Dating of marine aragonite by electron spin resonance

Marine aragonite, in the form of corals and/or shells, provides useful markers of geological and archaeological events. It is, therefore, important to have simple and accurate methods of dating these materials. Electron spin resonance (ESR) has previously been shown to be a reliable method for establishing the age of aragonitic coral samples in the time period approximately 100 ka B.P. The primary purpose of the present work is to discuss the problems encountered in extending this method to considerably older samples, up to 600 ka BP in age. In this time period there are questions about the stability of the ESR signal. The samples investigated are aragonitic corals from reef terraces of Barbados, West Indies, all of which have previously been dated by the methods, and by U-series disequilibrium, for samples below the limit of this method. There is generally good agreement for samples up to about 300 ka in age; older samples, even unrecrystallized, appear younger when dated by ESR than by . The source of this discrepancy is not clear. The explanation of thermal fading is not adequate. However, it appears likely that in most cases ESR will be able to be used to date materials up to this age. Further investigation is needed to determine tests that will distinguish datable samples from non-datable ones.     

Infrared spectroscopic investigation of hydroxyl in β-(Mg,Fe)2SiO4 and coexisting olivine: Implications for mantle evolution and dynamics

Wadsleyite (β-(Mg,Fe)₂SiO₄) is a major constituent of the Earth's transition zone and is known to accommodate OH. The portion of the transition zone between 400–550 km could be an important source or sink for hydroxyl in plumes and slabs intersecting this region. Micro-infrared spectroscopy has been carried out on the β-phase and coexisting metastable olivine synthesized in a multianvil apparatus at 14 GPa and 1550–1650 K under hydrous conditions. Single-crystal and polycrystal specimens of both phases were analyzed in the 1800–8500 cm^?1 frequency region to determine the speciation, abundances, and partitioning behavior of the hydrous components in coexisting β-phase and olivine. β-phase spectra consistently show three distinct OH bands at 3329, 3580, and 3615 cm^?1. OH concentrations range from 10000–65000 H/10⁶ Si. A strong positive correlation of grain size and extent of transformation with OH concentration in the β-phase indicates that grain-growth and transformation rates are enhanced in a hydrous environment. Olivine spectra are variable, but consistently show a prominent broad-band absorbance representing molecular H₂O, consistent with the infrared signature of the starting material. OH concentrations in olivine range from <300–1400 H/10⁶ Si. The highest OH concentrations measured for olivine and the β-phase may represent solubility limits, in which case the OH solubility ratio between these two phases is approximately 1∶40. Where both phases coexist and are undersaturated with OH, the partitioning ratio of OH between them is about 1∶100. The large solubility contrast between olivine and the β-phase suggests a mechanism for hydrating the transition zone via olivine carried down in subducting slabs. Plumes impinging on an OH-rich upper transition region could cause H₂ or H₂O to be released upon transformation of the β-phase to olivine, resulting in initiation of secondary upwellings. If dissolution of OH weakens the β-phase, and if OH is present in the mantle, the region between 400–550 km could be a zone of low viscosity.     

Genetic structure of bay anchovy (Anchoa mitchilli) populations in Chesapeake Bay

To determine the genetic structure of the bay anchovy (Anchoa mitchilli) within Chesapeake Bay, 16 isozyme systems encoding 21 loci for 20 population were examined using horizontal starch gel electrophoresis. Contingency Chisquare analysis revealed significant allelic frequency differences at nine loci (AAT-1, AAT-2, ALD-1, CPK-2, GAP-1, GLY-1, LDH-1, MDH-1, and MDH-2). Two loci, ALD-1 and MDH-1, were responsible for nine of 14 tests not conforming to Hardy-Weinberg expectations, with some of these deviations attributed to possible scoring and/or sampling error. Estimates for mean average heterozygosity were relatively high, ranging from 0.40 to 0.096, with 33–57% of the loci polymorphic. A low F_st value (0.041) along with high genetic identity estimates (I=0.997) indicated little substructuring of bay anchovy populations within Chesapeake Bay.     

