Further 40Ar39Ar evidence for the multi-collisional heating of the Kirin chondrite

Results of an ${}^{40}\text{Ar}{}^{39}\text{Ar}$Ar age spectrum obtained on a sample of the Kirin chondrite (K-5-13) show a similar character to previous published analyses of Kirin samples K-1 and K-2. The K-5-13 age spectrum shows clear evidence of having been substantially outgassed during a presumed collisional event about 0.5 Ga, ago, in good agreement with the estimate obtained from K-2, The differing amounts of ⁴⁰Ar loss registered by K-2 and K-5-13 during the 0.5 Ga event of about 60 and 50%, respectively, allows calculation of their vertical separation in the parent body at about 10cm.     

Stable carbon isotope ratio variations of organic matter in Orca Basin sediments

Orca Basin is a highly reducing basin on the slope of the Gulf of Mexico. Stable carbon isotope ratios and total organic carbon percentages were determined for two cores within the basin and one control core outside the basin. The results show that the organic carbon content of the basin cores is consistently 2–3 times greater than that of the control core. The Pleistocene-Holocene boundary, indicated by a break in the δ¹³C depth profile, occurs at a greater sediment depth in the basin cores than in the control core. A small sampling interval has made it possible to detect an unexplained fine structure in the δ¹³C profile not previously observed.     

Petrology and geochemistry of the island of Sarigan in the Mariana arc; calc-alkaline volcanism in an oceanic setting

Isotopic studies of rocks from oceanic island arcs such as the Marianas indicate that little, if any, recycling of continental material (e.g. oceanic sediments) occurs in these arcs. Because oceanic arcs are on the average more mafic than the dominantly andesitic continental arcs, an important question is whether the andesites of continental arcs are produced by a fundamentally different (more complex?) mechanism than the lavas of oceanic arcs. An excellent opportunity for study of this question is provided by the island of Sarigan, in the Mariana active arc, on which calc-alkaline andesites (including hornblende-bearing types) are exposed along with more mafic lavas. Available isotope data suggest the Sarigan lavas (including the andesites) were derived from mantle material with little or no involvement of continental components. Ratios of incompatible elements suggest that most of the Sarigan lavas were derived from similar source materials. Absolute abundances of incompatible elements vary irregularly within the eruptive sequence and indicate at least 5 distinct magma batches are represented on Sarigan. Major element data obtained on the lavas and mineral phases in them, combined with modal mineral abundances, suggest that the calc-alkaline nature of the volcanic rocks on Sarigan results from the fractional crystallization of titanomagnetite in combination with other anhydrous phases. Amphibole, although present in some samples, is mainly a late-crystallizing phase and did not produce the calc-alkline characteristics of these lavas. Gabbroic samples found in the volcanic sequence have mineralogc and geochemical characteristics that would be expected of residual solids produced during fractional crystallization of the Sarigan lavas. When combined, data on the lavas and the gabbros suggest the following crystallization sequence: olivine — plagioclase — clinopyroxene — titanomagnetite — orthopyroxene±hornblende, biotite and accessory phases. These results lead to the conclusion that calc-alkaline magmas can be generated directly from mantle sources.     

Investigations of an intrusive contact,northwest Nelson,New Zealand—I. Thermal,chronological and isotopic constraints

In the Nelson area of New Zealand, intrusion of the Separation Point Batholith 114 Ma ago caused thermal metamorphism in the adjacent Devonian Rameka Gabbro that allowed radiogenic ⁴⁰Ar to diffuse partially out of hornblendes in the gabbro.Comparison of mineral ages in the batholith (obtained by the K-Ar, ${}^{40}\text{Ar}{}^{39}\text{Ar}$, Rb-Sr, U-Pb and fission track methods) with closure temperature estimates for the various isotopic systems has allowed thermal histories of several samples to be resolved. These curves indicate that, following emplacement, the batholith cooled at an exponentially decreasing rate reaching 100°C by about 75 Ma ago.Oxygen isotope measurements on minerals from the gabbro and granodiorite give calculated equilibrium water compositions of +7 and +9 of δ¹⁸O_SMOW respectively. Measured porosities from samples of the gabbro yield a model permeability of 3 × 10^?17 m¹². These results confirm that heat transfer from the batholith to the gabbro was predominantly by conduction. A numerical heat flow model has been developed for the region, and shows that samples in the gabbro near the contact reached ~600°C. whereas 5 km away from the contact, the samples were only raised ~ 50°C above the ambient temperature.Excess ⁴⁰Ar was identified as causing a significant scatter in the K-Ar ages of hornblendes from the gabbro. Though obscured by this effect, these data suggest a crystallization age of the Rameka Gabbro of 367 Ma, which is consistent with geological evidence.     

