrix precursors? Did chondrule formation result in appreciable transfer of chondrule material into the matrix? Here, we consider three types of data: 1) compositional data for bulk chondrites and matrix, 2) mineralogical and textural information, and 3) the abundances and characteristics of presolar materials that reside in the matrix and rims. We use these data to evaluate the roles of evaporation and condensation, chondrule formation, mixing of different nebular components, and secondary processing both in the nebula and on the parent bodies. Our goal is to identify the things that are reasonably well established and to point out the areas that need additional work.

Isotopic signatures and distribution of nitrogen and trapped and radiogenic xenon in the Acapulco and FRO90011 meteorites

NASA Technical Reports Server (NTRS)

Kim, Y.; Marti, K.

1993-01-01

Acapulco metal and silicate show distinct N isotopic signatures. Trapped heavy noble gases are carried by 'magnetic' opx and radiogenic Xe-129 excesses are observed in phosphate and in minor surficial phases on metal grains. N and Xe isotopic signatures in FRO90011 do not agree with those observed in Acapulco. The Acapulco meteorite is unique in having achondritic texture and chondritic composition. Its mineralogical study shows the record of high temperature (1100 C) recrystallization. However, this meteorite shows abundances of volatile elements close to the levels observed in carbonaceous chondrites and concentrations of heavy noble gases comparable to those observed in type 4 ordinary chondrites, not expected for a presumed highly equilibrated object. Nitrogen measurements in bulk Acapulco revealed two different isotopic signatures, in apparent conflict with evidence for a high degree of recrystallization. N and Xe were studied in separated mineral phases to search for the carriers in order to better understand the formation and thermal history of the Acapulco parent body.

Paleomagnetism of a primitive achondrite parent body: The acapulcoite-lodranites

NASA Astrophysics Data System (ADS)

Schnepf, N. R.; Weiss, B. P.; Andrade Lima, E.; Fu, R. R.; Uehara, M.; Gattacceca, J.; Wang, H.; Suavet, C. R.

2014-12-01

Primitive achondrites are a recently recognized meteorite grouping with textures and compositions intermediate between unmelted meteorites (chondrites) and igneous meteorites (achondrites). Their existence demonstrates prima facie that some planetesimals only experienced partial rather than complete melting. We present the first paleomagnetic measurements of acapulcoite-lodranite meteorites to determine the existence and intensity of ancient magnetic fields on their parent body. Our paleomagnetic study tests the hypothesis that their parent body had an advecting metallic core, with the goal of providing one of the first geophysical constraints on its large-scale structure and the extent of interior differentiation. In particular, by analyzing samples whose petrologic textures require an origin on a partially differentiated body, we will be able to critically test a recent proposal that some achondrites and chondrite groups could have originated on a single body (Weiss and Elkins-Tanton 2013). We analyzed samples of the meteorites Acapulco and Lodran. Like other acapulcoites and lodranites, these meteorites are granular rocks containing large (~0.1-0.3 mm) kamacite and taenite grains along with similarly sized silicate crystals. Many silicate grains contain numerous fine (1-10 μm) FeNi metal inclusions. Our compositional measurements and rock magnetic data suggest that tetrataenite is rare or absent. Bulk paleomagnetic measurements were done on four mutually oriented bulk samples of Acapulco and one bulk sample of Lodran. Alternating field (AF) demagnetization revealed that the magnetization of the bulk samples is highly unstable, likely due to the large (~0.1-0.3 mm) interstitial kamacite grains throughout the samples. To overcome this challenge, we are analyzing individual ~0.2 mm mutually oriented silicate grains extracted using a wire saw micromill. Preliminary SQUID microscopy measurements of a Lodran silicate grain suggest magnetization stable to AF levels of at least 25-40 mT.

LEW 88180, LEW 87119, and ALH 85119: New EH6, EL7, and EL4 Enstatite Chondrites

NASA Astrophysics Data System (ADS)

Zhang, Y.; Benoit, P. H.; Sears, D. W. G.

1993-07-01

The EH and EL chondrites formed in a uniquely reducing environment, containing low-Fe pyroxene, abundant metal, and a number of unusual sulphides and other minerals [1]. An important aspect of their history is that while the EL chondrites consist predominantly of metamorphosed meteorites, the EH consist primarily of little-metamorphosed meteorites (e.g., [2]), and yet EL chondrites have lower equilibrium temperatures than EH chondrite [3,4]. To help understand this observation and its implication for the history of the classes, we have been searching for new enstatite chondrites, looking especially for meteorites of previously unknown chemical-petrologic class. Using our normal INAA methods [5] and sample splits of 100-200 mg, the bulk composition of nine Antarctic enstatite chondrites and one fall were determined. The data were used to assign the meteorites to chemical classes, the Ni/Ir vs. Al/V plot (Fig. 1) being especially useful since it uses the refractory element difference between EH and EL chondrites and is insensitive to metal-silicate heterogeneity. The well-analyzed Qingzhen was included to check our method. ALH84170, ALH84206, and EET87746, which Mason described as E3, E4, and E4 were all found to be EH chondrites [6]. Our data for the three paired EL3 chondrites were discussed earlier (MAC88136, 88180, and 88184) [7,8]. LEW88180, LEW87119, and ALH85119, which Mason described as type E6, E6, and E4 respectively [6], are EH, EL, and EL; thus LEW88180 and ALH85119 appear to be the first EH6 and EL4 chondrites. The compositions of kamacite, phosphide, and niningerite-alabandite (Fig. 2) for ALH84170, ALH84206, EET87746, LEW88180, and ALH85119 are consistent with Mason's petrologic type assignments [6]. The mineral composition of LEW88180 (2.7% Si and 9.4% Ni in the kamacite, 7.8% Ni in the phosphide, and 60% FeS in the niningerite) confirms our classification of this meteorite as EH6. ALH85119 contains kamacite with 0.5% Si and 7% Ni, phosphide with 46% Ni and alabandite with 22% FeS, confirming its classification as the first EL4 chondrite. The LEW87119 meteorite has kamacite with 1.5% Si and 9.1% Ni, troilite with 2.9% Cr and 0.64% Ti, and alabandite with the highest FeS (49%) recorded for EL chondrites. Since the meteorite does not appear to be shocked or impact melted (it has medium-grained texture with the slightest indication of chondrules and normal metal and sulfide distribution) and the phase chemistry clearly indicates a higher equilibration temperature than the EL6 chondrites, for the time being we propose to call LEW87119 an EL7 chondrite. With the discovery in the last decade or so of a number of low-petrologic-type EH chondrites and the present discovery of EH6 and EL7 chondrites, the EH class and the EL class now appear to be comparable in their range of mineral compositions and thereby equilibration temperatures. The highest equilibration temperature for the EL chondrites is now ~700 degrees C, which is close to that of EH6 chondrite (Fig. 2). Equilibration temperatures for the EL6 chondrites are similar to those of EH4 chondrites. It may be that EH and EL classes have more similar thermal histories than previously supposed and that it is purely the textures of the two classes that are widely different and in need of further research. References: [1] Keil K. (1968) JGR, 73, 6945-6976. [2] Sears D. W. G. and Weeks K. S. (1984) Nature, 308, 257-259. [3] Skinner B. J. and Luce F. D. (1971) Amer. Min., 56, 1269-1296. [4] Zhang Y. et al. (1992) Meteoritics, 27, 310-311. [5] Weeks K. S.and Sears D. W. G. (1985) GCA, 49, 1525-1536. [6] Mason in Antarctic Meteorite Newsletter (1986, 1987, 1989, and 1990) 9(3), 10(2), 12(1,3), and 13(2,3). [7] Lin Y. T. et al. (1991) LPSC XXII, 811-812. [8] Chang Y. et al. (1992) LPSC XXIII, 217-218.

Chemical and physical studies of type 3 chondrites 12: The metamorphic history of CV chondrites and their components

NASA Technical Reports Server (NTRS)

Guimon, R. Kyle; Symes, Steven J. K.; Sears, Derek W. G.

1995-01-01

The induced thermoluminescence (TL) properties of 16 CV and CV-related chondrites, four CK chondrites and Renazzo (CR2) have been measured in order to investigate their metamorphic history. The petrographic, mineralogical and bulk compositional differences among the CV chondrites indicate that the TL sensitivity of the approximately 130 C TL peak is reflecting the abundance of ordered feldspar, especially in chondrule mesostasis, which in turn reflects parent-body metamorphism. The TL properties of 18 samples of homogenized Allende powder heated at a variety of times and temperatures, and cathodoluminescence mosaics of Axtell and Coolidge, showed results consistent with this conclusion. Five refractory inclusions from Allende, and separates from those inclusions, were also examined and yielded trends reflecting variations in mineralogy indicative of high peak temperatures (either metamorphic or igneous) and fairly rapid cooling. The CK chondrites are unique among metamorphosed chondrites in showing no detectable induced TL, which is consistent with literature data that suggests very unusual feldspar in these meteorites. Using TL sensitivity and several mineral systems and allowing for the differences in the oxidized and reduced subgroups, the CV and CV-related meteorites can be divided into petrologic types analogous to those of the ordinary and CO type 3 chondrites. Axtell, Kaba, Leoville, Bali, Arch and ALHA81003 are type 3.0-3.1, while ALH84018, Efremovka, Grosnaja, Allende and Vigarano are type 3.2-3.3 and Coolidge and Loongana 001 are type 3.8. Mokoia is probably a breccia with regions ranging in petrologic type from 3.0 to 3.2. Renazzo often plots at the end of the reduced and oxidized CV chondrite trends, even when those trends diverge, suggesting that in many respects it resembles the unmetamorphosed precursors of the CV chondrites. The low-petrographic types and low-TL peak temperatures of all samples, including the CV3.8 chondrites, indicates metamorphism in the stability field of low feldspar (i.e., less than 800 C) and a metamorphic history similar to that of the CO chondrites but unlike that of the ordinary chondrites.

Santa Lucia (2008) (L6) Chondrite, a Recent Fall: Composition, Noble Gases, Nitrogen and Cosmic Ray Exposure Age

NASA Astrophysics Data System (ADS)

Mahajan, Ramakant R.; Varela, Maria Eugenia; Joron, Jean Louis

2016-04-01

The Santa Lucia (2008)—one the most recent Argentine meteorite fall, fell in San Juan province, Argentina, on 23 January 2008. Several masses (total ~6 kg) were recovered. Most are totally covered by fusion crust. The exposed interior is of light-grey colour. Chemical data [olivine (Fa24.4) and low-Ca pyroxene (En77.8 Fs20.7 Wo1.6)] indicate that Santa Luica (2008) is a member of the low iron L chondrite group, corresponding to the equilibrated petrologic type 6. The meteorite name was approved by the Nomenclature Committee (NomCom) of the Meteoritical Society (Meteoritic Bulletin, no. 97). We report about the chemical composition of the major mineral phases, its bulk trace element abundance, its noble gas and nitrogen data. The cosmic ray exposure age based on cosmogenic 3He, 21Ne, and 38Ar around 20 Ma is comparable to one peak of L chondrites. The radiogenic K-Ar age of 2.96 Ga, while the young U, Th-He are of 1.2 Ga indicates that Santa Lucia (2008) lost radiogenic 4He more recently. Low cosmogenic (22Ne/21Ne)c and absence of solar wind noble gases are consistent with irradiation in a large body. Heavy noble gases (Ar/Kr/Xe) indicated trapped gases similar to ordinary chondrites. Krypton and neon indicates irradiation in large body, implying large pre-atmospheric meteoroid.

Maribo—A new CM fall from Denmark

NASA Astrophysics Data System (ADS)

Haack, Henning; Grau, Thomas; Bischoff, Addi; Horstmann, Marian; Wasson, John; Sørensen, Anton; Laubenstein, Matthias; Ott, Ulrich; Palme, Herbert; Gellissen, Marko; Greenwood, Richard C.; Pearson, Victoria K.; Franchi, Ian A.; Gabelica, Zelimir; Schmitt-Kopplin, Philippe

2012-01-01

Maribo is a new Danish CM chondrite, which fell on January 17, 2009, at 19:08:28 CET. The fall was observed by many eye witnesses and recorded by a surveillance camera, an all sky camera, a few seismic stations, and by meteor radar observatories in Germany. A single fragment of Maribo with a dry weight of 25.8 g was found on March 4, 2009. The coarse-grained components in Maribo include chondrules, fine-grained olivine aggregates, large isolated lithic clasts, metals, and mineral fragments (often olivine), and rare Ca,Al-rich inclusions. The components are typically rimmed by fine-grained dust mantles. The matrix includes abundant dust rimmed fragments of tochilinite with a layered, fishbone-like texture, tochilinite-cronstedtite intergrowths, sulfides, metals, and carbonates often intergrown with tochilinite. The oxygen isotopic composition: (δ17O = -1.27‰; δ18O = 4.96‰; Δ17O = -3.85‰) plots at the edge of the CM field, close to the CCAM line. The very low Δ17O and the presence of unaltered components suggest that Maribo is among the least altered CM chondrites. The bulk chemistry of Maribo is typical of CM chondrites. Trapped noble gases are similar in abundance and isotopic composition to other CM chondrites, stepwise heating data indicating the presence of gas components hosted by presolar diamond and silicon carbide. The organics in Maribo include components also seen in Murchison as well as nitrogen-rich components unique to Maribo.

Potassium isotopic evidence for a high-energy giant impact origin of the Moon.

PubMed

Wang, Kun; Jacobsen, Stein B

2016-10-27

The Earth-Moon system has unique chemical and isotopic signatures compared with other planetary bodies; any successful model for the origin of this system therefore has to satisfy these chemical and isotopic constraints. The Moon is substantially depleted in volatile elements such as potassium compared with the Earth and the bulk solar composition, and it has long been thought to be the result of a catastrophic Moon-forming giant impact event. Volatile-element-depleted bodies such as the Moon were expected to be enriched in heavy potassium isotopes during the loss of volatiles; however such enrichment was never found. Here we report new high-precision potassium isotope data for the Earth, the Moon and chondritic meteorites. We found that the lunar rocks are significantly (>2σ) enriched in the heavy isotopes of potassium compared to the Earth and chondrites (by around 0.4 parts per thousand). The enrichment of the heavy isotope of potassium in lunar rocks compared with those of the Earth and chondrites can be best explained as the result of the incomplete condensation of a bulk silicate Earth vapour at an ambient pressure that is higher than 10 bar. We used these coupled constraints of the chemical loss and isotopic fractionation of K to compare two recent dynamic models that were used to explain the identical non-mass-dependent isotope composition of the Earth and the Moon. Our K isotope result is inconsistent with the low-energy disk equilibration model, but supports the high-energy, high-angular-momentum giant impact model for the origin of the Moon. High-precision potassium isotope data can also be used as a 'palaeo-barometer' to reveal the physical conditions during the Moon-forming event.

Differentiation of Asteroid 4 Vesta: Core Formation by Iron Rain in a Silicate Magma Ocean

NASA Technical Reports Server (NTRS)

Kiefer, Walter S.; Mittlefehldt, David W.

2017-01-01

Geochemical observations of the eucrite and diogenite meteorites, together with observations made by NASA's Dawn spacecraft while orbiting asteroid 4 Vesta, suggest that Vesta resembles H chondrites in bulk chemical composition, possible with about 25 percent of a CM-chondrite like composition added in. For this model, the core is 15 percent by mass (or 8 percent by volume) of the asteroid, with a composition of 73.7 percent by weight Fe, 16.0 percent by weight S, and 10.3 percent by weight Ni. The abundances of moderately siderophile elements (Ni, Co, Mo, W, and P) in eucrites require that essentially all of the metallic phase in Vesta segregated to form a core prior to eucrite solidification. The combination of the melting phase relationships for the silicate and metal phases, together with the moderately siderophile element concentrations together require that complete melting of the metal phase occurred (temperature is greater than1350 degrees Centigrade), along with substantial (greater than 40 percent) melting of the silicate material. Thus, core formation on Vesta occurs as iron rain sinking through a silicate magma ocean.

Identification of a Compound Spinel and Silicate Presolar Grain in a Chondritic Interplanetary Dust Particle

NASA Technical Reports Server (NTRS)

Nguyen, A. N.; Nakamura-Messenger, K.; Messenger, S.; Keller, L. P.; Kloeck, W.

2014-01-01

Anhydrous chondritic porous interplanetary dust particles (CP IDPs) have undergone minimal parent body alteration and contain an assemblage of highly primitive materials, including molecular cloud material, presolar grains, and material that formed in the early solar nebula [1-3]. The exact parent bodies of individual IDPs are not known, but IDPs that have extremely high abundances of presolar silicates (up to 1.5%) most likely have cometary origins [1, 4]. The presolar grain abundance among these minimally altered CP IDPs varies widely. "Isotopically primitive" IDPs distinguished by anomalous bulk N isotopic compositions, numerous 15N-rich hotspots, and some C isotopic anomalies have higher average abundances of presolar grains (375 ppm) than IDPs with isotopically normal bulk N (<10 ppm) [5]. Some D and N isotopic anomalies have been linked to carbonaceous matter, though this material is only rarely isotopically anomalous in C [1, 5, 6]. Previous studies of the bulk chemistry and, in some samples, the mineralogy of select anhydrous CP IDPs indicate a link between high C abundance and pyroxene-dominated mineralogy [7]. In this study, we conduct coordinated mineralogical and isotopic analyses of samples that were analyzed by [7] to characterize isotopically anomalous materials and to establish possible correlations with C abundance.

Copper and Zinc isotope composition of CR, CB and CH-like meteorites.

NASA Astrophysics Data System (ADS)

Russell, S.; Zhu, X.; Guo, Y.; Mullane, E.; Gounelle, M.; Mason, T.; Coles, B.

2003-04-01

Copper and zinc isotopes have recently been shown to be variable in isotopic composi-tion among terrestrial and extraterrestrial materials [1-3]. For this study, we have se-lected samples (bulk meteorite and chondrule separates) from the CR meteorite clan: Bencubbin (CB), Renazzo (CR2), NWA 801 (CR2), and HaH237 (CH-like). These meteorites were selected because meteorites from this clan have experienced very little alteration since their initial formation [4] and for their extremely high refrac-tory/volatile element ratios. The latter characteristic may allow a test of the correlation observed by [2] between element ratios and Cu isotope composition. Measurements were performed on NHM/IC Micromass Isoprobe and Oxford Nu MC-ICP-MS using techniques described elsewhere [1,5]. Each of the meteorites measured so far for Cu and Zn are isotopically light compared to the terrestrial mantle. This suggests that the terrestrial value may have been altered from the pristine solar system value, or else there were multiple early solar system components. Zinc isotopic com-positions lie on a fractionation line and range from δ66ZnNIST = -1.4±0.1ppm (bulk NWA801) to -1.9±0.1ppm (separated chondrule, NWA 801). Copper isotope compositions vary from δ65CuNIST976 = -1.5±0.1ppm (bulk Renazzo) to -3.1±0.1ppm (separated chondrule, NWA 801). Two chondrules from NWA 801 have differing Cu isotope values (-3.1±0.1 and -2.0±0.1ppm) and both are lighter than the bulk meteorite (-1.9±0.1ppm), suggesting a lack of equilibration with respect to Cu in this meteorite. The light values for the two separated chondrules, compared the bulk meteorite, hints that chondrules may be isotopically lighter than co-existing matrix, metal and sulphides with respect to Cu. The copper isotope compositions are not as isotopically light as expected for the high refractory/volatile element ratio observed in these chondrites. Thus a model to account for the Cu isotopes in chondrites may require greater com-plexity than one involving simple mixing of two primordial components. References: [1] Zhu et al., Chem. Geol. 163,139-149 (2000). [2] Luck et al., GCA 67 143 (2002). [3] Luck et al., MAPS 35 A100 (2000) [4] Krot et al., MAPS 37 1451-1490 (2002) [5] Mason et al. EOS Trans. AGU abstract V21A-0966 82 (2001)

Rhenium-osmium systematics of calcium-aluminium-rich inclusions in carbonaceous chondrites

USGS Publications Warehouse

Becker, H.; Morgan, J.W.; Walker, R.J.; MacPherson, G.J.; Grossman, J.N.

2001-01-01

The Re-Os isotopic systematics of calcium-aluminium-rich inclusions (CAIs) in chondrites were investigated in order to shed light on the behavior of the Re-Os system in bulk chondrites, and to constrain the timing of chemical fractionation in primitive chondrites. CAIs with relatively unfractionated rare earth element (REE) patterns (groups I, III, V, VI) define a narrow range of 187Re/188Os (0.3764-0.4443) and 187Os/188Os (0.12599-0.12717), and high but variable Re and Os abundances (3209-41,820 ppb Os). In contrast, CAIs that show depletions in highly refractory elements and strongly fractionated REE patterns (group II) also show a much larger range in 187Re/188Os (0.409-0.535) and 187Os/188Os (0.12695-0.13770), and greater than an order of magnitude lower Re and Os abundances than other groups (e.g., 75.7-680.2 ppb Os). Sixteen bulk CAIs and CAI splits plot within analytical uncertainty of a 4558 Ga reference isochron, as is expected for materials of this antiquity. Eight samples, however, plot off the isochron. Several possible reasons for these deviations are discussed. Data for multiple splits of one CAI indicate that the nonisochronous behavior for at least this CAI is the result of Re-Os reequilibration at approximately 1.6 Ga. Thus, the most likely explanation for the deviations of most of the nonisochronous CAIs is late-stage open-system behavior of Re and Os in the asteroidal environment. The 187Os/188Os-Os systematics of CAIs are consistent with previous models that indicate group II CAIs are mixtures of components that lost the bulk of their highly refractory elements in a previous condensation event and a minor second component that provided refractory elements at chondritic relative proportions. The high Re/Os of group II CAIs relative to other CAIs and chondrite bulk rocks may have been caused by variable mobilization of Re and Os during medium- to low-temperature parent body alteration ??4.5 Ga ago. This model is favored over nebular models, which pose several difficulties. The narrow range of 187Os/188Os in group I, III, V, and VI bulk CAIs, and the agreement with 187Os/188Os of whole rock carbonaceous chondrites suggest that on a bulk inclusion scale, secondary alteration only modestly fractionated Re/Os in these CAIs. The average of 187Os/188Os for group I, III, V, and VI CAIs is indistinguishable from average CI chondrites, indicating a modern solar system value for 187Os/188Os of 0.12650, corresponding to a 187Re/188Os of 0.3964. Copyright ?? 2001 Elsevier Science Ltd.

146Sm-142Nd systematics measured in enstatite chondrites reveals a heterogeneous distribution of 142Nd in the solar nebula.

PubMed

Gannoun, Abdelmouhcine; Boyet, Maud; Rizo, Hanika; El Goresy, Ahmed

2011-05-10

The short-lived (146)Sm-(142)Nd chronometer (T(1/2) = 103 Ma) is used to constrain the early silicate evolution of planetary bodies. The composition of bulk terrestrial planets is then considered to be similar to that of primitive chondrites that represent the building blocks of rocky planets. However for many elements chondrites preserve small isotope differences. In this case it is not always clear to what extent these variations reflect the isotope heterogeneity of the protosolar nebula rather than being produced by the decay of parent isotopes. Here we present Sm-Nd isotopes data measured in a comprehensive suite of enstatite chondrites (EC). The EC preserve (142)Nd/(144)Nd ratios that range from those of ordinary chondrites to values similar to terrestrial samples. The EC having terrestrial (142)Nd/(144)Nd ratios are also characterized by small (144)Sm excesses, which is a pure p-process nuclide. The correlation between (144)Sm and (142)Nd for chondrites may indicate a heterogeneous distribution in the solar nebula of p-process matter synthesized in supernovae. However to explain the difference in (142)Nd/(144)Nd ratios, 20% of the p-process contribution to (142)Nd is required, at odds with the value of 4% currently proposed in stellar models. This study highlights the necessity of obtaining high-precision (144)Sm measurements to interpret properly measured (142)Nd signatures. Another explanation could be that the chondrites sample material formed in different pulses of the lifetime of asymptotic giant branch stars. Then the isotope signature measured in SiC presolar would not represent the unique s-process signature of the material present in the solar nebula during accretion.

146Sm–142Nd systematics measured in enstatite chondrites reveals a heterogeneous distribution of 142Nd in the solar nebula

PubMed Central

Gannoun, Abdelmouhcine; Boyet, Maud; Rizo, Hanika; El Goresy, Ahmed

2011-01-01

The short-lived 146Sm–142Nd chronometer (T1/2 = 103 Ma) is used to constrain the early silicate evolution of planetary bodies. The composition of bulk terrestrial planets is then considered to be similar to that of primitive chondrites that represent the building blocks of rocky planets. However for many elements chondrites preserve small isotope differences. In this case it is not always clear to what extent these variations reflect the isotope heterogeneity of the protosolar nebula rather than being produced by the decay of parent isotopes. Here we present Sm–Nd isotopes data measured in a comprehensive suite of enstatite chondrites (EC). The EC preserve 142Nd/144Nd ratios that range from those of ordinary chondrites to values similar to terrestrial samples. The EC having terrestrial 142Nd/144Nd ratios are also characterized by small 144Sm excesses, which is a pure p-process nuclide. The correlation between 144Sm and 142Nd for chondrites may indicate a heterogeneous distribution in the solar nebula of p-process matter synthesized in supernovae. However to explain the difference in 142Nd/144Nd ratios, 20% of the p-process contribution to 142Nd is required, at odds with the value of 4% currently proposed in stellar models. This study highlights the necessity of obtaining high-precision 144Sm measurements to interpret properly measured 142Nd signatures. Another explanation could be that the chondrites sample material formed in different pulses of the lifetime of asymptotic giant branch stars. Then the isotope signature measured in SiC presolar would not represent the unique s-process signature of the material present in the solar nebula during accretion. PMID:21515828

Mineral and chemical composition of the Jezersko meteorite—A new chondrite from Slovenia

NASA Astrophysics Data System (ADS)

Miler, Miloš; Ambrožič, Bojan; Mirtič, Breda; Gosar, Mateja; Å turm, Sašo.; Dolenec, Matej; Jeršek, Miha

2014-10-01

The Jezersko meteorite is a newly confirmed stony meteorite found in 1992 in the Karavanke mountains, Slovenia. The meteorite is moderately weathered (W2), indicating short terrestrial residence time. Chondrules in partially recrystallized matrix are clearly discernible but often fragmented and have mean diameter of 0.73 mm. The meteorite consists of homogeneous olivine (Fa19.4) and low-Ca pyroxenes (Fs16.7Wo1.2), of which 34% are monoclinic, and minor plagioclase (Ab83An11Or6) and Ca-pyroxene (Fs6Wo45.8). Troilite, kamacite, zoned taenite, tetrataenite, chromite, and metallic copper comprise about 16.5 vol% of the meteorite. Phosphates are represented by merrillite and minor chlorapatite. Undulatory extinction in some olivine grains and other shock indicators suggests weak shock metamorphism between stages S2 and S3. The bulk chemical composition generally corresponds to the mean H chondrite composition. Low siderophile element contents indicate the oxidized character of the Jezersko parent body. The temperatures recorded by two-pyroxene, olivine-chromite, and olivine-orthopyroxene geothermometers are 854 °C, 737-787 °C, and 750 °C, respectively. Mg concentration profiles across orthopyroxenes and clinopyroxenes indicate relatively fast cooling at temperatures above 700 °C. A low cooling rate of 10 °C Myr-1 was obtained from metallographic data. Considering physical, chemical, and mineralogical properties, meteorite Jezersko was classified as an H4 S2(3) ordinary chondrite.

Nickel isotopic composition of the mantle

NASA Astrophysics Data System (ADS)

Gall, Louise; Williams, Helen M.; Halliday, Alex N.; Kerr, Andrew C.

2017-02-01

This paper presents a detailed high-precision study of Ni isotope variations in mantle peridotites and their minerals, komatiites as well as chondritic and iron meteorites. Ultramafic rocks display a relatively large range in δ60 Ni (permil deviation in 60 Ni /58 Ni relative to the NIST SRM 986 Ni isotope standard) for this environment, from 0.15 ± 0.07‰ to 0.36 ± 0.08‰, with olivine-rich rocks such as dunite and olivine cumulates showing lighter isotope compositions than komatiite, lherzolite and pyroxenite samples. The data for the mineral separates shed light on the origin of these variations. Olivine and orthopyroxene display light δ60 Ni whereas clinopyroxene and garnet are isotopically heavy. This indicates that peridotite whole-rock δ60 Ni may be controlled by variations in modal mineralogy, with the prediction that mantle melts will display variable δ60 Ni values due to variations in residual mantle and cumulate mineralogy. Based on fertile peridotite xenoliths and Phanerozoic komatiite samples it is concluded that the upper mantle has a relatively homogeneous Ni isotope composition, with the best estimate of δ60Nimantle being 0.23 ± 0.06‰ (2 s.d.). Given that >99% of the Ni in the silicate Earth is located in the mantle, this also defines the Ni isotope composition of the Bulk Silicate Earth (BSE). This value is nearly identical to the results obtained for a suite of chondrites and iron meteorites (mean δ60 Ni 0.26 ± 0.12‰ and 0.29 ± 0.10‰, respectively) showing that the BSE is chondritic with respect to its Ni isotope composition, with little to no Ni mass-dependent isotope fractionation resulting from core formation.

Chondritic Earth: comparisons, guidelines and status

NASA Astrophysics Data System (ADS)

McDonough, W. F.

2014-12-01

The chemical and isotopic composition of the Earth is rationally understood within the context of the chondritic reference frame, without recourse to hidden reservoirs, collision erosion, or strict interpretation of an enstatite chondrite model. Challenges to interpreting the array of recent and disparate chemical and isotopic observations from meteorites need to be understood as rich data harvests that inform us of the compositional heterogeneity in the early solar system. Our ability to resolve small, significant compositional differences between chondrite families provide critical insights into integrated compositional signatures at differing annuli distances from the Sun (i.e., 1-6 AU). Rigorous evaluation of chondritic models for planets requires treatment of both statistical and systematic uncertainties - to date these efforts are uncommonly practiced. Planetary olivine to pyroxene ratio reflects fO2 and temperature potentials in the nebular, given possible ISM compositional conditions; thus this ratio is a non-unique parameter of terrestrial bodies. Consequently the Mg/Si value of a planet (ie., olivine to pyroxene ratio) is a free variable; there is no singular chondritic Mg/Si value. For the Earth, there is an absence of physical and chemical evidence requiring a major element, chemical distinction between the upper and lower mantle, within uncertainties. Early Earth differentiation likely occurred, but there is an absence of chemical and isotopic evidence of its imprint. Chondrites, peridotites, komatiites, and basalts (ancient and modern) reveal a coherent picture of a chondritic compositional Earth, with compositionally affinities to enstatite chondrites. At present results from geoneutrino studies non-uniquely support these conclusions. Future experiments can provide true transformative insights into the Earth's thermal budget, define compositional BSE models, and will restrict discussions on Earth dynamics and its thermal evolution.

Enstatite chondrites EL3 as building blocks for the Earth: The debate over the 146Sm-142Nd systematics

NASA Astrophysics Data System (ADS)

Boyet, M.; Bouvier, A.; Frossard, P.; Hammouda, T.; Garçon, M.; Gannoun, A.

2018-04-01

The 146Sm-142Nd extinct decay scheme (146Sm half-life of 103 My) is a powerful tool to trace early Earth silicate differentiation. Differences in 142Nd abundance measured between different chondrite meteorite groups and the modern Earth challenges the interpretation of the 142Nd isotopic variations found in terrestrial samples because the origin of the Earth and the nature of its building blocks is still an ongoing debate. As bulk meteorites, the enstatite chondrites (EC) have isotope signatures that are the closest to the Earth value with an average small deficit of ∼10 ppm in 142Nd relative to modern terrestrial samples. Here we review all the Nd isotope data measured on EC so far, and present the first measurements on an observed meteorite fall Almahata Sitta containing pristine fragments of an unmetamorphosed enstatite chondrite belonging to the EL3 subgroup. Once 142Nd/144Nd ratios are normalized to a common chondritic evolution, samples from the EC group (both EL and EH) have a deficit in 142Nd but the dispersion is important (μ142 Nd = - 10 ± 12 (2SD) ppm). This scatter reflects their unique mineralogy associated to their formation in reduced conditions (low fO2 or high C/O). Rare-earth elements are mainly carried by the sulfide phase oldhamite (CaS) that is more easily altered than silicates by weathering since most of the EC meteorites are desert finds. The EL6 have fractionated rare-earth element patterns with depletion in the most incompatible elements. Deviations in Nd mass independent stable isotope ratios in enstatite chondrites relative to terrestrial standard are not resolved with the level of analytical precision achieved by modern mass spectrometry techniques. Here we show that enstatite chondrites from the EL3 and EL6 subgroups may come from different parent bodies. Samples from the EL3 subgroup have Nd (μ142 Nd = - 0.8 ± 7.0, 2SD) and Ru isotope ratios undistinguishable from that of the Bulk Silicate Earth. EL3 samples have never been analyzed for Mo isotopes. Because these enstatite chondrites are relatively small in size and number, they are usually not available for destructive isotopic measurements. Average values based on the measurement of EL6 samples should not be considered as representative of the whole EL group because of melting and thermal metamorphism events affecting the Sm/Nd ratios and prolonged open-system history. The EL3 chondrites are the best candidates as the Earth's building blocks. These new results remove the need to change the composition of refractory incompatible elements early in Earth's history.

Magnesium and 54Cr isotope compositions of carbonaceous chondrite chondrules – Insights into early disk processes

PubMed Central

Olsen, Mia B.; Wielandt, Daniel; Schiller, Martin; Van Kooten, Elishevah M.M.E.; Bizzarro, Martin

2016-01-01

We report on the petrology, magnesium isotopes and mass-independent 54Cr/52Cr compositions (μ54Cr) of 42 chondrules from CV (Vigarano and NWA 3118) and CR (NWA 6043, NWA 801 and LAP 02342) chondrites. All sampled chondrules are classified as type IA or type IAB, have low 27Al/24Mg ratios (0.04–0.27) and display little or no evidence for secondary alteration processes. The CV and CR chondrules show variable 25Mg/24Mg and 26Mg/24Mg values corresponding to a range of mass-dependent fractionation of ~500 ppm (parts per million) per atomic mass unit. This mass-dependent Mg isotope fractionation is interpreted as reflecting Mg isotope heterogeneity of the chondrule precursors and not the result of secondary alteration or volatility-controlled processes during chondrule formation. The CV and CR chondrule populations studied here are characterized by systematic deficits in the mass-independent component of 26Mg (μ26Mg*) relative to the solar value defined by CI chondrites, which we interpret as reflecting formation from precursor material with a reduced initial abundance of 26Al compared to the canonical 26Al/27Al of ~5 × 10−5. Model initial 26Al/27Al values of CV and CR chondrules vary from (1.5 ± 4.0) × 10−6 to (2.2 ± 0.4) × 10−5. The CV chondrules display significant μ54Cr variability, defining a range of compositions that is comparable to that observed for inner Solar System primitive and differentiated meteorites. In contrast, CR chondrites are characterized by a narrower range of μ54Cr values restricted to compositions typically observed for bulk carbonaceous chondrites. Collectively, these observations suggest that the CV chondrules formed from precursors that originated in various regions of the protoplanetary disk and were then transported to the accretion region of the CV parent asteroid whereas CR chondrule predominantly formed from precursor with carbonaceous chondrite-like μ54Cr signatures. The observed μ54Cr variability in chondrules from CV and CR chondrites suggest that the matrix and chondrules did not necessarily formed from the same reservoir. The coupled μ26Mg* and μ54Cr systematics of CR chondrules establishes that these objects formed from a thermally unprocessed and 26Al-poor source reservoir distinct from most inner Solar System asteroids and planetary bodies, possibly located beyond the orbits of the gas giants. In contrast, a large fraction of the CV chondrules plot on the inner Solar System correlation line, indicating that these objects predominantly formed from thermally-processed, 26Al-bearing precursor material akin to that of inner Solar System solids, asteroids and planets. PMID:27563152

Magnesium and 54Cr isotope compositions of carbonaceous chondrite chondrules - Insights into early disk processes

NASA Astrophysics Data System (ADS)

Olsen, Mia B.; Wielandt, Daniel; Schiller, Martin; Van Kooten, Elishevah M. M. E.; Bizzarro, Martin

2016-10-01

We report on the petrology, magnesium isotopes and mass-independent 54Cr/52Cr compositions (μ54Cr) of 42 chondrules from CV (Vigarano and NWA 3118) and CR (NWA 6043, NWA 801 and LAP 02342) chondrites. All sampled chondrules are classified as type IA or type IAB, have low 27Al/24Mg ratios (0.04-0.27) and display little or no evidence for secondary alteration processes. The CV and CR chondrules show variable 25Mg/24Mg and 26Mg/24Mg values corresponding to a range of mass-dependent fractionation of ∼500 ppm (parts per million) per atomic mass unit. This mass-dependent Mg isotope fractionation is interpreted as reflecting Mg isotope heterogeneity of the chondrule precursors and not the result of secondary alteration or volatility-controlled processes during chondrule formation. The CV and CR chondrule populations studied here are characterized by systematic deficits in the mass-independent component of 26Mg (μ26Mg∗) relative to the solar value defined by CI chondrites, which we interpret as reflecting formation from precursor material with a reduced initial abundance of 26Al compared to the canonical 26Al/27Al of ∼5 × 10-5. Model initial 26Al/27Al values of CV and CR chondrules vary from (1.5 ± 4.0) × 10-6 to (2.2 ± 0.4) × 10-5. The CV chondrules display significant μ54Cr variability, defining a range of compositions that is comparable to that observed for inner Solar System primitive and differentiated meteorites. In contrast, CR chondrites are characterized by a narrower range of μ54Cr values restricted to compositions typically observed for bulk carbonaceous chondrites. Collectively, these observations suggest that the CV chondrules formed from precursors that originated in various regions of the protoplanetary disk and were then transported to the accretion region of the CV parent asteroid whereas CR chondrule predominantly formed from precursor with carbonaceous chondrite-like μ54Cr signatures. The observed μ54Cr variability in chondrules from CV and CR chondrites suggest that the matrix and chondrules did not necessarily formed from the same reservoir. The coupled μ26Mg∗ and μ54Cr systematics of CR chondrules establishes that these objects formed from a thermally unprocessed and 26Al-poor source reservoir distinct from most inner Solar System asteroids and planetary bodies, possibly located beyond the orbits of the gas giants. In contrast, a large fraction of the CV chondrules plot on the inner Solar System correlation line, indicating that these objects predominantly formed from thermally-processed, 26Al-bearing precursor material akin to that of inner Solar System solids, asteroids and planets.

Rare-earth abundances in chondritic meteorites

NASA Technical Reports Server (NTRS)

Evensen, N. M.; Hamilton, P. J.; Onions, R. K.

1978-01-01

Fifteen chondrites, including eight carbonaceous chondrites, were analyzed for rare earth element abundances by isotope dilution. Examination of REE for a large number of individual chondrites shows that only a small proportion of the analyses have flat unfractionated REE patterns within experimental error. While some of the remaining analyses are consistent with magmatic fractionation, many patterns, in particular those with positive Ce anomalies, can not be explained by known magmatic processes. Elemental abundance anomalies are found in all major chondrite classes. The persistence of anomalies in chondritic materials relatively removed from direct condensational processes implies that anomalous components are resistant to equilibrium or were introduced at a late stage of chondrite formation. Large-scale segregation of gas and condensate is implied, and bulk variations in REE abundances between planetary bodies is possible.

Re-Os systematics of komatiites and komatiitic basalts at Dundonald Beach, Ontario, Canada: Evidence for a complex alteration history and implications of a late-Archean chondritic mantle source

NASA Astrophysics Data System (ADS)

Gangopadhyay, A.; Sproule, R. A.; Walker, R. J.; Lesher, C.

2004-12-01

Re-Os concentrations and isotopic compositions have been examined in one komatiite unit and one komatiitic basalt unit at Dundonald Beach, which is part of the spatially-extensive 2.7 Ga Kidd-Munro volcanic assemblage in the Abitibi greenstone belt, Ontario, Canada. The komatiitic rocks in this locality record at least three episodes of alteration of Re-Os elemental and isotope systematics. First, an average of 40% and as much as 75% Re was lost due to shallow degassing during eruption and/or hydrothermal leaching during or immediately after the lava emplacement. Second, the Re-Os isotope systematics of the rocks with 187Re/188Os ratios >1 were reset at ˜2.5 Ga, most likely due to a regional metamorphic event. Finally, there is evidence for relatively recent gain and loss of Re. The variations in Os concentrations in the Dundonald komatiites yield a relative bulk distribution coefficient for Os (DOs solid/liquid) of 2-4, consistent with those obtained for stratigraphically-equivalent komatiites in the nearby Alexo area and in Munro Township. This suggests that Os was moderately compatible during crystal-liquid fractionation of the magma parental to the Kidd-Munro komatiitic rocks. Furthermore, whole-rock samples and chromite separates with low 187Re/188Os ratios (<1) yield a precise chondritic average initial 187Os/188Os ratio of 0.1083 ± 0.0006 (\\gammaOs = 0.0 ± 0.6). The chondritic initial Os isotopic composition of the mantle source for the Dundonald rocks is consistent with that determined for komatiites in the Alexo area and in Munro Township. Our Os isotope results for the Dundonald komatiitic rocks, combined with those in the Alexo and Pyke Hill areas suggest that the mantle source region for the Kidd- Munro volcanic assemblage had evolved along a long-term chondritic Os isotopic trajectory until their eruption at ˜2.7 Ga. The chondritic initial Os isotopic composition of the Kidd-Munro komatiites is indistinguishable from that of the projected contemporaneous convective upper mantle. The uniform chondritic Os isotopic composition of the ˜2.7 Ga mantle source for the Kidd-Munro komatiites contrasts with the typical large-scale Os isotopic heterogeneity in the mantle sources for komatiites from the Gorgona Island, present-day ocean island basalts or arc-related lavas. This suggests a significantly more homogeneous mantle source in the Archean compared to the presentday mantle.

Re-Os systematics of komatiites and komatiitic basalts at Dundonald Beach, Ontario, Canada: Evidence for a complex alteration history and implications of a late-Archean chondritic mantle source

NASA Astrophysics Data System (ADS)

Gangopadhyay, Amitava; Sproule, Rebecca A.; Walker, Richard J.; Lesher, C. Michael

2005-11-01

Osmium isotopic compositions, and Re and Os concentrations have been examined in one komatiite unit and two komatiitic basalt units at Dundonald Beach, part of the 2.7 Ga Kidd-Munro volcanic assemblage in the Abitibi greenstone belt, Ontario, Canada. The komatiitic rocks in this locality record at least three episodes of alteration of Re-Os elemental and isotope systematics. First, an average of 40% and as much as 75% Re may have been lost due to shallow degassing during eruption and/or hydrothermal leaching during or immediately after emplacement. Second, the Re-Os isotope systematics of whole rock samples with 187Re/ 188Os ratios >1 were reset at ˜2.5 Ga, possibly due to a regional metamorphic event. Third, there is evidence for relatively recent gain and loss of Re in some rocks. Despite the open-system behavior, some aspects of the Re-Os systematics of these rocks can be deciphered. The bulk distribution coefficient for Os (D Ossolid/liquid) for the Dundonald rocks is ˜3 ± 1 and is well within the estimated D values obtained for komatiites from the nearby Alexo area and stratigraphically-equivalent komatiites from Munro Township. This suggests that Os was moderately compatible during crystal-liquid fractionation of the magmas parental to the Kidd-Munro komatiitic rocks. Whole-rock samples and chromite separates with low 187Re/ 188Os ratios (<1) yield a precise chondritic average initial 187Os/ 188Os ratio of 0.1083 ± 0.0006 (γ Os = 0.0 ± 0.6) for their well-constrained ˜2715 Ma crystallization age. The chondritic initial Os isotopic composition of the mantle source for the Dundonald rocks is consistent with that determined for komatiites in the Alexo area and in Munro Township, suggesting that the mantle source region for the Kidd-Munro volcanic assemblage had evolved with a long-term chondritic Re/Os before eruption. The chondritic initial Os isotopic composition of the Kidd-Munro komatiites is indistinguishable from that of the projected contemporaneous convective upper mantle. The uniform chondritic Os isotopic composition of the Kidd-Munro komatiites contrasts with the typical large-scale Os isotopic heterogeneity in the mantle sources for ca. 89 Ma komatiites from the Gorgona Island, arc-related rocks and present-day ocean island basalts. This suggests that the Kidd-Munro komatiites sampled a late-Archean mantle source region that was significantly more homogeneous with respect to Re/Os relative to most modern mantle-derived rocks.

Petrology and Geochemistry of LEW 88663 and PAT 91501: High Petrologic L Chondrites

NASA Astrophysics Data System (ADS)

Mittlefehldt, D. W.; Lindstrom, M. M.; Field, S. W.

1993-07-01

Primitive achondrites (e.g., Acapulco, Lodran) are believed to be highly metamorphosed chondritic materials, perhaps up to the point of anatexis in some types. Low petrologic grade equivalents of these achondrites are unknown, so the petrologic transition from chondritic to achondritic material cannot be documented. However, there are rare L chondrites of petrologic grade 7 that may have experienced igneous processes, and study of these may yield information relevant to the formation of primitive achondrites, and perhaps basaltic achondrites, from chondritic precursors. We have begun the study of the L7 chondrites LEW 88663 and PAT 91501 as part of our broader study of primitive achondrites. Here, we present our preliminary petrologic and geochemical data on these meteorites. Petrology and Mineral Compositions: LEW 88663 is a granular achondrite composed of equant, subhedral to anhedral olivine grains poikilitically enclosed in networks of orthopyroxene and plagioclase. Small grains of clinopyroxene are spatially associated with orthopyroxene. Troilite occurs as large anhedral and small rounded grains. The smaller troilite grains are associated with the orthopyroxene-plagioclase networks. PAT 91501 is a vesicular stone containing centimeter-sized troilite +/- metal nodules. Its texture consists of anhedral to euhedral olivine grains, anhedral orthopyroxene grains (some with euhedral clinopyroxene overgrowths), anhedral to euhedral clinopyroxene, and interstitial plagioclase and SiO2-Al2O3-K2O- rich glass. In some areas, olivine is poikilitically enclosed in orthopyroxene. Fine-grained troilite, metal, and euhedral chromite occur interstitial to the silicates. Average mineral compositions for LEW 88663 are olivine Fo(sub)75.8, orthopyroxene Wo(sub)3.4En(sub)76.2Fs(sub)20.4, clinopyroxene Wo(sub)42.6En(sub)47.8Fs(sub)9.6, plagioclase Ab(sub)75.0An(sub)21.6Or(sub)3.4. Mineral compositions for PAT 91501 are olivine Fo(sub)73.8, orthopyroxene Wo(sub)4.5En(sub)74.8Fs(sub)20.7, clinopyroxene Wo(sub)34.3En(sub)52.4Fs(sub)13.3, plagioclase Ab(sub)81.6An(sub)14.0Or(sub)44. Geochemistry: We have completed INM analysis of LEW 88663 only; analyses of PAT 91501 are in progress. The weighted mean lithophile element (refractory, moderately volatile, and volatile) content of LEW 88663 normalized to average L chondrites [1] is 0.97. The weighted mean siderophile element (excluding Fe) content is only 0.57x L. This supports the suggestion that LEW 88663 lost metal relative to average L chondrites, although not as complete as implied earlier [1]. The mean lithophile-element abundance is that of L chondrites, but the lithophile-element pattern is fractionated. Highly incompatible elements are enriched in LEW 88663 relative to L chondrites (e.g., La 2.6x, Sm 1.9x L chondrites), while the more compatible elements are near L chondrite levels or depleted (e.g., Lu 1.1x, Sc 0.94x, Cr 0.87x L chondrites). Discussion: LEW 88663 and PAT 91501 are texturally similar to the Shaw L7 chondrite [3] and to poikilitic textured clasts in LL chondrites [4]. Several textural and mineralogical characteristics of PAT 91501 indicate that this stone is in part igneous. Large rounded troilite +/- metal nodules imply that melting occurred in the metal-troilite system. Interstitial material consists of euhedral, zoned chromites, euhedral clinopyroxene overgrowths on orthopyroxene, and plagioclase + glass. Olivine often shows euhedral faces in contact with the interstitial regions. These textures indicate that the interstitial regions were molten. The average pyroxene compositions in PAT 91501 indicate equilibration at 1200 degrees C [5], above the ordinary chondrite solidus [6]. Although PAT 91501 is in part igneous in origin, we have yet to determine whether it represents an extension of parent body heating from that of metamorphosed L chondrites, or whether it represents impact melting on the parent body. We will evaluate shock features, cooling rates, and the bulk composition of PAT 91501 in order to investigate this further. Orthopyroxenes in LEW 88663 have a lower Wo content, and clinopyroxenes have a higher Wo content, than those in PAT 91501, and have equilibrated to lower temperatures, perhaps ~1000 degrees C [5]. References: [1] Wasson and Kallemeyn (1988) Phil. Trans. R. Soc. Lond., A325, 535. [2] Davis et al. (1993) LPS XXIV, 375. [3] Taylor et al. (1979) GCA, 43, 323. [4] Fodor and Keil (1975) Meteoritics, 10, 325. [5] Lindsley (1983) Am. Mineral., 68, 477. [6] Jurewicz et al. (1993) LPS XXIV, 739.

15N Fractionation in Star-Forming Regions and Solar System Objects

NASA Technical Reports Server (NTRS)

Wirstrom, Eva; Milam, Stefanie; Adande, GIlles; Charnley, Steven; Cordiner, Martin

2015-01-01

A central issue for understanding the formation and evolution of matter in the early Solar System is the relationship between the chemical composition of star-forming interstellar clouds and that of primitive Solar System materials. The pristinemolecular content of comets, interplanetary dust particles and carbonaceous chondrites show significant bulk nitrogen isotopic fractionation relative to the solar value, 14N15N 440. In addition, high spatial resolution measurements in primitive materials locally show even more extreme enhancements of 14N15N 100.

Laboratory Study of Aliphatic Organic Spectral Signatures and Applications to Ceres and Primitive Asteroids

NASA Astrophysics Data System (ADS)

Kaplan, H. H.; Milliken, R.

2017-12-01

Aliphatic organics were recently discovered on the surface of Ceres with Dawn's Visible and InfraRed (VIR) mapping spectrometer, which has implications for prebiotic chemistry of Ceres and other asteroids. An absorption in the spectrum at 3.4 µm was used to identify and provide initial estimates of the amount of organic material. We have studied the 3.4 µm absorption in reflectance spectra of bulk rock and meteorite powders and isolated organic materials in the NASA RELAB facility at Brown University to determine how organic composition and abundance affects absorption strength. Reflectance spectra of insoluble organic matter (IOM) extracted from carbonaceous chondrites were measured from 0.35 - 25 µm. These IOM have known elemental (H, C, N, O) and isotopic compositions that were compared with spectral properties. Bulk meteorites were measured as chips and particulates over the same wavelength range. Despite overall low reflectance values (albedo <0.01), the 3.4 µm absorption is observed for some IOM samples, specifically those with a H/C ratio greater than 0.4. The absorption strength (band depth) increases with increasing H/C ratio, which corroborates similar findings in our previous study of sedimentary rocks and isolated kerogens. The absorption strength in the bulk meteorites reflects both H/C of the IOM and the concentration of IOM in the inorganic (mineral) matrix. Overlapping absorptions from carbonates and phyllosilicates (OH/H2O) can also influence the aliphatic organic bands in bulk rocks and meteorites. This laboratory work provides a foundation that can be used to constrain the composition of Ceres' aliphatic organic matter using band depth as a proxy for H/C. Reflectance spectra collected for this work will also be used to model the Dawn VIR data and obtain abundance and H/C estimates assuming that the organic material on Ceres' surface is similar to carbonaceous chondrite IOM. These spectra and findings can aid interpretation of reflectance data from Ceres and other asteroid missions, such as OSIRIS-REx and Hayabusa2.

Collisional stripping of planetary crusts

NASA Astrophysics Data System (ADS)

Carter, Philip J.; Leinhardt, Zoë M.; Elliott, Tim; Stewart, Sarah T.; Walter, Michael J.

2018-02-01

Geochemical studies of planetary accretion and evolution have invoked various degrees of collisional erosion to explain differences in bulk composition between planets and chondrites. Here we undertake a full, dynamical evaluation of 'crustal stripping' during accretion and its key geochemical consequences. Crusts are expected to contain a significant fraction of planetary budgets of incompatible elements, which include the major heat producing nuclides. We present smoothed particle hydrodynamics simulations of collisions between differentiated rocky planetesimals and planetary embryos. We find that the crust is preferentially lost relative to the mantle during impacts, and we have developed a scaling law based on these simulations that approximates the mass of crust that remains in the largest remnant. Using this scaling law and a recent set of N-body simulations of terrestrial planet formation, we have estimated the maximum effect of crustal stripping on incompatible element abundances during the accretion of planetary embryos. We find that on average approximately one third of the initial crust is stripped from embryos as they accrete, which leads to a reduction of ∼20% in the budgets of the heat producing elements if the stripped crust does not reaccrete. Erosion of crusts can lead to non-chondritic ratios of incompatible elements, but the magnitude of this effect depends sensitively on the details of the crust-forming melting process on the planetesimals. The Lu/Hf system is fractionated for a wide range of crustal formation scenarios. Using eucrites (the products of planetesimal silicate melting, thought to represent the crust of Vesta) as a guide to the Lu/Hf of planetesimal crust partially lost during accretion, we predict the Earth could evolve to a superchondritic 176Hf/177Hf (3-5 parts per ten thousand) at present day. Such values are in keeping with compositional estimates of the bulk Earth. Stripping of planetary crusts during accretion can lead to detectable changes in bulk composition of lithophile elements, but the fractionation is relatively subtle, and sensitive to the efficiency of reaccretion.

Trace Element Study of H Chondrites: Evidence for Meteoroid Streams.

NASA Astrophysics Data System (ADS)

Wolf, Stephen Frederic

1993-01-01

Multivariate statistical analyses, both linear discriminant analysis and logistic regression, of the volatile trace elemental concentrations in H4-6 chondrites reveal compositionally distinguishable subpopulations. Observed difference in volatile trace element composition between Antarctic and non-Antarctic H4-6 chondrites (Lipschutz and Samuels, 1991) can be explained by a compositionaily distinct subpopulation found in Victoria Land, Antarctica. This population of H4-6 chondrites is compositionally distinct from non-Antarctic H4-6 chondrites and from Antarctic H4 -6 chondrites from Queen Maud Land. Comparisons of Queen Maud Land H4-6 chondrites with non-Antarctic H4-6 chondrites do not give reason to believe that these two populations are distinguishable from each other on the basis of the ten volatile trace element concentrations measured. ANOVA indicates that these differences are not the result of trivial causes such as weathering and analytical bias. Thermoluminescence properties of these populations parallels the results of volatile trace element comparisons. Given the differences in terrestrial age between Victoria Land, Queen Maud Land, and modern H4-6 chondrite falls, these results are consistent with a variation in H4-6 chondrite flux on a 300 ky timescale. This conclusion requires the existence of co-orbital meteoroid streams. Statistical analyses of the volatile trace elemental concentrations in non-Antarctic modern falls of H4-6 chondrites also demonstrate that a group of 13 H4-6 chondrites, Cluster 1, selected exclusively for their distinct fall parameters (Dodd, 1992) is compositionally distinguishable from a control group of 45 non-Antarctic modern H4-6 chondrites on the basis of the ten volatile trace element concentrations measured. Model-independent randomization-simulations based on both linear discriminant analysis and logistic regression verify these results. While ANOVA identifies two possible causes for this difference, analytical bias and group classification, a test validation experiment verifies that group classification is the more significant cause of compositional difference between Cluster 1 and non-Cluster 1 modern H4-6 chondrite falls. Thermoluminescence properties of these populations parallels the results of volatile trace element comparisons. This suggests that these meteorites are fragments of a co-orbital meteorite stream derived from a single parent body.

From Dust to Planets: The Tale Told by Moderately Volatile Element Depletion (MOVED)

NASA Technical Reports Server (NTRS)

Yin, Qing-Zhu

2004-01-01

The pronounced depletion of moderately volatile elements (MOVE, that condense or evaporate at temperatures in the range 1350-650K) relative to the average solar composition is a characteristic feature in most primitive chondrites and bulk terrestrial planets. It differs from the composition of the Sun and from the materials further away from the Sun (CI chondrites). None of the remaining planets or even meteorites shows an enrichment of volatile elements that would balance the depletion in the inner Solar System. Whether this depletion occurred in solar nebular stage or in planetary formation stage has been the subject of long lasting debate. The search for mysterite initiated in 1973 continues today in search of lost planets. Here I show that the MOVED patterns demonstrate a clear connection between the rocky materials of the inner solar system and the interstellar dust. The inheritance of interstellar materials by the solar system is not only documented by the presence of presolar grains, various isotopic anomalies, but also expressed in the chemical element distribution in the inner solar system.

Core Formation on Asteroid 4 Vesta: Iron Rain in a Silicate Magma Ocean

NASA Technical Reports Server (NTRS)

Kiefer, Walter S.; Mittlefehldt, David W.

2017-01-01

Geochemical observations of the eucrite and diogenite meteorites, together with observations made by NASA's Dawn spacecraft, suggest that Vesta resembles H chondrites in bulk chemical composition, possibly with about 25% of a CM-chondrite like composition added in. For this model, the core is 15% by mass (or 8 volume %) of the asteroid. The abundances of moderately siderophile elements (Ni, Co, Mo, W, and P) in eucrites require that essentially all of the metallic phase in Vesta segregated to form a core prior to eucrite solidification. Melting in the Fe-Ni-S system begins at a cotectic temperature of 940 deg. C. Only about 40% of the total metal phase, or 3-4 volume % of Vesta, melts prior to the onset of silicate melting. Liquid iron in solid silicate initially forms isolated pockets of melt; connected melt channels, which are necessary if the metal is to segregate from the silicate, are only possible when the metal phase exceeds about 5 volume %. Thus, metal segregation to form a core does not occur prior to the onset of silicate melting.

Relative amino acid concentrations as a signature for parent body processes of carbonaceous chondrites.

PubMed

Botta, Oliver; Glavin, Daniel P; Kminek, Gerhard; Bada, Jeffrey L

2002-04-01

Most meteorites are thought to have originated from objects in the asteroid belt. Carbonaceous chondrites, which contain significant amounts of organic carbon including complex organic compounds, have also been suggested to be derived from comets. The current model for the synthesis of organic compounds found in carbonaceous chondrites includes the survival of interstellar organic compounds and the processing of some of these compounds on the meteoritic parent body. The amino acid composition of five CM carbonaceous chondrites, two CIs, one CR, and one CV3 have been measured using hot water extraction-vapor hydrolysis, OPA/NAC derivatization and high-performance liquid chromatography (HPLC). Total amino acid abundances in the bulk meteorites as well as the amino acid concentrations relative to glycine = 1.0 for beta-alanine, alpha-aminoisobutyric acid and D-alanine were determined. Additional data for three Antarctic CM meteorites were obtained from the literature. All CM meteorites analyzed in this study show a complex distribution of amino acids and a high variability in total concentration ranging from approximately 15,300 to approximately 5800 parts per billion (ppb), while the CIs show a total amino acid abundance of approximately 4300 ppb. The relatively (compared to glycine) high AIB content found in all the CMs is a strong indicator that Strecker-cyanohydrin synthesis is the dominant pathway for the formation of amino acids found in these meteorites. The data from the Antarctic CM carbonaceous chondrites are inconsistent with the results from the other CMs, perhaps due to influences from the Antarctic ice that were effective during their residence time. In contrast to CMs, the data from the CI carbonaceous chondrites indicate that the Strecker synthesis was not active on their parent bodies.

Relative Amino Acid Concentrations as a Signature for Parent Body Processes of Carbonaceous Chondrites

NASA Technical Reports Server (NTRS)

Botta, Oliver; Glavin, Daniel P.; Kminek, Gerhard; Bada, Jeffrey L.

2002-01-01

Most meteorites are thought to have originated from objects in the asteroid belt. Carbonaceous chondrites, which contain significant amounts of organic carbon including complex organic compounds, have also been suggested to be derived from comets. The current model for the synthesis of organic compounds found in carbonaceous chondrites includes the survival of interstellar organic compounds and the processing of some of these compounds on the meteoritic parent body. The amino acid composition of five CM carbonaceous chondrites, two CIs, one CR, and one CV3 have been measured using hot water extraction-vapor hydrolysis, OPA/NAC derivatization and high-performance liquid chromatography (HPLC). Total amino acid abundances in the bulk meteorites as well as the amino acid concentrations relative to glycine = 1.0 for beta-alanine, alpha-aminoisobutyric acid and D-alanine were determined. Additional data for three Antarctic CM meteorites were obtained from the literature. All CM meteorites analyzed in this study show a complex distribution of amino acids and a high variability in total concentration ranging from approx. 15,300 to approx. 5800 parts per billion (ppb), while the CIs show a total amino acid abundance of approx. 4300 ppb. The relatively (compared to glycine) high AIB content found in all the CMs is a strong indicator that Strecker-cyanohydrin synthesis is the dominant pathway for the formation of amino acids found in these meteorites. The data from the Antarctic CM carbonaceous chondrites are inconsistent with the results from the other CMs, perhaps due to influences from the Antarctic ice that were effective during their residence time. In contrast to CMs, the data from the CI carbonaceous chondrites indicate that the Strecker synthesis was not active on their parent bodies.

Sm-Nd systematics of lunar ferroan anorthositic suite rocks: Constraints on lunar crust formation

NASA Astrophysics Data System (ADS)

Boyet, Maud; Carlson, Richard W.; Borg, Lars E.; Horan, Mary

2015-01-01

We have measured Sm-Nd systematics, including the short-lived 146Sm-142Nd chronometer, in lunar ferroan anorthositic suite (FAS) whole rocks (15415, 62236, 62255, 65315, 60025). At least some members of the suite are thought to be primary crystallization products formed by plagioclase flotation during crystallization of the lunar magma ocean (LMO). Most of these samples, except 62236, have not been exposed to galactic cosmic rays for a long period and thus require minimal correction to their 142Nd isotope composition. These samples all have measured deficits in 142Nd relative to the JNdi-1 terrestrial standard in the range -45 to -21 ppm. The range is -45 to -15 ppm once the 62236 142Nd/144Nd ratio is corrected from neutron-capture effects. Analyzed FAS samples do not define a single isochron in either 146Sm-142Nd or 147Sm-143Nd systematics, suggesting that they either do not have the same crystallization age, come from different sources, or have suffered isotopic disturbance. Because the age is not known for some samples, we explore the implications of their initial isotopic compositions for crystallization ages in the first 400 Ma of solar system history, a timing interval that covers all the ages determined for the ferroan anorthositic suite whole rocks as well as different estimates for the crystallization of the LMO. 62255 has the largest deficit in initial 142Nd and does not appear to have followed the same differentiation path as the other FAS samples. The large deficit in 142Nd of FAN 62255 may suggest a crystallization age around 60-125 Ma after the beginning of solar system accretion. This result provides essential information about the age of the giant impact forming the Moon. The initial Nd isotopic compositions of FAS samples can be matched either with a bulk-Moon with chondritic Sm/Nd ratio but enstatite-chondrite-like initial 142Nd/144Nd (e.g. 10 ppm below modern terrestrial), or a bulk-Moon with superchondritic Sm/Nd ratio and initial 142Nd/144Nd similar to ordinary chondrites.

DOE Office of Scientific and Technical Information (OSTI.GOV)

Boyet, Maud; Carlson, Richard W.; Borg, Lars E.

Here, we have measured Sm–Nd systematics, including the short-lived 146Sm– 142Nd chronometer, in lunar ferroan anorthositic suite (FAS) whole rocks (15415, 62236, 62255, 65315, 60025). At least some members of the suite are thought to be primary crystallization products formed by plagioclase flotation during crystallization of the lunar magma ocean (LMO). Most of these samples, except 62236, have not been exposed to galactic cosmic rays for a long period and thus require minimal correction to their 142Nd isotope composition. These samples all have measured deficits in 142Nd relative to the JNdi-1 terrestrial standard in the range –45 to –21 ppm.more » The range is –45 to –15 ppm once the 62236 142Nd/ 144Nd ratio is corrected from neutron-capture effects. Analyzed FAS samples do not define a single isochron in either 146Sm– 142Nd or 147Sm– 143Nd systematics, suggesting that they either do not have the same crystallization age, come from different sources, or have suffered isotopic disturbance. Because the age is not known for some samples, we explore the implications of their initial isotopic compositions for crystallization ages in the first 400 Ma of solar system history, a timing interval that covers all the ages determined for the ferroan anorthositic suite whole rocks as well as different estimates for the crystallization of the LMO. 62255 has the largest deficit in initial 142Nd and does not appear to have followed the same differentiation path as the other FAS samples. The large deficit in 142Nd of FAN 62255 may suggest a crystallization age around 60–125 Ma after the beginning of solar system accretion. This result provides essential information about the age of the giant impact forming the Moon. The initial Nd isotopic compositions of FAS samples can be matched either with a bulk-Moon with chondritic Sm/Nd ratio but enstatite-chondrite-like initial 142Nd/ 144Nd (e.g. 10 ppm below modern terrestrial), or a bulk-Moon with superchondritic Sm/Nd ratio and initial 142Nd/ 144Nd similar to ordinary chondrites.« less

Sm-Nd systematics of lunar ferroan anorthositic suite rocks: Constraints on lunar crust

DOE PAGES

Boyet, Maud; Carlson, Richard W.; Borg, Lars E.; ...

2014-09-28

Here, we have measured Sm–Nd systematics, including the short-lived 146Sm– 142Nd chronometer, in lunar ferroan anorthositic suite (FAS) whole rocks (15415, 62236, 62255, 65315, 60025). At least some members of the suite are thought to be primary crystallization products formed by plagioclase flotation during crystallization of the lunar magma ocean (LMO). Most of these samples, except 62236, have not been exposed to galactic cosmic rays for a long period and thus require minimal correction to their 142Nd isotope composition. These samples all have measured deficits in 142Nd relative to the JNdi-1 terrestrial standard in the range –45 to –21 ppm.more » The range is –45 to –15 ppm once the 62236 142Nd/ 144Nd ratio is corrected from neutron-capture effects. Analyzed FAS samples do not define a single isochron in either 146Sm– 142Nd or 147Sm– 143Nd systematics, suggesting that they either do not have the same crystallization age, come from different sources, or have suffered isotopic disturbance. Because the age is not known for some samples, we explore the implications of their initial isotopic compositions for crystallization ages in the first 400 Ma of solar system history, a timing interval that covers all the ages determined for the ferroan anorthositic suite whole rocks as well as different estimates for the crystallization of the LMO. 62255 has the largest deficit in initial 142Nd and does not appear to have followed the same differentiation path as the other FAS samples. The large deficit in 142Nd of FAN 62255 may suggest a crystallization age around 60–125 Ma after the beginning of solar system accretion. This result provides essential information about the age of the giant impact forming the Moon. The initial Nd isotopic compositions of FAS samples can be matched either with a bulk-Moon with chondritic Sm/Nd ratio but enstatite-chondrite-like initial 142Nd/ 144Nd (e.g. 10 ppm below modern terrestrial), or a bulk-Moon with superchondritic Sm/Nd ratio and initial 142Nd/ 144Nd similar to ordinary chondrites.« less

Gallium isotopic evidence for the fate of moderately volatile elements in planetary bodies and refractory inclusions

NASA Astrophysics Data System (ADS)

Kato, Chizu; Moynier, Frédéric

2017-12-01

The abundance of moderately volatile elements, such as Zn and Ga, show variable depletion relative to CI between the Earth and primitive meteorite (chondrites) parent bodies. Furthermore, the first solar system solids, the calcium-aluminum-rich inclusions (CAIs), are surprisingly rich in volatile element considering that they formed under high temperatures. Here, we report the Ga elemental and isotopic composition of a wide variety of chondrites along with five individual CAIs to understand the origin of the volatile elements and to further characterize the enrichment of the volatile elements in high temperature condensates. The δ71Ga (permil deviation of the 71Ga/69Ga ratio from the Ga IPGP standard) of carbonaceous chondrites decreases in the order of CI >CM >CO >CV and is inversely correlated with the Al/Ga ratio. This implies that the Ga budget of the carbonaceous chondrites parent bodies were inherited from a two component mixing of a volatile rich reservoir enriched in heavy isotope of Ga and a volatile poor reservoir enriched in light isotope of Ga. Calcium-aluminum-rich inclusions are enriched in Ga and Zn compared to the bulk meteorite and are both highly isotopically fractionated with δ71Ga down to -3.56‰ and δ66Zn down to -0.74‰. The large enrichment in the light isotopes of Ga and Zn in the CAIs implies that the moderately volatile elements were introduced in the CAIs during condensation in the solar nebula as opposed to secondary processing in the meteorite parent body and supports a change in gas composition in which CAIs were formed.

The mineralogy of ordinary chondrites and implications for asteroid spectrophotometry

NASA Technical Reports Server (NTRS)

Mcsween, Harry Y., Jr.; Bennett, Marvin E., III; Jarosewich, Eugene

1991-01-01

Published data from bulk chemical analyses of 94 ordinary chondrites are compiled in a table of normative mineralogy and discussed in detail. Significant variations in olivine, pyroxene, and metal abundance ratios are found within each chondrite class and attributed to redox processes superimposed on initial differences in metal/silicate ratios. The use of the diagrams constructed here to predict the mineralogic characteristics of asteroids on the basis of spectrophotometric observations is suggested.

Mineralogy, Reflectance Spectra, and Physical Properties of the Chelyabinsk LL5 Chondrite - Insight Into Shock Induced Changes in Asteroid Regoliths

NASA Astrophysics Data System (ADS)

Gritsevich, Maria; Muinonen, Karri; Kohout, Tomas; Grokhovsky, Victor; Yakovlev, Grigoriy; Haloda, Jakub; Halodova, Patricie; Michallik, Radoslaw; Penttilä, Antti

On February 15, 2013, at 9:22 am, an exceptionally bright and long duration fireball was observed by many eyewitnesses in the Chelyabinsk region, Russia. Two days later the first fragments of the Chelyabinsk meteorite were reported to be found in the area, located approximately 40 km south of Chelyabinsk. We have examined a large number of the recovered Chelyabinsk meteorite fragments. Three lithologies, the light-colored, dark-colored, and impact melt, were found within the recovered meteorites. The light colored lithology is a LL5 ordinary chondrite (Fa 28, Fs 23) shocked to S4 level. The dark colored lithology is of identical LL5 composition (Fa 28, Fs 23). However, it is shocked to higher level (shock-darkened) with fine grained metal and sulfide-rich melt forming a dense network of fine veins impregnating the inter- and intra-granular pore space within crushed silicate grains. The impact melt lithology is a whole-rock melt derived from the same LL5 source material and is present within the light-colored and dark-colored lithology as inter-granular veins. The measured bulk and grain densities and the porosity closely resemble other LL chondrites. Based on the magnetic susceptibility, the Chelyabinsk meteorites are richer in metallic iron as compared to database of other LL chondrites. All three Chelyabinsk lithologies are of identical LL5 composition and origin. Both impact melting and shock darkening cause a decrease in reflectance and a suppression of the silicate absorption bands in the reflectance spectra. Such spectral changes are similar to the space weathering effects observed on asteroids. However, space weathering of chondritic materials is often accompanied with a significant spectral slope change (reddening). In our case, only negligible to minor change in the spectral slope is observed. Thus, it is possible that some dark asteroids with invisible silicate absorption bands may be composed of relatively fresh shock-darkened chondritic material. The main spectral difference of chondritic asteroid surfaces dominated by impact melt, shock darkening, or space weathering, is a significant spectral slope change in the latter case. Thus, shock does not have significant effect on meteorite properties, but causes spectral darkening and suppression of silicate absorption bands.

Mineralogical, Spectral, and Compositional Changes During Heating of Hydrous Carbonaceous Chondrites

NASA Technical Reports Server (NTRS)

Nakamura, T.; Matsuoka, M.; Yamashita, S.; Sato, Y.; Mogi, K.; Enokido, Y.; Nakata, A.; Okumura, S.; Furukawa, Y.; Zolensky, M.

2017-01-01

Hydrous carbonaceous chondrites experienced hydration and subsequent dehydration by heating, which resulted in a variety of mineralogical and spectral features [e. g., 1-6]. The degree of heating is classified according to heating stage (HS) II to IV based on mineralogy of phyllosilicates [2], because they change, with elevating temperature, to poorly crystal-line phases and subsequently to aggregates of small secondary anhydrous silicates of mainly olivine. Heating of hydrous carbonaceous chondrites also causes spectral changes and volatile loss [3-6]. Experimental heating of Murchison CM chondrite showed flattening of whole visible-near infrared spectra, especially weakening of the 3µm band strength [1, 4, 7]. In order to understand mineralogical, spectral, and compositional changes during heating of hydrous carbonaceous chondrites, we have carried out systematic investigation of mineralogy, reflectance spectra, and volatile composition of hydrated and dehydrated carbonaceous chondrites as well as experimentally-heated hydrous carbonaceous chondrites. In addition, we investigated reflectance spectra of tochilinite that is a major phase of CM chondrites and has a low dehydration temperature (250degC).

Do L chondrites come from the Gefion family?

NASA Astrophysics Data System (ADS)

McGraw, Allison M.; Reddy, Vishnu; Sanchez, Juan A.

2018-05-01

Ordinary chondrites (H, L, and LL chondrites) are the most common type of meteorites comprising 80 per cent of the meteorites that fall on Earth. The source region of these meteorites in the main asteroid belt has been a basis of considerable debate in the small bodies community. L chondrites have been proposed to come from the Gefion asteroid family, based on dynamical models. We present results from our observational campaign to verify a link between the Gefion asteroid family and L chondrite meteorites. Near-infrared spectra of Gefion family asteroids (1839) Ragazza, (2373) Immo, (2386) Nikonov, (2521) Heidi, and (3860) Plovdiv were obtained at the NASA Infrared Telescope Facility (IRTF). Spectral band parameters including band centres and the band area ratio were measured from each spectrum and used to constrain the composition of these asteroids. Based on our results, we found that some members of the Gefion family have surface composition similar to that of H chondrites, primitive achondrites, and basaltic achondrites. No evidence was found for L chondrites among the Gefion family members in our small sample study. The diversity of compositional types observed in the Gefion asteroid family suggests that the original parent body might be partially differentiated or that the three asteroids with non-ordinary chondrite compositions might be interlopers.

TOF-SIMS Analysis of Crater Residues from Wild 2 Cometary on Stardust Aluminum Foil

NASA Technical Reports Server (NTRS)

Leutner, Jan; Stephan, Thomas; Kearsley, T.; Horz, Friedrich; Flynn, George J.; Sandford, Scott A.

2006-01-01

Impact residues of cometary particles on aluminum foils from the Stardust mission were investigated with TOF-SIMS for their elemental and organic composition. The residual matter from comet 81P/Wild 2 shows a wide compositional range, from nearly monomineralic grains to polymict aggregates. Despite the comparably small analyzed sample volume, the average element composition of the investigated residues is similar to bulk CI chondritic values. Analysis of organic components in impact residues is complicated, due to fragmentation and alteration of the compounds during the impact process and by the presence of contaminants on the aluminum foils. Nevertheless, polycyclic aromatic hydrocarbons (PAHs) that are unambiguously associated with the impact residues were observed, and thus are most likely of cometary origin.

Widespread hydrothermal alteration minerals in the fine-grained matrices of the Tieschitz unequilibrated ordinary chondrite

NASA Astrophysics Data System (ADS)

Dobricǎ, E.; Brearley, A. J.

2014-08-01

Mineralogic, textural, and compositional studies of black and white matrices in the unequilibrated ordinary chondrite Tieschitz (H/L, 3.6) show, for the first time in an ordinary chondrite, the presence of widespread, randomly distributed geode-like voids and veins. Scanning electron microscope (SEM) and transmission electron microscope (TEM) studies show that these voids and veins are partially or completely filled by sodic-calcic amphiboles (winchite and barroisite). The occurrence of amphiboles provides unequivocal evidence of the involvement of fluids in the metamorphic evolution of the parent body of Tieschitz. The presence of amphiboles as the main hydrous phases, rather than phyllosilicates, indicates that aqueous fluids were present at or close to the peak of thermal metamorphism, rather than during the waning stages of the cooling history of the parent body. In addition, ferrous olivine crystals, in association with the amphibole, also establish an important link between thermal metamorphism and hydrous phases formed at high temperatures. Mineralogic and textural evidence suggests that the white matrix and amphibole formed contemporaneously from the same hydrous fluid, prior to the formation of ferrous olivine crystals. Additionally, a dark inclusion identified in the host chondrite has mineralogic, petrologic, and bulk chemical characteristics that are similar to the black matrix of host Tieschitz, suggesting that this dark inclusion was emplaced before or during parent body metamorphism.

Magnesium and iron isotopes in 2.7 Ga Alexo komatiites: Mantle signatures, no evidence for Soret diffusion, and identification of diffusive transport in zoned olivine

NASA Astrophysics Data System (ADS)

Dauphas, Nicolas; Teng, Fang-Zhen; Arndt, Nicholas T.

