Engineering topics
Publications and source records attributed to Anders, E..
Within the accuracy of present data, elements of intermediate volatility (condensation temperatures between about 1100 and 600 K) do not show a correlation of abundance with volatility in equilibrated ordinary chondrites. There is no need to postulate continuous loss of gas during condensation.
The Ibitira eucrite is remarkable both for its vesicles and its unbrecciated nature. It consists of nearly 63 vol.% pyroxene (Wo14En38Fs48), 31% plagioclase (An95-96), nearly 2% of nickel-iron, troilite, ilmenite, titanian chromite, and 4% of a silica polymorph. It has a mean track density of 1.8 plus or minus 0.3 x 1,000,000 per sq cm, mainly due to cosmic rays. Its pre-atmospheric radius must have been at least 10 cm. The absence of complex radiation effects and presence of vesicles place constraints on the thickness of the Ibitira basalt flow. From the freezing time calculations of Provost and Bottinga, it appears that Ibitira came from a flow no less than 2.5 m and probably no more than 10 or 20 m thick. However, this estimate depends strongly on the viscosity of the melt, which is not well known.
A reply is made to previous criticisms of the claim that the range of accretion of ordinary chondrites can be narrowed to 500-420 K (from 560-405 K) using volatile metals as cosmothermometers. Questions concerning uncertainties in vapor pressure data, entropy of mixing, methods of analysis, uncertainties in condensation curves, metamorphic transport, alloy formation, condensation of Tl, condensation of In, and concordance with other thermometers (FeO contents of silicates) are addressed. It is concluded that the original claim is valid.
Two samples of the Murchinson C2 chondrite were analyzed for organic nitrogen compounds, using mass spectrometry in combination with paper and thin-layer chromatography. Under mild extraction conditions (water or formic acid), only alphatic amines and some alkylpyridines were seen. Drastic extraction conditions (hot 3-6 M HCL) a variety of nitrogen compounds appeared, including adenine (15 ppm), guanine (5ppm), melamine (20 ppm), cyanuric acid (20 to 30 ppm), guanylurea (30 to 45 ppm), and urea (25 ppm). It appears that these compounds are present mainly in macromolecular material. Failure of other investigators to identify these compounds in carboneceous chondrites is attributed to inadequate extraction conditions (water and formic acid rather than HCl).
The solar gas content of stony meteorites is used to determine their place of origin. The inert gas content and surface exposure age of meteorites and lunar regolith samples are compared, and the results suggest that gas implantation took place between 1 and 8 AU from the sun, i.e., in the asteroid belt. The prevalence of gas-rich meteorites is cited to indicate that the parent body must remain in the asteroid belt long enough to develop a substantial regolith, a condition which can be met by asteroids, but not by short period comets. It is concluded that all stony meteorite classes with gas-rich members, including carbonaceous chondrites, originated in asteroidal material.
Mineral separates from five carbonaceous chondrites were dated by extinct 16 million year I-129, in an attempt to establish the condensation time of the solar nebula. Two Fe3O4 or Fe3O4-FeS samples from the Murchison and Orgueil meteorites are older than any other material dated thus far, and apparently formed within 200,000 years of each other. The great age, close isochronism, and primitive nature of the samples suggest that the event recorded was the condensation stage of the solar nebula. It provides a suitable zero point for the chronology of the early solar system. The I-129/I-127 ratio during condensation of the nebula was (1.46 plus or minus 0.04) times 0.0001. The recrystallized C4 chondrite Karoonda began to retain Xe-129 1.8 plus or minus 0.5 million years after the above event. This short cooling time implies rapid accretion (not exceeding 1 million years) and a shallow origin (not exceeding 10 km) below the surface of its parent body.-
A description is presented of the preliminary results of interdisciplinary studies of matrix samples. The significance of the 73215 studies is considered and the relationship of 73215 to other Apollo 17 highland breccias is discussed. According to a tentative hypothesis 73215 is an aggregate of fragments plus melt generated in a very large impact, possibly the Serenitatis basin-forming event. If this is correct, studies of this sample will make it possible to date the Serenitatis event and will provide an insight into the breccia-forming processes associated with such events. Studies of the clasts in the breccia will provide an opportunity to formulate a partial characterization of the preimpact source terrain. An investigation of the deep lunar crust might perhaps also be possible.
In the reported studies of meteoritic material on the moon an attempt was made to characterize the nature of the projectile from the abundance pattern of certain diagnostic trace elements, such as Ir, Re, Ni, Au, Ge, Sb, and Bi. Analyses were conducted of 47 samples from 4 terrestrial meteorite craters. The main object in the investigation was to show that the nature of the projectile could be reliably inferred from the trace-element pattern of the ejecta. In this connection material was analyzed from two terrestrial craters where the projectile itself was known. A second objective was to characterize the projectile at two craters where no discrete meteoritic fragments had been found.
