Multiple origins of xenoliths and xenocrysts in the Elephant Moraine 79001 Lithology A olivine‐phyric shergottite

Petrographic examination of the xenolith and xenocryst populations in the olivine‐phyric shergottite Elephant Moraine 79001 Lithology A shows more chemical heterogeneity than previously documented. Analyses of olivine grains in 18 megacrysts and in 4 lithic fragments show that these two populations either do not have the same source or that this source is heterogeneous in terms of its time–temperature history. Additionally, among the four lithic fragments analyzed, two are distinctive (1) one contains a major‐element‐equilibrated, euhedral olivine grain and (2) the second contains high‐magnesium pyroxene cores. Furthermore, two populations of ferroan olivine were identified (1) one more ferroan than any other reported in EET 79001 and (2) a slightly less ferroan, unequilibrated olivine, but with a restricted range in Mg#. We have also observed an equilibrated pyroxene grain associated with a zoned olivine megacryst. As a result, we recognize that the xenolith/xenocryst population does not represent the incorporation of a single xeno‐lithology into Lithology A, and propose that it be subdivided into a suite of seven identified lithologies, with the understanding that more are likely to be identified with further study. The abundance of Ca in olivine in the xeno‐lithologies suggests a set of crustal, rather than deep mantle, lithologies. Diffusion rates in olivine suggest that the lithologies were incorporated shortly before rapid cooling of the host magma, preserving preexisting mineral chemical zoning. These mineral chemical zones could have been preserved at lower crustal temperatures for up to 10s of Ka. Trace‐element studies of these distinct populations would be required to test whether they are related by igneous processes from a common source magma.     

Mineralogy and geochemistry of atypical reduction spheroids from the Tumblagooda Sandstone,Western Australia

Reduction spheroids are small-scale, biogenic, redox-controlled, metal enrichments that occur within red beds globally. This study provides the first analysis of the compositionally unique reduction spheroids of the Tumblagooda Sandstone. The work aims to account for their composition and consequently improve existing models for reduction spheroids generally, which presently fail to account for the mineralogy of the Tumblagooda Sandstone reduction spheroids. Interstitial areas between detrital grains contained in the cores of these reduction spheroids are dominated by microplaty haematite, in addition to minor amounts of svanbergite, gorceixite, anatase, uraninite, monazite and illite. The haematite-rich composition, along with an absence of base metal phases and the vanadiferous mica roscoelite, makes these reduction spheroids notable in comparison to other global reduction spheroid occurrences. Analyses of illite crystallinity provide values for samples of the Tumblagooda Sandstone host rock corresponding to heating temperatures of ca 200°C. Consequently, while Tumblagooda Sandstone reduction spheroids formed via the typical metabolic processes of dissimilatory metal-reducing bacteria, the combination of a unique mineralogy and illite crystallinity analysis provides evidence of more complex late-stage heating and reoxidation. This has not previously been recognised in other reduction spheroids and therefore expands the existing model for reduction spheroid genesis by also considering the potential for late-stage alteration. As such, future reduction spheroid studies should consider the potential impact of post-formation modification, particularly where they are to be used as evidence of ancient microbial processes; such as in the search for early evidence of life in the geological record on Earth or other planets. Additionally, because of their potential for modification, reduction spheroids serve as a record of the redox history of red beds and their study could provide insights into the evolution of redox conditions within a given red bed during its diagenesis. Finally, this paper also provides insights into the relatively understudied diagenetic history of the Tumblagooda Sandstone; supplying the first reliable and narrow constraints on its thermal history. This has important implications for the thermal history of the Carnarvon Basin and its petroleum prospectivity more broadly.     

Radio-continuum study of the nearby Sculptor group Galaxies. Part 2: NGC 55 at λ=20, 13, 6 and 3 cm

A series of new radio-continuum (λ=20, 13, 6 and 3 cm) mosaic images focused on the NGC 55 galactic system were produced using archived observational data from the Australia Telescope Compact Array. These new images are both very sensitive (down to rms=33 μJy) and feature high angular resolution (down to <4″). Using these newly created images, 66 previously unidentified discrete sources are identified. Of these sources, 46 were classified as background sources, 11 as H?ii regions and 6 as supernova remnant candidates. This relatively low number of SNR candidates detected coupled with the low number of large H?ii regions is consistent with the estimated low star formation rate of the galaxy at 0.06 M _⊙?year^?1. Our spectral index map shows that the core of galaxy appears to have a shallow spectral index between α=?0.2 and ?0.4. This indicates that the core of the galaxy is a region of high thermal radiation output.     