2010-06-01

Komatiites from Alexo, Canada, are well preserved and represent high-degree partial mantle melts (˜50%). They are thus well suited for investigating the Mg and Fe isotopic compositions of the Archean mantle and the conditions of magmatic differentiation in komatiitic lavas. High precision Mg and Fe isotopic analyses of 22 samples taken along a 15-m depth profile in a komatiite flow are reported. The δ 25Mg and δ 26Mg values of the bulk flow are -0.138 ± 0.021‰ and -0.275 ± 0.042‰, respectively. These values are indistinguishable from those measured in mantle peridotites and chondrites, and represent the best estimate of the composition of the silicate Earth from analysis of volcanic rocks. Excluding the samples affected by secondary Fe mobilization, the δ 56Fe and δ 57Fe values of the bulk flow are +0.044 ± 0.030‰, and +0.059 ± 0.044‰, respectively. These values are consistent with a near-chondritic Fe isotopic composition of the silicate Earth and minor fractionation during komatiite magma genesis. In order to explain the early crystallization of pigeonite relative to augite in slowly cooled spinifex lavas, it was suggested that magmas trapped in the crystal mush during spinifex growth differentiated by Soret effect, which should be associated with large and coupled variations in the isotopic compositions of Mg and Fe. The lack of variations in Mg and Fe isotopic ratios either rules out the Soret effect in the komatiite flow or the effect is effaced as the solidification front migrates downward through the flow crust. Olivine separated from a cumulate sample has light δ 56Fe and slightly heavy δ 26Mg values relative to the bulk flow, which modeling shows can be explained by kinetic isotope fractionation associated with Fe-Mg inter-diffusion in olivine. Such variations can be used to identify diffusive processes involved in the formation of zoned minerals.

Petrology and mineralogy of the Ningqiang carbonaceous chondrite

NASA Astrophysics Data System (ADS)

Wang, Y.; Hsu, W.

2009-07-01

We report detailed chemical, petrological, and mineralogical studies on the Ningqiang carbonaceous chondrite. Ningqiang is a unique ungrouped type 3 carbonaceous chondrite. Its bulk composition is similar to that of CV and CK chondrites, but refractory lithophile elements (1.01 × CI) are distinctly depleted relative to CV (1.29 × CI) and CK (1.20 × CI) chondrites. Ningqiang consists of 47.5 vol% chondrules, 2.0 vol% Ca,Al-rich inclusions (CAIs), 4.5 vol% amoeboid olivine aggregates (AOAs), and 46.0 vol% matrix. Most chondrules (95%) in Ningqiang are Mgrich. The abundances of Fe-rich and Al-rich chondrules are very low. Al-rich chondrules (ARCs) in Ningqiang are composed mainly of olivine, plagioclase, spinel, and pyroxenes. In ARCs, spinel and plagioclase are enriched in moderately volatile elements (Cr, Mn, and Na), and low-Ca pyroxenes are enriched in refractory elements (Al and Ti). The petrology and mineralogy of ARCs in Ningqiang indicate that they were formed from hybrid precursors of ferromagnesian chondrules mixed with refractory materials during chondrule formation processes. We found 294 CAIs (55.0% type A, 39.5% spinel-pyroxene-rich, 4.4% hibonite-rich, and several type C and anorthite-spinelrich inclusions) and 73 AOAs in 15 Ningqiang sections (equivalent to 20 cm2 surface area). This is the first report of hibonite-rich inclusions in Ningqiang. They are texturally similar to those in CM, CH, and CB chondrites, and exhibit three textural forms: aggregates of euhedral hibonite single crystals, fine-grained aggregates of subhedral hibonite with minor spinel, and hibonite ± Al,Ti-diopside ± spinel spherules. Evidence of secondary alteration is ubiquitous in Ningqiang. Opaque assemblages, formed by secondary alteration of pre-existing alloys on the parent body, are widespread in chondrules and matrix. On the other hand, nepheline and sodalite, existing in all chondritic components, formed by alkali-halogen metasomatism in the solar nebula.

Oxygen-isotopic Compositions of Low-FeO relicts in High-FeO Host Chondrules in Acfer 094, a Type 3.0 Carbonaceous Chondrite Closely Related to CM

NASA Technical Reports Server (NTRS)

Rubin, Alan E.; Kunihiro, Tak; Wasson, John T.

2006-01-01

With one exception, the low-FeO relict olivine grains within high-FeO porphyritic chondrules in the type 3.0 Acfer 094 carbonaceous chondrite have DELTA O-17 ( = delta O-17 - 0.52 X delta O-18) values that are substantially more negative than those of the high-FeO olivine host materials. These results are similar to observations made earlier on chondrules in C03.0 chondrites and are consistent with two independent models: (1) Nebular solids evolved from low-FeO, low-DELTA O-17 compositions towards high-FeO, more positive DELTA O-17 compositions; and (2) the range of compositions resulted from the mixing of two independently formed components. The two models predict different trajectories on a DELTA O-17 vs. log Fe/Mg (olivine) diagram, but our sample set has too few values at intermediate Fe/Mg ratios to yield a definitive answer. Published data showing that Acfer 094 has higher volatile contents than CO chondrites suggest a closer link to CM chondrites. This is consistent with the high modal matrix abundance in Acfer 094 (49 vol.%). Acfer 094 may be an unaltered CM chondrite or an exceptionally matrix-rich CO chondrite. Chondrules in Acfer 094 and in CO and CM carbonaceous chondrites appear to sample the same population. Textural differences between Acfer 094 and CM chondrites are largely attributable to the high degree of hydrothermal alteration that the CM chondrites experienced in an asteroidal setting.

Reclassification of Hart and Northwest Africa 6047: Criteria for distinguishing between CV and CK3 chondrites

NASA Astrophysics Data System (ADS)

Dunn, Tasha L.; Gross, Juliane

2017-11-01

The single parent body model for the CV and CK chondrites (Greenwood et al.) was challenged by Dunn et al., who argued that magnetite compositions could not be reconciled by a single metamorphic sequence (i.e., CV3 → CK3 → CK4-6). Cr isotopic compositions, which are distinguishable between the CV and CK chondrites, also support two different parent bodies (Yin et al.). Despite this, there are many petrographic and mineralogical similarities between the unequilibrated (petrologic type 3) CK chondrites and the CV chondrites (also type 3), which may result in misclassification of samples. Hart and Northwest Africa 6047 (NWA 6047) are an excellent example of this. In this study, we revisit the classification of Hart and NWA 6047 using magnetite compositions, petrography, and compositions of olivine, the most ubiquitous mineral in both CV and CK chondrites. Not only do our results suggest that NWA 6047 and Hart were misclassified, but our assessment of CV and CK3 chondrites has also led to the development of criteria that can be used to distinguish between CV and CK3 chondrites. These criteria include: abundances of Cr2O3, TiO2, NiO, and Al2O3 in magnetite; Fa content and NiO abundance of matrix olivine; FeO content of chondrules; and the chondrule:matrix ratio. Classification as a CV chondrite is also supported by the presence of igneous chondrule rims, calcium-aluminum-rich inclusions, and an elongated petrofabric. However, none of these petrographic characteristics can be used conclusively to distinguish between CV and CK3 chondrites.

Magnesium isotopic composition of the Earth and chondrites

NASA Astrophysics Data System (ADS)

Teng, Fang-Zhen; Li, Wang-Ye; Ke, Shan; Marty, Bernard; Dauphas, Nicolas; Huang, Shichun; Wu, Fu-Yuan; Pourmand, Ali

2010-07-01

To constrain further the Mg isotopic composition of the Earth and chondrites, and investigate the behavior of Mg isotopes during planetary formation and magmatic processes, we report high-precision (±0.06‰ on δ 25Mg and ±0.07‰ on δ 26Mg, 2SD) analyses of Mg isotopes for (1) 47 mid-ocean ridge basalts covering global major ridge segments and spanning a broad range in latitudes, geochemical and radiogenic isotopic compositions; (2) 63 ocean island basalts from Hawaii (Kilauea, Koolau and Loihi) and French Polynesia (Society Island and Cook-Austral chain); (3) 29 peridotite xenoliths from Australia, China, France, Tanzania and USA; and (4) 38 carbonaceous, ordinary and enstatite chondrites including 9 chondrite groups (CI, CM, CO, CV, L, LL, H, EH and EL). Oceanic basalts and peridotite xenoliths have similar Mg isotopic compositions, with average values of δ 25Mg = -0.13 ± 0.05 (2SD) and δ 26Mg = -0.26 ± 0.07 (2SD) for global oceanic basalts ( n = 110) and δ 25Mg = -0.13 ± 0.03 (2SD) and δ 26Mg = -0.25 ± 0.04 (2SD) for global peridotite xenoliths ( n = 29). The identical Mg isotopic compositions in oceanic basalts and peridotites suggest that equilibrium Mg isotope fractionation during partial melting of peridotite mantle and magmatic differentiation of basaltic magma is negligible. Thirty-eight chondrites have indistinguishable Mg isotopic compositions, with δ 25Mg = -0.15 ± 0.04 (2SD) and δ 26Mg = -0.28 ± 0.06 (2SD). The constancy of Mg isotopic compositions in all major types of chondrites suggest that primary and secondary processes that affected the chemical and oxygen isotopic compositions of chondrites did not significantly fractionate Mg isotopes. Collectively, the Mg isotopic composition of the Earth's mantle, based on oceanic basalts and peridotites, is estimated to be -0.13 ± 0.04 for δ 25Mg and -0.25 ± 0.07 for δ 26Mg (2SD, n = 139). The Mg isotopic composition of the Earth, as represented by the mantle, is similar to chondrites. The chondritic composition of the Earth implies that Mg isotopes were well mixed during accretion of the inner solar system.

A IAB-Complex Iron Meteorite Containing Low-Ca Clinopyroxene: Northwest Africa 468 and its Relationship to Iodranites and Formation by Impact Melting

NASA Technical Reports Server (NTRS)

Rubin, Alan E.; Kallemeyn, Gregory W.; Wasson, John T.

2002-01-01

Northwest Africa 468 (NWA 468) is a new ungrouped, silicate-rich member of the IAB complex of nonmagmatic iron meteorites. The silicates contain relatively coarse (approximately 300 micron-size) grains of low-Ca clinopyroxene with polysynthetic twinning and inclined extinction. Low-Ca clinopyroxene is indicative of quenching from high temperatures (either from protoenstatite in a few seconds or high-temperature clinoenstatite in a few hours). It seems likely that NWA 468 formed by impact melting followed by rapid cooling to less than or equal to 660 C. After the loss of a metal-sulfide melt from the silicates, sulfide was reintroduced, either from impact-mobilized FeS or as an S2 vapor that combined with metallic Fe to produce FeS. The O-isotopic composition (delta O-17 = -1.39 %) indicates that the precursor material of NWA 468 was a metal-rich (e.g., CR) carbonaceous chondrite. Lodranites are similar in bulk chemical and O-isotopic composition to the silicates in NWA 468; the MAC 88177 lodranite (which also contains low-Ca clinopyroxene) is close in bulk chemical composition. Both NWA 468 and MAC 88177 have relatively low abundances of REE (rare earth elements) and plagiophile elements. Siderophiles in the metal-rich areas of NWA 468 are similar to those in the MAC 88177 whole rock; both samples contain low Ir and relatively high Fe, Cu and Se. Most unweathered lodranites contain approximately 20 - 38 wt. % metallic Fe-Ni. These rocks may have formed in an analogous manner to NWA 468 (i.e., by impact melting of metal-rich carbonaceous-chondrite precursors) but with less separation of metal-rich melts from silicates.

Petrology and Raman Spectroscopy of Shocked Phases in the Gujba CB Chondrite and the Shock History of the CB Parent Body

NASA Technical Reports Server (NTRS)

Weisberg, M. K.; Kimura, M.

2004-01-01

The CB chondrites are metal-rich chondritic meteorites having characteristics that sharply distinguish them from other chondrites [1], including (1) high metal abundances (60-80 vol.% metal), (2) most chondrules have cryptocrystalline or barred textures, (3) moderately volatile lithophile elements are highly depleted and (4) nitrogen is enriched in the heavy isotope. Similarities in mineral composition, as well as oxygen and nitrogen isotopic compositions of the CB to CR and CH chondrites are consistent with derivation of these chondrite groups from a common nebular reservoir, hence their grouping in the CR clan [1, 2, 3, 4]. CB chondrites have been divided into CBa (Gujba, Bencubbin, Weatherford) and CBb (Hammadah al Hamra 237 and QUE 94411) subgroups based on petrologic characteristics.

NEUTRON-POOR NICKEL ISOTOPE ANOMALIES IN METEORITES

DOE Office of Scientific and Technical Information (OSTI.GOV)

Steele, Robert C. J.; Coath, Christopher D.; Regelous, Marcel

2012-10-10

We present new, mass-independent, Ni isotope data for a range of bulk chondritic meteorites. The data are reported as {epsilon}{sup 60}Ni{sub 58/61}, {epsilon}{sup 62}Ni{sub 58/61}, and {epsilon}{sup 64}Ni{sub 58/61}, or the parts per ten thousand deviations from a terrestrial reference, the NIST SRM 986 standard, of the {sup 58}Ni/{sup 61}Ni internally normalized {sup 60}Ni/{sup 61}Ni, {sup 62}Ni/{sup 61}Ni, and {sup 64}Ni/{sup 61}Ni ratios. The chondrites show a range of 0.15, 0.29, and 0.84 in {epsilon}{sup 60}Ni{sub 58/61}, {epsilon}{sup 62}Ni{sub 58/61}, and {epsilon}{sup 64}Ni{sub 58/61} relative to a typical sample precision of 0.03, 0.05, and 0.08 (2 s.e.), respectively. The carbonaceousmore » chondrites show the largest positive anomalies, enstatite chondrites have approximately terrestrial ratios, though only EH match Earth's composition within uncertainty, and ordinary chondrites show negative anomalies. The meteorite data show a strong positive correlation between {epsilon}{sup 62}Ni{sub 58/61} and {epsilon}{sup 64}Ni{sub 58/61}, an extrapolation of which is within the error of the average of previous measurements of calcium-, aluminium-rich inclusions. Moreover, the slope of this bulk meteorite array is 3.003 {+-} 0.166 which is within the error of that expected for an anomaly solely on {sup 58}Ni. We also determined to high precision ({approx}10 ppm per AMU) the mass-dependent fractionation of two meteorite samples which span the range of {epsilon}{sup 62}Ni{sub 58/61} and {epsilon}{sup 64}Ni{sub 58/61}. These analyses show that 'absolute' ratios of {sup 58}Ni/{sup 61}Ni vary between these two samples whereas those of {sup 62}Ni/{sup 61}Ni and {sup 64}Ni/{sup 61}Ni do not. Thus, Ni isotopic differences seem most likely explained by variability in the neutron-poor {sup 58}Ni, and not correlated anomalies in the neutron-rich isotopes, {sup 62}Ni and {sup 64}Ni. This contrasts with previous inferences from mass-independent measurements of Ni and other transition elements which invoked variable contributions of a neutron-rich component. We have examined different nucleosynthetic environments to determine the possible source of the anomalous material responsible for the isotopic variations observed in Ni and other transition elements within bulk samples. We find that the Ni isotopic variability of the solar system cannot be explained by mixing with a component of bulk stellar ejecta from either SN II, Wolf-Rayet or, an asymptotic giant branch source and is unlikely to result from bulk mixing of material from an SN Ia. However, variable admixture of material from the Si/S zone of an SN II can create all the characteristics of Ni isotope variations in solar system materials. Moreover, these characteristics can also be provided by an SN II with a range of masses from 15 to 40 M{sub Sun }, showing that input from SN II is a robust source for Ni isotope variations in the solar system. Correlations of Ni isotope anomalies with O, Cr, and Ti isotope ratios and Pb/Yb in bulk meteorites suggest that the heterogeneous distribution of isotopic anomalies in the early solar system likely resulted from nebular sorting of chemically or physically different materials bearing different amounts of isotopes synthesized proximally to the collapse of the protosolar nebula.« less

The Chlorine Isotope Composition of the Solar Nebula & Implications to the Sources of Volatiles to the Terrestrial Planets

NASA Astrophysics Data System (ADS)

Gargano, A. M.; Sharp, Z. D.

2017-12-01

It was originally proposed by Sharp et al., 2016 that the solar nebula was isotopically light based on limited sampling of the Ol-phyric shergottites and two ordinary chondrites (Parnallee LL3.00, and NWA 8276 L3.00). Iron meteorites are remnants of early planetesimals which segregated cores <1Ma after CAI's and have δ37Cl values as low as -7‰, consistent with a light nebular source. Chondrules are relatively younger than iron meteorite parent bodies (2-3Ma after CAI's) and exhibit evidence for mixing with & recycling numerous isotopically distinct precursors as observed by Cl rich chondrules in Semarkona, and Qingzhen. The average δ37Cl values of chondrites are around 0‰, independent of petrologic type or [Cl], suggesting that chondrule forming regions have similar chlorine isotope sources. The average δ37Cl values of chondrites are consistent with a +3 to +6‰ isotopic fractionation of HCl clathrate from HCl gas, which occurred beyond the snow-line at 150K. The recycling of chondritic precursors mixed with HCl clathrate can account for pristine type 3.00 chondrites with δ37Cl values at approximately 0‰ independent of [Cl], or petrologic type. The source of volatiles to the terrestrial planets is commonly assumed to be chondritic in origin. These preliminary chlorine isotope data suggest that early planetesimals and planetary embryos had a solar Cl component at -7‰ or less, and secondary processes has since increased the δ37Cl values of Earth, Mars, and most chondrites. The chlorine isotope system therefore provides a new constraint regarding the sources of volatiles to the terrestrial planets. The δ37Cl value of the bulk Earth is around 0‰, inconsistent with a nebular source as measured in the Martian mantle but similar to that of chondrites with HCl clathrate precursors. The prolonged accretion of heavy chondritic material to Earth can account for the chlorine isotope discrepancy between the Earth and Mars, but is unconstrained by HSE abundances before complete core-mantle differentiation. Here, we examine the amount of chondritic chlorine and water that can added to the Earth allowable by HSE abundances and explore other potential sources of volatiles to the terrestrial planets to account for isotopic and elemental discrepancies.

Rare earth and other elements in components of the Abee enstatite chondrite

NASA Technical Reports Server (NTRS)

Frazier, R. M.; Boynton, W. V.

1985-01-01

Radiochemical and instrumental neutron activation analyses of REEs and other elements have been conducted for Abee clast samples, a matrix sample, a dark inclusion, magnetic and nonmagnetic samples, and bulk samples. Correlations of the REEs and oldhamite abundance for both the clasts and dark inclusions indicate that the REEs chiefly occur in oldhamite. The similar REE patterns for clasts and dark inclusions, and the similar mineral composition of oldhamite in clast and dark inclusions, suggest that the oldhamite in both the clasts and dark inclusions is of a common origin.

Mineralogies and source regions of near-Earth asteroids

NASA Astrophysics Data System (ADS)

Dunn, Tasha L.; Burbine, Thomas H.; Bottke, William F.; Clark, John P.

2013-01-01

Near-Earth Asteroids (NEAs) offer insight into a size range of objects that are not easily observed in the main asteroid belt. Previous studies on the diversity of the NEA population have relied primarily on modeling and statistical analysis to determine asteroid compositions. Olivine and pyroxene, the dominant minerals in most asteroids, have characteristic absorption features in the visible and near-infrared (VISNIR) wavelengths that can be used to determine their compositions and abundances. However, formulas previously used for deriving compositions do not work very well for ordinary chondrite assemblages. Because two-thirds of NEAs have ordinary chondrite-like spectral parameters, it is essential to determine accurate mineralogies. Here we determine the band area ratios and Band I centers of 72 NEAs with visible and near-infrared spectra and use new calibrations to derive the mineralogies 47 of these NEAs with ordinary chondrite-like spectral parameters. Our results indicate that the majority of NEAs have LL-chondrite mineralogies. This is consistent with results from previous studies but continues to be in conflict with the population of recovered ordinary chondrites, of which H chondrites are the most abundant. To look for potential correlations between asteroid size, composition, and source region, we use a dynamical model to determine the most probable source region of each NEA. Model results indicate that NEAs with LL chondrite mineralogies appear to be preferentially derived from the ν6 secular resonance. This supports the hypothesis that the Flora family, which lies near the ν6 resonance, is the source of the LL chondrites. With the exception of basaltic achondrites, NEAs with non-chondrite spectral parameters are slightly less likely to be derived from the ν6 resonance than NEAs with chondrite-like mineralogies. The population of NEAs with H, L, and LL chondrite mineralogies does not appear to be influenced by size, which would suggest that ordinary chondrites are not preferentially sourced from meter-sized objects due to Yarkovsky effect.

Isotopically distinct reservoirs in the solar nebula: Isotope anomalies in Vigarano meteorite inclusions

NASA Technical Reports Server (NTRS)

Loss, R. D.; Lugmair, G. W.; Davis, A. M.; Macpherson, G. J.

1994-01-01

The isotopic compositions of Mg, Ca, Ti, Cr, Zn, Sr, Ba, Nd, and Sm were measured in four relatively unaltered refractory inclusions from the Vigarano carbonaceous chondrite meteorite. Three of the inclusions (USNM 1623-2, 1623-3, and 1623-8) show similar Mg, Ca, Ti, and Cr isotopic compositions to those found in most inclusions in the Allende carbonaceous chondrite. This indicates that these Vigarano inclusions sampled the same isotopic reservoirs as the majority of the Allende inclusions that isotope signatures in the latter were not significantly modified by the secondary alteration that permeates most Allende inclusions. In contrast, inclusion 1623-5 has large deficits in Mg-26, Ca-48, and Ti-50 and small but distinct Cr-54, Zn-66, Sr-84, Ba-135, Ba-137, and Sm-144 anomalies. The magnitudes of these unusual anomalies in the refractory elements are within analytical uncertainty of those found in the Allende 'FUN" inclusion C1, yet 1623-5 has a very different bulk chemical composition from C1. The fact that 1623-5 and C1 have identical isotopic anomalies yet have significantly distinct major and trace element contents provide convincing evidence for the presence of isotopically distinct reservoirs in the early solar system.

Petrology of enstatite chondrites and anomalous enstatite achondrites

NASA Astrophysics Data System (ADS)

van Niekerk, Deon

2012-01-01

Chondrites are meteorites that represent unmelted portions of asteroids. The enstatite chondrites are one class of chondrites. They consist of reduced mineral assemblages that formed under low oxygen fugacity in the solar nebula, prior to accretion into asteroids. There are two groups of enstatite chondrites---EH and EL. I studied EL3 meteorites, which are understood to be unmetamorphosed and thus to only preserve primitive nebular products. I show in a petrographic study that the EL3s are in fact melt--breccias in which impact-melting produced new mineral assemblages and textures in portions of the host chondrites, after accretion. I document meta- land sulfide assemblages that are intergrown with silicate minerals (which are often euhedral), and occur outside chondrules; these assemblages probably represent impact-melting products, and are different from those in EH3 chondrites that probably represent nebular products. In situ siderophile trace element compositions of the metal in EL3s, obtained by laser ablation inductively coupled plasma mass spectrometry, are consistent with an impact-melting hypothesis. The trace element concentrations show no clear volatility trend, and are thus probably not the result of volatile-driven petrogenetic processes that operated in the solar nebula. Trace element modeling suggests that the character of the trace element patterns together with deviations from the mean bulk EL metal pattern is consistent with metal that crystallized in a coexisting liquid-solid metal system in which dissolved carbon influenced element partitioning. I also conducted a petrographic and mineral-chemistry study of several anomalous enstatite meteorites. These have igneous textures, but unfractionated mineralogy similar to unmelted chondrites. I show that with the exception of one, the meteorites are related to each other, and probably formed by crystallization from an impact melt instead of metamorphism through the decay of short lived radionuclides. The broad importance of these studies lies in documenting the petrology of extraterrestrial materials that reveal the geological history of the young solar system prior to the existence of planets. Furthermore, they serve to identify which mineral assemblages record nebular processes and which record processes on asteroids, so that future studies may select the correct material to address particular questions.

Cosmogenic Ne-21 Production Rates in H-Chondrites Based on Cl-36 - Ar-36 Ages

NASA Technical Reports Server (NTRS)

Leya, I.; Graf, Th.; Nishiizumi, K.; Guenther, D.; Wieler, R.

2000-01-01

We measured Ne-21 production rates in 14 H-chondrites in good agreement with model calculations. The production rates are based on Ne-21 concentrations measured on bulk samples or the non-magnetic fraction and Cl-36 - Ar-36 ages determined from the metal phase.

Mineralogy and chemistry of Rumuruti: The first meteorite fall of the new R chondrite group

NASA Astrophysics Data System (ADS)

Schulze, H.; Bischoff, A.; Palme, H.; Spettel, B.; Dreibus, G.; Otto, J.

1994-03-01

The Rumuruti meteorite shower fell in Rumuruti, Kenya, on 1934 January 28 at 10:45 p.m. Rumuruti is an olivine-rich chondritic breccia with light-dark structure. Based on the coexistence of highly recrystallized fragments and unequilibrated components, Rumuruti is classified as a type 3-6 chondrite breccia. The most abundant phase of Rumuruti is olivine (mostly Fa(approximately 39) with about 70 vol%. Feldspar (approximately 14 vol%; mainly plagioclase), Ca-pyroxene (5 vol%), pyrrhotite (4.4 vol%), and pentlandite (3.6 vol%) are major constituents. All other phases have abundances below 1 vol%, including low-Ca pyroxene, chrome spinels, phosphates (chlorapatite and whitlockite), chalcopyrite, ilemenite, tridymite, Ni-rich and Ge-containing metals, kamacite, and various particles enriched in noble metals like Pt, Ir, and Au. The chemical composition of Rumuruti is chondritic. The depletion in refractory elements (Sc, REE, etc.) and the comparatively high Mn, Na, and K contents are characteristic of ordinary chondrites and distinguish Rumuruti from carbonaceous chondrites. However, S, Se, and Zn contents in Rumuruti are significantly above the level expected for ordinary chondrites. The oxygen isotope composition of Rumuruti is high in delta O-17 (5.52%) and delta O-18 (5.07%). With Rumuruti, nine meteorites samples exist that are chemically and mineralogically very similar. These meteorites are attributed to at least eight different fall events. It is proposed in this paper to call this group R chondrites (rumurutites) after the first and only fall among these meteorites. The meteorites have a close relationship to ordinary chondrites. However, they are more oxidized than any of the existing groups of ordinary chondrites. Small, but significant differences in chemical composition and in oxygen isotopes between R chondrites and ordinary chondrites exclude formation of R chondrites from ordinary chondrites by oxidation. This implies a separate, independent R chondrite parent body.

Chemical composition of Mars

NASA Technical Reports Server (NTRS)

Morgan, J. W.; Anders, E.

1979-01-01

The chemical composition of Mars is estimated from the cosmochemical model of Ganapathy and Anders (1974) with additional petrological and geophysical constraints. The model assumes that planets and chondrites underwent the same fractionation processes in the solar nebula, and constraints are imposed by the abundance of the heat-producing elements, U, Th and K, the volatile-rich component and the high density of the mantle. Global abundances of 83 elements are presented, and it is noted that the mantle is an iron-rich garnet wehrlite, nearly identical to the bulk moon composition of Morgan at al. (1978) and that the core is sulfur poor (3.5% S). The comparison of model compositions for the earth, Venus, Mars, the moon and a eucrite parent body suggests that volatile depletion correlates mainly with size rather than with radial distance from the sun.

Evaluating Volatility-controlled Isotope Fractionation During Planet Formation: Kinetics versus Equilibrium

NASA Astrophysics Data System (ADS)

Young, E. D.

2017-12-01

Recent advances in our ability to measure stable isotope ratios of light, rock-forming elements, including those for Zn, K, Fe, Si, and Mg, among others, has resulted in an emerging hypothesis that collisions among rocky planetesimals, planetary embryos, and/or proto-planets caused losses of moderately volatile elements (e.g., K) and "common" or moderately refractory elements (e.g., Mg and Si). The primary evidence is in the form of heavy isotope enrichments in rock-forming elements relative to the chondrite groups that are thought to be representative of planetary precursors. Equilibrium volatility-controlled isotope fractionation for planetesimal magma oceans might have occurred for bodies larger than 0.1% of an Earth mass (½ the mass of Pluto) as these bodies had sufficient gravity to overpower the escape velocities of hot gas at 2000K. Both Jean's escape and viscous drag hydrodynamic escape can obviate the escape velocity limit but will fractionate by mass, not by volatility. Equilibrium vapor/melt fractionation is qualitatively consistent with the greater disparity in 29Si/28Si between Earth and chondrites than in 25Mg/24Mg. However, losses of large masses of vapor are required to record the fractionation in the melts. We consider that if Earth was derived from E chondrite-like materials, the bulk composition of the Earth, assuming refractory Ca was retained, requires > 60% loss of Mg. This is a lot of vapor loss for a process relying on at least intermittent equilibrium, although it comports with the isotopic lever-rule requirements. Paradoxically, the alternative of evaporative loss of rock-forming elements requires less total mass loss. For example, the calculated Mg and Si isotopic compositions of residues resulting from evaporation of chondritic melts can fit the Mg and Si isotopic compositions of Earth, Mars, and angrites with varying background pressures and with total mass losses of near 5% or less. These mass losses are closer to, and even lower than, those suggested by Ca concentrations relative to CI chondrite. Equilibrium models achieve greater Si than Mg isotope fractionation by large mass losses while evaporation models produce this effect for small mass losses. Additional constraints involving other isotope systems as well as models for vapor loss can distinguish between the two scenarios.

Distribution of 26Al in the CR chondrite chondrule-forming region of the protoplanetary disk

NASA Astrophysics Data System (ADS)

Schrader, Devin L.; Nagashima, Kazuhide; Krot, Alexander N.; Ogliore, Ryan C.; Yin, Qing-Zhu; Amelin, Yuri; Stirling, Claudine H.; Kaltenbach, Angela

2017-03-01

We report on the mineralogy, petrography, and in situ measured oxygen- and magnesium-isotope compositions of eight porphyritic chondrules (seven FeO-poor and one FeO-rich) from the Renazzo-like carbonaceous (CR) chondrites Graves Nunataks 95229, Grosvenor Mountains 03116, Pecora Escarpment 91082, and Queen Alexandra Range 99177, which experienced minor aqueous alteration and very mild thermal metamorphism. We find no evidence that these processes modified the oxygen- or Al-Mg isotope systematics of chondrules in these meteorites. Olivine, low-Ca pyroxene, and plagioclase within an individual chondrule have similar O-isotope compositions, suggesting crystallization from isotopically uniform melts. The only exceptions are relict grains in two of the chondrules; these grains are 16O-enriched relative to phenocrysts of the host chondrules. Only the FeO-rich chondrule shows a resolvable excesses of 26Mg, corresponding to an inferred initial 26Al/27Al ratio [(26Al/27Al)0] of (2.5 ± 1.6) × 10-6 (±2SE). Combining these results with the previously reported Al-Mg isotope systematics of CR chondrules (Nagashima et al., 2014, Geochem. J. 48, 561), 7 of 22 chondrules (32%) measured show resolvable excesses of 26Mg; the presence of excess 26Mg does not correlate with the FeO content of chondrule silicates. In contrast, virtually all chondrules in weakly metamorphosed (petrologic type 3.0-3.1) unequilibrated ordinary chondrites (UOCs), Ornans-like carbonaceous (CO) chondrites, and the ungrouped carbonaceous chondrite Acfer 094 show resolvable excesses of 26Mg. The inferred (26Al/27Al)0 in CR chondrules with resolvable excesses of 26Mg range from (1.0 ± 0.4) × 10-6 to (6.3 ± 0.9) × 10-6, which is typically lower than (26Al/27Al)0 in the majority of chondrules from UOCs, COs, and Acfer 094. Based on the inferred (26Al/27Al)0, three populations of CR chondrules are recognized; the population characterized by low (26Al/27Al)0 (<3 × 10-6) is dominant. There are no noticeable trends with major and minor element or O-isotope compositions between these populations. The weighted mean (26Al/27Al)0 of 22 CR chondrules measured is (1.8 ± 0.3) × 10-6. An apparent agreement between the 26Al-26Mg ages (using weighted mean value) and the revised (using 238U/235U ratio for bulk CR chondrites of 137.7789 ± 0.0085) 207Pb-206Pb age of a set of chondrules from CR chondrites (Amelin et al., 2002, Science297, 1678) is consistent with the initial 26Al/27Al ratio in the CR chondrite chondrule-forming region at the canonical level (∼5.2 × 10-5), allowing the use of 26Al-26Mg systematics as a chronometer for CR chondrules. To prove chronological significance of 26Al for CR chondrules, measurements of Al-Mg and U-Pb isotope systematics on individual chondrules are required. The presence of several generations among CR chondrules indicates some chondrules that accreted into the CR chondrite parent asteroid avoided melting by later chondrule-forming events, suggesting chondrule-forming processes may have occurred on relatively limited spatial scales. Accretion of the CR chondrite parent body occurred at >4.0-0.3+0.5 Ma after the formation of CAIs with the canonical 26Al/27Al ratio, although rapid accretion after formation of the major population of CR chondrules is not required by our data.

In-Situ Oxygen Isotopic Composition of Tagish Lake: An Ungrouped Type 2 Carbonaceous Chondrite

NASA Technical Reports Server (NTRS)

Zolensky, Michael E.; Engrand, Cecile; Gounelle, Matthieu; Zolensky, Mike E.

2001-01-01

We have measured the oxygen isotopic composition of several components of Tagish Lake by ion microprobe. This meteorite constitutes the best preserved sample of C2 matter presently available for study. It presents two different lithologies (carbonate-poor and -rich) which have fairly comparable oxygen isotopic composition, with regard to both the primary or secondary minerals. For the olivine and pyroxene grains, their delta O-18 values range from - 10.5% to + 7.4% in the carbonate-poor lithology, with a mean Delta O-17 value of - 3.7 2.4%. In the carbonate-rich lithology, delta O-18 varies from - 7.9% to + 3.3%, and the mean Delta O-17 value is - 4.7 +/- 1.4%. Olivine inclusions (Fo(sub >99)) with extreme O-16-enrichment were found in both lithologies: delta O-18 = - 46.1 %, delta O-187= - 48.3% and delta O-18 = - 40.6%, delta O-17 = - 41.2% in the carbonate-rich lithology; delta O-18 = - 41.5%, delta O-17 = -43.4%0 in the carbonate-poor lithology. Anhydrous minerals in the carbonate-poor lithology are slightly more O-16-rich than in the carbonate-rich one. Four low-iron manganese-rich (LIME) olivine grains do not have an oxygen isotopic composition distinct from the other "normal" olivines. The phyllosilicate matrix presents the same range of oxygen isotopic compositions in both lithologies: delta O-18 from approximately 11 % to approximately 6%, with an average Delta. O-17 approximately 0%. Because the bulk Tagish Lake oxygen isotopic composition given by Brown et al. is on the high end of our matrix analyses, we assume that this "bulk Tagish Lake" composition probably only represents that of the carbonate-rich lithology. Calcium carbonates have delta O-18 values up to 35%, with Delta O-17 approximately 0.5%0. Magnetite grains present very high Delta O-17 values approximately + 3.4%0 +/- 1.2%. Given our analytical uncertainties and our limited carbonate data, the matrix and the carbonate seem to have formed in isotopic equilibrium. In that case, their large isotopic fractionation would argue for a low temperature (CM-like, T approximately 0 deg) formation. Magnetite probably formed during a separate event. Tagish Lake magnetite data is surprisingly compatible with that of R-chondrites and unequilibrated ordinary (LL3) chondrites. Our oxygen isotope data strongly supports the hypothesis of a single precursor for both lithologies. Drastic mineralogical changes between the two lithologies not being accompanied with isotopic fractionation seem compatible with the alteration model presented by Young et aI. Tagish Lake probably represents the first well preserved large sample of the C2 matter that dominates interplanetary matter since the formation of the solar system.

A search for isotopic anomalies in uranium. [in chondritic meteorites and terrestrial basalt

NASA Technical Reports Server (NTRS)

Chen, J. H.; Wasserburg, G. J.

1980-01-01

The U-238/U-235 ratios for nine bulk chondritic meteorites and a terrestrial basalt were measured. The total range in U-238/U-235 determined for both total meteorites and for acid leaches was from 137.2 terrestrial U. The typical errors in a single determination are plus or minus 6 per thousand (2 sigma m) for a 2 ng U sample from a chondrite. Taking the extreme values of delta U-235 for each measurement the maximum amount of excess U-235 that can be allowed to be present ranges from 200 million to 2 billion atoms per gram of bulk meteorite. These results do not support the claims of variations in U-238/U-235 at the percentage levels or number of excess U-235 atoms in some of the same meteorites as reported by several other previous workers.

Petrogenesis of Alta'ameem meteorite (Iraq) inferred from major, trace, REE and PGE+Au content

NASA Astrophysics Data System (ADS)

Kettanah, Yawooz A.; Ismail, Sabah A.

2018-03-01

Alta'ameem Meteorite (AM) is an unaltered ordinary LL chondrite that hit an area near Kirkuk City in northern Iraq on 1977. It has an ash-gray colour with a thin black fusion crust, and consists of spheroidal chondrules and variously shaped clasts aggregated together by a fine grained matrix. The chondrules of Alta'ameem Meteorite include all known types in similar meteorites elsewhere. Mineralogically, the AM consists of silicates (olivine - Fa27.7; pyroxene - Fs23.2 (Opx) and 20.5 (Cpx); plagioclase - Ab73.5An22.1Or4.7), alloys and metals (taenite, tetrataenite, kamacite, and native copper), oxides (ilmenite and chromite), sulfides (troilite), and phosphates (apatite) as well as few unidentified minerals including a Fe-Ti-Cr oxide and Fe-Ni sulfide. The chemistry of AM is dominated by SiO2, MgO, and FeOt accounting for >91 wt% of the bulk composition with minor amounts of Al2O3, CaO, Na2O, S, Ni and Cr. It contains 3675 ppb REE which is within the range of most chondrites, with a negative (-0.8) Sm- and positive (+1.2) Tb-anomalies and a near flat normalized trend (LaN/YbN = 1.16). The concentration of PGEs and Au, Ni, Co, and Cr is low in comparison to most chondrites. The K/La, Ru/Rh vs. Pt/Pd, and Pd/Ir ratio (1.85), and low PGE indicates that the AM is somewhat distinct from other meteorites. The AM has W0 weathering grade and very weak (S2) shock metamorphism. Although the AM has some petrographical and geochemical differences with other chondrites, it still can be considered as LL5 chondrite.

Hf-W chronology of CR chondrites: Implications for the timescales of chondrule formation and the distribution of 26Al in the solar nebula

NASA Astrophysics Data System (ADS)

Budde, Gerrit; Kruijer, Thomas S.; Kleine, Thorsten

2018-02-01

Renazzo-type carbonaceous (CR) chondrites are distinct from most other chondrites in having younger chondrule 26Al-26Mg ages, but the significance of these ages and whether they reflect true formation times or spatial variations of the 26Al/27Al ratio within the solar protoplanetary disk are a matter of debate. To address these issues and to determine the timescales of metal-silicate fractionation and chondrule formation in CR chondrites, we applied the short-lived 182Hf-182W chronometer to metal, silicate, and chondrule separates from four CR chondrites. We also obtained Mo isotope data for the same samples to assess potential genetic links among the components of CR chondrites, and between these components and bulk chondrites. All investigated samples plot on a single Hf-W isochron and constrain the time of metal-silicate fractionation in CR chondrites to 3.6 ± 0.6 million years (Ma) after the formation of Ca-Al-rich inclusions (CAIs). This age is indistinguishable from a ∼3.7 Ma Al-Mg age for CR chondrules, suggesting not only that metal-silicate fractionation and chondrule formation were coeval, but also that these two processes were linked to each other. The good agreement of the Hf-W and Al-Mg ages, combined with concordant Hf-W and Al-Mg ages for angrites and CV chondrules, provides strong evidence for a disk-wide, homogeneous distribution of 26Al in the early solar system. As such, the young Al-Mg ages for CR chondrules do not reflect spatial 26Al/27Al heterogeneities but indicate that CR chondrules formed ∼1-2 Ma later than chondrules from most other chondrite groups. Metal and silicate in CR chondrites exhibit distinct nucleosynthetic Mo and W isotope anomalies, which are caused by the heterogeneous distribution of the same presolar s-process carrier. These data suggest that the major components of CR chondrites are genetically linked and therefore formed from a single reservoir of nebular dust, most likely by localized melting events within the solar protoplanetary disk. Taken together, the chemical, isotopic, and chronological data for components of CR chondrites imply a close temporal link between chondrule formation and chondrite accretion, indicating that the CR chondrite parent body is one of the youngest meteorite parent bodies. The relatively late accretion of the CR parent body is consistent with its isotopic composition (for instance the elevated 15N/14N) that suggests a formation at a larger heliocentric distance, probably beyond the orbit of Jupiter. As such, the accretion age of the CR chondrite parent body of ∼3.6 Ma after CAI formation provides the earliest possible time at which Jupiter's growth could have led to scattering of carbonaceous meteorite parent bodies from beyond its orbit into the inner solar system.

Mercury Abundances and Isotopic Compositions in the Murchison (CM) and Allende (CV)Carbonaceous Chondrites

NASA Technical Reports Server (NTRS)

Lauretta, D. S.; Klaue, B.; Blum, J. D.; Buseck, P. R.

2001-01-01

The abundance and isotopic composition of Hg was determined in bulk samples of both the Murchison (CM) and Allende (CV) carbonaceous chondrites using single- and multi-collector inductively coupled plasma mass spectrometry (ICP-MS). The bulk abundances of Hg are 294 6 15 ng/g in Murchison and 30.0 6 1.5 ng/g in Allende. These values are within the range of previous measurements of bulk Hg abundances by neutron activation analysis (NAA). Prior studies suggested that both meteorites contain isotopically anomalous Hg, with d l 96/202Hg values for the anomalous, thermal-release components from bulk samples ranging from 2260 %o to 1440 9/00 in Murchison and from 2620 9/00 to 1540 9/00 in Allende (Jovanovic and Reed, 1976a; 1976b; Kumar and Goel, 1992). Our multi-collector ICP-MS measurements suggest that the relative abundances of all seven stable Hg isotopes in both meteorites are identical to terrestrial values within 0.2 to 0.5 9/00m. On-line thermal-release experiments were performed by coupling a programmable oven with the singlecollector ICP-MS. Powdered aliquots of each meteorite were linearly heated from room temperature to 900 C over twenty-five minutes under an Ar atmosphere to measure the isotopic composition of Hg released fiom the meteorites as a h c t i o n of temperature. In separate experiments, the release profiles of S and Se were determined simultaneously with Hg to constrain the Hg distribution within the meteorites and to evaluate the possibility of Se interferences in previous NAA studies. The Hg-release patterns differ between Allende and Murchison. The Hg-release profile for Allende contains two distinct peaks, at 225" and 343"C, whereas the profile for Murchison has only one peak, at 344 C. No isotopically anomalous Hg was detected in the thermal-release experiments at a precision level of 5 to 30 9/00, depending on the isotope ratio. In both meteorites the Hg peak at ;340"C correlates with a peak in the S-release profile. This correlation suggests that Hg is associated with S-bearing phases and, thus, that HgS is a major Hg-bearing phase in both meteorites. The Hg peak at 225 C for Allende is similar to release patterns of physically adsorbed Hg on silicate and metal grains.

What is the iron isotope composition of the Moon?

NASA Astrophysics Data System (ADS)

Poitrasson, F.; Zambardi, T.; Magna, T.; Neal, C. R.

2016-12-01

It is difficult to estimate the bulk chemical and isotopic composition of the Moon because of severe limitations in our sampling. As a result, there is currently a debate on the bulk Fe isotope composition of the Moon despite the constraints on the lunar accretion modes or differentiation processes it may provide. For this, a proper mass balance estimation of essential planetary reservoirs is required. For instance, the dichotomy in δ57Fe between low- and high-Ti mare basalt varieties as a consequence of differences in degree of fractional crystallization of their respective lunar mantle sources should be rigorously tested. To investigate this, we performed new iron isotope measurements of 33 bulk lunar mare basalts and highland rocks, including KREEP-related materials. The new data show significant Fe isotope differences between high-Ti and low-Ti mare basalts, yielding mean δ57FeIRMM-014=0.277±0.020‰ and δ57FeIRMM-014=0.127±0.020‰, respectively. Assuming that lunar basalts mirror the iron isotope composition of their respective mantle protoliths, the estimated relative proportion of the low-Ti and high-Ti mantle source suggests that the lunar upper mantle should be close to δ57Fe=0.14±0.03‰. At present, it is unclear whether the bulk lunar Fe isotope composition is indistinguishable from that of the Earth (δ57FeIRMM-014=0.10±0.03‰), when estimated solely from mare basalts data, or if it is twice as heavy relative to chondrites, as initially proposed. A large scatter at δ57Fe=0.08±0.19‰ for ferroan anorthosites, Mg-suite rocks and a KREEP basalt imparts more complexities for global isotopic view of the Moon. A better understanding of the cause of Fe isotope heterogeneity among the lunar highland rocks will likely allow to better estimate the bulk Moon composition, and possibly to improve our knowledge about the genesis of the lunar crust itself.

The ruthenium isotopic composition of the oceanic mantle

NASA Astrophysics Data System (ADS)

Bermingham, K. R.; Walker, R. J.

2017-09-01

The approximately chondritic relative, and comparatively high absolute mantle abundances of the highly siderophile elements (HSE), suggest that their concentrations in the bulk silicate Earth were primarily established during a final ∼0.5 to 1% of ;late accretion; to the mantle, following the cessation of core segregation. Consequently, the isotopic composition of the HSE Ru in the mantle reflects an amalgamation of the isotopic compositions of late accretionary contributions to the silicate portion of the Earth. Among cosmochemical materials, Ru is characterized by considerable mass-independent isotopic variability, making it a powerful genetic tracer of Earth's late accretionary building blocks. To define the Ru isotopic composition of the oceanic mantle, the largest portion of the accessible mantle, we report Ru isotopic data for materials from one Archean and seven Phanerozoic oceanic mantle domains. A sample from a continental lithospheric mantle domain is also examined. All samples have identical Ru isotopic compositions, within analytical uncertainties, indicating that Ru isotopes are well mixed in the oceanic mantle, defining a μ100Ru value of 1.2 ± 7.2 (2SD). The only known meteorites with the same Ru isotopic composition are enstatite chondrites and, when corrected for the effects of cosmic ray exposure, members of the Main Group and sLL subgroup of the IAB iron meteorite complex which have a collective CRE corrected μ100Ru value of 0.9 ± 3.0. This suggests that materials from the region(s) of the solar nebula sampled by these meteorites likely contributed the dominant portion of late accreted materials to Earth's mantle.

Effects of Short-Term Thermal Alteration on Organic Matter in Experimentally-Heated Tagish Lake Observed by Raman Spectroscopy

NASA Technical Reports Server (NTRS)

Chan, Q. H. S.; Nakato, A.; Zolensky, M. E.; Nakamura, T.; Kebukawa, Y.

2007-01-01

Carbonaceous chondrites exhibit a wide range of aqueous and thermal alteration characteristics. Examples of the thermally metamorphosed carbonaceous chondrites (TMCCs) include the C2-ung/CM2TIVs Belgica (B)-7904 and Yamato (Y) 86720. The alteration extent is the most complete in these meteorites and thus they are considered typical end-members of TMCCs exhibiting complete dehydration of matrix phyllosilicates [1, 2]. The estimated heating conditions are 10 to 10(sup 3) days at 700 C to 1 to 100 hours at 890 C, i.e. short-term heating induced by impact and/or solar radiation [3]. The chemical and bulk oxygen isotopic compositions of the matrix of the carbonate (CO3)-poor lithology of the Tagish Lake (hereafter Tag) meteorite bears similarities to these TMCCs [4]. We investigated the experimentally-heated Tag with the use of Raman spectroscopy to understand how short-term heating affects the maturity of insoluble organic matter (IOM) in aqueously altered meteorites.

A model composition for Mars derived from the oxygen isotopic ratios of martian/SNC meteorites. [Abstract only

NASA Technical Reports Server (NTRS)

Delaney, J. S.

1994-01-01

Oxygen is the most abundant element in most meteorites, yet the ratios of its isotopes are seldom used to constrain the compositional history of achondrites. The two major achondrite groups have O isotope signatures that differ from any plausible chondritic precursors and lie between the ordinary and carbonaceous chondrite domains. If the assumption is made that the present global sampling of chondritic meteorites reflects the variability of O reservoirs at the time of planetessimal/planet aggregation in the early nebula, then the O in these groups must reflect mixing between known chondritic reservoirs. This approach, in combination with constraints based on Fe-Mn-Mg systematics, has been used previously to model the composition of the basaltic achondrite parent body (BAP) and provides a model precursor composition that is generally consistent with previous eucrite parent body (EPB) estimates. The same approach is applied to Mars exploiting the assumption that the SNC and related meteorites sample the martian lithosphere. Model planet and planetesimal compositions can be derived by mixing of known chondritic components using O isotope ratios as the fundamental compositional constraint. The major- and minor-element composition for Mars derived here and that derived previously for the basaltic achondrite parent body are, in many respects, compatible with model compositions generated using completely independent constraints. The role of volatile elements and alkalis in particular remains a major difficulty in applying such models.

Magnesium stable isotope composition of Earth's upper mantle

NASA Astrophysics Data System (ADS)

Handler, Monica R.; Baker, Joel A.; Schiller, Martin; Bennett, Vickie C.; Yaxley, Gregory M.

2009-05-01

The mantle is Earth's largest reservoir of Mg containing > 99% of Earth's Mg inventory. However, no consensus exists on the stable Mg isotope composition of the Earth's mantle or how variable it is and, in particular, whether the mantle has the same stable Mg isotope composition as chondrite meteorites. We have determined the Mg isotope composition of olivine from 22 mantle peridotites from eastern Australia, west Antarctica, Jordan, Yemen and southwest Greenland by pseudo-high-resolution MC-ICP-MS on Mg purified to > 99%. The samples include fertile lherzolites, depleted harzburgites and dunites, cryptically metasomatised ('dry') peridotites and modally metasomatised apatite ± amphibole-bearing harzburgites and wehrlites. Olivine from these samples of early Archaean through to Permian lithospheric mantle have δ25Mg DSM-3 = - 0.22 to - 0.08‰. These data indicate the bulk upper mantle as represented by peridotite olivine is homogeneous within current analytical uncertainties (external reproducibility ≤ ± 0.07‰ [2 sd]). We find no systematic δ25Mg variations with location, lithospheric age, peridotite fertility, or degree or nature of mantle metasomatism. Although pyroxene may have slightly heavier δ25Mg than coexisting olivine, any fractionation between mantle pyroxene and olivine is also within current analytical uncertainties with a mean Δ25Mg pyr-ol = +0.06 ± 0.10‰ (2 sd; n = 5). Our average mantle olivine δ25Mg DSM-3 = - 0.14 ± 0.07‰ and δ26Mg DSM-3 = - 0.27 ± 0.14‰ (2 sd) are indistinguishable from the average of data previously reported for terrestrial basalts, confirming that basalts have stable Mg isotope compositions representative of the mantle. Olivine from five pallasite meteorites have δ25Mg DSM-3 = - 0.16 to - 0.11‰ that are identical to terrestrial olivine and indistinguishable from the average δ25Mg previously reported for chondrites. These data provide no evidence for measurable heterogeneity in the stable Mg isotope composition of the source material in the proto-planetary disc from which Earth and chondrite and pallasite parent bodies accreted.

Enstatite Meteorites and the Original Heterogeneity of Mn-53 Distribution in the Solar Nebula

NASA Technical Reports Server (NTRS)

Lugmair, Guenter W.

1999-01-01

We have shown earlier that the relative abundance of radiogenic Cr-53 in bulk ordinary chondrites (approximately 0.48 epsilon) is clearly different from that in the earth-moon system (0 epsilon). The SNC parent body (Mars) is characterized by an intermediate Cr-53 excess (approximately 0.23 epsilon). We have also shown that the Mn-Cr systematics of the howardite-eucrite-diogenite parent body (HED PB, the asteroid Vesta) is consistent with the chondritic Mn/Cr ratio in the bulk HED PB and that it has a Cr-53 excess of approximately 0.5 epsilon units which is within error the same as that of chondrites. It appears that the excesses of Cr-53 in these planets are a function of their present heliocentric distance. The study of some other meteorite classes (angrites, pallasites, primitive achondrites) has shown that their Mn-CR systematics is consistent with that of the ordinary chondrites. The observed gradient in the radiogenic Cr-53 abundances can be explained by a). an early volatility controlled radial Mn/Cr fractionation in the nebula or b). an original heterogeneity of Mn-53. The first assumption, however, requires the Mn/Cr ratios of the bulk Earth and Mars to be considerably lower than the inferred model Mn/Cr ratios for these two planets. For this reason, we suggested that the observed gradient is due to an original radial Mn-53 heterogeneity in the late nebula.

Chemical evidence for differentiation, evaporation and recondensation from silicate clasts in Gujba

NASA Astrophysics Data System (ADS)

Oulton, Jonathan; Humayun, Munir; Fedkin, Alexei; Grossman, Lawrence

2016-03-01

The silicate and metal clasts in CB chondrites have been inferred to form as condensates from an impact-generated vapor plume between a metal-rich body and a silicate body. A detailed study of the condensation of impact-generated vapor plumes showed that the range of CB silicate clast compositions could not be successfully explained without invoking a chemically differentiated target. Here, we report the most comprehensive elemental study yet performed on CB silicates with 32 silicate clasts from nine slices of Gujba analyzed by laser ablation inductively coupled plasma mass spectrometry for 53 elements. Like in other studies of CBs, the silicate clasts are either barred olivine (BO) or cryptocrystalline (CC) in texture. In major elements, the Gujba silicate clasts ranged from chondritic to refractory enriched. Refractory element abundances ranged from 2 to 10 × CI, with notable anomalies in Ba, Ce, Eu, and U abundances. The two most refractory-enriched BO clasts exhibited negative Ce anomalies and were depleted in U relative to Th, characteristic of volatilization residues, while other BO clasts and the CC clasts exhibited positive Ce anomalies with excess U (1-3 × CI), and Ba (1-6 × CI) anomalies indicating re-condensation of ultra-refractory element depleted vapor. The Rare Earth Elements (REE) also exhibit light REE (LREE) enrichment or depletion in several clasts with a range of (La/Sm)CI of 0.9-1.8. This variation in the LREE is essentially impossible to accomplish by processes involving vapor-liquid or vapor-solid exchange of REE, and appears to have been inherited from a differentiated target. The most distinctive evidence for inherited chemical differentiation is observed in highly refractory element (Sc, Zr, Nb, Hf, Ta, Th) systematics. The Gujba clasts exhibit fractionations in Nb/Ta that correlate positively with Zr/Hf and span the range known from lunar and Martian basalts, and exceed the range in Zr/Hf variation known from eucrites. Variations of highly incompatible refractory elements (e.g., Th) against less incompatible elements (e.g., Zr, Sr, Sc) are not chondritic, but exhibit distinctly higher Th abundances requiring a differentiated crust to be admixed with depleted mantle in ratios that are biased to higher crust/mantle ratios than in a chondritic body. The possibility that these variations are due to admixture of refractory inclusion-debris into normal chondritic matter is raised but cannot be definitively tested because existing ;bulk; analyses of CAIs carry artifacts of unrepresentative sampling. The inferences drawn from the compositions of Gujba silicate clasts, here, complement what has been inferred from the compositions of metallic clasts, but provide surprisingly detailed insight into the structure of the target. Evidence that metal and silicate in CB chondrites both formed from impact-generated vapor plumes, taken together with recent work on metallic nodules in E chondrites, and on ordinary chondrites, indicates that chondrule formation occurs by this mechanism quite widely. However, the nature of the impact on the CB body is quite different than the popular conceptions of impact of partially or wholly molten chondritic bodies and the younger (5 Ma) age of CB chondrules is consistent with origin in a disk with more evolved targets and impactors gravitationally perturbed by nascent planets.

Evaluating Changes In the Elemental Composition of Micrometeorites During Entry into the Earth’s Atmosphere

NASA Astrophysics Data System (ADS)

Rudraswami, N. G.; Shyam Prasad, M.; Dey, S.; Plane, J. M. C.; Feng, W.; Taylor, S.

2015-11-01

We evaluate the heating of extraterrestrial particles entering the atmosphere using the comprehensive chemical ablation model (CABMOD). This model predicts the ablation rates of individual elements in a particle with a defined size, composition, entry velocity, and entry angle with respect to the zenith (ZA). In the present study, bulk chemical analyses of 1133 Antarctica micrometeorites (collected from the south pole water well) are interpreted using CABMOD. The marked spread in Fe/Si values in unmelted, partially melted, and melted micrometeorites is explained by the loss of relatively volatile Fe during atmospheric entry. The combined theoretical modeling and elemental composition of the micrometeorites (Mg/Si ratios) suggest that ˜85% of particles have a provenance of carbonaceous chondrites, the remaining ˜15% are either ordinary or enstatite chondrites. About 65% of the micrometeorites have undergone <20% ablation, while a further 20% have lost between 20% and 60% of their original mass. This has implications for understanding the micrometeorite flux that reaches the Earth's surface, as well as estimating the pre-atmospheric size of the particles. Our work shows that the unmelted particles that contribute ˜50% to the total micrometeorite collection on Earth's surface have a small entry zone: ZA = 60°-90° if the entry velocity is ˜11 km s-1, and ZA = 80°-90° for >11-21 km s-1.

Chromium on Eros: Further Evidence of Ordinary Chondrite Composition

NASA Technical Reports Server (NTRS)

Foley, C. N.; Nittler, L. R.; Brown, M. R. M.; McCoy, T. J.; Lim, L. F.

2005-01-01

The surface major element composition of the near-earth asteroid 433-Eros has been determined by x-ray fluorescence spectroscopy (XRS) on the NEAR-Shoemaker spacecraft [1]. The abundances of Mg, Al, Si, Ca and Fe match those of ordinary chondrites [1]. However, the observation that Eros appears to have a sulfur abundance at least a factor of two lower than ordinary chondrites, suggests either sulfur loss from the surface of Eros by impact and/or radiation processes (space weathering) or that its surface is comprised of a somewhat more differentiated type of material than an ordinary chondrite [1]. A definitive match for an ordinary chondrite parent body has very rarely been made, despite the conundrum that ordinary chondrites are the most prevalent type of meteorite found on Earth. Furthermore, Eros is classified as an S(IV) type asteroid [2] and being an S, it is the second most prevalent type of asteroid in the asteroid belt [3].

Oxygen isotopic composition of chondritic interplanetary dust particles: A genetic link between carbonaceous chondrites and comets

NASA Astrophysics Data System (ADS)

Aléon, J.; Engrand, C.; Leshin, L. A.; McKeegan, K. D.

2009-08-01

Oxygen isotopes were measured in four chondritic hydrated interplanetary dust particles (IDPs) and five chondritic anhydrous IDPs including two GEMS-rich particles (Glass embedded with metal and sulfides) by a combination of high precision and high lateral resolution ion microprobe techniques. All IDPs have isotopic compositions tightly clustered around that of solar system planetary materials. Hydrated IDPs have mass-fractionated oxygen isotopic compositions similar to those of CI and CM carbonaceous chondrites, consistent with hydration of initially anhydrous protosolar dust. Anhydrous IDPs have small 16O excesses and depletions similar to those of carbonaceous chondrites, the largest 16O variations being hosted by the two GEMS-rich IDPs. Coarse-grained forsteritic olivine and enstatite in anhydrous IDPs are isotopically similar to their counterparts in comet Wild 2 and in chondrules suggesting a high temperature inner solar system origin. The small variations in the 16O content of GEMS-rich IDPs suggest that most GEMS either do not preserve a record of interstellar processes or the initial interstellar dust is not 16O-rich as expected by self-shielding models, although a larger dataset is required to verify these conclusions. Together with other chemical and mineralogical indicators, O isotopes show that the parent-bodies of carbonaceous chondrites, of chondritic IDPs, of most Antarctic micrometeorites, and comet Wild 2 belong to a single family of objects of carbonaceous chondrite chemical affinity as distinct from ordinary, enstatite, K- and R-chondrites. Comparison with astronomical observations thus suggests a chemical continuum of objects including main belt and outer solar system asteroids such as C-type, P-type and D-type asteroids, Trojans and Centaurs as well as short-period comets and other Kuiper Belt Objects.

Clouds in Super-Earth Atmospheres: Chemical Equilibrium Calculations

NASA Astrophysics Data System (ADS)

Mbarek, Rostom; Kempton, Eliza M.-R.

2016-08-01

Recent studies have unequivocally proven the existence of clouds in super-Earth atmospheres. Here we provide a theoretical context for the formation of super-Earth clouds by determining which condensates are likely to form under the assumption of chemical equilibrium. We study super-Earth atmospheres of diverse bulk composition, which are assumed to form by outgassing from a solid core of chondritic material, following Schaefer & Fegley. The super-Earth atmospheres that we study arise from planetary cores made up of individual types of chondritic meteorites. They range from highly reducing to oxidizing and have carbon to oxygen (C:O) ratios that are both sub-solar and super-solar, thereby spanning a range of atmospheric composition that is appropriate for low-mass exoplanets. Given the atomic makeup of these atmospheres, we minimize the global Gibbs free energy of formation for over 550 gases and condensates to obtain the molecular composition of the atmospheres over a temperature range of 350-3000 K. Clouds should form along the temperature-pressure boundaries where the condensed species appear in our calculation. We find that the composition of condensate clouds depends strongly on both the H:O and C:O ratios. For the super-Earth archetype GJ 1214b, KCl and ZnS are the primary cloud-forming condensates at solar composition, in agreement with previous work. However, for oxidizing atmospheres, K2SO4 and ZnO condensates are favored instead, and for carbon-rich atmospheres with super-solar C:O ratios, graphite clouds appear. For even hotter planets, clouds form from a wide variety of rock-forming and metallic species.

Petrology and In Situ Trace Element Chemistry of a Suite of R Chondrites

NASA Astrophysics Data System (ADS)

Mittlefehldt, D. W.; Peng, Z. X.; Torrano, Z. A.

2015-07-01

Your eyes are not deceiving you: Duck has submitted an abstract to a chondrite session. We will present the results of our petrological and compositional studies of R chondrites of diverse petrological type.

Ultrafine-grained mineralogy and matrix chemistry of olivine-rich chondritic interplanetary dust particles

NASA Technical Reports Server (NTRS)

Rietmeijer, F. J. M.

1989-01-01

Olivine-rich chondritic interplanetary dust particles (IDPs) are an important subset of fluffy chondritic IDPs collected in the earth's stratosphere. Particles in this subset are characterized by a matrix of nonporous, ultrafine-grained granular units. Euhedral single crystals, crystals fragments, and platey single crystals occur dispersed in the matrix. Analytical electron microscopy of granular units reveals predominant magnesium-rich olivines and FeNi-sulfides embedded in amorphous carbonaceous matrix material. The variable ratio of ultrafine-grained minerals vs. carbonaceous matrix material in granular units support variable C/Si ratios, and some fraction of sulfur is associated with carbonaceous matrix material. The high Mg/(Mg+Fe) ratios in granular units is similar to this distribution in P/Comet Halley dust. The chondritic composition of fine-grained, polycrystalline IDPs gradually breaks down into nonchondritic, and ultimately, single mineral compositions as a function of decreased particle mass. The relationship between particle mass and composition in the matrix of olivine-rich chondritic IDPs is comparable with the relationship inferred for P/Comet Halley dust.

Parent Body Influences on Amino Acids in the Tagish Lake Meteorite

NASA Technical Reports Server (NTRS)

Glavin, D. P.; Callahan, M. P.; Dworkin, J. P.; Elsila, J. E.; Herd, C. D. K.

2010-01-01

The Tagish Lake meteorite is a primitive C2 carbonaceous chondrite with a mineralogy, oxygen isotope, and bulk chemical. However, in contrast to many CI and CM carbonaceous chondrites, the Tagish Lake meteorite was reported to have only trace levels of indigenous amino acids, with evidence for terrestrial L-amino acid contamination from the Tagish Lake meltwater. The lack of indigenous amino acids in Tagish Lake suggested that they were either destroyed during parent body alteration processes and/or the Tagish Lake meteorite originated on a chemically distinct parent body from CI and CM meteorites where formation of amino acids was less favorable. We recently measured the amino acid composition of three different lithologies (11h, 5b, and 11i) of pristine Tagish Lake meteorite fragments that represent a range of progressive aqueous alteration in order 11h < 5b < 11i as inferred from the mineralogy, petrology, bulk isotopes, and insoluble organic matter structure. The distribution and enantiomeric abundances of the one- to six-carbon aliphatic amino acids found in hot-water extracts of the Tagish Lake fragments were determined by ultra performance liquid chromatography fluorescence detection and time of flight mass spectrometry coupled with OPA/NAC derivatization. Stable carbon isotope analyses of the most abundant amino acids in 11h were measured with gas chromatography coupled with quadrupole mass spectrometry and isotope ratio mass spectrometry.

Ordinary chondrites - Multivariate statistical analysis of trace element contents

NASA Technical Reports Server (NTRS)

Lipschutz, Michael E.; Samuels, Stephen M.

1991-01-01

The contents of mobile trace elements (Co, Au, Sb, Ga, Se, Rb, Cs, Te, Bi, Ag, In, Tl, Zn, and Cd) in Antarctic and non-Antarctic populations of H4-6 and L4-6 chondrites, were compared using standard multivariate discriminant functions borrowed from linear discriminant analysis and logistic regression. A nonstandard randomization-simulation method was developed, making it possible to carry out probability assignments on a distribution-free basis. Compositional differences were found both between the Antarctic and non-Antarctic H4-6 chondrite populations and between two L4-6 chondrite populations. It is shown that, for various types of meteorites (in particular, for the H4-6 chondrites), the Antarctic/non-Antarctic compositional difference is due to preterrestrial differences in the genesis of their parent materials.

Comparative 187Re-187Os systematics of chondrites: Implications regarding early solar system processes

USGS Publications Warehouse

Walker, R.J.; Horan, M.F.; Morgan, J.W.; Becker, H.; Grossman, J.N.; Rubin, A.E.

2002-01-01

A suite of 47 carbonaceous, enstatite, and ordinary chondrites are examined for Re-Os isotopic systematics. There are significant differences in the 187Re/188Os and 187Os/188Os ratios of carbonaceous chondrites compared with ordinary and enstatite chondrites. The average 187Re/188Os for carbonaceous chondrites is 0.392 ?? 0.015 (excluding the CK chondrite, Karoonda), compared with 0.422 ?? 0.025 and 0.421 ?? 0.013 for ordinary and enstatite chondrites (1?? standard deviations). These ratios, recast into elemental Re/Os ratios, are as follows: 0.0814 ?? 0.0031, 0.0876 ?? 0.0052 and 0.0874 ?? 0.0027 respectively. Correspondingly, the 187Os/188Os ratios of carbonaceous chondrites average 0.1262 ?? 0.0006 (excluding Karoonda), and ordinary and enstatite chondrites average 0.1283 ?? 0.0017 and 0.1281 ?? 0.0004, respectively (1?? standard deviations). The new results indicate that the Re/Os ratios of meteorites within each group are, in general, quite uniform. The minimal overlap between the isotopic compositions of ordinary and enstatite chondrites vs. carbonaceous chondrites indicates long-term differences in Re/Os for these materials, most likely reflecting chemical fractionation early in solar system history. A majority of the chondrites do not plot within analytical uncertainties of a 4.56-Ga reference isochron. Most of the deviations from the isochron are consistent with minor, relatively recent redistribution of Re and/or Os on a scale of millimeters to centimeters. Some instances of the redistribution may be attributed to terrestrial weathering; others are most likely the result of aqueous alteration or shock events on the parent body within the past 2 Ga. The 187Os/188Os ratio of Earth's primitive upper mantle has been estimated to be 0.1296 ?? 8. If this composition was set via addition of a late veneer of planetesimals after core formation, the composition suggests the veneer was dominated by materials that had Re/Os ratios most similar to ordinary and enstatite chondrites. ?? 2002 Elsevier Science Ltd.

The chemistry and origin of the ordinary chondrites Implications from refractory-lithophile and siderophile elements

NASA Technical Reports Server (NTRS)

Fulton, C. R.; Rhodes, J. M.

1984-01-01

Thirty-eight ordinary chondrites (17 H, 20 L, and 1 LL) have been analyzed for major and selected trace elements. These data indicate that the lithophile elements Mg, Ca, Al, Cr, and V normalized to Si are in higher abundance in the H than in the L chondrites. The siderophile elements Ni, Co, and Fe show very good correlation within, as well as between, the two major ordinary chondrite groups. Twenty-four of the analyses are of Antarctic finds, while ten are samples of falls. Comparing the Antarctic data with the fall data reveals no evidence that any of the elements studied here have been mobilized by terrestrial weathering processes. Within the H and L chondrite groups there is little chemical variation, indicating that the source of these samples is remarkably homogeneous. Equilibrium condensate fractionation from a nebula of CI composition can result in the observed ordinary chondrite compositions. The fractionation of metal at about 1440 K (and 0.001 atm) into high and low iron groups, followed by a gas-solid fractionation at about 1380 K with the H group losing more solids than the L, will produce the observed H and L compositions and intragroup trends.

Titanium and Oxygen Isotope Compositions of Individual Chondrules from Ordinary Chondrites

NASA Astrophysics Data System (ADS)

Bauer, K. K.; Schönbächler, M.; Fehr, M. A.; Vennemann, T.; Chaumard, N.; Zanda, B.

2016-08-01

We measured Ti and triple-O isotope compositions of individual chondrules (characterized by CT scanning) from ordinary chondrites. We will discuss correlations between Ti and ∆17O and their implication for the origin of nucleosynthetic anomalies.

The ungrouped chondrite El Médano 301 and its comparison with other reduced ordinary chondrites

NASA Astrophysics Data System (ADS)

Pourkhorsandi, Hamed; Gattacceca, Jérôme; Devouard, Bertrand; D'Orazio, Massimo; Rochette, Pierre; Beck, Pierre; Sonzogni, Corinne; Valenzuela, Millarca

2017-12-01

El Médano 301 (EM 301) is an ungrouped chondrite with overall texture and trace-element distribution similar to those of ordinary chondrites (OCs), but with silicate (olivine and low-Ca pyroxene) compositions that are more reduced than those in OCs, with average olivine and low-Ca pyroxene of Fa3.9±0.3 and Fs12.8±4.9, respectively. These values are far lower than the values for OCs and even for chondrites designed as ;reduced; chondrites. Low-Ca pyroxene is the dominant mineral phase and shows zoning with higher MgO contents along the crystal rims and cracks (reverse zoning). The Co content of kamacite is also much lower than the concentrations observed in OCs (below detection limit of 0.18 wt% versus 0.44-37 wt%). Oxygen isotopic composition is Δ17O = +0.79,+0.78‰ and slightly different from that of OCs. The lower modal olivine/pyroxene ratio, different Infrared (IR) spectra, lower Co content of kamacite, lower mean FeO contents of olivine and pyroxene, different kamacite texture, and different oxygen-isotopic composition show that EM 301 does not belong to a known OC group. EM 301 shows similarities with chondritic clasts in Cumberland Falls aubrite, and with Northwest Africa 7135 (NWA 7135) and Acfer 370 ungrouped chondrites. However, dissimilar to NWA 7135 and the clasts, it does not contain highly reduced mineral phases like daubréelite. Our observations suggest the formation of EM 301 in a nebular region compositionally similar to OCs but with a different redox state, with oxygen fugacity (ƒO2) in this region lower than that of OCs and higher than that of enstatite chondrites condensation region. A second, possibly nebular, phase of reduction by the production of reducing gas phases (e.g., C-rich) could be responsible for the subsequent reduction of the primary material and the occurrence of reverse zoning in the low-Ca pyroxene and lower average Fa/Fs ratio. Based on the IR spectra of EM 301 we suggest the possibility that the parent body of this chondrite was a V-type asteroid.

What's Hot and What's Not: Multivariate Statistical Analysis of Ten Labile Trace Elements in H-Chondrite Population Pairs

NASA Astrophysics Data System (ADS)

Wolf, S. F.; Lipschutz, M. E.

1993-07-01

Dodd et al. [1] found that, from their circumstances of fall, 17 H chondrites ("H Cluster 1") which fell in May, from 1855 to 1895, are distinguishable from other H chondrite falls and apparently derive from a co-orbital stream of meteoroids. From data for 10 moderately to highly labile trace elements (Rb, Ag, Se, Cs, Te, Zn, Cd, Bi, Tl, In), they used two multivariate statistical techniques--linear discriminant analysis and logistic regression--to demonstrate that 1. 13 H Cluster 1 chondrites are compositionally distinguishable from 45 other H chondrite falls, probably because of differences in thermal histories of the meteorites' parent materials; 2. The reality of the compositional differences between the populations of falls are beyond any reasonable statistical doubt. 3. The compositional differences are inconsistent with the notion that the results reflect analytical bias. We have used these techniques to assess analogous data for various H chondrite populations [2-4] with results that are listed in Table 1. These data indicate that 1. There is no statistical reason to believe that random populations from Victoria Land, Antarctica, differ compositionally from each other. 2. There is significant statistical reason to believe that the H chondrite population recovered from Victoria Land, Antarctica, differs compositionally from that from Queen Maud Land, Antarctica, and from falls. 3. There is no reason to believe that the H chondrite population recovered from Queen Maud Land, Antarctica, differs compositionally from falls. 4. These observations can be made either by data obtained by one analyst or several. These results, coupled with earlier ones [5], demonstrate that trivial explanations cannot explain compositional differences involving labile trace elements in pairs of H chondrite populations. These differences must then reflect differences of preterrestrial thermal histories of the meteorites' parent materials. Acceptance of these differences as preterrestrial has led to predictions subsequently verified by others (meteoroid and asteroid stream discoveries, differencesin thermoluminescence or TL). We predict that a TL difference will be seen between the populations of falls defined by Dodd et al. [1]. References: [1] Dodd R. T. et al. (1993) JGR, submitted. [2] Lingner D. W. et al. (1987) GCA, 51, 727-739. [3] Dennison J. E. and Lipschutz M. E. (1987) GCA, 51, 741-754. [4] Wolf S. F. and Lipschutz M. E. (1993) in Advances in Analytical Geochemistry (M. Hyman and M. Rowe, eds.), in press. [5] Wang M.-S. et al. (1992) Meteoritics, 27, 303. [6] Lipschutz M. E. and Samuels S. M. (1991) GCA, 55, 19-47. Table 1, which appears in the hard copy, shows a multivariate statistical analysis of H chondrite population pairs using 10 labile trace elements (number of meteorites in population in parentheses).

A Weathering Index for CK and R Chondrites

NASA Technical Reports Server (NTRS)

Rubin, Alan E.; Huber, Heinz

2006-01-01

We present a new weathering index (wi) for the metallic-Fe-Ni-poor chondrite groups (CK and R) based mainly on transmitted light observations of the modal abundance of crystalline material that is stained brown in thin sections: wi-0, <5 vol%; wi-1, 5-25 vol%; wi-2,25-50 vol%; wi-3,50- 75 vol%; wi-4, 75-95 vol%; wi-5, >95 vol%, wi-6, significant replacement of mafic silicates by phyllosilicates. Brown staining reflects mobilization of oxidized iron derived mainly from terrestrial weathering of Ni-bearing sulfide. With increasing degrees of terrestrial weathering of CK and R chondrites, the sulfide modal abundance decreases, and S, Se, and Ni become increasingly depleted. In addition, bulk Cl increases in Antarctic CK chondrites, probably due to contamination from airborne sea mist.

Temperature and Oxygen Fugacity Constraints on CK and R Chondrites and Implications for Water and Oxidation in the Early Solar System

NASA Technical Reports Server (NTRS)

Righter, K.; Neff, K. E.

2007-01-01

Recent chondritic meteorite finds in Antarctica have included CB, CH, CK and R chondrites, the latter two of which are among the most oxidized materials found in meteorite collections. In this study we present petrographic and mineralogic data for a suite of CK and R chondrites, and compare to previous studies of CK and R, as well as some CV chondrites. In particular we focus on the opaque minerals magnetite, chromite, sulfides, and metal as well as unusual silicates hornblende, biotite, and plagioclase. Several mineral thermometers and oxy-barometers are utilized to calculate temperatures and oxygen fugacities for these unusual meteorites compared to other more common chondrite groups. R and CK chondrites show lower equilibrium temperatures than ordinary chondrites, even though they are at similar petrologic grades (e.g., thermal type 6). Oxygen fugacity calculated for CV and R chondrites ranges from values near the iron-wustite (IW) oxygen buffer to near the fayalite-magnetite-quartz (FMQ) buffer. In comparison, the fO2 recorded by ilmenite-magnetite pairs from CK chondrites are much higher, from FMQ+3.1 to FMQ+5.2. The latter values are the highest recorded for materials in meteorites, and place some constraints on the formation conditions of these magnetite-bearing chondrites. Differences between mineralogic and O isotopic compositions of CK and R chondrites suggest two different oxidation mechanisms, which may be due to high and low water: rock ratios during metamorphism, or to different fluid compositions, or both.