H-chondrites: Trace element clues to their origin

We have analyzed 10 H-chondrites for 20 trace elements, using RNAA. The meteorites included 4 of petrologic type 4 and 2 each of types 3, 5 and 6.The data show that H-chondrites are not isochemical. H3's are depleted by some 10% not only in Fe (Dodd, 1976), but also in the siderophiles Os, Re, Ir, Ni, Pd, Au, and Ge. Moreover, the abundance pattern of siderophiles varies systematically with petrologic type. As similar fractionations of REE have been observed by Nakamura (1974), it appears that both the proportions and compositions of the main nebular condensates varied slightly during accretion of the H-chondrites. Thus the higher petrologic types are independent nebular products, not metamorphosed descendants of lower petrologic types.Abundances of highly volatile elements (Cs, Br, Bi, Tl, In, Cd, Ar³⁶) correlate with petrologic type, declining by ≤ 10^?3 from Type 3 to Type 6. The trends differ from those for artificially heated Type 3's (Ikramuddinet al., 1977b; Herzoget al., 1979), but agree passably with theoretical curves for nebular condensation. Apparently the low volatile contents of higher petrologic types are a primary feature, not the result of metamorphic loss.The mineralogy of chondrites suggests that they accreted between 405 K (absence of Fe₃O₄) and 560 K (presence of FeS), and the abundances of Tl, Bi, and In further restrict this interval to 420–500 K. Accretion at 1070 ± 100 K, as proposed by Hutchisonet al. (1979, 1980), leads to some extraordinary problems. Volatiles must be injected into the parent body after cooling, which requires permeation of the body by 10¹¹ times its volume of nebular gas. This process must also achieve a uniform distribution of the less volatile elements (Rb, Cu, Ag, Zn, Ga, Ge, Sn, Sb, Se, F), without freezeout in the colder outer layers.Factor analysis of our data shows 3 groupings: siderophiles (Os, Re, Ir, Ni, Pd, Au, and Ge), volatiles (Ag, Br, In, Cd, Bi, and Tl) and alkalis (Rb and Cs). The remaining 5 elements (U, Zn, Te, Se, and Sb) remain unassociated.     

Thermal regime of the continental lithosphere

Thermally, the lithosphere may be defined as that outer portion of the earth in which heat is transferred primarily by conduction. It generally includes the crust and part of the mantle. The thermal regime of continental lithosphere is determined by many factors including heat flow from the asthenosphere, the vertical and lateral variation of both thermal conductivity and radiogenic heat production, tectonic history, and such superficial processes as climatic history and the shallow hydrothermal regime. From studies of the global heat flow data set, two generalizations regarding continental lithosphere have arisen, namely that: 1) there is a negative correlation between heat flow and tectonic age of continental lithosphere; and 2) the thermal evolution of continental lithosphere is similar to that of ocean basins with the result that the “stable geotherm” is similar in both environments. When continental heat-flow data are studied from a regional rather than a global point of view, considerable doubt arises as to the general applicability of either statement. R. U. M. Rao and his associates have demonstrated that while Precambrian terranes do have demonstrably lower heat flows than, say, Tertiary terranes, the data are not normally distributed and it is not possible to establish a negative correlation between heat flow and age in any rigorous statistical way. The scatter in the relation may be explained in terms of the variations in the duration, intensity and even the sign of continental thermotectonic events in contrast to the simple situation (creation of new oceanic lithosphere at mid-ocean ridges) which prevails in the oceans. The scatter also is partially attributable to the large and laterally variable radiogenic component of heat flow on continents. For a province for which a heat flow-heat production relation has been established, much of the scatter in surface heat flow due to crustal radiogenic heat production versus age is eliminated by determining reduced heat flow (surface heat flow minus radiogenic component) as a function of tectonic age, but much scatter remains, and it is still not possible to establish a heat flux-age relation in a rigorous way. Primarily because of the spatial variability in radiogenic heat production, no single geotherm can be used to characterize the thermal regime of a stable continental terrane. Thus, while some sites on stable continental blocks may have a geotherm fortuitously similar to that for old ocean basins, there is no reason to expect that this will be true generally, and many stable continental terranes will be characterized by geotherms markedly different from the geotherm for old ocean basins.     

High-Pressure crystal chemistry of spinel (MgAl2O4) and magnetite (Fe3O4): Comparisons with silicate spinels

High-pressure crystal structures and compressibilities have been determined by x-ray methods for MgAl₂O₄ spinel and its isomorph magnetite, Fe₃O₄. The measured bulk moduli, K, of spinel and magnetite (assuming K′=4) are 1.94±0.06 and 1.86±0.05 Mbar, respectively, in accord with previous ultrasonic determinations. The oxygen u parameter, the only variable atomic position coordinate in the spinel structure (Fd3m, Z=8), decreases with pressure in MgAl₂O₄, thus indicating that the magnesium tetrahedron is more compressible than the aluminum octahedron. In magnetite the u parameter is unchanged, and both tetrahedron and octahedron display the 1.9 Mbar bulk modulus characteristic of the entire crystal. This behavior contrasts with that of nickel silicate spinel (γ-Ni₂SiO₄), in which the u parameter increases with pressure because the silicon tetrahedron is relatively incompressible compared to the nickel octahedron.     

A study of intergranular and fissure permeability in Chalk and Permian aquifers,using double-packer injection testing

Double-packer injection tests have been carried out in a borehole in the Chalk of Hampshire and a borehole in the Permian Penrith Sandstone of Cumbria, England. The tests have been supplemented by borehole logging and television inspections and by laboratory measurements on cores. A new mathematical treatment has enabled results to be calculated for injection test intervals containing fissures. In both formations, transmissivity immediately around the borehole is dominated by a few major fissures. In the Penrith Sandstone there is good agreement between intergranular hydraulic conductivity measurements and packer-test results in the portions of the borehole which do not contain major fissures. In the Chalk, the packer-test values are always higher than the intergranular measurements, suggesting that some degree of fissuring is present throughout.