Hydrocarbons in surficial sediments from the Scotian Shelf

Surface sediments from 20 stations on the Scotian Shelf, collected on a transect from Halifax to Emerald Bank and around Sable Island, have been analyzed for hydrocarbon content and composition by gas chromatography and fluorescence spectrophotometry. Some samples were taken near abandoned exploratory drilling sites in the Sable Island area. Hydrocarbons appear to be mainly derived from biogenic terrestrial sources as evidenced by an inverse correlation of concentration with increasing distance from the mainland and a strong odd carbon preference in the n-alkanes. Contribution from petroleum sources, while minor, was most noticeable between Halifax and Emerald Bank. There is also evidence that the hydrocarbon composition at abandoned exploratory drilling sites has been slightly altered.     

Amino acid composition of organic matter associated with carbonate and non-carbonate sediments

Amino acids comprise from 15 to 36% by weight of humic substances from carbonate and non-carbonate sediments. Humic and fulvic acids extracted from carbonate sediments are characterized by an amino acid composition consisting primarily of the acidic amino acids, aspartic and glutamic acid. Humic substances from non-carbonate sediments have a distinctly different amino acid composition consisting primarily of glycine and alanine. Amino acid analyses of various molecular weight fractions of fulvic acids extracted from carbonates show that lower molecular weight fractions have appreciably higher relative abundances of the acidic amino acids compared to higher molecular weight fractions. Based on typical values for carboxyl group content in humic substances, acidic amino acids may be a significant contributor of these functional groups. Carbonate surfaces appear to selectively adsorb aspartic acid-enriched organic matter while non-carbonates do not have this property.     

The relationship of electron plasma oscillations to type III radio emissions and low-energy solar electrons

An extensive study of the IMP-6 and IMP-8 plasma and radio wave data has been performed to try to find electron plasma oscillations associated with type III radio noise bursts and low energy solar electrons. This study shows that electron plasma oscillations are seldom observed in association with solar electron events and type III radio bursts at 1.0 AU. In nearly four years of observations only one event was found in which electron plasma oscillations are clearly associated with solar electrons. Numerous cases were found in which no electron plasma oscillations with field strengths greater than 1 V/m could be detected even though electrons from the solar flare were clearly detected at the spacecraft.For the one case in which electron plasma oscillations are definitely produced by the electrons ejected by the solar flare, the electric field strength is very small, only about 100 V/m. This field strength is about a factor of ten smaller than the amplitude of electron plasma oscillations generated by electrons streaming into the solar wind from the bow shock. Electromagnetic radiation, believed to be similar to the type III radio emission, is also observed coming from the region of more intense electron plasma oscillations upstream of the bow shock. Quantitative calculations of the rate of conversion of the plasma oscillation energy to electromagnetic radiation are presented for plasma oscillations excited by both solar electrons and electrons from the bow shock. These calculations show that neither the type III radio emissions nor the radiation from upstream of the bow shock can be adequately explained by a current theory for the coupling of electron plasma oscillations to electromagnetic radiation. Possible ways of resolving these difficulties are discussed.     

The prominence-corona interface compared with the chromosphere-corona transition region

The intensities of 52 EUV emission lines from each of 9 hedgerow prominences observed at the limb with the Harvard experiment on ATM-Skylab have been compared with intensities from the interior of network cells at the center of the disk, in order to compare the prominence-corona (P-C) interface with the chromosphere-corona (C-C) transition region. The intensity ratio I _cell/I _prominence for each line varies systematically (in all of the prominences observed), with the temperature of formation of the line as T ^–0.6. The density sensitive C iii (formed at T 9 × 10⁴ K) line ratio I ₁₁₇₅/I ₉₇₇ implies an average density 1.3 × 10⁹ electrons cm^–3 in the P-C interface and 4 times this value in the C-C transition of the cells. The total optical thickness at the head of the Lyman continuum is 10 in most of the prominences studied; in two of the prominences, however, we cannot reject the possibility that _o is large. Methods of analysis of these EUV data are developed assuming both a resolved and an unresolved internal prominence structure. Although the systematic differences between the P-C interface and the C-C transition are stressed, the similarities are probably more remarkable and may be a result of fine structure in the C-C transition.Currently on leave from the Institute of Astronomy, Hawaii; at the Laboratory for Atmospheric and Space Physics, University of Colorado, Boulder, Colorado, 80309.     