Rhenium-osmium isotope systematics of carbonaceous chondrites

USGS Publications Warehouse

Walker, R.J.; Morgan, J.W.

1989-01-01

Rhenium and osmium concentrations and Os isotopic compositions of eight carbonaceous chondrites, one LL3 ordinary chondrite, and two iron meteorites were determined by resonance ionization mass spectrometry. Iron meteorite 187Re/186Os and 187OS/186Os ratios plot on the previously determined iron meteorite isochron, but most chondrite data plot 1 to 2 percent above this meteorite isochron. This suggests either that irons have significantly younger Re-Os closure ages than chondrites or that chondrites were formed from precursor materials with different chemical histories from the precursors of irons. Some samples of Semarkona (LL3) and Murray (C2M) meteorites plot 4 to 6 percent above the iron meteorite isochron, well above the field delineated by other chondrites. Murray may have lost Re by aqueous leaching during its preterrestrial history. Semarkona could have experienced a similar loss of Re, but only slight aqueous alteration is evident in the meteorite. Therefore, the isotopic composition of Semarkona could reflect assembly of isotopically heterogeneous components subsequent to 4.55 billion years ago or Os isotopic heterogeneities in the primordial solar nebula.

Chondritic Mn/Na ratio and limited post-nebular volatile loss of the Earth

NASA Astrophysics Data System (ADS)

Siebert, Julien; Sossi, Paolo A.; Blanchard, Ingrid; Mahan, Brandon; Badro, James; Moynier, Frédéric

2018-03-01

The depletion pattern of volatile elements on Earth and other differentiated terrestrial bodies provides a unique insight as to the nature and origin of planetary building blocks. The processes responsible for the depletion of volatile elements range from the early incomplete condensation in the solar nebula to the late de-volatilization induced by heating and impacting during planetary accretion after the dispersion of the H2-rich nebular gas. Furthermore, as many volatile elements are also siderophile (metal-loving), it is often difficult to deconvolve the effect of volatility from core formation. With the notable exception of the Earth, all the differentiated terrestrial bodies for which we have samples have non-chondritic Mn/Na ratios, taken as a signature of post-nebular volatilization. The bulk silicate Earth (BSE) is unique in that its Mn/Na ratio is chondritic, which points to a nebular origin for the depletion; unless the Mn/Na in the BSE is not that of the bulk Earth (BE), and has been affected by core formation through the partitioning of Mn in Earth's core. Here we quantify the metal-silicate partitioning behavior of Mn at deep magma ocean pressure and temperature conditions directly applicable to core formation. The experiments show that Mn becomes more siderophile with increasing pressure and temperature. Modeling the partitioning of Mn during core formation by combining our results with previous data at lower P-T conditions, we show that the core likely contains a significant fraction (20 to 35%) of Earth's Mn budget. However, we show that the derived Mn/Na value of the bulk Earth still lies on the volatile-depleted end of a trend defined by chondritic meteorites in a Mn/Na vs Mn/Mg plot, which tend to higher Mn/Na with increasing volatile depletion. This suggests that the material that formed the Earth recorded similar chemical fractionation processes for moderately volatile elements as chondrites in the solar nebula, and experienced limited post nebular volatilization.

The Chelyabinsk Fall Highly Siderophile Element Abundance and 187Os/188Os Composition and Comparison with Ordinary and Carbonaceous Chondrites

NASA Astrophysics Data System (ADS)

Day, J. M. D.; Corder, C. A.; Dhaliwal, J. K.; Liu, Y.; Taylor, L. A.

2014-09-01

New osmium isotope and highly siderophile element abundance data are presented for the Chelyabinsk ordinary chondrite fall (February 2013) and placed into context with new data for ordinary and carbonaceous chondrites.

Effects of mother lode-type gold mineralization on 187Os/188Os and platinum group element concentrations in peridotite: Alleghany District, California

USGS Publications Warehouse

Walker, R.J.; Böhlke, J.K.; McDonough, W.F.; Li, Ji

2007-01-01

Osmium isotope compositions and concentrations of Re, platinum group elements (PGE), and Au were determined for host peridotites (serpentinites and barzburgites) and hydrothermally altered ultramafic wall rocks associated with Mother Lode-type hydrothermal gold-quartz vein mineralization in the Alleghany district, California. The host peridotites have Os isotope compositions and Re, PGE, and Au abundances typical of the upper mantle at their presumed formation age during the late Proterozoic or early Paleozoic. The hydrothermally altered rocks have highly variable initial Os isotope compositions with ??os, values (% deviation of 187OS/188OS from the chondritic average calculated for the approx. 120 Ma time of mineralization) ranging from -1.4 to -8.3. The lowest Os isotope compositions are consistent with Re depletion of a chondritic source (e.g., the upper mantle) at ca. 1.6 Ga. Most of the altered samples are enriched in Au and have depleted and fractionated abundances of Re and PGE relative to their precursor peridotites. Geoehemical characteristics of the altered samples suggest that Re and some PGE were variably removed from the ultramafic rocks during the mineralization event. In addition to Re, the Pt and Pd abundances of the most intensely altered rocks appear to have been most affected by mineralization. The 187Os-depleted isotopic compositions of some altered rocks are interpreted to be a result of preferential 187Os loss via destruction of Re-rich phases during the event. For these rocks, Os evidently is not a useful tracer of the mineralizing fluids. The results do, however, provide evidence for differential mobility of these elements, and mobility of 187Os relative to the initial bulk Os isotope composition during hydrothermal metasomatic alteration of ultramafic rocks. ?? 2007 Society of Economic Geologists, Inc.

Trace element composition of Luna 24 Crisium VLT basalt

NASA Technical Reports Server (NTRS)

Haskin, L. A.

1978-01-01

The origins of the individual particles analyzed from the Luna 24 core and the information they provide on the trace-element composition of Mare Crisium basalt are considered. Previous analyses of several Luna 24 soil fragments are reviewed. It is concluded that: (1) the average trace-element concentrations for 12 VLT basalt fragments are the best available estimates for bulk samples of Crisium VLT basalt; (2) there is weak evidence that the average Crisium basalt might have a small positive Eu anomaly relative to chondritic matter; (3) the soils contain components from sources other than the Crisium VLT basalt; and (4) there is no convincing information in concentrations of rare-earth elements, Co, Sc, FeO, or Na2O among the analyzed fragments to indicate more than one parent basalt.

Could G Asteroids be the Parent Bodies of the CM Chondrites?

NASA Astrophysics Data System (ADS)

Burbine, T. H.; Binzel, R. P.

1995-09-01

Since almost all meteorites are believed to be derived from asteroidal source bodies, the comparison of asteroid and meteorite spectra should allow for possible meteorite parent bodies to be identified. However only two asteroids with unique spectral characteristics, 4 Vesta with the basaltic achondrites [1] and near-Earth asteroid 3103 Eger with the aubrites [2], have been convincingly linked with any meteorite type. Farinella et al. [3] has done a study of 2355 numbered main-belt asteroids to determine which asteroids have the highest probability of having their fragments injected into the 3:1 mean motion and the nu6 secular resonance regions. Interestingly, asteroids with the third (19 Fortuna), tenth (1 Ceres) and eleventh (13 Egeria) highest theoretical total fragment delivery efficiencies are G-asteroids, a moderately rare type of asteroid with approximately ten known members. (Vesta has the fifth highest theoretical total fragment delivery efficiency.) G-asteroids tend to have the strongest ultraviolet, 0.7 micrometers and 3 micrometers absorption features of all C-type (B, C, F and G) asteroids, appearing to indicate that G-asteroids are at the upper range of the aqueous alteration sequence in the asteroid population. (The 0.7 micrometers feature is apparently due to iron oxides in hydrated silicates and the 3 micrometers feature is apparently due to hydrated minerals.) Meteorites that have reflectance spectra with a 3 micrometers feature of comparable intensity to those of the G-asteroids are the CI, CM and CR chondrites. However, G-asteroids (like all C-types) have ultraviolet absorption features that are weaker than previously measured meteorite spectra. Comparisons of reflectance spectra between Ceres and meteorite samples appear to indicate that Ceres is compositionally different from almost all known carbonaceous chondrites. Both Fortuna and Egeria have an absorption feature centered around 0.7 micrometers [4] that is similar in structure and strength to those found in many CM chondrites. The visible and near-infrared spectrum of Fortuna [5] matches very well the spectra of CM chondrites Murchison (bulk powder) [6] and LEW90500 (particle sizes less than 100 micrometers) [7]. However, the ultraviolet absorption feature is still weaker in Fortuna's spectrum. A spectrum of a bulk powder of LEW90500 does have an ultraviolet feature that matches Fortuna's feature, but this spectrum is substantially bluer than Fortuna in the near-infrared. Egeria's ultraviolet absorption feature also matches very well the ultraviolet feature in LEW90500Us (bulk powder) spectrum, but this spectrum is slightly redder than Egeria [5] in the near-infrared. The question is how unique is any postulated linkage between the CM chondrites and the G-asteroids. The problem is that approximately two-thirds of all C-type asteroids have 3 micrometers absorption features [8] and approximately three-fourths have 0.7 micrometers absorption features [4]. However of all observed C-type asteroids, Fortuna and Egeria appear to be two of the best spectral matches for the CM chondrites. Coupled with the high probability that these two asteroids are injecting large numbers of fragments into meteorite-supplying resonances, G-asteroids Fortuna and Egeria appear to be possible CM chondrite parent bodies. Acknowledgments: This research is supported by NASA Grant Number NAGW-2049. References: [1] Binzel R. P. and Xu S. (1993) Science, 260, 186-191. [2] Gaffey M. J. et al. (1992) Icarus, 100, 95-109. [3] Farinella P. et al. (1993) Icarus, 101, 174-187. [4] Sawyer S. R. (1991) Ph.D. thesis, Univ. of Texas, Austin. [5] Bell J. F. et al. (1988) LPS XIX, 57-58. [6] Gaffey M. J. (1976) JGR, 81, 905-920. [7] Hiroi T. et al. (1993) Science, 261, 1016-1018. [8] Jones T. D. et al. (1990) Icarus, 88,172-192.

The parent body controls on cosmic spherule texture: Evidence from the oxygen isotopic compositions of large micrometeorites

NASA Astrophysics Data System (ADS)

van Ginneken, M.; Gattacceca, J.; Rochette, P.; Sonzogni, C.; Alexandre, A.; Vidal, V.; Genge, M. J.

2017-09-01

High-precision oxygen isotopic compositions of eighteen large cosmic spherules (>500 μm diameter) from the Atacama Desert, Chile, were determined using IR-laser fluorination - Isotope Ratio Mass spectrometry. The four discrete isotopic groups defined in a previous study on cosmic spherules from the Transantarctic Mountains (Suavet et al., 2010) were identified, confirming their global distribution. Approximately 50% of the studied cosmic spherules are related to carbonaceous chondrites, 38% to ordinary chondrites and 12% to unknown parent bodies. Approximately 90% of barred olivine (BO) cosmic spherules show oxygen isotopic compositions suggesting they are related to carbonaceous chondrites. Similarly, ∼90% porphyritic olivine (Po) cosmic spherules are related to ordinary chondrites and none can be unambiguously related to carbonaceous chondrites. Other textures are related to all potential parent bodies. The data suggests that the textures of cosmic spherules are mainly controlled by the nature of the precursor rather than by the atmospheric entry parameters. We propose that the Po texture may essentially be formed from a coarse-grained precursor having an ordinary chondritic mineralogy and chemistry. Coarse-grained precursors related to carbonaceous chondrites (i.e. chondrules) are likely to either survive atmospheric entry heating or form V-type cosmic spherules. Due to the limited number of submicron nucleation sites after total melting, ordinary chondrite-related coarse-grained precursors that suffer higher peak temperatures will preferentially form cryptocrystalline (Cc) textures instead of BO textures. Conversely, the BO textures would be mostly related to the fine-grained matrices of carbonaceous chondrites due to the wide range of melting temperatures of their constituent mineral phases, allowing the preservation of submicron nucleation sites. Independently of the nature of the precursors, increasing peak temperatures form glassy textures.

Formation of unequilibrated R chondrite chondrules and opaque phases

NASA Astrophysics Data System (ADS)

Miller, K. E.; Lauretta, D. S.; Connolly, H. C.; Berger, E. L.; Nagashima, K.; Domanik, K.

2017-07-01

Sulfide assemblages are commonly found in chondritic meteorites as small inclusions in the matrix or in association with chondrules. These assemblages are widely hypothesized to form through pre-accretionary corrosion of metal by H2S gas or through parent body processes. We report here on two unequilibrated R chondrite samples that contain large, chondrule-sized sulfide nodules in the matrix. Both samples are from Mount Prestrud (PRE) 95404. Chemical maps and spot and broad-beam electron microprobe analyses (EMPA) were used to assess the distribution, stoichiometry, and bulk composition of sulfide nodules and silicate chondrules in the clasts. Oxygen isotope data were collected via secondary ion mass spectrometry (SIMS) to assess the relationship of chondrules to other chondrite groups. Scanning electron microscopy (SEM), focused ion beam (FIB), and transmission electron microscopy (TEM) analyses were used to assess fine-scale features and identify crystal structures in sulfide assemblages. Thermodynamic models were used to assess the temperature, sulfur fugacity (fS2), total pressure, dust-to-gas ratio, and oxygen fugacity (fO2) conditions during sulfide nodule and chondrule formation. The unequilibrated clasts include a mixture of type I and type II chondrules, as well as non-porphyritic chondrules. Chondrule oxygen isotopes overlap with ordinary-chondrite chondrules. Sulfide nodules average 200 μm in diameter, have rounded shapes, and are primarily composed of pyrrhotite, pentlandite, and magnetite. Some are deformed around chondrules in a petrologic relationship similar in appearance to compound chondrules. Both nodules and sulfides in chondrules include phosphate inclusions and Cu-rich lamellae, which suggests a genetic relationship between sulfides in chondrules and in the matrix. Ni/Co ratios for matrix and chondrule sulfides are solar, while Fe and Ni are non-solar and inversely related. We hypothesize that sulfide nodules formed via pre-accretionary melt processes. During chondrule formation, precursors composed of a mixture of silicate and sulfide material were heated to form immiscible melt droplets, which separated and cooled to form Si-rich chondrules and S-rich nodules. Sulfide melt was stabilized by a high total pressure (∼1 atm) in a dust- or ice-enriched environment. Heating of this material contributed to a high fS2 (2 × 10-3 atm at 1138 °C), and high fO2 (IW - 1 to IW - 4), in an environment with peak temperatures between 1539 °C and 1750 °C. Oxygen isotopic compositions in this region were similar to those recorded by the LL-chondrite chondrules.

Collection of microparticles at high balloon altitudes in the stratosphere

NASA Technical Reports Server (NTRS)

Testa, John P., Jr.; Stephens, John R.; Berg, Walter W.; Cahill, Thomas A.; Onaka, Takashi

1990-01-01

Stratospheric particles were collected between 34 and 36 km, using a combination of cascade impactors and filters lofted by a large helium balloon, and the particle concentration, size distribution, and bulk elemental composition were determined using SEM and proton-induced X-ray emission (PEXE) instrument. In addition, datailed particle morphology, elemental analysis, and electron diffraction data were obtained on 23 particles using a TEM. The concentration of particles between 0.045 and 1.0 micron in radius was found to be orders of magnitude above the concentrations predicted by the model of Hunten et al. (1980), but was consistent with balloon and satellite observations. Elemental composition analysis showed the presence of Cl, S, Ti, Fe, Br, Ni, Zr, Zn, Sr, and Cu in decreasing order of concentration. The 23 particles analyzed by TEM ranged from Al-rich silicates to almost pure Fe to one containing almost exclusively Ba and S. None were definitely chondritic in composition.

Liquidus Phases of the Richardson H5 Chondrite at High Pressures and Temperatures

NASA Technical Reports Server (NTRS)

Channon, M.; Garber, J.; Danielson, L. R.; Righter, K.

2007-01-01

Part of early mantle evolution may include a magma ocean, where core formation began before the proto-Earth reached half of its present radius. Temperatures were high and bombardment and accretion were still occurring, suggesting that the proto-Earth consisted of a core and an at least partially liquid mantle, the magma ocean. As the Earth accreted, pressure near the core increased and the magma ocean decreased in volume and became shallower as it began to cool and solidify. As crystals settled, or floated, the composition of the magma ocean could change significantly and begin to crystallize different minerals from the residual liquid. Therefore, the mantle may be stratified following the P-T phase diagram for the bulk silicate Earth. To understand mantle evolution, it is necessary to know liquidus phase relations at high pressures and temperatures. In order to model the evolution of the magma ocean, high pressure and temperature experiments have been conducted to simulate the crystallization process using a range of materials that most likely resemble the bulk composition of the early Earth.

Oxygen Isotope Measurements of a Rare Murchison Type A CAI and Its Rim

NASA Technical Reports Server (NTRS)

Matzel, J. E. P.; Simon, J. I.; Hutcheon, I. D.; Jacobsen, B.; Simon, S. B.; Grossman, L.

2013-01-01

Ca-, Al-rich inclusions (CAIs) from CV chondrites commonly show oxygen isotope heterogeneity among different mineral phases within individual inclusions reflecting the complex history of CAIs in both the solar nebula and/or parent bodies. The degree of isotopic exchange is typically mineral-specific, yielding O-16-rich spinel, hibonite and pyroxene and O-16-depleted melilite and anorthite. Recent work demonstrated large and systematic variations in oxygen isotope composition within the margin and Wark-Lovering rim of an Allende Type A CAI. These variations suggest that some CV CAIs formed from several oxygen reservoirs and may reflect transport between distinct regions of the solar nebula or varying gas composition near the proto-Sun. Oxygen isotope compositions of CAIs from other, less-altered chondrites show less intra-CAI variability and 16O-rich compositions. The record of intra-CAI oxygen isotope variability in CM chondrites, which commonly show evidence for low-temperature aqueous alteration, is less clear, in part because the most common CAIs found in CM chondrites are mineralogically simple (hibonite +/- spinel or spinel +/- pyroxene) and are composed of minerals less susceptible to O-isotopic exchange. No measurements of the oxygen isotope compositions of rims on CAIs in CM chondrites have been reported. Here, we present oxygen isotope data from a rare, Type A CAI from the Murchison meteorite, MUM-1. The data were collected from melilite, hibonite, perovskite and spinel in a traverse into the interior of the CAI and from pyroxene, melilite, anorthite, and spinel in the Wark-Lovering rim. Our objectives were to (1) document any evidence for intra-CAI oxygen isotope variability; (2) determine the isotopic composition of the rim minerals and compare their composition(s) to the CAI interior; and (3) compare the MUM-1 data to oxygen isotope zoning profiles measured from CAIs in other chondrites.

The Nature and Origin of Aromatic Organic Matter in the Tagish Lake Meteorite

NASA Technical Reports Server (NTRS)

Clemett, S. J.; Keller, L. P.; Nakamura, K.; McKay, D. S.

2004-01-01

The Tagish Lake meteorite is an unusual carbonaceous chondrite that does not fit well within existing chondrite taxonomy. Bulk analyses suggest approx. 5 wt.% C of which approx. 1 wt.% is in the form of organic matter and the remainder is present as inorganic carbonate. The exact nature and form of this organic component is, as is the case with the other ordinary and carbonaceous chondrites, still poorly understood. Yet its significance has far reaching implications, from contributing to the abiotic evolution of the early Earth and Mars, to providing geothermal constraints in the evolution of the Solar nebula.

Assemblage of Presolar Materials and Early Solar System Condensates in Chondritic Porous Interplanetary Dust Particles

NASA Technical Reports Server (NTRS)

Nguyen, A. N.; Nakamura-Messenger, K.; Messenger, S.; Keller, L. P.; Kloeck, W.

2015-01-01

Anhydrous chondritic porous inter-planetary dust particles (CP IDPs) contain an assortment of highly primitive solar system components, molecular cloud matter, and presolar grains. These IDPs have largely escaped parent body processing that has affected meteorites, advocating cometary origins. Though the stardust abundance in CP IDPs is generally greater than in primitive meteorites, it can vary widely among individual CP IDPs. The average abundance of silicate stardust among isotopically primitive IDPs is approx. 375 ppm while some have extreme abundances up to approx. 1.5%. H and N isotopic anomalies are common in CP IDPs and the carrier of these anomalies has been traced to organic matter that has experienced chemical reactions in cold molecular clouds or the outer protosolar disk. Significant variations in these anomalies may reflect different degrees of nebular processing. Refractory inclusions are commonly observed in carbonaceous chondrites. These inclusions are among the first solar system condensates and display 16O-rich isotopic compositions. Refractory grains have also been observed in the comet 81P/Wild-2 samples re-turned from the Stardust Mission and in CP IDPs, but they occur with much less frequency. Here we conduct coordinated mineralogical and isotopic analyses of CP IDPs that were characterized for their bulk chemistry by to study the distribution of primitive components and the degree of nebular alteration incurred.

Analysis of Direct Samples of Extraterrestrial, Organic-Bearing, Aqueous Fluids

NASA Technical Reports Server (NTRS)

Zolensky, Michael

2016-01-01

I will describe water we have found in 4.5 billion year old extraterrestrial salt, and the organics that are also present. We hypothesize that organics being carried through the parent body of the halite have been deposited adjacent to the fluid inclusions, where they have been preserved against any thermal metamorphism. We are making bulk compositional, carbon and hydrogen isotopic measurements of solid organic phases associated with the aqueous fluid inclusions in the meteorites. We will compare these organics with those found in chondrites and Wild-2 comet coma particles to determine whether these classes of organics had an origin within aqueous solutions.

Chromite and olivine in type II chondrules in carbonaceous and ordinary chondrites - Implications for thermal histories and group differences

NASA Technical Reports Server (NTRS)

Johnson, Craig A.; Prinz, Martin

1991-01-01

Unequilibrated chromite and olivine margin compositions in type II chondrules are noted to differ systematically among three of the chondrite groups, suggesting that type II liquids differed in composition among the groups. These differences may be interpreted as indicators of different chemical compositions of the precursor solids which underwent melting, or, perhaps, as differences in the extent to which immiscible metal sulfide droplets were lost during chondrule formation. Because zinc is detectable only in type II chromites which have undergone reequilibration, the high zinc contents reported for chondritic chromites in other studies probably reflect redistribution during thermal metamorphism.

Terrestrial bitumen analogue of orgueil organic material demonstrates high sensitivity to usual HF-HCl treatment

NASA Technical Reports Server (NTRS)

Korochantsev, A. V.; Nikolaeva, O. V.

1993-01-01

The relationship between the chemical composition and the interlayer spacing (d002) of organic materials (OM's) is known for various terrestrial OM's. We improved this general trend by correlation with corresponding trend of natural solid bitumens (asphaltite-kerite-anthraxolite) up to graphite. Using the improved trend we identified bitumen analogs of carbonaceous chondrite OM's residued after HF-HCl treatment. Our laboratory experiment revealed that these analogs and, hence, structure and chemical composition of carbonaceous chondrite OM's are very sensitive to the HF-HCl treatment. So, usual extraction of OM from carbonaceous chondrites may change significantly structural and chemical composition of extracted OM.

Lunar and Planetary Science XXXV: Concerning Chondrites

NASA Technical Reports Server (NTRS)

2004-01-01

The Lunar and Planetary Science XXXV session entitled "Concerning Chondrites" includes the following topics: 1) Petrology and Raman Spectroscopy of Shocked Phases in the Gujba CB Chondrite and the Shock History of the CB Parent Body; 2) The Relationship Between CK and CV Chondrites: A Single Parent Body Source? 3) Samples of Asteroid Surface Ponded Deposits in Chondritic Meteorites; 4) Composition and Origin of SiO2-rich Objects in Carbonaceous and Ordinary Chondrites; 5) Re-Os Systematics and HSE distribution in Tieschitz (H3.6); Two Isochrons for One Meteorite; 6) Loss of Chromium from Olivine During the Metamorphism of Chondrites; 7) Very Short Delivery Times of Meteorites After the L-Chondrite Parent Body Break-Up 480 Myr Ago; and 8) The Complex Exposure History of a Very Large L/LL5 Chondrite Shower: Queen Alexandra Range 90201.

Chemical studies of H chondrites. 6: Antarctic/non-Antarctic compositional differences revisited

NASA Astrophysics Data System (ADS)

Wolf, Stephen F.; Lipschutz, Michael E.

1995-02-01

We report data for the trace elements Au, Co, Sb, Ga, Rb, Ag, Se, Cs, Te, Zn, Cd, Bi, T1, and In (ordered by putative volatility during nebular condensation and accretion) determined by radiochemical neutron activation analysis of 14 additional H5 and H6 chondrite falls. Data for the 10 most volatile elements (Rb to In) treated by the multivariate techniques of linear discriminant analysis and logistic regression in these and 44 other falls are compared with those of 59 H4-6 chondrites from Antarctica. Various populations are tested by the multivariate techniques, using the previously developed method of randomization-simulation to assess significance levels. An earlier conclusion, based on fewer examples, that H4-6 chondrite falls are compositionally distinguishable from the Antarctic suite is verified by the additional data. This distinctiveness is highly significant because of the presence of samples from Victoria Land in the Antarctic population, which differ compositionally from falls beyond any reasonable doubt. However, it cannot be proven unequivocally that falls and Antarctic samples from Queen Maud Land are compositionally distinguishable. Trivial causes (e.g., analyst bias, weathering) cannot explain the Victoria Land (Antarctic)/non-Antarctic compositional difference for paradigmatic H4-6 chondrites. This seems to reflect a time-dependent variation of near-Earth meteoroid source regions differing in average thermal history.

Chemical studies of H chondrites. 6: Antarctic/non-Antarctic compositional differences revisited

NASA Technical Reports Server (NTRS)

Wolf, Stephen F.; Lipschutz, Michael E.

1995-01-01

We report data for the trace elements Au, Co, Sb, Ga, Rb, Ag, Se, Cs, Te, Zn, Cd, Bi, T1, and In (ordered by putative volatility during nebular condensation and accretion) determined by radiochemical neutron activation analysis of 14 additional H5 and H6 chondrite falls. Data for the 10 most volatile elements (Rb to In) treated by the multivariate techniques of linear discriminant analysis and logistic regression in these and 44 other falls are compared with those of 59 H4-6 chondrites from Antarctica. Various populations are tested by the multivariate techniques, using the previously developed method of randomization-simulation to assess significance levels. An earlier conclusion, based on fewer examples, that H4-6 chondrite falls are compositionally distinguishable from the Antarctic suite is verified by the additional data. This distinctiveness is highly significant because of the presence of samples from Victoria Land in the Antarctic population, which differ compositionally from falls beyond any reasonable doubt. However, it cannot be proven unequivocally that falls and Antarctic samples from Queen Maud Land are compositionally distinguishable. Trivial causes (e.g., analyst bias, weathering) cannot explain the Victoria Land (Antarctic)/non-Antarctic compositional difference for paradigmatic H4-6 chondrites. This seems to reflect a time-dependent variation of near-Earth meteoroid source regions differing in average thermal history.

Effects of Short-Term Thermal Alteration on Organic Matter in Experimentally-Heated Tagish Lake Observed by Raman Spectroscopy

NASA Technical Reports Server (NTRS)

Chan, Q. H. S.; Nakato, A.; Zolensky, M. E.; Nakamura, T.; Kebukawa, Y.; Maisano, J.; Colbert, M.; Martinez, J. E.

2017-01-01

Carbonaceous chondrites exhibit a wide range of aqueous and thermal alteration characteristics, while some are known to demonstrate mineralogical and petrologic evidence of having been thermally metamorphosed after aqueous alteration. This group of meteorites are commonly referred as thermally met-amorphosed carbonaceous chondrites (TMCCs), and their reflectance spectra show resemblances to that of C-type asteroids which typically have low albedos. This suggests that the surfaces of the C-type asteroids are also composed of both hydrous and dehydrated minerals, and thus TMCCs are among the best samples that can be studied in laboratory to reveal the true nature of the C-type asteroids. Although TMCCs are usually meteorites that were previously categorized as CI and CM chondrites, they are not strictly CI/CM because they exhibit isotopic and petrographic characteristics that significantly deviate from typical CI/CM. More appropriately, they are called CI-like and/or CM-like chondrites. Typical examples of TMCCs include the C2-ung/CM2TIV Belgica (B)-7904 and Yamato (Y) 86720. Thermal alteration is virtually complete in these meteorites and thus they are considered typical end-members of TMCCs exhibiting complete dehydration of matrix phyllosilicates. The estimated heating conditions are 10 to 103 days at 700 C to 1 to 100 hours at 890 C, i.e. short-term heating induced by impact and/or solar radiation. While the petrology and chemistry of TMCCs have only recently been extensively characterized, we have just begun to study in detail their organic contents. In order to understand how short-term heating affects the maturity of insoluble organic matter (IOM) in hydrous chondrites, we investigated experimentally-heated Tagish Lake meteorite using Raman spectroscopy, as the chemical and bulk oxygen isotopic compositions of the matrix of the carbonate (CO3)-poor lithology of the Tagish Lake (hereafter Tag) meteorite bears similarities to the TMCCs.

Lunar anorthosite 60025, the petrogenesis of lunar anorthosites, and the composition of the moon

NASA Technical Reports Server (NTRS)

Ryder, G.

1982-01-01

The mineral chemistry of the lunar anorthosite 60025 is investigated, and a model for the differentiation of the moon is proposed based on these findings. Among other results, it is concluded that 60025 is a mixture of pieces from a related sequence of anorthosites, and that this sequence was generated by near-perfect accumulate growth during strong fractional crystallization. The parent liquid of the most primitive anorthosite was saturated with olivine, plagioclase, pigeonite, and chromite, and evolved to one saturated with plagioclase, pigeonite, high-Ca clinopyroxene, and ilmenite. The steep slope of anorthosites on an Mg (mafics) vs. Ab (plagioclase) diagram is a result of the very low alkali content of the magma and of the original magma ocean. The bulk moon had low Al2O3, a sub-chondritic Ca/Al ratio, and REE abundances and patterns which were probably close to chondritic. In addition, mare basalt sources were found to be too magnesian and some contain too much high Ca clinopyroxene to be directly or simply complementary to a floated anorthosite crust.

The radiation shielding potential of CI and CM chondrites

NASA Astrophysics Data System (ADS)

Pohl, Leos; Britt, Daniel T.

2017-03-01

Galactic Cosmic Rays (GCRs) and Solar Energetic Particles (SEPs) pose a serious limit on the duration of deep space human missions. A shield composed of a bulk mass of material in which the incident particles deposit their energy is the simplest way to attenuate the radiation. The cost of bringing the sufficient mass from the Earth's surface is prohibitive. The shielding properties of asteroidal material, which is readily available in space, are investigated. Solution of Bethe's equation is implemented for incident protons and the application in composite materials and the significance of various correction terms are discussed; the density correction is implemented. The solution is benchmarked and shows good agreement with the results in literature which implement more correction terms within the energy ranges considered. The shielding properties of CI and CM asteroidal taxonomy groups and major asteroidal minerals are presented in terms of stopping force. The results show that CI and CM chondrites have better stopping properties than Aluminium. Beneficiation is discussed and is shown to have a significant effect on the stopping power.

Manganese-Chromium Isotope Systematics of Ivuna, Kainsaz and Other Carbonaceous Chondrites

NASA Technical Reports Server (NTRS)

Shukolyukov, A.; Lugmair, G. W.; Bogdanovski, O.

2003-01-01

We have shown earlier that the bulk samples of carbonaceous chondrites [CC] reveal excesses in both Cr-53 (Cr-53*) and Cr-54 (Cr-54*) as compared to the terrestrial standard value. The Cr-53/52 ratios in bulk samples of Orgueil (CI), Murray (CM), Allende (CV), and the Bencubbin/CH-like meteorite Hammadah Al Hambra 237 (HH237) are correlated with the respective Mn/Cr ratios. In contrast to CC, HH237 is characterized by a deficit of Cr-53 (-0.15 +/- 0.10(epsilon)) at a low Mn/Cr ratio of 0.07. The HH237 data point, however, falls on the CC line. Here we report new Mn-53 - Cr-53 results for the CC Kainsaz (CO) and Ivuna (CI).

CLOUDS IN SUPER-EARTH ATMOSPHERES: CHEMICAL EQUILIBRIUM CALCULATIONS

DOE Office of Scientific and Technical Information (OSTI.GOV)

Mbarek, Rostom; Kempton, Eliza M.-R., E-mail: mbarekro@grinnell.edu, E-mail: kemptone@grinnell.edu

Recent studies have unequivocally proven the existence of clouds in super-Earth atmospheres. Here we provide a theoretical context for the formation of super-Earth clouds by determining which condensates are likely to form under the assumption of chemical equilibrium. We study super-Earth atmospheres of diverse bulk composition, which are assumed to form by outgassing from a solid core of chondritic material, following Schaefer and Fegley. The super-Earth atmospheres that we study arise from planetary cores made up of individual types of chondritic meteorites. They range from highly reducing to oxidizing and have carbon to oxygen (C:O) ratios that are both sub-solarmore » and super-solar, thereby spanning a range of atmospheric composition that is appropriate for low-mass exoplanets. Given the atomic makeup of these atmospheres, we minimize the global Gibbs free energy of formation for over 550 gases and condensates to obtain the molecular composition of the atmospheres over a temperature range of 350–3000 K. Clouds should form along the temperature–pressure boundaries where the condensed species appear in our calculation. We find that the composition of condensate clouds depends strongly on both the H:O and C:O ratios. For the super-Earth archetype GJ 1214b, KCl and ZnS are the primary cloud-forming condensates at solar composition, in agreement with previous work. However, for oxidizing atmospheres, K{sub 2}SO{sub 4} and ZnO condensates are favored instead, and for carbon-rich atmospheres with super-solar C:O ratios, graphite clouds appear. For even hotter planets, clouds form from a wide variety of rock-forming and metallic species.« less

Mercury (Hg) in meteorites: Variations in abundance, thermal release profile, mass-dependent and mass-independent isotopic fractionation

NASA Astrophysics Data System (ADS)

Meier, Matthias M. M.; Cloquet, Christophe; Marty, Bernard

2016-06-01

We have measured the concentration, isotopic composition and thermal release profiles of Mercury (Hg) in a suite of meteorites, including both chondrites and achondrites. We find large variations in Hg concentration between different meteorites (ca. 10 ppb to 14,000 ppb), with the highest concentration orders of magnitude above the expected bulk solar system silicates value. From the presence of several different Hg carrier phases in thermal release profiles (150-650 °C), we argue that these variations are unlikely to be mainly due to terrestrial contamination. The Hg abundance of meteorites shows no correlation with petrographic type, or mass-dependent fractionation of Hg isotopes. Most carbonaceous chondrites show mass-independent enrichments in the odd-numbered isotopes 199Hg and 201Hg. We show that the enrichments are not nucleosynthetic, as we do not find corresponding nucleosynthetic deficits of 196Hg. Instead, they can partially be explained by Hg evaporation and redeposition during heating of asteroids from primordial radionuclides and late-stage impact heating. Non-carbonaceous chondrites, most achondrites and the Earth do not show these enrichments in vapor-phase Hg. All meteorites studied here have however isotopically light Hg (δ202Hg = ∼-7 to -1) relative to the Earth's average crustal values, which could suggest that the Earth has lost a significant fraction of its primordial Hg. However, the late accretion of carbonaceous chondritic material on the order of ∼2%, which has been suggested to account for the water, carbon, nitrogen and noble gas inventories of the Earth, can also contribute most or all of the Earth's current Hg budget. In this case, the isotopically heavy Hg of the Earth's crust would have to be the result of isotopic fractionation between surface and deep-Earth reservoirs.

The Chlorine Isotopic Composition Of Lunar UrKREEP

NASA Technical Reports Server (NTRS)

Barnes, J. J.; Tartese, R.; Anand, M.; McCubbin, F. M.; Neal, C. R.; Franchi, I. A.

2016-01-01

Since the long standing paradigm of an anhydrous Moon was challenged there has been a renewed focus on investigating volatiles in a variety of lunar samples. However, the current models for the Moon’s formation have yet to fully account for its thermal evolution in the presence of H2O and other volatiles. When compared to chondritic meteorites and terrestrial rocks, lunar samples have exotic chlorine isotope compositions, which are difficult to explain in light of the abundance and isotopic composition of other volatile species, especially H, and the current estimates for chlorine and H2O in the bulk silicate Moon. In order to better understand the processes involved in giving rise to the heavy chlorine isotope compositions of lunar samples, we have performed a comprehensive in situ high precision study of chlorine isotopes, using NanoSIMS (Nanoscale Secondary Ion Mass Spectrometry) of lunar apatite from a suite of Apollo samples covering a range of geochemical characteristics and petrologic types.

Chemical characteristics and origin of H chondrite regolith breccias

NASA Technical Reports Server (NTRS)

Lipschutz, M. E.; Biswas, S.; Mcsween, H. Y., Jr.

1983-01-01

Petrologic data and contents of Ag, Bi, Cd, Co, Cs, Ga, In, Rb, Se, Te, Tl and Zn-trace elements spanning the volatility/mobility range-in light and dark portions of H chondrite regolith breccias and L chondrite fragmental breccias are reported. The chemical/petrologic characteristics of H chondrite regolith breccias differ from those of nonbrecciated chondrites or fragmental breccias. Petrologic characteristics and at least some trace element contents of H chondrite regolith breccias reflect primary processes; contents of the most volatile/mobile elements may reflect either primary or secondary processing, possibly within layered H chondrite parent object(s). Chemical/petrologic differences existed in different regions of the parent(s). Regoligh formation and gardening and meteoroid compaction were not so severe as to alter compositions markedly.

Anomalous REE patterns in unequilibrated enstatite chondrites: Evidence and implications

NASA Technical Reports Server (NTRS)

Crozaz, Ghislaine; Hsu, Weibiao

1993-01-01

We present here a study of Rare Earth Element (REE) microdistributions in unequilibrated enstatite chondrites (EOC's). Although the whole rock REE contents are similar in both unequilibrated and equilibrated chondrites, the host minerals of these refractory elements are different. In the least equilibrated ordinary chondrites (UOC's), the REE reside mainly in glass whereas, in their more equilibrated counterparts, the bulk of the REE is in calcium phosphate, a metamorphic mineral that formed by oxidation of phosphorous originally contained in metal. In the smaller group of enstatite (E) chondrites, calcium phosphate is absent and the phase that contains the highest REE concentrations is a minor mineral, CaS (oldhamite), which contains approximately 50 percent of the total Ca present. In E chondrites, elements typically considered to be lithophiles (such as Ca and Mn) occur in sulfides rather than silicates. This indicates formation under extremely reducing conditions, thus in a region of the solar nebula distinct from those that supplied the more abundant ordinary and carbonaceous chondrites. Previously, we observed a variety of REE patterns in the oldhamite of UEC's; they range from almost flat to some with pronounced positive Eu and Yb anomalies. Here, we searched for complementary REE patterns in other minerals from E chondrites and found them in the major mineral, enstatite. Whenever Eu and Yb anomalies are present in this mineral, they are always negative.

Carbonaceous Chondrite-Rich Howardites; The Potential for Hydrous Lithologies on the HED Parent

NASA Technical Reports Server (NTRS)

Herrin, J. S.; Zolensky, M. E.; Cartwright, J. A.; Mittlefehldt, D. W.; Ross, D. K.

2011-01-01

Howardites, eucrites, and diogenites, collectively referred to as the "HED's", are a clan of meteorites thought to represent three different lithologies from a common parent body. Collectively they are the most abundant type of achondrites in terrestrial collections. Eucrites are crustal basalts and gabbros, diogenites are mostly orthopyroxenites and are taken to represent lower crust or upper mantle materials, and howardites are mixed breccias containing both lithologies and are generally regarded as derived from the regolith or near-surface. The presence of exogenous chondritic material in howardite breccias has long been recognized. As a group, howardites exhibit divergence in bulk chemistry from what would be produced by mixing of diogenite and eucrite end-members exclusively, a phenomenon most evident in elevated concentrations of siderophile elements. Despite this chemical evidence for chondritic input in howardite breccias, chondritic clasts have only been identified in a minority of samples, and typically at levels of only a few percent. Three recent Antarctic howardite finds, the paired Mt. Pratt (PRA) 04401 and PRA 04402 and Scott Glacier (SCO) 06040, are notable for their high proportion of carbonaceous chondrite clasts. PRA 04401 is particularly well-endowed, with large chondritic clasts occupying more than half of the modal area of the sections we examined. Previously only a few percent chondritic clasts had been observed to occur in howardites. PRA 04401 is the most chondrite-rich howardite known

Primitive Fine-Grained Matrix in the Unequilbrated Enstatite Chondrites

NASA Technical Reports Server (NTRS)

Weisberg, M. K.; Zolensky, M. E.; Kimura, M.; Ebel, D. S.

2014-01-01

Enstatite chondrites (EC) have important implications for constraining conditions in the early solar system and for understanding the evolution of the Earth and other inner planets. They are among the most reduced solar system materials as reflected in their mineral compositions and assemblage. They are the only chondrites with oxygen as well as Cr, Ti, Ni and Zn stable isotope compositions similar to the earth and moon and most are completely dry, lacking any evidence of hydrous alteration; the only exception are EC clasts in the Kaidun breccia which have hydrous minerals. Thus, ECs likely formed within the snow line and are good candidates to be building blocks of the inner planets. Our goals are to provide a more detailed characterization the fine-grained matrix in E3 chondrites, understand its origin and relationship to chondrules, decipher the relationship between EH and EL chondrites and compare E3 matrix to matrices in C and O chondrites as well as other fine-grained solar system materials. Is E3 matrix the dust remaining from chondrule formation or a product of parent body processing or both?

Origin of the eclogitic clasts with graphite-bearing and graphite-free lithologies in the Northwest Africa 801 (CR2) chondrite: Possible origin from a Moon-sized planetary body inferred from chemistry, oxygen isotopes and REE abundances

NASA Astrophysics Data System (ADS)

Hiyagon, H.; Sugiura, N.; Kita, N. T.; Kimura, M.; Morishita, Y.; Takehana, Y.

2016-08-01

In order to clarify the origin of the eclogitic clasts found in the NWA801 (CR2) chondrite (Kimura et al., 2013), especially, that of the high pressure and temperature (P-T) condition (∼3 GPa and ∼1000 °C), we conducted ion microprobe analyses of oxygen isotopes and rare earth element (REE) abundances in the clasts. Oxygen isotopic compositions of the graphite-bearing lithology (GBL) and graphite-free lithology (GFL) show a slope ∼0.6 correlation slightly below the CR-CH-CB chondrites field in the O three-isotope-diagram, with a large variation for the former and almost homogeneous composition for the latter. The average REE abundances of the two lithologies show almost unfractionated patterns. Based on these newly obtained data, as well as mineralogical observations, bulk chemistry, and considerations about diffusion timescales for various elements, we discuss in detail the formation history of the clasts. Consistency of the geothermobarometers used by Kimura et al. (2013), suggesting equilibration of various elements among different mineral pairs, provides a strong constraint for the duration of the high P-T condition. We suggest that the high P-T condition lasted 102-103 years. This clearly precludes a shock high pressure (HP) model, and hence, strongly supports a static HP model. A static HP model requires a Moon-sized planetary body of ∼1500 km in radius. Furthermore, it implies two successive violent collisions, first at the formation of the large planetary body, when the clasts were placed its deep interior, and second, at the disruption of the large planetary body, when the clasts were expelled out of the parent body and later on transported to the accretion region of the CR chondrites. We also discuss possible origin of O isotopic variations in GBL, and presence/absence of graphite in GBL/GFL, respectively, in relation to smelting possibly occurred during the igneous process(es) which formed the two lithologies. Finally we present a possible formation scenario of the eclogitic clasts.

In Situ Mapping of the Organic Matter in Carbonaceous Chondrites and Mineral Relationships

NASA Technical Reports Server (NTRS)

Clemett, Simon J.; Messenger, S.; Thomas-Keprta, K. L.; Ross, D. K.

2012-01-01

Carbonaceous chondrite organic matter represents a fossil record of reactions that occurred in a range of physically, spatially and temporally distinct environments, from the interstellar medium to asteroid parent bodies. While bulk chemical analysis has provided a detailed view of the nature and diversity of this organic matter, almost nothing is known about its spatial distribution and mineralogical relationships. Such information is nevertheless critical to deciphering its formation processes and evolutionary history.

Thermal Profile of the Lunar Interior Constrained by Revised Estimates of Concentrations of Heat Producing Elements

NASA Astrophysics Data System (ADS)

Fuqua-Haviland, H.; Panovska, S.; Mallik, A.; Bremner, P. M.; McDonough, W. F.

2017-12-01

Constraining the heat producing element (HPE) concentrations of the Moon is important for understanding the thermal state of the interior. The lunar HPE budget is debated to be suprachondritic [1] to chondritic [2]. The Moon is differentiated, thus, each reservoir has a distinct HPE signature complicating this effort. The thermal profile of the lunar interior has been constructed using HPE concentrations of an ordinary chondrite (U = 0.0068 ppm; Th = 0.025 ppm; K = 17 ppm) which yields a conservative low estimate [2, 3, 4]. A later study estimated the bulk lunar mantle HPE concentrations (U = 0.039 ppm; Th = 0.15 ppm; K = 212 ppm) based on measurements of Apollo pyroclastic glasses [5] assuming that these glasses represent the least fractionated, near-primary lunar mantle melts, hence, are the best proxies for capturing mantle composition. In this study, we independently validate the revised estimate by using HPE concentrations [5] to construct a conductive lunar thermal profile, or selenotherm. We compare our conductive profile to the range of valid temperatures. We demonstrate the HPE concentrations reported by [5], when used in a simple 1D spherical thermal conduction equation, yield an impossibly hot mantle with temperatures in excess of 4,000 K (Fig 1). This confirms their revised estimate is not representative of the bulk lunar mantle, and perhaps only representative of a locally enriched mantle domain. We believe that their Low-Ti avg. source estimate (Th = 0.055 ppm, Th/U=4; K/U=1700), with the least KREEP assimilation is the closest representation of the bulk lunar mantle, producing 3E-12 W/kg of heat. This estimate is close to that of the Earth (5E-12 W/kg), indicating that the bulk Earth and lunar mantles are similar in their HPE constituents. We have used the lunar mantle heat production, in conjunction with HPE estimates of the Fe-Ti-rich cumulates (high Ti-source estimate from [5]) and measurements of crustal ferroan anorthite [6], to capture the present-day lunar interior thermal state. We also present plausible internal structures that best match the mass, moment of inertia and bulk silicate Moon composition along this conductive selenotherm. [1] Wanke et al (1973) LPSC; [2] Warren et al (1979) Rev Geophy; [3] Wieczorek et al (2000) JGR; [4] Grimm (2013) JGRP; [5] Hagerty et al (2006) GCA; [6] Peplowski et al (2016) JGR.

Carbon-rich Chondritic Clast PV1 from the Plainview H-chondrite Regolith Formation from H3 Chondrite Material by Possible Cometary Impact

NASA Technical Reports Server (NTRS)

Rubin, Alan E.; Trigo-Rodriguez, Josep M.; Kunihiro, Takuya; Kallemeyn, Gregory W.; Wasson, John T.

2006-01-01

Chondritic clast PV1 from the Plainview H-chondrite regolith breccia is a subrounded, 5-mm diameter unequilibrated chondritic fragment that contains 13 wt% C occurring mainly within irregularly shaped 30-400-micron-size opaque patches. The clast formed from H3 chondrite material as indicated by the mean apparent chondrule diameter (310 micron vs. approximately 300 micron in H3 chondrites), the mean Mg-normalized refractory lithophile abundance ratio (1.00 +/- 0.09 XH), the previously determined 0-isotopic composition (Delta O-17 = 0.66% vs. 0.68 +/- 0.04%0 in H3 chondrites and 0.73 +/- 0.09% in H4-6 chondrites), the heterogeneous olivine compositions in grain cores (with a minimum range of Fal-19), and the presence of glass in some chondrules. Although the clast lacks the fine-grained, ferroan silicate matrix material present in type 3 ordinary chondrites, PV1 contains objects that appear to be recrystallized clumps of matrix material. Similarly, the apparent dearth of radial pyroxene and cryptocrystalline chondrules in PV1 is accounted for by the presence of some recrystallized fragments of these chondrule textural types. All of the chondrules in PV1 are interfused indicating that temperatures must have briefly reached approximately 1100C (the approximate solidus temperature of H-chondrite silicate). The most likely source of this heating was by an impact. Some metal was lost during impact heating as indicated by the moderately low abundance of metallic Fe-Ni in PV1 (approximately 14 wt%) compared to that in mean H chondrites (approximately 18 wt%). The carbon enrichment of the clast may have resulted from a second impact event, one involving a cometary projectile, possibly a Jupiter-family comet. As the clast cooled, it experienced hydrothermal alteration at low water/rock ratios as evidenced by the thick rims of ferroan olivine around low-FeO olivine cores. The C-rich chondritic clast was later incorporated into the H-chondrite parent-body regolith and extensively fractured and faulted.

Molybdenum isotope fractionation in the mantle

NASA Astrophysics Data System (ADS)

Liang, Yu-Hsuan; Halliday, Alex N.; Siebert, Chris; Fitton, J. Godfrey; Burton, Kevin W.; Wang, Kuo-Lung; Harvey, Jason

2017-02-01

We report double-spike molybdenum (Mo) isotope data for forty-two mafic and fifteen ultramafic rocks from diverse locations and compare these with results for five chondrites. The δ98/95Mo values (normalized to NIST SRM 3134) range from -0.59 ± 0.04 to +0.10 ± 0.08‰. The compositions of one carbonaceous (CI) and four ordinary chondrites are relatively uniform (-0.14 ± 0.01‰, 95% ci (confidence interval)) in excellent agreement with previous data. These values are just resolvable from the mean of 10 mid-ocean ridge basalts (MORBs) (0.00 ± 0.02‰, 95% ci). The compositions of 13 mantle-derived ultramafic xenoliths from Kilbourne Hole, Tariat and Vitim are more diverse (-0.39 to -0.07‰) with a mean of -0.22 ± 0.06‰ (95% ci). On this basis, the isotopic composition of the bulk silicate Earth (BSE or Primitive Mantle) is within error identical to chondrites. The mean Mo concentration of the ultramafic xenoliths (0.19 ± 0.07 ppm, 95% ci) is similar in magnitude to that of MORB (0.48 ± 0.13 ppm, 95% ci), providing evidence, either for a more compatible behaviour than previously thought or for selective Mo enrichment of the subcontinental lithospheric mantle. Intraplate and ocean island basalts (OIBs) display significant isotopic variability within a single locality from MORB-like to strongly negative (-0.59 ± 0.04‰). The most extreme values measured are for nephelinites from the Cameroon Line and Trinidade, which also have anomalously high Ce/Pb and low Mo/Ce relative to normal oceanic basalts. δ98/95Mo correlates negatively with Ce/Pb and U/Pb, and positively with Mo/Ce, explicable if a phase such as an oxide or a sulphide liquid selectively retains isotopically heavy Mo in the mantle and fractionates its isotopic composition in low degree partial melts. If residual phases retain Mo during partial melting, it is possible that the [Mo] for the BSE may be misrepresented by values estimated from basalts. This would be consistent with the high Mo concentrations of all the ultramafic xenoliths of 40-400 ppb, similar to or, significantly higher than, current estimates for the BSE (39 ppb). On this basis a revised best estimate of the Mo content in the BSE based on these concentrations would be in the range 113-180 ppb, significantly higher than previously assumed. These values are similar to the levels of depletion in the other refractory moderately siderophile elements W, Ni and Co. A simpler explanation may be that the subcontinental lithospheric mantle has been selectively enriched in Mo leading to the higher concentrations observed. Cryptic melt metasomatism would be difficult to reconcile with the high Mo/Ce of the most LREE depleted xenoliths. Ancient Mo-enriched subducted components would be expected to have heavy δ98/95Mo, which is not observed. The Mo isotope composition of the BSE, cannot be reliably resolved from that of chondrites at this time despite experimental evidence for metal-silicate fractionation. An identical isotopic composition might result from core-mantle differentiation under very high temperatures such as were associated with the Moon-forming Giant Impact, or from the BSE inventory reflecting addition of moderately siderophile elements from an oxidised Moon-forming impactor (O'Neill, 1991). However, the latter would be inconsistent with the non-chondritic radiogenic W isotopic composition of the BSE. Based on mantle fertility arguments, Mo in the BSE could even be lighter (lower 98/95Mo) than that in chondrites, which might be explained by loss of S rich liquids from the BSE during core formation (Wade et al., 2012). Such a late removal model is no longer required to explain the Mo concentration of the BSE if its abundance is in fact much higher, and similar to the values for ultramafic xenoliths.

Pb-Pb dating of individual chondrules from the CBa chondrite Gujba: Assessment of the impact plume formation model

PubMed Central

Bollard, Jean; Connelly, James N.; Bizzarro, Martin

2016-01-01

The CB chondrites are metal-rich meteorites with characteristics that sharply distinguish them from other chondrite groups. Their unusual chemical and petrologic features and a young formation age of bulk chondrules dated from the CBa chondrite Gujba are interpreted to reflect a single-stage impact origin. Here, we report high-precision internal isochrons for four individual chondrules of the Gujba chondrite to probe the formation history of CB chondrites and evaluate the concordancy of relevant short-lived radionuclide chronometers. All four chondrules define a brief formation interval with a weighted mean age of 4562.49 ± 0.21 Myr, consistent with its origin from the vapor-melt impact plume generated by colliding planetesimals. Formation in a debris disk mostly devoid of nebular gas and dust sets an upper limit for the solar protoplanetary disk lifetime at 4.8 ± 0.3 Myr. Finally, given the well-behaved Pb-Pb systematics of all four chondrules, a precise formation age and the concordancy of the Mn-Cr, Hf-W, and I-Xe short-lived radionuclide relative chronometers, we propose that Gujba may serve as a suitable time anchor for these systems. PMID:27429545

Secondary overprinting of S-Se-Te signatures in the Earth's mantle: Implications for the Late Veneer

NASA Astrophysics Data System (ADS)

Koenig, S.; Luguet, A.; Lorand, J.; Pearson, D.

2013-12-01

Sulphur, Selenium and Tellurium are both chalcophile and highly siderophile elements (HSE) with near-chondritic ratios and absolute abundances in the terrestrial mantle that exceed those predicted by core-mantle differentiation[1]. These 'excess' HSE abundances have been attributed to addition of ca. 0.5% of chondrite-like material that hit the Earth in its accretionary stage between 4 to 3.8 billion years ago after core-mantle differentiation (Late Veneer[2]). Therefore, like other HSE, S, Se and Te are considered potential tracers for the composition of the Late Veneer, provided that their bulk silicate Earth abundances are properly constrained. In contrast to ca. 250 ppm S, Se and Te are ultra-trace elements in the terrestrial mantle. Like all HSE, they are furthermore controlled by base metal sulphides (BMS) and micrometric platinum group minerals (PGMs)[3]. This strong control exerted by the host mineralogy and petrology on the S-Se-Te systematics at both the micro-scale and the whole-rock scale makes detailed mineralogical and petrological studies of BMS and PGM a pre-requisite to fully understand and accurately interpret the whole-rock signatures. Here we combine in-situ sulphide data and detailed mineralogical observations with whole-rock S-Se-Te-HSE signatures of both lherzolites and harburgites from different geodynamic settings. We demonstrate that the near-chondritic Se and Te signature of 'fertile' mantle rocks (Se/Te ≈9×5) is not a primitive signature of the Earth's mantle, but rather reflects strong enrichment in metasomatic HSE host phases, which erased previous pristine signatures. Consequently, current attempts to identify a potential Late Veneer composition are seriously flawed because, neither refertilisation/metasomatism nor true melt depletion (e.g. harzburgitic residues) have been taken into account for the Primitive Upper Mantle composition estimate[4]. Our combined whole rock and in-situ sulphide data indicate a refertilisation trend towards sub-chondritic Se/Te ratios (i.e. Se/Te < 2). On the other hand, harzburgites that preserve depletion signatures show suprachondritic Se/Te ratios (< 31). Altogether this shows that metasomatic enrichment of mantle rocks may lead to a systematic bias and hence underestimation of the current Se/Te estimate of the primitive mantle. The metasomatic origin of the reported S, Se and Te ratios in peridotites that reflect the control of metasomatic BMS and PGMs[5;6] furthermore show that not all whole rock signatures in the Earth's mantle that scatter around near-chondritic values are primary and hence challenge the simple conception that these features may readily solve the long-standing conundrum of the Late Veneer composition. Refs: [1] Rose-Weston et al. (2009) GCA 73, 4598-4615; [2] Kimura et al. (1974) GCA 38, 683-701; [3] Lorand and Alard (2010) 67, 4137-4151; [4] Wang and Becker (2013) Nature 499, 328-331; [5] König et al. (2012) GCA 86, 354-366; [6] König et al. (2013, in press), EPSL.

The matrices of unequilibrated ordinary chondrites - Implications for the origin and history of chondrites

NASA Technical Reports Server (NTRS)

Huss, G. R.; Keil, K.; Taylor, G. J.

1981-01-01

The matrices of 16 unequilibrated chondrites were examined by optical microscopy, an electron microprobe, and a scanning electron microscope. The fine-grained, opaque, silicate matrix of type 3 unequilibrated chondrites was compositionally, mineralogically, and texturally different from the chondrules and their fragments; it may be the low temperature condensate proposed by Larimer and Anders (1967, 1970). Each meteorite has been metamorphosed by a combination of processes including thermal metamorphism and the passage of shock waves; the appearance of each chondrite results from the temperature and pressure conditions which formed it, and subsequent metamorphic alterations.

Deducing Wild 2 Components with a Statistical Dataset of Olivine in Chondrite Matrix

NASA Technical Reports Server (NTRS)

Frank, D. R.; Zolensky, M. E.; Le, L.

2012-01-01

Introduction: A preliminary exam of the Wild 2 olivine yielded a major element distribution that is strikingly similar to those for aqueously altered carbonaceous chondrites (CI, CM, and CR) [1], in which FeO-rich olivine is preferentially altered. With evidence lacking for large-scale alteration in Wild 2, the mechanism for this apparent selectivity is poorly understood. We use a statistical approach to explain this distribution in terms of relative contributions from different chondrite forming regions. Samples and Analyses: We have made a particular effort to obtain the best possible analyses of both major and minor elements in Wild 2 olivine and the 5-30 micrometer population in chondrite matrix. Previous studies of chondrite matrix either include larger isolated grains (not found in the Wild 2 collection) or lack minor element abundances. To overcome this gap in the existing data, we have now compiled greater than 10(exp 3) EPMA analyses of matrix olivine in CI, CM, CR, CH, Kakangari, C2-ungrouped, and the least equilibrated CO, CV, LL, and EH chondrites. Also, we are acquiring TEM/EDXS analyses of the Wild 2 olivine with 500s count times, to reduce relative errors of minor elements with respect to those otherwise available. Results: Using our Wild 2 analyses and those from [2], the revised major element distribution is more similar to anhydrous IDPs than previous results, which were based on more limited statistics (see figure below). However, a large frequency peak at Fa(sub 0-1) still persists. All but one of these grains has no detectable Cr, which is dissimilar to the Fa(sub 0-1) found in the CI and CM matrices. In fact, Fa(sub 0-1) with strongly depleted Cr content is a composition that appears to be unique to Kakangari and enstatite (highly reduced) chondrites. We also note the paucity of Fa(sub greater than 58), which would typically indicate crystallization in a more oxidizing environment [3]. We conclude that, relative to the bulk of anhydrous IDPs, Wild 2 may have received a larger contribution from the Kakangari and/or enstatite chondrite forming regions. Alternatively, Wild 2 may have undergone accretion in an anomalously reducing region, marked by nebular condensation of this atypical forsterite. In [4], a similar conclusion was reached with an Fe-XANES study. We will also use similar lines of reasoning, and our previous conclusions in [5], to constrain the relative contributions of silicates that appear to have been radially transported from different ordinary and carbonaceous chondrite forming regions to the Kuiper Belt. In addition, the widespread depletion of Cr in these FeO-rich (Fa(sub greater than 20)) fragments is consistent with mild thermal metamorphism in Wild 2.

Young Pb-Isotopic Ages of Chondrules in CB Carbonaceous Chondrites

NASA Technical Reports Server (NTRS)

Amelin, Yuri; Krot, Alexander N.

2005-01-01

CB (Bencubbin-type) carbonaceous chondrites differ in many ways from more familiar CV and CO carbonaceous chondrites and from ordinary chondrites. CB chondrites are very rich in Fe-Ni metal (50-70 vol%) and contain magnesian silicates mainly as angular to sub-rounded clasts (or chondrules) with barred olivine (BO) or cryptocrystalline (CC) textures. Both metal and silicates appear to have formed by condensation. The sizes of silicate clasts vary greatly between the two subgroups of CB chondrites: large (up to one cm) in CB(sub a) chondrites, and typically to much much less than 1 mm in CB(sub b) chondrites. The compositional and mineralogical differences between these subgroups and between the CB(sub s) and other types of chondrites suggest different environment and possibly different timing of chondrule formation. In order to constrain the timing of chondrule forming processes in CB(sub s) and understand genetic relationship between their subgroups, we have determined Pb-isotopic ages of silicate material from the CB(sub a) chondrite Gujba and CB(sub b) chondrite Hammadah al Hamra 237 (HH237 hereafter).

Chemical compositions of primitive solar system particles

NASA Technical Reports Server (NTRS)

Sutton, Steve R.; Bajt, S.

1994-01-01

Chemical studies of micrometeorites are of fundamental importance primarily because atmospheric entry selection effects (such as destruction of friable objects) are less significant than those for conventional meteorites. As a result, particles that have experienced very little postaccretional processing have a significant chance of surviving the Earth encounter and subsequent collection. Thus, chemical analyses of these relatively unaltered micrometeorites may lead to a better understanding of the compositions of the most primitive materials in the solar system and thereby constrain the conditions (physical and chemical) that existed in the early solar nebula. Micrometeorites have been collected from the stratosphere, polar ices, and ocean sediments, but the stratospheric collection is the best source for the most unaltered material because they are small and are not heated to their melting points. Despite the fact that the stratospheric micrometeorites have masses in the nanogram range, a variety of microanalytical techniques have been applied to bulk chemical analyses with part-per-million sensitivity. In some cases, multi-disciplinary studies (e.g., chemistry and mineralogy) have been performed on individual particles. The first-order conclusion is that the chondrite-like particles are chemically similar to carbonaceous chondrites but in detail are distinct from members of the conventional meteorite collection. The purpose of this paper is to provide an overview of the results to date and identify important areas for further study.

Chronology of formation of early solar system solids from bulk Mg isotope analyses of CV3 chondrules

NASA Astrophysics Data System (ADS)

Chen, Hsin-Wei; Claydon, Jennifer L.; Elliott, Tim; Coath, Christopher D.; Lai, Yi-Jen; Russell, Sara S.

2018-04-01

We have analysed the petrography, major element abundances and bulk Al-Mg isotope systematics of 19 ferromagnesian chondrules from the CV3 chondrites Allende, Mokoia, and Vigarano, together with an Al-rich chondrule and refractory olivine from Mokoia. Co-variations of Al/Mg with Na/Mg and Ti/Mg in our bulk chondrules suggest their compositions are dominantly controlled by reworking of different proportions of chondrule components (e.g. mafic minerals and mesostatis); their precursors are thus fragments from prior generations of chondrules. Our samples show a range in fractionation corrected 26Mg/24Mg (Δ‧26Mg) ∼ 60 ppm, relative to precisions <±5 ppm (2se) and these values broadly covary with 27Al/24Mg. The data can be used to calculate model initial 26Al/27Al, or (26Al/27Al)0, of the chondrule precursors. Our resolvably radiogenic chondrules yield model (26Al/27Al)0 ∼ 1-2 × 10-5, equivalent to model "ages" of precursor formation ≦1 Ma post CAI. However, many of our chondrules show near solar Δ‧26Mg and no variability despite a range in 27Al/24Mg. This suggests their derivation either from younger precursor chondrules or open system behaviour once 26Al was effectively extinct ((26Al/27Al)0 < 0.8 × 10-5, given the resolution here). Evidence for the latter explanation is provided by marked rims of orthopyroxene replacing olivine, indicating reaction of chondrules with a surrounding silicate vapour. Concurrent isotopic exchange of Mg with a near chondritic vapour during late reworking could explain their isotopic systematics. One ferromagnesian object is dominated by a high Mg# olivine with elevated Ti and Ca abundances. This refractory olivine has a markedly negative Δ‧26Mg = -16 ± 3 ppm (2se), reflecting its early removal (model age of <0.5 Ma post CAI), from a reservoir with evolving Δ‧26Mg. If representative of the chondrule forming region, this grain defines a minimum interval of radiogenic ingrowth for CV chondrites commensurate with (26Al/27Al)0 > 3.4 ± 0.6 × 10-5. Overall, our samples record a sequence of events from the formation of ferromagnesian objects within 0.5 Ma of CAI to re-equilibration of chondrules and silicate vapour >2 Ma post CAI, assuming an initially homogeneous 26Al/27Al. Metamorphism on the asteroid parent body may have played a subsequent role in affecting Mg isotope composition, but we argue this had a minor influence on the observations here.

Comparing Wild 2 Particles to Chondrites and IDPS

NASA Technical Reports Server (NTRS)

Zolensky, Michael; Nakamura-Messenger, Keiko; Rietmeijer, Frans; Leroux, Hugues; Mikouchi, Takashi; Ohsumi, Kazumasa; Simon, Steven; Grossman, Lawrence; Stephan, Thomas; Weisberg, Michael;

The Oxygen Isotopic Composition of MIL 090001: A CR2 Chondrite with Abundant Refractory Inclusions

NASA Technical Reports Server (NTRS)

Keller, Lindsay P.; McKeegan, K. D.; Sharp, Z. D.

2012-01-01

MIL 090001 is a large (>6 kg) carbonaceous chondrite that was classified as a member of the CV reduced subgroup (CVred) that was recovered during the 2009-2010 ANSMET field season [1]. Based on the abundance of refractory inclusions and the extent of aqueous alteration, Keller [2] suggested a CV2 classification. Here we report additional mineralogical and petrographic data for MIL 090001, its whole-rock oxygen isotopic composition and ion microprobe analyses of individual phases. The whole rock oxygen isotopic analyses show that MIL 090001 should be classified as a CR chondrite.

Martian regolith in Elephant Moraine 79001 shock melts? Evidence from major element composition and sulfur speciation

NASA Astrophysics Data System (ADS)

Walton, E. L.; Jugo, P. J.; Herd, C. D. K.; Wilke, M.

2010-08-01

Shock veins and melt pockets in Lithology A of Martian meteorite Elephant Moraine (EETA) 79001 have been investigated using electron microprobe (EM) analysis, petrography and X-ray Absorption Near Edge Structure (XANES) spectroscopy to determine elemental abundances and sulfur speciation (S 2- versus S 6+). The results constrain the materials that melted to form the shock glasses and identify the source of their high sulfur abundances. The XANES spectra for EETA79001 glasses show a sharp peak at 2.471 keV characteristic of crystalline sulfides and a broad peak centered at 2.477 keV similar to that obtained for sulfide-saturated glass standards analyzed in this study. Sulfate peaks at 2.482 keV were not observed. Bulk compositions of EETA79001 shock melts were estimated by averaging defocused EM analyses. Vein and melt pocket glasses are enriched in Al, Ca, Na and S, and depleted in Fe, Mg and Cr compared to the whole rock. Petrographic observations show preferential melting and mobilization of plagioclase and pyrrhotite associated with melt pocket and vein margins, contributing to the enrichments. Estimates of shock melt bulk compositions obtained from glass analyses are biased towards Fe- and Mg- depletions because, in general, basaltic melts produced from groundmass minerals (plagioclase and clinopyroxene) will quench to a glass, whereas ultramafic melts produced from olivine and low-Ca pyroxene megacrysts crystallize during the quench. We also note that the bulk composition of the shock melt pocket cannot be determined from the average composition of the glass but must also include the crystals that grew from the melt - pyroxene (En 72-75Fs 20-21Wo 5-7) and olivine (Fo 75-80). Reconstruction of glass + crystal analyses gives a bulk composition for the melt pocket that approaches that of lithology A of the meteorite, reflecting bulk melting of everything except xenolith chromite. Our results show that EETA79001 shock veins and melt pockets represent local mineral melts formed by shock impedance contrasts, which can account for the observed compositional anomalies compared to the whole rock sample. The observation that melts produced during shock commonly deviate from the bulk composition of the host rock has been well documented from chondrites, rocks from terrestrial impact structures and other Martian meteorites. The bulk composition of shock melts reflects the proportions of minerals melted; large melt pockets encompass more minerals and approach the whole rock whereas small melt pockets and thin veins reflect local mineralogy. In the latter, the modal abundance of sulfide globules may reach up to 15 vol%. We conclude the shock melt pockets in EETA79001 lithology A contain no significant proportion of Martian regolith.

Yes, Kakangari is a unique chondrite. [meteoritic composition

NASA Technical Reports Server (NTRS)

Davis, A. M.; Grossman, L.; Ganapathy, R.

1977-01-01

The position of the Kakangari chondrite as the representative of a new class of chondrites is considered, taking into account the results of the analysis of a 17.1-mg piece of Kakangari for 20 elements. Elemental concentration data are compared for Kakangari and other meteorite groups. Data for the most similar groups, C2, C3(V), L, and E4 chondrites are represented in a graph along with Kakangari data. It is found that pronounced differences exist between Kakangari and the other meteorite classes.

Ureilites - Trace element clues to their origin

NASA Technical Reports Server (NTRS)

Janssens, Marie-Josee; Hertogen, Jan; Wolf, Rainer; Ebihara, Mitsuru; Anders, Edward

1987-01-01

The question of the origin of ureilites was reexamined using new data obtained by radiochemical NAA for Ag, Au, Bi, Br, Cd, Cs, Ge, In, Ir, Ni, Pd, Os, Rb, Re, Sb, Se, Te, Tl, U, and Zn in two vein separates from Haveroe and Kenna and a bulk sample of Kenna. Vein material was found to be enriched in all elements analyzed, except Zn, and to account for most of the carbon, noble gases, and, presumably, siderophiles in the meteorite. The results support the earlier interpretation of Higuchi et al. (1976) on the composition of ureilite parent body (similar to C3V or H3, but not C3O chondrites).

HFSE systematics of rutile-bearing eclogites: New insights into subduction zone processes and implications for the earth’s HFSE budget

NASA Astrophysics Data System (ADS)

Schmidt, Alexander; Weyer, Stefan; John, Timm; Brey, Gerhard P.

2009-01-01

The depleted mantle and the continental crust are generally thought to balance the budget of refractory and lithophile elements of the Bulk Silicate Earth (BSE), resulting in complementary trace element patterns. However, the two high field strength elements (HFSE) niobium and tantalum appear to contradict this mass balance. All reservoirs of the silicate Earth exhibit subchondritic Nb/Ta ratios, possibly as a result of Nb depletion. In this study a series of nineteen orogenic MORB-type eclogites from different localities was analyzed to determine their HFSE concentrations and to contribute to the question of whether subducted oceanic crust could form a hidden reservoir to account for the mass imbalance of Nb/Ta between BSE and the chondritic reservoir. Concentrations of HFSE were analyzed with isotope dilution (ID) techniques. Additionally, LA-ICPMS analyses of clinopyroxene, garnet and rutile have been performed. Rutile is by far the major host for Nb and Ta in all analyzed eclogites. However, many rutiles revealed zoning in Nb/Ta ratios, with cores being higher than rims. Accordingly, in situ analyses of rutiles have to be evaluated carefully and rutile cores do not necessarily reflect a bulk rock Nb and Ta composition, although over 90% of these elements reside in rutile. The HFSE concentration data in bulk rocks show that the orogenic eclogites have subchondritic Nb/Ta ratios and near chondritic Zr/Hf ratios. The investigated eclogites show neither enrichment of Nb compared to similarly incompatible elements (e.g. La), nor fractionation of Nb/Ta ratios relative to MOR-basalts, the likely precursor of these rocks. This indicates that during the conversion of the oceanic crust to eclogites in most cases, (1) HFSE and REE have similar mobility on average, possibly because both element groups remain in the down going slab, and (2) no significant fractionation of Nb/Ta occurs in subducted oceanic crust. With an average Nb/Ta ratio of 14.2 ± 1.4 (2s.e.), the investigated eclogites cannot balance the differences between BSE and chondrite. Additionally, as their average Nb/Ta is indistinguishable from the Nb/Ta of MORB, they are also an unlikely candidate to balance the potentially small differences in Nb/Ta between the continental crust and the mantle.

Mixing and Transport of Dust in the Early Solar Nebula as Inferred from Titanium Isotope Variations among Chondrules

DOE Office of Scientific and Technical Information (OSTI.GOV)

Gerber, Simone; Burkhardt, Christoph; Budde, Gerrit

2017-05-20

Chondrules formed by the melting of dust aggregates in the solar protoplanetary disk and as such provide unique insights into how solid material was transported and mixed within the disk. Here, we show that chondrules from enstatite and ordinary chondrites show only small {sup 50}Ti variations and scatter closely around the {sup 50}Ti composition of their host chondrites. By contrast, chondrules from carbonaceous chondrites have highly variable {sup 50}Ti compositions, which, relative to the terrestrial standard, range from the small {sup 50}Ti deficits measured for enstatite and ordinary chondrite chondrules to the large {sup 50}Ti excesses known from Ca–Al-rich inclusionsmore » (CAIs). These {sup 50}Ti variations can be attributed to the addition of isotopically heterogeneous CAI-like material to enstatite and ordinary chondrite-like chondrule precursors. The new Ti isotopic data demonstrate that isotopic variations among carbonaceous chondrite chondrules do not require formation over a wide range of orbital distances, but can instead be fully accounted for by the incorporation of isotopically anomalous “nuggets” into chondrule precursors. As such, these data obviate the need for disk-wide transport of chondrules prior to chondrite parent body accretion and are consistent with formation of chondrules from a given chondrite group in localized regions of the disk. Finally, the ubiquitous presence of {sup 50}Ti-enriched material in carbonaceous chondrites and the lack of this material in the non-carbonaceous chondrites support the idea that these two meteorite groups derive from areas of the disk that remained isolated from each other, probably through the formation of Jupiter.« less

Oxygen isotopic relationships between the LEW85332 carbonaceous chondrite and CR chondrites

NASA Technical Reports Server (NTRS)

Prinz, M.; Weisberg, M. K.; Clayton, R. N.; Mayeda, T. K.

1993-01-01

LEW85332, originally described as a unique C3 chondrite, was shown to be a C2 chondrite with important linkages to the CR clan. An important petrologic aspect of LEW85332 is that it contains anhydrous chondrules and hydrated matrix, and new oxygen isotopic data on chondrules, matrix and whole rock are consistent with the petrology. Chondrules fall on the equilibrated chondrite line (ECL), with a slope near 1, which goes through ordinary chondrite chondrules. This contrasts with the CR chondrule line which has a lower slope due to hydrated components. LEW85332 chondrules define a new carbonaceous chondrite chondrule line, parallel to the anhydrous CV chondrule line (CCC), consistent with the well-established concept of two oxygen isotopic reservoirs. Matrix and whole rock fall on the CR line. The whole rock composition indicates that the chondrite is dominated by chondrules, and that most of them contain light oxygen similar to that of anhydrous olivine and pyroxene separates in the Renazzo and Al Rais CR chondrites.

A Comprehensive Study of Chelyabinsk Meteorite: Physical, Mineralogical, Spectral Properties and Solar System Orbit

NASA Astrophysics Data System (ADS)

Gritsevich, Maria; Kohout, T.; Grokhovsky, V.; Yakovlev, G.; Lyytinen, E.; Vinnikov, V.; Haloda, J.; Halodova, P.; Michallik, R.; Penttilä, A.; Muinonen, K.; Peltoniemi, J.; Lupovka, V.; Dmitriev, V.

2013-10-01

On February 15, 2013, at 9:22 am, an exceptionally bright and long duration fireball was observed by many eyewitnesses in the Chelyabinsk region, Russia. A strong shock wave associated with the fireball caused significant damage such as destroyed windows and parts of buildings in Chelyabinsk and the surrounding territories. A number of video records of the event are available and have been used to reconstruct atmospheric trajectory, velocity, deceleration rate, and parent asteroid Apollo-type orbit in the Solar System. Two types of meteorite material are present among recovered fragments of the Chelyabinsk meteorite. These are described as the light-colored and dark-colored lithology. Both types are of LL5 composition with the dark-colored one being an impact-melt shocked to a higher level. Based on the magnetic susceptibility measurements, the Chelyabinsk meteorite is richer in metallic iron as compared to other LL chondrites. The measured bulk and grain densities and the porosity closely resemble other LL chondrites. Shock darkening does not have a significant effect on the material physical properties, but causes a decrease of reflectance and decrease in silicate absorption bands in the reflectance spectra. This is similar to the space weathering effects observed on asteroids. However, no spectral slope change similar to space weathering is observed as a result of shock-darkening. Thus, it is possible that some dark asteroids with invisible silicate absorption bands may be composed of relatively fresh shock darkened chondritic material.

Organic matter in primitive meteorites: a study of the hydrogen isotopic distribution in CM-type carbonaceous chondrites

NASA Astrophysics Data System (ADS)

Piani, L.; Yurimoto, H.; Remusat, L.; Gonzales, A.; Marty, B.

