Composition-Induced Variations in SIMS Instrumental Mass Fractionation during Boron Isotope Ratio Measurements of Silicate Glasses

An analytical artefact is reported here related to differences in instrumental mass fractionation between NIST SRM glasses and natural geological glasses during SIMS boron isotope determinations. The data presented demonstrated an average 3.4‰ difference between the NIST glasses and natural basaltic to rhyolitic glasses mainly in terms of their sputtering-induced fractionation of boron isotopes. As no matrix effect was found among basaltic to rhyolitic glasses, instrumental mass fractionation of most natural glass samples can be corrected by using appropriate glass reference materials. In order to confirm the existence of the compositionally induced variations in boron SIMS instrumental mass bias, the observed offset in SIMS instrumental mass bias has been independently reproduced in two laboratories and the phenomenon has been found to be stable over a period of more than one year. This study highlights the need for a close match between the chemical composition of the reference material and the samples being investigated.     

Late Quaternary megafloods from Glacial Lake Atna, Southcentral Alaska, U.S.A.

Geomorphic, stratigraphic, geotechnical, and biogeographic evidence indicate that failure of a Pleistocene ice dam between 15.5 and 26 ka generated a megaflood from Glacial Lake Atna down the Matanuska Valley. While it has long been recognized that Lake Atna occupied ≥ 9000 km² of south-central Alaska's Copper River Basin, little attention has focused on the lake's discharge locations and behaviors. Digital elevation model and geomorphic analyses suggest that progressive lowering of the lake level by decanting over spillways exposed during glacial retreat led to sequential discharges down the Matanuska, Susitna, Tok, and Copper river valleys. Lake Atna's size, ∼ 50 ka duration, and sequential connection to four major drainages likely made it a regionally important late Pleistocene freshwater refugium. We estimate a catastrophic Matanuska megaflood would have released 500–1400 km³ at a maximum rate of ≥ 3 × 10⁶ m³ s^{− 1}. Volumes for the other outlets ranged from 200 to 2600 km³ and estimated maximum discharges ranged from 0.8 to 11.3 × 10⁶ m³ s^{− 1}, making Lake Atna a serial generator of some of the largest known freshwater megafloods.     

Mineral dissolution in the Cape Cod aquifer, Massachusetts, USA: I . Reaction stoichiometry and impact of accessory feldspar and glauconite on strontium isotopes, solute concentrations, and REY distribution

To compare relative reaction rates of mineral dissolution in a mineralogically simple groundwater aquifer, we studied the controls on solute concentrations, Sr isotopes, and rare earth element and yttrium (REY) systematics in the Cape Cod aquifer. This aquifer comprises mostly carbonate-free Pleistocene sediments that are about 90% quartz with minor K-feldspar, plagioclase, glauconite, and Fe-oxides. Silica concentrations and pH in the groundwater increase systematically with increasing depth, while Sr isotopic ratios decrease. No clear relationship between ⁸⁷Sr/⁸⁶Sr and Sr concentration is observed. At all depths, the ⁸⁷Sr/⁸⁶Sr ratio of the groundwater is considerably lower than the Sr isotopic ratio of the bulk sediment or its K-feldspar component, but similar to that of a plagioclase-rich accessory separate obtained from the sediment. The Si-⁸⁷Sr/⁸⁶Sr-depth relationships are consistent with dissolution of accessory plagioclase. In addition, solutes such as Sr, Ca, and particularly K show concentration spikes superimposed on their respective general trends. The K-Sr-⁸⁷Sr/⁸⁶Sr systematics suggests that accessory glauconite is another major solute source to Cape Cod groundwater. Although the authigenic glauconite in the Cape Cod sediment is rich in Rb, it is low in in-grown radiogenic ⁸⁷Sr because of its young Pleistocene age. The low ⁸⁷Sr/⁸⁶Sr ratios are consistent with equilibration of glauconite with seawater. The impact of glauconite is inferred to vary due to its variable abundance in the sediments. In the Cape Cod groundwater, the variation of REY concentrations with sampling depth resembles that of K and Rb, but differs from that of Ca and Sr. Shale-normalized REY patterns are light REY depleted, show negative Ce anomalies and super-chondritic Y/Ho ratios, but no Eu anomalies. REY input from feldspar, therefore, is insignificant compared to input from a K-Rb-bearing phase, inferred to be glauconite. These results emphasize that interpretation of groundwater chemistry, even in relatively simple aquifers, may be complicated by solute contributions from “exotic” accessory minerals such as glauconite. To detect such peculiarities, groundwater studies should combine the study of elemental concentration and isotopic composition of several solutes that show different geochemical behavior.     

