Petrology and geochemistry of feldspathic impact‐melt breccia Abar al' Uj 012, the first lunar meteorite from Saudi Arabia

Abar al' Uj (AaU) 012 is a clast‐rich, vesicular impact‐melt (IM) breccia, composed of lithic and mineral clasts set in a very fine‐grained and well‐crystallized matrix. It is a typical feldspathic lunar meteorite, most likely originating from the lunar farside. Bulk composition (31.0 wt% Al₂O₃, 3.85 wt% FeO) is close to the mean of feldspathic lunar meteorites and Apollo FAN‐suite rocks. The low concentration of incompatible trace elements (0.39 ppm Th, 0.13 ppm U) reflects the absence of a significant KREEP component. Plagioclase is highly anorthitic with a mean of An_96.9Ab_3.0Or_0.1. Bulk rock Mg# is 63 and molar FeO/MnO is 76. The terrestrial age of the meteorite is 33.4 ± 5.2 kyr. AaU 012 contains a ~1.4 × 1.5 mm² exotic clast different from the lithic clast population which is dominated by clasts of anorthosite breccias. Bulk composition and presence of relatively large vesicles indicate that the clast was most probably formed by an impact into a precursor having nonmare igneous origin most likely related to the rare alkali‐suite rocks. The IM clast is mainly composed of clinopyroxenes, contains a significant amount of cristobalite (9.0 vol%), and has a microcrystalline mesostasis. Although the clast shows similarities in texture and modal mineral abundances with some Apollo pigeonite basalts, it has lower FeO and higher SiO₂ than any mare basalt. It also has higher FeO and lower Al₂O₃ than rocks from the FAN‐ or Mg‐suite. Its lower Mg# (59) compared to Mg‐suite rocks also excludes a relationship with these types of lunar material.     

The hydrogen balmer lines and the structure of the quiet solar chromosphere

Spectra of Hα, Hβ and Hδ have been taken under good seeing conditions with the vacuum tower telescope of Sacramento Peak Observatory. Intensity curves are given at various wavelengths in these lines to permit further comparison with a theoretical model. Moreover, considering in each case the range of height in which the lines are almost optically thin and using a few approximations, the following results are derived: between 2000 and 6000 km above the limb the average thermal + turbulent velocity of the atoms is found to increase from 20 km s^?1 to 30 km s^?1 and the mean number of hydrogen atoms per cm³ in level 2 is given by $$\log n_2 {\text{ = }}4.5{\text{ }} - {\text{ 0}}{\text{.00056(}}z - 2000)$$ z being the altitude above the limb in km. For line profile computations a new interpolation formula is presented; it gives good profiles with a small number of scans, saving microphotometer time.     

Surface complexation effects on phosphate adsorption to ferric iron oxyhydroxides along pH and salinity gradients in estuaries and coastal aquifers

Non-conservative behavior of dissolved inorganic phosphate (DIP) in estuaries is generally ascribed to desorption from iron and aluminum (hydr)oxides with increasing salinity. Here, we assess this hypothesis by simulating the reversible adsorption of phosphate onto a model oxide (goethite) along physico-chemical gradients representative of surface and subsurface estuaries. The simulations are carried out using a surface complexation model (SCM), which represents the main aqueous speciation and adsorption reactions of DIP, plus the ionic strength-dependent coulombic interactions in solution and at the mineral-solution interface. According to the model calculations, variations in pH and salinity alone are unlikely to explain the often reported production of DIP in surface estuaries. In particular, increased aqueous complexation of phosphate by Mg²⁺ and Ca²⁺ ions with increasing salinity is offset by the formation of ternary Mg-phosphate surface complexes and the drop in electrical potential at the mineral-water interface. However, when taking into account the downstream decrease in the abundance of sorption sites, the model correctly simulates the observed release of DIP in the Scheldt estuary. The sharp increase in pH accompanying the admixing of seawater to fresh groundwater should also cause desorption of phosphate from iron oxyhydroxides during seawater intrusion in coastal aquifers. As for surface estuaries, the model calculations indicate that significant DIP release additionally requires a reduction in the phosphate sorption site density. In anoxic aquifers, this can result from the supply of seawater sulfate and the subsequent reductive dissolution of iron oxyhydroxides coupled to microbial sulfate reduction.     