2017-12-01

Chondrite meteorites are fragments of rocks coming from small bodies of the asteroid belt and constitute witnesses of the volatile-rich reservoirs present in the inner protoplanetary disk. Among these meteorites, carbonaceous chondrites contain the largest quantity of water and organic matter and are one of the most probable candidates for the delivery of water and molecular origin of life to Earth. Organic matter in carbonaceous chondrites is intimately mixed with hydrated minerals challenging its in situ characterization and the determination of its H-isotope composition (Le Guillou et al., GCA 131, 2014). Organic matter occurs as soluble components (in water or organic solvents) and an insoluble macromolecule. The insoluble organic matter (IOM) is efficiently isolated after acid leaching of the chondrite minerals. IOM has thus been investigated by a large set of analytical techniques allowing its structural organization, chemical composition and isotopic composition to be determined at several scales (e.g. Derenne and Robert, MAPS 45, 2010). In the soluble counterpart (SOM), targeted studies have shown large ranges of D/H ratios in the different classes of soluble organic compounds (i.e. carboxylic acids, ketones and aldehydes, amino-acids etc.) (Remusat, Planetary Mineralogy 15, 2015 and references therein). This D/H distribution indicates a complex and probably multiple-stage synthesis of this organic compounds occurring at different stages of the disk evolution. Nevertheless, inventories of the known C-bearing species in carbonaceous chondrites (carbonates, SOM and IOM) show that about 40-50 % of the carbon is hidden within the matrix (Alexander et al., MAPS 50, 2015). In this study, we perform in situ hydrogen isotope analyses at the micrometer scale by secondary ion mass spectrometry to investigate the distribution of organic matter in primitive chondrites without the use of any chemical treatment. Correlated analyses of the D/H and C/H ratios allow us to decipher the H contribution of water-bearing minerals and to estimate the hydrogen isotopic composition of water in chondrites (Piani et al., submitted). Comparison of spot analyses and isotope images obtained in situ and on isolated IOM gives clues on the nature of the organic components of carbonaceous asteroid rocks.

ALH85085: a unique volatile-poor carbonaceous chondrite with possible implications for nebular fractionation processes

USGS Publications Warehouse

Grossman, J.N.; Rubin, A.E.; MacPherson, G.J.

1988-01-01

Allan Hills 85085 is a unique chondrite with affinities to the Al Rais-Renazzo clan of carbonaceous chondrites. Its constituents are less than 50 ??m in mean size. Chondrules and microchondrules of all textures are present; nonporphyritic chondrules are unusually abundant. The mean compositions of porphyritic, nonporphyritic and barred olivine chondrules resemble those in ordinary chondrites except that they are depleted in volatile elements. Ca-, Al-rich inclusions are abundant and largely free of nebular alteration; they comprise types similar to those in CM and CO chondrites, as well as unique types. Calcium dialuminate occurs in several inclusions. Metal, silicate and sulfide compositions are close to those in CM-CO chondrites and Al Rais and Renazzo. C1-chondrite clasts and metal-rich "reduced" clasts are present, but opaque matrix is absent. Siderophile abundances in ALH85085 are extremely high (e.g., Fe Si = 1.7 ?? solar), and volatiles are depleted (e.g., Na Si = 0.25 ?? solar, S Si = 0.03 ?? solar). Nonvolatile lithophile abundances are similar to those in Al Rais, Renazzo, and CM and CO chondrites. ALH85085 agglomerated when temperatures in the nebula were near 1000 K, in the same region where Renazzo, Al Rais and the CI chondrites formed. Agglomeration of high-temperature material may thus be a mechanism by which the fractionation of refractory lithophiles occurred in the nebula. Chondrule formation must have occurred at high temperatures when clumps of precursors were small. After agglomeration, ALH85085 was annealed and lightly shocked. C1 and other clasts were subsequently incorporated during late-stage brecciation. ?? 1988.

Chemical composition of Mars

USGS Publications Warehouse

Morgan, J.W.; Anders, E.

1979-01-01

The composition of Mars has been calculated from the cosmochemical model of Ganapathy and Anders (1974) which assumes that planets and chondrites underwent the same 4 fractionation processes in the solar nebula. Because elements of similar volatility stay together in these processes, only 4 index elements (U, Fe, K and Tl or Ar36) are needed to calculate the abundances of all 83 elements in the planet. The values chosen are U = 28 ppb, K = 62 ppm (based on K U = 2200 from orbital ??-spectrometry and on thermal history calculations by Tokso??z and Hsui (1978) Fe = 26.72% (from geophysical data), and Tl = 0.14 ppb (from the Ar36 and Ar40 abundances measured by Viking). The mantle of Mars is an iron-rich [Mg/(Mg + Fe) = 0.77] garnet wehrlite (?? = 3.52-3.54 g/cm3), similar to McGetchin and Smyth's (1978) estimate but containing more Ca and Al. It is nearly identical to the bulk Moon composition of Morgan et al. (1978b). The core makes up 0.19 of the planet and contains 3.5% S-much less than estimated by other models. Volatiles have nearly Moon-like abundances, being depleted relative to the Earth by factors of 0.36 (K-group, Tcond = 600-1300 K) or 0.029 (Tl group, Tcond < 600 K). The water abundance corresponds to a 9 m layer, but could be higher by as much as a factor of 11. Comparison of model compositions for 5 differentiated planets (Earth, Venus, Mars, Moon, and eucrite parent body) suggests that volatile depletion correlates mainly with size rather than with radial distance from the Sun. However, the relatively high volatile content of shergottites and some chondrites shows that the correlation is not simple; other factors must also be involved. ?? 1979.

A New Titanium-Bearing Calcium Aluminosilicate Phase. 1; Meteoritic Occurrences and Formation in Synthetic Systems

NASA Technical Reports Server (NTRS)

Paque, Julie M.; Beckett, John R.; Barber, David J.; Stolper, Edward M.

1994-01-01

A new titanium-bearing calcium aluminosilicate mineral has been identified in coarse-grained calcium-aluminum-rich inclusions (CAIs) from carbonaceous chondrites. The formula for this phase, which we have temporarily termed "UNK," is Ca3Ti(AlTi)2(Si,Al)3O14, and it is present in at least 8 of the 20 coarse-grained CAIs from the Allende CV3 chondrite examined as part of this project. The phase occurs in Types A and B1 inclusions as small tabular crystals oriented along two mutually perpendicular planes in melilite. UNK crystallizes from melts in dynamic crystallization experiments conducted in air from four bulk compositions modeled after Types A, B1, B2 and C inclusions. Cooling rates resulting in crystallization of UNK ranged from 0.5 to 200 C/h from maximum (initial) temperatures of 1375 to 1580 C. Only below 1190 C does UNK itself begin to crystallize. To first order, the presence or absence of UNK from individual experiments can be understood in terms of the compositions of residual melts and nucleation probabilities. Compositions of synthetic and meteoritic LINK are very similar in terms of major oxides, differing only in the small amounts of trivalent Ti (7-13% of total Ti) in meteoritic samples. UNK crystallized from the Type A analog is similar texturally to that found in CAls, although glass, which is typically associated with synthetic UN& is not observed in meteoritic occurrences. A low Ti end-member of UNK ("Si-UNK") with a composition new that of Ca3Al2Si4O14 was produced in a few samples from the Type B1 analog. This phase has not been found in the meteoritic inclusions.

A new titanium-bearing calcium aluminosilicate phase. 1: Meteoritic occurrences and formation in synthetic systems

NASA Technical Reports Server (NTRS)

Paque, Julie M.; Beckett, John R.; Barber, David J.; Stolper, Edward M.

1994-01-01

A new titanium-bearing calcium aluminosilicate mineral has been identified in coarse-grained calcium-aluminum-rich inclusions (CAIs) from carbonaceous chondrites. The formula for this phase, which we have temporarily termed 'UNK,' is Ca3Ti(Al,Ti)2(Si,Al)3O14, and it is present in at least 8 of the 20 coarse-grained CAIs from the Allende CV3 chondrite examined as part of this project. The phase occurs in Types A and B1 inclusions as small tabular crystal oriented along two mutually perpendicular planes in melilite. UNK crystallizes from melts in dynamic crystallization experiments conducted in air from four bulk compositions modeled after Types A, B1, B2 and C inclusions. Cooling rates resulting in crystallization of UNK ranged from 0.5 to 200 C/h from maximum (initial) temperatures of 1375 to 1580 C. Only below 1190 C does UNK itself begin to crystallize. To first order, the presence or absence of UNK from individual experiments can be understood in terms of the compositions of residual melts and nucleation probabilities. Compositions of synthetic and meteoritic UNK are very similar in terms of major oxides, differing only in the small amounts of trivalent Ti(7-13% of total Ti) in meteoritic samples. UNK crystallized from the Type A analog is similar texturally to that found in CAIs, although glass, which is typically associated with synthetic UNK, is not observed in the meteoritic occurrences. A low Ti end-member of UNK ('Si-UNK') with a composition near that of Ca3Al2Si4O14 was produced in a few samples from the Type B1 analog. This phase has not been found in the meteoritic inclusions.

Planetary and meteoritic Mg/Si and δ30 Si variations inherited from solar nebula chemistry

NASA Astrophysics Data System (ADS)

Dauphas, Nicolas; Poitrasson, Franck; Burkhardt, Christoph; Kobayashi, Hiroshi; Kurosawa, Kosuke

2015-10-01

The bulk chemical compositions of planets are uncertain, even for major elements such as Mg and Si. This is due to the fact that the samples available for study all originate from relatively shallow depths. Comparison of the stable isotope compositions of planets and meteorites can help overcome this limitation. Specifically, the non-chondritic Si isotope composition of the Earth's mantle was interpreted to reflect the presence of Si in the core, which can also explain its low density relative to pure Fe-Ni alloy. However, we have found that angrite meteorites display a heavy Si isotope composition similar to the lunar and terrestrial mantles. Because core formation in the angrite parent-body (APB) occurred under oxidizing conditions at relatively low pressure and temperature, significant incorporation of Si in the core is ruled out as an explanation for this heavy Si isotope signature. Instead, we show that equilibrium isotopic fractionation between gaseous SiO and solid forsterite at ∼1370 K in the solar nebula could have produced the observed Si isotope variations. Nebular fractionation of forsterite should be accompanied by correlated variations between the Si isotopic composition and Mg/Si ratio following a slope of ∼1, which is observed in meteorites. Consideration of this nebular process leads to a revised Si concentration in the Earth's core of 3.6 (+ 6.0 / - 3.6) wt% and provides estimates of Mg/Si ratios of bulk planetary bodies.

Chondrule formation, metamorphism, brecciation, an important new primary chondrule group, and the classification of chondrules

NASA Technical Reports Server (NTRS)

Sears, Derek W. G.; Shaoxiong, Huang; Benoit, Paul H.

1995-01-01

The recently proposed compositional classification scheme for meteoritic chondrules divides the chondrules into groups depending on the composition of their two major phases, olivine (or pyroxene) and the mesostasis, both of which are genetically important. The scheme is here applied to discussions of three topics: the petrographic classification of Roosevelt County 075 (the least-metamorphosed H chondrite known), brecciation (an extremely important and ubiquitous process probably experienced by greater than 40% of all unequilibrated ordinary chondrites), and the group A5 chondrules in the least metamorphosed ordinary chondrites which have many similarities to chondrules in the highly metamorphosed 'equilibrated' chondrites. Since composition provides insights into both primary formation properties of the chondruies and the effects of metamorphism on the entire assemblage it is possible to determine the petrographic type of RC075 as 3.1 with unique certainty. Similarly, the near scheme can be applied to individual chondrules without knowledge of the petrographic type of the host chondrite, which makes it especially suitable for studying breccias. Finally, the new scheme has revealed the existence of chondrules not identified by previous techniques and which appear to be extremely important. Like group A1 and A2 chondrules (but unlike group B1 chondrules) the primitive group A5 chondruies did not supercool during formation, but unlike group A1 and A2 chondrules (and like group B1 chondrules) they did not suffer volatile loss and reduction during formation. It is concluded that the compositional classification scheme provides important new insights into the formation and history of chondrules and chondrites which would be overlooked by previous schemes.

Evidence against a chondritic Earth.

PubMed

Campbell, Ian H; O'Neill, Hugh St C

2012-03-28

The (142)Nd/(144)Nd ratio of the Earth is greater than the solar ratio as inferred from chondritic meteorites, which challenges a fundamental assumption of modern geochemistry--that the composition of the silicate Earth is 'chondritic', meaning that it has refractory element ratios identical to those found in chondrites. The popular explanation for this and other paradoxes of mantle geochemistry, a hidden layer deep in the mantle enriched in incompatible elements, is inconsistent with the heat flux carried by mantle plumes. Either the matter from which the Earth formed was not chondritic, or the Earth has lost matter by collisional erosion in the later stages of planet formation.

Fe-Ni metal and sulfide minerals in CM chondrites: An indicator for thermal history

USGS Publications Warehouse

Kimura, M.; Grossman, J.N.; Weisberg, M.K.

2011-01-01

CM chondrites were subjected to aqueous alteration and, in some cases, to secondary metamorphic heating. The effects of these processes vary widely, and have mainly been documented in silicate phases. Herein, we report the characteristic features of Fe-Ni metal and sulfide phases in 13 CM and 2 CM-related chondrites to explore the thermal history of these chondrites. The texture and compositional distribution of the metal in CM are different from those in unequilibrated ordinary and CO chondrites, but most have similarities to those in highly primitive chondrites, such as CH, CR, and Acfer 094. We classified the CM samples into three categories based on metal composition and sulfide texture. Fe-Ni metal in category A is kamacite to martensite. Category B is characterized by pyrrhotite grains always containing blebs or lamellae of pentlandite. Opaque mineral assemblages of category C are typically kamacite, Ni-Co-rich metal, and pyrrhotite. These categories are closely related to the degree of secondary heating and are not related to degree of the aqueous alteration. The characteristic features of the opaque minerals can be explained by secondary heating processes after aqueous alteration. Category A CM chondrites are unheated, whereas those in category B experienced small degrees of secondary heating. CMs in category C were subjected to the most severe secondary heating process. Thus, opaque minerals can provide constraints on the thermal history for CM chondrites. ?? The Meteoritical Society, 2011.

LEW85332: A C2 Chondrite in the CR Clan

NASA Astrophysics Data System (ADS)

Prinz, M.; Weisberg, M. K.; Brearley, A.; Grady, M. M.; Pillinger, C.; Clayton, R. N.; Mayeda, T. K.

1992-07-01

Introduction. LEW85332 was described as a unique C3 chondrite [1] and we undertook this study to learn more about its relationship to other carbonaceous chondrites. We find it to be a C2 chondrite with significant similarites to CR2 chondrites. This linkage extends to the ALH85085 [2] and Acfer 182 [3,4] chondrites, although there are some important differences among them. Petrologic and isotopic similarities define the CR clan, which consists of CR chondrites and their three relatives noted above (and Bencubbin). Some differences are due to major component abundances (chondrules, matrix, metal), and some to minor differences between components, but the similarities are greater and define the clan. Results. Petrogically, LEW85332 has over 60% (vol) chondrules, about 30% matrix and matrix clasts, and about 4-7% metal. Extensive weathering makes modal abundances uncertain. Chondrules are anhydrous, about 170 micrometers wide [1] and of all textural types. ALH85085 chondrules average 20 micrometers and are mainly pyroxene-rich, whereas Acfer 182 is more like LEW85332. Matrix is hydrous and occurs as interstitial matrix, matrix clasts, and chondrule rims [5]. The matrix contains phyllosilicates and magnetite framboids. Matrix clasts are not foreign [1], but part of the chondrite, making it C2. This is also the case for Acfer 182 [3], and perhaps ALH85085. Phyllosilicates are mainly saponite and serpentine [5], and their composition is similar to that in CR chondrites. The water/rock ratio was low. Metal abundances in LEW85332 [1] are lower than in Acfer 182 (9.3 vol%) [4] and ALH85085 (22%) [6]. However, FeNi composition is the same, with a positive Ni-Co trend equivalent to the solar abundance ratio. This is the same as that in CR chondrites [7]. LEW85332 contains 0.5% carbon, combusting between 200 and 500 degrees C, indicating fine-grained, poorly crystalline carbon, or organic material. It contains 259 ppm nitrogen with delta^15N = +249o/oo. Most nitrogen is released between 200 and 500 degrees C, but at 325 C the delta^15N reaches +306o/oo indicating at least two N-bearing components with differing C/N atomic ratios. The LEW85332 nitrogen isotopic composition is intermediate between ALH85085, Acfer 182 and CR chondrites, closer to CR. The extremely heavy, high- temperature component found in ALH85085 is absent (or nearly so) in LEW85332. Nitrogen abundance is similar to ALH85085, but lower than in CRs. The oxygen isotopic composition of LEW85332 is delta^18O = -0.92, delta^17O = -1.93. This, plus ALH85085 and Acfer 182 define a line (figure) identical to that of the CR chondrite mixing line (slope = 0.7) [7]. The composition of LEW85332 is close to that of unaltered olivine and pyroxene in Renazzo and Al Rais. Conclusions. (1) The important similarities between components in LEW85332 and CR2 chondrites put it in the CR clan. (2) Recognition of LEW85332, Acfer 182, and ALH85085 as relatives in the CR clan indicates that carbonaceous chondrites can no longer be classified only into coherent groups with highly similar characteristics. Recognition of clan relationships will be needed for IDPs and micrometeorites. (3) LEW85332, Acfer 182, and ALH85085 contain hydrous matrices and anhydrous chondrules, and the implications of this observation requires further study. References. [1] Rubin, A.E. and Kallemeyn, G.W. (1990) Meteoritics 25, 215-225. [2] Weisberg, M.K. et al. (1990) Meteoritics 25, 269-279. [3] Prinz, M. and Weisberg, M.K. (1992) LPSCXXIII, 1109-1110. [4] Bischoff, A. et al. (1992) Acfer 182 ms. GCA (in press). [5] Brearley, A.J. (1992) LPSCXXIII, 155-156. [6] Weisberg, M.K. et al. (1988) EPSL 91, 19-32. [7] Weisberg, M.K. et al. (1992) CR chondrite ms. GCA (in press).

Australasian microtektites: Impactor identification using Cr, Co and Ni ratios

NASA Astrophysics Data System (ADS)

Folco, L.; Glass, B. P.; D'Orazio, M.; Rochette, P.

2018-02-01

Impactor identification is one of the challenges of large-scale impact cratering studies due to the dilution of meteoritic material in impactites (typically < 1 wt%). The nature of the impactor that generated the Australasian tektite/microtektite strewn field, i.e., the largest Cenozoic strewn field (∼15% of the Earth's surface), the youngest (∼0.78 Myr old) on Earth, and the only one without an associated impact crater so far, is an outstanding issue. We identify a chondritic impactor signature in 77 Australasian microtektites (size range: ∼200-700 μm) from within 3000 km from the hypothetical impact location in Indochina (∼17°N, 107°E) based on variations of Cr, Co and Ni interelement ratios in a Co/Ni vs Cr/Ni space (46 microtektites analyzed in this work by Laser Ablation-Inductively Coupled Plasma -Mass Spectrometry and 31 from literature by means of Neutron Activation Analyses with Cr, Co and Ni concentrations up to ∼370, 50 and 680 μg/g, respectively). Despite substantial overlap in Cr/Ni versus Co/Ni composition for several meteorite types with chondritic composition (chondrites and primitive achondrites), regression calculation based on ∼85% of the studied microtektites best fit a mixing line between crustal compositions and an LL chondrite. However, due to some scatter mainly in the Cr versus Ni ratios in the considered dataset, an LL chondrite may not be the best fit to the data amongst impactors of primitive compositions. Eight high Ni/Cr and five low Ni/Cr outlier microtektites (∼15% in total) deviate from the above mixing trend, perhaps resulting from incomplete homogenization of heterogeneous impactor and target precursor materials at the microtektite scale, respectively. Together with previous evidence from the ∼35 Myr old Popigai impact spherules and the ∼1 Myr old Ivory Coast microtektites, our finding suggests that at least three of the five known Cenozoic distal impact ejecta were generated by the impacts of large stony asteroids of chondritic composition, and possibly of ordinary chondritic composition. The impactor signature found in Australasian microtektites documents mixing of target and impactor melts upon impact cratering. This requires target-impactor mixing in both the two competing models in literature for the formation of the Australasian tektites/microtektites: the impact cratering and low-altitude airburst plume models.

The classification and complex thermal history of the enstatite chondrites

NASA Technical Reports Server (NTRS)

Zhang, Yanhong; Benoit, Paul H.; Sears, Derek W. G.

1995-01-01

We have carried out instrumental neutron activation analysis of 11 enstatite chondrites and electron microprobe analyses of 17 enstatite chondrites, most of which were previously little described. We report here the third known EH5 chondrite (LEW 88180) and an unusual EL6 chondrite (LEW 87119), new data on four EL3 chondrites (ALH 85119, EET 90299, PCA 91020, and MAC 88136, which is paired with MAC 88180 and MAC 88184), the second EL5 chondrite (TIL 91714), and an unusual metal-rich and sulfide-poor EL3 chondrite (LEW 87223). The often discussed differences in mineral composition displayed by the EH and EL chondrites are not as marked after the inclusion of the new samples in the database, and the two classes apparently experienced a similar range of equilibrium temperatures. However, texturally the EL chondrites appear to have experienced much higher levels of metamorphic alteration than EH chondrites of similar equilibration temperatures. Most of the petrologic type criteria are not applicable to enstatite chondrites and, unlike the ordinary chondrites, texture and mineralogy reflect different aspects of the meteorite history. We therefore propose that the existing petrologic type scheme not be used for enstatite chondrites. We suggest that while 'textural type' reflects peak metamorphic temperatures, the 'mineralogical type' reflects equilibration during postmetamorphic (probably regolith) processes. Unlike the ordinary chondrites and EH chondrites, EL chondrites experienced an extensive low-temperature metamorphic episode. There are now a large number of enstatite meteorite breccias and impact melts, and apparently surface processes were important in determining the present nature of the enstatite chondrites.

Exploring Chondrule and CAI Rims Using Micro- and Nano-Scale Petrological and Compositional Analysis

NASA Astrophysics Data System (ADS)

Cartwright, J. A.; Perez-Huerta, A.; Leitner, J.; Vollmer, C.

2017-12-01

As the major components within chondrites, chondrules (mm-sized droplets of quenched silicate melt) and calcium-aluminum-rich inclusions (CAI, refractory) represent the most abundant and the earliest materials that solidified from the solar nebula. However, the exact formation mechanisms of these clasts, and whether these processes are related, remains unconstrained, despite extensive petrological and compositional study. By taking advantage of recent advances in nano-scale tomographical techniques, we have undertaken a combined micro- and nano-scale study of CAI and chondrule rim morphologies, to investigate their formation mechanisms. The target lithologies for this research are Wark-Lovering rims (WLR), and fine-grained rims (FGR) around CAIs and chondrules respectively, present within many chondrites. The FGRs, which are up to 100 µm thick, are of particular interest as recent studies have identified presolar grains within them. These grains predate the formation of our Solar System, suggesting FGR formation under nebular conditions. By contrast, WLRs are 10-20 µm thick, made of different compositional layers, and likely formed by flash-heating shortly after CAI formation, thus recording nebular conditions. A detailed multi-scale study of these respective rims will enable us to better understand their formation histories and determine the potential for commonality between these two phases, despite reports of an observed formation age difference of up to 2-3 Myr. We are using a combination of complimentary techniques on our selected target areas: 1) Micro-scale characterization using standard microscopic and compositional techniques (SEM-EBSD, EMPA); 2) Nano-scale characterization of structures using transmission electron microscopy (TEM) and elemental, isotopic and tomographic analysis with NanoSIMS and atom probe tomography (APT). Preliminary nano-scale APT analysis of FGR morphologies within the Allende carbonaceous chondrite has successfully discerned complex chondritic mineralogies and compositional differences across boundaries, which is one of the first applications of in-situ APT techniques to chondrites. Further data reduction will allow us to characterize the exact phases present, and further chondrite analyses are in progress.

Chromium isotopic homogeneity between the Moon, the Earth, and enstatite chondrites

NASA Astrophysics Data System (ADS)

Mougel, Bérengère; Moynier, Frédéric; Göpel, Christa

2018-01-01

Among the elements exhibiting non-mass dependent isotopic variations in meteorites, chromium (Cr) has been central in arguing for an isotopic homogeneity between the Earth and the Moon, thus questioning physical models of Moon formation. However, the Cr isotopic composition of the Moon relies on two samples only, which define an average value that is slightly different from the terrestrial standard. Here, by determining the Cr isotopic composition of 17 lunar, 9 terrestrial and 5 enstatite chondrite samples, we re-assess the isotopic similarity between these different planetary bodies, and provide the first robust estimate for the Moon. In average, terrestrial and enstatite samples show similar ε54Cr. On the other hand, lunar samples show variables excesses of 53Cr and 54Cr compared to terrestrial and enstatite chondrites samples with correlated ε53Cr and ε54Cr (per 10,000 deviation of the 53Cr/52Cr and 54Cr/52Cr ratios normalized to the 50Cr/52Cr ratio from the NIST SRM 3112a Cr standard). Unlike previous suggestions, we show for the first time that cosmic irradiation can affect significantly the Cr isotopic composition of lunar materials. Moreover, we also suggest that rather than spallation reactions, neutron capture effects are the dominant process controlling the Cr isotope composition of lunar igneous rocks. This is supported by the correlation between ε53Cr and ε54Cr, and 150Sm/152Sm ratios. After correction of these effects, the average ε54Cr of the Moon is indistinguishable from the terrestrial and enstatite chondrite materials reinforcing the idea of an Earth-Moon-enstatite chondrite system homogeneity. This is compatible with the most recent scenarios of Moon formation suggesting an efficient physical homogenization after a high-energy impact on a fast spinning Earth, and/or with an impactor originating from the same reservoir in the inner proto-planetary disk as the Earth and enstatite chondrites and having similar composition.

Boulders on Ceres

NASA Technical Reports Server (NTRS)

Schroder, S. E.; Carsenty, U.; Neesemann, A.; Jaumann, R.; Marchi, S.; Mcfadden, L. A.; Otto, K.; Schenk, P.; Schulzeck, F.; Raymond, C. A.;

Elemental compositions of two extrasolar rocky planetesimals

DOE Office of Scientific and Technical Information (OSTI.GOV)

Xu, S.; Jura, M.; Klein, B.

2014-03-10

We report Keck/HIRES and Hubble Space Telescope/COS spectroscopic studies of extrasolar rocky planetesimals accreted onto two hydrogen atmosphere white dwarfs, G29-38 and GD 133. In G29-38, eight elements are detected, including C, O, Mg, Si, Ca, Ti, Cr, and Fe while in GD 133, O, Si, Ca, and marginally Mg are seen. These two extrasolar planetesimals show a pattern of refractory enhancement and volatile depletion. For G29-38, the observed composition can be best interpreted as a blend of a chondritic object with some refractory-rich material, a result from post-nebular processing. Water is very depleted in the parent body accreted ontomore » G29-38, based on the derived oxygen abundance. The inferred total mass accretion rate in GD 133 is the lowest of all known dusty white dwarfs, possibly due to non-steady state accretion. We continue to find that a variety of extrasolar planetesimals all resemble to zeroth order the elemental composition of bulk Earth.« less

The thermal and physical characteristics of the Gao-Guenie (H5) meteorite

NASA Astrophysics Data System (ADS)

Beech, Martin; Coulson, Ian M.; Nie, Wenshuang; McCausland, Phil

2009-06-01

Measurements of the bulk density, grain density, porosity, and magnetic susceptibility of 19 Gao-Guenie H5 chondrite meteorite samples are presented. We find average values of bulk density < ρbulk>=3.46±0.07 g/cm 3, grain density < ρgrain>=3.53±0.08 g/cm 3, porosity < P(%)>=2.46±1.39, and bulk mass magnetic susceptibility =5.23±0.11. Measurements of the specific heat capacity for a 3.01-g Gao-Guenie sample, a 61.37-g Gao-Guenie sample, a 62.35-g Jilin H5 chondrite meteorite sample, and a 51.37-g Sikhote-Alin IIAB Iron meteorite sample are also presented. Temperature interpolation formula are further provided for the specific heat capacity, thermal conductivity, and thermal diffusivity of the 3.01-g Gao-Guenie sample in the temperature range 300< T (K)<800. We briefly review the possible effects of the newly deduced specific heat and thermal conductivity values on the ablation of meteoroids within the Earth's atmosphere, the modeling of asteroid interiors and the orbital evolution of meteoroids through the Yarkovsky-O'Keefe-Radzievskii-Paddack (YORP) effect.

Osmium Isotope Evidence for an S-Process Carrier in Primitive Chondrites

NASA Technical Reports Server (NTRS)

Brandon, A. D.; Puchtel, I. S.; Humayun, M.; Zolensky, M.

2005-01-01

The degree of isotopic mixing in the solar nebula and the nature of pre-solar components that have contributed to our solar system remain subjects of vigorous debate. Isotopic anomalies have been identified in Ca-Al inclusions in chondrites [1-4]. This indicates that refractory pre-solar components were not completely homogenized or processed away at the high temperatures experienced by CAIs. Pre-solar grains (SiC, C, etc.) are prevalent in primitive chondrites, and preserve isotopic heterogeneity resulting from the nucleosynthetic processes occurring in the stars from which these grains formed [2,4]. Several recent studies employing precise techniques for measuring Ru, Mo and Zr isotopes in bulk meteorites, have come up with varying conclusions on the degree of effectiveness of nebular mixing on the scale of bulk meteorite material. Some of these studies have reported isotopic anomalies in Mo and Ru [3,5-7], while others have not observed anomalies in Mo, Ru, or Zr [8-10]. Debate over the quality of the data, the normalization techniques employed, the absence or presence of isobaric interferences during the measurements on different types of instruments (e.g. TIMS versus ICP-MS), and other factors, has ensued [11,12].

Iron Isotopes in Meteorites

NASA Astrophysics Data System (ADS)

Kehm, K.; Alexander, C. M.; Hauri, E. H.

2001-12-01

The recent identification of naturally occurring isotopic mass fractionation of the transition met-als on the Earth has prompted a search for similar variability in meteorites. Studies of Cu, Zn, and Fe, for example, have revealed per-mil level and larger mass fractionations between different bulk meteorites. Such variations can result from temperature-sensitive isotope exchange reactions and kinetic processes, and therefore may reflect conditions in the solar nebula and on meteorite parent bodies. Recent advances in ICP-MS have permitted isotope studies of transition metals and other elements with similarly small isotopic mass dispersions. Among the transition metals, Fe is perhaps the most difficult to analyze by ICP-MS because plasma sources are copious producers of argide molecules that interfere with the measurement of iron isotopes. However, the stable isotope behavior of Fe is of special interest because it is a non-refractory major element in meteorites, present in a variety of mineral associations and redox states. Considerable effort has gone into overcoming the inherent analytical difficulties of measuring Fe using ICP-MS. We recently reported on a technique that achieves argide reduction by operating the plasma source in so-called 'cold' mode. In this presentation, we report results from this ongoing work. To date, analyses of nine different meteorites, and eight individual Tieschitz (H3) chondrules have been completed, along with a number of measurements of the Hawaiian basalt sample Kil1919. All of the bulk meteorite compositions, which include both chondrites and irons, have identical 56Fe/54Fe to within ~ 0.14 per mil (2 sigma), and are indistinguishable from the composition of the terrestrial basalt. The Tieschitz chondrules, on the other hand, tend to have isotopically light compositions. This could reflect formation from fractionated starting material. Alternatively, Fe condensation, under non-equilibrium conditions can enrich light isotopes. Future work will focus on determining the extent of Fe mass fractionation in chondrules from Tieschitz as well as other chondrites. This growing database will help us to understand the conditions in which chondrules formed, potentially placing stringent constraints on theories of their formation.

Hydrothermal Habitats: Measurements of Bulk Microbial Elemental Composition, and Models of Hydrothermal Influences on the Evolution of Dwarf Planets

NASA Astrophysics Data System (ADS)

Neveu, Marc Francois Laurent

Finding habitable worlds is a key driver of solar system exploration. Many solar system missions seek environments providing liquid water, energy, and nutrients, the three ingredients necessary to sustain life. Such environments include hydrothermal systems, spatially-confined systems where hot aqueous fluid circulates through rock by convection. I sought to characterize hydrothermal microbial communities, collected in hot spring sediments and mats at Yellowstone National Park, USA, by measuring their bulk elemental composition. To do so, one must minimize the contribution of non-biological material to the samples analyzed. I demonstrate that this can be achieved using a separation method that takes advantage of the density contrast between cells and sediment and preserves cellular elemental contents. Using this method, I show that in spite of the tremendous physical, chemical, and taxonomic diversity of Yellowstone hot springs, the composition of microorganisms there is surprisingly ordinary. This suggests the existence of a stoichiometric envelope common to all life as we know it. Thus, future planetary investigations could use elemental fingerprints to assess the astrobiological potential of hydrothermal settings beyond Earth. Indeed, hydrothermal activity may be widespread in the solar system. Most solar system worlds larger than 200 km in radius are dwarf planets, likely composed of an icy, cometary mantle surrounding a rocky, chondritic core. I enhance a dwarf planet evolution code, including the effects of core fracturing and hydrothermal circulation, to demonstrate that dwarf planets likely have undergone extensive water-rock interaction. This supports observations of aqueous products on their surfaces. I simulate the alteration of chondritic rock by pure water or cometary fluid to show that aqueous alteration feeds back on geophysical evolution: it modifies the fluid antifreeze content, affecting its persistence over geological timescales; and the distribution of radionuclides, whose decay is a chief heat source on dwarf planets. Interaction products can be observed if transported to the surface. I simulate numerically how cryovolcanic transport is enabled by primordial and hydrothermal volatile exsolution. Cryovolcanism seems plausible on dwarf planets in light of images recently returned by spacecrafts. Thus, these coupled geophysical-geochemical models provide a comprehensive picture of dwarf planet evolution, processes, and habitability.

The Oxygen Isotope Composition of Dark Inclusions in HEDs, Ordinary and Carbonaceous Chondrites

NASA Technical Reports Server (NTRS)

Greenwood, R. C.; Zolensky, M. E.; Buchanan, P. C.; Franchi, I. A.

2015-01-01

Dark inclusions (DIs) are lithic fragments that form a volumetrically small, but important, component in carbonaceous chondrites. Carbonaceous clasts similar to DIs are also found in some ordinary chondrites and HEDs. DIs are of particular interest because they provide a record of nebular and planetary processes distinct from that of their host meteorite. DIs may be representative of the material that delivered water and other volatiles to early Earth as a late veneer. Here we focus on the oxygen isotopic composition of DIs in a variety of settings with the aim of understanding their formational history and relationship to the enclosing host meteorite.

Non-LTE spectral models for the gaseous debris-disk component of Ton 345

NASA Astrophysics Data System (ADS)

Hartmann, S.; Nagel, T.; Rauch, T.; Werner, K.

2014-11-01

Context. For a fraction of single white dwarfs with debris disks, an additional gaseous disk was discovered. Both dust and gas are thought to be created by the disruption of planetary bodies. Aims: The composition of the extrasolar planetary material can directly be analyzed in the gaseous disk component, and the disk dynamics might be accessible by investigating the temporal behavior of the Ca ii infrared emission triplet, hallmark of the gas disk. Methods: We obtained new optical spectra for the first helium-dominated white dwarf for which a gas disk was discovered (Ton 345) and modeled the non-LTE spectra of viscous gas disks composed of carbon, oxygen, magnesium, silicon, sulfur, and calcium with chemical abundances typical for solar system asteroids. Iron and its possible line-blanketing effects on the model structure and spectral energy distribution was still neglected. A set of models with different radii, effective temperatures, and surface densities as well as chondritic and bulk-Earth abundances was computed and compared with the observed line profiles of the Ca ii infrared triplet. Results: Our models suggest that the Ca ii emission stems from a rather narrow gas ring with a radial extent of R = 0.44-0.94 R⊙, a uniform surface density Σ = 0.3 g cm-2, and an effective temperature of Teff ≈ 6000 K. The often assumed chemical mixtures derived from photospheric abundances in polluted white dwarfs - similar to a chondritic or bulk-Earth composition - produce unobserved emission lines in the model and therefore have to be altered. We do not detect any line-profile variability on timescales of hours, but we confirm the long-term trend over the past decade for the red-blue asymmetry of the double-peaked lines. Based on observations collected at the Centro Astronómico Hispano Alemán (CAHA) at Calar Alto, operated jointly by the Max-Planck-Institut für Astronomie and the Instituto de Astrofísica de Andalucía (CSIC).

Highly siderophile elements in chondrites

USGS Publications Warehouse

Horan, M.F.; Walker, R.J.; Morgan, J.W.; Grossman, J.N.; Rubin, A.E.

2003-01-01

The abundances of the highly siderophile elements (HSE), Re, Os, Ir, Ru, Pt and Pd, were determined by isotope dilution mass spectrometry for bulk samples of 13 carbonaceous chondrites, 13 ordinary chondrites and 9 enstatite chondrites. These data are coupled with corresponding 187Re-187Os isotopic data reported by Walker et al. [Geochim. Cosmochim. Acta, 2002] in order to constrain the nature and timing of chemical fractionation relating to these elements in the early solar system. The suite of chondrites examined displays considerable variations in absolute abundances of the HSE, and in the ratios of certain HSE. Absolute abundances of the HSE vary by nearly a factor of 80 among the chondrite groups, although most vary within a factor of only 2. Variations in concentration largely reflect heterogeneities in the sample aliquants. Different aliquants of the same chondrite may contain variable proportions of metal and/or refractory inclusions that are HSE-rich, and sulfides that are HSE-poor. The relatively low concentrations of the HSE in CI1 chondrites likely reflect dilution by the presence of volatile components. Carbonaceous chondrites have Re/Os ratios that are, on average, approximately 8% lower than ratios for ordinary and enstatite chondrites. This is also reflected in 187Os/188Os ratios that are approximately 3% lower for carbonaceous chondrites than for ordinary and enstatite chondrites. Given the similarly refractory natures of Re and Os, this fractionation may have occurred within a narrow range of high temperatures, during condensation of these elements from the solar nebula. Superimposed on this major fractionation are more modest movements of Re or Os that occurred within the last 0-2 Ga, as indicated by minor open-system behavior of the Re-Os isotope systematics of some chondrites. The relative abundances of other HSE can also be used to discriminate among the major classes of chondrites. For example, in comparison to the enstatite chondrites, carbonaceous and ordinary chondrites have distinctly lower ratios of Pd to the more refractory HSE (Re, Os, Ir, Ru and Pt). Differences are particularly well resolved for the EH chondrites that have Pd/Ir ratios that average more than 40% higher than for carbonaceous and ordinary chondrite classes. This fractionation probably occurred at lower temperatures, and may be associated with fractionation processes that also affected the major refractory lithophile elements. Combined, 187Os/188Os ratios and HSE ratios reflect unique early solar system processing of HSE for each major chondrite class. ?? 2002 Elsevier Science B.V. All rights reserved.

Distribution of p-process 174Hf in early solar system materials and the origin of nucleosynthetic Hf and W isotope anomalies in Ca-Al rich inclusions

NASA Astrophysics Data System (ADS)

Peters, Stefan T. M.; Münker, Carsten; Pfeifer, Markus; Elfers, Bo-Magnus; Sprung, Peter

2017-02-01

Some nuclides that were produced in supernovae are heterogeneously distributed between different meteoritic materials. In some cases these heterogeneities have been interpreted as the result of interaction between ejecta from a nearby supernova and the nascent solar system. Particularly in the case of the oldest objects that formed in the solar system - Ca-Al rich inclusions (CAIs) - this view is confirm the hypothesis that a nearby supernova event facilitated or even triggered solar system formation. We present Hf isotope data for bulk meteorites, terrestrial materials and CAIs, for the first time including the low-abundance isotope 174Hf (∼0.16%). This rare isotope was likely produced during explosive O/Ne shell burning in massive stars (i.e., the classical "p-process"), and therefore its abundance potentially provides a sensitive tracer for putative heterogeneities within the solar system that were introduced by supernova ejecta. For CAIs and one LL chondrite, also complementary W isotope data are reported for the same sample cuts. Once corrected for small neutron capture effects, different chondrite groups, eucrites, a silicate inclusion of a IAB iron meteorite, and terrestrial materials display homogeneous Hf isotope compositions including 174Hf. Hafnium-174 was thus uniformly distributed in the inner solar system when planetesimals formed at the <50 ppm level. This finding is in good agreement with the evidently homogeneous distributions of p-process isotopes 180W, 184Os and possibly 190Pt between different iron meteorite groups. In contrast to bulk meteorite samples, CAIs show variable depletions in p-process 174Hf with respect to the inner solar system composition, and also variable r-process (or s-process) Hf and W contributions. Based on combined Hf and W isotope compositions, we show that CAIs sampled at least one component in which the proportion of r- and s-process derived Hf and W deviates from that of supernova ejecta. The Hf and W isotope anomalies in CAIs are therefore best explained by selective processing of presolar carrier phases prior to CAI formation, and not by a late injection of supernova materials. Likewise, other isotope anomalies in additional elements in CAIs relative to the bulk solar system may reflect the same process. The isotopic heterogeneities between the first refractory condensates may have been eradicated partially during CAI formation, because W isotope anomalies in CAIs appear to decrease with increasing W concentrations as inferred from time-integrated 182W/184W. Importantly, the 176Lu-176Hf and 182Hf-182W chronometers are not significantly affected by nucleosynthetic heterogeneity of Hf isotopes in bulk meteorites, but may be affected in CAIs.

Silicon Isotopic Fractionation of CAI-like Vacuum Evaporation Residues

DOE Office of Scientific and Technical Information (OSTI.GOV)

Knight, K; Kita, N; Mendybaev, R

2009-06-18

Calcium-, aluminum-rich inclusions (CAIs) are often enriched in the heavy isotopes of magnesium and silicon relative to bulk solar system materials. It is likely that these isotopic enrichments resulted from evaporative mass loss of magnesium and silicon from early solar system condensates while they were molten during one or more high-temperature reheating events. Quantitative interpretation of these enrichments requires laboratory determinations of the evaporation kinetics and associated isotopic fractionation effects for these elements. The experimental data for the kinetics of evaporation of magnesium and silicon and the evaporative isotopic fractionation of magnesium is reasonably complete for Type B CAI liquidsmore » (Richter et al., 2002, 2007a). However, the isotopic fractionation factor for silicon evaporating from such liquids has not been as extensively studied. Here we report new ion microprobe silicon isotopic measurements of residual glass from partial evaporation of Type B CAI liquids into vacuum. The silicon isotopic fractionation is reported as a kinetic fractionation factor, {alpha}{sub Si}, corresponding to the ratio of the silicon isotopic composition of the evaporation flux to that of the residual silicate liquid. For CAI-like melts, we find that {alpha}{sub Si} = 0.98985 {+-} 0.00044 (2{sigma}) for {sup 29}Si/{sup 28}Si with no resolvable variation with temperature over the temperature range of the experiments, 1600-1900 C. This value is different from what has been reported for evaporation of liquid Mg{sub 2}SiO{sub 4} (Davis et al., 1990) and of a melt with CI chondritic proportions of the major elements (Wang et al., 2001). There appears to be some compositional control on {alpha}{sub Si}, whereas no compositional effects have been reported for {alpha}{sub Mg}. We use the values of {alpha}Si and {alpha}Mg, to calculate the chemical compositions of the unevaporated precursors of a number of isotopically fractionated CAIs from CV chondrites whose chemical compositions and magnesium and silicon isotopic compositions have been previously measured.« less

On the chemical composition of L-chondrites

NASA Technical Reports Server (NTRS)

Neal, C. W.; Dodd, R. T.; Jarosewich, E.; Lipschutz, M. E.

1980-01-01

Radiochemical neutron activation analysis of Ag, As, Au, Bi, Co, Cs, Ga, In, Rb, Sb, Te, Tl, and Zn and major element data in 14 L4-6 and 3 LL5 chondrites indicates that the L group is unusually variable and may represent at least 2 subgroups differing in formation history. Chemical trends in the S/Fe rich subgroup support textural evidence indicating late loss of a shock formed Fe-Ni-S melt; the S/Fe poor subgroup seemingly reflects nebular fractionation only. Highly mobile In and Zn apparently reflect shock induced loss from L chondrites. However, contrasting chemical trends in several L chondrite sample sets indicate that these meteorites constitute a more irregular sampling of, or more heterogeneous parent material than do carbonaceous or enstatite chondrites. Data for 15 chondrites suggest higher formation temperatures and/or degrees of shock than for LL5 chondrites.

Antarctic Meteorite Newsletter, Volume 29, Number 1

NASA Technical Reports Server (NTRS)

Satterwhite, Cecilia (Editor); Righter, Kevin (Editor)

2006-01-01

This newsletter contains classifications for 597 new meteorites from the 2003 and 2004 ANtarctic Search for METeorites (ANSMET) seasons. They include samples from the Cumulus Hills, Dominion Range, Grosvenor Mountains, LaPaz Icefield, MacAlpine Hills, and the Miller Range. Macroscopic and petrographic descriptions are given for 25 of the new meteorites: 1 acapulcoite/Iodranite, 1 howardite, 1 diogenite, 2 eucrites, 1 enstatite chondrite, four L3 and two H3 chondrites, 2 CM, 3 CK and 1 CV chondrites, three R chondrites, and four impact melt breccias (with affinities for H and L). Likely the most interesting sample announced in this newsletter is LAP04840, with affinity to R chondrites. This meteorite contains approximately 15% horneblende, and has mineral compositional ranges and oxygen isotopic values similar to those of R chondrites. The presence of an apparently hydrous phase in this petrologic grade 6 chondrite is very unusual, and should be of great interest to many meteoriticists.

Petrology and In Situ Trace Element Chemistry of a Suite of R Chondrites

NASA Technical Reports Server (NTRS)

Mittlefehldt, D. W.; Peng, Z. X.; Torrano, Z. A.

2015-01-01

Rumuruti (R) chondrites are characterized by low chondrule/matrix modal ratios, high oxidation state, small mean chondrule size, abundant sulfides and low metal contents, and are of petrologic types 3 to 6 [1, 2]. LAP 04840 (R5, [3]) and MIL 11207 (R6), contain the high-T hydrous phases amphibole and mica [3, 4]; not all equilibrated R chondrites contain these [2]. R chondrites thus can provide evidence on whether there are compositional effects caused by high-T, high-fluid metamorphism of nebular materials. We are investigating a suite of R chondrites of diverse petrologic grades to further understand the nature of the metamorphic processes that engendered them [5]. We report on our petrological studies, plus preliminary in situ analyses of trace elements in amphibole-bearing R chondrites.

A mutli-technique search for the most primitive CO chondrites

NASA Astrophysics Data System (ADS)

Alexander, C. M. O'D.; Greenwood, R. C.; Bowden, R.; Gibson, J. M.; Howard, K. T.; Franchi, I. A.

2018-01-01

As part of a study to identify the most primitive COs and to look for weakly altered CMs amongst the COs, we have conducted a multi-technique study of 16 Antarctic meteorites that had been classified as primitive COs. For this study, we have determined: (1) the bulk H, C and N abundances and isotopes, (2) bulk O isotopic compositions, (3) bulk modal mineralogies, and (4) for some selected samples the abundances and compositions of their insoluble organic matter (IOM). Two of the 16 meteorites do appear to be CMs - BUC 10943 seems to be a fairly typical CM, while MIL 090073 has probably been heated. Of the COs, DOM 08006 appears to be the most primitive CO identified to date and is quite distinct from the other members of its pairing group. The other COs fall into two groups that are less primitive than DOM 08006 and ALH 77307, the previously most primitive CO. The first group is composed of members of the DOM 08004 pairing group, except DOM 08006. The second group is composed of meteorites belonging to the MIL 03377 and MIL 07099 pairing groups. These two pairing groups should probably be combined. There is a dichotomy in the bulk O isotopes between the primitive (all Antarctic finds) and the more metamorphosed COs (mostly falls). This dichotomy can only partly be explained by the terrestrial weathering experienced by the primitive Antarctic samples. It seems that the more equilibrated samples interacted to a greater extent with 16O-poor material, probably water, than the more primitive meteorites.

Primitive ultrafine matrix in ordinary chondrites

NASA Technical Reports Server (NTRS)

Rambaldi, E. R.; Fredriksson, B. J.; Fredriksson, K.

1981-01-01

Ultrafine matrix material has been concentrated by sieving and filtering disaggregated samples of six ordinary chondrites of different classes. This component(s), 'Holy Smoke' (HS), is enriched in both volatile, e.g. Na, K, Zn, Sb, and Pb, as well as refractory elements, e.g. W and REE; however, the element ratios vary greatly among the different chondrites. SEM studies show that HS contains fragile crystals, differing in composition, and apparently in gross disequilibrium not only among themselves but also with the major mineral phases and consequently thermodynamic equilibration did not occur. Thus HS must have originated from impacting bodies and/or was inherent in the 'primitive' regolith. Subsequent impact brecciation and reheating appears to have altered, to varying degrees, the original composition of this ultrafine matrix material. Recent 'cosmic dust' studies may indicate that HS still exists in the solar system. Survival of such delicate material must be considered in all theories for the origin of chondrites.

Origin and history of chondrite regolith, fragmental and impact-melt breccias from Spain

NASA Technical Reports Server (NTRS)

Casanova, I.; Keil, K.; Wieler, R.; San Miguel, A.; King, E. A.

1990-01-01

Six ordinary chondrite breccias from the Museo Nacional de Ciencias Naturales, Madrid (Spain), are described and classified as follows: the solar gas-rich regolith breccia Oviedo (H5); the premetamorphic fragmental breccias Cabezo de Mayo (type 6, L-LL), and Sevilla (LL4); the fragmental breccias Canellas (H4) and Gerona (H5); and the impact melt breccia, Madrid (L6). It is confirmed that chondrites with typical light-dark structures and petrographic properties typical of regolith breccias may (Oviedo) or may not (Canellas) be solar gas-rich. Cabezo de Mayo and Sevilla show convincing evidence that they were assembled prior to peak metamorphism and were equilibrated during subsequent reheating. Compositions of olivine and low-Ca pyroxene in host chondrite and breccia clasts in Cabezo de Mayo are transitional between groups L and LL. It is suggested, based on mineralogic and oxygen isotopic compositions of host and clasts, that the rock formed on the L parent body by mixing, prior to peak metamorphism. This was followed by partial equilibrium of two different materials: the indigenous L chondrite host and exotic LL melt rock clasts.

Origin and history of chondrite regolith, fragmental and impact-melt breccias from Spain

NASA Astrophysics Data System (ADS)

Casanova, I.; Keil, K.; Wieler, R.; San Miguel, A.; King, E. A.

1990-06-01

Six ordinary chondrite breccias from the Museo Nacional de Ciencias Naturales, Madrid (Spain), are described and classified as follows: the solar gas-rich regolith breccia Oviedo (H5); the premetamorphic fragmental breccias Cabezo de Mayo (type 6, L-LL), and Sevilla (LL4); the fragmental breccias Canellas (H4) and Gerona (H5); and the impact melt breccia, Madrid (L6). It is confirmed that chondrites with typical light-dark structures and petrographic properties typical of regolith breccias may (Oviedo) or may not (Canellas) be solar gas-rich. Cabezo de Mayo and Sevilla show convincing evidence that they were assembled prior to peak metamorphism and were equilibrated during subsequent reheating. Compositions of olivine and low-Ca pyroxene in host chondrite and breccia clasts in Cabezo de Mayo are transitional between groups L and LL. It is suggested, based on mineralogic and oxygen isotopic compositions of host and clasts, that the rock formed on the L parent body by mixing, prior to peak metamorphism. This was followed by partial equilibrium of two different materials: the indigenous L chondrite host and exotic LL melt rock clasts.

SXRF determination of trace elements in chondrule rims in the unequilibrated CO3 chondrite, ALH A77307

NASA Technical Reports Server (NTRS)

Brearley, Adrian J.; Bajt, Sasa; Sutton, Steve R.; Papike, J. J.

1993-01-01

The concentrations of Ni, Cu, Zn, Ga, Ge, and Se in five chondrule rims in the CO3 chondrite ALH A77307 (3.0) using the synchrotron x-ray fluorescence (SXRF) microprobe at Brookhaven National Laboratory were determined. The data show that the trace element chemistry of rims on different chondrules is remarkably similar, consistent with data obtained for the major elements by electron microprobe. These results support the idea that rims are not genetically related to individual chondrules, but all sampled the same reservoir of homogeneously mixed dust. Of the trace elements analyzed Zn and Ga show depletions relative to CI chondrite values, but in comparison with bulk CO chondrites all the elements are enriched by approximately 1.5 to 3.5 x CO. The high concentrations of the highly volatile elements Se and Ga and moderately volatile Zn (1.5 to 2 x CO) in rims show that matrix is the major reservoir of volatile elements in ALH A77307.

Elemental Compositions of Extrasolar Planetesimals

NASA Astrophysics Data System (ADS)

Xu, Siyi; Jura, M.

2014-01-01

The composition of extrasolar rocky planets is essential for understanding the formation and evolution of these alien worlds. Studying externally-polluted white dwarfs provides the only method to directly measure the elemental compositions of extrasolar planetesimals, the building blocks of planets. The standard model is that some planetesimals can survive to the white dwarf phase, get perturbed, enter into the tidal radius of the white dwarf and get accreted, polluting its pure hydrogen or helium atmosphere. We have been performing high-resolution spectroscopic observations on a number of polluted white dwarfs to measure the bulk compositions of the accreted objects. To have a full picture of the abundance pattern, we gathered data from both Keck/HIRES and HST/COS. I will present the analysis for one of the most interesting objects -- G29-38. It is the first white dwarf identified with an infrared excess from debris of pulverized planetesimals and among the very first identified polluted hydrogen atmosphere white dwarfs. Our analysis indicates that the accreted extrasolar planetesimal is enhanced in refractory elements and depleted in volatile elements. A detailed comparison with solar system objects show that the observed composition can be best interpreted as a blend of chondritic object with some refractory-rich material, a result from post-nebular processing. When all polluted white dwarfs are viewed as an ensemble, we find that the elemental compositions of accreted extrasolar planetesimals resemble to those of solar system objects to zeroth order. (i) The big four elements, O, Fe, Mg and Si are also dominant. Objects with exotic compositions, e.g. diamond planets and refractory-dominated planets, are yet to be found. (ii) Volatiles, such as carbon and water, are only trace constituents. In terms of bulk composition, solar system objects are essentially normal.

Trace element content of chondritic cosmic dust: Volatile enrichments, thermal alterations, and the possibility of contamination

NASA Technical Reports Server (NTRS)

Flynn, G. J.; Sutton, S. R.; Bajt, S.

1993-01-01

Trace element abundances in 51 chondritic Interplanetary Dust Particles (IDP's) were measured by Synchrotron X-Ray Fluorescence (SXRF). The data allow us to determine an average composition of chondritic IDP's and to examine the questions of volatile loss during the heating pulse experienced on atmospheric entry and possible element addition due to contamination during atmospheric entry, stratospheric residence, and curation.

The relationship between CK and CV chondrites

NASA Astrophysics Data System (ADS)

Greenwood, R. C.; Franchi, I. A.; Kearsley, A. T.; Alard, O.

2010-03-01

CK chondrites are highly oxidized meteorites containing abundant magnetite and trace amounts of Fe,Ni metal. Although the group is predominately composed of equilibrated meteorites (types 4-6), in recent years a significant number of new samples have been classified as being either CK3 or CK3-anomalous. These unequilibrated CKs often display a close affinity with members of the CV oxidized subgroup. CKs and CVs (oxidized subgroup) may therefore form a continuum and by implication could be derived from a single common parent body. To investigate the relationship between these two groups a detailed study of the oxygen isotope composition, opaque mineralogy and major and trace element geochemistry of a suite of CV and CK chondrites has been undertaken. The results of oxygen isotope analysis confirm the close affinity between CV and CK chondrites, while excluding the possibility of a linkage between the CO and CK groups. Magnetites in both CV and CK chondrites show significant compositional similarities, but high Ti contents are a diagnostic feature of the latter group. The results of major and trace element analysis demonstrate that both CV and CK chondrites show overlapping variation. Supporting evidence for a single common source for both groups comes from their similar cosmic-ray exposure age distributions. Recent reflectance spectral analysis is consistent with both the CVs and CKs being derived from Eos family asteroids, which are believed to have formed by the catastrophic disruption of a single large asteroid. Thus, a range of evidence appears to be consistent with CV and CK chondrites representing samples from a single thermally stratified parent body. In view of the close similarity between CV and CK chondrites some modification of the present classification scheme may be warranted, possibly involving integration of the two groups. One means of achieving this would be to reassigned CK chondrites to a subgroup of the oxidized CVs. It is recognized that a full evaluation of this proposal may require further study of the still poorly understood CK3 chondrites.

Chondrites and the Protoplanetary Disk, Part 3

NASA Technical Reports Server (NTRS)

2004-01-01

Contents include the following: Ca-, Al-Rich Inclusions and Ameoboid Olivine Aggregates: What We Know and Don t Know About Their Origin. Aluminium-26 and Oxygen Isotopic Distributions of Ca-Al-rich Inclusions from Acfer 214 CH Chondrite. The Trapping Efficiency of Helium in Fullerene and Its Implicatiion to the Planetary Science. Constraints on the Origin of Chondritic Components from Oxygen Isotopic Compositions. Role of Planetary Impacts in Thermal Processing of Chondrite Materials. Formation of the Melilite Mantle of the Type B1 CAIs: Flash Heating or Transport? The Iodine-Xenon System in Outer and Inner Portions of Chondrules from the Unnamed Antarctic LL3 Chondrite. Nucleosynthesis of Short-lived Radioactivities in Massive Stars. The Two-Fluid Analysis of the Kelvin-Helmholtz Instability in the Dust Layer of a Protoplanetary Disk: A Possible Path to the Planetesimal Formation Through the Gravitational Instability. Shock-Wave Heating Model for Chonodrule Formation: Heating Rate and Cooling Rate Constraints. Glycine Amide Hydrolysis with Water and OH Radical: A Comparative DFT Study. Micron-sized Sample Preparation for AFM and SEM. AFM, FE-SEM and Optical Imaging of a Shocked L/LL Chondrite: Implications for Martensite Formation and Wave Propagation. Infrared Spectroscopy of Chondrites and Their Components: A Link Between Meteoritics and Astronomy? Mid-Infrared Spectroscopy of CAI and Their Mineral Components. The Origin of Iron Isotope Fractionation in Chondrules, CAIs and Matrix from Allende (CV3) and Chainpur (LL3) Chondrites. Protoplanetary Disk Evolution: Early Results from Spitzer. Kinetics of Evaporation-Condensation in a Melt-Solid System and Its Role on the Chemical Composition and Evolution of Chondrules. Oxygen Isotope Exchange Recorded Within Anorthite Single Crystal in Vigarano CAI: Evidence for Remelting by High Temperature Process in the Solar Nebula. Chondrule Forming Shock Waves in Solar Nebula by X-Ray Flares. Organic Globules with Anormalous Nitrogen Isotopic Compositions in the Tagish Lake Meteorite: Products of Primitive Organic Reactions. Yet Another Chondrule Formation Scenario. CAIs are Not Supernova Condensates. Microcrystals and Amorphous Material in Comets and Primitive Meteorites: Keys to Understanding Processes in the Early Solar System. A Nearby Supernova Injected Short-lived Radionuclides into Our Protoplanetary Disk. REE+Y Systematics in CC and UOC Chondrules. Meteoritic Constraints on Temperatures, Pressures, Cooling Rates, Chemical Compositions, and Modes of Condensation in the Solar Nebula. The I-Xe Record of Long Equilibration in Chondrules from the Unnamed Antarctic Meteorite L3/LL3. Early Stellar Evolution.

Aubrite and Impact Melt Enstatite Chondrite Meteorites as Potential Analogs to Mercury

NASA Technical Reports Server (NTRS)

Wilbur, Z. E.; Udry, A.; Mccubbin, Francis M.; McCubbin, F. M.; Combs, L. M.; Rahib, R. R.; McCoy, C.; McCoy, T. J.

2018-01-01

The MESSENGER (MErcury Sur-face, Space ENvironment, GEochemistry and Ranging) orbiter measured the Mercurian surface abundances of key rock-forming elements to help us better understand the planet's surface and bulk geochemistry. A major discovery is that the Mercurian surface and interior are characterized by an extremely low oxygen fugacity (ƒO2; Iron-Wüstite (IW) -7.3 to IW-2.6. This is supported by low Fe and high S abundances on the surface. This low ƒO2 causes a different elemental partioning from what is observed on Earth. Using surface composition, it was shown that the Mercurian surface mainly consists of normative plagioclase, pyroxene, olivine, and exotic sulfides, such as niningerite ((Mg,Mn, Fe)S) and oldhamite (CaS).

Chelyabinsk meteorite explains unusual spectral properties of Baptistina Asteroid Family

NASA Astrophysics Data System (ADS)

Reddy, Vishnu; Sanchez, Juan A.; Bottke, William F.; Cloutis, Edward A.; Izawa, Matthew R. M.; O'Brien, David P.; Mann, Paul; Cuddy, Matthew; Le Corre, Lucille; Gaffey, Michael J.; Fujihara, Gary

2014-07-01

We investigated the spectral and compositional properties of Chelyabinsk meteorite to identify its possible parent body in the main asteroid belt. Our analysis shows that the meteorite contains two spectrally distinct but compositionally indistinguishable components of LL5 chondrite and shock blackened/impact melt material. Our X-ray diffraction analysis confirms that the two lithologies of the Chelyabinsk meteorite are extremely similar in modal mineralogy. The meteorite is compositionally similar to LL chondrite and its most probable parent asteroid in the main belt is a member of the Flora family. Our work confirms previous studies (e.g., Vernazza et al. [2008]. Nature 454, 858-860; de León, J., Licandro, J., Serra-Ricart, M., Pinilla-Alonso, N., Campins, H. [2010]. Astron. Astrophys. 517, A23; Dunn, T.L., Burbine, T.H., Bottke, W.F., Clark, J.P. [2013]. Icarus 222, 273-282), linking LL chondrites to the Flora family. Intimate mixture of LL5 chondrite and shock blackened/impact melt material from Chelyabinsk provides a spectral match with (8) Flora, the largest asteroid in the Flora family. The Baptistina family and Flora family overlap each other in dynamical space. Mineralogical analysis of (298) Baptistina and 11 small family members shows that their surface compositions are similar to LL chondrites, although their absorption bands are subdued and albedos lower when compared to typical S-type asteroids. A range of intimate mixtures of LL5 chondrite and shock blackened/impact melt material from Chelyabinsk provides spectral matches for all these BAF members. We suggest that the presence of a significant shock/impact melt component in the surface regolith of BAF members could be the cause of lower albedo and subdued absorption bands. The conceptual problem with part of this scenario is that impact melts are very rare within ordinary chondrites. Of the ∼42,000 ordinary chondrites, less than 0.5% (203) of them contain impact melts. A major reason that impact melts are rare in meteorites is that high impact velocities (V > 10 km/s) are needed to generate the necessary shock pressures and temperatures (e.g., Pierazzo, E., Melosh, H.J. [1998]. Hydrocode modeling of oblique impacts: The fate of the projectile. In: Origin of the Earth and Moon, Proceedings of the Conference. LPI Contribution No. 957) unless the target material is highly porous. Nearly all asteroid impacts within the main belt are at ∼5 km/s (Bottke, W.F., Nolan, M.C., Greenberg, R., Kolvoord, R.A. [1994]. Collisional lifetimes and impact statistics of near-Earth asteroids. In: Tucson, Gehrels T. (Ed.), Hazards Due to Comets and Asteroids. The University of Arizona Press, Arizona, pp. 337-357), which prevents them from producing much impact melt unless they are highly porous. However, shock darkening is an equally efficient process that takes place at much lower impact velocities (∼2 km/s) and can cause the observed spectral effects. Spectral effects of shock darkening and impact melt are identical. The parent asteroid of BAF was either a member of the Flora family or had the same basic composition as the Floras (LL Chondrite). The shock pressures produced during the impact event generated enough impact melt or shock blackening to alter the spectral properties of BAF, but keep the BAF composition largely unchanged. Collisional mixing of shock blackened/impact melt and LL5 chondritic material could have created the Baptistina Asteroid Family with composition identical to those of the Floras, but with subdued absorption bands. Shock darkening and impact melt play an important role in altering the spectral and albedo properties of ordinary chondrites and our work confirms earlier work by Britt and Pieters (Britt, D.T., Pieters, C.M. [1994]. Geochimica et Cosmochimica Acta 58, 3905-3919).

Evidence for Reduced, Carbon-rich Regions in the Solar Nebula from an Unusual Cometary Dust Particle

NASA Astrophysics Data System (ADS)

De Gregorio, Bradley T.; Stroud, Rhonda M.; Nittler, Larry R.; Kilcoyne, A. L. David

2017-10-01

Geochemical indicators in meteorites imply that most formed under relatively oxidizing conditions. However, some planetary materials, such as the enstatite chondrites, aubrite achondrites, and Mercury, were produced in reduced nebular environments. Because of large-scale radial nebular mixing, comets and other Kuiper Belt objects likely contain some primitive material related to these reduced planetary bodies. Here, we describe an unusual assemblage in a dust particle from comet 81P/Wild 2 captured in silica aerogel by the NASA Stardust spacecraft. The bulk of this ˜20 μm particle is comprised of an aggregate of nanoparticulate Cr-rich magnetite, containing opaque sub-domains composed of poorly graphitized carbon (PGC). The PGC forms conformal shells around tiny 5-15 nm core grains of Fe carbide. The C, N, and O isotopic compositions of these components are identical within errors to terrestrial standards, indicating a formation inside the solar system. Magnetite compositions are consistent with oxidation of reduced metal, similar to that seen in enstatite chondrites. Similarly, the core-shell structure of the carbide + PGC inclusions suggests a formation via FTT reactions on the surface of metal or carbide grains in warm, reduced regions of the solar nebula. Together, the nanoscale assemblage in the cometary particle is most consistent with the alteration of primary solids condensed from a C-rich, reduced nebular gas. The nanoparticulate components in the cometary particle provide the first direct evidence from comets of reduced, carbon-rich regions that were present in the solar nebula.

Modes of planetary-scale Fe isotope fractionation

NASA Astrophysics Data System (ADS)

Schoenberg, Ronny; von Blanckenburg, Friedhelm

2006-12-01

A comprehensive set of high-precision Fe isotope data for the principle meteorite types and silicate reservoirs of the Earth is used to investigate iron isotope fractionation at inter- and intra-planetary scales. 14 chondrite analyses yield a homogeneous Fe isotope composition with an average δ56Fe/ 54Fe value of - 0.015 ± 0.020‰ (2 SE) relative to the international iron standard IRMM-014. Eight non-cumulate and polymict eucrite meteorites that sample the silicate portion of the HED (howardite-eucrite-diogenite) parent body yield an average δ56Fe/ 54Fe value of - 0.001 ± 0.017‰, indistinguishable to the chondritic Fe isotope composition. Fe isotope ratios that are indistinguishable to the chondritic value have also been published for SNC meteorites. This inner-solar system homogeneity in Fe isotopes suggests that planetary accretion itself did not significantly fractionate iron. Nine mantle xenoliths yield a 2 σ envelope of - 0.13‰ to + 0.09‰ in δ56Fe/ 54Fe. Using this range as proxy for the bulk silicate Earth in a mass balance model places the Fe isotope composition of the outer liquid core that contains ca. 83% of Earth's total iron to within ± 0.020‰ of the chondritic δ56Fe/ 54Fe value. These calculations allow to interprete magmatic iron meteorites ( δ56Fe/ 54Fe = + 0.047 ± 0.016‰; N = 8) to be representative for the Earth's inner metallic core. Eight terrestrial basalt samples yield a homogeneous Fe isotope composition with an average δ56Fe/ 54Fe value of + 0.072 ± 0.016‰. The observation that terrestrial basalts appear to be slightly heavier than mantle xenoliths and that thus partial mantle melting preferentially transfers heavy iron into the melt [S. Weyer, A.D. Anbar, G.P. Brey, C. Munker, K. Mezger and A.B. Woodland, Iron isotope fractionation during planetary differentiation, Earth and Planetary Science Letters 240(2), 251-264, 2005.] is intriguing, but also raises some important questions: first it is questionable whether the Fe isotope composition of lithospheric mantle xenoliths are representative for an undisturbed melt source, and second, HED and SNC meteorites, representing melting products of 4Vesta and Mars silicate mantles would be expected to show a similar fractionation towards heavy isotope compositions. This is not observed. Four international granitoid standards with SiO 2 contents between 60 and 70 wt.% yield δ56Fe/ 54Fe values between 0.118‰ and 0.132‰. An investigation of the alpine Bergell igneous rock suite revealed a positive correlation between Fe isotope compositions and SiO 2 contents — from gabbros and tonalites ( δ56Fe/ 54Fe ≈ 0.03 to 0.09‰) to granodiorites and silicic dykes ( δ56Fe/ 54Fe ≈ 0.14 to 0.23‰). Although in this suite δ56Fe/ 54Fe correlates with δ18O values and radiogenic isotopes, open-system behavior to explain the heavy iron is not undisputed. This is because an obvious assimilant with the required heavy Fe isotope composition has so far not been identified. Alternatively, the relatively heavy granite compositions might be obtained by fractional crystallisation of the melt. Ultimately, further detailed studies on natural rocks and the experimental determination of mineral/melt fractionation factors at magmatic conditions are required to unravel whether or not iron isotope fractionation takes place during partial mantle melting and crystal fractionation.

High precision Al-Mg systematics of forsterite-bearing Type B CAIs from CV3 chondrites

NASA Astrophysics Data System (ADS)

MacPherson, G. J.; Bullock, E. S.; Tenner, T. J.; Nakashima, D.; Kita, N. T.; Ivanova, M. A.; Krot, A. N.; Petaev, M. I.; Jacobsen, S. B.

2017-03-01

In order to further elucidate possible temporal relationships between different varieties of calcium-, aluminum-rich inclusions (CAIs), we measured the aluminum-magnesium isotopic systematics of seven examples of the rare type known as forsterite-bearing Type B (FoB) inclusions from four different CV3 carbonaceous chondrites: Allende, Efremovka, NWA 3118, and Vigarano. The primary phases (forsterite, Al-Ti-rich diopside, spinel, melilite, and anorthite) in each inclusion were analyzed in situ using high-precision secondary ion mass-spectrometry (SIMS). In all cases, minerals with low Al/Mg ratios (all except anorthite) yield well-defined internal Al-Mg isochrons, with a range of initial 26Al/27Al ratios [(26Al/27Al)0] ranging from (5.30 ± 0.22) × 10-5 down to (4.17 ± 0.43) × 10-5. Anorthite in all cases is significantly disturbed relative to the isochrons defined by the other phases in the same CAIs, and in several cases contains no resolved excesses of radiogenic 26Mg (δ26Mg∗) even at 27Al/24Mg ratios greater than 1000. The fact that some FoBs preserve (26Al/27Al)0 of ∼5.2 × 10-5, close to the canonical value of (5.23 ± 0.13) × 10-5 inferred from bulk magnesium-isotope measurements of CV CAIs (B. Jacobsen et al., 2008), demonstrates that FoBs began forming very early, contemporaneous with other more-refractory CAIs. The range of (26Al/27Al)0 values further shows that FoBs continued to be reprocessed over ∼200,000 years of nebular history, consistent with results obtained for other types of igneous CAIs in CV chondrites. The absence of any correlation between of CAI + FoB formation or reprocessing times with bulk composition or CAI type means that there is no temporal evolutionary sequence between the diverse CAI types. The initial δ26Mg∗ value in the most primitive FoB (SJ101) is significantly lower than the canonical solar system value of -0.040 ± 0.029‰.

Pyroxene structures, cathodoluminescence and the thermal history of the enstatite chondrites

NASA Technical Reports Server (NTRS)

Zhang, Yanhong; Huang, Shaoxiong; Schneider, Diann; Benoit, Paul H.; Sears, Derek W. G.; DeHart, John M.; Lofgren, Gary E.

1996-01-01

In order to explore the thermal history of enstatite chondrites, we examined the cathodoluminescence (CL) and thermoluminescence (TL) properties of 15 EH chondrites and 21 EL chondrites, including all available petrographic types, both textural types 3-6 and mineralogical types alpha-delta. The CL properties of EL3(alpha) and EH3(alpha) chondrites are similar. Enstatite grains high in Mn and other transition metals display red CL, while enstatite with low concentrations of these elements show blue CL. A few enstatite grains with greater than 5 wt% FeO display no CL. In contrast, the luminescent properties of the metamorphosed EH chondrites are very different from those of metamorphosed EL chondrites. While the enstatites in metamorphosed EH chondrites display predominantly blue CL, the enstatites in metamorphosed EL chondrites display a distinctive magenta CL with blue and red peaks of approximately equal intensity in their spectra. The TL sensitivities of the enstatite chondrites correlate with the intensity of the blue CL and, unlike other meteorite classes, are not simply related to metamorphism. The different luminescent properties of metamorphosed EH and EL chondrites cannot readily be attributed to compositional differences. But x-ray diffraction data suggests that the enstatite in EH5(gamma),(delta) chondrites is predominantly disordered orthopyroxene, while enstatite in EL6(beta) chondrites is predominantly ordered orthopyroxene. The difference in thermal history of metamorphosed EL and EH chondrites is so marked that the use of single 'petrographic' types is misleading, and separate textural and mineralogical types are preferable. Our data confirm earlier suggestions that metamorphosed EH chondrites underwent relatively rapid cooling, and the metamorphosed EL chondrites cooled more slowly and experienced prolonged heating in the orthopyroxene field.

Preliminary Compositional Comparisons of H-Chondrite Falls to Antarctic H-Chondrite Populations

NASA Astrophysics Data System (ADS)

Kallemeyn, G. W.; Krot, A. N.; Rubin, A. E.

1993-07-01

In a series of papers [e.g., 1,2], Lipschutz and co-workers compared trace- element RNAA data from Antarctic and non-Antarctic H4-6 chondrites and concluded that the two populations have significantly different concentrations of several trace elements including Co, Se, and Sb. They interpreted their data as indicating that these Antarctic H chondrites form different populations than observed H falls and may have originated in separate parent bodies. Recent work by Sears and co-workers [e.g., 3] has shown that there seem to be distinct populations of Antarctic H chondrites, distinguishable on the bases of induced thermoluminescence (TL) peak temperature, metallographic cooling rate, and cosmic ray exposure age. They showed that a group of Antarctic H chondrites having abnormally high induced TL peak temperatures (>=190 degrees C) also has cosmic ray exposure ages <20 Ma (mostly ~8 Ma) and fast metallographic cooling rates (~100 K/Ma). Another group having induced TL peak temperatures <190 degrees C has exposure ages >20 Ma and slower cooling rates (~10-20 K/Ma). We studied 24 H4-6 chondrites from Victoria Land (including 12 previously analyzed by the Lipschutz group) by optical microscopy and electron microprobe. Many of the Antarctic H chondrites studied by Lipschutz and co- workers are unsuitable for proper compositional comparisons with H chondrite falls: Four are very weathered, five are extensively shocked, and two are extensively brecciated. Furthermore, at least five of the samples contain solar-wind gas (and hence are regolith breccias) [4]. These samples were rejected because of possible compositional modification by secondary processes. For our INAA study we chose a suite of relatively unweathered and unbrecciated Antarctic H chondrites (including nine from the Lipschutz set): ALHA 77294 (H5, S3); ALHA 79026 (H5, S3); ALHA 79039 (H5, S3); ALHA 80131 (H5, S3); ALHA 80132 (H5, S4); ALHA 81037 (H6, S3); EETA 79007 (H5, S4); LEW 85320 (H6, S4); LEW 85329 (H6, S3); RKPA 78002 (H5, S2); and RKPA 78004 (H4, S4). Single samples were each analyzed for 27 elements. Only four of our samples have been analyzed by TL. Concentrations of siderophile elements (Fe, Co, Ni, Ga, As, Au) in the Antarctic H chondrites tend to scatter more than those of 24 H falls studied in replicate at UCLA. This is probably due in part to the fact that replicate samples of the Antarctic chondrites have not yet been analyzed. The median concentrations of siderophile elements also tend to be slightly lower in Antarctic H chondrites, although 95% confidence intervals on the medians overlap with those of H falls for every element. Concentration ranges and median values of two chalcophile elements, Se and Zn, are nearly identical between the Antarctic H chondrites and H falls. Kolmogorov-Smirnov two-tailed tests on these elements show no significant differences between the two populations. Three of the elements analyzed in this study (Co, Se, Sb) are among those reported to vary significantly between Antarctic H chondrites and H falls by Dennison and Lipschutz [1], who found that median concentrations of these elements were slightly higher in Antarctic H chondrites. As noted earlier, we determined slightly lower median concentrations for Co and Sb in Antarctic H chondrites than in H falls; median Se concentrations were identical. The slightly lower median concentration values that we found for siderophile elements in general are probably indicative of a slight weathering loss of metal. Based on our compositional data, the Victoria Land H chondrites and non-Antarctic H falls do not require derivation from separate parent populations. References: [1] Dennison J. E. and Lipschutz M. E. (1987) GCA, 51, 741-754. [2] Lipschutz M. E. and Samuels S. M. (1991) GCA, 55, 19-34. [3] Benoit P. H. and Sears D. W. G. (1993) Icarus, 101, 188-200. [4] Schultz L. et al. (1991) GCA, 55, 59-66.

