Alteration in CM carbonaceous chondrites inferred from modal and chemical variations in matrix

The modal abundance of matrix in CM chondrites appears to vary from 57–85 vol%. The concentrations of volatile elements that should occur in matrix remain approximately constant despite differences in the proportions of matrix, suggesting that the differing matrix contents may not be real primary variations but are optical effects due to aqueous alteration processes that make other petrologic components unrecognizable. Apparent matrix content can be used as a qualitative measure of the degree of alteration experienced by each CM chondrite. Fe/Si ratios in matrices decrease progressively with increasing alteration due to the formation of new phyllosilicate phases with higher Mg/Fe ratios and optically recognizable opaque minerals that are not counted as matrix. The aqueous alteration process in CM chondrites appears to have been largely isochemical if the bulk meteorites are considered as the reacting systems, although depletion patterns and isotopic anomalies indicate open-system behavior for a few highly mobile components.     

Solar and meteoritic abundance of silicon

Recent lifetime measurements on excited electronic states of neutral silicon (Beckeret al., Phys. Lett. In press, 1980) lead to a reassessment of widely used experimental transition probabilities Garz, Astron. Astrophys., 26, 471–477, 1973 of Si I lines. This translates into a 25% downward revision of the Si abundance determined from the solar spectrum.A solar atomic ratio, Si/Ca = 15.5 is inferred. This value coincides with that found in carbonaceous chondrites, but contrasts with ordinary and enstatite chondrites.     

Rank of coal beds of the Narragansett basin,Massachusetts and Rhode Island

Coal of the Narragansett basin generally has been considered to be anthracite and/or meta-anthracite. However, no single reliable method has been used to distinguish these two ranks in this basin. Three methods — chemical, X-ray, and petrographic — have been used with some degree of success on coal of the Narragansett basin, but too often the results are in conflict. Chemical methods have been limited by inadequate sampling on a coal-bed-by-coal-bed basis and by a lack of analyses made according to (American Society for Testing and Materials, 1974) standard specifications.In addition, when corrections are made by using the Parr formulas, as required by the ASTM (1974) procedures, the generally high to very high ash content of coal from the Narragansett basin causes the fixed-carbon content to appear higher than it actually is. X-ray methods using the degree of graphitization as a measure of rank are not reliable because some of the graphite is related to shearing and brecciation associated with folding and faulting. Petrographic methods using reflectance on vitrinite give results that are generally consistent with results from chemical determinations. However, it is not clear whether the mean maximum reflectance or mean bireflectance is a better indicator of similar rank of such high-rank coals that have been structurally deformed.Coal from the Cranston Mine, RI, is probably meta-anthracite and coal from the Portsmouth Mine is probably anthracite. These ranks are based on chemical,X-ray, and petrographic data and are supported by associated metamorphic mineral assemblages that indicate that the Cranston Mine is in a higher metamorphic zone than the zone containing the Porthmouth Mine. Interpretation of the rank of Mansfield, MA, coal on the basis of extant chemical data is difficult because it is an impure coal with an ash content of 33 to 50%. Reflectance data indicate that the Mansfield, Foxborough, and Plainville coals in the northern part of the Narragansett basin are meta-anthracite but this is in disagreement with the rank suggested by the low degree of metamorphism of the associated rocks.     

A new type of chondritic meteorite found in lunar soil

A fragment found in soil from the Apollo 12 site (12037, from the rim of Bench Crater) appears to be a unique type of chondrite, petrologically and chemically distinct from other chondrites and lunar rocks. Inclusions consisting of shocked pyroxene rimmed by euhedral troilite crystals are set in a black aphanitic matrix. Abundant magnetite in the matrix exhibits microscopic morphologies (framboids and plaquets) characteristic of C1 chondrites. The bulk composition of this sample has high Mg/Si and low Fe/Si relative to other chondrites, and P and S are strongly enriched. Most compositional differences between this meteorite and other chondrites may be explained by fractionation of Fe phases, such as magnetite and troilite. Low refractory element contents preclude mixing with lunar materials. This sample may be a surviving fragment of the meteoritic component present in the lunar regolith. Its characteristics suggest that ancient meteoritic debris sampled by the moon may be significantly different from that captured by the present-day earth.     

Resolving climate change in the period 15–23 ka in Greenland ice cores: a new application of spectral trend analysis

Northern Hemisphere climate history through and following the Last Glacial Maximum is recorded in detail in ice cores from Greenland. However, the period between Greenland Interstadials 1 and 2 (15–23 ka), i.e. the period of deglaciation following the last major glaciation, has been difficult to resolve in great detail. We here offer a new subdivision of this in the NGRIP, GRIP and GISP2 ice cores, by newly introducing spectral trend analysis to the study of climate-related data series from ice cores. This analysis reveals patterns of change and discontinuity in the waveform properties of a data series, relating to the environmental (including climatic) history of accumulation of the rock or ice record. The application allows high-resolution correlation between the ice cores, and a greatly improved subdivision of the study interval. Nine climatic phases are recognized, within which more identifiable events can also be correlated between the three locations.     

MIL 03443, a dunite from asteroid 4 Vesta: Evidence for its classification and cumulate origin

Abstract– The absence of dunite (>90 vol% olivine) in the howardite, eucrite, and diogenite (HED) meteorite suite, when viewed with respect to spectroscopic and petrologic evidence for olivine on Vesta, is problematic. Herein, we present petrologic, geochemical, and isotopic evidence confirming that Miller Range (MIL) 03443, containing 91 vol% olivine, should be classified with the HED clan rather than with mesosiderites. Similarities in olivine and pyroxene FeO/MnO ratios, mineral compositions, and unusual mineral inclusions between MIL 03443 and the diogenites support their formation on a common parent body. This hypothesis is bolstered by oxygen isotopic and bulk geochemical data. Beyond evidence for its reclassification, we present observations and interpretations that MIL 03443 is probably a crustal cumulate rock like the diogenites, rather than a sample of the Vestan mantle.