Magnetic evidence for a partially differentiated carbonaceous chondrite parent body
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ABSTRACT:
SUBMITTER: Carporzen L
PROVIDER: S-EPMC3081022 | biostudies-literature | 2011 Apr
REPOSITORIES: biostudies-literature
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Project description:Comparative planetology studies are key for understanding the main processes driving planetary formation and evolution. None have been yet applied to pristine asteroids formed in the solar protoplanetary disk, mainly because of their comminution during their 4.5-billion-year collisional lifetime. From remarkable textural, mineralogical, chemical, and thermodynamic similarities, we show that the high-temperature Kudryavy volcano fumarolic environment from Kurile Islands is a likely proxy of the Fe-alkali-halogen metasomatism on the CV and CO carbonaceous chondrite parent bodies. Ca-Fe-rich and Na-Al-Cl-rich secondary silicates in CV and CO chondrites are, thus, inferred to be fumarolic-like incrustations that precipitate from hot and reduced hydrothermal vapors after interactions with the wallrocks during buoyancy-driven Darcy flow percolation. These vapors may originate from the progressive heating and devolatilization of a chondritic protolith on their parent body or are remnant of the cooling of residual local nebular gases at the time of their primary planetesimal accretion.
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Project description:Carbonaceous chondrite meteorites record the earliest stages of Solar System geo-logical activities and provide insight into their parent bodies' histories. Some carbonaceous chondrites are volumetrically dominated by hydrated minerals, providing evidence for low temperature and pressure aqueous alteration1. Others are dominated by anhydrous minerals and textures that indicate high temperature metamorphism in the absence of aqueous fluids1. Evidence of hydrous metamorphism at intermediate pressures and temperatures in carbonaceous chondrite parent bodies has been virtually absent. Here we show that an ungrouped, aqueously altered carbonaceous chondrite fragment (numbered 202) from the Almahata Sitta (AhS) meteorite contains an assemblage of minerals, including amphibole, that reflect fluid-assisted metamorphism at intermediate temperatures and pressures on the parent asteroid. Amphiboles are rare in carbonaceous chondrites, having only been identified previously as a trace component in Allende (CV3oxA) chondrules2. Formation of these minerals requires prolonged metamorphism in a large (~640-1800 km diameter), unknown asteroid. Because Allende and AhS 202 represent different asteroidal parent bodies, intermediate conditions may have been more widespread in the early Solar System than recognized from known carbonaceous chondrite meteorites, which are likely a biased sampling.
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Project description:A long-standing question regarding carbonaceous chondrites (CCs) is how the CCs’ organics were sourced and converted before and after the accretion of their parent bodies. Growing evidence shows that amino acid abundances in CCs decrease with an elongated aqueous alteration. However, the underlying chemical processes are unclear. If CCs’ parent bodies were water-rock differentiated, pH and redox gradients can drive electrochemical reactions by using H2 as an electron source. Here, we simulate such redox conditions and demonstrate that α-amino acids are electrochemically altered to monoamines and α-hydroxy acids on FeS and NiS catalysts at 25 °C. This conversion is consistent with their enrichment compared to amino acid analogs in heavily altered CCs. Our results thus suggest that H2 can be an important driver for organic evolution in water-rock differentiated CC parent bodies as well as the Solar System icy bodies that might possess similar pH and redox gradients. Researchers at Earth-Life Science Institute (ELSI) discovered a chemical process that can explain the very low amino acid abundances in aqueously altered carbonaceous chondrites, deepening our understanding on the Solar System chemical evolution.
