On the chondrite—achondrite transition: mineralogy and chemistry of Yamato 74160 (LL7)

We report on the petrology, mineralogic properties and contents of major elements and trace elements Ag, Au, Bi, Cd, Co, Cs, Ga, In, Rb, Se, Te, Tl, U and Zn (determined by radiochemical neutron activation analysis) in Yamato 74160, interpreted as an LL7 chondrite. All properties are consistent with this meteorite having been recrystallized and partially melted locally once at temperatures well above 1090°C under conditions such that some minerals (e.g. plagioclase, euhedral pyroxene, tetrataenite) grew from melt pockets and siderophilic and chalcophilic elements were lost by extraction into eutectic melt that drained away. Inhomogeneous plagioclase compositions and mobile element loss suggest shock as the most likely heat source. Yamato 74160, while inferentially chondritic, is a larval achondrite: even higher temperatures and longer times would have been required to cause the separations necessary to transform it to an identifiable achondrite type.     

Particulate pollution monitoring in the Elefsis Gulf: The role of mineral magnetic studies

Measurements of ‘quadrature’ susceptibility (X_q) at low and high frequency on seabottom sediments of the Gulf of Elefsis supplement the results derived from the study of magnetic susceptibility (X) and saturation isothermal remanent magnetization (SIRM) (Scoullos et al., 1979) and make possible the distinction between the background soil erosional fraction and that of anthropogenic combustion origin. New devices speed up the on-site appraisal of the impact of discharges on marine sediment quality.     

Abundance of Boron in International Geochemical Standards by Prompt-Gamma Neutron Activation Analysis

Eighteen international reference standards, mostly geochemical standards, have been analysed for boron using prompt-gamma neutron activation analysis (PGNAA). There is good agreement between the results for samples with high boron abundances and the few published values using PGNAA and other methods. However, correlation is poor at low boron abundances, especially in those standards with low boron/sodium ratios. Corrections for sodium interference on boron have been critically evaluated and the data corrected using two different methods.     

Mechanism of continental crust subsidence in the Alpine Belt

Formation of deep basins on continental crust in fold belts is often explained by stretching. This mechanism inevitably produces large deformations in the upper crust. No deformations typical of significant stretching were revealed in the predominant part of deep basins on continental crust in the Alpine Belt. This means that these basins were not produced by stretching. Most basins were formed during a short period of time of a few million years. The short duration of the subsidences eliminates thermal relaxation as the mechanism. The space and time relationships between the subsidence and orogeny and the profile of the basin floor exclude thrust loading as a cause of formation for practically all large basins. Gabbro to eclogite transformation is suggested as a mechanism of rapid subsidence. This occurs under the upwelling of hydrous asthenosphere at moderate temperature to the base of the crust. Eclogite sinking into the mantle results in a strong attenuation of the crust and lithosphere, which permits intense subsequent folding. The major part of deep basins in continental crust that formed by rapid subsidence was intensely shortened in the Alpine Belt. Significant crustal shortening did not spread over the cratonic lithosphere.     

Structure and viscosity of rhyolitic composition melts

The average local structure of a rhyolitic composition glass has been determined at 25°C using X-ray radial distribution analysis (RDA) and quasi-crystalline modelling and is best described as similar to that in a stuffed framework composed principally of six-membered rings of Si and Al tetrahedra (basically a stuffed tridymite-like model). Using this model it is possible to calculate a density (2.41 g/cm³) which compares well with the measured density (2.40 g/cm³); a structural model based on four-membered rings (an albite-like model) results in a substantially higher calculated density (2.60 g/cm³). We suggest that the rhyolite glass structural model is appropriate for rhyolitic melts, based on evidence from the recent literature. New viscosity data for an anhydrous rhyolite composition measured between 1200°C and 1500°C are presented and interpreted in terms of our proposed structural model and previous melt structure models for the major normative components of rhyolite. A mechanism for diffusion and viscous flow in framework silicate melts (including rhyolite composition) is proposed on the basis of recent molecular orbital calculations and molecular dynamics simulations of silicate and fluoride melts.     

