Chemical fractionations in meteorites. VI - Accretion temperatures of H-, LL-, and E-chondrites, from abundance of volatile trace elements.
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Laul, J. C.↗
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Chemical fractionations in meteorites. IX - C3 chondrites
Radiochemical neutron activation is applied to the analysis of four C3V chondrites and three C3O chondrites for 17 trace elements (U, Re, Ir, Ni, Au, Sb, Ge, Ag, Rb, Cs, Bi, Tl, Br, Se, Te, In, and Cd). It is shown that both classes exhibit a typical chondritic step pattern, reflecting loss of volatiles during chondrule formation. It appears that the H2S/H2 ratio is the key variable to account for the condensation of chalcophile elements as a function of H2S. C3O's seem to have condensed in a region where enough metallic Fe was present to buffer the H2S pressure, whereas C3V's condensed in a more oxidized region where H2S was in excess. Accretion temperatures for both subclasses is determined. Sb and Au show variable depletion, presumably reflecting variable loss during chondrule formation.
Anders, E.↗
Chemical fractionations in meteorites. X - Ureilites
An investigation involving the measurement of 17 trace elements in 4 ureilites was conducted with the objective to obtain information for the characterization of the two components of the ureilites. The groundmass of the mineral is an olivine-clinopyroxene rock which is presumably the residue left after partial melting of a more primitive precursor. This ultramafic rock is permeated by a network of veins containing diamond, graphite, nickel-iron, and primordial noble gases. Attention is given to the vein material, the origin of the vein material, the 'constant' siderophile component and ultramafic rock, and questions concerning the origin of ureilites.
Higuchi, H.↗
Chemical fractionation of Ru and Os in the moon
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Jovanovic, S.↗
Is osmium chemically fractionated in the moon
An investigation was conducted involving the determination of Os in 53 highland samples from the Apollo 14-17 missions. The Os/Ir ratio was found to remain essentially constant at 1.05 as Os and Ir abundances vary over four orders of magnitude. The Os-Au and the Os-Ni correlation in highland samples is presented in graphs. The graphs show that the majority of highland samples have Os/Au and Os/Ni ratios somewhat below the cosmic value. But there is no reason to attribute this trend to a loss of Os by local processes, because two other refractory siderophiles, Ir and Re, show exactly the same trend. Results on more than 150 analyzed highland samples show that meteoritic groups of low (Ir, Re, Os)/Au ratio are much more common at the Apollo landing sites than are groups of high ratio.
Hertogen, J.↗
Chemical fractionation in the solar system
The cosmochemical and geochemical history of planetary material is reflected in relative and absolute abundances of two groups of trace elements; siderophiles and volatiles. Many of these elements can be determined at the required levels only by radiochemical neutron activation analysis. The abundance patterns of elements in chondritic meteorites result from condensation processes in the solar nebula. The composition of planetisimals which bombarded the moon is characterized from trace elements in lunar breccias, and is also related to nebula processes. Trace elements in anorthosites and basalts from earth and moon suggest that the moon is refractory-rich and volatile-poor relative to the earth.
Morgan, J. W.↗
Chemical fractionations in meteorites. XI - C2 chondrites
Measurements of the compositions of 20 trace elements in the representative C2 chondrites Boriskino, Cold Bokkeveld, Erakot, Essebi, Haripura, Santa Cruz and Al Rais are reported. The contents of Ag, Au, Bi, Cd, Cs, Ge, In, Ir, Ni, Os, Pd, Rb, Re, Sb, Se, Sn, Te, Tl, U, and Zn were determined by radiochemical neutron activation analysis. The siderophile abundances of the C2 chondrites are found to be less uniform than those of other carbonaceous chondrites, while the C2R chondrite Al Rais is systematically lower in 12 volatiles than the C2M chondrites. Enrichment of Bi and Tl found in Erakot and Haripura indicate the possible presence of the late condensate mysterite. Volatile abundances are shown to agree with matrix contents for meteorites that have suffered little aqueous alteration, however to be 20-30% lower for the more altered meteorites. Finally, the decline of element abundance with volatility is shown to be consistent with the sigmoid curve explained by the two-component model.
Wolf, R.↗
Extreme early solar system chemical fractionation recorded by alkali-rich clasts contained in ordinary chondrite breccias
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Tatsunori Yokoyama↗
The lunar regolith - Chemistry and petrology of Luna 24 grain size fractions
Chemical data obtained by instrumental neutron activation analysis are reported for 30 elements in eight lunar soil size fractions from 370 to less than 2 microns, as well as petrology for five size fractions down to 40-10 microns in two Luna 24 soils. While the compositions of coarser fractions are similar to each other, they differ from the fractions smaller than 10 microns; these become increasingly feldspathic and enriched in large ion lithophile elements (LILE) with decreasing grain size. The high concentrations of the Ni, Au and Ir meteoritic indicator elements in these finer fractions are consistent with comminution by meteoritic impact. Size distributions, petrology and LILE patterns indicate that Luna 24 soils are less reworked than most lunar soils.