1H and 13C NMR of marine humic acids

¹³C and ¹H NMR spectra were obtained for humic acids isolated from marine sediments. NMR shows great promise in identifying structural components of humic acids as some new and interesting structural features are identified. Aliphatic structures were found to constitute a much larger fraction of humic acids than previously thought, and they appeared to be highly branched. Although the aromatic content of terrestrial humic acid was found to be lower than expected, the aromaticity appears to be a specific discriminator of terrestrial/aquatic source types. A humic acid isolated from an anoxic algal sapropel was found to be composed predominantly of polyuronic acids and different than other aquatic sedimentary humic substances.     

Pacific Pleistocene paleoclimatic stratigraphies: A comparative analysis of results

Global atmospheric and oceanic circulation effects of expansion of continental ice sheets initiated upwelling in the western equatorial Pacific and simultaneously intensified upwelling in the eastern equatorial Pacific; contraction of the ice sheets reversed the process. Published Pleistocene paleoclimatic stratigraphies correlated across the entire equatorial Pacific exhibit eight such cycles in the Brünhes epoch. The extrapolated chronostratigraphies for the equatorial Pacific compare favorably with published paleoclimatic schemes for the southeastern, eastern, and northern Pacific Ocean. The Southern Ocean record exhibits fewer, and possibly also consistently older, climatic variations. A time progression or lack of synchrony of marine Pleistocene climatic events is not inconsistent with modified “Milankovitch” hypotheses, such as that involving Antarctic ice-sheet instability.     

40Ar/39Ar age and thermal history of the Kirin chondrite

The Kirin meteorite, a large (2800kg) H5 chondrite, fell in Kirin Province, China in 1976. A sample from each of the two largest fragments (K-1, K-2) yield⁴⁰Ar/³⁹Ar total fusion ages of 3.63 ± 0.02b.y. and 2.78 ± 0.02b.y. respectively.⁴⁰Ar/³⁹Ar age spectra show typical diffusional argon loss profiles. Maximum apparent ages of 4.36 b.y. (K-1) and ～4.0 b.y. (K-2) are interpreted as possible minimum estimates for the age of crystallization of the parent body.The⁴⁰Ar/³⁹Ar ages found for gas released at low temperature are about 2.2 b.y. for K-1 and about 0.5 b.y. for K-2, suggesting that this meteorite may have suffered two discrete collisional events that caused degassing of radiogenic argon. Modelling of possible thermal events in the parent body indicates that samples K-1 and K-2 were at a depth of less than 3 m from the base of an impact melt of a thickness less than 7 m and separated by no more than ～2 m from one another at the time of the heating event about 0.5 b.y. ago. Further, the duration of heating was probably less than a few years.Calculations from³⁸Ar data yield exposure ages for samples K-1 and K-2 of about 5 m.y., similar to that found for many other H chondrites.     

Arma models for earthquake ground motions

This paper outlines the use of discrete, autoregressive/moving-average (ARMA) models for identification and estimation of parameters in models derived from analysis of uniformly digitized earthquake ground motion acceleration data. Such models are of equal generality as compared to continuous-time models and have a number of significant advantages for purposes of digital analysis and simulation. The structure of ARMA models is briefly described, their relation to continuous models noted, and results of their application to a number of recorded accelerograms summarized.     

Calculation of multicomponent chemical equilibria and reaction processes in systems involving minerals,gases and an aqueous phase

The compositional characteristics of many geochemical systems which involve the interaction of natural aqueous solutions with minerals and gases are conveniently described using the following thermodynamic components: Cl^?, SO₄⁼, HS^?, CO₃⁼, H⁺, Na⁺, K⁺, Ca⁺⁺, Mg⁺⁺, Fe⁺⁺, Zn⁺⁺, Cu⁺, Al⁺⁺⁺, SiO₂ and H₂O. A set of mass balance and mass action equations equal in number to the number of components plus the number of saturated minerals (and gases) is defined for a specified temperature, pressure and bulk composition. The mass balance equations include terms for minerals, gases and the molalities of aqueous complexes and dissociated species. This set of non-linear equations can be solved with the aid of a computer using'a Newton-Raphson technique. The calculation takes account of aqueous ion complexing, oxidation-reduction equilibria, activity coefficients, non-unit water activity and solid solutions. The use of H⁺, SO₄⁼, HS^? and H₂O as components allows straightforward treatment of processes involving oxidation-reduction, evaporation, boiling and changes of total aqueous H⁺ due to hydrolysis, mineral reaction or temperature change. One product of this approach is a technique for calculating pH at high temperature from measurement of pH at room temperature.By linking a series of discrete overall heterogeneous equilibrium calculations in which incremental changes of bulk composition, temperature or pressure are made, dynamic geochemical processes can be modeled. Example calculations for two such processes are given. These are the heating of seawater from 25° to 300°C and the isothermal irreversible reaction of rhyolite with an aqueous solution at 250°C.