The presolar grain inventory of fine‐grained chondrule rims in the Mighei‐type (CM) chondrites

We investigated the inventory of presolar silicate, oxide, and silicon carbide (SiC) grains of fine‐grained chondrule rims in six Mighei‐type (CM) carbonaceous chondrites (Banten, Jbilet Winselwan, Maribo, Murchison, Murray and Yamato 791198), and the CM‐related carbonaceous chondrite Sutter's Mill. Sixteen O‐anomalous grains (nine silicates, six oxides) were detected, corresponding to a combined matrix‐normalized abundance of ~18 ppm, together with 21 presolar SiC grains (~42 ppm). Twelve of the O‐rich grains are enriched in ¹⁷O, and could originate from low‐mass asymptotic giant branch stars. One grain is enriched in ¹⁷O and significantly depleted in ¹⁸O, indicative of additional cool bottom processing or hot bottom burning in its stellar parent, and three grains are of likely core‐collapse supernova origin showing enhanced ¹⁸O/¹⁶O ratios relative to the solar system ratio. We find a presolar silicate/oxide ratio of 1.5, significantly lower than the ratios typically observed for chondritic meteorites. This may indicate a higher degree of aqueous alteration in the studied meteorites, or hint at a heterogeneous distribution of presolar silicates and oxides in the solar nebula. Nevertheless, the low O‐anomalous grain abundance is consistent with aqueous alteration occurring in the protosolar nebula and/or on the respective parent bodies. Six O‐rich presolar grains were studied by Auger Electron Spectroscopy, revealing two Fe‐rich silicates, one forsterite‐like Mg‐rich silicate, two Al‐oxides with spinel‐like compositions, and one Fe‐(Mg‐)oxide. Scanning electron and transmission electron microscopic investigation of a relatively large silicate grain (490 nm × 735 nm) revealed that it was crystalline åkermanite (Ca₂Mg[Si₂O₇]) or a an åkermanite‐diopside (MgCaSi₂O₆) intergrowth.     

Magnetic properties of the LL5 ordinary chondrite Chelyabinsk (fall of February 15, 2013)

Here we characterize the magnetic properties of the Chelyabinsk chondrite (LL5, S4, W0) and constrain the composition, concentration, grain size distribution, and mineral fabric of the meteorite's magnetic mineral assemblage. Data were collected from 10 to 1073 K and include measurements of low‐field magnetic susceptibility (χ₀), the anisotropy of χ₀, hysteresis loops, first‐order reversal curves, Mössbauer spectroscopy, and X‐ray microtomography. The REM and REM′ paleointensity protocols suggest that the only magnetizations recorded by the chondrite are components of the Earth's magnetic field acquired during entry into our planet's atmosphere. The Chelyabinsk chondrite consists of light and dark lithologies. Fragments of the light lithology show logχ₀ = 4.57 ± 0.09 (s.d.) (n = 135), while the dark lithology shows 4.65 ± 0.09 (n = 39) (where χ₀ is in 10^?9 m³ kg^?1). Thus, Chelyabinsk is three times more magnetic than the average LL5 fall, but is similar to a subgroup of metal‐rich LL5 chondrites (Paragould, Aldsworth, Bawku, Richmond) and L/LL5 chondrites (Glanerbrug, Knyahinya). The meteorite's room‐temperature magnetization is dominated by multidomain FeNi alloys taenite and kamacite (no tetrataenite is present). However, below approximately 75 K remanence is dominated by chromite. The metal contents of the light and dark lithologies are 3.7 and 4.1 wt%, respectively, and are based on values of saturation magnetization.     

