Geochemistry and chronology of the Bunburra Rockhole ungrouped achondrite

Bunburra Rockhole is a unique basaltic achondrite that has many mineralogical and petrographic characteristics in common with the noncumulate eucrites, but differs in its oxygen isotope composition. Here, we report a study of the mineralogy, petrology, geochemistry, and chronology of Bunburra Rockhole to better understand the petrogenesis of this meteorite and compare it to the eucrites. The geochemistry of bulk samples and of pyroxene, plagioclase, and Ca‐phosphate in Bunburra Rockhole is similar to that of typical noncumulate eucrites. Chronological data for Bunburra Rockhole indicate early formation, followed by slow cooling and perhaps multiple subsequent heating events, which is also similar to some noncumulate eucrites. The ²⁶Al‐²⁶Mg extinct radionuclide chronometer was reset in Bunburra Rockhole after the complete decay of ²⁶Al, but a slight excess in the radiogenic ²⁶Mg in a bulk sample allows the determination of a model ²⁶Al‐²⁶Mg age that suggests formation of the parent melt for this meteorite from its source magma within the first ~3 Ma of the beginning of the solar system. The ²⁰⁷Pb‐²⁰⁶Pb absolute chronometer is also disturbed in Bunburra Rockhole minerals, but a whole‐rock isochron provides a re‐equilibration age of ~4.1 Ga, most likely caused by impact heating. The mineralogy, geochemistry, and chronology of Bunburra Rockhole demonstrate the similarities of this achondrite to the eucrites, and suggest that it formed from a parent melt with a composition similar to that for noncumulate eucrites and subsequently experienced a thermal history and evolution comparable to that of eucritic basalts. This implies the formation of multiple differentiated parent bodies in the early solar system that had nearly identical bulk elemental compositions and petrogenetic histories, but different oxygen isotope compositions inherited from the solar nebula.     

Carbon isotopes in the rivers from the Lesser Antilles: origin of the carbonic acid consumed by weathering reactions in the Lesser Antilles

In this paper, we use carbon isotopes in the dissolved load of rivers from the Lesser Antilles volcanic arc (Guadeloupe, Martinique and Dominica islands) to constrain the source of the carbon dioxide (CO₂) involved in the neutralization reactions during water–rock interactions. The δ¹³C data span a large range of variations, from –19‰ to –5 · 2‰ for DIC (dissolved inorganic carbon) concentrations ranging from 11 μM to 2000 μM. Coupled with major element concentrations, carbon isotopic ratios are interpreted as reflecting a mixture of magmatic CO₂ (enriched in heavy carbon (δ¹³C ≈ –3 · 5‰) and biogenic CO₂ produced in soils (enriched in light carbon (δ¹³C < –17‰)). Carbon isotopes show that, at the regional scale, 23 to 40% of CO₂ consumed by weathering reactions is of magmatic origin and is transferred to the river system through aquifers under various thermal regimes. These numbers remain first‐order estimates as the major uncertainty in using carbon isotopes as a source tracer is that carbon isotopes can be fractionated by a number of processes, including soil and river degassing. Chemical weathering is clearly, at least, partly controlled by the input of magmatic CO₂, either under hydrothermal (hot) or surficial (cold) weathering regimes. This study shows that the contribution of magmatic CO₂ to chemical weathering is an additional parameter that could explain the high weathering rates of volcanic rocks. The study also shows that a significant part of the carbon degassed from the Earth's interior is not released as CO₂ to the atmosphere, but as DIC to the ocean because it interacts with the groundwater system. This study calls for a better understanding of the contributions of deep carbon to the hydrosphere and its influence on the development of the Critical Zone. Copyright © 2013 John Wiley & Sons, Ltd.     

Performance characteristics of a new electronic snow water equivalent sensor in different climates

The US Army ERDC CRREL and the US Department of Agriculture Natural Resources Conservation Service developed a square electronic snow water equivalent (e‐SWE) sensor as an alternative to using fluid‐filled snow pillows to measure SWE. The sensors consist of a centre panel to measure SWE and eight outer panels to buffer edge stress concentrations. Seven 3 m square e‐SWE sensors were installed in five different climate zones. During the 2011–2012 winter, 1.8 and 1.2 m square e‐SWE sensors were installed and operated in Oregon. With the exception of New York State and Newfoundland, the e‐SWE sensors accurately measured SWE, with R² values between the sensor and manual SWE measurements of between 0.86 and 0.98. The e‐SWE sensor at Hogg Pass, Oregon, accurately measured SWE during the past 8 years of operations. In the thin, icy snow of New York during midwinter 2008–2009, the e‐SWE sensors overmeasured SWE because of edge stress concentrations associated with strong icy layers and a shallow snow cover. The New York e‐SWE sensors' measurement accuracy improved in spring 2009 and further improved during the 2011–2012 winter with operating experience. At Santiam Junction, measured SWE from the 1.8 and 1.2 m square e‐SWE sensors agreed well with the snow pillow, 3 m square e‐SWE sensor, and manual SWE measurements until February 2013, when dust and gravel blew onto the testing area resulting in anomalous measurements. © 2014 The Authors. Hydrological Processes published by John Wiley & Sons Ltd.     