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Project description:Early Solar System planetesimal thermal models predict the heating of the chondritic protolith and the preservation of a chondritic crust on differentiated parent bodies. Petrological and geochemical analyses of chondrites have suggested that secondary alteration phases formed at low temperatures (<300 °C) by fluid-rock interaction where reduced and oxidized Vigarano type Carbonaceous (CV) chondrites witness different physicochemical conditions. From a thermodynamical survey of Ca-Fe-rich secondary phases in CV3 chondrites including silica activity (aSiO2), here we show that the classical distinction between reduced and oxidized chondrites is no longer valid and that their Ca-Fe-rich secondary phases formed in similar reduced conditions near the iron-magnetite redox buffer at low aSiO2 (log(aSiO2) <-1) and moderate temperature (210-610 °C). The various lithologies in CV3 chondrites are inferred to be fragments of an asteroid percolated heterogeneously via porous flow of hydrothermal fluid. Putative 'onion shell' structures are not anymore a requirement for the CV parent body crust.Meteorites may unlock the history of the early solar system. Here, the authors find, through Ca-Fe-rich secondary phases, that the distinction between reduced and oxidized CV chondrites is invalid; therefore, CV3 chondrites are asteroid fragments that percolated heterogeneously via porous flow of hydrothermal fluid.
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Project description:Recent isotopic and paleomagnetic data point to a possible connection between carbonaceous chondrites and differentiated planetary materials, suggesting the existence, perhaps ephemeral, of transitional objects with a layered structure whereby a metal-rich core is enclosed by a silicate mantle, which is itself overlain by a crust containing an outermost layer of primitive solar nebula materials. This idea has not received broad support, mostly because of a lack of samples in the meteoritic record that document incipient melting at the onset of planetary differentiation. Here, we report the discovery and the petrologic-isotopic characterization of UH154-11, a ferroan trachybasalt fragment enclosed in a Renazzo-type carbonaceous chondrite (CR). Its chemical and oxygen isotopic compositions are consistent with very-low-degree partial melting of a Vigarano-type carbonaceous chondrite (CV) from the oxidized subgroup at a depth where fluid-assisted metamorphism enhanced the Na content. Its microdoleritic texture indicates crystallization at an increasing cooling rate, such as would occur during magma ascent through a chondritic crust. This represents direct evidence of magmatic activity in a carbonaceous asteroid on the verge of differentiating and demonstrates that some primitive outer Solar System objects related to icy asteroids and comets underwent a phase of magmatic activity early in the Solar System. With its peculiar petrology, UH154-11 can be considered the long-sought first melt produced during partial differentiation of a carbonaceous chondritic planetary body, bridging a previously persistent gap in differentiation processes from icy cometary bodies to fully melted iron meteorites with isotopic affinities to carbonaceous chondrites.
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Project description:The abundances of highly siderophile elements (HSE: Re, Os, Ir, Ru, Pt, Pd), as well as 187Re-187Os and 182Hf-182W isotopic systematics were determined for separated metal, slightly magnetic, and nonmagnetic fractions from seven H4 to H6 ordinary chondrites. The HSE are too abundant in nonmagnetic fractions to reflect metal-silicate equilibration. The disequilibrium was likely a primary feature, as 187Re-187Os data indicate only minor open-system behavior of the HSE in the slightly and non-magnetic fractions. 182Hf-182W data for slightly magnetic and nonmagnetic fractions define precise isochrons for most meteorites that range from 5.2 ± 1.6 Ma to 15.2 ± 1.0 Ma after calcium aluminum inclusion (CAI) formation. By contrast, 182W model ages for the metal fractions are typically 2-5 Ma older than the slope-derived isochron ages for their respective, slightly magnetic and nonmagnetic fractions, with model ages ranging from 1.4 ± 0.8 Ma to 12.6 ± 0.9 Ma after CAI formation. This indicates that the W present in the silicates and oxides was not fully equilibrated with the metal when diffusive transport among components ceased, consistent with the HSE data. Further, the W isotopic compositions of size-sorted metal fractions from some of the H chondrites also differ, indicating disequilibrium among some metal grains. The chemical/isotopic disequilibrium of siderophile elements among H chondrite components is likely the result of inefficient diffusion of siderophile elements from silicates and oxides to some metal and/or localized equilibration as H chondrites cooled towards their respective Hf-W closure temperatures. The tendency of 182Hf-182W isochron ages to young from H5 to H6 chondrites may indicate derivation of these meteorites from a slowly cooled, undisturbed, concentrically-zoned parent body, consistent with models that have been commonly invoked for H chondrites. Overlap of isochron ages for H4 and H5 chondrites, by contrast, appear to be more consistent with shallow impact disruption models. The W isotopic composition of metal from one CR chondrite was examined to compare with H chondrite metals. In contrast to the H chondrites, the CR chondrite metal is characterized by an enrichment in 183W that is consistent with nucleosynthetic s-process depletion. Once corrected for the correlative nucleosynthetic effect on 182W, the 182W model age for this meteorite of 7.0 ± 3.6 Ma is within the range of model ages of most metal fractions from H chondrites. The metal is therefore too young to be a direct nebular condensate, as proposed by some prior studies.
