RESUMO
A long-standing paradigm assumes that the chemical and isotopic compositions of many elements in the bulk silicate Earth are the same as in chondrites. However, the accessible Earth has a greater (142)Nd/(144)Nd ratio than do chondrites. Because (142)Nd is the decay product of the now-extinct (146)Sm (which has a half-life of 103 million years), this (142)Nd difference seems to require a higher-than-chondritic Sm/Nd ratio for the accessible Earth. This must have been acquired during global silicate differentiation within the first 30 million years of Solar System formation and implies the formation of a complementary (142)Nd-depleted reservoir that either is hidden in the deep Earth, or lost to space by impact erosion. Whether this complementary reservoir existed, and whether or not it has been lost from Earth, is a matter of debate, and has implications for determining the bulk composition of Earth, its heat content and structure, as well as for constraining the modes and timescales of its geodynamical evolution. Here we show that, compared with chondrites, Earth's precursor bodies were enriched in neodymium that was produced by the slow neutron capture process (s-process) of nucleosynthesis. This s-process excess leads to higher (142)Nd/(144)Nd ratios; after correction for this effect, the (142)Nd/(144)Nd ratios of chondrites and the accessible Earth are indistinguishable within five parts per million. The (142)Nd offset between the accessible silicate Earth and chondrites therefore reflects a higher proportion of s-process neodymium in the Earth, and not early differentiation processes. As such, our results obviate the need for hidden-reservoir or super-chondritic Earth models and imply a chondritic Sm/Nd ratio for the bulk Earth. Although chondrites formed at greater heliocentric distances and contain a different mix of presolar components than Earth, they nevertheless are suitable proxies for Earth's bulk chemical composition.
Assuntos
Planeta Terra , Evolução Planetária , Meia-Vida , Meteoroides , Sistema SolarRESUMO
The age of secondary carbonate mineralization in the martian meteorite ALH84001 was determined to be 3.90 +/- 0.04 billion years by rubidium-strontium (Rb-Sr) dating and 4.04 +/- 0.10 billion years by lead-lead (Pb-Pb) dating. The Rb-Sr and Pb-Pb isochrons are defined by leachates of a mixture of high-graded carbonate (visually estimated as approximately 5 percent), whitlockite (trace), and orthopyroxene (approximately 95 percent). The carbonate formation age is contemporaneous with a period in martian history when the surface is thought to have had flowing water, but also was undergoing heavy bombardment by meteorites. Therefore, this age does not distinguish between aqueous and impact origins for the carbonates.
Assuntos
Carbonatos , Marte , Meteoroides , Cálcio/análise , Fosfatos de Cálcio , Carbonatos/análise , Ferro/análise , Isótopos/análise , Chumbo/análise , Magnésio/análise , Minerais , Radioisótopos de Rubídio/análise , Isótopos de Estrôncio/análiseRESUMO
We examined lithic breccias from the Apollo sample collection in order to identify ferroan anorthosite samples suitable for geochronology, and better define the age relationships between rocks of the lunar highlands. Clast 3A is a previously unstudied noritic anorthosite from Apollo 16 lithic breccia 60016 with textural evidence of slow subsolidus recrystallization. We estimate a cooling rate of ~10 °C/Myr and calculate a pyroxene solvus temperature of 1,100-1,000 °C. Pyroxene exsolution lamellae (1-3 µm) indicate that the last stage of cooling was rapid at ~0.2 °C/year, typical of rates observed in thick ejecta blankets. We calculate concordant ages from the 147Sm-143Nd, 146Sm-142Nd, Rb-Sr, and Ar-Ar isotopic systems of 4,302 ± 28, 4,296 + 39/-53, 4,275 ± 38, and 4,311 ± 31 Ma, respectively, with a weighted average of 4,304 ± 12 Ma. The closure temperature of the Sm-Nd system is ~855 ± 14 °C, whereas the closure temperature of the Ar-Ar system is 275 ± 25 °C. Cooling from 855 to 275 °C at 10 °C/Myr should result in an age difference between the two isotopic systems of ~60 Myr. The concordant Sm-Nd, Rb-Sr, and Ar-Ar ages imply that they record the time the rock was excavated by a large impact from the midcrust. The ages clearly predate various late accretion scenarios in which an uptick in impacts at 3.8 Ga is preceded by a period of relative quiescence between 4.4 and ~4.1 Ga, and instead are consistent with decreasing accretion rates following the formation of the Moon.
RESUMO
Chemical compositions of impact melt glass veins, called Lithology C (Lith C) in Martian meteorite EET79001 were determined by electron microprobe analysis. A large enrichment of S, and significant enrichments of Al, Ca, and Na were observed in Lith C glass compared to Lithology A (Lith A). The S enrichment is due to mixing of plagioclase- enriched Lith A material with Martian soil, either prior to or during impact on Mars. A mixture of 87% Lith A, 7% plagioclase, and 6% Martian soil reproduces the average elemental abundances observed in Lith C. Shock melting of such a mixture of plagioclase-enriched, fine-grained Lith A host rock and Martian soil could yield large excesses of S (observed in this study) and Martian atmospheric noble gases (found by Bogard et al., 1983) in Lith C. These mixing proportions can be used to constrain the elemental abundance of phosphorus in Martian soil.