Laul, J. C.↗
Condensation of solids in space. Isotope fractionation in the model system C-O
The reported chemical fractionation of a single isotope O-16 under simulated space conditions provides the first experimental proof for the hypothesis that the oxygen isotopic anomaly (and other similar anomalies) seen in meteorites is a product of chemical fractionation in interstellar or circumstellar space. Work proposed on this subject was discontinued because a peer review determined that such effects could not possibly exist and that continued support of this project would be a wasted effort. A bibliography is included of articles generated during research in this area.
Arrhenius, G.↗
Single isotope fractionation of (16)O(-) implications for early history of solar system
Chemical fractionation processes are investigated with emphasis on selective single isotope fractionation in polyisotopic systems, particularly in oxygen. The related temperature parameters of meteoritic condensates and of their source medium are investigated by a thermometric method that is independent of assumptions regarding temperatures and pressures in the solar nebula. The crucial nonlinear chemical fractionation of O-16 was demonstrated experimentally. The effect was achieved in condensed CO2 formed from CO with C-12 O-16 selectively excited by H Ly alpha. The effect was verified by mass spectrometric measurements. The meteorite paleotemperature estimates were advanced from defining only thermal exposure to evaluating time and temperature independently. Grain temperatures at condensation of refractory inclusion materials are indicated to be less than 900 K in agreement with radiation temperature considerations and observations in circumstellar dust shells.
Arrhenius, G.↗
Zr-Hf fractionation in chemically defined lunar rock groups
Zirconium and hafnium, a geochemically coherent pair of elements, are strongly fractionated in lunar rocks, as evidenced by a wide range of Zr/Hf mass ratios from 12 for the anorthosite 60015,65A to 50 for the KREEP breccia 14321. This may be explained in part by selective reduction of Zr(4+) to Zr(3+) and exclusion of the Zr(3+) from early crystallized Fe-Ti minerals.
Garg, A. N.↗
Constraints placed on the chondrule-forming process by merrihueite in the Mezoe-Madaras chondrite
A few unusual chondrules in the Mezoe-Madaras L3 chondrite contain the peralkaline mineral merrihueite, (K, Na)2(Fe, Mg)5Si12O30, formed by reaction of free silica in the chondrules with K, Na, Fe-rich nebular gas. Vapor fractionation was required to create chondrules poor in Al and rich in Si, and the fractionated condensate produced had to aggregate into protochondrules very promptly (on the order of hours or less) to prevent it from mixing with dust of more generalized composition in the nebula. The traditional paradigm for chondrule formation, involving a series of unrelated events (chemical fractionation of precursor dust; clumping of the dust; melting of the dust-clumps), is inadequate for making these chondrules. A rapid process, all stages of which are related, is required. We propose that this occurred during the cooling and contraction of the volume of hot gas created by a small transient high-energy event in the nebula, of unspecified nature. Microdroplets of silicate melt created by condensation from the cooling, contracting gas had velocity vectors directed toward the center of the volume. Coalescence occurred in the crowded central zone where the microdroplets converged. The Mezoe-Madaras merriihueite-bearing chondrules may have been formed by an atypically low-energy nebular event, which achieved the needed chemical fractionations by only partially vaporizing precursor dust. More commonplace chondrule types may have been created by the same basic process, but involving higher-energy events in which precursor dust was completely vaporized and recondensed.
Wood, John A.↗
In-Situ and Experimental Evidence for Acidic Weathering of Rocks and Soils on Mars
Experimental data for alteration of synthetic Martian basalts at pH=0-1 indicate that chemical fractionations at low pH are vastly different from those observed during terrestrial weathering. Rock analyses from Gusev crater are well described by the relationships apparent from low pH experimental alteration data. A model for rock surface alteration is developed which indicates that a leached alteration zone is present on rock surfaces at Gusev. This zone is not chemically fractionated to a large degree from the underlying rock interior, indicating that the rock surface alteration process has occurred at low fluid-to-rock ratio. The geochemistry of natural rock surfaces analyzed by APXS is consistent with a mixture between adhering soil/dust and the leached alteration zone. The chemistry of rock surfaces analyzed after brushing with the RAT is largely representative of the leached alteration zone. The chemistry of rock surfaces analyzed after grinding with the RAT is largely representative of the interior of the rock, relatively unaffected by the alteration process occurring at the rock surface. Elemental measurements from the Spirit, Opportunity, Pathfinder and Viking 1 landing sites indicate that soil chemistry from widely separated locations is consistent with the low-pH, low fluid to rock ratio alteration relationships developed for Gusev rocks. Soils are affected principally by mobility of FeO and MgO, consistent with alteration of olivine-bearing basalt and subsequent precipitation of FeO and MgO bearing secondary minerals as the primary control on soil geochemistry.