An in situ investigation of the preservation and alteration of presolar silicates in the Miller Range 07687 chondrite

Dust grains that formed around ancient stars and in stellar explosions seeded the early solar protoplanetary disk. While most of such presolar grains were destroyed during solar system formation, a fraction of such grains were preserved in primitive materials such as meteorites. These grains can provide constraints on stellar origins and secondary processing such as aqueous alteration and thermal metamorphism on their parent asteroids. Here, we report on the nature of aqueous alteration in the Miller Range (MIL) 07687 chondrite through the analysis of four presolar silicates and their surrounding material. The grains occur in the Fe-rich and Fe-poor lithologies, reflecting relatively altered and unaltered material, respectively. The O-isotopic compositions of two grains, one each from the Fe-rich and Fe-poor matrix, are consistent with formation in the circumstellar envelopes of low-mass Asymptotic Giant Branch (AGB)/Red Giant Branch (RGB) stars. The other two grains, also one each from the Fe-rich and Fe-poor matrix, have O-isotopic compositions consistent with formation in the ejecta of type-II supernovae (SNe). The grains derived from AGB/RGB stars include two polycrystalline pyroxene grains that contain Fe-rich rims. The SNe grains include a polycrystalline Ca-bearing pyroxene and a polycrystalline assemblage consistent with a mixture of olivine and pyroxene. Ferrihydrite is observed in all focused ion beam sections, consistent with parent-body aqueous alteration of the fine-grained matrix under oxidizing conditions. The Fe-rich rims around presolar silicates in this study are consistent with Fe-diffusion into the grains resulting from early-stage hydrothermal alteration, but such alteration was not extensive enough to lead to isotopic equilibration with the surrounding matrix.     

Seasonal and depth-dependent variations in the size and lipid contents of stage 5 copepodites of Calanus finmarchicus in the waters of the Newfoundland Shelf and the Labrador Sea

We report on the variation in energy reserves of individual C5 copepodites of Calanus finmarchicus from the Newfoundland continental shelf and the Labrador Sea collected from surface and overwintering (or bottom) depths prior to, during and after the expected timing of the onset of diapause. Overall, the trend was for a decreasing average prosome length as the year progressed for all locations although the decline was smallest in the Labrador Sea and greatest in the deep waters of the continental shelf. The size of the oil sac was closely linked to the weight of the copepodite but the form of this relationship showed substantial variations with depth and season. We show a clear increase in the relative oil sac volume for C. finmarchicus between late spring and late summer, by which time some animals had descended to diapause depths. The progressive decrease in oil sac volume of animals sampled at depth in the Labrador Sea between September and December suggests a significant loss of energy reserves during diapause. From the distribution of volumes and body sizes in December we estimate that 23–53% of individuals would not be able to meet the energetic cost of moulting and early gonad development. Overall, some of our observations appear to invalidate earlier hypotheses concerning the governing role of lipids in the life history of C. finmarchicus. However, assessment of the factors that influence entry into dormancy should be based on the relative probabilities of alternative strategies for successful reproduction (e.g. entering dormancy vs. continuing into a second generation).     

Evidence for a warmer period during the 12th and 13th centuries AD from chironomid assemblages in Southampton Island, Nunavut, Canada

This study presents the Late-Holocene evolution of a northern Southampton Island (Nunavut, Canada) lake, using fossil chironomids supported by sedimentological evidences (XRF, grain size and CNS). All proxies revealed a relatively stable environment during the last millennium with short-lived events driving changes in the entire lake ecosystem. The chironomid-based paleotemperatures revealed variations of significant amplitude coincident with changes in the sediment density and chemical composition of the core. Higher temperature intervals were generally correlated to lower sediment density with higher chironomid concentration and diversity. Higher temperatures were recorded from cal yr AD 1160 to AD 1360, which may correspond to the Medieval Warm Period. Between cal yr AD 1360 and AD 1700, lower temperatures were probably related to a Little Ice Age event. This study presents new information on the timing of known climatic events which will refine our knowledge of the paleoclimate and climatic models of the Foxe Basin region. It also provides a new framework for the evolution of such freshwater ecosystems under the “Anthropocene” and underlines the importance of including sedimentological proxies when interpreting chironomid remains as this combined approach provides an extended overview of the past hydrological and geochemical changes and their impacts on lake biota.