First identification and characterization of Borrobol‐type tephra in the Greenland ice cores: new deposits and improved age estimates

Contiguous sampling of ice spanning key intervals of the deglaciation from the Greenland ice cores of NGRIP, GRIP and NEEM has revealed three new silicic cryptotephra deposits that are geochemically similar to the well‐known Borrobol Tephra (BT). The BT is complex and confounded by the younger closely timed and compositionally similar Penifiler Tephra (PT). Two of the deposits found in the ice are in Greenland Interstadial 1e (GI‐1e) and an older deposit is found in Greenland Stadial 2.1 (GS‐2.1). Until now, the BT was confined to GI‐1‐equivalent lacustrine sequences in the British Isles, Sweden and Germany, and our discovery in Greenland ice extends its distribution and geochemical composition. However, the two cryptotephras that fall within GI‐1e ice cannot be separated on the basis of geochemistry and are dated to 14358 ± 177 a b2k and 14252 ± 173 a b2k, just 106 ± 3 years apart. The older deposit is consistent with BT age estimates derived from Scottish sites, while the younger deposit overlaps with both BT and PT age estimates. We suggest that either the BT in Northern European terrestrial sequences represents an amalgamation of tephra from both of the GI‐1e events identified in the ice‐cores or that it relates to just one of the ice‐core events. A firm correlation cannot be established at present due to their strong geochemical similarities. The older tephra horizon, found within all three ice‐cores and dated to 17326 ± 319 a b2k, can be correlated to a known layer within marine sediment cores from the North Iceland Shelf (ca. 17179‐16754 cal a BP). Despite showing similarities to the BT, this deposit can be distinguished on the basis of lower CaO and TiO₂ and is a valuable new tie‐point that could eventually be used in high‐resolution marine records to compare the climate signals from the ocean and atmosphere.     

Diffusion and solubility of hydrogen and water in periclase

Cylinders of synthetic periclase single crystals were annealed at 0.15–0.5 GPa and 900–1200 °C under water-saturated conditions for 45 min to 72 h. Infrared spectra measured on the quenched products show bands at 3,297 and 3,312 cm^?1 indicating V _OH ^? centers (OH-defect stretching vibrations in a half-compensated cation vacancy) in the MgO structure as a result of proton diffusion into the crystal. For completely equilibrated specimens, the OH-defect concentration, expressed as H₂O equivalent, was calculated to 3.5 wt ppm H₂O at 1,200 °C and 0.5 GPa based on the calibration method of Libowitzky and Rossmann (Am Min 82:1111–1115, 1997). This value was confirmed via Raman spectroscopy, which shows OH-defect-related bands at identical wavenumbers and yields an H₂O equivalent concentration of about 9 wt ppm using the quantification scheme of Thomas et al. (Am Min 93:1550–1557, 2008), revised by Mrosko et al. (Am Mineral 96:1748–1759, 2011). Results of both independent methods give an overall OH-defect concentration range of 3.5–9 (+4.5/?2.6) ppm H₂O. Proton diffusion follows an Arrhenius law with an activation energy E _a = 280 ± 64 kJ mol^?1 and the logarithm of the pre-exponential factor logD_o (m² s^?1) = ?2.4 ± 1.9. IR spectra taken close to the rims of MgO crystals that were exposed to water-saturated conditions at 1,200 °C and 0.5 GPa for 24 h show an additional band at 3,697 cm^?1, which is related to brucite precipitates. This may be explained by diffusion of molecular water into the periclase, and its reaction with the host crystal during quenching. Diffusion of molecular water may be described by logD_H2O (m² s^?1) = ?14.1 ± 0.4 (2σ) at 1,200 °C and 0.5 GPa, which is ~ 2 orders of magnitude slower than proton diffusion at identical P-T conditions.     