Barium uptake into the shells of the common mussel (Mytilus edulis) and the potential for estuarine paleo-chemistry reconstruction

In this study we test if calcite shells of the common mussel, Mytilus edulis, contain barium in proportion to the water in which they grew. Similar to all bivalves analyzed to date, the [Ba/Ca]_shell profiles are characterized by a relatively flat background [Ba/Ca]_shell, interrupted by sharp [Ba/Ca]_shell peaks. Previous studies have focused on these [Ba/Ca]_shell peaks, but not on the background [Ba/Ca]_shell. We show that in both laboratory and field experiments, there is a direct relationship between the background [Ba/Ca]_shell and [Ba/Ca]_water in M. edulis shells. The laboratory and field data provided background Ba/Ca partition coefficients (D_Ba) of 0.10 ± 0.02 and 0.071 ± 0.001, respectively. This range is slightly higher than the D_Ba previously determined for inorganic calcite, and slightly lower than foraminiferal calcite. These data suggest that M. edulis shells can be used as an indicator of [Ba/Ca]_water, and therefore, fossil or archaeological M. edulis shells could be used to extend knowledge of estuarine dissolved Ba throughputs back in time. Moreover, considering the inverse relationship between [Ba/Ca]_water and salinity, background [Ba/Ca]_shell data could be used as an estuary specific indicator of salinity. The cause of the [Ba/Ca]_shell peaks is more confusing, both the laboratory and field experiments indicate that they cannot be used as a direct proxy of [Ba/Ca]_water or phytoplankton production, but may possibly be caused by barite ingestion.     

Origin of SiO2-rich components in ordinary chondrites

Silica-rich objects are common minor components in ordinary chondrites (OC), occurring as fragments and as chondrules. Their typical paragenesis is orthopyroxene + SiO₂ (with bulk SiO₂ >65 wt%) and occasionally with additional olivine and/or spinel. Individual silica-rich components (SRC) have previously been studied in various types of OCs, although there is only one comprehensive study of these objects by Brigham et al. [Brigham, C.A., Murrell, M.T., Yabuki, H., Ouyang, Z., El Goresy, A., 1986. Silica-bearing chondrules and clasts in ordinary chondrites. Geochim. Cosmochim. Acta 50, 1655-1666]. Several different explanations of how SRCs formed have been published. The main question is how silica-enrichment was achieved, because CI-chondritic atomic Mg/Si-ratio is 1.07 and as a consequence only olivine and pyroxene, but no free silica should be stable. There are two basic possibilities for the SiO₂-enrichment: (1) a RedOx-mechanism or magmatic fractionation on the parent body and (2) fractional condensation or recycling of chondrule mesostasis in the solar nebula. To better constrain the origin of these objects, we measured major and rare earth elements in SRCs of various types of ordinary chondrites, and in addition, we studied silica polymorphism in these objects using an in situ micro-Raman technique. Bulk chondrule compositions define mixing lines between the compositions of olivine and pyroxene. The SRCs extend these lines to an SiO₂ end member. In contrast, magmatic trends grossly deviate from these mixing lines. Concentrations of CaO, Al₂O₃, and REE in the pyroxenes of the SRCs are low (0.01 to 1× CI) and the CI-normalized REE-patterns are virtually flat, typical of bulk chondrules, but untypical of magmatic trends. We therefore conclude that SiO₂-rich objects are not of magmatic origin. They are the result of fractional condensation in the solar nebula. The silica in SRCs occurs mainly as tridymite and sometimes as cristobalite or—in very rare cases—as quartz. Some SiO₂-phases yielded a yet unknown micro-Raman spectrum, which we were unable to identify. The often chondrule-like shape of SRCs as well as the presence of high-temperature SiO₂-polymorphs lead to the following model for the origin of SRCs: formation of SiO₂-rich precursors in the solar nebula by fractional condensation, reheating to temperatures between 1140 and >1968 K, thereby forming the SRCs,—probably during the chondrule-forming process—followed by rapid cooling.     