Benthic foraminifera in sandy (siliciclastic) coastal sediments of the Arabian Gulf (Saudi Arabia): a technical report

The Uromia–Dokhtar Magmatic Arc (UDMA) is a northwest–southeast trending magmatic belt which is formed due to oblique subduction of Neotethys underneath Central Iran and dominantly comprises magmatic rocks. The Jebal-e-Barez Plutonic Complex (JBPC) is located southeast of the UDMA and composed of quartz diorite, granodiorite, granite, and alkali granite. Magmatic enclaves, ranging in composition from felsic to mafic, are abundant in the studied rocks. Based on the whole rock and mineral chemistry study, the granitoids are typically medium-high K calc-alkaline and metaluminous to peraluminous that show characteristics of I-type granitoids. The high field strength (HFS) and large ionic radius lithophile (LIL) element geochemistry suggests fractional crystallization as a major process in the evolution of the JBPC. The tectonomagmatic setting of the granitoids is compatible with the arc-related granitic suite, a pre-plate collision granitic suite, and a syncollision granitic suite. Field observations and petrographic and geochemical studies suggest that the rocks in this area are I-type granitoids and continental collision granitoids (CCG), continental arc granitoids (CAG), and island arc granitoid (IAG) subsections. The geothermobarometry based on the electron probe microanalysis of amphibole, feldspars, and biotite from selected rocks of JBPC implies that the complex formed at high-level depths (i.e., 9–12 km; upper continental crust) and at temperatures ranging from 650 to 750 °C under oxidation conditions. It seems that JBPC is located within a shear zone period, and structural setting of JBPC is extensional shear fractures which are product of transpression tectonic regime. All available data suggested that these granitoids may be derived from a magmatic arc that was formed by northeastern ward subduction of the Neotethyan oceanic crust beneath the Central Iran in Paleogene and subsequent collision between the Arabian and Iranian plates in Miocene.

     

Chemistry of alkali extraction of brown coals—I. Kinetics, characterisation and implications to coalification

Three Australian brown coals have been separated into humin and humic acid fractions and studied by high resolution solid state ¹³C NMR spectroscopy and Fourier transform IR spectroscopy. The aromatic rings of the humic acids are highly substituted showing that extensive cross linking must have occurred during formation from wood lignin and tannin. However, the humins contain more aliphatic carbon and hydrogen than the corresponding humic acids. This shows that little cross linking has occurred with other components of the brown coal such as resins, waxes cutin and algal detritus, and cross linking has not rendered the aromatics alkali insoluble. The kinetics of extraction are complex and not simple first order. This is reflected in the chemical composition of the humic acid which is extraction temperature dependent. We also observed that there is a conversion of aromatic carbon to aliphatic carbon and gas during extraction, probably by alkaline oxidation, resulting in ring opening. A range of suitable model compounds have been studied to confirm this finding. Such a mechanism may account for the modification of lignin in oxidising environments such as those occurring in the initial stages of coalification (lignite or brown coal formation) and in soils.     

Constraints on the composition of the Venus atmosphere from microwave measurements near 1.35 cm wavelength

The determination of the brightness temperature of Venus near 1.35 cm wavelength is reviewed. The observed brightness temperature is compared with models for the microwave emission based on the physical and chemical structure of the atmosphere as obtained from spacecraft. Upper limits are set on the concentrations of microwave-absorbing minor constituents. In particular, upper limits are determined for SO₂ (180 ppm) and H₂O (0.3%) for a mixing-ratio profile that is uniformly mixed up to the cloud bottom at 50 km and is rapidly depleted ($\text{scale height}\text{? 1}\text{km}\text{)}$ at higher altitudes. The total optical depth of the cloud region at or above 50 km is <0.17 at 1.35 cm wavelength. The SO₂ upper limit is only in marginal agreement with the spacecraft results, and it may be that the latter have been overestimated, or that the distribution of SO₂ is more complex than given by the uniform mixing model.