Temperature calibration of expendable bathythermographs

A non-destructive temperature calibration system for expendable bathythermographs (XBT) is described. A transfer standard technique has been used to estimate XBT thermistor probe-to-probe temperature variability. One-point calibration results suggest that a standard deviation of 0.025°C is typical at 10°C. Additional calibration data from nine XBT thermistors suggest that probe-to-probe temperature variability is largest at 0°C (ca. 0.03°C) and decreases uniformly to a minimum at 30°C (ca. 0.01°C).     

Acoustic Emissions Monitoring during Inelastic Deformation of Porous Sandstone: Comparison of Three Modes of Deformation

In some reservoirs, large deformations can occur during oil or gas production because of the effective stress change. For very porous rocks, these production operations can be sufficient to cause inelastic deformation and irreversible damage. Rock formations can undergo deformation by different mechanisms, including dilatancy or pore collapse. In the laboratory, it has been shown that the inelastic deformation and failure mode of porous rocks are pressure sensitive. Indeed, when subjected to an overall compressive loading, a porous rock may fail by shear localization, compaction localization, or by cataclastic compaction. Acoustic emission (AE) records provide important information to understand the failure mode of rocks: the spatial evolution of damage as well as the source mechanisms can be followed using this technique. In this paper, we present three different laboratory axisymmetric compression experiments, performed on Bleurswiller sandstone, which enable us to compare the acoustic emission signature of these three modes of deformation. Our data show that compaction localization and cataclastic compaction are characterized by similar acoustic signatures (in terms of AE sources characteristics and evolution of AE number), in comparison to the acoustic signature from shear localization. This implies similar micromechanisms involved during compaction bands formation and cataclastic compaction.     

Phytoplankton distribution and productivity in a highly turbid, tropical coastal system (Bach Dang Estuary, Vietnam)

Phytoplankton diversity, primary and bacterial production, nutrients and metallic contaminants were measured during the wet season (July) and dry season (March) in the Bach Dang Estuary, a sub-estuary of the Red River system, Northern Vietnam. Using canonical correspondence analysis we show that phytoplankton community structure is potentially influenced by both organometallic species (Hg and Sn) and inorganic metal (Hg) concentrations. During March, dissolved methylmercury and inorganic mercury were important factors for determining phytoplankton community composition at most of the stations. In contrast, during July, low salinity phytoplankton community composition was associated with particulate methylmercury concentrations, whereas phytoplankton community composition in the higher salinity stations was more related to dissolved inorganic mercury and dissolved mono and tributyltin concentrations. These results highlight the importance of taking into account factors other than light and nutrients, such as eco-toxic heavy metals, in understanding phytoplankton diversity and activity in estuarine ecosystems.     

The effect of silica and natural organic matter on the Fe(II)-catalysed transformation and reactivity of Fe(III) minerals

The Fe(II)-catalysed transformation of synthetic schwertmannite, ferrihydrite, jarosite and lepidocrocite to more stable, crystalline Fe(III) oxyhydroxides is prevented by high, natural concentrations of Si and natural organic matter (NOM). Adsorption isotherms demonstrate that Si adsorbs to the iron minerals investigated and that increasing amounts of adsorbed Si results in a decrease in isotope exchange between aqueous Fe(II) and the Fe(III) mineral. This suggests that the adsorption of Si inhibits the direct adsorption of Fe(II) onto the mineral surface, providing an explanation for the inhibitory effect of Si on the Fe(II)-catalysed transformation of Fe(III) minerals. During the synthesis of lepidocrocite and ferrihydrite, the presence of equimolar concentrations of Si and Fe resulted in the formation of 2-line ferrihydrite containing co-precipitated Si in both cases. Isotope exchange experiments conducted with this freeze-dried Si co-precipitated ferrihydrite species (Si-ferrihydrite) demonstrated that the rate and extent of isotope exchange between aqueous Fe(II) and solid ⁵⁵Fe(III) was very similar to that of 2-line ferrihydrite formed in the absence of Si and which had not been allowed to dry. In contrast to un-dried ferrihydrite formed in the absence of Si, Si-ferrihydrite did not transform into a more crystalline Fe(III) mineral phase over the 7-day period of investigation. Reductive dissolution studies using ascorbic acid demonstrated that both dried Si-ferrihydrite and un-dried 2-line ferrihydrite were very reactive, suggesting these species may be major contributors to the rapid release of dissolved iron following flooding and the onset of conditions conducive to reductive dissolution in acid sulphate soil environments.