An experimental study of anorthosite dissolution in lunar picritic magmas: Implications for crustal assimilation processes

Experiments characterizing the kinetics of anorthosite dissolution in lunar picritic magmas (very low-Ti, low-Ti, and high-Ti picritic glasses) were conducted at 0.6 GPa and 1250-1400 °C using the dissolution couple method. Reaction between the anorthosite and lunar picritic magmas at 1250-1300 °C produced a spinel + melt layer. Reaction between the anorthosite and an olivine-saturated low-Ti magma at 1250-1300 °C produced a crystal-free region between the spinel + melt layer and the olivine-saturated magma. The anorthosite dissolution experiments conducted at 1400 °C simply dissolved anorthosite and did not result in a crystal-bearing region. The rate of anorthosite dissolution strongly depends on temperature and composition of the reacting melt. Concentration profiles that develop during anorthosite dissolution are nonlinear and extend from the picritic glass compositions to anorthite. These profiles feature a large and continuous variation in melt density and viscosity from the anorthosite-melt interface to the initial picritic magmas. In both the low-Ti and high-Ti magmas the diffusive fluxes of TiO₂, Al₂O₃, and SiO₂ are strongly coupled to the concentration gradients of CaO and FeO. Anorthosite dissolution may play an important role in producing the chemical variability of the lunar picritic magmas, the origin of spinel in the lunar basalts and picritic glasses, and the petrogenesis of the high-Al basalts.     

A pronounced dry event recorded around 4.2 ka in brine sediments from the northern Red Sea

Partly laminated sediments were sampled from the brine-filled, anoxic Shaban Deep basin in the northern Red Sea. At about 4200 cal yr BP more than two millennia of anoxic sedimentation is replaced by a sub-oxic facies strongly suggesting the episodic absence of the brine. At the same time stable oxygen isotopes from surface dwelling foraminifera show a sharp increase (within less than 100 yr) pointing to a strong positive salinity anomaly at the sea surface. This major evaporation event significantly enhanced the renewal of deep water and the subsequent ventilation of the small Shaban Deep basin. The timing and strength of the reconstructed environmental changes around 4200 cal yr BP suggest that this event is the regional expression of a major drought event, which is widely observed in the neighboring regions, and which strongly affected Middle East agricultural civilizations.     

GGR Critical Review of Analytical Developments in 2004–2005

In 2005 Geostandards and Geoanalytical Research embarked upon a new initiative for its readers. Key researchers in various fields of geoanalytical technique development and their application were identified and invited to provide reviews pertinent to their expertise. As noted in the first of these publications "…instead of revisiting the historical context or decades of development in each analytical technique, the goal here has been to capture a snapshot of "hot topics" across a range of fields as represented in the… literature" (Hergt et al . 2005). Rather than prepare an annual review, a decision was taken earlier this year to provide a biennial summary of progress and accomplishments, in this case for the years 2004–2005. The principal techniques employed in Earth and environmental sciences are covered here, and include laser ablation and multicollector ICP-MS, ICP-AES, thermal ionisation and secondary ion mass spectrometry, as well as neutron activation analysis, X-ray fluorescence and atomic absorption spectrometry. A comprehensive review of the development of reference materials, often essential to these techniques, is also provided. The contributions assembled serve both to keep readers informed of advances they may be unfamiliar with, but also as a means of showcasing examples of the breadth and depth of work being conducted in these fields.