Structure proof and significance of stereoisomeric 28,30-bisnorhopanes in petroleum and petroleum source rocks

Two C₂₈H₄₈-pentacyclic triterpanes were isolated from Monterey shale. X-ray crystallography of a crystal containing both compounds proved their structures as 17β,18α,21α(H)-28,30-bisnorhopane and 17β,18α,21β(H)-28,30-bisnorhopane. Several differences are found between 28,30-bisnorhopanes and the regular hopanes. Unlike the regular hopane epimers, for practical purposes the three epimeric 28,30-bisnorhopanes [17α,21β(H)-, 17β,21α(H)-, and 17β,21β(H)-]cannot be distinguished by their mass spectra. Special conditions are needed to separate them by gas chromatography. The diagenetically first-formed epimer is thought to be 17α,21β(H)- because it predominates in immature shales. The order of thermodynamic stability is 17β,2lα(H) < > 17α,21β(H) > 17β,21β(H), and all three epimers are present in petroleum. 25,28,30-Trisnorhopanes can be analyzed in similar fashion and are found to have similar thermodynamic characteristics. The percent of the ring D/E cis epimer of 28,30-bisnorhopane and/or 25,28,30-trisnorhopane is a useful maturation parameter similar to the 20S/20R sterane ratio. Evidence indicates 25-demethylation of 28,30-bisnorhopane to 25,28,30-trisnorhopane during advanced stages of biodegradation. Hence, percent ring $\text{D}\text{E}$cis 25,28,30-trisnorhopane has an application to maturation assessment in heavily biodegraded oils.     

Nitrogen and carbon isotopic composition of bone collagen from marine and terrestrial animals

The stable nitrogen and carbon isotope ratios of bone collagen prepared from more than 100 animals representing 66 species of birds, fish, and mammals are presented. The δ¹⁵N values of bone collagen from animals that fed exclusively in the marine environment are, on average, 9%. more positive than those from animals that fed exclusively in the terrestrial environment; ranges for the two groups overlap by less than 1%. Bone collagen δ¹⁵N values also serve to separate marine fish from the small number of freshwater fish we analyzed. The bone collagen δ¹⁵N values of birds and fish that spent part of their life cycles feeding in the marine environment and part in the freshwater environment are intermediate between those of animals that fed exclusively in one or the other system. Further, animals that fed at successive trophic levels in the marine and terrestrial environment are separated, on average, by a 3%. difference in the δ¹⁵N values of their bone collagen. Specifically, carnivorous and herbivorous terrestrial animals have mean δ¹⁵N values for bone collagen of + 8.0 and + 5.3%., respectively. Among marine animals, those that fed on fish have a mean δ¹⁵N value for bone collagen of + 16.5%., whereas those that fed on invertebrates have a mean δ¹⁵N value of + 13.3%. These results support previous suggestions of a 3%. enrichment in δ¹⁵N values at each successively higher trophic level. In contrast to the results for δ¹⁵N values, the ranges of bone collagen δ¹³C values from marine and terrestrial feeders overlap to a great extent. Additionally, bone collagen δ¹³C values do not reflect the trophic levels at which the animals fed. These results indicate that bone collagen δ¹⁵N values will be useful in determining relative dependence on marine and terrestrial food sources and in investigating trophic level relationships among different animal species within an ecosystem. This approach should be applicable to animals represented by prehistoric or fossilized bone in which collagen is preserved.     

Fossil mammoths from Santa Cruz Island, California

Mammoth remains on Santa Cruz Island, one of the four Northern Channel Islands of California, are very sparse, in marked contrast to those reported from Santa Rosa and San Miguel Islands of the same island group. A probable major reason for this scarcity is that Quaternary deposits are greatly restricted on Santa Cruz Island. It is proposed, contrary to popular opinion, that fossils found on Santa Cruz Island were derived from animals which died on the island, and were not transported there by humans. Reasons for this conclusion are that the size and geological context of the fossils are similar to those of the largest mammoth fossils of Santa Rosa Island, and that, in spite of extensive investigations by many persons, mammoth remains have not been found in middens, either on the islands or on the adjacent mainland.     

Volatile contents of phlogopite micas from South African kimberlite

Phlogopite micas from nodules in South African kimberlites were analyzed for major elements with the electron microprobe and for volatile contents by high temperature mass spectrometry. The micas are from primary- (deformed) and secondary- (undeformed) textured grains in perodotite xenoliths, glimmerites, MARID (mica-amphibole-rutile-ilmenite-diopside) suite nodules and a mica megacryst. The major element and volatile contents of micas exhibiting these modes of occurrence overlap to a greater extent than indicated in previous studies. Concentrations of volatile species occupying structurally defined crystallographic sites (H₂O, F, Cl) are greater for many of the micas than predicted on the basis of the mica formula, particularly for the glimmerite and MARID suite samples. A correlation exists between micas with tetrahedral and octahedral cation deficiencies and those with excess H₂O, F and Cl. Substitution of H⁺ for tetrahedral and possibly octahedral cations may be responsible for the excess H₂O in these micas. Except for one sample, the major element and volatile data for the peridotite, glimmerite and MARID suite micas indicate that they crystallized at oxygen fugacities below the quartz-fayalite-magnetite buffer. F and K₂O are in the correct proportion in the micas to provide the source for these elements in alkali basalts, but not in mid-ocean ridge basalts. Kaersutite amphibole is a more likely source of potassium and fluorine in mid-ocean ridge basalts.