scholarly journals Magnesium isotopic composition of olivine from the Earth, Mars, Moon, and pallasite parent body

2006 ◽  
Vol 33 (15) ◽  
Author(s):  
M. D. Norman ◽  
G. M. Yaxley ◽  
V. C. Bennett ◽  
A. D. Brandon
Keyword(s):  
Isotopic Composition ◽  
Parent Body ◽  
The Earth

Core formation in the shergottite parent body and comparison with the Earth

1987 ◽  
Vol 92 (B4) ◽  
pp. E627-E632 ◽  
Author(s):  
Allan H. Treiman ◽  
John H. Jones ◽  
Michael J. Drake
Keyword(s):  
Parent Body ◽  
Core Formation ◽  
The Earth

Machiite, Al2Ti3O9, a new oxide mineral from the Murchison carbonaceous chondrite: A new ultra-refractory phase from the solar nebula

2020 ◽  
Vol 105 (2) ◽  
pp. 239-243 ◽  
Author(s):  
Alexander N. Krot ◽  
Kazuhide Nagashima ◽  
George R. Rossman
Keyword(s):  
Isotopic Composition ◽  
Solar Nebula ◽  
Carbonaceous Chondrite ◽  
Parent Body ◽  
Oxygen Isotopic Composition ◽  
New Mineral ◽  
Calculated Density ◽  
California Institute Of Technology ◽  
Oxygen Isotopic ◽  
Institute Of Technology

Abstract Machiite (IMA 2016-067), Al2Ti3O9, is a new mineral that occurs as a single euhedral crystal, 4.4 μm in size, in contact with an euhedral corundum grain, 12 μm in size, in a matrix of the Murchison CM2 carbonaceous chondrite. The mean chemical composition of holotype machiite by electron probe microanalysis is (wt%) TiO2 59.75, Al2O3 15.97, Sc2O3 10.29, ZrO2 9.18, Y2O3 2.86, FeO 1.09, CaO 0.44, SiO2 0.20, MgO 0.10, total 99.87, giving rise to an empirical formula (based on 9 oxygen atoms pfu) of (Al1.17Sc0.56Y0.10Ti0.084+Fe0.06Ca0.03Mg0.01)(Ti2.714+Zr0.28Si0.01)O9. The general formula is (Al,Sc)2(Ti4+,Zr)3O9. The end-member formula is Al2Ti3O9. Machiite has the C2/c schreyerite-type structure with a = 17.10 Å, b = 5.03 Å, c = 7.06 Å, β = 107°, V = 581 Å3, and Z = 4, as revealed by electron backscatter diffraction. The calculated density using the measured composition is 4.27 g/cm3. The machiite crystal is highly 16O-depleted relative to the coexisting corundum grain (Δ17O = –0.2 ± 2.4‰ and –24.1 ± 2.6‰, respectively; where Δ17O = δ17O – 0.52 × δ18O). Machiite is a new member of the schreyerite (V2Ti3O9) group and a new Sc,Zr-rich ultrarefractory phase formed in the solar nebula, either by gas-solid condensation or as a result of crystallization from a Ca,Al-rich melt having solar-like oxygen isotopic composition (Δ17O~ –25‰) under high-temperature (~1400–1500 °C) and low-pressure (~10-4–10-5 bar) conditions in the CAI-forming region near the protosun. The currently observed disequilibrium oxygen isotopic composition between machiite and corundum may indicate that machiite subsequently experienced oxygen isotopic exchange with a planetary-like 16O-poor gaseous reservoir either in the solar nebula or on the CM chondrite parent body. The name machiite is in honor of Chi Ma, mineralogist at California Institute of Technology, for his contributions to meteorite mineralogy and discovery of many new minerals representing extreme conditions of formation.