Hurowitz, J. A.↗
Observations of Carbon Isotopic Fractionation in Interstellar Formaldehyde
Primitive Solar System materials (e.g. chondrites. IDPs, the Stardust sample) show large variations in isotopic composition of the major volatiles (H, C, N, and O ) even within samples, witnessing to various degrees of processing in the protosolar nebula. For ex~ ample. the very pronounced D enhancements observed in IDPs [I] . are only generated in the cold. dense component of the interstellar medium (ISM), or protoplanetary disks, through ion-molecule reactions in the presence of interstellar dust. If this isotopic anomaly has an interstellar origin, this leaves open the possibility for preservation of other isotopic signatures throughout the form ation of the Solar System. The most common form of carbon in the ISM is CO molecules, and there are two potential sources of C-13 fractionation in this reservoir: low temperature chemistry and selective photodissociation. While gas-phase chemistry in cold interstellar clouds preferentially incorporates C-13 into CO [2], the effect of self-shielding in the presence of UV radiation instead leads to a relative enhancement of the more abundant isotopologue, 12CO. Solar System organic material exhibit rather small fluctuations in delta C-13 as compared to delta N-15 and delta D [3][1], the reason for which is still unclear. However, the fact that both C-13 depleted and enhanced material exists could indicate an interstellar origin where the two fractionation processes have both played a part. Formaldehyde (H2CO) is observed in the gas-phase in a wide range of interstellar environments, as well as in cometary comae. It is proposed as an important reactant in the formation of more complex organic molecules in the heated environments around young stars, and formaldehyde polymers have been suggested as the common origin of chondritic insoluable organic matter (IOM) and cometary refractory organic solids [4]. The relatively high gas-phase abundance of H2CO observed in molecular clouds (10(exp- 9) - 10(exp- 8) relative to H2) makes it feasible to observe its less common isotopologues. As a step in our investigation of C-13 fractionation patterns in the ISM, we here present comparisons between observations of the C-13 fraction in formaldehyde, and chemical fractionation models.
Wirstrom, E. S.↗
Nonbiological fractionation of iron isotopes
Laboratory experiments demonstrate that iron isotopes can be chemically fractionated in the absence of biology. Isotopic variations comparable to those seen during microbially mediated reduction of ferrihydrite are observed. Fractionation may occur in aqueous solution during equilibration between inorganic iron complexes. These findings provide insight into the mechanisms of iron isotope fractionation and suggest that nonbiological processes may contribute to iron isotope variations observed in sediments.
NASA Discipline Exobiology↗
The SNC Meteorites Are From Mars
The thirteen SNC meteorites are all igneous rocks, either basalts or basaltic cumulates. They are inferred to be from Mars, based on direct comparison with martian materials and on consistency with inferences about Mars. Most telling is that the SNC meteorites contain traces of gas which is very similar in elemental and isotopic compositions to the modem Martian atmosphere as measured by Viking. The martian atmosphere appears to be unique in the solar system, so its presence in the SNCs is accepted as virtually unequivocal proof that they formed on Mars. Independent of this link, the SNC meteorites must be from a planet with a significant atmosphere because they contain several abundant gas components, some of which carry large isotopic fractionations characteristic of atmospheric processing. The chemical compositions of the SNC meteorites are also consistent with data from in situ analyses of martian soils and rocks, and are quite different from compositions of other meteorites, rocks from the Earth, and rocks from the Moon. The range of formation ages for the SNC meteorites, 4.5 Ga to 0. 18 Ga, is consistent with the varied ages of the Martian surface (based on its cratering record) and inconsistent with surface ages on any other solar system body. The extreme chemical fractionations in the SNC meteorites suggest complex internal processes on a large planet, which is inconsistent with an asteroidal origin. Some SNCs were altered by aqueous solutions at greater than 0.7 Ga, consistent with the recent presence of liquid groundwater in Mars inferred independently from the geology of its surface. There seems little likelihood that the SNCs are not from Mars. If they were from another planetary body, it would have to be substantially identical to Mars as it now is understood.
Treiman, Allan H.↗
Mineral equilibrium in fractionated nebular systems
We investigated the equilibrium mineral assemblages in chemically fractionated nebular systems, using a computer routine that finds the set of minerals and gases which minimizes the Gibbs free energy of a system with stipulated elemental abundances. Diagrams are presented showing the equilibrium mineralogy, as a function of temperature (400-2300 K), for unfractionated solar material and five fractionated systems. The fractionated systems were defined by mixing, in various proportions, the following four volatility components that solar material can be divided into: refractory dust, carbonaceous matter, ices, and H2 gas. Dust enrichment is seen to increase temperatures of condensation/evaporation and the Fe(2+) content of mafic minerals and to permit existence of stable melt phases. Enrichment of dust and organic matter produces mineral assemblages that are similar in many ways to those of enstatite chondrites, but with mafic minerals that are far more reduced than those in primitive enstatite chondrites. Enrichment of dust, organics, and ices leads to highly ferrous mineralogies even at the highest temperatures but does not predict the stability of hydrous phases above about 450 K.
Wood, John A.↗