Organic Analysis in the Miller Range 090657 CR2 Chondrite: Part 3 C and N Isotopic Imaging

NASA Technical Reports Server (NTRS)

Messenger, S.; Nakamura-Messenger, K.; Elsila, J. E.; Berger, E. L.; Burton, A. S.; Clemett, S. J.; Cao, T.

2016-01-01

Primitive carbonaceous chondrites contain a wide variety of organic material, ranging from soluble discrete molecules to insoluble nanoglobules of macro-molecular carbon. The relationship between the soluble organic molecules, macromolecular organic material, and host minerals are poorly understood. Large H, C and N isotopic anomalies suggest some organic components formed in low-T interstellar or outer Solar System environments. The highest isotope anomalies occur in m-scale inclusions in the most primitive materials, such as cometary dust and the least altered carbonaceous chondrites. Often, the hosts of these isotopically anomalous 'hotspots' are discrete organic nanoglobules that probably formed in the outermost reaches of the protosolar disk or cold molecular cloud. Molecular and isotopic studies of meteoritic organic matter are aimed at identifying the chemical properties and formation processes of interstellar organic materials and the subsequent chemical evolutionary pathways in various Solar System environments. The combination of soluble and insoluble analyses with in situ and bulk studies provides powerful constraints on the origin and evolution of organic matter in the Solar System. Using macroscale extraction and analysis techniques as well as microscale in situ observations we have been studying both insoluble and soluble organic material in primitive astromaterial samples. Here, we present results of bulk C and N isotopic measurements and coordinated in situ C and N isotopic imaging and mineralogical and textural studies of carbonaceous materials in a Cr2 carbonaceous chondrite. In accompanying abstracts we discuss the morphology and distribution of carbonaceous components and soluble organic species of this meteorite.

Silver contents and Cu/Ag ratios in Martian meteorites and the implications for planetary differentiation

NASA Astrophysics Data System (ADS)

Wang, Zaicong; Becker, Harry

2017-11-01

Silver and Cu show very similar partitioning behavior in sulfide melt-silicate melt and metal-silicate systems at low and high pressure-temperature (P-T) experimental conditions, implying that mantle melting, fractional crystallization and core-mantle differentiation have at most modest (within a factor of 3) effects on Cu/Ag ratios. For this reason, it is likely that Cu/Ag ratios in mantle-derived magmatic products of planetary bodies reflect that of the mantle and, in some circumstances, also the bulk planet composition. To test this hypothesis, new Ag mass fractions and Cu/Ag ratios in different groups of Martian meteorites are presented and compared with data from chondrites and samples from the Earth's mantle. Silver contents in lherzolitic, olivine-phyric and basaltic shergottites and nakhlites range between 1.9 and 12.3 ng/g. The data display a negative trend with MgO content and correlate positively with Cu contents. In spite of displaying variable initial Ɛ143Nd values and representing a diverse spectrum of magmatic evolution and physiochemical conditions, shergottites and nakhlites display limited variations of Cu/Ag ratios (1080 ± 320, 1 s, n = 14). The relatively constant Cu/Ag suggests limited fractionation of Ag from Cu during the formation and evolution of the parent magmas, irrespectively of whether sulfide saturation was attained or not. The mean Cu/Ag ratio of Martian meteorites thus reflects that of the Martian mantle and constrains its Ag content to 1.9 ± 0.7 ng/g (1 s). Carbonaceous and enstatite chondrites display a limited range of Cu/Ag ratios of mostly 500-2400. Ordinary chondrites show a larger scatter of Cu/Ag up to 4500, which may have been caused by Ag redistribution during parent body metamorphism. The majority of chondrites have Cu/Ag ratios indistinguishable from the Martian mantle value, indicating that Martian core formation strongly depleted Cu and Ag contents, but probably did not significantly change the Cu/Ag ratio of the mantle compared to bulk Mars. Bulk Mars is richer in moderately volatile elements than Earth, however, the Martian mantle displays a much stronger depletion of the moderately volatile elements Cu and Ag, e.g., by a factor of 15 for Cu. This observation is consistent with experimental studies suggesting that core formation at low P-T conditions on Mars led to more siderophile behavior of Cu and Ag than at high P-T conditions as proposed for Earth. In contrast, Cu/Ag ratios of the mantles of Mars and Earth (Cu/AgEarth = 3500 ± 1000) display only a difference by a factor of 3, which implies restricted fractionation of Cu and Ag even at high P-T conditions. The concentration data support the notion that siderophile element partitioning during planetary core formation scales with the size of the planetary body, which is particularly important for the differentiation of large terrestrial planets such as Earth. Collectively, the Ag and Cu data on magmatic products from the mantles of Mars and Earth and the data on chondrites confirm experimental predictions and support the limited fractionation of Cu and Ag during planetary core formation and high-temperature magmatic evolution, and probably also in early solar nebular processes.

Aqueous fluid composition in CI chondritic materials: Chemical equilibrium assessments in closed systems

NASA Astrophysics Data System (ADS)

Zolotov, Mikhail Yu.

2012-08-01

Solids of nearly solar composition have interacted with aqueous fluids on carbonaceous asteroids, icy moons, and trans-neptunian objects. These processes altered mineralogy of accreted materials together with compositions of aqueous and gaseous phases. We evaluated chemistry of aqueous solutions coexisted with CI-type chondritic solids through calculations of chemical equilibria in closed water-rock-gas systems at different compositions of initial fluids, water/rock mass ratios (0.1-1000), temperatures (<350 °C), and pressures (<2 kbars). The calculations show that fluid compositions are mainly affected by solubilities of solids, the speciation of chlorine in initial water-rock mixtures, and the occurrence of Na-bearing secondary minerals such as saponite. The major species in modeled alkaline solutions are Na+, Cl-, CO32-,HCO3-, K+, OH-, H2, and CO2. Aqueous species of Mg, Fe, Ca, Mn, Al, Ni, Cr, S, and P are not abundant in these fluids owing to low solubility of corresponding solids. Typical NaCl type alkaline fluids coexist with saponite-bearing mineralogy that usually present in aqueously altered chondrites. A common occurrence of these fluids is consistent with the composition of grains emitted from Enceladus. Na-rich fluids with abundant CO32-,HCO3-, and OH- anions coexist with secondary mineralogy depleted in Na. The Na2CO3 and NaHCO3 type fluids could form via accretion of cometary ices. NaOH type fluids form in reduced environments and may locally occur on parent bodies of CR carbonaceous chondrites. Supposed melting of accreted HCl-bearing ices leads to early acidic fluids enriched in Mg, Fe and other metals, consistent with signs of low-pH alteration in chondrites. Neutralization of these solutions leads to alkaline Na-rich fluids. Sulfate species have negligible concentrations in closed systems, which remain reduced, especially at elevated pressures created by forming H2 gas. Hydrogen, CO2, and H2O dominate in the gaseous phase, though the abundance of methane cannot be fairly estimated.

Primitive material surviving in chondrites - Mineral grains

NASA Astrophysics Data System (ADS)

Steele, Ian M.

Besides chondrules and various kinds of polymineralic inclusion, carbonaceous chondrites commonly contain, embedded in their matrices, isolated grains of mafic silicates and metallic iron. Most of the silicate grains probably originated in chondrules, but some appear to predate chondrule formation and may have formed as individual grains in the solar nebula. If that was the case, their compositions suggest some departure from equilibrium condensation from a gas of solar composition. Metal-grain compositions are broadly suggestive of nebular formation but the exact nature of the conditions in which they were formed remains problematical.

Olivine Composition of the Mars Trojan 5261 Eureka: Spitzer IRS Data

NASA Technical Reports Server (NTRS)

Lim, L. F.; Burt, B. J.; Emery, J. P.; Mueller, M.; Rivkin, A. S.; Trilling, D.

2011-01-01

The largest Mars trojan, 5261 Eureka, is one of two prototype "Sa" asteroids in the Bus-Demeo taxonomy. Analysis of its visible/near-IR spectrum led to the conclusion that it might represent either an angritic analog or an olivine-rich composition such as an R chondrite. Spitzer IRS data (5-30 micrometers) have enabled us to resolve this ambiguity. The thermal-IR spectrum exhibits strong olivine reststrahlen features consistent with a composition of approximately equals Fo60-70. Laboratory spectra of R chondrites, brachinites, and chassignites are dominated by similar features.

Carbon abundances, major element chemistry, and mineralogy of hydrated interplanetary dust particles

NASA Technical Reports Server (NTRS)

Keller, L. P.; Thomas, K. L.; Mckay, D. S.

1993-01-01

Hydrated interplanetary dust particles (IDP's) comprise a major fraction of the interplanetary dust particles collected in the stratosphere. While much is known about the mineralogy and chemistry of hydrated IDP's, little is known about the C abundance in this class of IDP's, the nature of the C-bearing phases, and how the C abundance is related to other physical properties of hydrated IDP's. Bulk compositional data (including C and O) for 11 hydrated IDP's that were subsequently examined by the transition electron microscopy (TEM) to determine their mineralogy and mineral chemistry are reported. Our analysis indicates that these hydrated IDP's are strongly enriched in C relative to the most C-rich meteorites. The average abundance of C in these hydrated IDP's is 4X CI chondrite values. The bulk compositions (including C and O) of 11 hydrated IDP's were determined by thin-window, energy-dispersive x ray (EDX) spectroscopy of the uncoated IDP's on Be substrates in the scanning electron microscopy (SEM). As a check on our C measurements, one of the IDP's (L2006H5) was embedded in glassy S, and microtome thin sections were prepared and placed onto Be substrates. Thin-film EDX analyses of multiple thin sections of L2006H5 show good agreement with the bulk value determined in the SEM. Following EDX analysis, the mineralogy and mineral chemistry of each IDP was determined by analyzing ultramicrotome thin sections in a TEM equipped with an EDX spectrometer.

Re — Os isotopic constraints on the origin of volcanic rocks, Gorgona Island, Colombia: Os isotopic evidence for ancient heterogeneities in the mantle

NASA Astrophysics Data System (ADS)

Walker, R. J.; Echeverria, L. M.; Shirey, S. B.; Horan, M. F.

1991-04-01

The Re — Os isotopic systematics of komatiites and spatially associated basalts from Gorgona Island, Colombia, indicate that they were produced at 155±43 Ma. Subsequent episodes of volcanism produced basalts at 88.1±3.8 Ma and picritic and basaltic lavas at ca. 58 Ma. The age for the ultramafic rocks is important because it coincides with the late-Jurassic, early-Cretaceous disassembly of Pangea, when the North- and South-American plates began to pull apart. Deep-seated mantle upwelling possibly precipitated the break-up of these continental plates and caused a tear in the subducting slab west of Gorgona, providing a rare, late-Phanerozoic conduit for the komatiitic melts. Mantle sources for the komatiites were heterogeneous with respect to Os and Pb isotopic compositions, but had homogeneous Nd isotopic compositions (ɛNd+9±1). Initial 187Os/186Os normalized to carbonaceous chondrites at 155 Ma (γOs) ranged from 0 to +22, and model-initial μ values ranged from 8.17 to 8.39. The excess radiogenic Os, compared with an assumed bulk-mantle evolution similar to carbonaceous chondrites, was likely produced in portions of the mantle with long-term elevated Re concentrations. The Os, Pb and Nd isotopic compositions, together with major-element constraints, suggest that the sources of the komatiites were enriched more than 1 Ga ago by low (<20%) and variable amounts of a basalt or komatiite component. This component was added as either subducted oceanic crust or melt derived from greater depths in the mantle. These results suggest that the Re — Os isotope system may be a highly sensitive indicator of the presence of ancient subducted oceanic crust in mantle-source regions.

Re - Os isotopic constraints on the origin of volcanic rocks, Gorgona Island, Colombia: Os isotopic evidence for ancient heterogeneities in the mantle

USGS Publications Warehouse

Walker, R.J.; Echeverria, L.M.; Shirey, S.B.; Horan, M.F.

1991-01-01

The Re - Os isotopic systematics of komatiites and spatially associated basalts from Gorgona Island, Colombia, indicate that they were produced at 155??43 Ma. Subsequent episodes of volcanism produced basalts at 88.1??3.8 Ma and picritic and basaltic lavas at ca. 58 Ma. The age for the ultramafic rocks is important because it coincides with the late-Jurassic, early-Cretaceous disassembly of Pangea, when the North- and South-American plates began to pull apart. Deep-seated mantle upwelling possibly precipitated the break-up of these continental plates and caused a tear in the subducting slab west of Gorgona, providing a rare, late-Phanerozoic conduit for the komatiitic melts. Mantle sources for the komatiites were heterogeneous with respect to Os and Pb isotopic compositions, but had homogeneous Nd isotopic compositions (??Nd+9??1). Initial 187Os/186Os normalized to carbonaceous chondrites at 155 Ma (??Os) ranged from 0 to +22, and model-initial ?? values ranged from 8.17 to 8.39. The excess radiogenic Os, compared with an assumed bulk-mantle evolution similar to carbonaceous chondrites, was likely produced in portions of the mantle with long-term elevated Re concentrations. The Os, Pb and Nd isotopic compositions, together with major-element constraints, suggest that the sources of the komatiites were enriched more than 1 Ga ago by low (<20%) and variable amounts of a basalt or komatiite component. This component was added as either subducted oceanic crust or melt derived from greater depths in the mantle. These results suggest that the Re - Os isotope system may be a highly sensitive indicator of the presence of ancient subducted oceanic crust in mantle-source regions. ?? 1991 Springer-Verlag.

Sm-Nd, K-Ar and petrologic study of some kimberlites from eastern United States and their implication for mantle evolution

USGS Publications Warehouse

Basu, A.R.; Rubury, E.; Mehnert, H.; Tatsumoto, M.

1984-01-01

We provide new data on Sm-Nd systematics, K-Ar dating and the major element chemistry of kimberlites from the eastern United States (mostly from central New York State) and their constituent mineral phases of olivine, clinopyroxene, garnet, phlogopite and perovskite. In addition, we report Nd-isotopes in a few kimberlites from South Africa, Lesotho and from the eastern part of China. The major element compositions of the New York dike rocks and of their constituent minerals including a xenolith of eclogite are comparable with those from the Kimberley area in South Africa. The K-Ar age of emplacement of the New York dikes is further established to be 143 Ma. We have analyzed the Nd-isotopic composition of the following kimberlites and related rocks: Nine kimberlite pipes from South Africa and Lesotho, two from southern India; one from the U.S.S.R., fifteen kimberlite pipes and related dike rocks from eastern and central U.S. and two pipes from the Shandong Province of eastern China. The age of emplacement of these kimberlites ranges from 1300 million years to 90 million years. The initial Nd-isotopic compositions of these kimberlitic rocks expressed as e{open}NdIwith respect to a chondritic bulk-earth growth-curve show a range between 0 and +4, with the majority of the kimberlites being in the range 0 to +2. This range is not matched by any other suite of mantle-derived igneous rocks. This result strengthens our earlier conclusion that kimberlitic liquids are derived from a relatively primeval and unique mantle reservoir with a nearly chondritic Sm/Nd ratio. ?? 1984 Springer-Verlag.

The Shaw chondrite. I - The case of the missing metal

NASA Technical Reports Server (NTRS)

Rambaldi, E. R.; Larimer, J. W.

1976-01-01

The mineralogy as well as the elemental and isotopic composition of the Shaw meteorite indicate that it is a highly metamorphosed L-group chondrite which has lost a portion of its metal and sulfide. The metal which remains has an unusual composition relative to that in other L-group chondrites. It is enriched in Ga, Ge, Ir, Mo, Os, Pt, Re, and Ru but depleted in As, Au, Cu, and Sb. A comparison of the relative enrichments and depletions in Shaw with those observed in San Cristobal, the extreme end-member of group IAB iron meteorites, shows that the metal phases in these two meteorites have complementary compositions. This implies that the metal in Shaw represents the residual solid of a partial melting process while the missing metal, which drained away, may have gone to form an iron meteorite, like San Cristobal.

Distribution of some highly volatile elements in chondrules

NASA Astrophysics Data System (ADS)

Kim, J. S.; Marti, K.

1994-07-01

As chondrule apparently were melted before accretion into chondritic parent bodies, we carried out a N and Xe isotopic study to obtain information on the partitioning of some of the most volatile as well as incompatible elements: noble gases, N, I, REE, and Pu. In separated silicates in Forest Vale, consisting of mostly broken chondrules, we observed rather large Xe concentrations, and since noble gases in chondrites are associated with C-rich phases, we decided to study the core portion of a suite of chondrules after removing the chondrule rim portion and adhering matrix. We selected sets of rounded chondrules from four meteorites: Allende (CV3), Dhajala (H3.8), Forest Vale (H4), and Bjurbole (L4). We compare measured N and Xe concentrations and isotopic abundances in cores of chondrules to those obtained from unetched chondrules. We discuss results obtained from melting steps, because N and Xe in the silicate lattice are mostly released at T greater than 1000 C. All cores of chondrules contain less than 1% of the Xe in the respective bulk samples. Moreover, they released much less trapped Xe in the melting step than did untreated bulk chondrites. However, the radiogenic Xer-129 and fissiogenic Xef is not or is only slightly depleted, and spallogenic Xe is a major component, particularly in Forest Vale. We can not deduce the signature of trapped Xe in the chondrules. The release systematics are completely different from those observed in primitive achondrites, which contain noble gas in the 'dusty' silicate inclusions. Allende chondrules differ from those of ordinary chondrite in the N release pattern. This represents possibly a signature of the local environment during chondrule formation, since N may exist in chondrule minerals in chemically bound forms. In contrast, all three sets of ordinary chondrite chondrules released less than 0.6 ppm N in the melting step, and these signatures reveal substantial components of cosmic-ray-produced N.

Halogens in chondritic meteorites and terrestrial accretion

NASA Astrophysics Data System (ADS)

Clay, Patricia L.; Burgess, Ray; Busemann, Henner; Ruzié-Hamilton, Lorraine; Joachim, Bastian; Day, James M. D.; Ballentine, Christopher J.

2017-11-01

Volatile element delivery and retention played a fundamental part in Earth’s formation and subsequent chemical differentiation. The heavy halogens—chlorine (Cl), bromine (Br) and iodine (I)—are key tracers of accretionary processes owing to their high volatility and incompatibility, but have low abundances in most geological and planetary materials. However, noble gas proxy isotopes produced during neutron irradiation provide a high-sensitivity tool for the determination of heavy halogen abundances. Using such isotopes, here we show that Cl, Br and I abundances in carbonaceous, enstatite, Rumuruti and primitive ordinary chondrites are about 6 times, 9 times and 15-37 times lower, respectively, than previously reported and usually accepted estimates. This is independent of the oxidation state or petrological type of the chondrites. The ratios Br/Cl and I/Cl in all studied chondrites show a limited range, indistinguishable from bulk silicate Earth estimates. Our results demonstrate that the halogen depletion of bulk silicate Earth relative to primitive meteorites is consistent with the depletion of lithophile elements of similar volatility. These results for carbonaceous chondrites reveal that late accretion, constrained to a maximum of 0.5 ± 0.2 per cent of Earth’s silicate mass, cannot solely account for present-day terrestrial halogen inventories. It is estimated that 80-90 per cent of heavy halogens are concentrated in Earth’s surface reservoirs and have not undergone the extreme early loss observed in atmosphere-forming elements. Therefore, in addition to late-stage terrestrial accretion of halogens and mantle degassing, which has removed less than half of Earth’s dissolved mantle gases, the efficient extraction of halogen-rich fluids from the solid Earth during the earliest stages of terrestrial differentiation is also required to explain the presence of these heavy halogens at the surface. The hydropilic nature of halogens, whereby they track with water, supports this requirement, and is consistent with volatile-rich or water-rich late-stage terrestrial accretion.

Stardust (Comet) Samples and the Meteorite Record

NASA Astrophysics Data System (ADS)

Weisberg, M.; Connolly, H.; Zolensky, M.; Bland, P.; Bradley, J.; Braerley, A.; Bridges, J.; Brownlee, D.; Butterworth, A.; Dai, Z.; Ebel, D.; Genge, M.; Gounelle, M.; Graham, G.; Grossman, J.; Grossman, L.; Harvey, R.; Ishii, H.; Kearsley, A.; Keller, L.; Krot, A.; Langenhorst, F.; Lanzirotti, A.; Leroux, H.; Matrajt, G.; Messenger, K.; Mikouchi, T.; Nakamura, T.; Ohsumi, K.; Okudaira, K.; Perronnet, M.; Simon, S.; Stephan, T.; Stroud, R.; Taheri, M.; Tomeoka, K.; Toppani, A.; Tsou, P.; Tsuchiyama, A.; Velbel, M.; Weber, I.; Westphal, A.; Yano, H.; Zega, T.

2006-12-01

Perhaps the most intriguing aspect of the material collected by Stardust from `comet Wild 2 is the preponderance of high temperature and reduced crystalline phases, which are characteristic of chondrites thought to derive from the main Asteroid Belt (2-4 AU) [1]. Here we compare the mineralogy of Stardust samples to that of chondrite groups. Results: Investigation by the Preliminary Examination Team (PET) of particles from Wild 2 shows a mineral assemblage typical of chondrites, with olivine, pyroxene, FeNi-metal and sulfide as common components. Olivine and low-Ca pyroxene have a range of mg# (Fa0.5-41 and Fs0-48, respectively), which indicates that the material is unequilibrated, similar to types 2 and 3 chondrites. Some forsterite with <1 wt% FeO has up to 6.4 wt% MnO and 1.4 wt% Cr2O3. Other silicates observed are Ti-bearing aluminus diopside and rare melilite, typical of some calcium, aluminum-rich inclusions (CAIs) in carbonaceous (C) chondrites. Additionally, FeNi- metal and sulfides including pentlandite [(FeNi)9S8)] and Fe-Ni-Cu and Fe-Zn sulfide, phases observed in C and enstatite (E) chondrites, are present in some particles. V-bearing osbornite (TiN), a phase also observed in some C and E chondrites, occurs associated with unidentified Zr-rich phase(s). Discussion: The observations by the PET are based on work done in a short period of time on a limited number of particles less than several microns in size, and, hence, conclusions based on these data are tentative. Many C chondrite groups have the wide range of ferromagnesian silicate compositions found in the Stardust samples. However, the range of olivine and pyroxene compositions, occurrence of Mn-, Cr-rich olivine, metal and pentlandite are features most consistent with CR and CH chondrites, though a CM-like lithology cannot be ruled out. Mn-, Cr- rich forsterite is found in the matrix and in amoeboid olivine aggregates in CR chondrites [2, 3]; Osbornite-bearing CAIs have been identified in the ALH 85085 CH chondrite [4] and the Isheyevo CH/CB chondrite [5]. Thus, the Stardust samples analyzed thus far have mineral assemblages close to those of CR and CH chondrites, members of the CR chondrite clan. References: [1] Scott and Krot (2005) Chondrules and the Protoplanetary Disk, 15-54. [2] Weisberg et al. (1993) GCA 57, 1567-1586. [3] Weisberg et al. (2004) MAPS 39, 1741-1753. [4] Weisberg et al. (1988) EPSL 91, 19-32. [5] Krot et al. (2006) MAPS #1506.

Vesta is not an intact protoplanet

NASA Astrophysics Data System (ADS)

Consolmagno, G.; Turrini, D.; Golabek, G.; Svetsov, V.; Sirono, S.; Tsiganis, K.

2014-07-01

The Dawn mission was designed to explore ''remnant intact protoplanets from the earliest epoch of solar system formation'' [1]. However, models of Vesta composed of an iron core, olivine mantle, and HED crust in chondritic proportions cannot match the joint constraints from Dawn [1] of Vesta's density, core size, and the extremely limited presence of exposed olivine on its surface. Vesta has a mean density of 3456 kg/m3 and its surface composition is well matched by howardites. The Dawn gravity data suggest a nickel-iron core of radius 110 km and density 7500--7800 kg/m3. The Rheasilvia impact basin, formed within a pre-existing large basin, Veneneia, should have excavated material from a depth of 50 km to 80 km or more below Vesta's surface [2]. If the howardite crust were thinner than 50--80 km, a significant amount of olivine-rich material, derived from depth, would have been exposed within this basin; models suggest that olivine would also be distributed both on Vesta's surface and in space as meteorite-source Vestoids. Such olivine is rare on Vesta, among the Vestoids, or in our meteorite collection. Vesta's density is similar to an L chondrite, but the Na and K abundances in Vesta are strongly depleted compared to chondrites and the average metal content of an L chondrite, 8.4% by mass, would give a core radius less than 90 km. A 110 km radius metallic core, via the Dawn data, represents 15% of Vesta's mass. The Mg/Al ratio in cosmic abundances is about 10:1, but roughly 1:1 within the eucrites; thus if Vesta started with cosmic abundances, the eucrites can only represent 10% of the parent body total mass. Likewise the 10 x chondritic rare earth trace elements (REE) abundance seen in most eucrites demands that, regardless of formation mechanism, these basalts were crystallized from a melt representing 10% of the mass of the source region [3]. Thus the howardite crust of a chondritic HED parent body, mixing all the available eucritic and diogenitic material (in a 2:1 ratio), represents no more than 15% of its total mass. This leaves 70% of Vesta's mass as olivine. Assuming no porosity in this mantle, the radius and density of Vesta can be matched only with a howardite crust (average grain density [4] of 3270 kg/m3) that was 27 km thick with a porosity of nearly 45%, comparable to sand. If the mantle porosity is 8%, similar to Chassigny, the necessary crust porosity would be 30%, but its thickness would drop to 21 km. In both cases, this crust is too thin to accommodate the lack of olivine in Rheasilvia or its ejecta. Absent some unknown process to hide large amounts of olivine on the surface of Vesta and among the Vestoids, chondritic models do not fit the observational constraints. A larger, lower density core of olivine and metal mixed in equal proportions (by mass), of density 5000 kg/m3 and radius 145 km may also fit the Dawn gravity data [5]. The remaining volume of Vesta would be a 115 km thick howardite crust, thick enough to allow the metal/olivine core to remain unexposed. (In this case Vesta would be composed only of core and crust, but the core would be rich in olivine.) To match Vesta's density, this thick crust only needs an average porosity of 4%. Since 50% of Vesta's mass in this model would be eucrites, the REE abundances for the whole of Vesta would have to be five times chondritic values. Either Vesta accreted from a highly unusual cosmochemical setting, or 80% of its primordial olivine and iron were removed at some time after the REE trace elements were extracted from the bulk proto-Vesta into the eucritic melt. This proto-Vesta would have to have at least three times the mass of the current Vesta, with a radius of at least 375 km (still smaller than Ceres). Either Vesta formed with a very non-chondritic composition or it was subjected to a radical change in composition, presumably due to the intense collisional environment [6,7] where and when it formed. In any event, Vesta is not a remnant protoplanet but a chemically stripped and reaccreted body.

The Osmium Isotopic Composition of Tagish Lake and Other Chondrites, Implications for Late Terrestrial Planetary Accretion

NASA Technical Reports Server (NTRS)

Brandon, A. D.

2003-01-01

The goals of this investigation are twofold. First, obtain high-precision Os isotope measurements of Tagish Lake and other chondrites by TIMS. Second, measure Re, Os, Pt, and other HSE concentrations by isotope dilution using TIMS and ICPMS. These measurements will determine whether this meteorite does in fact represent C-chondrite material with timeintegrated elevated Re/Os and Pt/Os with the implications to late accretion material characteristics.

Recondensation of chondritic material in the early solar system: Results of thermodynamic simulation

NASA Technical Reports Server (NTRS)

Dorofeyeva, V. A.; Makalkin, A. B.; Mironenko, M. V.; Vityazev, A. V.

1993-01-01

We have performed a thermodynamic simulation of the recondensation of evaporated meteoritic material. We suggest that evaporation and recondensation occurred in impact events during the intercollision of planetesimals during the early evolution of the solar system. The source materials adopted for our model are the chondrites CI Orgueil and H5 Richardton. These chondrites are representative examples of the two extremes regarding volatile content and oxidation state. We calculated equilibrium mineral compositions of the closed systems of the Orgueil's and Richardton's elemental composition at the P-T conditions characteristic of the explosion cloud formed at a planetesimal collision. The P-T conditions are as follows: 10(exp -4) bar, and 1500 and 2000 K. The results are presented.

Bunburra Rockhole: Exploring the Geology of a New Differentiated Basaltic Asteroid

NASA Technical Reports Server (NTRS)

Benedix, G.K.; Bland, P. A.; Friedrich, J. M.; Mittlefehldt, D.; Sanborn, M. E.; Yin, Q.-Z.; Greenwood, R. C; Franchi, L. A.; Bevan, A. W. R.; Towner, M. C.;

Chemistry of Earth's Putative Steam Atmosphere

NASA Astrophysics Data System (ADS)

Fegley, B.; Schaefer, L.

2007-12-01

The concept of a steam atmosphere generated by impact devolatilization of planetesimals accreted during Earth's formation is over 20 years old (Matsui and Abe, 1986; Lange and Ahrens, 1982). Surprisingly, with the possible exception of a few qualitative remarks, no one has critically assessed this scenario. We use thermochemical equilibrium and, where relevant, thermochemical kinetic calculations to model the chemistry of the "steam" atmosphere produced by impact volatilization of different types of accreting material. We present results for our nominal conditions (1500 K, total P = 100 bar). We also studied the effects of variable temperature and total pressure. The composition of the accreting material is modeled using average compositions of the Orgueil CI chondrite, the Murchison CM2 chondrite, the Allende CV3 chondrite, average ordinary (H, L, LL) chondrites, and average enstatite (EH, EL) chondrites. The major gases released from CI and CM chondritic material are H2O, CO2, H2, H2S, CO, CH4, and SO2 in decreasing order of abundance. About 10% of the atmosphere is CO2. The major gases released from CV chondritic material are CO2, H2O, CO, H2, and SO2 in decreasing order of abundance. About 20% of the total atmosphere is steam. The major gases released from average ordinary chondritic material are H2, CO, H2O, CO2, CH4, H2S, and N2 in decreasing order of abundance. The "steam" atmosphere is predominantly H2 + CO with steam being about 10% of the total atmosphere. The major gases released from EH chondritic material are H2, CO, H2O, CO2, N2, and CH4 in decreasing order of abundance. The "steam" atmosphere is predominantly H2 + CO with about 10% of the total atmosphere as steam. This work was supported by the NASA Astrobiology and Origins Programs.

Late Eocene 3He and Ir anomalies associated with ordinary chondritic spinels

NASA Astrophysics Data System (ADS)

Boschi, Samuele; Schmitz, Birger; Heck, Philipp R.; Cronholm, Anders; Defouilloy, Céline; Kita, Noriko T.; Monechi, Simonetta; Montanari, Alessandro; Rout, Surya S.; Terfelt, Fredrik

2017-05-01

During the late Eocene there was an enigmatic enhancement in the flux of extraterrestrial material to Earth. Evidence comes from sedimentary 3He records indicating an increased flux of interplanetary dust during ca. 2 Myr, as well as two very large impact structures, Popigai (100 km diameter) and Chesapeake Bay (40-85 km), that formed within 10-20 kyr at the peak of the 3He delivery. The Massignano section in Italy has one of the best sedimentary records of these events, including a well-defined 3He record, an Ir-rich ejecta bed related to the Popigai impact event, and two smaller Ir anomalies. Recently we showed that the Popigai ejecta is associated with a significant enrichment of chromite grains (>63 μm) with an H-chondritic elemental composition (17 grains in 100 kg of rock). Most likely these grains are unmelted fragments from the impactor. Slightly higher up (ca. 20 cm) in the section, where a small Ir anomaly possibly related to the Chesapeake Bay impact has been measured, we found a weak enrichment in L-chondritic grains (8 grains in 208 kg of rock). Here we report an extended data set increasing the total amount of sediment dissolved in acid and searched for extraterrestrial chromite grains from 658 to 1168 kg. In altogether 760 kg of background sediment from 17 levels over 14 m of strata outside the interval corresponding to the Popigai and Chesapeake Bay impacts, we only found 2 extraterrestrial chromite grains. Both grains have L-chondritic compositions and were found in a 100 kg sample from the ca. 10.25 m level in the section where the second of the smaller Ir anomalies has been reported. A correlation appears to exist between Ir, 3He and chromite from ordinary chondrites. We also report oxygen three-isotope measurements of the extraterrestrial chromite grains associated with the Popigai ejecta and confirm an H-chondritic composition. The new results strengthen our scenario that the upper Eocene 3He and Ir enrichments originate from the asteroid belt rather than the Oort cloud as originally proposed when the 3He anomaly was discovered. The generally low background concentrations of extraterrestrial chromite through the section speak against any major single asteroid breakup event such as in the mid-Ordovician after the break-up of the L-chondrite parent body. Instead the data reconcile with a small, possibly a factor of 2-3, increase in the flux of extraterrestrial material to Earth, but of both H- and L-chondritic composition. We also report the composition of all the 2310 terrestrial chrome spinel grains recovered, and show that their chemical composition indicates a dominantly regional ophiolitic source. Four anomalous chrome spinel grains with high Ti and V concentrations were found in the Popigai ejecta. These grains originate from Siberian Traps basalts in the Popigai crater at the time of impact.

Molecular Isotopic Characterization of the ALH 85013.50 Meteorite: Defining the Extraterrestrial Organic Compounds

NASA Technical Reports Server (NTRS)

Fuller, M.; Huang, Y.

2003-01-01

The Antarctic Meteorite Program has returned over 16,000 meteorites from the ice sheets of the Antarctic. This more than doubles the number of preexisting meteorite collection and adds important and rare specimens to the assemblage. The CM carbonaceous chondrites are of particular interest because of their high organic component. The Antarctic carbonaceous chondrites provide a large, previously uninvestigated suite of meteorites. Of the 161 CM chondrites listed in the Catalogue of Meteorites 138 of them have been recovered from the Antarctic ice sheets,. However, these meteorites have typically been exposed to Earth s conditions for long periods of time. The extent of terrestrial organic contamination and weathering that has taken place on these carbonaceous chondrites is unknown. In the past, stable isotope analysis was used to identify bulk organics that were extraterrestrial in origin. Although useful, this method could not exclude the possibility of terrestrial contamination contributing to the isotopic measurement. Compound specific isotope analysis of organic meteorite material has provided the opportunity to discern the terrestrial contamination from extraterrestrial organic compounds on the molecular level.

Tellurium stable isotope fractionation in chondritic meteorites and some terrestrial samples

NASA Astrophysics Data System (ADS)

Fehr, Manuela A.; Hammond, Samantha J.; Parkinson, Ian J.

2018-02-01

New methodologies employing a 125Te-128Te double-spike were developed and applied to obtain high precision mass-dependent tellurium stable isotope data for chondritic meteorites and some terrestrial samples by multiple-collector inductively coupled plasma mass spectrometry. Analyses of standard solutions produce Te stable isotope data with a long-term reproducibility (2SD) of 0.064‰ for δ130/125Te. Carbonaceous and enstatite chondrites display a range in δ130/125Te of 0.9‰ (0.2‰ amu-1) in their Te stable isotope signature, whereas ordinary chondrites present larger Te stable isotope fractionation, in particular for unequilibrated ordinary chondrites, with an overall variation of 6.3‰ for δ130/125Te (1.3‰ amu-1). Tellurium stable isotope variations in ordinary chondrites display no correlation with Te contents or metamorphic grade. The large Te stable isotope fractionation in ordinary chondrites is likely caused by evaporation and condensation processes during metamorphism in the meteorite parent bodies, as has been suggested for other moderately and highly volatile elements displaying similar isotope fractionation. Alternatively, they might represent a nebular signature or could have been produced during chondrule formation. Enstatite chondrites display slightly more negative δ130/125Te compared to carbonaceous chondrites and equilibrated ordinary chondrites. Small differences in the Te stable isotope composition are also present within carbonaceous chondrites and increase in the order CV-CO-CM-CI. These Te isotope variations within carbonaceous chondrites may be due to mixing of components that have distinct Te isotope signatures reflecting Te stable isotope fractionation in the early solar system or on the parent bodies and potentially small so-far unresolvable nucleosynthetic isotope anomalies of up to 0.27‰. The Te stable isotope data of carbonaceous and enstatite chondrites displays a general correlation with the oxidation state and hence might provide a record of the nebular formation environment. The Te stable isotope fractionation of the carbonaceous chondrites CI and CM (and CO potentially) overlap within uncertainty with data for terrestrial Te standard solutions, sediments and ore samples. Assuming the silicate Earth displays similar Te isotope fractionation as the studied terrestrial samples, the data indicate that the late veneer might have been delivered by material similar to CI or CM (or possibly) CO carbonaceous chondrites in terms of Te isotope composition. Nine terrestrial samples display resolvable Te stable isotope fractionation of 0.85 and 0.60‰ for δ130/125Te for sediment and USGS geochemical exploration reference samples, respectively. Tellurium isotopes therefore have the potential to become a new geochemical sedimentary proxy, as well as a proxy for ore-exploration.

Les minéraux accessoires des granitoïdes de la suite taourirt, Hoggar (Algérie): conséquences pétrogénétiques

NASA Astrophysics Data System (ADS)

Azzouni-Sekkal, Abla; Bonin, Bernard

1998-01-01

The post-Pan-African 'taourirt' suite of Hoggar (Algeria) is made up by themagmatic suite: G I monzogranite, G IIa monzogranite+syenogranite, G IIb subsolvus alkali feldspar granite (alaskite), GIII hypersolvus alkali feldspar syenite + granite. Silicates (zircon, thorite, allanite, chevkinite, titanite), oxides (magnetite, ilmenite, fergusonite) and phosphates (apatite, monazite), often abundant, constitute various accessory mineral associations. Crystal morphology, place in the sequence of crystallisation and mineral chemistry change as a function of parageneses. The constant titanite + magnetite + ilmenite assemblage in G I and G II rocks illustrates more oxidising conditions than in G III group, where hedenbergite + magnetite + ilmenite coexist. Two groups of accessory minerals are distinguished: (1) LREE rich (3×10 4 to 3×10 5 × chondrites) and Y rich (50 to 10 4 × chondrites), such as allanite, chevkinite and monazite, (2) LREE poor (100 to 10 4 × chondrites) and Y rich (1000 to 10 5 × chondrites), such as zircon, thorite, titanite and fergusonite. Shapes of chondrite-normalised patterns and evolutionary trends of REE, as well as of other HFSE, such as Nb, Zr, U and Th, in bulk rocks are dependent on relative abundances of the different accessory minerals.

Rotational spectral variations of asteroid (8) Flora Implications for the nature of the S-type asteroids and for the parent bodies of the ordinary chondrites

NASA Technical Reports Server (NTRS)

Gaffey, M. J.

1984-01-01

The surface material and the surface material heterogeneities of the asteroid Flora are characterized using the best available data sets and the most sophisticated interpretive calibrations. Five spectrally derived mineralogic and patrologic properties of the surface assemblage of Flora which are relevant to whether this body is a differentiated or undifferentiated object are considered: bulk mineralogy, mafic mineral assemblage, metallic phase, pyroxene composition and structural type, and mineralogic variation. All of these properties indicate that Flora is a differentiated body. Flora is probably the residual core of an intensely heated, thermally evolved, and magnetically differentiated planetesimal which was subsequently disrupted. The present surface sample layers formed at or near the core-mantle boundary in the parent body.

The stable Cr isotopic compositions of chondrites and silicate planetary reservoirs

NASA Astrophysics Data System (ADS)

Schoenberg, Ronny; Merdian, Alexandra; Holmden, Chris; Kleinhanns, Ilka C.; Haßler, Kathrin; Wille, Martin; Reitter, Elmar

2016-06-01

The depletion of chromium in Earth's mantle (∼2700 ppm) in comparison to chondrites (∼4400 ppm) indicates significant incorporation of chromium into the core during our planet's metal-silicate differentiation, assuming that there was no significant escape of the moderately volatile element chromium during the accretionary phase of Earth. Stable Cr isotope compositions - expressed as the ‰-difference in 53Cr/52Cr from the terrestrial reference material SRM979 (δ53/52CrSRM979 values) - of planetary silicate reservoirs might thus yield information about the conditions of planetary metal segregation processes when compared to chondrites. The stable Cr isotopic compositions of 7 carbonaceous chondrites, 11 ordinary chondrites, 5 HED achondrites and 2 martian meteorites determined by a double spike MC-ICP-MS method are within uncertainties indistinguishable from each other and from the previously determined δ53/52CrSRM979 value of -0.124 ± 0.101‰ for the igneous silicate Earth. Extensive quality tests support the accuracy of the stable Cr isotope determinations of various meteorites and terrestrial silicates reported here. The uniformity in stable Cr isotope compositions of samples from planetary silicate mantles and undifferentiated meteorites indicates that metal-silicate differentiation of Earth, Mars and the HED parent body did not cause measurable stable Cr isotope fractionation between these two reservoirs. Our results also imply that the accretionary disc, at least in the inner solar system, was homogeneous in its stable Cr isotopic composition and that potential volatility loss of chromium during accretion of the terrestrial planets was not accompanied by measurable stable isotopic fractionation. Small but reproducible variations in δ53/52CrSRM979 values of terrestrial magmatic rocks point to natural stable Cr isotope variations within Earth's silicate reservoirs. Further and more detailed studies are required to investigate whether silicate differentiation processes, such as partial mantle melting and crystal fractionation, can cause stable Cr isotopic fractionation on Earth and other planetary bodies.

Relict chondrules in primitive achondrites: Remnants from their precursor parent bodies

NASA Astrophysics Data System (ADS)

Schrader, Devin L.; McCoy, Timothy J.; Gardner-Vandy, Kathryn

2017-05-01

We studied the petrography, analyzed the chemical compositions, constrained the closure temperatures (via geothermometry), and determined the oxidation states of relict chondrules in Campo del Cielo (IAB iron meteorite), Graves Nunataks (GRA) 98028 (acapulcoite), and Netschaëvo (IIE iron meteorite) to constrain their formation conditions and investigate links to known meteorite groups. Despite having been thermally metamorphosed, mineral phases within relict chondrules retain information about their precursor compositions. The sizes and textures of relict chondrules, and silicate and chromite compositions indicate that Campo del Cielo, GRA 98028, and Netschaëvo had distinct parent bodies that were similar to, but different from, known chondrite groups. To determine the utility of relict chondrule sizes in thermally metamorphosed meteorites, we determined the chondrule size distributions in the LL chondrites Semarkona (LL3.00), Soko-Banja (LL4), Siena (LL5), and Saint-Séverin (LL6), and the H chondrites Clovis (No. 1) (H3.6), Kesen (H4), Arbol Solo (H5), and Estacado (H6). As expected, mean chondrule diameters increase with degree of thermal metamorphism. We find that Campo del Cielo and GRA 98028 were reduced during thermal metamorphism, consistent with previous studies, indicating that their precursors were initially more FeO-rich than their current compositions. In contrast to previous studies, we find no evidence for reduction of silicates in Netschaëvo. Normal zoning of olivine in Netschaëvo is consistent with crystallization and suggests its silicates are near their primary FeO-contents. The presence of elongated chromite grains along olivine grain boundaries in Netschaëvo indicates formation during thermal metamorphism under oxidizing conditions. Due to the absence of reduction and the composition of chromite being distinct from that of metamorphosed H chondrites, we conclude that Netschaëvo, and by extension the IIE iron meteorites, are not from the H chondrite parent body.

Redox Conditions Among the Terrestrial Planets

NASA Technical Reports Server (NTRS)

Jones, J. H.

2004-01-01

Early solar system conditions should have been extremely reducing. The redox state of the early solar nebula was determined by the H2O/H2 of the gas, which is calculated (based on solar composition) to have been about IW-5. At high temperature under such conditions, ferrous iron would exist only as a trace element in silicates and the most common type of chondritic material should have been enstatite chondrites. The observation that E-chondrites form only a subset of the chondrite suite and that the terrestrial planets (Earth, Moon, Mars, Venus, 4 Vesta) contain ferrous and ferric iron as major and minor elements, respectively, implies that either most chondritic materials formed under conditions that were not solar or that early-formed metals oxidized at low temperature, producing FeO. For example, equilibrated ordinary chondrites (by definition, common chondritic materials), by their phase assemblage of olivine, orthopyroxene and metal, must fall not far from the QFI (Quartz-Fayalite-Iron) oxygen buffer. The QFI buffer is about IW-0.5 and, as we shall see, this fo2 is close to that inferred for many materials in the inner solar system.

Photomosaics of the cathodoluminescence of 60 sections of meteorites and lunar samples

USGS Publications Warehouse

Akridge, D.G.; Akridge, J.M.C.; Batchelor, J.D.; Benoit, P.H.; Brewer, J.; DeHart, J.M.; Keck, B.D.; Jie, L.; Meier, A.; Penrose, M.; Schneider, D.M.; Sears, D.W.G.; Symes, S.J.K.; Yanhong, Z.

2004-01-01

Cathodoluminescence (CL) petrography provides a means of observing petrographic and compositional properties of geological samples not readily observable by other techniques. We report the low-magnification CL images of 60 sections of extraterrestrial materials. The images we report include ordinary chondrites (including type 3 ordinary chondrites and gas-rich regolith breccias), enstatite chondrites, CO chondrites and a CM chondrite, eucrites and a howardite, lunar highland regolith breccias, and lunar soils. The CL images show how primitive materials respond to parent body metamorphism, how the metamorphic history of EL chondrites differs from that of EH chondrites, how dark matrix and light clasts of regolith breccias relate to each other, how metamorphism affects eucrites, the texture of lunar regolith breccias and the distribution of crystallized lunar spherules ("lunar chondrules"), and how regolith working affects the mineral properties of lunar soils. More particularly, we argue that such images are a rich source of new information on the nature and history of these materials and that our efforts to date are a small fraction of what can be done. Copyright 2004 by the American Geophysical Union.

Sayama CM2 Chondrite: Fresh but Heavily Altered

NASA Technical Reports Server (NTRS)

Takaoka, N.; Nakamura, T.; Noguchi, T.; Tonui, E.; Gounelle, M.; Zolensky, M. E.; Ebisawa, N.; Osawa, T.; Okazaki, R.; Nagao, K.;

Ti(3+) in meteoritic and synthetic hibonite

NASA Technical Reports Server (NTRS)

Beckett, John R.; Stolper, Edward; Live, David; Tsay, Fun-Dow; Grossman, Lawrence

1988-01-01

This paper describes the first direct determination (performed by electron spin resonance spectroscopy) of Ti(3+) in hibonite from inclusion SH-7 of the Murchison C2 chondrite and in synthetic hibonites of four compositions, three of which corresponded to the compositions of blue hibonites and one to that of an orange hibonite. The Ti(3+) concentration in the hibonite from SH-7 was found to range from 0.35 to 0.44 percent, while the Ti(3+) contents in three synthetic blue hibonites ranged from 0.02 to 0.64 percent. Orange hibonite contained no Ti(3+), supporting an earlier conclusion that the orange-to-blue transition is associated with the presence of Ti(3+). At constant temperature and oxygen fugacity, the Ti(3+)/Ti(4+) ratio in synthetic hibonites was found to increase with decreasing V, but was not strongly dependent on bulk Ti. Fe and Cr contents did not have a significant effect on the amount of Ti(3+).

Ti(3+) in meteoritic and synthetic hibonite

NASA Astrophysics Data System (ADS)

Beckett, John R.; Live, David; Tsay, Fun-Dow; Grossman, Lawrence; Stolper, Edward

1988-06-01

This paper describes the first direct determination (performed by electron spin resonance spectroscopy) of Ti(3+) in hibonite from inclusion SH-7 of the Murchison C2 chondrite and in synthetic hibonites of four compositions, three of which corresponded to the compositions of blue hibonites and one to that of an orange hibonite. The Ti(3+) concentration in the hibonite from SH-7 was found to range from 0.35 to 0.44 percent, while the Ti(3+) contents in three synthetic blue hibonites ranged from 0.02 to 0.64 percent. Orange hibonite contained no Ti(3+), supporting an earlier conclusion that the orange-to-blue transition is associated with the presence of Ti(3+). At constant temperature and oxygen fugacity, the Ti(3+)/Ti(4+) ratio in synthetic hibonites was found to increase with decreasing V, but was not strongly dependent on bulk Ti. Fe and Cr contents did not have a significant effect on the amount of Ti(3+).

Original structures, and fragmentation and reassembly histories of asteroids - Evidence from meteorites

NASA Technical Reports Server (NTRS)

Taylor, G. Jeffrey; Maggiore, Peter; Scott, Edward R. D.; Rubin, Alan E.; Keil, Klaus

1987-01-01

The validity of an onion shell model (OSM) for chondrite parent asteroids was assessed using metallographic cooling rates (MCR) derived from the compositions of metallic Fe-Ni grains. The hypothesis evaluated was that the hottest materials in chondrites would have been buried the deepest and cooled the slowest. The survey covered breccia from regolith and 13 different chondrites. The MCRs agreed well with cooling rates predicted by fission-track thermometry and Ar-40/Ar-39 ages. The OSM predicts an inverse correlation between the cooling rate and the petrographic type. Low correlations found between the MCRs and petrographic type indicate that chondrite parent asteroids were not assembled with onion shell structures.

Rapid Classification of Ordinary Chondrites Using Raman Spectroscopy

NASA Technical Reports Server (NTRS)

Fries, M.; Welzenbach, L.

2014-01-01

Classification of ordinary chondrites is typically done through measurements of the composition of olivine and pyroxenes. Historically, this measurement has usually been performed via electron microprobe, oil immersion or other methods which can be costly through lost sample material during thin section preparation. Raman microscopy can perform the same measurements but considerably faster and with much less sample preparation allowing for faster classification. Raman spectroscopy can facilitate more rapid classification of large amounts of chondrites such as those retrieved from North Africa and potentially Antarctica, are present in large collections, or are submitted to a curation facility by the public. With development, this approach may provide a completely automated classification method of all chondrite types.

The composition of phobos: evidence for carbonaceous chondrite surface from spectral analysis.

PubMed

Pang, K D; Pollack, J B; Veverka, J; Lane, A L; Ajello, J M

1978-01-06

A reflectance spectrum of Phobos (from 200 to 1100 nanometers) has been compiled from the Mariner 9 ultraviolet spectrometer, Viking lander imaging, and ground-based photometric data. The reflectance of the martian satellite is approximately constant at 5 percent from 1100 to 400 nanometers but drops sharply below 400 nanometers, reaching a value of 1 percent at 200 nanometers. The spectral albedo of Phobos bears a striking resemblance to that of asteroids (1) Ceres and (2) Pallas. Comparison of the reflectance spectra of asteroids with those of meteorites has shown that the spectral signature of Ceres is indicative of a carbonaceous chondritic composition. A physical explanation of how the compositional information is imposed on the reflectance spectrum is given. On the basis of a good match between the reflectance spectra of Phobos and Ceres and the extensive research that has been done to infer the composition of Ceres, it seems reasonable to believe that the surface composition of Phobos is similar to that of carbonaceous chondrites. This suggestion is consistent with the recently determined low density of Mars's inner satellite. Our result and recent Viking noble gas measurements suggest different modes of origin for Mars and Phobos.

Evidence for Reduced, Carbon-rich Regions in the Solar Nebula from an Unusual Cometary Dust Particle

DOE Office of Scientific and Technical Information (OSTI.GOV)

De Gregorio, Bradley T.; Stroud, Rhonda M.; Nittler, Larry R.

Geochemical indicators in meteorites imply that most formed under relatively oxidizing conditions. However, some planetary materials, such as the enstatite chondrites, aubrite achondrites, and Mercury, were produced in reduced nebular environments. Because of large-scale radial nebular mixing, comets and other Kuiper Belt objects likely contain some primitive material related to these reduced planetary bodies. Here, we describe an unusual assemblage in a dust particle from comet 81P/Wild 2 captured in silica aerogel by the NASA Stardust spacecraft. The bulk of this ∼20 μ m particle is comprised of an aggregate of nanoparticulate Cr-rich magnetite, containing opaque sub-domains composed of poorlymore » graphitized carbon (PGC). The PGC forms conformal shells around tiny 5–15 nm core grains of Fe carbide. The C, N, and O isotopic compositions of these components are identical within errors to terrestrial standards, indicating a formation inside the solar system. Magnetite compositions are consistent with oxidation of reduced metal, similar to that seen in enstatite chondrites. Similarly, the core–shell structure of the carbide + PGC inclusions suggests a formation via FTT reactions on the surface of metal or carbide grains in warm, reduced regions of the solar nebula. Together, the nanoscale assemblage in the cometary particle is most consistent with the alteration of primary solids condensed from a C-rich, reduced nebular gas. The nanoparticulate components in the cometary particle provide the first direct evidence from comets of reduced, carbon-rich regions that were present in the solar nebula.« less

A volatile topic: Parsing out the details of Earth's formation through experimental metal-silicate partitioning of volatile and moderately volatile elements

NASA Astrophysics Data System (ADS)

Mahan, B. M.; Siebert, J.; Blanchard, I.; Badro, J.; Sossi, P.; Moynier, F.

2017-12-01

Volatile and moderately volatile elements display different volatilities and siderophilities, as well as varying sensitivity to thermodynamic controls (X, P, T, fO2) during metal-silicate differentiation. The experimental determination of the metal-silicate partitioning of these elements permits us to evaluate processes controlling the distribution of these elements in Earth. In this work, we have combined metal-silicate partitioning data and results for S, Sn, Zn and Cu, and input these characterizations into Earth formation models. Model parameters such as source material, timing of volatile delivery, fO2 path, and degree of impactor equilibration were varied to encompass an array of possible formation scenarios. These models were then assessed to discern plausible sets of conditions that can produce current observed element-to-element ratios (e.g. S/Zn) in the Earth's present-day mantle, while also satisfying current estimates on the S content of the core, at no more than 2 wt%. The results of our models indicate two modes of accretion that can maintain chondritic element-to-element ratios for the bulk Earth and can arrive at present-day mantle abundances of these elements. The first mode requires the late addition of Earth's entire inventory of these elements (assuming a CI-chondritic composition) and late-stage accretion that is marked by partial equilibration of large impactors. The second, possibly more intuitive mode, requires that Earth accreted - at least initially - from volatile poor material preferentially depleted in S relative to Sn, Zn, and Cu. From a chemical standpoint, this source material is most similar to type I chondrule rich (and S poor) materials (Hewins and Herzberg, 1996; Mahan et al., 2017; Amsellem et al., 2017), such as the metal-bearing carbonaceous chondrites.

The Stubenberg meteorite—An LL6 chondrite fragmental breccia recovered soon after precise prediction of the strewn field

NASA Astrophysics Data System (ADS)

Bischoff, Addi; Barrat, Jean-Alix; Bauer, Kerstin; Burkhardt, Christoph; Busemann, Henner; Ebert, Samuel; Gonsior, Michael; Hakenmüller, Janina; Haloda, Jakub; Harries, Dennis; Heinlein, Dieter; Hiesinger, Harald; Hochleitner, Rupert; Hoffmann, Viktor; Kaliwoda, Melanie; Laubenstein, Matthias; Maden, Colin; Meier, Matthias M. M.; Morlok, Andreas; Pack, Andreas; Ruf, Alexander; Schmitt-Kopplin, Philippe; SchöNbäChler, Maria; Steele, Robert C. J.; Spurný, Pavel; Wimmer, Karl

2017-08-01

On March 6, 2016 at 21:36:51 UT, extended areas of Upper Austria, Bavaria (Germany) and the southwestern part of the Czech Republic were illuminated by a very bright bolide. This bolide was recorded by instruments in the Czech part of the European Fireball Network and it enabled complex and precise description of this event including prediction of the impact area. So far six meteorites totaling 1473 g have been found in the predicted area. The first pieces were recovered on March 12, 2016 on a field close to the village of Stubenberg (Bavaria). Stubenberg is a weakly shocked (S3) fragmental breccia consisting of abundant highly recrystallized rock fragments embedded in a clastic matrix. The texture, the large grain size of plagioclase, and the homogeneous compositions of olivine (Fa31.4) and pyroxene (Fs25.4) clearly indicate that Stubenberg is an LL6 chondrite breccia. This is consistent with the data on O, Ti, and Cr isotopes. Stubenberg does not contain solar wind-implanted noble gases. Data on the bulk chemistry, IR spectroscopy, cosmogenic nuclides, and organic components also indicate similarities to other metamorphosed LL chondrites. Noble gas studies reveal that the meteorite has a cosmic ray exposure (CRE) age of 36 ± 3 Ma and that most of the cosmogenic gases were produced in a meteoroid with a radius of at least 35 cm. This is larger than the size of the meteoroid which entered the Earth's atmosphere, which is constrained to <20 cm from short-lived radionuclide data. In combination, this might suggest a complex exposure history for Stubenberg.

Chemical and oxygen isotopic properties of ordinary chondrites (H5, L6) from Oman: Signs of isotopic equilibrium during thermal metamorphism

NASA Astrophysics Data System (ADS)

Ali, Arshad; Nasir, Sobhi J.; Jabeen, Iffat; Al Rawas, Ahmed; Banerjee, Neil R.; Osinski, Gordon R.

2017-10-01

Mean bulk chemical data of recently found H5 and L6 ordinary chondrites from the deserts of Oman generally reflect isochemical features which are consistent with the progressive thermal metamorphism of a common, unequilibrated starting material. Relative differences in abundances range from 0.5-10% in REE (Eu = 14%), 6-13% in siderophile elements (Co = 48%), and >10% in lithophile elements (exceptions are Ba, Sr, Zr, Hf, U = >30%) between H5 and L6 groups. These differences may have accounted for variable temperature conditions during metamorphism on their parent bodies. The CI/Mg-normalized mean abundances of refractory lithophile elements (Al, Ca, Sm, Yb, Lu, V) show no resolvable differences between H5 and L6 suggesting that both groups have experienced the same fractionation. The REE diagram shows subtle enrichment in LREE with a flat HREE pattern. Furthermore, overall mean REE abundances are 0.6 × CI with enriched La abundance ( 0.9 × CI) in both groups. Precise oxygen isotope compositions demonstrate the attainment of isotopic equilibrium by progressive thermal metamorphism following a mass-dependent isotope fractionation trend. Both groups show a slope-1/2 line on a three-isotope plot with subtle negative deviation in Δ17O associated with δ18O enrichment relative to δ17O. These deviations are interpreted as the result of liberation of water from phyllosilicates and evaporation of a fraction of the water during thermal metamorphism. The resultant isotope fractionations caused by the water loss are analogous to those occurring between silicate melt and gas phase during CAI and chondrule formation in chondrites and are controlled by cooling rates and exchange efficiency.

Laboratory synthesis of silicate glass spherules: Application to impact ejecta

NASA Astrophysics Data System (ADS)

Stoddard, P. S.; Pahlevan, K.; Tumber, S.; Weber, R.; Lee, K. K.

2012-12-01

To investigate the process by which molten droplets of impact ejecta solidify into glassy spherule tektites, we employed laser levitation experiments to recreate the hot temperatures of falling molten rock. Following models for Earth composition based on enstatite chondrites, we levitated mixtures of oxide powders in a stream of gas and melted them with a laser, producing silicate glass beads. After quenching, we polished the ~1 mm diameter samples in cross-section and analyzed with electron probe microanalysis (EPMA). Fine and coarsely-spaced EPMA transects across each bead displayed diffusion profiles at their edges, particularly in their SiO2 and MgO content. Heating altered the beads' bulk composition as well; all of the glassy spherules were compositionally different from the initial combination of powders. By comparing these changes to the environmental factors acting on the bead (e.g., temperature, type of levitation gas, duration of heating and amount of rotation), we produced a model for how molten ejecta change chemically and physically as they solidify into a glass. We find that high temperatures likely generated on impact have a strong effect on the composition of tektites; therefore, attempts to correlate tektites to their parent rocks should correct for this effect.

Petrology and geochemistry of Antarctic micrometeorites

NASA Astrophysics Data System (ADS)

Kurat, Gero; Koeberl, Christian; Presper, Thomas; Brandstätter, Franz; Maurette, Michel

1994-09-01

The petrology and geochemistry of twentythree chondritic dust particles with masses of 1-47 μg (sizes 100-400 μm) were recovered from blue ice near Cap Prudhomme, Antarctica, and studied by INAA, ASEM, EMPA, and optical microscopy. Sample selection criteria were irregular shape and (for a subsample) black color, with the aim of studying as many unmelted micrometeorites (MMs) as possible. Of thirteen unmelted MMs, six were phyllosilicate-dominated MMs, and seven were coarsegrained crystalline MMs consisting mainly of olivine and pyroxene. The remaining ten particles were largely melted and consisted of a foamy melt with variable amounts of relic phases (scoriaceous MMs). Thus, of the black particles selected, an astonishing portion, 40% (by number), consisted of largely unmelted MMs. Although unmelted, most phyllosilicate MMs have been thermally metamorphosed to a degree that most of the phyllosilicates were destroyed, but not melted. The original preterrestrial mineralogy is occasionally preserved and consists of serpentine-like phyllosilicates with variable amounts of cronstedtite, tochilinite-like oxides, olivine, and pyroxene. The crystalline MMs consist of olivine, low-Ca pyroxene, tochilinite-like oxides, and occasional Ni-poor metal. Relics in scoriaceous MMs consist of the same phases. Mineral compositions and the coexistence of phyllosilicates with anhydrous phases are typical of CM and CR-type carbonaceous chondrites. However, the olivine/pyroxene ratio (~ 1) and the lack of carbonates, sulfates, and of very Fe-poor, refractory element-rich olivines and pyroxenes sets the MMs apart from CM and CR chondrites. The bulk chemistry of the phyllosilicate MMs is similar to that of CM chondrites. However, several elements are either depleted (Ca, Ni, S, less commonly Na, Mg, and Mn) or enriched (K, Fe, As, Br, Rb, Sb, and Au) in MMs as compared to CM chondrites. Similar depletions and enrichments are also found in the scoriaceous MMs. We suggest that the depletions are probably due to terrestrial leaching of sulfates and carbonates from unmelted MMs. The overabundance of some elements may also be due to processes acting during atmospheric passage such as the recondensation of meteoric vapors in the high atmosphere. Most MMs are coated by magnetite of platy or octahedral habit, which is rich in Mg, Al, Si, Mn, and Ni. We interpret the magnetites to be products of recondensation processes in the high (>90 km) atmosphere, which are, therefore, probably the first refractory aerominerals identified.

Filling in the Gaps: Xenoliths in Meteorites are Samples of "Missing" Asteroid Lithologies

NASA Technical Reports Server (NTRS)

Zolensky, Mike

2016-01-01

We know that the stones that fall to earth as meteorites are not representative of the full diversity of small solar system bodies, because of the peculiarities of the dynamical processes that send material into Earth-crossing paths [1] which result in severe selection biases. Thus, the bulk of the meteorites that fall are insufficient to understand the full range of early solar system processes. However, the situation is different for pebble- and smaller-sized objects that stream past the giant planets and asteroid belts into the inner solar system in a representative manner. Thus, micrometeorites and interplanetary dust particles have been exploited to permit study of objects that do not provide meteorites to earth. However, there is another population of materials that sample a larger range of small solar system bodies, but which have received little attention - pebble-sized foreign clasts in meteorites (also called xenoliths, dark inclusions, clasts, etc.). Unfortunately, most previous studies of these clasts have been misleading, in that these objects have simply been identified as pieces of CM or CI chondrites. In our work we have found this to be generally erroneous, and that CM and especially CI clasts are actually rather rare. We therefore test the hypothesis that these clasts sample the full range of small solar system bodies. We have located and obtained samples of clasts in 81 different meteorites, and have begun a thorough characterization of the bulk compositions, mineralogies, petrographies, and organic compositions of this unique sample set. In addition to the standard e-beam analyses, recent advances in technology now permit us to measure bulk O isotopic compositions, and major- though trace-element compositions of the sub-mm-sized discrete clasts. Detailed characterization of these clasts permit us to explore the full range of mineralogical and petrologic processes in the early solar system, including the nature of fluids in the Kuiper belt and the outer main asteroid belt, as revealed by the mineralogy of secondary phases.

Low-Degree Partial Melting Experiments of CR and H Chondrite Compositions: Implications for Asteroidal Magmatism Recorded in GRA 06128 and GRA 06129 T

NASA Technical Reports Server (NTRS)

Usui, T.; Jones, John H.; Mittlefehldt, D. W.

2010-01-01

Studies of differentiated meteorites have revealed a diversity of differentiation processes on their parental asteroids; these differentiation mechanisms range from whole-scale melting to partial melting without the core formation [e.g., 1]. Recently discovered paired achondrites GRA 06128 and GRA 06129 (hereafter referred to as GRA) represent unique asteroidal magmatic processes. These meteorites are characterized by high abundances of sodic plagioclase and alkali-rich whole-rock compositions, implying that they could originate from a low-degree partial melt from a volatile-rich oxidized asteroid [e.g., 2, 3, 4]. These conditions are consistent with the high abundances of highly siderophile elements, suggesting that their parent asteroid did not segregate a metallic core [2]. In this study, we test the hypothesis that low-degree partial melts of chondritic precursors under oxidizing conditions can explain the whole-rock and mineral chemistry of GRA based on melting experiments of synthesized CR- and H-chondrite compositions.

Cobalt and precious metals in sulphides of peridotite xenoliths and inferences concerning their distribution according to geodynamic environment: A case study from the Scottish lithospheric mantle

NASA Astrophysics Data System (ADS)

Hughes, Hannah S. R.; McDonald, Iain; Faithfull, John W.; Upton, Brian G. J.; Loocke, Matthew

2016-01-01

Abundances of precious metals and cobalt in the lithospheric mantle are typically obtained by bulk geochemical analyses of mantle xenoliths. These elements are strongly chalcophile and the mineralogy, texture and trace element composition of sulphide phases in such samples must be considered. In this study we assess the mineralogy, textures and trace element compositions of sulphides in spinel lherzolites from four Scottish lithospheric terranes, which provide an ideal testing ground to examine the variability of sulphides and their precious metal endowments according to terrane age and geodynamic environment. Specifically we test differences in sulphide composition from Archaean-Palaeoproterozoic cratonic sub-continental lithospheric mantle (SCLM) in northern terranes vs. Palaeozoic lithospheric mantle in southern terranes, as divided by the Great Glen Fault (GGF). Cobalt is consistently elevated in sulphides from Palaeozoic terranes (south of the GGF) with Co concentrations > 2.9 wt.% and Co/Ni ratios > 0.048 (chondrite). In contrast, sulphides from Archaean cratonic terranes (north of the GGF) have low abundances of Co (< 3600 ppm) and low Co/Ni ratios (< 0.030). The causes for Co enrichment remain unclear, but we highlight that globally significant Co mineralisation is associated with ophiolites (e.g., Bou Azzer, Morocco and Outokumpu, Finland) or in oceanic peridotite-floored settings at slow-spreading ridges. Thus we suggest an oceanic affinity for the Co enrichment in the southern terranes of Scotland, likely directly related to the subduction of Co-enriched oceanic crust during the Caledonian Orogeny. Further, we identify a distinction between Pt/Pd ratio across the GGF, such that sulphides in the cratonic SCLM have Pt/Pd ≥ chondrite whilst Palaeozoic sulphides have Pt/Pd < chondrite. We observe that Pt-rich sulphides with discrete Pt-minerals (e.g., PtS) are associated with carbonate and phosphates in two xenolith suites north of the GGF. This three-way immiscibility (carbonate-sulphide-phosphate) indicates carbonatitic metasomatism is responsible for Pt-enrichment in this (marginal) cratonic setting. These Co and Pt-enrichments may fundamentally reflect the geodynamic setting of cratonic vs. non-cratonic lithospheric terranes and offer potential tools to facilitate geochemical mapping of the lithospheric mantle.

A New Modal Analysis Method to put Constraints on the Aqueous Alteration of CR Chondrites and Estimate the Unaltered CR Composition

NASA Technical Reports Server (NTRS)

Perronnet, M.; Zolensky, M. E.; Gounelle, M.; Schwandt, C. S.

2007-01-01

CR carbonaceous chondrites are of the major interest since they contain one of the most primitive organic matters. However, aqueous alteration has more or less overprinted their original features in a way that needed to be assessed. That was done in the present study by comparing the mineralogy of the most altered CR1 chondrite, GRO 95577, to a less altered CR2, Renazzo. Their modal analyses were achieved thanks to a new method, based on X-ray elemental maps acquired on electron microprobe, and on IDL image treatment. It allowed the collection of new data on the composition of Renazzo and confirmed the classification of GRO 95577 as a CR1. New alteration products for CRs, vermiculite and clinochlore, were observed. The homogeneity of the Fe-poor clays in the CR1 and the distinctive matrix composition in the two chondrites suggest a wide-range of aqueous alteration on CRs. The preservation of the outlines of the chondrules in GRO 95577 and the elemental transfers of Al, Fe and Ca throughout the chondrule and of Fe and S from the matrix to the chondrule favor the idea of an asteroidal location of the aqueous alteration. From their mineralogical descriptions and modal abundances, the element repartitions in Renazzo and GRO 95577 were computed. It indicates a possible relationship between these two chondrites via an isochemical alteration process. Knowing the chemical reactions that occurred during the alteration, it was thus possible to decipher the mineralogical modal abundances in the unaltered CR body.

A New Modal Analysis Method to put Constraints on the Aqueous Alteration of CR Chondrites and Estimate the Unaltered CR Composition

NASA Technical Reports Server (NTRS)

Perronnet, M.; Zolensky, M. E.; Gounelle, M.; Schwandt, C. S.

2007-01-01

carbonaceous chondrites are of the major interest since they contain one of the most primitive organic matters. However, aqueous alteration has more or less overprinted their original features in a way that needed to be assessed. That was done in the present study by comparing the mineralogy of the most altered CR1 chondrite, GRO 95577, to a less altered CR2, Renazzo. Their modal analyses were achieved thanks to a new method, based on X-ray elemental maps acquired on electron microprobe, and on IDL image treatment. It allowed the collection of new data on the composition of Renazzo and confirmed the classification of GRO 95577 as a CR1. New alteration products for CRs, vermiculite and clinochlore, were observed. The homogeneity of the Fe-poor clays in the CR1 and the distinctive matrix composition in the two chondrites suggest a wide-range of aqueous alteration on CRs. The preservation of the outlines of the chondrules in GRO 95577 and the elemental transfers of Al, Fe and Ca throughout the chondrule and of Fe and S from the matrix to the chondrule favor the idea of an asteroidal location of the aqueous alteration. From their mineralogical descriptions and modal abundances, the element repartitions in Renazzo and GRO 95577 were computed. It indicates a possible relationship between these two chondrites via an isochemical alteration process. Knowing the chemical reactions that occurred during the alteration, it was thus possible to decipher the mineralogical modal abundances in the unaltered CR body.

Magnetic Evidence for a Partially Differentiated Carbonaceous Chondrite Parent Body and Possible Implications for Asteroid 21 Lutetia

NASA Astrophysics Data System (ADS)

Weiss, Benjamin; Carporzen, L.; Elkins-Tanton, L.; Shuster, D. L.; Ebel, D. S.; Gattacceca, J.; Binzel, R. P.

2010-10-01

The origin of remanent magnetization in the CV carbonaceous chondrite Allende has been a longstanding mystery. The possibility of a core dynamo like that known for achondrite parent bodies has been discounted because chondrite parent bodies are assumed to be undifferentiated. Here we report that Allende's magnetization was acquired over several million years (Ma) during metasomatism on the parent planetesimal in a > 20 microtesla field 8-9 Ma after solar system formation. This field was present too recently and directionally stable for too long to have been the generated by the protoplanetary disk or young Sun. The field intensity is in the range expected for planetesimal core dynamos (Weiss et al. 2010), suggesting that CV chondrites are derived from the outer, unmelted layer of a partially differentiated body with a convecting metallic core (Elkins-Tanton et al. 2010). This suggests that asteroids with differentiated interiors could be present today but masked under chondritic surfaces. In fact, CV chondrites are spectrally similar to many members of the Eos asteroid family whose spectral diversity has been interpreted as evidence for a partially differentiated parent asteroid (Mothe-Diniz et al. 2008). CV chondrite spectral and polarimetric data also resemble those of asteroid 21 Lutetia (e.g., Belskaya et al. 2010), recently encountered by the Rosetta spacecraft. Ground-based measurements of Lutetia indicate a high density of 2.4-5.1 g cm-3 (Drummond et al. 2010), while radar data seem to rule out a metallic surface composition (Shepard et al. 2008). If Rosetta spacecraft measurements confirm a high density and a CV-like surface composition for Lutetia, then we propose Lutetia may be an example of a partially differentiated carbonaceous chondrite parent body. Regardless, the very existence of primitive achondrites, which contain evidence of both relict chondrules and partial melting, are prima facie evidence for the formation of partially differentiated bodies.

A petrologic, thermodynamic and experimental study of brachinites: Partial melt residues of an R chondrite-like precursor

NASA Astrophysics Data System (ADS)

Gardner-Vandy, Kathryn G.; Lauretta, Dante S.; McCoy, Timothy J.

2013-12-01

The primitive achondrites provide a window into the initial melting of asteroids in the early solar system. The brachinites are olivine-dominated meteorites with a recrystallized texture that we and others interpret as evidence of partial melting and melt removal on the brachinite parent body. We present a petrologic, thermodynamic and experimental study of the brachinites to evaluate the conditions under which they formed and test our hypothesis that the precursor material to the brachinites was FeO-rich compared to the precursors of other primitive achondrites. Petrologic analysis of six brachinites (Brachina, Allan Hills (ALH) 84025, Hughes 026, Elephant Moraine (EET) 99402, Northwest Africa (NWA) 3151, and NWA 4969) and one brachinite-like achondrite (NWA 5400) shows that they are meteorites with recrystallized texture that are enriched in olivine (⩾80 vol.%) and depleted in other minerals with respect to a chondritic mineralogy. Silicates in the brachinites are FeO-rich (Fa32-36). Brachinite-like achondrite Northwest Africa 5400 is similar in mineralogy and texture to the brachinites but with a slightly lower FeO-content (Fa30). Thermodynamic calculations yield equilibration temperatures above the Fe,Ni-FeS cotectic temperature (∼950 °C) for all meteorites studied here and temperatures above the silicate eutectic (∼1050 °C) for all but two. Brachina formed at an fO2 of ∼IW, and the other brachinites and NWA 5400 formed at ∼IW - 1. All the meteorites show great evidence of formation by partial melting having approximately chondritic to depleted chondritic mineralogies, equilibrated mineral compositions, and recrystallized textures, and having reached temperatures above that required for melt generation. In an attempt to simulate the formation of the brachinite meteorites, we performed one-atmosphere, gas-mixing partial melting experiments of R4 chondrite LaPaz Ice Field 03639. Experiments at 1250 °C and an oxygen fugacity of IW - 1 produce residual phases that are within the mineralogy and mineral compositions of the brachinites. These experiments provide further evidence for the formation of brachinites as a result of partial melting of a chondritic precursor similar in mineralogy and mineral compositions to the R chondrites.

Oxygen, Magnesium, and Aluminum Isotopes in the Ivuna CAI: Re-Examining High-Temperature Fractionations in CI Chondrites

NASA Astrophysics Data System (ADS)

Frank, D. R.; Huss, G. R.; Nagashima, K.; Zolensky, M. E.; Le, L.

2017-07-01

The only whole CAI preserved in the aqueously altered CI chondrites is 16O-rich and has no resolvable radiogenic Mg. Accretion of CAIs by the CI parent object(s) may limit the precision of cosmochemical models that require a CI starting composition.

Determining the relative extent of alteration in CM chondrites

NASA Technical Reports Server (NTRS)

Browning, Lauren B.; Mcsween, Harry Y., Jr.; Zolensky, Michael

1993-01-01

The aqueous alteration of CM chondrites provides a record of the processes attending the earliest stages of parent body evolution. However, resolving the alteration pathways of chondritic evolution requires a means for distinguishing the relative extent of alteration that individual samples have experienced. Three new indices for gauging the relative degree of alteration in CM chondrites based on modal and compositional analyses of 7 CM falls were proposed. The proposed alteration parameters are consistent with the basic tenets of several previous models and correlate with additional indices to produce an integrated method for determining the relative extent of alteration. The model predicts the following order of progressive alteration: Murchison (MC) is less than or equal to Bells (BL) is less than Murray (MY) is less than Cochabamba (CC) is less than Mighei (MI) is less than Nogoya (NG) is less than or equal to Cold Bokkeveld (CB). The broad range of CM phyllosilicate compositions observed within individual meteorites is fundamental to the characterization of the aqueous alteration process. Chemical analyses of CM phyllosilicates suggest that these phases became systematically enriched in Mg and depleted in Fe with increasing alteration.

Carbynes - Carriers of primordial noble gases in meteorites

NASA Technical Reports Server (NTRS)

Whittaker, A. G.; Watts, E. J.; Lewis, R. S.; Anders, E.