Constitution of terrestrial planets

1981 ◽  
Vol 303 (1477) ◽  
pp. 287-302 ◽  
Keyword(s):  
Bulk Composition ◽  
Parent Body ◽  
The Moon ◽  
Volatile Elements ◽  
Earth’S Mantle ◽  
The Earth ◽  
History Of ◽  
Relationship Of ◽  
Reduced State

Reliable estimates of the bulk composition are so far restricted to the three planetary objects from which we have samples for laboratory investigation, i.e. the Earth, the Moon and the eucrite parent asteroid. The last, the parent body of the eucrite— diogenite family of meteorites, an object that like Earth and Moon underwent magmatic differentiations, seems to have an almost chondritic composition except for a considerable depletion of all moderately volatile (Na, K, Rb, F, etc.) and highly volatile (Cl, Br, Cd, Pb, etc.) elements. The Moon is also depleted in moderately volatile and volatile elements compared to carbonaceous chondrites of type 1 (Cl) and also compared to the Earth. Again normalized to Cl and Si the Earth’s mantle and the Moon are slightly enriched in refractory lithophile elements and in magnesium. It might be that this enrichment is fictitious and only due to the normalization to Si and that both Earth’s mantle and Moon are depleted in Si, which partly entered the Earth’s core in metallic form. The striking depletion of the Earth’s mantle for the elements V, Cr and Mn can also be explained by their partial removal into the core. The similar abundances of V, Cr and Mn in the Moon and in the Earth’s mantle indicate the strong genetic relationship of Earth and Moon. Apart from their contents of metallic iron, all siderophile elements, moderately volatile and volatile elements, Earth and Moon are chemically very similar. It might well be that, with these exceptions and that of a varying degree of oxidation, all the inner planets have a similar chemistry. The chemical composition of the Earth’s mantle, for which reliable and accurate data have recently been obtained from the study of ultramafic nodules, yields important information about the accretion history of the Earth and that of the inner planets. It seems that accretion started with highly reduced material, with all Fe as metal and even Si and Cr, V and Mn partly in reduced state, followed by the accretion of more and more oxidized matter.

scholarly journals Evaporative fractionation of volatile stable isotopes and their bearing on the origin of the Moon

2014 ◽  
Vol 372 (2024) ◽  
pp. 20130259 ◽  
Author(s):  
James M. D. Day ◽  
Frederic Moynier
Keyword(s):  
Global Scale ◽  
Parent Body ◽  
The Moon ◽  
Magma Ocean ◽  
Volatile Elements ◽  
Giant Impact ◽  
The Earth ◽  
Present Distribution ◽  
Volatile Loss

The Moon is depleted in volatile elements relative to the Earth and Mars. Low abundances of volatile elements, fractionated stable isotope ratios of S, Cl, K and Zn, high μ ( 238 U/ 204 Pb) and long-term Rb/Sr depletion are distinguishing features of the Moon, relative to the Earth. These geochemical characteristics indicate both inheritance of volatile-depleted materials that formed the Moon and planets and subsequent evaporative loss of volatile elements that occurred during lunar formation and differentiation. Models of volatile loss through localized eruptive degassing are not consistent with the available S, Cl, Zn and K isotopes and abundance data for the Moon. The most probable cause of volatile depletion is global-scale evaporation resulting from a giant impact or a magma ocean phase where inefficient volatile loss during magmatic convection led to the present distribution of volatile elements within mantle and crustal reservoirs. Problems exist for models of planetary volatile depletion following giant impact. Most critically, in this model, the volatile loss requires preferential delivery and retention of late-accreted volatiles to the Earth compared with the Moon. Different proportions of late-accreted mass are computed to explain present-day distributions of volatile and moderately volatile elements (e.g. Pb, Zn; 5 to >10%) relative to highly siderophile elements (approx. 0.5%) for the Earth. Models of early magma ocean phases may be more effective in explaining the volatile loss. Basaltic materials (e.g. eucrites and angrites) from highly differentiated airless asteroids are volatile-depleted, like the Moon, whereas the Earth and Mars have proportionally greater volatile contents. Parent-body size and the existence of early atmospheres are therefore likely to represent fundamental controls on planetary volatile retention or loss.

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