A stepwise heating technique was used to analyze eight silicate samples from the Orgueil carbonaceous chondrite for He, Ne, Ar, and Xe. Six samples, of which two were etched with NaOH, were density fractions. The other two samples were grain-size fractions separated according to their ability to form a colloid at pH 11.5. Results showed the LiCl separation procedure to be gentler than the NaOH procedure. All fractions were found to be deficient in cosmogenic neon. Above 950 C the fractions gave low 20Ne/22Ne ratios particularly in the low-density and noncolloidal fraction. Compared to the other fractions the fraction from 2.35 to 2.45 g/cu cm contained less Xe and released it more rapidly at low temperatures.
To determine the compound distribution formed by surface catalysis, mixtures of CO, D2, and ND2 were heated with nickel-iron or montmorillonite clay catalysts for 49-214 hours at 250 to 300 C. Compounds identified include most of the known polyatomic interstellar molecules, as well as homologous series of acetylenes, dienes, alcohols, aldehydes, ketones, ethers, esters, nitriles, amines, etc., and cyclic compounds such as furans and pyrroles. These homologous series are uniquely characteristic of surface catalysis. A search for the heavier members of these series, predicted to occur at 1/10th to 1/1,000th the abundance of the lightest members, thus comprises a crucial test of this mechanism.
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Of six samples from boulder 1 at Station 2, four contain a unique meteoritic component, which is attributed to the Crisium projectile. The other two samples are meteorite free, igneous rocks: an unusual, alkali- and Ge-rich pigeonitic basalt, and an alkali-poor norite of unexceptional trace element chemistry.
Micrometeorites, ancient planetesimal debris from the early intense bombardment, and debris of recent, crater-forming projectiles are discussed and their amounts and compositions have been determined from trace element studies. The micrometeorite component is uniformly distrubuted over the entire lunar surface, but is seen most clearly in mare soils whereas, the ancient component is seen in highland breccias and soils. A few properties of the basin-forming objects are inferred from the trace element data. An attempt is made to reconstruct the bombardment history of the moon from the observation that only basin-forming objects fell on the moon after crustal differentiation. The apparent half-life of basin-forming bodies is close to the calculated value for earth-crossing planetesimals. It is shown that a gap in radiometric ages is expected between the Imbrium and Nectaris impacts, because all 7 basins formed in this interval lie on the farside or east limb.
The present work calculates the bulk compositions of the earth and moon, based on the assumption that these planets formed by the same processes as chondrites. In terms of the model presented, the earth contains 9.2% early condensate and 1.5% carbonaceous, volatile-rich silicate. For the moon these percentages are 30.1 and 0.04, respectively. When lunar and terrestrial basalt data are normalized to these model compositions, element abundance patterns based on the percentages (assuming that each component carried its cosmic complement of trace elements) demonstrate the essential identity of igneous processes on both celestial bodies.
Recent evidence from two sources provides a basis for a reexamination of the relationship between the stratigraphy at the Apollo 16 site and the trace element distribution. Information concerning the surface exposure ages makes it possible to relate many samples to specific local impact events. At least five ancient meteoritic components have been tentatively assigned to individual basin-forming impacts on the basis of trace element analyses of Apollo 17 rocks. Attention is given to a petrographic examination of separates from two soils from Station 11 (North Ray Crater).
The ancient meteoritic components are considered, taking into account the significance of high siderophile abundances in highland rocks. Because this component occurs in breccias which have remained closed systems for at least 3.9 aeons, it can properly be called an ancient meteoritic component. It appears that the ancient meteoritic bodies represent a distinct population, different from present-day meteorites. Attention is given to the assignment of the lunar meteorite groups to individual basins and to the origin of basin-forming objects.
The problem of whether organic compounds originated in meteorites as a primary condensate from a solar gas or whether they were introduced as a secondary product into the meteorite during its residence in a parent body is examined by initially attempting to reconstruct the physical conditions during condensation (temperature, pressure, time) from clues in the inorganic matrix of the meteorite. The condensation behavior of carbon under these conditions is then analyzed on the basis of thermodynamic calculations, and compounds synthesized in model experiments on the condensation of carbon are compared with those actually found in meteorites. Organic compounds in meteorites seem to have formed by catalytic reactions of carbon monoxide, hydrogen, and ammonia in the solar nebula at 360 to 400 K temperature and about 3 to 7.6 microtorr pressure. The onset of these reactions was triggered by the formation of suitable catalysts (magnetite, hydrated silicates) at these temperatures.
Three types of meteoritic material are found on the moon: micrometeorites, ancient planetesimal debris from the 'early intense bombardment,' and debris of recent, crater-forming projectiles. Their amounts and compositions have been determined from trace element studies. The micrometeorite component is uniformly distributed over the entire lunar surface, but is seen most clearly in mare soils. It has a primitive, Cl-chondrite-like composition, and comprises 1-1.5% of mature soils. The ancient component is seen in highland breccias and soils more than 3.9 AE old. It has a fractionated composition, with volatiles depleted relative to siderophiles. The abundance pattern does not match that of any known meteorite class. The crater-forming component has remained elusive. Only a possible hint of this component has been seen, in ejecta from Dune Crater and Apollo 12 KREEP glasses of possibly Copernican origin.