1980-01-01

Five carbynes (triply bonded allotropes of carbon) have been found by electron diffraction in the Allende and Murchison carbonaceous chondrites: carbon VI, VIII, X, XI, and (tentatively) XII. From the isotopic composition of the associated noble-gas components, it appears that the carbynes in Allende (C3V chondrite) are local condensates from the solar nebula, whereas at least two carbynes in Murchison (C2 chondrite) are of exotic, presolar origin. They may be dust grains that condensed in stellar envelopes and trapped isotropically anomalous matter from stellar nucleosynthesis.

Chondrites and the Protoplanetary Disk, Part 2

NASA Technical Reports Server (NTRS)

2004-01-01

Contents include the following: On the Dynamical Evolution of a Nebula and Its Effect on Dust Coagulation and the Formation of Centimeter-sized Particles. The Mineralogy and Grain Properties of the Disk Surfaces in Three Herbig Ae/Be Stars. Astrophysical Observations of Disk Evolution Around Solar Mass Stars. The Systematic Petrology of Chondrites: A Consistent Approach to Assist Classification and Interpretation. Understanding Our Origins: Formation of Sun-like Stars in H II Region Environments. Chondrule Crystallization Experiments. Formation of SiO2-rich Chondrules by Fractional Condensation. Refractory Forsterites from Murchison (CM2) and Yamato 81020 (CO3.0) Chondrites: Cathodoluminescence, Chemical Compositions and Oxygen Isotopes. Apparent I-Xe Cooling Rates of Chondrules Compared with Silicates from the Colomera Iron Meteorite. Chondrule Formation in Planetesimal Bow Shocks: Physical Processes in the Near Vicinity of the Planetesimal. Genetic Relationships Between Chondrules, Rims and Matrix. Chondrite Fractionation was Cosmochemical; Chondrule Fractionation was Geochemical. Chondrule Formation and Accretion of Chondrite Parent Bodies: Environmental Constraints. Amoeboid Olivine Aggregates from the Semarkona LL3.0 Chondrite. The Evolution of Solids in Proto-Planetary Disks. New Nickel Vapor Pressure Measurements: Possible Implications for Nebular Condensates. Chemical, Mineralogical and Isotopic Properties of Chondrules: Clues to Their Origin. Maximal Size of Chondrules in Shock-Wave Heating Model: Stripping of Liquid Surface in Hypersonic Rarefied Gas Flow. The Nature and Origin of Interplanetary Dust: High Temperature Components. Refractory Relic Components in Chondrules from Ordinary Chondrites. Constraints on the Origin of Chondrules and CAIs from Short-lived and Long-lived Radionuclides. The Genetic Relationship Between Refractory Inclusions and Chondrules. Contemporaneous Chondrule Formation Between Ordinary and Carbonaceous Chondrites. Chondrules and Isolated Grains in the Fountain Hills Bencubbinite. Implications of Chondrule Formation in a Gas of Solar Composition. Implications of Meteoritic Cl-36 Abundance for the Origin of Short-lived Radionuclides in the Early Solar System. Size Sorting and the Chondrule Size Spectrum. Comparative Study of Refractory Inclusions from Different Groups of Chondrites. In Situ Investigation of Mg Isotope Distributions in an Allende CAI by Combined LA-ICPMS and SIMS Analyses Photochemical Speciation of Oxygen Isotopes in the Solar Nebula.

Al-rich objects in ordinary chondrites - Related origin of carbonaceous and ordinary chondrites and their constituents

NASA Technical Reports Server (NTRS)

Bischoff, A.; Keil, K.

1984-01-01

A description is given of 169 Al-rich objects (arbitrarily defined as having 10 wt pct or more of Al2O3) from 24 ordinary chondrites of types 3 and 4, five regolith breccias containing unequilibrated material, the unique meteorite Kakangari, and a few ordinary chondrites of types 5 and 6. On the basis of shape and texture, the Al-rich objects are divided into chondrules (round, with igneous textures), irregularly shaped inclusions (similar to type F and spinel-rich complex Ca-Al-rich inclusions), and fragments (probably fragments of Al-rich chondrules and inclusions). For descriptive purposes, the Al-rich chondrules are further subdivided into compositional subgroups, although they are entirely transitional.

Amino Acids and Chirality

NASA Technical Reports Server (NTRS)

Cook, Jamie E.

2012-01-01

Amino acids are among the most heavily studied organic compound class in carbonaceous chondrites. The abundance, distributions, enantiomeric compositions, and stable isotopic ratios of amino acids have been determined in carbonaceous chondrites fi'om a range of classes and petrographic types, with interesting correlations observed between these properties and the class and typc of the chondritcs. In particular, isomeric distributions appear to correlate with parent bodies (chondrite class). In addition, certain chiral amino acids are found in enantiomeric excess in some chondrites. The delivery of these enantiomeric excesses to the early Earth may have contributed to the origin of the homochirality that is central to life on Earth today. This talk will explore the amino acids in carbonaceous chondritcs and their relevance to the origin of life.

Evidence for the presence of planetesimal material among the precursors of magnesian chondrules of nebular origin

NASA Astrophysics Data System (ADS)

Libourel, Guy; Krot, Alexander N.

2007-02-01

Chondrules are the major high-temperature components of chondritic meteorites, which are conventionally viewed as the samples from the very first generation of undifferentiated planetesimals. Growing evidences from long- and short-lived radionuclide chronologies indicate however that chondrite parent asteroids accreted after or contemporaneously with igneous activities on differentiated asteroids, questioning the pristine nature of chondrites. Here we report a discovery of metal-bearing olivine aggregates with granoblastic textures inside magnesian porphyritic (Type I) chondrules from the CV carbonaceous chondrite Vigarano. Formation of the granoblastic textures requires sintering and prolonged, high-temperature (> 1000 °C) annealing - conditions which are not expected in the solar nebula during chondrule formation, but could have been achieved on parent bodies of olivine-rich differentiated or thermally metamorphosed meteorites. The mineralogy and petrography of the metal-olivine aggregates thus indicate that they are relict, dunite-like lithic fragments which resulted from fragmentation of such bodies. The very old Pb-Pb absolute ages and Al-Mg relative model ages of bulk CV chondrules suggest that such planetesimals may have formed as early as the currently accepted age of the Solar System (4567.2 ± 0.6 Ma).

Cometary Evolution: Clues on Physical Properties from Chondritic Interplanetary Dust Particles

NASA Technical Reports Server (NTRS)

Rietmeijer, Frans J. M.; Mackinnon, Ian D. R.

1989-01-01

The degree of diversity or similarity detected in comets depends primarily on the lifetimes of the individual cometary nuclei at the time of analysis. It is inherent in our understanding of cometary orbital dynamics and the seminal model of comet origins by Oort that cometary evolution is the natural order of events in our Solar System. Thus, predictions of cometary behaviour in terms of bulk physical, mineralogical or chemical parameters should contain an appreciation of temporal variation(s). Previously, Rietmeijer and Mackinnon developed mineralogical bases for the chemical evolution of cometary nuclei primarily with regard to the predominantly silicate fraction of comet nuclei. We suggested that alteration of solids in cometary nuclei should be expected and that indications of likely reactants and products can be derived from judicious comparison with terrestrial diagenetic environments which include hydrocryogenic and low-temperature aqueous alterations. In a further development of this concept, Rietmeijer provides indirect evidence for the formation of sulfides and oxides in comet nuclei. Furthermore, Rietmeijer noted that timescales for hydrocryogenic and low-temperature reactions involving liquid water are probably adequate for relatively mature comets, e.g. P/comet Halley. In this paper, we will address the evolution of comet nuclei physical parameters such as solid particle grain size, porosity and density. In natural environments, chemical evolution (e.g. mineral reactions) is often accompanied by changes in physical properties. These concurrent changes are well-documented in the terrestrial geological literature, especially in studies of sediment diagenesis and we suggest that similar basic principles apply within the upper few meters of active comet nuclei. The database for prediction of comet nuclei physical parameters is, in principle, the same as used for the proposition of chemical evolution. We use detailed mineralogical studies of chondritic interplanetary dust particles (IDPS) as a guide to the likely constitution of mature comets traversing the inner Solar System. While there is, as yet, no direct proof that a specific sub-group or type of chondritic IDP is derived from a specific comet, it is clear that these particles are extraterrestrial in origin and that a certain portion of the interplanetary flux received by the Earth is cometary in origin. Two chondritic porous (CP) MPs, sample numbers W7010A2 and W7029Cl, from the Johnson Space Center Cosmic Dust Collection have been selected for this study of putative cometary physical parameters. This particular type of particle is considered a likely candidate for a cometary origin on the basis of mineralogy, bulk composition and morphology. While many IDPs have been subjected to intensive study over the past decade, we can develop a physical parameter model on only these two CP IDPs because few others have been studied in sufficient detail.

Cometary Evolution: Clues on Physical Properties from Chondritic Interplanetary Dust Particles

NASA Technical Reports Server (NTRS)

Reitmeijer, Frans J. M.; Mackinnon, Ian D. R.

1997-01-01

The degree of diversity or similarity detected in comets depends primarily on the lifetimes of the individual cometary nuclei at the time of analysis. It is inherent in our understanding of cometary orbital dynamics and the seminal model of comet origins that cometary evolution is the natural order of events in our Solar System. Thus, predictions of cometary behaviour in terms of bulk physical, mineralogical or chemical parameters should contain an appreciation of temporal variation(s). Previously, Rietmeijer and Mackinnon [1987] developed mineralogical bases for the chemical evolution of cometary nuclei primarily with regard to the predominantly silicate fraction of comet nuclei. We suggested that alteration of solids in cometary nuclei should be expected and that indications of likely reactants and products can be derived from judicious comparison with terrestrial diagenetic environments which include hydrocryogenic and low-temperature aqueous alterations. In a further development of this concept, Rietmeijer [1988] provides indirect evidence for the formation of sulfides and oxides in comet nuclei. Furthermore, Rietmeijer [1988] noted that timescales for hydrocryogenic and low-temperature reactions involving liquid water are probably adequate for relatively mature comets, e.g. P/comet Halley. In this paper, we will address the evolution of comet nuclei physical parameters such as solid particle grain size, porosity and density. In natural environments, chemical evolution (e.g. mineral reactions) is often accompanied by changes in physical properties. These concurrent changes are well-documented in the terrestrial geological literature, especially in studies of sediment diagenesis and we suggest that similar basic principles apply within the upper few meters of active comet nuclei. The database for prediction of comet nuclei physical parameters is, in principle, the same as used for the proposition of chemical evolution. We use detailed mineralogical studies of chondritic interplanetary dust particles (IDPS) as a guide to the likely constitution of mature comets traversing the inner Solar System. While there is, as yet, no direct proof that a specific sub-group or type of chondritic IDP is derived from a specific comet, it is clear that these particles are extraterrestrial in origin and that a certain portion of the interplanetary flux received by the Earth is cometary in origin. Two chondritic porous (CP) IDPS, sample numbers W701OA2 and W7029CI, from the Johnson Space Center Cosmic Dust Collection have been selected for this study of putative cometary physical parameters. This particular type of particle is considered a likely candidate for a cometary origin on the basis of mineralogy, bulk composition and morphology. While many IDPs have been subjected to intensive study over the past decade, we can develop a physical parameter model on only these two CP IDPs because few others have been studied in sufficient detail.

A Procedure to Determine the Coordinated Chromium and Calcium Isotopic Composition of Astromaterials Including the Chelyabinsk Meteorite

NASA Technical Reports Server (NTRS)

Tappa, M. J.; Mills, R. D.; Ware, B.; Simon, J. I.

2014-01-01

The isotopic compositions of elements are often used to characterize nucelosynthetic contributions in early Solar System objects. Coordinated multiple middle-mass elements with differing volatilities may provide information regarding the location of condensation of early Solar System solids. Here we detail new procedures that we have developed to make high-precision multi-isotope measurements of chromium and calcium using thermal ionization mass spectrometry, and characterize a suite of chondritic and terrestrial material including two fragments of the Chelyabinsk LL-chondrite.

Classification of six ordinary chondrites from Texas

NASA Astrophysics Data System (ADS)

Ehlmann, Arthur J.; Keil, Klaus

1988-12-01

Based on optical microscopy, modal and electron microprobe analyses, six ordinary chondrites from Texas were classified in compositional groups, petrologic types, and shock facies. These meteorites are Comanche (stone), L5c; Haskell, L5c; Deport (a), H4b; Naruna (a), H4b; Naruna (b), H4b; and Clarendon (b), H5d.

Applications of the 190Pt-186Os isotope system to geochemistry and cosmochemistry

USGS Publications Warehouse

Walker, R.J.; Morgan, J.W.; Beary, E.S.; Smoliar, M.I.; Czamanske, G.K.; Horan, M.F.

1997-01-01

Platinum is fractionated from osmium primarily as a consequence of processes involving sulfide and metal crystallization. Consequently, the 190Pt-186Os isotope system (190Pt ??? 186Os + ??) shows promise for dating some types of magmatic sulfide ores and evolved iron meteorites. The first 190Pt-186Os isochrons are presented here for ores from the ca. 251 Ma Noril'sk, Siberia plume, and for group IIAB magmatic iron meteorites. Given the known age of the Noril'sk system, a decay constant for 190Pt is determined to be 1.542 ?? 10-12a-1, with ??1% uncertainty. The isochron generated for the IIAB irons is consistent with this decay constant and the known age of the group. The 186Os/188Os ratios of presumably young, mantle-derived osmiridiums and also the carbonaceous chondrite Allende were measured to high-precision to constrain the composition of the modern upper mantle. These compositions overlap, indicating that the upper mantle is chondritic within the level of resolution now available. Our best estimate for this 186Os/188Os ratio is 0.119834 ?? 2 (2??M). The 190Pt/186Os ratios determined for six enstatite chondrites average 0.001659 ?? 75, which is very similar to published values for carbonaceous chondrites. Using this ratio and the presumed composition of the modern upper mantle and chondrites, a solar system initial 186Os/188Os ratio of 0.119820 is calculated. In comparison to the modern upper mantle composition, the 186Os/188Os ratio of the Noril'sk plume was approximately 0.012% enriched in 186Os. Possible reasons for this heterogeneity include the recycling of Pt-rich crust into the mantle source of the plume and derivation of the osmium from the outer core. Derivation of the osmium from the outer core is our favored model. Copyright ?? 1997 Elsevier Science Ltd.

Samples of Asteroid Surface Ponded Deposits in Chondritic Meteorites

NASA Technical Reports Server (NTRS)

Zolensky, M. E.; Lee, R.; Le, L.

2004-01-01

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%.

Petrography and Geochemistry of Metals in Almahata Sitta Ureilites

NASA Technical Reports Server (NTRS)

Ross, A. J.; Herrin, J. S.; Mittlefehldt, D. W.; Downes, H.; Smith, C. L.; Lee, M. R.; Jones, A. P.; Jenniskens, P.; Shaddad, M. H,

2011-01-01

Ureilites are ultramafic achondrites, predominantly composed of olivine and pyroxenes with accessory carbon, metal and sulfide. The majority of ureilites are believed to represent the mantle of the ureilite parent body (UPB) [1]. Although ureilites have lost much of their original metal [2], the metal that remains retains a record of the formative processes. Almahata Sitta is predominantly composed of unbrecciated ureilites with a wide range of silicate compositions [3,4]. As a fall it presents a rare opportunity to examine fresh ureilite metal in-situ, and analyzing their highly siderophile element (HSE) ratios gives clues to their formation. Bulk siderophile element analyses of Almahata Sitta fall within the range observed in other ureilites [5]. We have examined the metals in seven ureilitic samples of Almahata Sitta (AS) and one associated chondrite fragment (AS#25).

Thermal evolution of a partially differentiated H chondrite parent body

NASA Astrophysics Data System (ADS)

Abrahams, J. N. H.; Bryson, J. F. J.; Weiss, B. P.; Nimmo, F.

2016-12-01

It has traditionally been assumed that planetesimals either melted entirely or remained completely undifferentiated as they accreted. The unmelted textures and cooling histories of chondrites have been used to argue that these meteorites originated from bodies that never differentiated. However, paleomagnetic measurements indicate that some chondrites (e.g., the H chondrite Portales Valley and several CV chondrites) were magnetized by a core dynamo magnetic field, implying that their parent bodies were partially differentiated. It has been unclear, however, whether planetesimal histories consistent with dynamo production can also be consistent with the diversity of chondrite cooling rates and ages. To address this, we modeled the thermal evolution of the H chondrite parent body, considering a variety of accretion histories and parent body radii. We considered partial differentiation using two-stage accretion involving the initial formation and differentiation of a small body, followed by the later addition of low thermal conductivity chondritic material that remains mostly unmelted. We were able to reproduce the measured thermal evolution of multiple H chondrites for a range of parent body parameters, including initial radii from 70-150 km, chondritic layer thicknesses from 50 km to over 100 km, and second stage accretion times of 2.5-3 Myr after solar system formation. Our predicted rates of core cooling and crystallization are consistent with dynamo generation by compositional convection beginning 60-200 Myr after solar system formation and lasting for at least tens of millions of years. This is consistent with magnetic studies of Portales Valley [Bryson et al., this meeting]. In summary, we find that thermal models of partial differentiation are consistent the radiometric ages, magnetization, and cooling rates of a diversity H chondrites.

Extraterrestrial amino acids identified in metal-rich CH and CB carbonaceous chondrites from Antarctica

NASA Astrophysics Data System (ADS)

Burton, Aaron S.; Elsila, Jamie E.; Hein, Jason E.; Glavin, Daniel P.; Dworkin, Jason P.

2013-03-01

Carbonaceous chondrites contain numerous indigenous organic compounds and could have been an important source of prebiotic compounds required for the origin of life on Earth or elsewhere. Extraterrestrial amino acids have been reported in five of the eight groups of carbonaceous chondrites and are most abundant in CI, CM, and CR chondrites but are also present in the more thermally altered CV and CO chondrites. We report the abundance, distribution, and enantiomeric and isotopic compositions of simple primary amino acids in six metal-rich CH and CB carbonaceous chondrites that have not previously been investigated for amino acids: Allan Hills (ALH) 85085 (CH3), Pecora Escarpment (PCA) 91467 (CH3), Patuxent Range (PAT) 91546 (CH3), MacAlpine Hills (MAC) 02675 (CBb), Miller Range (MIL) 05082 (CB), and Miller Range (MIL) 07411 (CB). Amino acid abundances and carbon isotopic values were obtained by using both liquid chromatography time-of-flight mass spectrometry and fluorescence, and gas chromatography isotope ratio mass spectrometry. The δ13C/12C ratios of multiple amino acids fall outside of the terrestrial range and support their extraterrestrial origin. Extracts of CH chondrites were found to be particularly rich in amino acids (13-16 parts per million, ppm) while CB chondrite extracts had much lower abundances (0.2-2 ppm). The amino acid distributions of the CH and CB chondrites were distinct from the distributions observed in type 2 and 3 CM and CR chondrites and contained elevated levels of β-, γ-, and δ-amino acids compared to the corresponding α-amino acids, providing evidence that multiple amino acid formation mechanisms were important in CH and CB chondrites.

Chemical studies of H chondrites. II - Weathering effects in the Victoria Land, Antarctic population and comparison of two Antarctic populations with non-Antarctic falls

NASA Astrophysics Data System (ADS)

Dennison, J. E.; Lipschutz, M. E.

1987-03-01

The authors report RNAA data for 14 siderophile, lithophile and chalcophile volatile/mobile trace elements in interior portions of 45 different H4-6 chondrites (49 samples) from Victoria Land, Antarctica and 5 H5 chondrites from the Yamato Mts., Antarctica. Relative to H5 chondrites of weathering types A and B, all elements are depleted (10 at statistically significant levels) in extensively weathered (types B/C and C) samples. Chondrites of weathering types A and B seem compositionally uncompromised and as useful as contemporary falls for trace-element studies. When data distributions for these 14 trace elements in non-Antarctic H chondrite falls and unpaired samples from Victoria Land and from the Yamato Mts. (Queen Maud Land) are compared statistically, numerous significant differences are apparent. These and other differences give ample cause to doubt that the various sample populations derive from the same parent population. The observed differences do no reflect weathering, chance or other trivial causes: a preterrestrial source must be responsible.

H/L chondrite LaPaz Icefield 031047 - A feather of Icarus?

DOE Office of Scientific and Technical Information (OSTI.GOV)

Wittmann, Axel; Friedrich, Jon M; Troiano, Julianne

2011-10-28

Antarctic meteorite LAP 031047 is an ordinary chondrite composed of loosely consolidated chondritic fragments. Its petrography, oxygen isotopic composition and geochemical inventory are ambiguous and indicate an intermediate character between H and L chondrites. Petrographic indicators suggest LAP 031047 suffered a shock metamorphic overprint below ~10 GPa, which did not destroy its unusually high porosity of ~27 vol%. Metallographic textures in LAP 031047 indicate heating above ~700 °C and subsequent cooling, which caused massive transformation of taenite to kamacite. The depletion of thermally labile trace elements, the crystallization of chondritic glass to microcrystalline plagioclase of unusual composition, and the occurrencemore » of coarsely crystallized chondrule fragments is further evidence for post-metamorphic heating to ~700-750 °C. However, this heating event had a transient character because olivine and low-Ca pyroxene did not equilibrate. Nearly complete degassing up to very high temperatures is indicated by the thorough resetting of LAP 031047's Ar-Ar reservoir ~100 ± 55 Ma ago. A noble gas cosmic-ray exposure age indicates it was reduced to a meter-size fragment at <0.5 Ma. In light of the fact that shock heating cannot account for the thermal history of LAP 031047 in its entirety, we test the hypothesis that this meteorite belonged to the near-surface of an Aten or Apollo asteroid that underwent heating during orbital passages close to the Sun.« less

The Origin of the Compositional Diversity of Mercury's Surface Constrained From Experimental Melting of Enstatite Chondrites

NASA Technical Reports Server (NTRS)

Boujibar, A.; Righter, K.; Pando, K.; Danielson, L.

2015-01-01

Mercury is known as an endmember planet as it is the most reduced terrestrial planet with the highest core/mantle ratio. MESSENGER spacecraft has shown that its surface is FeO-poor (2-4 wt%) and Srich (up to 6-7 wt%), which confirms the reducing nature of its silicate mantle. Moreover, high resolution images revealed large volcanic plains and abundant pyroclastic deposits, suggesting important melting stages of the Mercurian mantle. This interpretation was confirmed by the high crustal thickness (up to 100 km) derived from Mercury's gravity field. This is also corroborated by a recent experimental result that showed that Mercurian partial melts are expected to be highly buoyant within the Mercurian mantle and could have risen from depths as high as the core-mantle boundary. In addition MESSENGER spacecraft provided relatively precise data on major elemental compositions of Mercury's surface. These results revealed important chemical and mineralogical heterogeneities that suggested several stages of differentiation and re-melting processes. However, the extent and nature of compositional variations produced by partial melting remains poorly constrained for the particular compositions of Mercury (very reducing conditions, low FeO-contents and high sulfur-contents). Therefore, in this study, we investigated the processes that lead to the various compositions of Mercury's surface. Melting experiments with bulk Mercury-analogue compositions were performed and compared to the compositions measured by MESSENGER.

The origin of chromitic chondrules and the volatility of Cr under a range of nebular conditions

NASA Technical Reports Server (NTRS)

Krot, Alexander; Ivanova, Marina A.; Wasson, John T.

1993-01-01

We characterize ten chromatic chondrules, two spinelian chondrules andd one spinel-bearing chondrule and summarize data for 120 chromitic inclusions discovered in an extensive survey of ordinary chondrites. Compositional and petrographic evidence suggests that chromitic chondrules and inclusions are closely related. The Cr/(Cr + Al) ratios in the spinal of these objects range from 0.5 to 0.9 and bulk Al2O3 contents are uniformly high (greater than 10 wt%, except for one with 8 wt%). No other elements having comparable solar abundances are so stongly enriched, and alkali feldspar and merrillite are more common than in normal chondrules. The Cr/Mg ratios in chromitic chondrules are 180-750 times the ratios in the bulk chondrite. With the possible exception of magnetic clumping of chromite in the presolar cloud, mechanical processes cannot account for this enrichment. Examination of nebular equilibrium processes shows that 50%-condensation temperatures of Cr at pH2/pH2O of 1500 are several tens of degrees below those of Mg as Mg2SiO4; the condensation of Cr is primarily as MgCr2O4 dissolved in MgAl2O4 at nebular pressures of 10(exp -4) atm or below. At pH2 = 10(exp -3) atm condesation as Cr in Fe-Ni is favored. Making the nebula much more oxidizing reduces the difference in condensation temperatures but Mg remains more refractory. We conclude that nebular equilibrium processes are not responsible for the enhanced Cr/Mg ratios. We propose that both Cr and Al became enriched in residues formed by incomplete evaporation of presolar lumps. We suggest that spinals remained as solid phases when the bulk of the silicates were incorporated into the evaporating melt; vaporization of Al and Cr were inhibited by the slow kinetics of diffusion. Subsequent melting and crystallization of these residues fractionated Cr from Al. The resulting materials constituted major components in the precursors of chromitic chondrules. Our model implies that chromitic chondrules and inclusions preserve the Cr isotopic record of presolar sources.

Density of very small meteoroids

NASA Astrophysics Data System (ADS)

Kikwaya Eluo, Jean-Baptiste

2015-08-01

Knowing the density of meteoroids helps to determine the physical structure and gives insight into the composition of their parent bodies. The density of meteoroids can provide clues to their origins, whether cometary or asteroidal. Density helps also to characterize the risk meteoroids may pose to artificial satellites.Ceplecha (1968) calculated the density of small meteoroids based on a parameter KB (meteoroid beginning height) and classified them in four categories (A,B,C,D) with densities going from 2700 to 180 kgm-3.Babadzhanov(2002) applied a model based on quasi-continuous fragmentation (QCF) on 413 photographic Super-Schmidt meteors by solely fitting their light curves. Their densities range from 400 to 7800 kgm-3. Bellot Rubio et al. (2002) analyzed the same 413 photographic meteors assuming the single body theory based on meteoroid dynamical properties and found densities ranging from 400 to 4800 kgm-3. A thermal erosion model was used by Borovicka et al. (2007) to analyze, simultaneously, the observed decelerations and light curves of six Draconid meteors. The density was found to be 300 kgm-3, consistent with the fact that the Draconid meteors are porous aggregates of grains associated with the Jupiter-family-comet 21P/Giacobini-Zinner (Jacchia, L.G., 1950).We used the Campbell-Brown and Koschny (2004) model of meteoroid ablation to determine the density of faint meteoroids from the analysis of both observed decelerations and light curves of meteoroids (Kikwaya et al., 2009; Kikwaya et al., 2011). Our work was based on a collection of six and ninety-two sporadic meteors. The grain masses used in the modeling ranged from 10-12 Kg to 10-9 Kg. We computed the orbit of each meteoroid and determined its Tisserand parameter. We found that meteoroids with asteroidal orbits have bulk densities ranging from 3000-5000 kgm-3. Meteoroids consistent with HTC/NIC parents have bulk densities from 400 kgm-3 to 1600 kg m-3. JFC meteoroids were found to have surprisingly chondritic-like bulk densities, suggesting either the sintering of the meteoroids through evolutionary processes, or the original radial transportation of chondritic materials up to the Kuiper Belt region.

Thermal and impact history of the H chondrite parent asteroid during metamorphism: Constraints from metallic Fe-Ni

NASA Astrophysics Data System (ADS)

Scott, Edward R. D.; Krot, Tatiana V.; Goldstein, Joseph I.; Wakita, Shigeru

2014-07-01

We have studied cloudy taenite, metallographic cooling rates, and shock effects in 30 H3-6 chondrites to elucidate the thermal and early impact history of the H chondrite parent body. We focused on H chondrites with old Ar-Ar ages (>4.4 Gyr) and unshocked and mildly shocked H chondrites, as strongly shocked chondrites with such old ages are very rare. Cooling rates for most H chondrites at 500 °C are 10-50 °C/Myr and do not decrease systematically with increasing petrologic type as predicted by the onion-shell model in which types 3-5 are arranged in concentric layers around a type 6 core. Some type 4 chondrites cooled slower than some type 6 chondrites and type 3 chondrites did not cool faster than other types, contrary to the onion-shell model. Cloudy taenite particle sizes, which range from 40 to 120 nm, are inversely correlated with metallographic cooling rates and show that the latter were not compromised by shock heating. The three H4 chondrites that were used to develop the onion-shell model, Ste. Marguerite, Beaver Creek, and Forest Vale, cooled through 500 °C at ⩾5000 °C/Myr. Our thermal modeling shows that these rates are 50× higher than could be achieved in a body that was heated by 26Al and cooled without disturbance by impact. Published Ar-Ar ages do not decrease systematically with increasing petrologic type but do correlate inversely with cloudy taenite particle size suggesting that impact mixing decreased during metamorphism. Metal and silicate compositions in regolith breccias show that impacts mixed material after metamorphism without causing significant heating. Impacts during metamorphism created Portales Valley and two other H6 chondrites with large metallic veins, excavated the fast-cooled H4 chondrites around 3-4 Myr after accretion, and mixed petrologic types. Metallographic data do not require catastrophic disruption by impact during cooling.

Chondritic late accretion to Mars and the nature of shergottite reservoirs

NASA Astrophysics Data System (ADS)

Tait, Kim T.; Day, James M. D.

2018-07-01

Mars is considered to have formed as a planetary embryo that experienced extensive differentiation early in its history. Shergottite meteorites preserve evidence for this history, and for late accretion events that affected their mantle sources within Mars. Here we report the first coupled 187Re-187Os, 87Sr/86Sr, highly siderophile element (HSE: Os, Ir, Ru, Pt, Pd, Re) and major element abundance dataset for martian shergottites that span a range of MgO contents, from 6.4 to 30.3 wt.%. The shergottites range from picro-basalt to basaltic-andesite compositions, have enriched to depleted incompatible trace-element compositions, and define fractional crystallization trends, enabling the determination of HSE compatibility for martian magmatism in the order: Os > Ir ≥ Ru ≫ Pt ≥ Pd ≥ Re. This order of compatibility is like that defined previously for Earth and the Moon, but the fractionation of strongly compatible Os, Ir and Ru appears to take place at higher MgO contents in martian magmas, due to early onset of sulfide fractionation. In general, enriched shergottites have lower MgO contents than intermediate or depleted shergottites and have fractionated HSE patterns (Re + Pd + Pt > Ru + Ir + Os) and more radiogenic measured 87Sr/86Sr (0.7127-0.7235) and 187Os/188Os (0.140-0.247) than intermediate or depleted shergottite meteorites (87Sr/86Sr = 0.7010-0.7132; 187Os/188Os = 0.127-0.141). Osmium isotope compositions, corrected for crystallization age, define compositions that are implausibly unradiogenic in some enriched shergottites, implying recent mobilization of Re in some samples. Filtering for the effects of alteration and high Re/Os through crystal-liquid fractionation leads to a positive correlation between age-corrected Sr and Os isotope compositions. Mixing between hypothetical martian crustal and mantle reservoirs are unable to generate the observed Sr-Os isotope compositions of shergottites, which require either distinct and discrete long-term incompatible-element depleted and enriched mantle sources, or originate from hybridized melting of deep melts with metasomatized martian lithosphere. Using MgO-regression methods, we obtain a modified estimate of the bulk silicate Mars HSE composition of (in ng g-1) 0.4 [Re], 7.4 [Pd], 9.6 [Pt], 6.2 [Ru], 3.7 [Ir], 4 [Os], and a long-term chondritic 187Os/188Os ratio (∼0.1312). This result does not permit existing models invoking high-pressure and temperature partitioning of the HSE. Instead, our estimate implies 0.6-0.7% by mass of late accretion of broadly chondritic material to Mars. Our results indicate that Mars could have accreted earlier than Earth, but that disproportional accretion of large bodies and a relative constant flux of accretion of available materials in the first 50-100 Ma of Solar System led to the broad similarity in HSE abundances between Earth and Mars.

Modification of REE distribution of ordinary chondrites from Atacama (Chile) and Lut (Iran) hot deserts: Insights into the chemical weathering of meteorites

NASA Astrophysics Data System (ADS)

Pourkhorsandi, Hamed; D'Orazio, Massimo; Rochette, Pierre; Valenzuela, Millarca; Gattacceca, Jérôme; Mirnejad, Hassan; Sutter, Brad; Hutzler, Aurore; Aboulahris, Maria

2017-09-01

The behavior of rare earth elements (REEs) during hot desert weathering of meteorites is investigated. Ordinary chondrites (OCs) from Atacama (Chile) and Lut (Iran) deserts show different variations in REE composition during this process. Inductively coupled plasma-mass spectrometry (ICP-MS) data reveal that hot desert OCs tend to show elevated light REE concentrations, relative to OC falls. Chondrites from Atacama are by far the most enriched in REEs and this enrichment is not necessarily related to their degree of weathering. Positive Ce anomaly of fresh chondrites from Atacama and the successive formation of a negative Ce anomaly with the addition of trivalent REEs are similar to the process reported from Antarctic eucrites. In addition to REEs, Sr and Ba also show different concentrations when comparing OCs from different hot deserts. The stability of Atacama surfaces and the associated old terrestrial ages of meteorites from this region give the samples the necessary time to interact with the terrestrial environment and to be chemically modified. Higher REE contents and LREE-enriched composition are evidence of contamination by terrestrial soil. Despite their low degrees of weathering, special care must be taken into account while working on the REE composition of Atacama meteorites for cosmochemistry applications. In contrast, chondrites from the Lut desert show lower degrees of REE modification, despite significant weathering signed by Sr content. This is explained by the relatively rapid weathering rate of the meteorites occurring in the Lut desert, which hampers the penetration of terrestrial material by forming voluminous Fe oxide/oxyhydroxides shortly after the meteorite fall.

Lunar and Planetary Science XXXVI, Part 1

NASA Technical Reports Server (NTRS)

2005-01-01

Contents include the following: Observations with Near Infrared Spectrometer for Hayabusa Mission in the Cruising Phase. First Results of Quadrantid Meteor Spectrum. Compositional Investigation of Binary Near-Earth Asteroid 66063 (1998 RO1): A Potentially Undifferentiated Assemblage. Impact-induced Hydrothermal Activity on Early Mars. HRTEM and EFTEM Studies of Phyllosilicate-Organic Matter Associations in Matrix and Dark Inclusions in the EET92042 CR2 Carbonaceous Chondrite. Volumetric Analysis of Martian Rampart Craters. High Pressure Melting of H-Chondrite: A Match for the Martian Basalt Source Mantle. MERView: A New Computer Program for Easy Display of MER-acquired M ssbauer Data. Distribution, Exchange, and Topographic Control of Subsurface Ice on Mars. Shock-induced Damage Beneath Normal and Oblique Impact Craters. Amphitrites Patera Studied from the Mars Express HRSC Data. Oxygen Isotope Microanalysis of Enveloping Compound Chondrules in CV3 and LL3 Chondrites. Gamma-Ray Irradiation in the Early Solar System and the Conundrum of the Lu-176 Decay Constant. Magnesium Isotope Mapping of Silica-rich Grains Having. Extreme Oxygen Isotope Anomalies Extreme Oxygen Isotopic Anomalies from Irradiation in the Early Solar System, Re-Examining the Role of Chondrules in Producing the Elemental Fractionations in Chondrites. Meteorite Data on the Solar Modulation of Galactic Cosmic Rays and an Inference on the Solar Activity Influence on Climate of the Earth. Volatiles Enrichments and Composition of Jupiter. Thinking Like a Wildcatter Prospecting for Methane in Arabia Terra, Mars. Size Distribution of Genesis Solar Wind Array Collector Fragments. Initial Subdivision of Genesis Early Science Polished Aluminum Collector. Presolar Graphite and Its Noble Gases. Young Pb-Isotopic Ages of Chondrules in CB Carbonaceous Chondrites. Fe Isotopic Composition of Martian Meteorites. Petrology and Geochemistry of Nakhlite MIL 03346: A New Martian Meteorite from Antarctica.

Lu-Hf systematics of meteorites

NASA Astrophysics Data System (ADS)

Bizzarro, M.; Baker, J. A.; Haack, H.

2003-04-01

We have measured Lu-Hf concentrations and Hf isotope ratios on a number of solar system objects with a new digestion and chemical separation technique (1). The analysed materials include a variety of carbonaceous and ordinary chondrites (CC and OC), basaltic eucrites and a diogenite, and work is ongoing on angrites, aubrites and mesosiderites. Nineteen analyses of OC and CC define, for the first time, a statistically significant Lu-Hf isochron with a slope of 0.09465 ± 145 and intercept of 0.279628 ± 47 (2). In contrast to the CC and type 3 OC (176Lu/177Hf = 0.032-0.034), the more highly metamorphosed OC have a large range of 176Lu/177Hf ratios (0.026-0.036). The large range of 176Lu/177Hf values may be related to heterogeneous variations in phosphate abundances in equilibrated OC, which is supported by the observation that most of the observed variation is defined by this type of material. The present-day bulk-earth 176Hf/177Hf ratio calculated from this study, and a 176Lu/177Hf ratio of 0.0332, is identical to the value of (3) and confirms that the chondritic Hf-Hd isotopic composition is displaced (3 ɛ units) to unradiogenic Hf compared to the terrestrial array. The slope and intercept derived from individual regressions of either the OC or the L type alone are identical within analytical uncertainty. Using a mean age of 4.56 Ga for the chondrite forming event, we derive a value for λ176Lu = 1.983 ± 33 time 10-11 y-1 from the regression of the chondrite meteorites, ca. 6% faster than a recent calibration based on terrestrial material, which has important implications for the differentiation of the early Earth (2, 4). The four basaltic eucrites analysed align on the same array as the chondrites and, as such, chondrites and basaltic eucrites also define a statistically significant isochron with a slope of 0.09462 ± 68 and intercept of 0.279627 ± 20, identical to the values derived from the chondrites alone. Moreover, a recent Lu-Hf study of basaltic eucrites also yielded a slope and intercept identical to that determined here (5). In contrast, three cumulate eucrites of (5) and our analysis of the Bilanga diogenite align on a statistically significant Lu-Hf isochron defining an age of 4.349 ± 0.073 Ga. This implies a genetic relationship between diogenites and cumulate eucrites, and further confirms that cumulate eucrites are at least 100 Myr younger than basaltic eucrites. (1) Bizzarro, M., Baker, J.A. &Ulfbeck D. (in review) Geostandards Newsletter. (2) Bizzarro, M., Baker, J.A., Haack, H., Ulfbeck D. &Rosing M. (In press) Nature. (3) Blichert-Toft, J. &Albarede, F. (1997) EPSL 148, 243-258. (4) Scherer, E., Münker, C. &Mezger, K. (2001) Science 293, 683-686. (5) Blichert-Toft, J., Boyet, M., Télouk, P &Albarède, F. (2002) EPSL 204, 167-181.

New insights into Mo and Ru isotope variation in the nebula and terrestrial planet accretionary genetics

NASA Astrophysics Data System (ADS)

Bermingham, K. R.; Worsham, E. A.; Walker, R. J.

2018-04-01

When corrected for the effects of cosmic ray exposure, Mo and Ru nucleosynthetic isotope anomalies in iron meteorites from at least nine different parent bodies are strongly correlated in a manner consistent with variable depletion in s-process nucleosynthetic components. In contrast to prior studies, the new results show no significant deviations from a single correlation trend. In the refined Mo-Ru cosmic correlation, a distinction between the non-carbonaceous (NC) group and carbonaceous chondrite (CC) group is evident. Members of the NC group are characterized by isotope compositions reflective of variable s-process depletion. Members of the CC group analyzed here plot in a tight cluster and have the most s-process depleted Mo and Ru isotopic compositions, with Mo isotopes also slightly enriched in r- and possibly p-process contributions. This indicates that the nebular feeding zone of the NC group parent bodies was characterized by Mo and Ru with variable s-process contributions, but with the two elements always mixed in the same proportions. The CC parent bodies sampled here, by contrast, were derived from a nebular feeding zone that had been mixed to a uniform s-process depleted Mo-Ru isotopic composition. Six molybdenite samples, four glacial diamictites, and two ocean island basalts were analyzed to provide a preliminary constraint on the average Mo isotope composition of the bulk silicate Earth (BSE). Combined results yield an average μ97Mo value of +3 ± 6. This value, coupled with a previously reported μ100Ru value of +1 ± 7 for the BSE, indicates that the isotopic composition of the BSE falls precisely on the refined Mo-Ru cosmic correlation. The overlap of the BSE with the correlation implies that there was homogeneous accretion of siderophile elements for the final accretion of 10 to 20 wt% of Earth's mass. The only known cosmochemical materials with an isotopic match to the BSE, with regard to Mo and Ru, are some members of the IAB iron meteorite complex and enstatite chondrites.

Low-temperature aqueous alteration on the CR chondrite parent body: Implications from in situ oxygen-isotope analyses

NASA Astrophysics Data System (ADS)

Jilly-Rehak, Christine E.; Huss, Gary R.; Nagashima, Kazu; Schrader, Devin L.

2018-02-01

The presence of hydrated minerals in chondrites indicates that water played an important role in the geologic evolution of the early Solar System; however, the process of aqueous alteration is still poorly understood. Renazzo-like carbonaceous (CR) chondrites are particularly well-suited for the study of aqueous alteration. Samples range from being nearly anhydrous to fully altered, essentially representing snapshots of the alteration process through time. We studied oxygen isotopes in secondary-minerals from six CR chondrites of varying hydration states to determine how aqueous fluid conditions (including composition and temperature) evolved on the parent body. Secondary minerals analyzed included calcite, dolomite, and magnetite. The O-isotope composition of calcites ranged from δ18O ≈ 9 to 35‰, dolomites from δ18O ≈ 23 to 27‰, and magnetites from δ18O ≈ -18 to 5‰. Calcite in less-altered samples showed more evidence of fluid evolution compared to heavily altered samples, likely reflecting lower water/rock ratios. Most magnetite plotted on a single trend, with the exception of grains from the extensively hydrated chondrite MIL 090292. The MIL 090292 magnetite diverges from this trend, possibly indicating an anomalous origin for the meteorite. If magnetite and calcite formed in equilibrium, then the relative 18O fractionation between them can be used to extract the temperature of co-precipitation. Isotopic fractionation in Al Rais carbonate-magnetite assemblages revealed low precipitation temperatures (∼60 °C). Assuming that the CR parent body experienced closed-system alteration, a similar exercise for parallel calcite and magnetite O-isotope arrays yields "global" alteration temperatures of ∼55 to 88 °C. These secondary mineral arrays indicate that the O-isotopic composition of the altering fluid evolved upon progressive alteration, beginning near the Al Rais water composition of Δ17O ∼ 1‰ and δ18O ∼ 10‰, and becoming increasingly 16O-enriched toward a final fluid composition of Δ17O ∼ -1.2‰ and δ18O ∼ -15‰.

The Aqueous Alteration of CR Chondrites: Experiments and Geochemical Modeling

NASA Technical Reports Server (NTRS)

Perronnet, M.; Berger, G.; Zolensky, M. E.; Toplis, M. J.; Kolb, V. M.; Bajagic, M.

2007-01-01

CR carbonaceous chondrites are of major interest since they contain some of the most primitive organic matter known. However, aqueous alteration has more or less overprinted their original features in a way that needs to be assessed. This study was initiated by comparing the mineralogy and modal abundances of the most altered CR1 chondrite, GRO 95577, to a less altered CR2. Calculated element distributions imply that GRO 95577 may result from aqueous alteration of Renazzo by an isochemical process on their parent asteroid, whose mineralogical composition was estimated ( Unaltered CR shown included table).

Neon isotopes show that Earth was accreted from irradiated material

NASA Astrophysics Data System (ADS)

Moreira, M. A.

2015-12-01

Since the 1980s, the notion that the Earth's mantle has a "solar" isotopic signature for neon has been favoured. Indeed, the 20Ne/22Ne ratio is above 12.5 in the mantle sources of OIB and MORB, close to the solar composition (13.4 for the Sun or 13.8 for the solar wind) and different from both atmospheric and chondritic compositions (Phase Q, Neon A). The most well accepted process invoked to explain this observed solar composition in the mantle is dissolution into a magma ocean of solar gases captured by gravity around the proto-Earth. However, Earth was accreted after gas from the proto-planetary disk had evaporated, suggesting that Earth itself could not have captured such a solar primordial atmosphere. Only planetary embryos were formed when the gas was still present in the disk. However, these planetary embryos with the mass of Mars are not massive enough to capture a solar dense atmosphere able to incorporate enough neon into the mantle. New estimates of the neon isotopic compositions of both the Earth's mantle and of the implanted solar wind into grains suggest that the origin of the neon on Earth is related to solar wind irradiation on μm grains before planetary accretion started and not dissolution. Although incorporation of solar ions by this process is only significant for very volatiles (depleted) elements, the irradiation by x-rays has important consequences for the bulk chemistry of irradiated grains as it has been demonstrated that it produces depletion in Mg and Si, relatively to O (e.g Bradley et al., 1994), a pattern also observed for the Bulk silicate Earth. References Bradley, J. (1994). "Chemically Anomalous, Preaccretionally irradiated Grains in Interplanetary fust from Comets." Science 265: 925-929.

The solar nebula redox state as recorded by the most reduced chondrules of five primitive chondrites

NASA Technical Reports Server (NTRS)

Johnson, M. C.

1986-01-01

Mafic minerals in the most reduced chondrules of five primitive meteorites were analyzed with an electron microprobe to determine the lower limit on their FeO contents. The accuracy obtained was + or - 0.01 weight percent FeO. The thermodynamic relationship between mole fraction FeSiO3 and pO2 of the ambient nebular gas at the time of mineral equilibration was established, and was used to infer the local O/H ratio of the nebular gas during chondrule formation. The lowest ferrosilite compositions reflected equilibration at 1500 K with a gas 2-18 times more oxidizing than a gas of solar composition. Olivines in low-FeO unequilibrated ordinary chondrites (UOC) chondrules are uniformly more FeO-rich than coexisting pyroxenes. This discrepancy suggests that a significant change in the O/H ratio of the nebular gas occurred between the time of olivine and pyroxene crystallization in the region of the nebula where UOCs formed. Mineral compositions in the chondrules of two C2 chondrites studied suggest they formed in a more homogeneous region of the nebula than the UOCs.

Experimental Studies of Phase Equilibria of Meteorites and Planetary Bodies

NASA Technical Reports Server (NTRS)

Stolper, Edward M.

2005-01-01

The primary theme of this project was the application of experimental petrology and geochemistry to a variety of problems in meteoritics and planetary geology. The studies were designed to help develop constraints on the histories of primitive meteorites and their components, the environments in which they formed and evolved, and to understand quantitatively the processes involved in the evolution of igneous rocks on the earth and other planetary bodies. We undertook several projects relating to the origin of CAIs and chondrules. Systematics in the thermodynamic properties of CAI-like liquids were investigated and used to elucidate speciation of multi-valent cations and sulfide capacity of silicate melts and to constrain redox conditions and the vapor pressures of volatile species over molten chondrules. We experimentally determined vanadium speciation in meteoritic pyroxenes and in pyroxenes crystallized from CAI-like melts under very reducing conditions. We also found that bulk oxygen isotope compositions of chondrules in the moderately unequilibrated LL chondrites are related to the relative timing of plagioclase crystallization. We completed an experimental study on the vaporization of beta-SiC and SiO2 (glass or cristobalite) in reducing gases and established the conditions under which these presolar grains could have survived in the solar nebula. We expanded our technique for determining the thermodynamic properties of minerals and liquids to iron-bearing systems. We determined activity-composition relationships in Pt-Fe, Pt-Cr and Pt-Fe-Cr alloys. Results were used to determine the thermodynamic properties of chromite-picrochromite spinels including the free energy of formation of end-member FeCr2O4. We also established a new approach for evaluating Pt-Fe saturation experiments. We calculated the T-fO2 relationships in equilibrated ordinary chondrites and thereby constrained the conditions of metamorphism in their parent bodies.

A volatile rich Earth's core?

NASA Astrophysics Data System (ADS)

Morard, G.; Antonangeli, D.; Andrault, D.; Nakajima, Y.

2017-12-01

The composition of the Earth's core is still an open question. Although mostly composed of iron, it contains impurities that lower its density and melting point with respect to pure Fe. Knowledge of the nature and abundance of light elements (O, S, Si, C or H) in the core has major implications for establishing the bulk composition of the Earth and for building the model of Earth's differentiation. Geochemical models of the Earth's formation point out that its building blocks were depleted in volatile elements compared to the chondritic abundance, therefore light elements such as S, H or C cannot be the major elements alloyed with iron in the Earth's core. However, such models should be compatible with the comparison of seismic properties of the Earth's core and physical properties of iron alloys under extreme conditions, such as sound velocity or density of solid and liquid. The present work will discuss the recent progress for compositional model issued from studies of phase diagrams and elastic properties of iron alloys under core conditions and highlight the compatibility of volatile elements with observed properties of the Earth's core, in potential contradiction with models derived from metal-silicate partitioning experiments.

A Raman Study of Carbonates and Organic Contents in Five CM Chondrites

NASA Technical Reports Server (NTRS)

Chan, Q. H. S.; Zolensky, M. E.; Bodnar, R. J.; Farley, C.; Cheung, J. C. H.

2016-01-01

Carbonates comprise the second most abundant class of carbon-bearing phases in carbonaceous chondrites after organic matter (approximately 2 wt.%), followed by other C-bearing phases such as diamond, silicon carbide, and graphite. Therefore, understanding the abundances of carbonates and the associated organic matter provide critical insight into the genesis of major carbonaceous components in chondritic materials. Carbonates in CM chondrites mostly occur as calcite (of varying composition) and dolomite. Properly performed, Raman spectroscopy provides a non-destructive technique for characterizing meteorite mineralogy and organic chemistry. It is sensitive to many carbonaceous phases, allows the differentiation of organic from inorganic materials, and the interpretation of their spatial distribution. Here, with the use of Raman spectroscopy, we determine the structure of the insoluble organic matter (IOM) in the matrix and carbonate phases in five CM chondrites: Jbilet Winselwan, Murchison, Nogoya, Santa Cruz, and Wisconsin Range (WIS) 91600, and interpret the relative timing of carbonate precipitation and the extent of the associated alteration events.

Aqueous Alteration of Carbonaceous Chondrites: New Insights from Comparative Studies of Two Unbrecciated CM2 Chondrites, Y 791198 and ALH 81002

NASA Technical Reports Server (NTRS)

Chizmadia, L. J.; Brearley, A. J.

2004-01-01

Carbonaceous chondrites are an important resource for understanding the physical and chemical conditions in the early solar system. In particular, a long-standing question concerns the role of water in the cosmochemical evolution of carbonaceous chondrites. It is well established that extensive hydration of primary nebular phases occurred in the CM and CI chondrites, but the location where this alteration occurred remains controversial. In the CM2 chondrites, hydration formed secondary phases such as serpentine, tochilinite, pentlandite, carbonate and PCP. There are several textural observations which suggest that alteration occurred before the accretion of the final CM parent asteroid, i.e. preaccretionary alteration. Conversely, there is a significant body of evidence that supports parent-body alteration. In order to test these two competing hypotheses further, we studied two CM chondrites, Y-791198 and ALH81002, two meteorites that exhibit widely differing degrees of aqueous alteration. In addition, both meteorites have primary accretionary textures, i.e. experienced minimal asteroidal brecciation. Brecciation significantly complicates the task of unraveling alteration histories, mixing components that have been altered to different degrees from different locations on the same asteroidal parent body. Alteration in Y-791198 is mostly confined to chondrule mesostases, FeNi metal and fine-grained matrix and rims. In comparison, the primary chondrule silicates in ALH81002 have undergone extensive replacement by secondary hydrous phases. This study focuses on compositional and textural relationships between chondrule mesostasis and the associated rim materials. Our hypothesis is: both these components are highly susceptible to aqueous alteration and should be sensitive recorders of the alteration process. For parent body alteration, we expect systematic coupled mineralogical and compositional changes in rims and altered mesostasis, as elemental exchange between these components occurs. Conversely, for preaccretionary alteration, there should be no clear relationships between the rims and mesostases.

In situ analysis of Refractory Metal Nuggets in carbonaceous chondrites

NASA Astrophysics Data System (ADS)

Daly, Luke; Bland, Phil A.; Dyl, Kathryn A.; Forman, Lucy V.; Evans, Katy A.; Trimby, Patrick W.; Moody, Steve; Yang, Limei; Liu, Hongwei; Ringer, Simon P.; Ryan, Christopher G.; Saunders, Martin

2017-11-01

Micrometre to sub-micrometre-scale alloys of platinum group elements (PGEs) known as Refractory Metal Nuggets (RMNs) have been observed in primitive meteorites. The Australian Synchrotron X-ray Fluorescence (XRF) beamline, in tandem with the Maia detector, allows rapid detection of PGEs in concentrations as low as 50-100 ppm at 2 μm resolution. Corroborating these analyses with traditional electron microscopy techniques, RMNs can be rapidly identified in situ within carbonaceous chondrites. These results dispute the assumption of most previous studies: that RMNs are unique to Ca-Al-rich inclusions (CAIs). We find that RMNs are, in fact, observed within all components of carbonaceous chondrites, such as the matrix, chondrules (consistent with observations from Schwander et al. (2015b) and Wang et al. (2007)), and sulphides; though the majority of RMNs are still found in CAIs. The chemistry of RMNs reveals a complex diversity of compositions, which nevertheless averages to CI chondrite abundance ratios. This implies that RMNs are the dominant, if not sole host phase for PGEs. One hundred and thirteen RMNs from this study are combined with reported compositions in the literature, and compared to condensation model compositions similar to Berg et al. (2009), RMNs derived experimentally by precipitation (Schwander et al., 2015a), host phase and host meteorite. Comparisons reveal only weak correlations between parent body processes (sulphidation) and nebular processes (condensation and precipitation) with RMN compositions. It appears that none of these processes acting in isolation or in tandem can explain the diversity observed in the RMN population. Our interpretation is that the Solar Nebula inherited an initially compositionally diverse population of RMNs from the Giant Molecular Cloud; that a variety of Solar System processes have acted on that population; but none have completely homogenised it. Most RMNs have experienced disk and asteroidal processing, but some may have retained a primordial composition. RMNs have been identified in pre-solar graphite grains (Croat et al., 2013). We anticipate that pre-solar RMNs will be present elsewhere in primitive meteorites.

Genealogy of Iron and Pallasite Meteorites as Revealed by Cr Isotopes

NASA Astrophysics Data System (ADS)

Sanborn, M.; Yin, Q. Z.; Ziegler, K. G.

2017-12-01

The parent bodies and/or chemical reservoirs from which iron and stony-iron meteorites originated are not very well understood. It is unclear if particular groups of iron or stony-iron meteorites originated from melting of already known chondritic parent bodies or are representating new chemical reservoirs. Potential connections between iron meteorites and pallasites and known parent bodies have been suggested based on oxygen isotopes. Proposed genetic relationships include the IVA irons with ordinary chondrites1 and the anomalous pallasite Eagle Station with the CV chondrites2. Here, we use the power of Cr isotopes to further resolve potential connections between IVA irons and pallasites and specific parent bodies. Our new measurements of Cr isotopic composition of silicate inclusions from two IVA irons, Steinbach and São João Nepomuceno, are shown to be indistinguishable from that of the ordinary chondrites. Coupling Cr with oxygen indicates the IVA irons likely originated from the same source as LL chondrites. In contrast with Eagle Station, the new Cr isotope measurements combined with oxygen indicates the MGP Brenham and Krasnojarsk sampled a source material similar to that of the anomalous HEDs. As with Eagle Station, the Milton pallasite exhibits a carbonaceous chondrite (CC) Cr isotope composition, indicating that Eagle Station was not the lone case of a pallasite originating from a CC reservoir. By establishing these genetic relationships using Cr isotopes, it is now evident that the differentiation activity sampled by IVA irons and pallasites represents processes occurring on a diverse set of parent bodies in the early Solar System. [1] Ruzicka and Hutson (2006) MAPS, 41, 1959. [2] Shukolyukov and Lugmair (2006) EPSL, 250, 200.

Geochemical and oxygen isotope perspective of a new R chondrite Dhofar 1671: Affinity with ordinary chondrites

NASA Astrophysics Data System (ADS)

Ali, Arshad; Nasir, Sobhi J.; Jabeen, Iffat; Al Rawas, Ahmed; Banerjee, Neil R.; Osinski, Gordon R.

2017-09-01

Dhofar 1671 is a relatively new meteorite that previous studies suggest belongs to the Rumuruti chondrite class. Major and REE compositions are generally in agreement with average values of the R chondrites (RCs). Moderately volatile elements such as Se and Zn abundances are lower than the R chondrite values that are similar to those in ordinary chondrites (OCs). Porphyritic olivine pyroxene (POP), radial pyroxene (RP), and barred olivine (BO) chondrules are embedded in a proportionately equal volume of matrix, one of the characteristic features of RCs. Microprobe analyses demonstrate compositional zoning in chondrule and matrix olivines showing Fa-poor interior and Fa-rich outer zones. Precise oxygen isotope data for chondrules and matrix obtained by laser-assisted fluorination show a genetic isotopic relationship between OCs and RCs. On the basis of our data, we propose a strong affinity between these groups and suggest that OC chondrule precursors could have interacted with a 17O-rich matrix to form RC chondrules (i.e., ∆17O shifts from 1‰ to 3‰). These interactions could have occurred at the same time as "exotic" clasts in brecciated samples formed such as NWA 10214 (LL3-6), Parnallee (LL3), PCA91241 (R3.8-6), and Dhofar 1671 (R3.6). We also infer that the source of the oxidation and 17O enrichment is the matrix, which may have been enriched in 17O-rich water. The abundance of matrix in RCs relative to OCs, ensured that these rocks would be apparently more oxidized and appreciably 17O-enriched. In situ analysis of Dhofar 1671 is recommended to further strengthen the link between OCs and RCs.

Effect of Tube-Based X-Ray Microtomography Imaging on the Amino Acid and Amine Content of the Murchison CM2 Chondrite

NASA Technical Reports Server (NTRS)

Glavin, D. P.; Friedrich, J. M.; Aponte, J. C.; Dworkin, J. P.; Ebel, D. S.; Elsila, J. E.; Hill, M.; McLain, H. L.; Towbin, W. H.

2017-01-01

X-ray and synchrotron X-ray micro-computed tomography (micro-CT) are increasingly being used for three dimensional reconnaissance imaging of chondrites and returned extraterrestrial material prior to detailed chemical and mineralogical analyses. Although micro-CT imaging is generally considered to be a non-destructive technique since silicate and metallic minerals in chondrites are not affected by X-ray exposures at the intensities and wavelengths typically used, there are concerns that the use of micro-CT could be detrimental to the organics in carbonaceous chondrites. We recently conducted a synchrotron micro-CT experiment on a powdered sample of the Murchison CM2 carbonaceous chondrite exposed to a monochromatic high energy (approximately 48 kiloelectronvolts) total X-ray radiation dose of approximately 1 kilogray (kGy) using the Advanced Photon Source beamline 13-BMD (13-Bending Magnet-D Beamline) at Argonne National Laboratory and found that there were no detectable changes in the amino acid abundances or enantiomeric compositions in the chondrite after exposure relative to a Murchison control sample that was not exposed. However, lower energy bremsstrahlung X-rays could interact more with amino acids and other lower molecular weight amines in meteorites. To test for this possibility, three separate micro-CT imaging experiments of the Murchison meteorite using the GE Phoenix v/tome/x s 240 kilovolt microfocus high resolution tungsten target X-ray tube instrument at the American Museum of Natural History (AMNH) were conducted and the amino acid abundances and enantiomeric compositions were determined. We also investigated the abundances of the C1-C5 amines in Murchison which were not analyzed in the first study.

The Divnoe meteorite: Petrology, chemistry, oxygen isotopes and origin

NASA Technical Reports Server (NTRS)

Petaev, M. I.; Barsukova, L. D.; Lipschultz, M. E.; Wang, M.-S.; Ariskin, A. A.; Clayton, R. N.; Mayeda, T. K.

1994-01-01

The Divnoe meteorite is an olivine-rich primitive achondrite with subchondritic chemistry and mineralogy. It has a granoblastic, coarse-grained, olivine groundmass (CGL: coarse-grained lithology) with relatively large pyroxene-plagioclase poiklitic patches (PP) and small fine-grained domains of an opaque-rich lithology (ORL). Both PP and ORL are inhomogeneously distributed and display reaction boundaries with the groundmass. Major silicates, olivine Fa(20-28) and orthopyroxyene Fs(20-28 Wo(0.5-2.5), display systematic differences in composition between CGL and ORL as well as a complicated pattern of variations within CGL. Accessory plagioclase has low K content and displays regular igneous zoning with core compositions An(40-45) and rims An(32-37). The bulk chemical composition of Divnoe is similar to that of olivine-rich primitive achondrites, except for a depletion of incompatible elements and minor enrichment of refractory siderophiles. Oxygen isotope compositions for whole-rock and separated minerals from Divnoe fall in a narrow range, with mean delta O-18 = +4.91, delta O-17 = +2.24, and Delta O-17 = -0.26 +/- 0.11. The isotopic composition is not within the range of any previously recognized group but is very close to that of the brachinites. To understand the origin of Divnoe lithologies, partial melting and crystallization were modelled using starting compositions equal to that of Divnoe and some chondritic meteorites. It was found that the Divnoe composition could be derived from a chondritic source region by approximately 20 wt% partial melting at Ta approximately 1300 C and log(fO2) = IW-1.8, followed by approximtely 60 wt% crystallization of the partial melt formed, and removal of the still-liquid portion of the partial melt. Removal of the last partial melt resulted in depletion of the Divnoe plagioclase in Na and K. In this scenario, CGL represents the residue of partial melting, and PP is a portion of the partial melt that crystallized in situ. The ORL was formed during the final stages of partial melting by reaction between gaseous sulfur and residual olivine in the source region. A prominent feature of Divnoe is fine micron-scale chemical variations within olivine grains, related to lamellar structures the olivines display. The origin of these structures is not known.

Chemically anomalous, pre-accretionally irradiated grains in interplanetary dust -- interstellar grains?. [Abstract only

NASA Technical Reports Server (NTRS)

Bradley, J. P.

1994-01-01

Ultrafine-grained matrix is a unique and fundamental building block of chondritic porous (CP) interplanetary dust particles. Most IDPs so far determined to be of cometary origin belong to the CP class. The matrix in CP IDPs is not homogeneous but rather a loose mixture of discrete single crystals (e.g., olivine, pyroxene, Fe sulfides) and polyphase grains. The petrographic diversity observed among the polyphase grains suggest that they were formed under variable physiochemical conditions. One particular class of polyphase grains are a dominant component in cometary IDPs. Although their occurrence is well documented, the terminology used to describe them is confused. They have been called many names. Here they are simply called GEMS (Glass with Embedded Metal and Sulfides). The bulk compositions of GEMS are within a factor of 3 chondritic (solar) for all major elements except C. Quantitative thin-film X-ray (EDS) analyses have shown that GEMS are systematically depleted in Mg and Si, enriched in S, Fe, and Ni, and stoichiometrically enriched in O. Electron energy-loss spectroscopy (EELS) suggests that the excess O is present as hydroxyl (-OH) groups. These same chemical 'anomalies' were observed in solar-wind-irradiated amorphous rims on the surfaces of IDPs, suggesting that the compositions of GEMS reflect prior exposure to ionizing radiation. In order to test this hypothesis, a sample of Allende (CV3) matrix was exposed to proton flux. Radiation-damaged amorphous rims on olivine and pyroxene crystals in the Allende sample were found to be depleted in Mg and Ca, enriched in S, Fe, and Ni, and stoichiometrically enriched in O. Thus, the compositions of GEMS are indeed consistent with exposure to ionizing radiation. This study suggests that chemical as well as isotopic anomalies may be used to identify presolar interstellar grains in primitive meteoritic materials.

Experimental Constraints on a Vesta Magma Ocean

NASA Technical Reports Server (NTRS)

Hoff, C.; Jones, J. H.; Le, L.

2014-01-01

A magma ocean model was devised to relate eucrites (basalts) and diogenites (orthopyroxenites), which are found mixed together as clasts in a suite of polymict breccias known as howardites. The intimate association of eucritic and diogenitic clasts in howardites argues strongly that these three classes of achondritic meteorites all originated from the same planetoid. Reflectance spectral evidence (including that from the DAWN mission) has long suggested that Vesta is indeed the Eucrite Parent Body. Specifically, the magma ocean model was generated as follows: (i) the bulk Vesta composition was taken to be 0.3 CV chondrite + 0.7 L chondrite but using only 10% of the Na2O from this mixture; (ii) this composition is allowed to crystallize at 500 bar until approx. 80% of the system is solid olivine + low-Ca pyroxene; (iii) the remaining 20% liquid crystallizes at one bar from 1250C to 1110C, a temperature slightly above the eucrite solidus. All crystallization calculations were performed using MELTS. In this model, diogenites are produced by cocrystallization of olivine and pyroxene in the >1250C temperature regime, with Main Group eucrite liquids being generated in the 1300-1250C temperature interval. Low-Ca pyroxene reappears at 1210C in the one-bar calculations and fractionates the residual liquid to produce evolved eucrite compositions (Stannern Trend). We have attempted to experimentally reproduce the <1250C portion of the MELTS Vesta magma ocean. In the MELTS calculation, the change from 500 bar to one bar results in a shift of the olivine:low-Ca pyroxene boundary so that the 1250C liquid is now in the olivine field and, consequently, olivine should be the first-crystallizing phase, followed by low-Ca pyroxene at 1210C, and plagioclase at 1170C. Because at one bar the olivine:low-Ca pyroxene boundary is a peritectic, fractional crystallization of the 1210C liquid proceeds with only pyroxene crystallization until plagioclase appears. Thus, the predictions of the MELTS calculation are clear and straightforward.

Studies of Brazilian meteorites. XIII - Mineralogy, petrology, and chemistry of the Putinga, Rio Grande do Sul, chondrite

NASA Technical Reports Server (NTRS)

Keil, K.; Lange, D.; Ulbrich, M. N. C.; Gomes, C. B.; Jarosewich, E.; Roisenberg, A.; Souza, M. J.

1978-01-01

The Putinga, Rio Grande do Sul chondrite is described and classified as an L6. The mineral composition and some significant ratios of elements are reported, and the reasons for assignment to the L group and to petrologic type 6 are explained. The analysis suggests that maskelynite of oligoclase composition was formed by solid-state shock transformation of previously existing well-crystallized plagioclase at estimated shock pressures of about 250-350 kbar. This finding indicates that recrystallization (formation of well-crystallized oligoclase) preceded shock transformation formation of the maskelynite.

Extraterrestrial Amino Acids Identified in Metal-Rich CH and CB Carbonaceous Chondrites from Antarctica

NASA Technical Reports Server (NTRS)

Burton, Aaron S.; Elsila, Jamie E.; Hein, Jason E.; Glavin, Daniel P.; Dworkin, Jason P.

2013-01-01

Carbonaceous chondrites contain numerous indigenous organic compounds and could have been an important source of prebiotic compounds required for the origin of life on Earth or elsewhere. Extraterrestrial amino acids have been reported in five of the eight groups of carbonaceous chondrites and are most abundant in CI, CM, and CR chondritesbut are also present in the more thermally altered CV and CO chondrites. We report the abundance, distribution, and enantiomeric and isotopic compositions of simple primary amino acids in six metal-rich CH and CB carbonaceous chondrites that have not previously been investigated for amino acids: Allan Hills (ALH) 85085 (CH3), Pecora Escarpment(PCA) 91467 (CH3), Patuxent Range (PAT) 91546 (CH3), MacAlpine Hills (MAC) 02675(CBb), Miller Range (MIL) 05082 (CB), and Miller Range (MIL) 07411 (CB). Amino acid abundances and carbon isotopic values were obtained by using both liquid chromatography time-of-flight mass spectrometry and fluorescence, and gas chromatography isotope ratiomass spectrometry. The (delta D, delta C-13, delta N-15) ratios of multiple amino acids fall outside of the terrestrial range and support their extraterrestrial origin. Extracts of CH chondrites were found to be particularly rich in amino acids (1316 parts per million, ppm) while CB chondrite extracts had much lower abundances (0.22 ppm). The amino acid distributions of the CH and CB chondrites were distinct from the distributions observed in type 2 and 3 CM and CR chondrites and contained elevated levels of beta-, gamma-, and delta-amino acids compared to the corresponding alpha-amino acids, providing evidence that multiple amino acid formation mechanisms were important in CH and CB chondrites.

Planetary Protection Considerations in EVA System Design

NASA Technical Reports Server (NTRS)

Eppler, Dean B.; Kosmo, Joseph J.

2011-01-01

To better constrain their origin, we have performed systematic studies of the siderophile element distribution in metal from Enstatite achondrites and iron-rich meteorites linked to Enstatite achondrites. Humayun (2010) reported 20 siderophile elements in the metal of Horse Creek, Mt. Egerton and Tucson, three iron meteorites known for their high Si content in their metal. The Horse Creek and Mt. Egerton irons have elemental patterns identical to metallic solids derived from partially molten enstatite chondrites. Tucson has an unusual siderophile element pattern that is reminiscent of IVA irons, except for the most volatile siderophiles with condensation temperatures below that of Cu (Sb, Ge, Sn) which are more depleted. The origin of Tucson metal is likely linked to an impact involving a reduced chondritic body that provided the silicates, and IVA iron. In a related study, van Acken et al. (2010) reported siderophile element abundances in metal and sulfides from aubrites, chondritic inclusions in aubrites, and other enstatite achondrites (including a separate section of Mt. Egerton). They found that aubrite metal was linked to metal in enstatite chondrites by low degree partial melting forming sulfur-rich metallic liquids. A restite origin of aubrites is not consistent with these metal compositions. The link between the metal compositions and cumulate silicates is not simple. The metal must have been incorporated from enstatite chondritic material that was assimilated by the aubrite magma. A manuscript is in preparation (van Acken et al., 2010). In a related study, van Acken et al. (2010, submitted) reported new precise Os isotope ratios and highly siderophile element abundances in Enstatite chondrites, Enstatite achondrites, Rumurutite chondrites to explore the range of nucleosynthetic variation in s-process Os. They observed nucleosynthetic anomalies, deficiencies of s-process Os, in most primitive enstatite chondrites, but showed the Rumurutite chondrites have very little expression of these anomalies. hardware from the human-occupied area may limit (although not likely eliminate) external materials in the human habitat. Definition of design-to requirements is critical to understanding technical feasibility and costs. The definition of Planetary Protection needs in relation to EVA mission and system element development cost impacts should be considered and interpreted in terms of Plausible Protection criteria. Since EVA operations will have the most direct physical interaction with the Martian surface, PP needs should be considered in the terms of mitigating hardware and operations impacts and costs.

Noble Gases in the LEW 88663 L7 Chondrite

NASA Astrophysics Data System (ADS)

Miura, Y. N.; Sugiura, N.; Nagao, K.

1995-09-01

LEW88663 and some meteorites (e.g. Shaw) are the most highly metamorphosed meteorites among L group chondrites. Although the abundances of lithophile elements and oxygen isotopic compositions of the L7 chondrite LEW88663 (total recovered mass: 14.5g) are close to those of the range for L chondrites [1,2], metallic iron is absent and concentrations of siderophile elements are about half of typical values for L chondrites [3,4]. Petrographical and geochemical observation suggested that this meteorite has experienced partial melting [5]. As a part of our study on differentiated meteorites, we also investigated noble gases in this meteorite. We present here noble gas compositions of LEW88663 and discuss history of this meteorite. In addition, we will consider whether there is any evidence for bridging between chondrites and achondrites. Noble gases were extracted from a whole rock sample weighing 66.31 mg by total fusion, and all stable noble gas isotopes as well as cosmogenic radioactive 81Kr were analyzed using a mass spectrometer at ISEI, Okayama University. The results are summarized in the table. The concentrations of cosmogenic ^3He, ^21Ne, and ^38Ar are 7.3, 1.6 and 3.1x10^-8 cm^3STP/g, respectively. The cosmic-ray exposure ages based on them are calculated to be 4.7, 6.9 and 8.8 m.y., respectively, using the production rates proposed by [6, 7] and mean chemical compositions of L chondrites. The shorter cosmic-ray exposure ages T(sub)3 and T(sub)21 than T(sub)38 would be due to diffusive loss of lighter noble gases from the meteorite. The concentrations of trapped Kr and Xe in LEW88663 are lower than those for L6 chondrites [8], supporting thermal metamorphism for the meteorite higher than that for L6 chondrites. The Kr and Xe are isotopically close to those of the terrestrial atmospheric Kr and Xe, and elemental abundance ratios for Ar, Kr and Xe suggest adsorbed noble gas patterns of the terrestrial atmosphere. The terrestrial atmospheric Ar, Kr and Xe (most likely terrestrial contamination in origin) rather than chondritic ones seem to be dominant in LEW88663. A K-Ar age of 4.3 +/- 0.2 b.y. is obtained assuming K content of 660 ppm by [9], implying radiogenic ^40Ar is almost retained. Because of low abundance of trapped Xe in the meteorite compared with the abundances in other chondrites, ^244Pu-derived fission Xe could be evaluated more precisely. According to the measured Xe data (for this, three isotope plots such as ^134Xe/^130Xe versus ^136Xe/^130Xe are useful), we conclude that Xe in LEW88663 is the mixture of ^244Pu-derived fission Xe and the terrestrial atmospheric Xe with possibility that a small amount of chondritic Xe is contained. Using the same procedure described in [10], we obtained excess ^136Xe concentration, 1.4 x 10^-12 cm^3STP/g with about 20% uncertainty, of which about 3% is from contribution of ^238U-derived ^136Xe if average U content for L chondrite (14 ppb) is assumed. The calculated Pu abundance of 0.21 ppb is slightly higher than those reported for L chondrites Barwell (0.11 +/- 0.05 ppb [11]) and Marion (0.10+/-0.40 ppb [11]). Acknowledgments: We thank Meteorite Working Group for providing the sample. We are also grateful to Dr. D. Mittlefehldt for showing us his chemical composition data. This work is supported by Research Fellowships of the Japan Society for the Promotion of Science for Young Scientists. References: [1] Mason B. et al. (1992) Antarc. Meteorite Newsletter, 15(2), 30. [2] Mason B. and Marlow R. (1992) Antarc. Meteorite Newsletter, 15(1), 16. [3] Davis A. M. et al. (1993) LPS XXIV, 375-376. [4] Mittlefehldt D. W. (1993) Meteoritics, 28, 401-402. [5] Hervey R. P. (1993) Meteoritics, 28, 360. [6] Eugster O. (1988) GCA, 52, 1649-1662. [7] Marti K. and Graf T.(1992) Annu. Rev. Earth Planet Sci., 20, 221-243. [8] E.g. Marti K. (1967) EPSL, 2, 193-196. [9] Mittlefehldt D. W., personal communication. [10] Miura Y. et al. (1993) GCA, 57, 1857-1866. [11] Hagee B. et al. (1990) GCA, 54, 2847-2858. Table 1 shows noble gases in L7 chondrite LEW88663 (66.31 mg).

Phase equilibrium constraints on angrite petrogenesis

NASA Astrophysics Data System (ADS)

Longhi, John

1999-02-01

Parameterizations of liquidus boundaries and solid solution in the CMAS + Fe system (Shi, 1992) have been employed to depict the liquidus equilibria relevant to the petrogenesis of angrites. Angrites are basaltic achondrites characterized by highly aluminous augite (fassaite), intermediate Mg-Fe olivine, and late-stage CaFe-olivine (kirschsteinite). Two important features of the equilibria on the olivine liquidus surface relevant to angrite petrogenesis are: 1) the presence of a thermal divide on the ol + aug + plag + liq boundary curve, which separates the compositions of source materials that produce low-silica angritic melts that crystallize highly aluminous augite from those that produce higher silica melts with tholeiitic to eucritic crystallization patterns; and 2) the change in the pseudo-invariant point on the low-silica side of the thermal divide from a plagioclase-peritectic involving spinel ( ol + aug + plag + sp + liq) at high to intermediate Mg' (Mg/[Mg + Fe]) to two pseudo-eutectics involving kirschsteinite ( ol + aug + plag + kir + liq and ol + kir + plag + sp + liq) at low Mg'. The fassaitic (aluminous augite) pyroxene composition in Angra Dos Reis (ADOR), the presence of minor green spinel, and the absence of primary kirschsteinite (Prinz et al., 1977) indicate that crystallization of the ADOR parental liquid was governed by the intermediate-Mg' set of equilibria such that, following crystallization of ol + aug + plag, the plagioclase reacted completely at the plagioclase-peritectic with the interstitial liquid, which subsequently crystallized beyond the plagioclase-peritectic onto the ol + aug + sp liquidus boundary curve. The ADOR bulk composition is consistent with trapping ˜10% of the parental liquid in a cumulate with cotectic proportions of fassaite and olivine. Lewis Cliff (LEW)86010 crystallized from a liquid with Mg' similar to that of ADOR, but on the ol + plag cotectic closer to the thermal divide such that the first pyroxene to crystallize had much lower Al content than that of ADOR. In the late stages of crystallization the 86010 residual liquid (and that of LEW87051) encountered the low Mg' set of equilibria involving kirschsteinite. These relationships require either a higher degree of melting for the 86010 parent magma or source region different than ADOR's. These relationships are also consistent with compositionally dependent REE partition coefficients between fassaite and the ADOR liquid being as much as 1.5-2 times higher than those for the 86010 liquid at the onset of pyroxene crystallization. The combination of a trapped liquid component, higher partition coefficients, and smaller degrees of melting help to explain the observation that ADOR, an apparent cumulate, has REE concentrations twice as high as those in 86010 (Mittlefehdlt and Lindstrom, 1990), an apparent chilled liquid. The absence of a strong negative Eu-anomaly in the ADOR parent liquid, however, requires relatively high degrees of partial melting to eliminate plagioclase in the source region (resorption of plagioclase at the peritectic eliminates the Eu-anomaly that develops during crystallization), so ultimately different source regions are required. Progressive iron loss from devolatilized primitive chondrites (Allende, Murchison) produces source regions capable of producing a wide range of melt compositions with angritic to eucritic crystallization behavior. The compositions of carbonaceous and ordinary chondrite provide a similar range of potential source region compositions. However, primitive chondrite(±Fe) source regions that produce angrite-like melts have Mg' that is too low, whereas chondrite(±Fe) sources that have Mg' sufficiently high to yield the Mg' in angrite minerals have too much silica (or orthopyroxene) component to yield angrite-like liquids. No single group of meteorites ± Fe simultaneously satisfies the constraints of Mg' and silica component. However, mixtures of Fe-depleted chondrite plus a low-silica component similar to Ca-Al-rich inclusions (CAIs) can satisfy the constraints. The absence in angrites of 48Ca and 50Ti anomalies, typical of CAIs (Lugmair and Galer, 1992), suggests that the low-silica component was not simply an enrichment of CAIs, but was the result of direct accretion of high-temperature condensate (Grossman, 1972) into sizable, thermally shielded planetesimals. Thus angrites cryptically record mixing of planetesimal-sized heterogeneities in the early solar system.