Insights into the Hadean Earth from experimental studies of zircon

Geologists investigate the evolution of the atmosphere, crust, and mantle through time by direct study of the rock record. However, the Hadean eon (>3.85 Ga) has been traditionally viewed as inaccessible due to the absence of preserved rocks. The discovery of >4.0 Ga detrital zircons from Western Australia in the 1980s — coupled with the development of new micro-analytical capabilities — made possible new avenues of early Earth research. The prevailing view that emerged is that the early Earth may have contained a stable hydrosphere, water-saturated or (near watersaturated) granitic magmas, and volcanic emanations dominated by neutral gas species (e.g., CO₂, H₂O, and SO₂). The Hadean Earth may have been capable of supporting life ～200 Ma after accretion and perhaps earlier. Many of these models are formulated — or have been subsequently supported — by laboratory experiments of zircon. Important petrological variables such as temperature, pressure, oxygen fugacity, and component activities (e.g., SiO₂/TiO₂-activities) can be controlled. These experiments are fundamental for extrapolation to ‘deep time’ because they provide a means to understand primary chemistry preserved in ancient zircons. This review paper specifically focuses on zircon experimental studies (oxygen isotope fractionations, Ti-thermometry, and redox sensitive element incorporation into zircon), which have influenced our view of the very early Earth.     

Revisiting the Borrobol Tephra

The Borrobol Tephra has been identified as one of the key tephra horizons for the Lateglacial time period but it also exemplifies many of the promises and problems of tephrochronology. Additional horizons with similar major element composition and approximately the same age have been identified around the North Atlantic region. Here, we revisit the Borrobol Tephra identified at two Swedish sites, Hässeldala port and Skallahult, and also the Borrobol type‐site in Scotland. We present the first set of minor element data (trace and rare earth analyses) along with new analyses of major elements from these three sites. The analysed minor and the trace elements have a similar signature; however, the glass from the Scottish type‐site seems to imply two populations. To answer if this truly represents two populations, or if it reflects magmatic differentiation additional and larger data sets of minor elements are needed. The new major elements are compared to other Borrobol‐type tephras identified in the North Atlantic region. Our results are in line with earlier investigations, which showed no differences in major elements. Further, comparison of minor elements from glass analyses from our sites with those for eruptions associated with Icelandic central volcanoes implies an Icelandic origin for the Borrobol‐type tephras.     

Bioavailability of sediment-bound metals to marine bivalve molluscs: An overview

Coastal marine sediments are commonly enriched in metals, including potentially toxic trace metals, by natural processes and human activities. These sediments have long been regarded as the final repositories of contaminants, but in recent years it has been recognized that they can also serve as potentially important sources of metal contaminants for benthic organisms and benthic food chains in general. The geochemical and biological factors governing the bioavailability of diverse metals (Ag, Cd, Co, Cr, Se, Zn) that are bound to different kinds of marine sediments are reviewed. Particular attention has been paid to those species of marine bivalve mollusks that are used as bioindicators of coastal contamination. Both deposit-feeding and suspension-feeding bivalves can accumulate metals appreciably by assimilating sediment-bound metals that are ingested, although important differences have been recognized between these two feeding modes as well as between metals. The properties of the digestive tracts of deposit and suspension-feeding bivalves that influence metal bioaccumulation from food are also discussed. Through kinetic modeling, the relative importance of ingestion as a route of metal uptake has been compared quantitatively with uptake from the dissolved phase, including from pore water and from overlying water, and has been shown to account for the high concentrations in bivalve tissues for a number of contaminant metals.     

Holocene dune formation at Ash Meadows National Wildlife Area,Nevada, USA

Small isolated dune fields in the northern Mojave Desert are important centers of biodiversity and archaeological occupation sites. Currently dunes at Ash Meadows, Nevada, are stabilized by vegetation and are experiencing erosion of their upwind margins, indicating a negative sediment budget. New OSL ages from dunes at Ash Meadows indicate continuous eolian accumulation from 1.5 to 0.8 ka, with further accumulation around 0.2 ka. Prior studies (e.g., Mehringer and Warren, 1976) indicate periods of dune accumulation prior to 3.3 ka; 1.9–1 ka; and after 0.9 ka. These periods of eolian accumulation are largely synchronous with those identified elsewhere in the Mojave Desert. The composition of the Ash Meadows dunes indicates their derivation from regional fluvial sources, most likely during periods when axial washes were active as a result of enhanced winter precipitation.