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Project description:Chemical fingerprints of impacts are usually compromised by extreme conditions in the impact plume, and the contribution of projectile matter to impactites does not often exceed a fraction of per cent. Here we use chromium and oxygen isotopes to identify the impactor and impact-plume processes for Zhamanshin astrobleme, Kazakhstan. ε54Cr values up to 1.54 in irghizites, part of the fallback ejecta, represent the 54Cr-rich extremity of the Solar System range and suggest a CI-like chondrite impactor. Δ17O values as low as -0.22‰ in irghizites, however, are incompatible with a CI-like impactor. We suggest that the observed 17O depletion in irghizites relative to the terrestrial range is caused by partial isotope exchange with atmospheric oxygen (Δ17O = -0.47‰) following material ejection. In contrast, combined Δ17O-ε54Cr data for central European tektites (distal ejecta) fall into the terrestrial range and neither impactor fingerprint nor oxygen isotope exchange with the atmosphere are indicated.Identifying the original impactor from craters remains challenging. Here, the authors use chromium and oxygen isotopes to indicate that the Zhamanshin astrobleme impactor was a carbonaceous chrondrite by demonstrating that depleted 17O values are due to exchange with atmospheric oxygen.
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Project description:The Paris carbonaceous chondrite represents the most pristine carbonaceous chondrite, providing a unique opportunity to investigate the composition of early solar system materials prior to the onset of significant aqueous alteration. A dual origin (namely from the inner and outer solar system) has been demonstrated for water in the Paris meteorite parent body (Piani et al. 2018). Here, we aim to evaluate the contribution of outer solar system (cometary-like) water ice to the inner solar system water ice using Xe isotopes. We report Ar, Kr, and high-precision Xe isotopic measurements within bulk CM 2.9 and CM 2.7 fragments, as well as Ne, Ar, Kr, and Xe isotope compositions of the insoluble organic matter (IOM). Noble gas signatures are similar to chondritic phase Q with no evidence for a cometary-like Xe component. Small excesses in the heavy Xe isotopes relative to phase Q within bulk samples are attributed to contributions from presolar materials. CM 2.7 fragments have lower Ar/Xe relative to more pristine CM 2.9 fragments, with no systematic difference in Xe contents. We conclude that Kr and Xe were little affected by aqueous alteration, in agreement with (1) minor degrees of alteration and (2) no significant differences in the chemical signature of organic matter in CM 2.7 and CM 2.9 areas (Vinogradoff et al. 2017). Xenon contents in the IOM are larger than previously published data of Xe in chondritic IOM, in line with the Xe component in Paris being pristine and preserved from Xe loss during aqueous alteration/thermal metamorphism.
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Project description:We report on the detection of primordial organic matter within the carbonaceous chondrite Maribo that is distinct from the majority of organics found in extraterrestrial samples. We have applied high-spatial resolution techniques to obtain C-N isotopic compositions, chemical, and structural information of this material. The organic matter is depleted in 15N relative to the terrestrial value at around ?15N?~?-200‰, close to compositions in the local interstellar medium. Morphological investigations by electron microscopy revealed that the material consists of µm- to sub-µm-sized diffuse particles dispersed within the meteorite matrix. Electron energy loss and synchrotron X-ray absorption near-edge structure spectroscopies show that the carbon functional chemistry is dominated by aromatic and C=O bonding environments similar to primordial organics from other carbonaceous chondrites. The nitrogen functional chemistry is characterized by C-N double and triple bonding environments distinct from what is usually found in 15N-enriched organics from aqueously altered carbonaceous chondrites. Our investigations demonstrate that Maribo represents one of the least altered CM chondrite breccias found to date and contains primordial organic matter, probably originating in the interstellar medium.
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