Impact splash chondrule formation during planetesimal recycling

NASA Astrophysics Data System (ADS)

Lichtenberg, Tim; Golabek, Gregor J.; Dullemond, Cornelis P.; Schönbächler, Maria; Gerya, Taras V.; Meyer, Michael R.

2018-03-01

Chondrules, mm-sized igneous-textured spherules, are the dominant bulk silicate constituent of chondritic meteorites and originate from highly energetic, local processes during the first million years after the birth of the Sun. So far, an astrophysically consistent chondrule formation scenario explaining major chemical, isotopic and textural features, in particular Fe,Ni metal abundances, bulk Fe/Mg ratios and intra-chondrite chemical and isotopic diversity, remains elusive. Here, we examine the prospect of forming chondrules from impact splashes among planetesimals heated by radioactive decay of short-lived radionuclides using thermomechanical models of their interior evolution. We show that intensely melted planetesimals with interior magma oceans became rapidly chemically equilibrated and physically differentiated. Therefore, collisional interactions among such bodies would have resulted in chondrule-like but basaltic spherules, which are not observed in the meteoritic record. This inconsistency with the expected dynamical interactions hints at an incomplete understanding of the planetary growth regime during the lifetime of the solar protoplanetary disk. To resolve this conundrum, we examine how the observed chemical and isotopic features of chondrules constrain the dynamical environment of accreting chondrite parent bodies by interpreting the meteoritic record as an impact-generated proxy of early solar system planetesimals that underwent repeated collision and reaccretion cycles. Using a coupled evolution-collision model we demonstrate that the vast majority of collisional debris feeding the asteroid main belt must be derived from planetesimals which were partially molten at maximum. Therefore, the precursors of chondrite parent bodies either formed primarily small, from sub-canonical aluminum-26 reservoirs, or collisional destruction mechanisms were efficient enough to shatter planetesimals before they reached the magma ocean phase. Finally, we outline the window in parameter space for which chondrule formation from planetesimal collisions can be reconciled with the meteoritic record and how our results can be used to further constrain early solar system dynamics.

Are C1 chondrites chemically fractionated - A trace element study

NASA Technical Reports Server (NTRS)

Ebihara, M.; Wolf, R.; Anders, E.

1982-01-01

Six C1 chondrite samples and a C2 xenolith from the Plainview H5 chondrite were analyzed by radiochemical neutron activation for a large variety of elements, including rare earths. The sample processing is described, including the irradiation, chemical procedure, rare earths separation, counting techniques, radiochemical purity check, and chemical yields. The results of consistency checks on a number of elements are discussed. Abundances for siderophiles, volatiles, and rare earths are presented and discussed. Tests are presented for fractionation of rare earths and other refractories, compositional uniformity of C1's, and interelement correlations. There is no conclusive evidence for nebular fractionation affecting C1's. Three fractionation-prone rare earths have essentially the same relative abundances in C1's and all other chondrite classes, and hence are apparently not fractionated in C1's.

Petrogenesis of Miller Range 07273, a new type of anomalous melt breccia: Implications for impact effects on the H chondrite asteroid

NASA Astrophysics Data System (ADS)

Ruzicka, Alex M.; Hutson, Melinda; Friedrich, Jon M.; Rivers, Mark L.; Weisberg, Michael K.; Ebel, Denton S.; Ziegler, Karen; Rumble, Douglas; Dolan, Alyssa A.

2017-09-01

Miller Range 07273 is a chondritic melt breccia that contains clasts of equilibrated ordinary chondrite set in a fine-grained (<5 μm), largely crystalline, igneous matrix. Data indicate that MIL was derived from the H chondrite parent asteroid, although it has an oxygen isotope composition that approaches but falls outside of the established H group. MIL also is distinctive in having low porosity, cone-like shapes for coarse metal grains, unusual internal textures and compositions for coarse metal, a matrix composed chiefly of clinoenstatite and omphacitic pigeonite, and troilite veining most common in coarse olivine and orthopyroxene. These features can be explained by a model involving impact into a porous target that produced brief but intense heating at high pressure, a sudden pressure drop, and a slower drop in temperature. Olivine and orthopyroxene in chondrule clasts were the least melted and the most deformed, whereas matrix and troilite melted completely and crystallized to nearly strain-free minerals. Coarse metal was largely but incompletely liquefied, and matrix silicates formed by the breakdown during melting of albitic feldspar and some olivine to form pyroxene at high pressure (>3 GPa, possibly to 15-19 GPa) and temperature (>1350 °C, possibly to ≥2000 °C). The higher pressures and temperatures would have involved back-reaction of high-pressure polymorphs to pyroxene and olivine upon cooling. Silicates outside of melt matrix have compositions that were relatively unchanged owing to brief heating duration.

Composition and evolution of the eucrite parent body - Evidence from rare earth elements. [extraterrestrial basaltic melts

NASA Technical Reports Server (NTRS)

Consolmagno, G. J.; Drake, M. J.

1977-01-01

Quantitative modeling of the evolution of rare earth element (REE) abundances in the eucrites, which are plagioclase-pigeonite basalt achondrites, indicates that the main group of eucrites (e.g., Juvinas) might have been produced by approximately 10% equilibrium partial melting of a single type of source region with initial REE abundances which were chondritic relative and absolute. Since the age of the eucrites is about equal to that of the solar system, extensive chemical differentiation of the eucrite parent body prior to the formation of eucrites seems unlikely. If homogeneous accretion is assumed, the bulk composition of the eucrite parent body can be estimated; two estimates are provided, representing different hypotheses as to the ratio of metal to olivine in the parent body. Since a large number of differentiated olivine meteorites, which would represent material from the interior of the parent body, have not been detected, the eucrite parent body is thought to be intact. It is suggested that the asteroid 4 Vesta is the eucrite parent body.

CM and CO chondrites: A common parent body or asteroidal neighbors? Insights from chondrule silicates

NASA Astrophysics Data System (ADS)

Schrader, Devin L.; Davidson, Jemma

2017-10-01

By investigating the petrology and chemical composition of type II (FeO-rich) chondrules in the Mighei-like carbonaceous (CM) chondrites we constrain their thermal histories and relationship to the Ornans-like carbonaceous (CO) chondrites. We identified FeO-rich relict grains in type II chondrules by their Fe/Mn ratios; their presence indicates chondrule recycling among type II chondrules. The majority of relict grains in type II chondrules are FeO-poor olivine grains. Consistent with previous studies, chemical similarities between CM and CO chondrite chondrules indicate that they had similar formation conditions and that their parent bodies probably formed in a common region within the protoplanetary disk. However, important differences such as mean chondrule size and the lower abundance of FeO-poor relicts in CM chondrite type II chondrules than in CO chondrites suggest CM and CO chondrules did not form together and they likely originate from distinct parent asteroids. Despite being aqueously altered, many CM chondrites contain pre-accretionary anhydrous minerals (i.e., olivine) that are among the least thermally metamorphosed materials in chondrites according to the Cr2O3 content of their ferroan olivine. The presence of these minimally altered pre-accretionary chondrule silicates suggests that samples to be returned from aqueously altered asteroids by the Hayabusa2 and OSIRIS-REx asteroid sample return missions, even highly hydrated, may contain silicates that can provide information about the pre-accretionary histories and conditions of asteroids Ryugu and Bennu, respectively.

Multicolor observations of phobos with the viking lander cameras: evidence for a carbonaceous chondritic composition.

PubMed

Pollack, J B; Veverka, J; Pang, K; Colburn, D; Lane, A L; Ajello, J M

1978-01-06

The reflectivity of Phobos has been determined in the spectral region from 0.4 to 1.1 micrometers from images taken with a Viking lander camera. The reflectivity curve is flat in this spectral interval and the geometric albedo equals 0.05 +/- 0.01. These results, together with Phobos's reflectivity spectrum in the ultraviolet, are compared with laboratory spectra of carbonaceous chondrites and basalts. The spectra of carbonaceous chondrites are consistent with the observations, whereas the basalt spectra are not. These findings raise the possibility that Phobos may be a captured object rather than a natural satellite of Mars.

The petrogenesis of L-6 chondrites - Insights from the chemistry of minerals

NASA Technical Reports Server (NTRS)

Curtis, D. B.; Schmitt, R. A.

1979-01-01

Measurements of the major, minor and trace element abundances of the major minerals of the L-6 chondrites Alfianello, Colby (WI) and Leedey are used to investigate the formation mechanisms of L-6 chondrites. Electron microprobe analysis was performed on individual grains of each mineral, and separated minerals were analyzed by instrumental and radiochemical neutron activation analysis. The compositions of the three meteorites are observed to be generally uniform, however different abundances and distributions of rare earth elements and Co and Ni indicate that the meteorites have different petrogenetic histories. Alkali element distributions are found to be incompatible with internal equilibration of a closed system.

Molybdenum Isotopic Composition of Iron Meteorites, Chondrites and Refractory Inclusions

NASA Technical Reports Server (NTRS)

Becker, H.; Walker, R. J.

2003-01-01

Recent Mo isotopic studies of meteorites reported evidence for differences in isotopic compositions for whole rocks of some primitive and differentiated meteorites relative to terrestrial materials. Enrichments of r- and p-process isotopes of up to 3-4 units (e unit = parts in 10(exp 4) over s-process dominated isotopes are the most prominent features. Certain types of presolar grains show large enrichments in s-process isotopes, however, it was concluded on grounds of mass balance that incomplete digestion of such grains cannot explain the enrichments of r- and p-process isotopes in whole rocks of primitive chondrites. If the reported variability in r- and p-process isotope enrichments reflects the true isotopic characteristics of the whole rocks, the implications are quite profound. It would suggest the presence of large scale Mo isotopic heterogeneity within the solar accretion disk with likely collateral effects for other elements. However, such effects were not found for Ru isotopes, nor for Zr isotopes. Another recent Mo isotopic study by multi collector ICP-MS could not confirm the reported deviations in Allende, Murchison or iron meteorites. Here, we present new results for the Mo isotopic composition of iron meteorites, chondrites and CAIs obtained by negative thermal ionization mass spectrometry (NTIMS). We discuss analytical aspects and the homogeneity of Mo isotopic compositions in solar system materials.

Green spherules from Apollo 15 - Inferences about their origin from inert gas measurements.

NASA Technical Reports Server (NTRS)

Lakatos, S.; Yaniv, A.; Heymann, D.

1973-01-01

Green spherules from the 'clod' 15426 and from fines 15421 contain about 100 times less trapped inert gases than normal bulk fines from Apollo 15. These spherules have apparently never been directly exposed to the solar wind. Spherules from other fines contain about 10 times more trapped gas than those from the 'clod.' The gas in the former is surface correlated. However, spherules from fines 15401 are exceptionally gas-poor. The trapped gases can be of solar-wind origin, but this origin requires a two-stage model for the spherules from the clods. Another possibility is that the gases were absorbed from an ambient gas phase. The trapped gases may also be assumed to represent primordial lunar gas. The composition of this gas is then similar to the 'solar' or 'unfractionated' component of gas-rich meteorites, but unlike that in most of the carbonaceous chondrites.

Metal-Silicate Segregation in Asteroidal Meteorites

NASA Technical Reports Server (NTRS)

Herrin, Jason S.; Mittlefehldt, D. W.

2006-01-01

A fundamental process of planetary differentiation is the segregation of metal-sulfide and silicate phases, leading eventually to the formation of a metallic core. Asteroidal meteorites provide a glimpse of this process frozen in time from the early solar system. While chondrites represent starting materials, iron meteorites provide an end product where metal has been completely concentrated in a region of the parent asteroid. A complimentary end product is seen in metal-poor achondrites that have undergone significant igneous processing, such as angrites, HED's and the majority of aubrites. Metal-rich achondrites such as acapulcoite/lodranites, winonaites, ureilites, and metal-rich aubrites may represent intermediate stages in the metal segregation process. Among these, acapulcoite-lodranites and ureilites are examples of primary metal-bearing mantle restites, and therefore provide an opportunity to observe the metal segregation process that was captured in progress. In this study we use bulk trace element compositions of acapulcoites-lodranites and ureilites for this purpose.

On the origin of the moon, with emphasis on bulk composition

NASA Technical Reports Server (NTRS)

Kaula, W. M.

1977-01-01

A new analysis of altimetric, gravimetric, and seismological results, together with petrological and thermal history constraints, obtains an estimated Al2O3 content of 5.0%, 2.1 times chondritic. Hence the moon definitely has a refractory lithophile excess as well as an iron deficiency. In addition, the lunar surface is characterized by refractory siderophile depletions. The combination of these properties appears to require a previous stage of differentiation in a planetary body or bodies. Siderophile and chalcolphile depletions and dispersions in eucrites suggest that these bodies are not necessarily large. Possible mechanisms of lunar formation include impacting of a very large body into the earth; tidal disruption of sizeable differentiated planetesimals by the earth; and selective capture of differentiated planetesimal material by small moonlets. Each mechanism has its difficulties; the major unknown affecting all of them is the size distribution of planetesimals.

The effects of parent body processes on amino acids in carbonaceous chondrites

NASA Astrophysics Data System (ADS)

Glavin, Daniel P.; Callahan, Michael P.; Dworkin, Jason P.; Elsila, Jamie E.

2010-12-01

To investigate the effect of parent body processes on the abundance, distribution, and enantiomeric composition of amino acids in carbonaceous chondrites, the water extracts from nine different powdered CI, CM, and CR carbonaceous chondrites were analyzed for amino acids by ultra performance liquid chromatography-fluorescence detection and time-of-flight mass spectrometry (UPLC-FD/ToF-MS). Four aqueously altered type 1 carbonaceous chondrites including Orgueil (CI1), Meteorite Hills (MET) 01070 (CM1), Scott Glacier (SCO) 06043 (CM1), and Grosvenor Mountains (GRO) 95577 (CR1) were analyzed using this technique for the first time. Analyses of these meteorites revealed low levels of two- to five-carbon acyclic amino alkanoic acids with concentrations ranging from approximately 1 to 2,700 parts-per-billion (ppb). The type 1 carbonaceous chondrites have a distinct distribution of the five-carbon (C5) amino acids with much higher relative abundances of the γ- and δ-amino acids compared to the type 2 and type 3 carbonaceous chondrites, which are dominated by α-amino acids. Much higher amino acid abundances were found in the CM2 chondrites Murchison, Lonewolf Nunataks (LON) 94102, and Lewis Cliffs (LEW) 90500, the CR2 Elephant Moraine (EET) 92042, and the CR3 Queen Alexandra Range (QUE) 99177. For example, α-aminoisobutyric acid (α-AIB) and isovaline were approximately 100 to 1000 times more abundant in the type 2 and 3 chondrites compared to the more aqueously altered type 1 chondrites. Most of the chiral amino acids identified in these meteorites were racemic, indicating an extraterrestrial abiotic origin. However, nonracemic isovaline was observed in the aqueously altered carbonaceous chondrites Murchison, Orgueil, SCO 06043, and GRO 95577 with L-isovaline excesses ranging from approximately 11 to 19%, whereas the most pristine, unaltered carbonaceous chondrites analyzed in this study had no detectable L-isovaline excesses. These results are consistent with the theory that aqueous alteration played an important role in amplification of small initial left handed isovaline excesses on the parent bodies.

The Effects of Parent Body Processes on Amino Acids in Carbonaceous Chondrites

NASA Technical Reports Server (NTRS)

Glavin, Daniel P.; Callahan, Michael P.; Dworkin, Jason P.; Elsila, Jamie E.

2010-01-01

To investigate the effect of parent body processes on the abundance, distribution, and enantiomeric composition of amino acids in carbonaceous chondrites, the water extracts from nine different powdered Cl, CM, and CR carbonaceous chondrites were analyzed for amino acids by ultrahigh performance liquid chromatography-fluorescence detection and time-of-flight mass spectrometry (UPLC-FD/ToF-MS). Four aqueously altered type 1 carbonaceous chondrites including Orgueil (C11), Meteorite Hills (MET) 01070 (CM1), Scott Glacier (SCO) 06043 (CM1), and Grosvenor Mountains (GRO) 95577 (CR1) were analyzed using this technique for the first time. Analyses of these meteorites revealed low levels of two- to five-carbon acyclic amino alkanoic acids with concentrations ranging from -1 to 2,700 parts-per-billion (ppb). The type 1 carbonaceous chondrites have a distinct distribution of the five-carbon (C5) amino acids with much higher relative abundances of the gamma- and delta-amino acids compared to the type 2 and type 3 carbonaceous chondrites, which are dominated by a-amino acids. Much higher amino acid abundances were found in the CM2 chondrites Murchison, Lonewolf Nunataks (LON) 94102, and Lewis Cliffs (LEW) 90500, the CR2 Elephant Moraine (EET) 92042, and the CR3 Queen Alexandra Range (QUE) 99177. For example, a-aminoisobutyric acid ((alpha-AIB) and isovaline were approximately 100 to 1000 times more abundant in the type 2 and 3 chondrites compared to the more aqueously altered type 1 chondrites. Most of the chiral amino acids identified in these meteorites were racemic, indicating an extraterrestrial abiotic origin. However, non-racemic isovaline was observed in the aqueously altered carbonaceous chondrites Murchison, Orgueil, SCO 06043, and GRO 95577 with L-isovaline excesses ranging from approximately 11 to 19%, whereas the most pristine, unaltered carbonaceous chondrites analyzed in this study had no detectable L-isovaline excesses. These results are consistent with the theory that aqueous alteration played an important role in amplification of small initial left handed isovaline excesses on the parent bodies.

Condensation and Evaporation of Solar System Materials

NASA Astrophysics Data System (ADS)

Davis, A. M.; Richter, F. M.

2003-12-01

It is widely believed that the materials making up the solar system were derived from a nebular gas and dust cloud that went through an early high-temperature stage during which virtually all of the material was in the gas phase. At one time, it was thought that the entire inner solar nebula was hot, but it is now believed that most material was processed through regions where high temperatures were achieved. Certainly some material, such as presolar grains (cf., Mendybaev et al., 2002a), has never been exposed to high temperatures. As the system cooled, solids and perhaps liquids began to condense, but at some point the partially condensed materials became isolated from the remaining gas. Various lines of evidence support this view. At the largest scale, there is the observation that the Earth, Moon, Mars, and all chondritic meteorites except for the CI chondrites are depleted to varying degrees in the abundances of moderately volatile elements relative to bulk solar system composition. The CI chondrites reflect the bulk composition of the solar system for all but hydrogen, carbon, nitrogen, oxygen, and the rare gases, the most volatile elements (see Chapter 1.03; Palme et al., 1988; McDonough and Sun, 1995; Humayun and Cassen, 2000). The depletions in moderately volatile elements are, to a significant degree, correlated with condensation temperature, suggesting progressive removal of gas as condensation proceeded ( Cassen, 1996). Additional observations that can be explained by partial condensation are that various particularly primitive components of meteorites (e.g., calcium-, aluminum-rich refractory inclusions, and certain metal grains) have mineralogy and/or details of their chemical composition that are remarkably similar to what is calculated for equilibrium condensates from a solar composition gas. For example, the calcium-, aluminum-rich inclusions (CAIs) in chondritic meteorites have compositions very similar to that calculated for the first 5% of total condensable matter (see Chapter 1.08; Grossman, 1973; Wänke et al., 1974; Grossman and Ganapathy, 1976; Grossman et al., 1977), where CI chondrites are taken to represent total condensable matter.Elemental abundance patterns ordered by volatility certainly could have been produced by partial condensation, but they could also have been caused by partial evaporation. The relative importance of these opposite processes is still subject to debate and uncertainty. It should be remembered that condensation calculations typically assume chemical equilibrium in a closed system, in which case the system has no memory of the path by which it arrived at a given state, and thus the chemical and isotopic composition of the condensed phase cannot be used to distinguish between partial condensation and partial evaporation. Humayun and Clayton (1995) have taken a somewhat different view by arguing that condensation and evaporation are distinguishable, in that evaporation, but not condensation, will produce isotopically fractionated residues. With this idea in mind, they carefully measured the potassium isotopic compositions of a broad range of solar system materials with different degrees of potassium depletion and found them to be indistinguishable. This they took as evidence that evaporation could not have been a significant process in determining the diverse elemental abundance patterns of the various solar system materials they measured, because had evaporation been important in fractionating potassium it would have also fractionated the potassium isotopes. We will qualify this line of reasoning by arguing that evaporation and condensation can under certain conditions produce isotopically fractionated condensed phases (i.e., that partial evaporation can produce isotopically heavy residues and that partial condensation can produce isotopically light condensates) but that under other conditions both can produce elemental fractionations without significant isotopic fractionation. The absence of isotopic fractionation in a volatile element-depleted condensed phase is more a measure of the degree to which the system maintained thermodynamic equilibrium than a diagnostic of whether the path involved condensation or evaporation.The pervasive volatile element depletion of inner solar system planets and the asteroidal parent bodies of most meteorites is a major, but by no means the only reason to consider evaporation and condensation processes in the early history of the solar system. Chondrules appear to have been rapidly heated and then cooled over a period of minutes to hours (see Chapter 1.07). If this occurred in a gas of solar composition under nonequilibrium conditions, chondrules should have partially evaporated and an isotopic fractionation record should remain. The absence of such effects can be used to chonstrain the conditions of chondrule formation (e.g., Alexander et al., 2000; Alexander and Wang, 2001). There is good petrologic, chemical, and isotopic evidence suggesting that certain solar system materials such as the coarse-grained CAIs are likely evaporation residues. For example, the type B CAIs are often found to have correlated enrichments in the heavy isotopes of silicon and magnesium ( Figure 1), and these isotopic fractionations are very much like those of evaporation residues produced in laboratory experiments. Condensation also appears to be a major control of elemental zoning patterns in metal grains in CH chondrites (Meibom et al., 1999, 2001; Campbell et al., 2001; Petaev et al., 2001; Campbell et al., 2002). A more contemporary example is the isotopic and chemical compositions of deep-sea spherules that have been significantly affected by evaporative loss during atmospheric entry ( Davis et al., 1991a; Davis and Brownlee, 1993; Herzog et al., 1994, 1999; Xue et al., 1995; Alexander et al., 2002). (7K)Figure 1. Isotopic mass fractionation effects in CAIs. Most coarse-grained CAIs have enrichments of a few ‰ amu-1 in magnesium and silicon, whereas "fractionation and unknown nuclear" (FUN) CAIs are isotopically heavier. The volatile element depletion patterns of planetary size objects and the chemical and isotopic composition of numerous smaller objects such as chondrules and CAIs provide the motivation to consider evaporation and condensation process in the early solar system. The key point is that the processes that led to chondrules and planets appear to have occurred under conditions very close to equilibrium, whereas the processes that led to CAIs involved significant departures from equilibrium.

Nitrogen isotopic signatures in the Acapulco meteorite

NASA Technical Reports Server (NTRS)

Sturgeon, G.; Marti, K.

1991-01-01

N isotopic abundances are reported for a bulk sample of the unique meteorite Acapulco. Although the mineral chemistry indicates a high degree of recrystallization under redox conditions between those of H and E chondrites (Palme et al., 1981), the presence of two distinct N isotopic signatures shows that the carriers of these N components were not equilibrated. In stepwise pyrolysis, the larger (65 percent) N component is released mostly below 1000 C and reveals a signature of delta(N-15) = 8.9 + or - 1.2 per mil, which is within the range observed in chondrites. A second 'light' component appears above 1000 C and has a signature of delta(N-15) less than or equal to -110.5 + or - 4.0 per mil (uncorrected for spallation N-15).

Partial melting of ordinary chondrites: Lost City (H) and St. Severin (LL)

NASA Technical Reports Server (NTRS)

Jurewicz, Amy J. G.; Jones, John H.; Weber, Egon T.; Mittlefehldt, David W.

1993-01-01

Eucrites and diogenites are examples of asteroidal basalts and orthopyroxenites, respectively. As they are found intermingled in howardites, which are inferred to be regolith breccias, eucrites and diogenites are thought to be genetically related. But the details of this relationship and of their individual origins remain controversial. Work by Jurewicz et al. showed that 1170-1180 C partial melts of the (anhydrous) Murchison (CM) chondrite have major element compositions extremely similar to primitive eucrites, such as Sioux County. However, the MnO contents of these melts were about half that of Sioux County, a problem for the simple partial melting model. In addition, partial melting of Murchison could not produce diogenites, because residual pyroxenes in the Murchison experiments were too Fe- and Ca-rich and were minor phases at all but the lowest temperatures. A parent magma for diogenites needs an expanded low-calcium pyroxene field. In their partial melting study of an L6 chondrite, Kushiro and Mysen found that ordinary chondrites did have an expanded low-Ca pyroxene field over that of CV chondrites (i.e., Allende), probably because ordinary chondrites have lower Mg/Si ratios. This study expands that of both Kushiro and Mysen and Jurewicz et al. to the Lost City (H) and St. Severin (LL) chondrites at temperatures ranging from 1170 to 1325 C, at an fO2 of one log unit below the iron-wuestite buffer (IW-1).

Surface composition of near-Earth Asteroid (4953) 1990 MU: Possible fragment of (6) Hebe

NASA Astrophysics Data System (ADS)

Kelley, Michael S.; Gaffey, Michael J.; Reddy, Vishnu; Sanchez, Juan A.

2014-05-01

Near-Earth asteroids (NEAs) are interesting as both a threat to the Earth and as the immediate parent bodies of most meteorites. We observed NEA (4953) 1990 MU using the NASA Infrared Telescope Facility (IRTF) and University of Hawaii (U.H.) telescopes on Mauna Kea to constrain its surface composition and origin. The surface composition of 1990 MU is similar to ordinary chondrites (H chondrites). The calculated olivine and pyroxene chemistry of 1990 MU (Fa13.5±1.3 and Fs12.7±1.4) are consistent with the olivine and pyroxene chemistry ranges for H chondrites (Fa15-21 and Fs13-19) (Dunn, T.L., McCoy, T.J., Sunshine, J.M., McSween, H.Y. [2010]. Icarus 208, 789-797), although the estimated Fa value is at the lower end of the H chondrite range. The olivine abundance ratio of 1990 MU (0.57 ± 0.03) is slightly higher but not inconsistent with H chondrites (0.47-0.55 ± 0.03). The radar circular polarization ratio (same circular polarization state or SC/opposite circular polarization state or OC) (Benner, L.A.M., Ostro, S.J., Magri, C., Nolan, M.C., Howell, E.S., Giorgini, J.D., Jurgens, R.F., Margot, J.L., Taylor, P.A., Busch, M.W., Shepard, M.K. [2008]. Icarus, 198, 294-304) of 1990 MU is 0.36 ± 0.03, which is higher than the mean SC/OC ratio for S-type NEAs (0.270 ± 0.079). The 1990 MU SC/OC is also higher than those of (25143) Itokawa (0.27 ± 0.04), (4179) Toutatis (0.29 ± 0.01) and (433) Eros (0.28 ± 0.06) suggesting a rougher surface at decimeter scale (Benner, L.A.M., Ostro, S.J., Magri, C., Nolan, M.C., Howell, E.S., Giorgini, J.D., Jurgens, R.F., Margot, J.L., Taylor, P.A., Busch, M.W., Shepard, M.K. [2008]. Icarus, 198, 294-304). We constrained the diameter of 1990 MU (4.4 km) using the average albedo at 0.55 μm of H chondrites (0.21) and absolute magnitude (H) of 14.1 (Flower, J.W., Chillemi J.R. [1992]. IRAS Asteroid Data Processing: The IRAS Minor Planet Survey, Philips Laboratory Technical Report PL-TR-92-2049. Jet Propulsion Laboratory, Pasadena, California, pp. 17-43). This diameter is higher than the 2.8 km value from Harris et al. (Harris, A.W. et al. [2011]. Astron. J. 141, 10) using an albedo of 0.52 for 1990 MU. This albedo value is unusually high for H chondrites, which have an albedo range of 0.12-0.30. We compared olivine and pyroxene chemistries of 1990 MU with main belt Asteroid (6) Hebe, probable parent body of H chondrite meteorites and IIE irons (Gaffey, M.J., Gilbert, S.L. [1998]. Meteor. Planet. Sci. 33, 1281-1295), and found that 1990 MU has more high-calcium pyroxene than Hebe. Fayalite and ferrosilite values of the two asteroids are consistent with H chondrites but do not overlap each other. The differences could be due to compositional variations observed on Hebe by Gaffey and Gilbert (Gaffey, M.J., Gilbert, S.L. [1998]. Meteor. Planet. Sci. 33, 1281-1295), although the observed rotational variation in spectral parameters does not match well with those of 1990 MU.

High-temperature rims around calcium-aluminum-rich inclusions from the CR, CB and CH carbonaceous chondrites

NASA Astrophysics Data System (ADS)

Krot, Alexander N.; Nagashima, Kazuhide; van Kooten, Elishevah M. M.; Bizzarro, Martin

2017-03-01

We describe the mineralogy, petrology and oxygen isotopic compositions of high-temperature rims around mineralogically pristine calcium-aluminum-rich inclusions (CAIs) from the CR, CB and CH carbonaceous chondrites. In CR chondrites, nearly all CAIs are surrounded by single- or multi-layered rims composed of CAI-like minerals; relict CAIs inside chondrules in which the rims were resorbed by the host chondrule melt (Aléon et al., 2002; Makide et al., 2009) are the only exception. A complete multi-layered rim sequence (from inside outward: spinel + hibonite + perovskite → melilite → anorthite replacing melilite → Al-diopside → forsterite) is rarely observed; Al-diopside ± forsterite rims are more common. The CR CAIs and all rim layers are uniformly 16O-rich (Δ17O ∼-24‰), indicating formation in a 16O-rich gaseous reservoir. The mineralogy, petrology and 16O-rich compositions of these rims suggest formation by evaporation/condensation, melting (?), and thermal annealing in the formation region of the host CAIs. We define such rims as the primordial Wark-Lovering (WL) rims. In CH chondrites, most CAIs are uniformly 16O-rich and surrounded by the primordial WL rims. One of the 16O-rich CAIs is surrounded by an anorthite-Al-diopside WL rim showing a range of Δ17O values, from ∼-24‰ to ∼-6‰; Δ17O decreases towards the CAI core. We infer that this rim experienced incomplete melting and O-isotope exchange in an 16O-poor nebular gas, most likely during chondrule formation. Most CAIs in CB chondrites and about 10% of CAIs in CH chondrites are uniformly 16O-depleted igneous inclusions; Δ17O values between individual CAIs vary from ∼-12‰ to ∼-5‰. These CAIs have diverse mineralogies (grossite-rich, hibonite-rich, melilite-rich, spinel-rich, and Al,Ti-diopside ± forsterite-rich), but are surrounded by the mineralogically similar igneous rims composed of ±melilite, Al-diopside and Ca-rich forsterite (0.5-1.4 wt% CaO). The igneous rims and the host igneous CAIs have identical (within uncertainties of our SIMS measurements) O-isotope compositions, suggesting that they crystallized from isotopically similar, but chemically distinct melts. We suggest that the uniformly 16O-depleted igneous rims around the uniformly 16O-depleted igneous CAIs in CB and CH chondrites formed during melting of pre-existing CAIs in an impact-generated plume invoked for the origin of CB chondrites (Krot et al., 2005), followed by O-isotope exchange with an 16O-poor plume gas (Δ17O ∼-2‰), condensation of gaseous SiO and Mg into CAI melt, and its subsequent crystallization. We conclude that high-temperature rims around CAIs from CR, CH and CB chondrites recorded thermal processing in gaseous reservoirs with different oxygen isotopic compositions. In contrast to the isotopically heterogeneous WL rims around CV CAIs, our data provide no evidence that CAIs were transported between 16O-rich and 16O-poor gaseous reservoirs multiple times. We suggest instead that oxygen-isotope heterogeneity in the CV WL rims resulted from a fluid-rock interaction on the CV parent asteroid.

Long-period seismology on Europa: 1. Physically consistent interior models

NASA Astrophysics Data System (ADS)

Cammarano, F.; Lekic, V.; Manga, M.; Panning, M.; Romanowicz, B.

2006-12-01

In order to examine the potential of seismology to determine the interior structure and properties of Europa, it is essential to calculate seismic velocities and attenuation for the range of plausible interiors. We calculate a range of models for the physical structure of Europa, as constrained by the satellite's composition, mass, and moment of inertia. We assume a water-ice shell, a pyrolitic or a chondritic mantle, and a core composed of pure iron or iron plus 20 weight percent of sulfur. We consider two extreme mantle thermal states: hot and cold. Given a temperature and composition, we determine density, seismic velocities, and attenuation using thermodynamical models. While anelastic effects will be negligible in a cold mantle and the brittle part of the ice shell, strong dispersion and dissipation are expected in a hot convective mantle and the bulk of the ice shell. There is a strong relationship between different thermal structures and compositions. The ``hot'' mantle may maintain temperatures consistent with a liquid core made of iron plus light elements. For the ``cold scenarios,'' the possibility of a solid iron core cannot be excluded, and it may even be favored. The depths of the ocean and core-mantle boundary are determined with high precision, 10 km and 40 km, respectively, once we assume a composition and thermal structure. Furthermore, the depth of the ocean is relatively insensitive (4 km) to the core composition used.

Surface Mineralogy Mapping of Ceres from the Dawn Mission

NASA Astrophysics Data System (ADS)

McCord, T. B.; Zambon, F.

2017-12-01

Ceres' surface composition is of special interest because it is a window into the interior state and the past evolution of this dwarf planet. Disk-integrated telescopic spectral observations indicated that Ceres' surface is hydroxylated, similar to but not exactly the same as some of the carbonaceous chondrite classes of meteorites. Furthermore, Ceres' bulk density is low, indicating significant water content. The Dawn mission in orbit around Ceres, provided a new and larger set of observations on the mineralogy, molecular and elemental composition, and their distributions in association with surface features and geology. A set of articles was prepared, from which this presentation is derived, that is the first treatment of the entire surface composition of Ceres using the complete High Altitude Mapping Orbit (HAMO) Dawn Ceres data set and the calibrations from all the Dawn instruments. This report provides a current and comprehensive view of Ceres' surface composition and integrates them into general conclusions. Ceres' surface composition shows a fairly uniform distribution of NH4- and Mg-phyllosilicates, carbonates, mixed with a dark component. The widespread presence of phyllosilicates, and salts on Ceres' surface is indicative of the presence of aqueous alteration processes, which involved the whole dwarf planet. There is also likely some contamination by low velocity infall, as seen on Vesta, but it is more difficult to distinguish this infall from native Ceres material, unlike for the Vesta case.

Comparison of the Mineralogy of Comet Wild 2 Coma Grains to Other Astromaterials

NASA Technical Reports Server (NTRS)

Frank, David; Zolensky, Michael

2010-01-01

We propose that Kuiper Belt samples (in this case comet coma grains from the Jupiter family comet Wild 2) are recognizably different from the bulk of materials in outer belt asteroids, because of their different formation positions and times in the early solar system. We believe this despite similarities found between some Wild 2 grains and components of carbonaceous chondrites (i.e. some CAI and chondrules). Kuiper Belt samples must preserve measurable mineralogical and compositional evidence of formation at unique positions and times in the early solar nebula, and these formational differences must have imparted recognizable special characteristics. We hypothesize that these characteristics include: (1) Unique major element compositional ranges of common astromaterial minerals, especially olivine and pyroxene; (2) Unique minor element compositions of major silicate phases, especially olivine and low-Ca pyroxene; (3) Degree and effects of radiation processing -- including amorphous rims, metal coatings, and Glass with Embedded Metal and Sulfides (GEMS); (4) Presence of abundant presolar silicate grains as recognized by anomalous oxygen in silicates; (5) Oxidation state of the mineral assemblage. We are working our way through all available Wild 2 samples, selecting 1-2 non-consecutive viable TEM grids from each possible extracted Wild 2 grain. We especially prefer TEM grids from grains for which complete mineralogical details have not been published (which is to say the majority of the extracted grains). We are performing a basic mineralogic survey by E-beam techniques, to establish the essential features of the extracted Wild 2 grains. We are making a particular effort to carefully and accurately measure minor elements of olivine and pyroxene, as these minerals are widespread in astromaterials, and comparisons of their compositions will serve to place the Wild 2 silicates in contact with asteroids, meteorites and chondritic interplanetary dust particles processing. We are also making a special effort to search for mineralogical products of aqueous alteration, since their presence would reveal that Wild 2 was once internally heated, a result with dramatic implications for models of early solar system primitive bodies. Thus far carbonates are the only potential evidence for aqueous alteration for Wild 2.

Sulfide in the core and the composition of the silicate Earth

NASA Astrophysics Data System (ADS)

Burton, K. W.

2015-12-01

The chemical composition of the Earth is traditionally explained in terms of evolution from a solar-like composition, similar to that found in primitive 'chondritic' meteorites. It now appears, however, that the silicate Earth is not 'chondritic', but depleted in incompatible elements, including refractory lithophile and heat-producing elements. Either Earth lost material during planet-building due to collisional erosion or else internal differentiation processes produced a hidden reservoir deep in the early Earth. Sulfide in the core may provide a reservoir capable of balancing the composition of the silicate Earth. Recent experimental work suggests that the core contains a significant proportion of sulfide, added during the final stages of accretion and new data suggests that at high pressures sulfide can incorporate a substantial amount of refractory lithophile and heat-producing elements [1]. Pioneering work using the short-lived 146Sm-142Nd system strongly suggests that Earth's silicate mantle is non-chondritic [e.g. 2]. The drawback of such radiogenic isotope systems is that it is not possible to distinguish the fractionation of Sm/Nd that occurs during silicate melting from that occurring during the segregation of a sulfide-melt to form the core. Neodymium stable isotopes have the potential to provide just such a tracer of sulfide segregation, because there is a significant contrast in bonding environment between sulfide and silicate, where heavy isotopes should be preferentially incorporated into high force-constant bonds involving REE3+ (i.e. the silicate mantle). Preliminary data indicate that mantle rocks do indeed possess heavier 146Nd/144Nd values than chondritic meteorites, consistent with the removal of light Nd into sulfide in the core, driving the residual mantle to heavy values. Overall, our isotope and elemental data indicate that the rare earths and other incompatible elements are substantially incorporated into sulfide. While Nd Stable isotope data for chondritic meteorites and mantle rocks, are consistent with the segregation of sulfide to the core. [1] Wohlers &Wood, Nature 520, 337 (2015) [2] Boyet & Carlson, Science 309, 576 (2005)

LEW 88516: A Meteorite Compositionally Close to the "Martian Mantle"

NASA Astrophysics Data System (ADS)

Dreibus, G.; Jochum, K. H.; Palme, H.; Spettel, B.; Wlotzka, F.; Wanke, H.

1992-07-01

Several samples from a total of 250 mg of the recently discovered Antarctic shergottite LEW 88516 were analysed for major and trace elements by neutron activation techniques, SSMS, and a carbon-sulfur analyser. Results are presented in Table 1, together with data on ALHA 77005 (Wanke et al., 1976). This and earlier results (Boynton et al., 1992; Lindstrom et al.,1992) show the close compositional similarity of Lew 88516 to ALHA 77005. A major difference between the two shergottites is the much lower iodine content of the ALHA 77005 meteorite. The absence of similar variations in Br and Cl confirms earlier suggestions of an Antarctic source for the I excess. In a Mg/Si vs. Al/Si diagram (Fig. 1) the LEW 88516 meteorite plots at the intersection of a Shergotty parent (SPB) body fractionation trend and a line connecting enstatite chondrites and CM chondrites. The position of LEW 88516 and also of ALHA 77005 in the vicinity of ordinary chondrites is indicative of their relatively primitive composition. Lithophile trace elements show some enhancement of Sc and V over heavy REE and depletion of light REE, suggesting either a residual character for the two meteorites or assimilation of a cumulate phase during their formation. Comparatively high Ni and Co also reflect the more mafic character of the two meteorites. The present analysis and the earlier data on ALHA 77005 unambiguously demonstrate the presence of Ir in an abundance range typical for the terrestrial upper mantle. A similar Ir level was found in Chassigny, but the more fractionated Shergotty has 100 times lower Ir contents. The presence of Ir in the martian mantle samples may be the result of sulfide-silicate equilibration. The sulfides in Lew 88516 are small pyrrhotite grains (5-30 micron, 52 atom% S) and occur often together with ilmenite, at grain boundaries of the major silicate minerals. Sulfides contain an average of 1.8% Ni. However, the major fraction of Ni must reside in oxides and/or silicates as the bulk Ni/S-ratio is 0.25 as compared to 0.05 in sulfides. References: Boynton W.V., Hill D.H. and Kring D.A. (1992) Lunar Planet. Sci. (abstract) 23, 147. Lindstrom M.M., Mittlefehldt D.W., Treiman A.H., Wentworth S.J., Gooding J.L., Morris R.V., Keller L.P. and McKay G.A. (1992) Lunar Planet. Sci. (abstract) 23, 783. Wanke H., Dreibus G., Jagoutz E., Palme H., Spettel B. and Weckwerth G. (1986) Lunar Planet. Sci. (abstract) 17, 919. Table 1, which in the hard copy appears here, shows the chemical composition of Shergottite LEW 55816 and comparison with ALHA 77005.

Experimental and Analytical Studies of Solar System Chemistry

NASA Technical Reports Server (NTRS)

Burnett, Donald S.

2003-01-01

The cosmochemistry research funded by this grant resulted in the publications given in the attached Publication List. The research focused in three areas: (1) Experimental studies of trace element partitioning. (2) Studies of the minor element chemistry and O isotopic compositions of MgAlO4 spinels from Ca-Al-Rich Inclusions in carbonaceous chondrite meteorites, and (3) The abundances and chemical fractionations of Th and U in chondritic meteorites.

Noble gases, nitrogen, cosmic ray exposure history and mineralogy of Beni M'hira (L6) chondrite

NASA Astrophysics Data System (ADS)

Mahajan, Ramakant R.; Nejia, Laridhi Ouazaa; Ray, Dwijesh; Naik, Sekhar

2018-03-01

The concentrations and isotopic composition of noble gases helium (He), neon (Ne), argon (Ar), krypton (Kr), xenon(Xe) and nitrogen were measured in the Beni M'hira L6 chondrite. The cosmic ray exposure age of Beni M'hira is estimated of 15.6 ± 3.7 (Ma). The radiogenic age, of around 485 ± 64 Ma, derived from 4He, and of around 504 ± 51 Ma from 40Ar, suggests an age resetting indicating the event impact. The heavy noble gases (Ar, Kr and Xe) concentrations imply that the gas is a mixture of trapped component Q and solar wind. The measured nitrogen abundance of 0.74 ppm and the isotopic signature of δ15N = 14.6‰ are within the range of ordinary chondrites. The homogeneous chemical composition of olivine (Fa:26 ± 0.25) and low-Ca pyroxene (Fs:22.4 ± 0.29) suggest that the Beni M'hira meteorite is an equilibrated chondrite. This is further corroborated by strong chondrule-matrix textural integration (lack of chondrules, except a few relict clast). Shock metamorphism generally corresponds to S5 (>45 GPa), however, locally disequilibrium melting (shock-melt veins) suggests, that the peak shock metamorphism was at ∼75 GPa, 950 °C.

Carbon in weathered ordinary chondrites from Roosevelt County

NASA Technical Reports Server (NTRS)

Ash, R. D.; Pillinger, C. T.

1993-01-01

A suite of Roosevelt County ordinary chondrites of known terrestrial age have been analyzed for carbon content and isotopic composition. Initial results indicate that significant carbon contamination is evident only in samples with a terrestrial age greater than 40 ka. These samples are of weathering grade D and E and contain three times more carbon than the less weathered samples. The soil in which they were preserved has a carbon content of ca. 1.5 percent. Over 200 meteorites have been recovered from a series of soil depleted areas of New Mexico and West Texas. Most have been recovered from blowouts near Clovis in Roosevelt County (RC) on the high plains of New Mexico. The mineralogical and petrologic Al effects of weathering upon these samples have been studied previously and show that the degree of weathering is largely depend ant upon the terrestrial residence time. The study was undertaken to determine the effects of prolonged exposure to the soil and climate of Roosevelt County upon ordinary chondrites in the hope that this will enable a better understanding of the problems associated with the collection of meteoritic falls. A suite of ten grade 4 to 6 H, L, and LL ordinary chondrites were analyzed for carbon content and isotopic composition.

A vaporization model for iron/silicate fractionation in the Mercury protoplanet

NASA Technical Reports Server (NTRS)

Fegley, Bruce, Jr.; Cameron, A. G. W.

1987-01-01

A study has been carried out on the vaporization of a totally molten silicate magma of chondritic composition heated into the range 2500-3500 K. The motivation for this was to determine the changes in the composition of the mantle that would occur in the Mercury protoplanet should that body have been subjected to the high-temperature phase in the evolution of the primitive solar nebula, but the results are of more general interest. An empirical model based on ideal mixing of complex components was used to describe the nonideal magma. It is found that vaporization of about 70-80 percent of the original amount of silicate from a chondritic planet is required to produce an iron-rich body with a mean uncompressed density equal to that deduced for Mercury. At this point the silicate is depleted in the alkalis, FeO, and SiO2, and enriched in CaO, MgO, Al2O3, and TiO2 relative to chondritic material.

Mineral Composition and Structure of the Sverdlovsk Meteorite (H4-5)

NASA Astrophysics Data System (ADS)

Berzin, S. V.; Koroteev, V. A.; Ivanov, K. S.; Kleimenov, D. A.; Kiseleva, D. V.; Cherednichenko, N. V.

2018-03-01

A fragment of the Sverdlovsk Meteorite, which was found in 1985 in the Central Urals, is studied by modern analytical methods. It belongs to H chondrites of petrologic type 4-5; shock stage of meteorite is S1-2, terrestrial weathering is W1. The composition of minerals of the meteorite is studied. It is found for the first time that the metal and sulfides are concentrated in fine veinlets of the recrystallized matrix of the chondrite and are accompanied by segregations of metal and troilite inside these veinlets. The distribution of trace elements of the metal phase of the meteorite is studied.

Origins and Distribution of Chondritic Olivine Inferred from Wild 2 and Chondrite Matrix

NASA Technical Reports Server (NTRS)

Frank, D. R.; Zolensky, M. E.

2014-01-01

To date, only 180 particle impact tracks from Wild 2 have been extracted from the Stardust aerogel collector and even fewer have been thoroughly characterized. In order to provide a cohesive compositional dataset that can be compared to the meteorite record, we have made both major and minor element analyses (TEM/EDXS) of olivine and low-Ca pyroxene for 39 particles harvested from 26 tracks. However, the dearth of equivalent analyses for these phases in chondrite matrix hinders their comparison to the Wild 2 samples. To properly permit comparison of chondritic olivine and pyroxene to the Wild 2 samples, we have also provided a large, comprehensive EPMA dataset (greater than10(exp 3) analyses) of analogous grains (5-30 micrometers) isolated in L/LL3.0-4, CI, CM, CR, CH, CO, CV, Acfer 094, EH3, EL6, and Kakangari matrix

Extraterrestrial Amino Acids in Orgueil and Ivuna: Tracing the Parent Body of CI Type Carbonaceous Chondrites

NASA Technical Reports Server (NTRS)

Meyer, Michael (Technical Monitor); Ehrenfreund, Pascale; Glavin, Daniel P.; Bota, Oliver; Cooper, George; Bada, Jeffrey

2001-01-01

Amino acid analyses using HPLC of pristine interior pieces of the CI carbonaceous chondrites Orgueil and Ivuna have found that beta-alanine, glycine, and gamma-amino-n-butyric acid (ABA) are the most abundant amino acids in these two meteorites, with concentrations ranging from approx. 600 to 2,000 parts per billion (ppb). Other alpha-amino acids such as alanine, alpha-ABA, alpha-aminoisobutyric acid (AIB), and isovaline are present only in trace amounts (less than 200 ppb). Carbon isotopic measurements of beta-alanine and glycine and the presence of racemic (D/L 1) alanine and beta-ABA in Orgueil suggest that these amino acids are extraterrestrial in origin. In comparison to the CM carbonaceous chondrites Murchison and Murray, the amino acid composition of the CIs is strikingly distinct, suggesting that these meteorites came from a different type of parent body, possibly an extinct comet, than did the CM carbonaceous chondrites.

Actinide abundances in ordinary chondrites

NASA Technical Reports Server (NTRS)

Hagee, B.; Bernatowicz, T. J.; Podosek, F. A.; Johnson, M. L.; Burnett, D. S.

1990-01-01

Measurements of actinide and light REE (LREE) abundances and of phosphate abundances in equilibrated ordinary chondrites were obtained and were used to define the Pu abundance in the solar system and to determine the degree of variation of actinide and LREE abundances. The results were also used to compare directly the Pu/U ratio with the earlier obtained ratio determined indirectly, as (Pu/Nd)x(Nd/U), assuming that Pu behaves chemically as a LREE. The data, combined with high-accuracy isotope-dilution data from the literature, show that the degree of gram-scale variability of the Th, U, and LREE abundances for equilibrated ordinary chondrites is a factor of 2-3 for absolute abundances and up to 50 percent for relative abundances. The observed variations are interpreted as reflecting the differences in the compositions and/or proportions of solar nebula components accreted to ordinary chondrite parent bodies.

DOE Office of Scientific and Technical Information (OSTI.GOV)

Spitz, A.H.; Boynton, W.V.

Six ureilites (ALHA77257, ALHA81101, ALH82130, PCA82506, Kanna, and Novo Urei) were analyzed using neutron activation analysis for Ca, Sc, Cr, Mn, Fe, Co, Ni, Zn, Ga, REE, W, Re, Os, Ir, and Au. The authors examined bulk samples as well as acid-treated samples. In bulk samples the refractory siderophiles' concentrations range from approximately 0.1 to 1.0 times CI chondrites while the volatile siderophiles' concentrations range from approximately 0.1 to 1.0 times CI chondrites while the volatile siderophiles range from about 0.07 to 0.3 times CI chondrites. Rare earth elements (REEs) in ureilites are quite depleted and display light and heavymore » rare earth enrichments. The Antarctic meteorites display either much less pronounced v-shaped patterns or no enrichment in the light rare earths at all. In terms of the new trace-element results, ureilites do not fall into the coherent groups that other workers have defined by chemical or petrographic characteristics. Trace elements do provide additional constraints on the models for the petrogenesis of ureilites. In particular, the siderophile element abundances call for simplified models of chemical processing rather than the complex, multistage processing called for in silicate fractionation models. REE concentrations, on the other hand, imply multistage processing to produce the ureilites. None of the ureilite petrogenesis models extant account for the trace element data. These new data and the considerations of them with respect to the proposed ureilite petrogenesis models indicate that the direction of modeling should be toward contemplation of mixtures and how the components the authors observe in ureilites behave under such conditions.« less

Microscale Variations in the 13C Content of the Murchison Meteorite

NASA Astrophysics Data System (ADS)

Romanek, C.; Gibson, E.; Socki, R.; Burkett, P. J.

1993-07-01

Heretofore unresolved micrometer-scale carbon isotopic zonation in the Murchison meteorite (CM3) is documented using a laser microprobe mass spectrometer. High-resolution isotopic gradients and heterogeneities between high- and low-temperature textural components help to constrain the processes that have shaped the physiochemical character of this carbonaceous chondrite. Previous bulk samples of Murchison yield an average delta ^13C value of - 5.7 +/- 4.3 per mil [1] while individual components such as micrometer-sized mineral separates (e.g., C(sub)graphite , C(sub)diamond, and SiC), acid- soluble extracts (e.g., CaCO3 and polar hydrocarbons), and insoluble residues (e.g., polycyclic aromatic hydrocarbons) are isotopically diverse (delta ^13C of -1000 to 29,000 per mil). While these studies shed light on the origin and occurrence of C-bearing phases, they fail to constrain intrinsic spatial isotopic heterogeneities. The power of the laser microprobe lies in the fact that in situ chemical and isotopic compositions are measured simultaneously for volatiles extracted from extremely small sample volumes (i.e., 0.025 mm^3 for 5 wt% C). Nd-YAG laser irradiation (1.06 micrometers) is directed onto texturally defined targets (>=50 micrometers wide) from which solid material is volatilized. Condensible gaseous phases are collected in a variable-temperature cold trap while the more volatile species (CH4 and CO) are quantified using an ion trap mass spectrometer. All gases are then converted to CO2 in a CuO furnace (containing Pt) held at 600 degrees C and analyzed for carbon and oxygen isotope ratios. The concentration and isotopic composition of condensed species are determined by stepped sublimation of unstable components and conversion to CO2. Preliminary isotopic analyses of the total volatile C content (i.e., bulk microanalysis) from distinct textural components at least 0.05 mm^3 in volume are described below. The most ^13C-depleted components within Murchison reside within the cores of chondrules and/or aggregates. Three typical cores were analyzed, with an average bulk composition of -21.0 +/- 0.5 per mil (n = 7). The bulk ^13C content of C-bearing phases increases monotonically outward in all directions within 100 to 200 micrometers of each core (i.e., within dust mantles) to a constant matrix value of -12.5 +/- 0.5 per mil (n = 40). The most isotopically enriched textural component found in Murchison is a regolith breccia clast without chondrules that has an average bulk delta ^13C value of -10 +/-0.5 per mil (n = 5). The clast was originally detectable only under cathodoluminescence, but with the aid of the laser microprobe it is now characterized by an unusually low volatile content and enriched ^13C composition. In general, the most isotopically enriched components also produce the lowest yield of gas (normalized to sampling volume). This trend of isotopic enrichment from chondrule to matrix has been documented previously for oxygen isotopes in carbonaceous chondrites [2]. Carbon isotopic gradients and heterogeneities within Murchison reflect fundamental changes in the chemical speciation and/or isotopic content of the main C-bearing components (i.e., acid-soluble and insoluble hydrocarbon fractions) within the meteorite. Perhaps core interiors and dust mantles are responding to environmental changes reflected in the speciation of C-bearing species distributed within the solar nebula or the parent body. Inverse correlations between hydrocarbon atomic mass number and ^13C abundance in the acid-soluble [3] and insoluble residues [4] of Murchison have been documented. Alternatively, micrometer-scale isotopic gradients may reflect fundamental changes in the isotopic composition of individual C-bearing species through time. Enrichments may represent kinetically controlled processes related to hydrocarbon formation. In contrast, assuming an equilibrium fractionation mechanism, isotopic enrichments may record a temperature-dependent component to hydrocarbon delta ^13C values. These opposing alternatives will be discussed in light of the isotopic composition of individual C-bearing components volatilized from tightly constrained sample volumes within Murchison. References: [1] Kerridge J. F. (1985) GCA, 49, 1707-1714. [2] Clayton R. N. and Mayeda T. K. (1984) EPSL, 67, 151-161. [3] Yuen G. et al. (1984) Nature, 307, 254. [4] Gilmour I. et al. (1991) Meteoritics, 26, 337-338.

Hungaria Asteroid Region Telescopic Spectral Survey (HARTSS): Stony Asteroids Abundant in the Background and Family Populations

NASA Astrophysics Data System (ADS)

Lucas, Michael P.; Emery, Joshua P.; Pinilla-Alonso, Noemi; Lindsay, Sean S.; Lorenzi, Vania

2016-10-01

The Hungaria region represents a "purgatory" for the closest, preserved samples of the material from which the terrestrial planets accreted. The Hungaria region harbors a collisional family of Xe-type asteroids, which are situated among a background of predominantly S-complex asteroids. Deciphering their surface composition may provide constraints on the nature of the primordial building blocks of the terrestrial planets. We hypothesize that planetesimals in the inner part of the primordial asteroid belt experienced partial- to full-melting and differentiation, the Hungaria region should retain any petrologically-evolved material that formed there.We have undertaken an observational campaign entitled the Hungaria Asteroid Region Telescopic Spectral Survey (HARTSS) to record near-infrared (NIR) spectra to characterize taxonomy, surface mineralogy, and potential meteorite analogs. We used NIR instruments at two ground-based facilities (NASA IRTF; TNG). Our data set includes spectra of 82 Hungaria asteroids (61 background; 21 family), 65 were observed during HARTSS. We compare S-complex background asteroids to calibrations developed via laboratory analyses of ordinary chondrites, and to our analyses (EPMA, XRD, VIS+NIR spectra) of 11 primitive achondrite (acapulcoite-lodranite clan) meteorites.We find that stony S-complex asteroids dominate the Hungaria background population (~80%). Background objects exhibit considerable spectral diversity, when quantified by spectral band parameter measurements, translates to a variety of surface compositions. Two main meteorite groups are represented within the Hungaria background: unmelted, nebular L chondrites (and/or L chondrites), and partially-melted primitive achondrites. H-chondrite mineralogies appear to be absent from the Hungaria background. Xe-type Hungaria family members exhibit spectral homogeneity, consistent with the hypothesis that the family was derived from the disruption of a parent body analogous to an enstatite achondrite (i.e., aubrite) composition. Hungaria region asteroids exhibit a full range of petrologic evolution, from nebular, unmelted ordinary chondrites, through partially-melted primitive achondrites, to fully-melted igneous aubrite meteorites.

Closed System Step Etching of CI chondrite Ivuna reveals primordial noble gases in the HF-solubles

NASA Astrophysics Data System (ADS)

Riebe, My E. I.; Busemann, Henner; Wieler, Rainer; Maden, Colin

2017-05-01

We analyzed all the noble gases in HF-soluble phases in the CI chondrite Ivuna by in-vacuum gas release using the "Closed System Step Etching" (CSSE) technique, which allows for direct noble gas measurements of acid-soluble phases. The main motivation was to investigate if there are primordial noble gases in HF-soluble phases in Ivuna, something that has not been done before in CI chondrites, as most primordial noble gases are known to reside in HF-resistant phases. The first steps under mild etching released He, Ne, and Ar with solar-like elemental and isotopic compositions, confirming that Ivuna contains implanted solar wind (SW) noble gases acquired in the parent body regolith. The SW component released in some etch steps was elementally unfractionated. This is unusual as trapped SW noble gases are elementally fractionated in most meteoritic material. In the intermediate etch steps under slightly harsher etching, cosmogenic noble gases were more prominent than SW noble gases. The HF-soluble portion of Ivuna contained primordial Ne and Xe, that was most visible in the last etch steps after all cosmogenic and most SW gases had been released. The primordial Ne and Xe in the HF-solubles have isotopic and elemental ratios readily explained as a mixture of the two most abundant primordial noble gas components in Ivuna bulk samples: HL and Q. Only small fractions of the total HL and Q in Ivuna were released during CSSE analysis; ∼3% of 20NeHL and ∼4% of 132XeQ. HL is known to reside in nanodiamond-rich separates and Q-gases are most likely carried by a carbonaceous phase known as phase Q. Q-gases were likely released from an HF-soluble portion of phase Q. However, nanodiamonds might not be the source of the HL-gases released upon etching, since nanodiamond-rich separates are very HF-resistant and the less tightly bound nanodiamond component P3 was not detected.

Element Abundances in Meteorites and the Earth: Implication for the Accretion of Planetary Bodies

NASA Astrophysics Data System (ADS)

Mezger, K.; Vollstaedt, H.; Maltese, A.

2017-12-01

Essentially all known inner solar system materials show near chondritic relative abundances of refractory elements and depletion in volatile elements. To a first approximation volatile element depletion correlates with the respective condensation temperature (TC) of the elements. Possible mechanisms for this depletion are incomplete condensation and partial loss by evaporation caused by heating prior to or during the planetesimal accretion. The stable isotope compositions of almost all moderately volatile elements in different meteorite classes show only minor, or no evidence for a Rayleigh-type fractionation that could be attributed to partial condensation or evaporation. The different classes of meteorites also show that the degree of depletion in their parent bodies (i.e. mostly planetesimals) is quite variable, but nevertheless systematic. For primitive and least disturbed carbonaceous chondrites the element depletion pattern is a smooth function of TC. The accessible silicate Earth also shows this general depletion pattern, but in detail it is highly complex and requires differentiation processes that are not solely controlled by TC. If only highly lithophile elements are considered the depletion pattern of the silicate Earth reveals a step function that shows that moderately volatile lithophile elements have abundances that are ca. 0.1 times the chondritic value, irrespective of their TC. This element pattern observed for bulk silicate Earth can be modelled as a mixture of two distinct components: ca. 90% of a strongly reduced planetary body that is depleted in highly volatile elements and ca. 10% of a more volatile element rich and oxidized component. This mixture can account for the apparent Pb- paradox observed in melts derived from the silicate Earth and provides a time constraint for the mixing event, which is ca. 70 My after the beginning of the solar system. This event corresponds to the giant impact that also formed the Moon.

Spectral nature of CO2 adsorption onto meteorites

USGS Publications Warehouse

Berlanga, Genesis; Hibbitts, Charles A; Takir, Driss; Dyar, Draby M; Elizabeth Sklute,

2016-01-01

Previous studies have identified carbon dioxide (CO2) on the surfaces of Jovian and Galilean satellites in regions of non-ice material that are too warm for CO2 ice to exist. CO2 ice would quickly sublimate if not retained by a less-volatile material. To ascertain what non-ice species may be responsible for stabilizing this CO2, we performed CO2 gas adsorption experiments on thirteen powdered CM, CI, and CV carbonaceous chondrite meteorites. Reflectance spectra of the ν3 feature associated with adsorbed CO2 near 4.27 μm were recorded. Results show that many meteorites adsorbed some amount of CO2, as evidenced by an absorption feature that was stable over several hours at ultra-high vacuum (UHV) and high vacuum, (1.0×10−8 and 1.0×10−7 Torr, respectively). Ivuna, the only CI chondrite studied, adsorbed significantly more CO2 than the others. We found that CO2 abundance did not vary with ‘water’ abundance, organics, or carbonates as inferred from the area of the 3-μm band, the 3.2-3.4 μm C-H feature, and the ∼3.8-μm band respectively, but did correlate with hydrous/anhydrous phyllosilicate ratios. Furthermore, we did not observe CO2 ice because the position of the CO2 feature was generally shifted 3-10 nm from that of the 4.27 μm absorption characteristic of ice. The strongest compositional relationship observed was a possible affinity of CO2 for total FeO abundance and complex clay minerals, which make up the bulk of the CI chondrite matrix. This finding implies that the most primitive refractory materials in the Solar System may also act as reservoirs of CO2, and possibly other volatiles, delivering them to parts of the Solar System where their ices would not be stable.

Constraints on the Composition and Evolution of the Lunar Crust from Meteorite NWA 3163

NASA Technical Reports Server (NTRS)

McLeod, C. L.; Brandon, A. D.; Fernandes, V. A.; Peslier, A. H.; Lapen, T. J.; Irving, A. J.

2013-01-01

The lunar meteorite NWA 3163 (paired with NWA 4881, 4483) is a ferroan, feldspathic granulitic breccia characterized by pigeonite, augite, olivine, maskelynite and accessory Tichromite, ilmenite and troilite. Bulk rock geochemical signatures indicate the lack of a KREEP- derived component (Eu/Eu* = 3.47), consistent with previously studied lunar granulites and anorthosites. Bulk rock chondrite-normalized signatures are however distinct from the anorthosites and granulites sampled by Apollo missions and are relatively REE-depleted. In-situ analyses of maskelynite reveal little variation in anorthite content (average An% is 96.9 +/- 1.6, 2 sigma). Olivine is relatively ferroan and exhibits very little variation in forsterite content with mean Fo% of 57.7 +/- 2.0 (2 sigma). The majority of pyroxene is low-Ca pigeonite (En57Fs33Wo10). Augite (En46Fs21Wo33) is less common, comprising approximately 10% of analyzed pyroxene. Two pyroxene thermometry on co-existing orthopyroxene and augite yield an equilibrium temperature of 1070C which is in reasonable agreement with temperatures of 1096C estimated from pigeonite compositions. Rb-Sr isotopic systematics of separated fractions yield an average measured Sr-87/Sr-87 of 0.699282+/-0.000007 (2 sigma). Sr model ages are calculated using a modern day Sr-87/Sr-86 Basaltic Achondrite Best Initial (BABI) value of 0.70475, from an initial BABI value Sr-87/Sr-86 of 0.69891 and a corresponding Rb-87/Sr-97 of 0.08716. The Sr model Thermomechanical analysis (TMA) age, which represents the time of separation of a melt from a source reservoir having chondritic evolution, is 4.56+/-0.1 Ga. A Sr model T(sub RD) age, which is a Rb depletion age and assumes no contribution from Rb in the sample in the calculation, yields 4.34+/-0.1 Ga (i.e. a minimum age). The Ar-Ar dating of paired meteorite NWA 4881 reveals an age of c. 2 Ga, likely representing the last thermal event this meteorite experienced. An older Ar-40/Ar-39 age of c. 3.5 Ga may record the thermal event which produced the granulitic texture. Additional chronological constraints will be provided by Sm-Nd systematics. Ferroan Anorthosites like NWA 3163 have been interpreted to represent direct lunar magma ocean (LMO) crystallization products. If this is the case, trace element concentrations in NWA 3163 primary mineral phases should be in equilibrium with residual LMO liquids present during crystallization of those phases. Results from petrogenetic modeling suggest that the NWA 3163 protolith did not form from crystallization of an initially LREE depleted LMO but rather require an initially chondritic LMO with early garnet crystallization. Furthermore, a two-stage crystallization model where plagioclase crystalized prior to pyroxene (93% vs. 99.5% of LMO crystallization) is implied.

Na, K-Rich Rim Around a Chondrule in Unequilibrated Ordinary Chondrite Lew 86018 (L3.1)

NASA Technical Reports Server (NTRS)

Mishra, R. K.; Simon, J. I.; Ross, D. K.; Needham, A. W.; Messenger, S.; Keller, L. P.; Han, J.; Marhas, K. K.

2015-01-01

Ordinary chondrites represent the most abundant early Solar system extra-terrestrial (approximately 85% abundance) material available for laboratory studies and expectedly record the most extensive range of alterations effects from unmetamorphosed chondritic material to the highest temperatures of thermal metamorphism. The least metamorphosed chondrites belonging to petrologic type 3, the so called unequili-brated ordinary chondrites (UOCs), provide insights into alteration that happened during the primeval, ear-liest stage of Solar system formation. The higher grade petrologic types 4-6 ordinary chondrites on the other hand document up to near textural equilibrium (in type 6) extensive thermal metamorphism consisting of minerals and phases providing evidence of equilibration of heterogeneous mineral composition, solid-state recrystallization. Despite being the most abundant, the effect of alteration is less explicitly understood in ordinary chondrites (even less in UOCs) compared to other groups (e.g. CV, CO, CR). Additionally, the relationship between metasomatism (also referred as aqueous alteration or fluid-assisted metamorphism) and metamorphism (primarily thermal driven) has not been studied and alterations in the ordinary chondrites have been considered to have occurred in absence of fluids in general. Despite this conventional view, UOCs of lowest grades (3.0-3.2) show some evidence of low temperature (approximately 200 C), fluid assisted metamorphism in the form of the presence of phyllosilicates, ferroan olivine, and magnetites in their matrices and occasionally in chondrules. Here, we present petrographic and mineralogical studies of UOC, Lewis Hills (LEW) 86018 to further our understanding of the extent and relative importance of metasomatism and/or metamorphism in UOCs.

Oxygen Isotopic Compositions of Solar Corundum Grains

NASA Astrophysics Data System (ADS)

Makide, Kentaro; Nagashima, Kazuhide; Krot, Alexander N.; Huss, Gary R.

2009-11-01

Oxygen is one of the major rock-forming elements in the solar system and the third most abundant element of the Sun. Oxygen isotopic composition of the Sun, however, is not known due to a poor resolution of astronomical spectroscopic measurements. Several Δ17O values have been proposed for the composition of the Sun based on (1) the oxygen isotopic measurements of the solar wind implanted into metallic particles in lunar soil (< -20‰ by Hashizume & Chaussidon and ~ +26‰ by Ireland et al.), (2) the solar wind returned by the Genesis spacecraft (-27‰ ± 6‰ by McKeegan et al.), and (3) the mineralogically pristine calcium-aluminum-rich inclusions (CAIs) (-23.3‰ ± 1.9‰ by Makide et al. and -35‰ by Gounelle et al.). CAIs are the oldest solar system solids, and are believed to have formed by evaporation, condensation, and melting processes in hot nebular region(s) when the Sun was infalling (Class 0) or evolved (Class 1) protostar. Corundum (Al2O3) is thermodynamically the first condensate from a cooling gas of solar composition. Corundum-bearing CAIs, however, are exceptionally rare, suggesting either continuous reaction of the corundum condensates with a cooling nebular gas and their replacement by hibonite (CaAl12O19) or their destruction by melting together with less refractory condensates during formation of igneous CAIs. In contrast to the corundum-bearing CAIs, isolated micrometer-sized corundum grains are common in the acid-resistant residues from unmetamorphosed chondrites. These grains could have avoided multistage reprocessing during CAI formation and, therefore, can potentially provide constraints on the initial oxygen isotopic composition of the solar nebula, and, hence, of the Sun. Here we report oxygen isotopic compositions of ~60 micrometer-sized corundum grains in the acid-resistant residues from unequilibrated ordinary chondrites (Semarkona (LL3.0), Bishunpur (LL3.1), Roosevelt County 075 (H3.2)) and unmetamorphosed carbonaceous chondrites (Orgueil (CI1), Murray (CM2), and Alan Hills A77307 (CO3.0)) measured with a Cameca ims-1280 ion microprobe. All corundum grains, except two, are 16O-rich (Δ17O = -22.7‰ ± 8.5‰, 2σ), and compositionally similar to the mineralogically pristine CAIs from the CR carbonaceous chondrites (-23.3‰ ± 1.9‰, 2σ), and solar wind returned by the Genesis spacecraft (-27‰ ± 6‰, 2σ). One corundum grain is highly 17O-enriched (δ17O ~ +60‰, δ18O ~ -40‰) and is probably of the presolar origin; the origin of another 17O-rich grain (δ17O ~ -15‰, δ18O ~ -35‰) is unclear. We conclude that the 16O-rich corundum grains in the acid-resistant residues from unequilibrated ordinary and unmetamorphosed carbonaceous chondrites recorded initial oxygen isotopic composition of the solar nebula, and, hence, of the Sun. Our inferred oxygen isotopic composition of the Sun is inconsistent with the more extreme 16O-rich value (Δ17O ~ -35‰) proposed by Gounelle et al. on the basis of two extremely 16O-rich CAIs from the CH/CB-like chondrite Isheyevo and with the 16O-poor value observed as a component of the solar wind implanted into the metallic particles in lunar soil (Ireland et al.).

Mineralogy and Microstructures of Shock-Induced Melt Veins in Chondrites

NASA Technical Reports Server (NTRS)

Sharp, Thomas G.

2000-01-01

The applicability of phase equilibrium data to the interpretation of shock-induced melt veins can only be tested by a detailed study of melt- vein mineralogy to see how high-pressure assemblages vary as a function of shock conditions inferred from other indicators. We have used transmission electron microscopy (TEM), analytical electron microscopy (AEM), scanning electron microscopy (SEM), electron microprobe analysis (EMA) and optical petrography to characterize the mineralogy, microstructures, and compositions of melt veins and associated high-pressure minerals in shocked chondrites and SNC meteorites. In the processes, we have gained a better understanding of what melt veining can tell us about shock conditions and we have discovered new mineral phases in chondritic and SNC meteorites.

An Ordinary Chondrite Impactor Composition for the Bosumtwi Impact Structure, Ghana, West Africa: Discussion of Siderophile Element Contents and Os and Cr Isotope Data

NASA Technical Reports Server (NTRS)

Koeberl, Christian; Shukolyukov, Alex; Lugmair, Guenter

2004-01-01

Osmium isotope data had shown that Ivory Coast tektites contain an extraterrestrial component, but do not allow distinction between chondritic and iron meteorite contamination. PGE abundances of Ivory Coast tektites and impactites and target rocks from the Bosumtwi crater, the source crater of the Ivory Coast tektites, were all relatively high and did not allow to resolve the presence, or identify the nature, of the meteoritic component. However, Cr isotope analyses of an Ivory Coast tektite yielded a distinct 53Cr excess of 0.30+/-0.06, which indicates that the Bosumtwi impactor was an ordinary chondrite.

New constraints on the formation of shergottite Elephant Moraine 79001 lithology A

NASA Astrophysics Data System (ADS)

Liu, Yang; Balta, J. Brian; Goodrich, Cyrena A.; McSween, Harry Y.; Taylor, Lawrence A.

2013-05-01

Previous studies of Elephant Moraine (EET) 79001 disagreed upon the nature of the magnesian olivine and orthopyroxene grains, and generally considered the formation of EET 79001 at low pressure conditions. New observations on mineral associations, and trace-element abundances of olivine-hosted melt inclusions, in lithology A (EET-A) of EET 79001 lead to new constraints on the formation of this meteorite. The abundances and chondrite-normalized REE pattern of the average melt inclusions in olivine of Mg# 75-61 are similar to those of the bulk-rock composition of lithology A, suggesting that the Mg# <77 olivines are phenocrysts. We also report the widespread occurrence of round orthopyroxene (En78.9-77.9Wo2.2-2.5) inclusions in disequilibrium contact with their olivine hosts (Mg# 73-68). Compositions of these inclusions are similar to xenocrystic cores (Mg# ⩾77; Wo ⩽4) in pyroxene megacrysts. These observations indicate that orthopyroxene xenocrysts were being resorbed while Mg# 77-73 olivine was crystallizing. Combined, these observations suggest that only small portions of the megacrysts are xenocrystic, namely orthopyroxene of Mg# ⩾77 and Wo ⩽4, and possibly also olivine of Mg# ⩾77. The volume percentages of the xenocrystic materials in the rock are small (⩽1 vol.% for each mineral). Compositions of the xenocrystic minerals are similar to cores of megacrysts in olivine-phyric shergottite Yamato (Y) 980459 and Northwest Africa (NWA) 5789. Considering the small fraction of xenocrysts and the similarity between REE abundances of the early-trapped melt and those in bulk EET-A, we re-evaluated the possibility that the bulk-rock composition of EET-A is close to that of its parent melt. Results of pMELTS modeling indicate that polybaric crystallization of the EET-A bulk composition (corrected by removal of xenocryst material) can reproduce the crystallization sequence of EET-A, in contrast to the conclusions of previous workers. We estimate that the EET-A parent magma began crystallizing at ∼0.7 GPa (∼60 km depth), followed a near-isobaric path at 0.5-0.7 GPa during crystallization of most olivine and pyroxene megacrysts, and then crystallized at shallower depth during the formation of megacryst rims and groundmass. Combined with recent reports of high-pressure crystallization for three other olivine-phyric samples, our results strongly support the interpretation that these relatively primitive samples may have begun to crystallize at much greater depths than previously inferred, at the base of martian crust.

Consortium study of the unusual H chondrite regolith breccia, Noblesville

NASA Technical Reports Server (NTRS)

Lipschutz, Michael E.; Wolf, Stephen F.; Vogt, Stephan; Michlovich, Edward; Lindstrom, Marilyn M.; Zolensky, Michael E.; Mittlefehldt, David W.; Satterwhite, Cecilia; Schultz, Ludolf; Loeken, Thomas

1993-01-01

The Noblesville meteorite is a genomict, regolith breccia (H6 clasts in H4 matrix). Moessbauer analysis confirms that Noblesville is unusually fresh, not surprising in view of its recovery immediately after its fall. It resembles 'normal' H4-6 chondrites in its chemical composition and induced thermoluminescence (TL) levels. Thus, at least in its contents of volatile trace elements, Noblesville differs from other H chondrite, class A regolith breccias. Noblesville's small pre-atmospheric mass and fall near solar maximum and/or its peculiar orbit (with perihelion less than 0.8 AU as shown by natural TL intensity) may partly explain its levels of cosmogenic radionuclides. Its cosmic ray exposure age of about 44 Ma is long, is equalled or exceeded by less than 3 percent of all H chondrites, and also differs from the 33 +/- 3 Ma mean exposure age peak of other H chondrite regolith breccias. While Noblesville is now among the chondritic regolithic breccias richest in solar gases, elemental ratios indicate some loss, especially of He, perhaps by impacts in the regolith that heated individual grains. While general shock-loading levels in Noblesville did not exceed 4 GPa, individual clasts record shock levels of 5-10 GPa, doubtless acquired prior to lithification of the whole-rock meteoroid.

Clouds Composition in Super-Earth Atmospheres: Chemical Equilibrium Calculations

NASA Astrophysics Data System (ADS)

Kempton, Eliza M.-R.; Mbarek, Rostom

2015-12-01

Attempts to determine the composition of super-Earth atmospheres have so far been plagued by the presence of clouds. Yet the theoretical framework to understand these clouds is still in its infancy. For the super-Earth archetype GJ 1214b, KCl, Na2S, and ZnS have been proposed as condensates that would form under the condition of chemical equilibrium, if the planet’s atmosphere has a bulk composition near solar. Condensation chemistry calculations have not been presented for a wider range of atmospheric bulk composition that is to be expected for super-Earth exoplanets. Here we provide a theoretical context for the formation of super-Earth clouds in atmospheres of varied composition by determining which condensates are likely to form, under the assumption of chemical equilibrium. We model super-Earth atmospheres assuming they are formed by degassing of volatiles from a solid planetary core of chondritic material. Given the atomic makeup of these atmospheres, we minimize the global Gibbs free energy of over 550 gases and condensates to obtain the molecular composition of the atmospheres over a temperature range of 350-3,000 K. Clouds should form along the temperature-pressure boundaries where the condensed species appear in our calculations. The super-Earth atmospheres that we study range from highly reducing to oxidizing and have carbon to oxygen (C:O) ratios that are both sub-solar and super-solar, thereby spanning a diverse range of atmospheric composition that is appropriate for low-mass exoplanets. Some condensates appear across all of our models. However, the majority of condensed species appear only over specific ranges of H:O and C:O ratios. We find that for GJ 1214b, KCl is the primary cloud-forming condensate at solar composition, in agreement with previous work. However, for oxidizing atmospheres, where H:O is less than unity, K2SO4 clouds form instead. For carbon-rich atmospheres with super-solar C:O ratios, graphite clouds additionally appear. At higher temperatures, clouds are formed from a variety of materials including metals, metal oxides, and aluminosilicates.

Simulations of defense strategies for Bennu: Material characterization and impulse delivery

DOE PAGES

Herbold, E. B.; Owen, J. M.; Swift, D. C.; ...

2015-05-19

Assessments of asteroid deflection strategies depend on material characterization to reduce the uncertainty in predictions of the deflection velocity resulting from impulsive loading. In addition to strength, equation of state, the initial state of the material including its competency (i.e. fractured or monolithic) and the amount of micro- or macroscopic porosity are important considerations to predict the thermomechanical response. There is recent interest in observing near-Earth asteroid (101955) Bennu due to its classification of being potentially hazardous with close approaches occurring every 6 years. Bennu is relatively large with a nominal diameter of 492 m, density estimates ranging from 0.9-1.26more » g/cm³ and is composed mainly of carbonaceous chondrite. There is a lack of data for highly porous carbonaceous chondrite at very large pressures and temperatures. In the absence of the specific material composition and state (e.g. layering, porosity as a function of depth) on Bennu we introduce a continuum constitutive model based on the response of granular materials and provide impact and standoff explosion simulations to investigate the response of highly porous materials to these types of impulsive loading scenarios. Simulations with impact speeds of 5 km/s show that the shock wave emanating from the impact site is highly dispersive and that a 10% porous material has a larger compacted volume compared with a 40% porous material with the same bulk density due to differences in compaction response.« less

Rare earth element abundances in presolar SiC

NASA Astrophysics Data System (ADS)

Ireland, T. R.; Ávila, J. N.; Lugaro, M.; Cristallo, S.; Holden, P.; Lanc, P.; Nittler, L.; Alexander, C. M. O'D.; Gyngard, F.; Amari, S.

2018-01-01

Individual isotope abundances of Ba, lanthanides of the rare earth element (REE) group, and Hf have been determined in bulk samples of fine-grained silicon carbide (SiC) from the Murchison CM2 chondrite. The analytical protocol involved secondary ion mass spectrometry with combined high mass resolution and energy filtering to exclude REE oxide isobars and Si-C-O clusters from the peaks of interest. Relative sensitivity factors were determined through analysis of NIST SRM reference glasses (610 and 612) as well as a trace-element enriched SiC ceramic. When normalised to chondrite abundances, the presolar SiC REE pattern shows significant deficits at Eu and Yb, which are the most volatile of the REE. The pattern is very similar to that observed for Group III refractory inclusions. The SiC abundances were also normalised to s-process model predictions for the envelope compositions of low-mass (1.5-3 M⊙) AGB stars with close-to-solar metallicities (Z = 0.014 and 0.02). The overall trace element abundances (excluding Eu and Yb) appear consistent with the predicted s-process patterns. The depletions of Eu and Yb suggest that these elements remained in the gas phase during the condensation of SiC. The lack of depletion in some other moderately refractory elements (like Ba), and the presence of volatile elements (e.g. Xe) indicates that these elements were incorporated into SiC by other mechanisms, most likely ion implantation.

Magnesium isotope compositions of Solar System materials determined by double spiking

NASA Astrophysics Data System (ADS)

Hin, R.; Lai, Y. J.; Coath, C.; Elliott, T.

2015-12-01

As a major element, magnesium is of interest for investigating large scale processes governing the formation and evolution of rocky planetary bodies. Determining the Mg isotope composition of the Earth and other planetary bodies has hence been a topic of interest ever since mass-dependent fractionation of 'non-traditional' stable isotopes has been used to study high-temperature processes. Published results, however, suffer from disagreement on the Mg isotope compositions of the Earth and chondrites [1-5], which is attributed to residual matrix effects. Nonetheless, most recent studied have converged towards a homogeneous (chondritic) Mg isotope composition in the Solar System [2-5]. However, in several of the recent studies there is a hint of a systematic difference of about 0.02-0.06‰ in the 26Mg/24Mg isotope compositions of chondrites and Earth. Such difference, however, is only resolvable by taking standard errors, which assumes robust data for homogenous sample sets. The discrepancies between various studies unfortunately undermine the confidence in such robustness and homogeneity. The issues with matrix effects during isotopic analyses can be overcome by using a double spike approach. Such methodology generally requires three isotope ratios to solve for three unknowns, a requirement that cannot be met for Mg. However, using a newly developed approach, we present Mg isotope compositions obtained by critical mixture double spiking. This new approach should allow greater confidence in the robustness of the data and hence enable improvement of. Preliminary data indicate that chondrites have a resolvable ~0.04‰ lighter 26Mg/24Mg than (ultra)mafic rocks from Earth, Mars and the eucrite parent body, which appear indistinguishable from each other. It seems implausible that this difference is caused by magmatic process such as partial melting or crystallisation. More likely, Mg isotopes are fractionated by a non-magmatic process during the formation of planets, e.g. by vapour-condensate fractionation. [1] Wiechert and Halliday, 2007. EPSL 256, 360-371. [2] Bourdon et al., 2010. GCA 74, 5069-5083. [3] Teng et al., 2010. GCA 74, 4150-4166. [4] Chakrabarti and Jacobsen, 2010. EPSl 293, 349-358. [5] Von Strandmann, 2011. GCA 75, 5247-5268.

Mineralogical Composition of the Mexican Ordinary Chondrite Type Meteorite: A Raman, Infrared and XRD Study

NASA Astrophysics Data System (ADS)

Ostrooumov, M.

2016-08-01

The Raman microprobe (RMP), infrared (IR) and XRD analysis have been applied to the examination of mineralogical composition of seven mexican meteorites: Aldama, Cosina, El Pozo, Escalon, Nuevo Mercurio,Pacula, Zapotitlan Salinas.

Physical properties of the ESA Rosetta target asteroid (21) Lutetia. I. The triaxial ellipsoid dimensions, rotational pole, and bulk density

NASA Astrophysics Data System (ADS)

Drummond, J. D.; Conrad, A.; Merline, W. J.; Carry, B.; Chapman, C. R.; Weaver, H. A.; Tamblyn, P. M.; Christou, J. C.; Dumas, C.

2010-11-01

Context. Asteroid (21) Lutetia was the target of the ESA Rosetta mission flyby in 2010 July. Aims: We seek the best size estimates of the asteroid, the direction of its spin axis, and its bulk density, assuming its shape is well described by a smooth featureless triaxial ellipsoid. We also aim to evaluate the deviations from this assumption. Methods: We derive these quantities from the outlines of the asteroid in 307 images of its resolved apparent disk obtained with adaptive optics (AO) at Keck II and VLT, and combine these with recent mass determinations to estimate a bulk density. Results: Our best triaxial ellipsoid diameters for Lutetia, based on our AO images alone, are a × b × c = 132 × 101 × 93 km, with uncertainties of 4 × 3 × 13 km including estimated systematics, with a rotational pole within 5° of ECJ2000 [λβ] = [45° - 7°] , or EQJ2000 [RA Dec] = [44° + 9°] . The AO model fit itself has internal precisions of 1 × 1 × 8 km, but it is evident both from this model derived from limited viewing aspects and the radius vector model given in a companion paper, that Lutetia significantly departs from an idealized ellipsoid. In particular, the long axis may be overestimated from the AO images alone by about 10 km. Therefore, we combine the best aspects of the radius vector and ellipsoid model into a hybrid ellipsoid model, as our final result, of diameters 124 ± 5 × 101 ± 4 × 93 ± 13 km that can be used to estimate volumes, sizes, and projected areas. The adopted pole position is within 5° of [λβ] = [52° - 6°] or [RA Dec] = [52° + 12°]. Conclusions: Using two separately determined masses and the volume of our hybrid model, we estimate a density of 3.5±1.1 or 4.3±0.8 g cm-3. From the density evidence alone, we argue that this favors an enstatite-chondrite composition, although other compositions are formally allowed at the extremes (low-porosity CV/CO carbonaceous chondrite or high-porosity metallic). We discuss this in the context of other evidence. Based on observations collected at the W. M. Keck Observatory and the European Southern Observatory Very Large Telescope (program ID:079.C-0493, PI: E. Dotto). The W. M. Keck Observatory is operated as a scientific partnership among the California Institute of Technology, the University of California, and the National Aeronautics and Space Administration. The Observatory was made possible by the generous financial support of the W. M. Keck Foundation.

The cali meteorite fell: A new H/L ordinary chondrite

USGS Publications Warehouse

Rodriguez, J.M.T.; Llorca, J.; Rubin, A.E.; Grossman, J.N.; Sears, D.W.G.; Naranjo, M.; Bretzius, S.; Tapia, M.; Sepulveda, M.H.G.

2009-01-01

The fall of the Cali meteorite took place on 6 July 2007 at 16 h 32 ?? 1 min local time (21 h 32 ?? 1 min UTC). A daylight fireball was witnessed by hundreds of people in the Cauca Valley in Colombia from which 10 meteorite samples with a total mass of 478 g were recovered near 3??24.3'N, 76??30.6'W. The fireball trajectory and radiant have been reconstructed with moderate accuracy. From the computed radiant and from considering various plausible velocities, we obtained a range of orbital solutions that suggest that the Cali progenitor meteoroid probably originated in the main asteroid belt. Based on petrography, mineral chemistry, magnetic susceptibility, fhermoluminescence, and bulk chemistry, the Cali meteorite is classified as an H/L4 ordinary chondrite breccia.

Near-infrared spectroscopy of 3:1 Kirkwood Gap asteroids III

NASA Astrophysics Data System (ADS)

Fieber-Beyer, Sherry K.; Gaffey, Michael J.

2015-09-01

The research is an integrated effort beginning with telescopic observations and extending through detailed mineralogical characterizations to provide constraints on the composition and meteorite affinities of a subset of fourteen asteroids in/near the 3:1 Kirkwood Gap. Eight asteroids were identified as having either one or two absorption features, while six were deemed featureless. The compositional analysis of Asteroids (355) Gabriella and (1447) Utra reveal Fs and Fa values which are consistent with values for the L-type ordinary chondrites (Fs19-22 and Fa22-26). The location of these two bodies with respect to each other and to the previously identified L-chondrite parent body Asteroid (1722) Goffin, suggests a small L-chondrite genetic family. These results support the model that the L-chondrites come from an asteroid family rather than from a single object. Asteroids (1368) Numidia, (1587) Kahrstadt, (1854) Skvortsov, (2497) Kulikovskij, and (5676) Voltaire were analyzed and determined to have "basaltic" silicate mineralogies similar to those of the HED (howardite-eucrite-diogenite) meteorite group. In particular, we found that the compositions of (1368), (1587) and (1854) are consistent with olivine-orthopyroxenitic diogenites, while (2497) and (5676)'s compositions are consistent with harzburgitic diogenites. The Band I and Band II absorption feature depths are much shallower than seen in diogenite spectra, typically ∼70% depth (Burbine, T.H. et al. [2000]. Forging asteroid-meteorite relationships through reflectance spectroscopy. Lunar Planet. Sci. XXXI. Abstract 1844). The nature of the weak features seen in the asteroid spectra when compared to measured band depths of in situ diogenite samples indicate an additional mechanism(s) acting to weaken the features, most likely space weathering. The aforementioned five asteroids are plausible sources for the olivine-orthopyroxenitic diogenites and harzburgitic diogenites, and very well may be fragments of Vesta. Asteroid (46) Hestia is an interesting object whose surface minerals may be consistent with a CR2 chondrite; however, the unique spectrum deserves further study in the future. Featureless Asteroids (248) Lameia, (1960) Guisan, (3345) Tarkovskij and (6212) 1993 MS1 surface materials are likely organic assemblages consistent with the Type 1 or 2 carbonaceous chondrite meteorite class; however specific terrestrial meteorite analog could not be identified. The spectra of Asteroids (3228) Pire and (3999) Aristarchus are consistent with each other and have been assigned to the Eulalia by Walsh et al. (Walsh, K.J. et al. [2013]. Icarus 225, 283-297). Spectrally they are similar to (495) in terms of blue-slope and albedo (Fieber-Beyer, S.K., et al. [2012]. Icarus 221, 593-602), thus increasing our confidence the three bodies are truly related dynamically and genetically. By extrapolation and due to their location adjacent to the 3:1 Kirkwood Gap, (3228) and (3999) are plausible sources of the CV3OXB carbonaceous chondrites.

The Abundance and Isotopic Composition of Hg in Extraterrestrial Materials

NASA Technical Reports Server (NTRS)

Blum, J. D.; Klaue, Bjorn

2005-01-01

During the three year grant period we made excellent progress in our study of the abundances and isotopic compositions of Hg and other volatile trace elements in extraterrestrial materials. At the time the grant started, our collaborating PI, Dante Lauretts, was a postdoctoral research associate working with Peter Buseck at Arizona State University. The work on chondritic Hg was done in collaboration with Dante Lauretta and Peter Buseck and this study was published in Lauretta et a1 (2001a). In July, 2001 Dante Lauretta accepted a position as an Assistant Professor in the Lunar and Planetary Laboratory at the University of Arizona. His funding was transferred and this grant has supported much of his research activities during his first two years at the U of A. Several other papers are in preparation and will be published soon. We presented papers on this topic at Goldschmidt Conferences, the Lunar and Planetary Science Conferences, and the Annual Meetings of the Meteoritical Society. The work done under this grant has spurred several new directions of inquiry, which we are still pursuing. Included in this paper are the studies of bulk abundances and isotopic compositions of metreoritic Mercury, and the development of a thermal analysis ICP-MS technique applied to thermally liable elements.

The moon: Composition determined by nebular processes

USGS Publications Warehouse

Morgan, J.W.; Hertogen, J.; Anders, E.

1978-01-01

The bulk composition of the Moon was determined by the conditions in the solar nebula during its formation, and may be quantitatively estimated from the premise that the terrestrial planets were formed by cosmochemical processes similar to those recorded in the chondrites. The calculations are based on the Ganapathy-Anders 7-component model using trace element indicators, but incorportate improved geophysical data and petrological constraints. A model Moon with 40 ppb U, a core 2% by weight (1.8% metal with ???35% Ni and 0.2% FeS) and Mg/(Fe2++Mg)?????0.75 meets the trace element restrictions, and has acceptable density, heat flow and moment of inertia ratio. The high Ni content of the core permits low-Ti mare basalts to equilibrate with metal, yet still retain substantial Ni. The silicate resembles the Taylor-Jakes?? composition (and in some respects the waif Ganapathy-Anders Model 2a), but has lower SiO2. Minor modifications of the model composition (U=30-35 ppb) yield a 50% melt approximating Apollo 15 green glass and a residuum of olivine plus 3 to 4% spinel; the low SiO2, favors spinel formation, and, contrary to expectation, Cr is not depleted in the liquid. There may no longer be any inconsistency between the cosmochemical approach and arguments based on experimental petrology. ?? 1978 D. Reidel Publishing Company.

Heterogeneities in the solar nebula

NASA Technical Reports Server (NTRS)

Clayton, R. N.; Grossman, L.; Mayeda, T. K.; Onuma, N.

1977-01-01

Oxygen isotopic compositions of the high-temperature phases in carbonaceous chondrites define a mixing line with an 0-16-rich component and show little superimposed chemical isotope fractionation. Within a single inclusion in Allende, variations of delta 0-18 and delta 0-17 of 39 thousands are found. The ordinary chondrites are slightly displaced from the terrestrial fractionation trend, implying that at least 0.2 percent of the oxygen in terrestrial rocks was derived from the 0-16-rich component.

Ion Microprobe Measurements of Comet Dust and Implications for Models of Oxygen Isotope Heterogeneity in the Solar System

NASA Technical Reports Server (NTRS)

Snead, C. J.; McKeegan, K. D.; Keller, L. P.; Messenger, S.

2017-01-01

The oxygen isotopic compositions of anhydrous minerals in carbonaceous chondrites reflect mixing between a O-16-rich and O-17, O18-rich reservoir. The UV photodissociation of CO (i.e. selfshielding) has been proposed as a mass-independent mechanism for producing these isotopically distinct reservoirs. Self-shielding models predict the composition for the CO gas reservoir to be O-16-rich, and that the accreting primordial dust was in isotopic equilibrium with the gaseous reservoir [1, 2]. Self-shielding also predicts that cometary water, presumed to represent the O-17, O-18-rich reservoir, should be enriched in O-17 and O-18, with compositions of 200 -1000per mille, and that the interaction with this O-17, O-18-rich H2O reservoir altered the compositions of the primordial dust toward planetary values. The bulk composition of the solar nebula, which may be an approximation to the 16O-rich gaseous reservoir, has been constrained by the Genesis results [3]. However, material representing the O-17, O-18-rich end-member is rare [4], and dust representing the original accreting primordial dust has been challenging to conclusively identify in current collections. Anhydrous dust from comets, which accreted in the distal cold regions of the nebula at temperatures below approximately 30K, may provide the best opportunity to measure the oxygen isotope composition of primordial dust. Chondritic porous interplanetary dust particles (CP-IDPs) have been suggested as having cometary origins [5]; however, until direct comparisons with dust from a known comet parent body were made, link between CP-IDPs and comets remained circumstantial. Oxygen isotope analyses of particles from comet 81P/Wild 2 collected by NASA's Stardust mission have revealed surprising similarities to minerals in carbonaceous chondrites which have been interpreted as evidence for large scale radial migration of dust components from the inner solar nebula to the accretion regions of Jupiter- family comets [6]. These studies have been largely focused on the coarse-grained terminal particles extracted from aerogel collectors; hypervelocity capture into aerogel resulted in fine-grained material that was melted and intimately mixed with the SiO2 capture medium. Hypervelocity impacts into Al foils surrounding the aerogel tiles produced impact craters that captured material from the impactor without significant oxygen contamination, allowing for analysis of both the coarse and fine-grained components of the Wild 2 dust. To date, no particles with definitive hydrated mineralogy have been observed in Stardust samples, though this may be a result of alteration due to hypervelocity capture. High-carbon hydrated CS-IDPs have been suggested as resulting from the aqueous alteration of CP-IDPs [7], and may retain evidence for interaction with O-17, O-18-enriched "cometary" water predicted by CO self-shielding. Here we present results of oxygen isotope measurements of twelve Stardust foil craters and four C-rich hydrated IDPs [8, 9], and discuss implications for models of oxygen isotope heterogeneity in the early solar system.

Antarctic and non-Antarctic meteorites form different populations

NASA Technical Reports Server (NTRS)

Dennison, J. E.; Lingner, D. W.; Lipschutz, M. E.

1986-01-01

The trace element differences between Victoria Land H5 chondrites and non-Antarctic H5 chondrites are studied. The focus on common meteorites was stimulated by Antarctic and non-Antarctic differences in meteorite types and in the trace element contents of congeners of rare type. Thirteen elements were analyzed by neutron activation analysis with radiochemical separation, and eight differed significantly. Eliminating test biasing and the possibility of compositional difference due to Antarctic weathering of the 300,000 year-old (on the average) Victoria Land falls, it is concluded that the two sets of chondrites differ due to extraterrestrial causes. The three possibilities discussed, differences in sample population, physical properties, orbital characteristics, and meteoroid flux with time, are all seen as problematic.

Gallium-bearing sphalerite in a metal-sulfide nodule of the Qingzhen (EH3) chondrite

NASA Technical Reports Server (NTRS)

Rambaldi, E. R.; Rajan, R. S.; Housley, R. M.; Wang, D.

1986-01-01

The composition and possible history of the Qingshen (EH3) chondrite is presented. The chondrite contains a population of spheroidal metal-sulfide nodules, which display textural evidence of reheating and melting. Evidence of metal sulfuration is also present, suggesting replacement of metal by sulfide during melting. This process has led to the nucleation of perryite along metal-sulfide interfaces. The Ga-bearing sphalerite that was found may have formed by injection of molten sulfide droplets into the metal followed by subsolidus diffusion of Ga from the metal into the sulfide. The latter may occur because of Ga supersaturation in the metal during progressive sulfuration and its decreased affinity for the metal phase during cooling below the taenite-kamacite transition point.

Compositions and microstructures of CB sulfides: Implications for the thermal history of the CB chondrite parent body

NASA Astrophysics Data System (ADS)

Srinivasan, Poorna; Jones, Rhian H.; Brearley, Adrian J.

2017-10-01

We studied textures and compositions of sulfide inclusions in unzoned Fe,Ni metal particles within CBa Gujba, CBa Weatherford, CBb HH 237, and CBb QUE 94411 in order to constrain formation conditions and secondary thermal histories on the CB parent body. Unzoned metal particles in all four chondrites have very similar metal and sulfide compositions. Metal particles contain different types of sulfides, which we categorize as: homogeneous low-Cr sulfides composed of troilite, troilite-containing exsolved daubreelite lamellae, arcuate sulfides that occur along metal grain boundaries, and shock-melted sulfides composed of a mixture of troilite and Fe, Ni metal. Our model for formation proposes that the unzoned metal particles were initially metal droplets that formed from splashing by a partially molten impacting body. Sulfide inclusions later formed as a result of precipitation of excess S from solid metal at low temperatures, either during single stage cooling or during a reheating event by impacts. Sulfides containing exsolution lamellae record temperatures of ≪600 °C, and irregular Fe-FeS intergrowth textures suggest localized shock melting, both of which are indicative of heterogeneous heating by impact processes on the CB parent body. Our study shows that CBa and CBb chondrites formed in a similar environment, and also experienced similar secondary impact processing.

A Russian record of a Middle Ordovician meteorite shower: Extraterrestrial chromite at Lynna River, St. Petersburg region

NASA Astrophysics Data System (ADS)

Lindskog, Anders; Schmitz, Birger; Cronholm, Anders; Dronov, Andrei

2012-08-01

Numerous fossil meteorites and high concentrations of sediment-dispersed extraterrestrial chromite (EC) grains with ordinary chondritic composition have previously been documented from 467 ± 1.6 Ma Middle Ordovician (Darriwilian) strata. These finds probably reflect a temporarily enhanced influx of L-chondritic matter, following the disruption of the L-chondrite parent body in the asteroid belt 470 ± 6 Ma. In this study, a Volkhovian-Kundan limestone/marl succession at Lynna River, northwestern Russia, has been searched for EC grains (>63 μm). Eight samples, forming two separate sample sets, were collected. Five samples from strata around the Asaphus expansus-A. raniceps trilobite Zone boundary, in the lower-middle Kundan, yielded a total of 496 EC grains in 65.5 kg of rock (average 7.6 EC grains kg-1, but up to 10.2 grains kg-1). These are extremely high concentrations, three orders of magnitude higher than "background" levels in similar condensed sediment from other periods. EC grains are typically about 50 times more abundant than terrestrial chrome spinel in the samples and about as common as terrestrial ilmenite. Three stratigraphically lower lying samples, close to the A. lepidurus-A. expansus trilobite Zone boundary, at the Volkhov-Kunda boundary, yielded only two EC grains in 38.2 kg of rock (0.05 grains kg-1). The lack of commonly occurring EC grains in the lower interval probably reflects that these strata formed before the disruption of the L-chondrite parent body. The great similarity in EC chemical composition between this and other comparable studies indicates that all or most EC grains in these Russian mid-Ordovician strata share a common source--the L-chondrite parent body.

Ruthenium isotopic evidence for an inner Solar System origin of the late veneer

NASA Astrophysics Data System (ADS)

Fischer-Gödde, Mario; Kleine, Thorsten

2017-01-01

The excess of highly siderophile elements in the Earth’s mantle is thought to reflect the addition of primitive meteoritic material after core formation ceased. This ‘late veneer’ either comprises material remaining in the terrestrial planet region after the main stages of the Earth’s accretion, or derives from more distant asteroidal or cometary sources. Distinguishing between these disparate origins is important because a late veneer consisting of carbonaceous chondrite-like asteroids or comets could be the principal source of the Earth’s volatiles and water. Until now, however, a ‘genetic’ link between the late veneer and such volatile-rich materials has not been established or ruled out. Such genetic links can be determined using ruthenium (Ru) isotopes, because the Ru in the Earth’s mantle predominantly derives from the late veneer, and because meteorites exhibit Ru isotope variations arising from the heterogeneous distribution of stellar-derived dust. Although Ru isotopic data and the correlation of Ru and molybdenum (Mo) isotope anomalies in meteorites were previously used to argue that the late veneer derives from the same type of inner Solar System material as do Earth’s main building blocks, the Ru isotopic composition of carbonaceous chondrites has not been determined sufficiently well to rule them out as a source of the late veneer. Here we show that all chondrites, including carbonaceous chondrites, have Ru isotopic compositions distinct from that of the Earth’s mantle. The Ru isotope anomalies increase from enstatite to ordinary to carbonaceous chondrites, demonstrating that material formed at greater heliocentric distance contains larger Ru isotope anomalies. Therefore, these data refute an outer Solar System origin for the late veneer and imply that the late veneer was not the primary source of volatiles and water on the Earth.

The distribution of evaporitic weathering products on Antarctic meteorites

NASA Technical Reports Server (NTRS)

Velbel, Michael A.

1987-01-01

White evaporite deposits of terrestrial origin occur on some 5 percent of Antarctic meteorites. The few previous studies, and new mineralogical analyses, indicate that the deposits are predominately carbonates and/or sulfates of magnesium. The distribution of white evaporitic salt deposits differs among different meteorite compositional groups and weathering categories. Salts occur with unusual frequency on carbonaceous chondrites, and are especially common in carbonaceous chondrites of weathering categories A and B. Among achondrites, weathering categories A and A/B show the most examples of salt weathering. Unlike carbonaceous chondrites and achrondites, most salt-bearing ordinary (H and L) chondrites are from rustier meteorites of weathering categories B, and to a lesser degree, B/C and C. The LL chondrites are conspicuous by their complete lack or any salt-weathering product. Almost two-thirds of all evaporite-bearing meteorites belong to weathering categories, A, A/B, and B. Where chemical and/or mineralogical data are available, there is a persistent suggestion that evaporite formation is accompanied by elemental redistribution from meteorite interiors. Meteorites of weathering categories B, A/B, and even A may have experienced significant element redistribution and/or contamination as a result of terrestrial exposure.

Early Solar System Alkali Fractionation Events Recorded by K-Ca Isotopes in the Yamato-74442 LL-Chondritic Breccia

NASA Technical Reports Server (NTRS)

Tatsunori, T.; Misawa, K.; Okano, O.; Shih, C.-Y.; Nyquist, L. E.; Simon, J. I.; Tappa, M. J.; Yoneda, S.

2015-01-01

Radiogenic ingrowth of Ca-40 due to decay of K-40 occurred early in the solar system history causing the Ca-40 abundance to vary within different early-former reservoirs. Marshall and DePaolo ] demonstrated that the K-40/Ca-40 decay system could be a useful radiogenic tracer for studies of terrestrial rocks. Shih et al. [3,4] determined 40K/40Ca ages of lunar granitic rock fragments and discussed the chemical characteristics of their source materials. Recently, Yokoyama et al. [5] showed the application of the K-40/Ca-40 chronometer for high K/Ca materials in ordinary chondrites (OCs). High-precision calcium isotopic data are needed to constrain mixing processes among early solar system materials and the time of planetesimal formation. To better constrain the solar system calcium isotopic compositions among astromaterials, we have determined the calcium isotopic compositions of OCs and an angrite. We further estimated a source K/Ca ratio for alkali-rich fragments in a chondritic breccia using the estimated solar system initial Ca-40/Ca-44.

Compositional Homogeneity of CM Parent Bodies

NASA Astrophysics Data System (ADS)

Vernazza, P.; Marsset, M.; Beck, P.; Binzel, R. P.; Birlan, M.; Cloutis, E. A.; DeMeo, F. E.; Dumas, C.; Hiroi, T.

2016-09-01

CM chondrites are the most common type of hydrated meteorites, making up ˜1.5% of all falls. Whereas most CM chondrites experienced only low-temperature (˜0°C-120°C) aqueous alteration, the existence of a small fraction of CM chondrites that suffered both hydration and heating complicates our understanding of the early thermal evolution of the CM parent body(ies). Here, we provide new constraints on the collisional and thermal history of CM-like bodies from a comparison between newly acquired spectral measurements of main-belt Ch/Cgh-type asteroids (70 objects) and existing laboratory spectral measurements of CM chondrites. It first appears that the spectral variation observed among CM-like bodies is essentially due to variations in the average regolith grain size. Second, the spectral properties of the vast majority (unheated) of CM chondrites resemble both the surfaces and the interiors of CM-like bodies, implying a “low” temperature (<300°C) thermal evolution of the CM parent body(ies). It follows that an impact origin is the likely explanation for the existence of heated CM chondrites. Finally, similarly to S-type asteroids and (2) Pallas, the surfaces of large (D > 100 km)—supposedly primordial—Ch/Cgh-type main-belt asteroids likely expose the interiors of the primordial CM parent bodies, a possible consequence of impacts by small asteroids (D < 10 km) in the early solar system.

Non-destructive elemental analysis of a carbonaceous chondrite with direct current Muon beam at MuSIC.

PubMed

Terada, K; Sato, A; Ninomiya, K; Kawashima, Y; Shimomura, K; Yoshida, G; Kawai, Y; Osawa, T; Tachibana, S

2017-11-13

Electron- or X-ray-induced characteristic X-ray analysis has been widely used to determine chemical compositions of materials in vast research fields. In recent years, analysis of characteristic X-rays from muonic atoms, in which a muon is captured, has attracted attention because both a muon beam and a muon-induced characteristic X-ray have high transmission abilities. Here we report the first non-destructive elemental analysis of a carbonaceous chondrite using one of the world-leading intense direct current muon beam source (MuSIC; MUon Science Innovative Channel). We successfully detected characteristic muonic X-rays of Mg, Si, Fe, O, S and C from Jbilet Winselwan CM chondrite, of which carbon content is about 2 wt%, and the obtained elemental abundance pattern was consistent with that of CM chondrites. Because of its high sensitivity to carbon, non-destructive elemental analysis with a muon beam can be a novel powerful tool to characterize future retuned samples from carbonaceous asteroids.

Using the Fe/Mn Ratio of FeO-Rich Olivine In WILD 2, Chondrite Matrix, and Type IIA Chondrules to Disentangle Their Histories

NASA Technical Reports Server (NTRS)

Frank, David R.; Le, L.; Zolensky, M. E.

2012-01-01

The Stardust Mission returned a large abundance of impactors from Comet 81P/Wild2 in the 5-30 m range. The preliminary examination of just a limited number of these particles showed that the collection captured abundant crystalline grains with a diverse mineralogy [1,2]. Many of these grains resemble those found in chondrite matrix and even contain fragments of chondrules and CAIs [1-3]. In particular, the olivine found in Wild 2 exhibits a wide compositional range (Fa0-97) with minor element abundances similar to the matrix olivine found in many carbonaceous chondrites (CCs) and unequilibrated ordinary chondrites (UOCs). Despite the wide distribution of Fa content, the olivine found in the matrices of CCs, UOCs, and Wild 2 can be roughly lumped into two types based solely on fayalite content. In fact, in some cases, a distinct bi-modal distribution is observed.

Extraterrestrial amino acids in Orgueil and Ivuna: Tracing the parent body of CI type carbonaceous chondrites

PubMed Central

Ehrenfreund, Pascale; Glavin, Daniel P.; Botta, Oliver; Cooper, George; Bada, Jeffrey L.

2001-01-01

Amino acid analyses using HPLC of pristine interior pieces of the CI carbonaceous chondrites Orgueil and Ivuna have found that β-alanine, glycine, and γ-amino-n-butyric acid (ABA) are the most abundant amino acids in these two meteorites, with concentrations ranging from ≈600 to 2,000 parts per billion (ppb). Other α-amino acids such as alanine, α-ABA, α-aminoisobutyric acid (AIB), and isovaline are present only in trace amounts (<200 ppb). Carbon isotopic measurements of β-alanine and glycine and the presence of racemic (D/L ≈ 1) alanine and β-ABA in Orgueil suggest that these amino acids are extraterrestrial in origin. In comparison to the CM carbonaceous chondrites Murchison and Murray, the amino acid composition of the CIs is strikingly distinct, suggesting that these meteorites came from a different type of parent body, possibly an extinct comet, than did the CM carbonaceous chondrites. PMID:11226205

Watson: A new link in the IIE iron chain

NASA Technical Reports Server (NTRS)

Olsen, Edward; Davis, Andrew; Clarke, Roy S., Jr.; Schultz, Ludolf; Weber, Hartwig W.; Clayton, Robert; Mayeda, Toshiko; Jarosewich, Eugene; Sylvester, Paul; Grossman, Lawrence

1994-01-01

Watson, which was found in 1972 in South Australia, contains the largest single silicate rock mass seen in any known iron meteorite. A comprehensive study has been completed on this unusual meteorite: petrography, metallography, analyses of the silicate inclusion (whole rock chemical analysis, INAA, RNAA, noble gases, and oxygen isotope analysis) and mineral compositions (by electron microprobe and ion microprobe). The whole rock has a composition of an H-chondrite minus the normal H-group metal and troilite content. The oxygen isotope composition is that of the silicates in the IIE iron meteorites and lies along an oxygen isotope fractionation line with the H-group chondrites. Trace elements in the metal confirm Watson is a new IIE iron. Whole rock Watson silicate shows an enrichment in K and P (each approximately 2X H-chondrites). The silicate inclusion has a highly equilibrated igneous (peridotite-like) texture with olivine largely poikilitic within low-Ca pyroxene: olivine (Fa20), opx (Fs17Wo3), capx (Fs9Wo14)(with very fine exsolution lamellae), antiperthite feldspar (An1-3Or5) with less than 1 micron exsolution lamellae (An1-3Or greater than 40), shocked feldspar with altered stoichiometry, minor whitlockite (also a poorly characterized interstitial phosphate-rich phase) and chromite, and only traces of metal and troilite. The individual silicate minerals have normal chondritic REE patterns, but whitlockite has a remarkable REE pattern. It is very enriched in light REE (La is 720X C1, and Lu is 90X C1, as opposed to usual chonditic values of approximately 300X and 100-150X, respectively) with a negative Eu anomaly. The enrichment of whole rock K is expressed both in an unusually high mean modal Or content of the feldspar, Or13, and in the presence of antiperthite.

Origin of mantle peridotite: Constraints from melting experiments to 16.5 GPa

NASA Astrophysics Data System (ADS)

Herzberg, Claude; Gasparik, Tibor; Sawamoto, Hiroshi

1990-09-01

Experimental data are reported for the melting of komatiite, peridotite, and chondrite compositions in the pressure range 5-16.5 GPa. All experiments were run using the multiple-anvil apparatus facilities at Nagoya and Stony Brook. Equilibrium between coexisting crystals and liquid is demonstrated to occur in less than 3 min in the 2100°C range. The anhydrous solidus in CaO-MgO-Al2O3-SiO2 has been calibrated and is shown to be about 100° higher than that for naturally occurring peridotite (KLB1). All melting curves have positive dT/dP. The effect of pressure is to expand the crystallization field of garnet at the expense of all other phases, resulting in a change in the liquidus phase from olivine to garnet at high pressures. The melting of rocks which contain the four crystalline phases olivine, orthopyroxene, clinopyroxene, and garnet is restricted to enstatite-rich compositions such as chondrite. For these it is demonstrated that melting is peritectic, rather than eutectic, and takes the form L+Opx = Ol+Cpx+Gt. Partial melting yields liquids with the following properties: 5 GPa for komatiite; and 10-15 GPa for liquid peridotite with about 40% MgO, but one that is unlike mantle peridotite in that it is distinctly enriched in silica. These results provide a test and refutation of the model that upper mantle peridotite originated by direct initial melting of a chondritic mantle (Herzberg and O'Hara, 1985). Unlike chondrite, partial melting of peridotite does not usually involve orthopyroxene. Instead, it occurs by the generation of ultrabasic liquids along a cotectic involving L+Ol+Cpx+Gt. Although the thermal and compositional characteristics of this cotectic have not been fully calibrated, it is very likely that it will degenerate into a thermal minimum (L+Ol+Cpx+Gt), compositionally similar to komatiite at 5 GPa and mantle peridotite at 10-15 GPa. Peridotite liquids that occupy a thermal minimum can be derived from those formed from the melting of chondrite by removal of orthopyroxene, followed by fractional crystallization of olivine, clinopyroxene, and garnet. The possibility exists that the thermal minimum is compositionally identical to mantle peridotite in the 10-15 GPa range. If this can be confirmed by experiment, the upper mantle can be understood as having originated by the fractional crystallization of peridotite liquids in a large-scale differentiation event, consistent with magma ocean models for an early Earth.

Variation of mineralogy and organic material during the early stages of aqueous activity recorded in Antarctic micrometeorites

NASA Astrophysics Data System (ADS)

Noguchi, T.; Yabuta, H.; Itoh, S.; Sakamoto, N.; Mitsunari, T.; Okubo, A.; Okazaki, R.; Nakamura, T.; Tachibana, S.; Terada, K.; Ebihara, M.; Imae, N.; Kimura, M.; Nagahara, H.

2017-07-01

Micrometeorites (MMs) recovered from surface snow near the Dome Fuji Station, Antarctica are almost free from terrestrial weathering and contain very primitive materials, and are suitable for investigation of the evolution and interaction of inorganic and organic materials in the early solar system. We carried out a comprehensive study on seven porous and fluffy MMs [four Chondritic porous (CP) MMs and three fluffy fine-grained (Fluffy Fg) MMs] and one fine-grained type 1 (Fg C1) MM for comparison with scanning electron microscope, transmission electron microscope, X-ray absorption near-edge structure analysis, and secondary ion mass spectrometer. They show a variety of early aqueous activities. Four out of the seven CP MMs contain glass with embedded metal and sulfide (GEMS) and enstatite whiskers/platelets and do not have hydrated minerals. Despite the same mineralogy, organic chemistry of the CP MMs shows diversity. Two of them contain considerable amounts of organic materials with high carboxyl functionality, and one of them contains nitrile (Ctbnd N) and/or nitrogen heterocyclic groups with D and 15N enrichments, suggesting formation in the molecular cloud or a very low temperature region of the outer solar system. Another two CP MMs are poorer in organic materials than the above-mentioned MMs. Organic material in one of them is richer in aromatic C than the CP MMs mentioned above, being indistinguishable from those of hydrated carbonaceous chondrites. In addition, bulk chemical compositions of GEMS in the latter organic poor CP MMs are more homogeneous and have higher Fe/(Si + Mg + Fe) ratios than those of GEMS in the former organic-rich CP MMs. Functional group of the organic materials and amorphous silicate in GEMS in the organic-poor CP MMs may have transformed in the earliest stage of aqueous alteration, which did not form hydrated minerals. Three Fluffy Fg MMs contain abundant phyllosilicates, showing a clear evidence of aqueous alteration. Phyllosilicates in thee MMs are richer in Fe than those in hydrated IDPs, typical fine-grained hydrated (Fg C1) MMs, and hydrated carbonaceous chondrites. One of the Fluffy Fg MMs contains amorphous silicate, which is richer in Fe than GEMS and contains little or no nanophase Fe metal but contains Fe sulfide. Because the chemical compositions of the amorphous silicate are within the compositional field of GEMS in CP IDPs, the amorphous silicate may be alteration products of GEMS. The entire compositional field of GEMS in the CP MMs and the amorphous silicate in the Fluffy Fg MM matches that of the previously reported total compositional range of GEMS in IDPs. One Fluffy Fg MM contains Mg-rich phyllosilicate along with Fe-rich phyllosilicate and Mg-Fe carbonate. Mg-rich phyllosilicate and Mg-Fe carbonate may have been formed through the reaction of Fe-rich phyllosilicate, Mg-rich olivine and pyroxene, and water with C-bearing chemical species. These data indicate that CP MMs and Fluffy Fg MMs recovered from Antarctic surface snow contain materials that throw a light on the earliest stages of aqueous alteration on very primitive solar system bodies. Because mineralogy and isotopic and structural features of organic materials in D10IB009 are comparable with isotopically primitive IDPs, its parent body could be comets or icy asteroids showing mass ejection (active asteroids). By contrast, organic-poor CP MMs may have experienced the earliest stage of aqueous alteration and Fluffy Fg MMs experienced weak aqueous alteration. The precursor materials of the parent bodies of Fluffy Fg MMs probably contained abundant GEMS or GEMS-like materials like CP IDPs, which is common to fine-grained matrices of very primitive carbonaceous chondrites such as CR3s. However, highly porous nature of organic-poor CP MMs and Fluffy Fg MMs suggests that parent bodies of these MMs must have been much more porous than the parent bodies of primitive carbonaceous chondrites. Given no phyllosilicate among the returned samples of 81P/Wild 2 comet, the MMs may have been derived from porous icy asteroids such as active asteroids as well as P- and D-type asteroids rather than comets.

Post-metamorphic brecciation in type 3 ordinary chondrites

NASA Technical Reports Server (NTRS)

Scott, E. R. D.; Mccoy, T. J.; Keil, K.

1993-01-01

Type 3.1-3.9 ordinary chondrites can be divided into two kinds: those in which the compositions of chondrule silicates are entirely consistent with metamorphism of type 3.0 material, and those in which the computational heterogeneity appears to be too extreme for in situ metamorphism. We present petrologic data for three LL3 chondrites of the second kind--Ngawi, ALH A77278 (both type 3.6), and Hamlet (type 3.9)--and compare these data with results for the first kind of LL3-4 chondrites. Given that chondrules form in the nebula and that metamorphic equilibration occurs in asteroids, our new data imply that Ngawi, A77278, Hamlet, and many other type 3 ordinary chondrites are post-metamorphic breccias containing materials with diverse metamorphic histories; they are not metamorphic rocks or special kinds of 'primitive breccias.' We infer also that metamorphism to type 3.1-3.9 levels produces very friable material that is easily remixed into breccias and lithified by mild shock. Thus, petrologic types and subtypes of chondrites indicate the mean metamorphic history of the ingredients, not the thermal history of the rock. The metamorphic history of individual type 1 or 2 porphyritic chondrules in type 3 breccias is best derived from olivine and pyroxene analyses and the data of McCoy et al. for unbrecciated chondrites. The new chondrule classification schemes of Sears, DeHart et al., appears to provide less information about the original state and metamorphic history of individual porphyritic chondrules and should not replace existing classification schemes.

Post-metamorphic brecciation in type 3 ordinary chondrites

NASA Astrophysics Data System (ADS)

Scott, E. R. D.; McCoy, T. J.; Keil, K.

1993-03-01

Type 3.1-3.9 ordinary chondrites can be divided into two kinds: those in which the compositions of chondrule silicates are entirely consistent with metamorphism of type 3.0 material, and those in which the computational heterogeneity appears to be too extreme for in situ metamorphism. We present petrologic data for three LL3 chondrites of the second kind--Ngawi, ALH A77278 (both type 3.6), and Hamlet (type 3.9)--and compare these data with results for the first kind of LL3-4 chondrites. Given that chondrules form in the nebula and that metamorphic equilibration occurs in asteroids, our new data imply that Ngawi, A77278, Hamlet, and many other type 3 ordinary chondrites are post-metamorphic breccias containing materials with diverse metamorphic histories; they are not metamorphic rocks or special kinds of 'primitive breccias.' We infer also that metamorphism to type 3.1-3.9 levels produces very friable material that is easily remixed into breccias and lithified by mild shock. Thus, petrologic types and subtypes of chondrites indicate the mean metamorphic history of the ingredients, not the thermal history of the rock. The metamorphic history of individual type 1 or 2 porphyritic chondrules in type 3 breccias is best derived from olivine and pyroxene analyses and the data of McCoy et al. for unbrecciated chondrites. The new chondrule classification schemes of Sears, DeHart et al., appears to provide less information about the original state and metamorphic history of individual porphyritic chondrules and should not replace existing classification schemes.

Hungaria asteroid region telescopic spectral survey (HARTSS) I: Stony asteroids abundant in the Hungaria background population

NASA Astrophysics Data System (ADS)

Lucas, Michael P.; Emery, Joshua P.; Pinilla-Alonso, Noemi; Lindsay, Sean S.; Lorenzi, Vania

2017-07-01

The Hungaria asteroids remain as survivors of late giant planet migration that destabilized a now extinct inner portion of the primordial asteroid belt and left in its wake the current resonance structure of the Main Belt. In this scenario, the Hungaria region represents a ;purgatory; for the closest, preserved samples of the asteroidal material from which the terrestrial planets accreted. Deciphering the surface composition of these unique samples may provide constraints on the nature of the primordial building blocks of the terrestrial planets. We have undertaken an observational campaign entitled the Hungaria Asteroid Region Telescopic Spectral Survey (HARTSS) to record near-infrared (NIR) reflectance spectra in order to characterize their taxonomy, surface mineralogy, and potential meteorite analogs. The overall objective of HARTSS is to evaluate the compositional diversity of asteroids located throughout the Hungaria region. This region harbors a collisional family of Xe-type asteroids, which are situated among a background (i.e., non-family) of predominantly S-complex asteroids. In order to assess the compositional diversity of the Hungaria region, we have targeted background objects during Phase I of HARTSS. Collisional family members likely reflect the composition of one original homogeneous parent body, so we have largely avoided them in this phase. We have employed NIR instruments at two ground-based telescope facilities: the NASA Infrared Telescope Facility (IRTF), and the Telescopio Nazionale Galileo (TNG). Our data set includes the NIR spectra of 42 Hungaria asteroids (36 background; 6 family). We find that stony S-complex asteroids dominate the Hungaria background population (29/36 objects; ∼80%). C-complex asteroids are uncommon (2/42; ∼5%) within the Hungaria region. Background S-complex objects exhibit considerable spectral diversity as band parameter measurements of diagnostic absorption features near 1- and 2-μm indicate that several different S-subtypes are represented therein, which translates to a variety of surface compositions. We identify the Gaffey S-subtype (Gaffey et al. [1993]. Icarus 106, 573-602) and potential meteorite analogs for 24 of these S-complex background asteroids. Additionally, we estimate the olivine and orthopyroxene mineralogy for 18 of these objects using spectral band parameter analysis established from laboratory-based studies of ordinary chondrite meteorites. Nine of the asteroids have band parameters that are not consistent with ordinary chondrites. We compared these to the band parameters measured from laboratory VIS+NIR spectra of six primitive achondrite (acapulcoite-lodranite) meteorites. These comparisons suggest that two main meteorite groups are represented among the Hungaria background asteroids: unmelted, nebular L- (and possibly LL-ordinary chondrites), and partially-melted primitive achondrites of the acapulcoite-lodranite meteorite clan. Our results suggest a source region for L chondrite like material from within the Hungarias, with delivery to Earth via leakage from the inner boundary of the Hungaria region. H chondrite like mineralogies appear to be absent from the Hungaria background asteroids. We therefore conclude that the Hungaria region is not a source for H chondrite meteorites. Seven Hungaria background asteroids have spectral band parameters consistent with partially-melted primitive achondrites, but the probable source region of the acapulcoite-lodranite parent body remains inconclusive. If the proposed connection with the Hungaria family to fully-melted enstatite achondrite meteorites (i.e., aubrites) is accurate (Gaffey et al. [1992]. Icarus 100, 95-109; Kelley and Gaffey [2002]. Meteorit. Planet. Sci. 37, 1815-1827), then asteroids in the Hungaria region exhibit a full range of petrologic evolution: from nebular, unmelted ordinary chondrites, through partially-melted primitive achondrites, to fully-melted igneous aubrite meteorites.

Accretion and Preservation of Organic Matter in Carbonaceous Chondrites as Revealed by NanoSIMS Imaging.

NASA Astrophysics Data System (ADS)

Remusat, L.; Guan, Y.; Eiler, J.

2008-12-01

Carbonaceous chondrites are the most primitive known meteorites. Their parent bodies accreted several discrete components of the early solar system: CAIs, other silicates, oxides, sulfides, ice, organics, and noble gases. Radioactive decay of short live radionucleides quickly heated these parent bodies and drove thermal metamorphism and aqueous alteration of their constituents. Despite this post-acretionary modification, at least some components of the organic matter in the carbaceous chondrites retained distinctive isotopic and molecular properties that may relate to their pre-acretionary origins in the protosolar nebula or in the molecular cloud that gave birth to it [1]. These processes that gave rise to early solar-system organic matter and the extent to which it was modified by parent body processes are still a matter of debate [2]. We have acquired NanoSIMS images of matrices of several CI, CM, CR and CV chondrites to document, in- situ, the distribution of organics and their textural and chemical relationships to co-existing inorganic components. Importantly, we performed these analyses on essentially unmodified fragments of matrix material pressed into indium, rather than on extracts, which have been the focus of most previous work on meteoritic organic matter. Specifically, we simultaneously collected H, D, 12C, 18O, 26CN, 28Si and 32S with a spatial resolution of 200 nm. Inorganic constituents of the imaged domains were determined by SEM imaging and EDS analysis. We identify two textural classes of organic constituents: diffuse organic matter and organic particles ~ 1 micron in diameter. The particles are common and do not exhibit any textural association with any inorganic matrix constituent. This distribution is consistent with previous observations by fluorescence optical microscopy [3]. These organic particles are likely primarily composed of insoluble organic matter (IOM) that grew prior to accretion as pure organic particules and was preserved in the matrix. In contrast to some observations of nm-scale HRTEM observations of chondritic matrices [4], organics do not seem to be associated with sulfides or sulfates. Instead, they are found intermixed with clay minerals within the matrix. We also found that a subset of organic particles in the matrices of CI, CM and CR chondrites are D rich (as previously reported by [5]). Profiles across these particles reveal that no significant isotopic exchange has occurred between these D-rich organic grains and the surrounding clays. This suggests that the isotopic composition of these grains remained unchanged during the parent body evolution, in contrast with conclusions from bulk measurements [2]. It has been previously suggested that relatively D-depleted water circulated through the parent bodies of the volatile-rich carbonaceous chondrites for 3 My. Known rates of water mobility through polymerized organic compounds and of D/H exchange between organic hydrogen and water lead one to predict that organic particles should have fully equilibrated with their surrounding phases in much less time than this. We speculate that this paradox might be evidence for exceptionally refractory character of H-C bonds in meteoritic IOM, or extreme D-exchange behavior of some organic moieties like radicals evidenced in IOM. [1] Pizzarello et al. (2006) in MESS II 625-651; [2] Alexander et al. (2007) GCA 71, 4380-4403 ; [3] Alpern and Benkheiri (1973) EPSL 19, 422-428; [4] Brearley and Abreu 32th LPSC; [5] Busemann et al (2006) Science 312, 727-730.

Metamorphism and partial melting of ordinary chondrites: Calculated phase equilibria

NASA Astrophysics Data System (ADS)

Johnson, T. E.; Benedix, G. K.; Bland, P. A.

2016-01-01

Constraining the metamorphic pressures (P) and temperatures (T) recorded by meteorites is key to understanding the size and thermal history of their asteroid parent bodies. New thermodynamic models calibrated to very low P for minerals and melt in terrestrial mantle peridotite permit quantitative investigation of high-T metamorphism in ordinary chondrites using phase equilibria modelling. Isochemical P-T phase diagrams based on the average composition of H, L and LL chondrite falls and contoured for the composition and abundance of olivine, ortho- and clinopyroxene, plagioclase and chromite provide a good match with values measured in so-called equilibrated (petrologic type 4-6) samples. Some compositional variables, in particular Al in orthopyroxene and Na in clinopyroxene, exhibit a strong pressure dependence when considered over a range of several kilobars, providing a means of recognising meteorites derived from the cores of asteroids with radii of several hundred kilometres, if such bodies existed at that time. At the low pressures (<1 kbar) that typify thermal metamorphism, several compositional variables are good thermometers. Although those based on Fe-Mg exchange are likely to have been reset during slow cooling, those based on coupled substitution, in particular Ca and Al in orthopyroxene and Na in clinopyroxene, are less susceptible to retrograde diffusion and are potentially more faithful recorders of peak conditions. The intersection of isopleths of these variables may allow pressures to be quantified, even at low P, permitting constraints on the minimum size of parent asteroid bodies. The phase diagrams predict the onset of partial melting at 1050-1100 °C by incongruent reactions consuming plagioclase, clinopyroxene and orthopyroxene, whose compositions change abruptly as melting proceeds. These predictions match natural observations well and support the view that type 7 chondrites represent a suprasolidus continuation of the established petrologic types at the extremes of thermal metamorphism. The results suggest phase equilibria modelling has potential as a powerful quantitative tool in investigating, for example, progressive oxidation during metamorphism, the degree of melting and melt loss or accumulation required to produce the spectrum of differentiated meteorites, and whether the onion shell or rubble pile model best explains the metamorphic evolution of asteroid parent bodies in the early solar system.

Geochemical arguments for an Earth-like Moon-forming impactor

PubMed Central

Dauphas, Nicolas; Burkhardt, Christoph; Warren, Paul H.; Fang-Zhen, Teng

2014-01-01

Geochemical evidence suggests that the material accreted by the Earth did not change in nature during Earth's accretion, presumably because the inner protoplanetary disc had uniform isotopic composition similar to enstatite chondrites, aubrites and ungrouped achondrite NWA 5363/5400. Enstatite meteorites and the Earth were derived from the same nebular reservoir but diverged in their chemical evolutions, so no chondrite sample in meteorite collections is representative of the Earth's building blocks. The similarity in isotopic composition (Δ17O, ε50Ti and ε54Cr) between lunar and terrestrial rocks is explained by the fact that the Moon-forming impactor came from the same region of the disc as other Earth-forming embryos, and therefore was similar in isotopic composition to the Earth. The heavy δ30Si values of the silicate Earth and the Moon relative to known chondrites may be due to fractionation in the solar nebula/protoplanetary disc rather than partitioning of silicon in Earth's core. An inversion method is presented to calculate the Hf/W ratios and ε182W values of the proto-Earth and impactor mantles for a given Moon-forming impact scenario. The similarity in tungsten isotopic composition between lunar and terrestrial rocks is a coincidence that can be explained in a canonical giant impact scenario if an early formed embryo (two-stage model age of 10–20 Myr) collided with the proto-Earth formed over a more protracted accretion history (two-stage model age of 30–40 Myr). PMID:25114316

Geological and geochemical record of 3400-million-year-old terrestrial meteorite impacts

NASA Technical Reports Server (NTRS)

Lowe, Donald R.; Byerly, Gary R.; Asaro, Frank; Kyte, Frank T.

1989-01-01

Beds of sand-sized spherules in the 3400-million-year-old Fig Tree Group, Barberton Greenstone belt, South Africa, formed by the fall of quenched liquid silicate droplets into a range of shallow- to deep-water depositional environments. The regional extent of the layers, their compositional complexity, and lack of included volcanic debris suggest that they are not products of volcanic activity. The layers are greatly enriched in iridium and other platinum group elements in roughly chondritic proportions. Geochemical modeling based on immobile element abundances suggests that the original average spherule composition can be approximated by a mixture of fractionated tholeiitic basalt, komatiite, and CI carbonaceous chondrite. The spherules are thought to be the products of large meteorite impacts on the Archean earth.

Chondrulelike objects in short-period comet 81P/Wild 2.

PubMed

Nakamura, Tomoki; Noguchi, Takaaki; Tsuchiyama, Akira; Ushikubo, Takayuki; Kita, Noriko T; Valley, John W; Zolensky, Michael E; Kakazu, Yuki; Sakamoto, Kanako; Mashio, Etsuko; Uesugi, Kentaro; Nakano, Tsukasa

2008-09-19

The Stardust spacecraft returned cometary samples that contain crystalline material, but the origin of the material is not yet well understood. We found four crystalline particles from comet 81P/Wild 2 that were apparently formed by flash-melting at a high temperature and are texturally, mineralogically, and compositionally similar to chondrules. Chondrules are submillimeter particles that dominate chondrites and are believed to have formed in the inner solar nebula. The comet particles show oxygen isotope compositions similar to chondrules in carbonaceous chondrites that compose the middle-to-outer asteroid belt. The presence of the chondrulelike objects in the comet suggests that chondrules have been transported out to the cold outer solar nebula and spread widely over the early solar system.

Early Archean Spherule Beds: Chromium Isotopes Confirm Origin Through Multiple Impacts of Projectiles of Carbonaceous Chondrite Type

NASA Technical Reports Server (NTRS)

Kyte, Frank T.; Shukolyukov, Alex; Lugmair, Guenter W.; Lowe, Donald R.; Byerly, Gary R.

2003-01-01

Three Early Archean spherule beds from Barberton, South Africa, have anomalous Cr isotope compositions in addition to large Ir anomalies, confirming the presence of meteoritic material with a composition similar to that in carbonaceous chondrites. The extra-terrestrial components in beds S2, S3, and S4 are estimated to be approx. l%, 50% - 60%, and 15% - 30%, respectively. These beds are probably the distal, and possibly global, ejecta from major large-body impacts. These impacts were probably much larger than the Cretaceous-Tertiary event, and all occurred over an interval of approx. 20 m.y., implying an impactor flux at 3.2 Ga that was more than an order of magnitude greater than the present flux.

Chemical characterization of seven Large Area Collector particles by SXRF. [cosmic dust composition

NASA Technical Reports Server (NTRS)

Flynn, G. J.; Sutton, S. R.

1991-01-01

Optical microscopy and synchrotron X-ray fluorescence (SXRF) are used to analyze the chemical composition of seven dark-appearing cosmic-dust particles obtained in the stratosphere during NASA Johnson Large Area Collector flights. The experimental setup and procedures are outlined, and the results are presented in extensive tables. Three of the particles had abundances similar to those of chondrites (except for low Ca values in one particle); two had a metallic appearance and spectra dominated by Fe and Zn; one contained Cu and Cr plus small amounts of Fe and Zn; and one had igneous-type abundances of minor and trace elements while containing all of the elements seen in chondritic particles, suggesting it may be of extraterrestrial origin.

A Case for Nebula Scale Mixing Between Non-Carbonaceous and Carbonaceous Chondrite Reservoirs: Testing the Grand Tack Model with Chromium Isotopic Composition of Almahata Sitta Stone 91A

NASA Technical Reports Server (NTRS)

Sanborn, M. E.; Yin, Q.-Z.; Goodrich, C. A.; Zolensky, M.; Fioretti, A. M.

2017-01-01

There is an increasing number of Cr-O-Ti isotope studies that show solar system materials are divided into two main populations, one carbonaceous chondrite (CC)-like and the other is non-carbonaceous (NC)-like, with minimal mixing attributed to a gap opened in the protoplanetary disk due to Jupiter's formation. The Grand Tack model suggests there should be large-scale mixing between S- and C-type asteroids, an idea supported by our recent work on chondrule (Delta)17O-e54Cr isotope systematics. The Almahata Sitta (AhS) meteorite provides a unique opportunity to test the Grand Tack model. The meteorite fell to Earth in October 2008 and has been linked to the asteroid 2008 TC3 which was discovered just prior to the fall of the AhS stones. The AhS meteorite is composed of up to 700 individual pieces with approx.140 of those pieces having some geochemical and/or petrologic studies. Almahata Sitta is an anomalous polymict ureilite with other meteorite components, including enstatite, ordinary, and carbonaceous chondrites with an approximate abundance of 70% ureilites and 30% chondrites. This observation has lead to the suggestion that TC3 2008 was a loosely aggregated rubble pile-like asteroid with the non-ureilite sample clasts within the rubble-pile. Due to the loosely-aggregated nature of AhS, the object disintegrated during atmospheric entry resulting in the weakly held clasts falling predominantly as individual stones in the AhS collection area. However, recent work has identified one sample of AhS, sample 91A, which may represent two different lithologies coexisting within a single stone. The predominate lithology type in 91A appears to be that of a C2 chondrite based on mineralogy but also contains olivine, pyroxene, and albite that have ureilite-like compositions. Previous Cr isotope investigations into AhS stones are sparse and what data is available show nearly uniform isotopic composition similar to that of typical ureilites with negative e54Cr values.

Striking Graphite Bearing Clasts Found in Two Ordinary Chondrite Samples; NWA6169 and NWA8330

NASA Technical Reports Server (NTRS)

Johnson, Jessica M.; Zolensky, Michael E.; Chan, Queenie; Kring, David A.

2015-01-01

Meteorites play an integral role in understanding the history of the solar system. Not only can they contain some of the oldest material found in the solar system they also can contain material that is unique. Many lithologies are only found as foreign clasts within distinctly different host meteorites. In this investigation two foreign clasts within the meteorites, NWA6169 and NWA8330 were studied. The purpose of this investigation was to examine the mineralogy and petrography of the clasts within the samples. From there an identification and possible origin were to be inferred. NWA6169 is an unclassified ordinary chondrite that has a presumed petrologic type of L3. NWA8330 is a classified ordinary chondrite that has a petrologic type of LL3. Both meteorites were found to contain clasts that were similar; both modally were comprised of about 5% acicular graphite. Through SEM and Raman Spectroscopy it was found that they contained olivine, pyroxene, plagioclase, Fe-Ni sulfides, graphite, and metals. They were found to portray an igneous texture with relationships that suggest concurrent growth. Analytical microprobe results for NWA6169 revealed mineral compositions of Fa31-34, Fs23-83, and Ab7-85. For NWA8330 these were Fa28-32, Fs10-24, and Ab4-83. Only one similar material has been reported, in the L3 chondrite Krymka (Semenenko & Girich, 1995). The clast they described exhibited similar mineralogies including the unusual graphite. Krymka data displayed compositional values of Fa28.5-35.0 and Fs9-25.9. These ranges are fairly similar to that of NWA6169 and NWA8330. These samples may all be melt clasts, probably of impact origin. Two possibilities are (1) impact of a C-type asteroid onto the L chondrite parent asteroid, and (2) a piece of proto-earth ejected from the moon-forming collision event. These possibilities present abundant questions, and can be tested. The measurement of oxygen isotope compositions from the clasts should reveal the original source of the melt clasts. It may also be possible to perform Ar dating of the plagioclase present. Former analyses are now being performed.

Highly siderophile elements were stripped from Earth’s mantle by iron sulfide segregation

NASA Astrophysics Data System (ADS)

Rubie, David C.; Laurenz, Vera; Jacobson, Seth A.; Morbidelli, Alessandro; Palme, Herbert; Vogel, Antje K.; Frost, Daniel J.

2016-09-01

Highly siderophile elements (HSEs) are strongly depleted in the bulk silicate Earth (BSE) but are present in near-chondritic relative abundances. The conventional explanation is that the HSEs were stripped from the mantle by the segregation of metal during core formation but were added back in near-chondritic proportions by late accretion, after core formation had ceased. Here we show that metal-silicate equilibration and segregation during Earth’s core formation actually increased HSE mantle concentrations because HSE partition coefficients are relatively low at the high pressures of core formation within Earth. The pervasive exsolution and segregation of iron sulfide liquid from silicate liquid (the “Hadean matte”) stripped magma oceans of HSEs during cooling and crystallization, before late accretion, and resulted in slightly suprachondritic palladium/iridium and ruthenium/iridium ratios.

U-Th-Pb age of the Barwell chondrite - Anatomy of a 'discordant' meteorite

NASA Technical Reports Server (NTRS)

Unruh, D. M.; Tatsumoto, M.; Hutchison, R.

1979-01-01

A Pb-Pb internal isochron for the Barwell L5-6 chondrite yields an age of 4.530 plus or minus 0.005 billion years, using the measured U-238/U-235 ratio of 135.24 plus or minus .17. If the terrestrial U isotope composition is used, an age of 4.559 billion years is obtained. The Pb isotopic composition is distinctly different from that of a terrestrial contaminant found in the fusion crust of the Barwell stone. When the U-Th-Pb data are plotted on the concordia diagram, the data define a line that intersects the concordia curve at approximately 4.53 and 0 billion years, and nearly all of the data plot above the concordia curve, regardless of the initial Pb correction. This discordancy and the Pb isotopic composition of the triolite are attributed to a recent reequilibration of Pb and not to terrestrial contamination.

The oxygen isotope composition of Almahata Sitta

NASA Astrophysics Data System (ADS)

Rumble, Douglas; Zolensky, Michael E.; Friedrich, Jon M.; Jenniskens, Peter; Shaddad, Muawia H.

2010-10-01

Eleven fragments of the meteorite Almahata Sitta (AHS) have been analyzed for oxygen isotopes. The fragments were separately collected as individual stones from the meteorite's linear strewn field in the Nubian Desert. Each of the fragments represents a sample of a different and distinct portion of asteroid 2008 TC3. Ten of the fragments span the same range of values of δ18O, δ17O, and Δ17O, and follow the same trend along the carbonaceous chondrite anhydrous minerals (CCAM) line as monomict and polymict members of the ureilite family of meteorites. The oxygen isotope composition of fragment #25 is consistent with its resemblance petrographically to an H5 ordinary chondrite. Our results demonstrate that a single small asteroidal parent body, asteroid 2008 TC3, only 4 m in length, encompassed the entire range of variation in oxygen isotope compositions measured for monomict and polymict ureilites.

Mass independent sulfur isotope signatures in CMs: Implications for sulfur chemistry in the early solar system

NASA Astrophysics Data System (ADS)

Labidi, J.; Farquhar, J.; Alexander, C. M. O.'D.; Eldridge, D. L.; Oduro, H.

2017-01-01

We have investigated the quadruple sulfur isotopic composition of inorganic sulfur-bearing phases from 13 carbonaceous chondrites of CM type. Our samples include 4 falls and 9 Antarctic finds. We extracted sulfur from sulfides, sulfates, and elemental sulfur (S0) from all samples. On average, we recover a bulk sulfur (S) content of 2.11 ± 0.39 wt.% S (1σ). The recovered sulfate, S0 and sulfide contents represent 25 ± 12%, 10 ± 7% and 65 ± 15% of the bulk S, respectively (all 1σ). There is no evidence for differences in the bulk S content between falls and finds, and there is no correlation between the S speciation and the extent of aqueous alteration. We report ranges of Δ33S and Δ36S values in CMs that are significantly larger than previously observed. The largest variations are exhibited by S0, with Δ33S values ranging between -0.104 ± 0.012‰ and +0.256 ± 0.018‰ (2σ). The Δ36S/33S ratios of S0 are on average -3.1 ± 1.0 (2σ). Two CMs show distinct Δ36S/33S ratios, of +1.3 ± 0.1 and +0.9 ± 0.1. We suggest that these mass independent S isotopic compositions record H2S photodissociation in the nebula. The varying Δ36S/Δ33S ratios are interpreted to reflect photodissociation that occurred at different UV wavelengths. The preservation of these isotopic features requires that the S-bearing phases were heterogeneously accreted to the CM parent body. Non-zero Δ33S values are also preserved in sulfide and sulfate, and are positively correlated with S0 values. This indicates a genetic relationship between the S-bearing phases: We argue that sulfates were produced by the direct oxidation of S0 (not sulfide) in the parent body. We describe two types of models that, although imperfect, can explain the major features of the CM S isotope compositions, and can be tested in future studies. Sulfide and S0 could both be condensates from the nebula, as the residue and product, respectively, of incomplete H2S photodissociation by UV light (wavelength <150 nm). This idea requires that FeS formation and the S0 condensation co-occur. As an alternative, ice accretion to the CM parent body could allow the delivery of S-MIF in CMs. In that case, sulfides would have been the only S-bearing condensate in CM precursors, and S0 would have been derived from the oxidation of H2S trapped in ices, after its photodissociation at low temperature (<500 K) in the nebula. In our models, the observations of H2S UV photodissociation is required to occur at the disk surface, and allowed in nebular environments with canonical C/O ratios. Vertical motions in the disk would redistribute phases that condensed at high altitude to the midplane, where they accreted in the phases that make up the chondritic matrix.

Variability in Abundances of Meteorites in the Ordovician

NASA Astrophysics Data System (ADS)

Heck, P. R.; Schmitz, B.; Kita, N.

2017-12-01

The knowledge of the flux of extraterrestrial material throughout Earth's history is of great interest to reconstruct the collisional evolution of the asteroid belt. Here, we present a review of our investigations of the nature of the meteorite flux to Earth in the Ordovician, one of the best-studied time periods for extraterrestrial matter in the geological record [1]. We base our studies on compositions of extraterrestrial chromite and chrome-spinel extracted by acid dissolution from condensed marine limestone from Sweden and Russia [1-3]. By analyzing major and minor elements with EDS and WDS, and three oxygen isotopes with SIMS we classify the recovered meteoritic materials. Today, the L and H chondrites dominate the meteorite and coarse micrometeorite flux. Together with the rarer LL chondrites they have a type abundance of 80%. In the Ordovician it was very different: starting from 466 Ma ago 99% of the flux was comprised of L chondrites [2]. This was a result of the collisional breakup of the parent asteroid. This event occurred close to an orbital resonance in the asteroid belt and showered Earth with >100x more L chondritic material than today during more than 1 Ma. Although the flux is much lower at present, L chondrites are still the dominant type of meteorites that fall today. Before the asteroid breakup event 467 Ma ago the three groups of ordinary chondrites had about similar abundances. Surprisingly, they were possibly surpassed in abundance by achondrites, materials from partially and fully differentiated asteroids [3]. These achondrites include HED meteorites, which are presumably fragments released during the formation of the Rheasilvia impact structure 1 Ga ago on asteroid 4 Vesta. The enhanced abundance of LL chondrites is possibly a result of the Flora asteroid family forming event at 1 Ga ago. The higher abundance of primitive achondrites was likely due to smaller asteroid family forming events that have not been identified yet but that did not generate a supply of fragments that was long-lived enough to be still important today. Our results imply that the composition of the flux of meteorites to Earth is biased by discrete collisional events in the asteroid belt. [1] Schmitz B (2013) Chem Erde 73, 117; [2] Heck PR et al (2016) GCA 177, 120; [3] Heck PR et al (2017) Nat Astron 1, 35, DOI: 10.1038/s41550-016-0035.

Tungsten isotopes in bulk meteorites and their inclusions—Implications for processing of presolar components in the solar protoplanetary disk

PubMed Central

Holst, J. C.; Paton, C.; Wielandt, D.; Bizzarro, M.

2016-01-01

We present high precision, low- and high-resolution tungsten isotope measurements of iron meteorites Cape York (IIIAB), Rhine Villa (IIIE), Bendego (IC), and the IVB iron meteorites Tlacotepec, Skookum, and Weaver Mountains, as well as CI chondrite Ivuna, a CV3 chondrite refractory inclusion (CAI BE), and terrestrial standards. Our high precision tungsten isotope data show that the distribution of the rare p-process nuclide 180W is homogeneous among chondrites, iron meteorites, and the refractory inclusion. One exception to this pattern is the IVB iron meteorite group, which displays variable excesses relative to the terrestrial standard, possibly related to decay of rare 184Os. Such anomalies are not the result of analytical artifacts and cannot be caused by sampling of a protoplanetary disk characterized by p-process isotope heterogeneity. In contrast, we find that 183W is variable due to a nucleosynthetic s-process deficit/r-process excess among chondrites and iron meteorites. This variability supports the widespread nucleosynthetic s/r-process heterogeneity in the protoplanetary disk inferred from other isotope systems and we show that W and Ni isotope variability is correlated. Correlated isotope heterogeneity for elements of distinct nucleosynthetic origin (183W and 58Ni) is best explained by thermal processing in the protoplanetary disk during which thermally labile carrier phases are unmixed by vaporization thereby imparting isotope anomalies on the residual processed reservoir. PMID:27445452

Sources of osmium to the modern oceans: New evidence from the 190Pt-186Os system

USGS Publications Warehouse

McDaniel, D.K.; Walker, R.J.; Hemming, S.R.; Horan, M.F.; Becker, H.; Grauch, R.I.

2004-01-01

High precision Os isotope analysis of young marine manganese nodules indicate that whereas the composition of modern seawater is radiogenic with respect to 187Os/188Os, it has 186Os/188Os that is within uncertainty of the chondritic value. Marine Mn nodule compositions thus indicate that the average continental source of Os to modern seawater had long-term high Re/Os compared to Pt/Os. Analyses of loess and freshwater Mn nodules support existing evidence that average upper continental crust (UCC) has resolvably suprachondritic 186Os/188Os, as well as radiogenic 187Os/188Os. Modeling the composition of seawater as a two-component mixture of oceanic/cosmic Os with chondritic Os compositions and continentally-derived Os demonstrates that, insofar as estimates for the composition of average UCC are accurate, congruently weathered average UCC cannot be the sole continental source of Os to seawater. Our analysis of four Cambrian black shales confirm that organic-rich sediments can have 187Os/188Os ratios that are much higher than average UCC, but 186Os/188Os compositions that are generally between those of chondrites and average-UCC. Preferential weathering of black shales can result in dissolved Os discharged to the ocean basins that has a much lower 186Os/188Os than does average upper crust. Modeling the available data demonstrates that augmentation of estimated average UCC compositions with less than 0.1% additional black shale and 1.4% additional ultramafic rock can produce a continental end-member Os isotopic composition that satisfies the requirements imposed by the marine Mn nodule data. The interplay of these two sources provides a mechanism by which the 187Os/188Os of seawater can change as sources and weathering conditions change, yet seawater 186Os/188Os varies only minimally. ?? 2004 Elsevier Ltd.

Sub-Micrometer Scale Minor Element Mapping in Interplanetary Dust Particles: A Test for Stratospheric Contamination

NASA Technical Reports Server (NTRS)

Flynn, G. J.; Keller, L. P.; Sutton, S. R.

2004-01-01

Combined X-ray microprobe (XRM), energy dispersive x-ray fluorescence using a Transmission Electron Microscope (TEM), and electron microprobe measurements have determined that the average bulk chemical composition of the interplanetary dust particles (IDPs) collected from the Earth s stratosphere is enriched relative to the CI meteorite composition by a factor of 2 to 4 for carbon and for the moderately volatile elements Na, K, P, Mn, Cu, Zn, Ga, Ge, and Se, and enriched to approximately 30 times CI for Br. However, Jessberger et al., who have reported similar bulk enrichments using Proton Induced X-ray Emission (PIXE), attribute the enrichments to contamination by meteor-derived atmospheric aerosols during the several weeks these IDPs reside in the Earth s atmosphere prior to collection. Using scanning Auger spectroscopy, a very sensitive surface analysis technique, Mackinnon and Mogk have observed S contamination on the surface of IDPs, presumably due to the accretion of sulfate aerosols during stratospheric residence. But the S-rich layer they detected was so thin (approximately 100 angstroms thick) that the total amount of S on the surface was too small to significantly perturb the bulk S-content of a chondritic IDP. Stephan et al. provide support for the contamination hypothesis by reporting the enrichment of Br on the edges of the IDPs using Time-of-Flight Secondary-Ion Mass-Spectrometry (TOFSIMS), but TOF-SIMS is notorious for producing false edge-effects, particularly on irregularly-shaped samples like IDPs. Sutton et al. mapped the spatial distribution of Fe, Ni, Zn, Br, and Sr, at the approximately 2 m scale, in four IDPs using element-specific x-ray fluorescence (XRF) computed microtomography. They found the moderately volatile elements Zn and Br, although spatially inhomogeneous, were not concentrated on the surface of any of the IDPs they examined, suggesting that the Zn and the Br enrichments in the IDPs are not due to contamination during stratospheric residence.