Partial melting due to breakdown of an epidote‐group mineral during exhumation of ultrahigh‐pressure eclogite: An example from the North‐East Greenland Caledonides

In the North‐East Greenland Caledonides, P–T conditions and textures are consistent with partial melting of ultrahigh‐pressure (UHP) eclogite during exhumation. The eclogite contains a peak assemblage of garnet, omphacite, kyanite, coesite, rutile, and clinozoisite; in addition, phengite is inferred to have been present at peak conditions. An isochemical phase equilibrium diagram, along with garnet isopleths, constrains peak P–T conditions to be subsolidus at 3.4 GPa and 940°C. Zr‐in‐rutile thermometry on inclusions in garnet yields values of ~820°C at 3.4 GPa. In the eclogite, plagioclase may exhibit cuspate textures against surrounding omphacite and has low dihedral angles in plagioclase–clinopyroxene–garnet aggregates, features that are consistent with former melt–solid–solid boundaries and crystallized melt pockets. Graphic intergrowths of plagioclase and amphibole are present in the matrix. Small euhedral neoblasts of garnet against plagioclase are interpreted as formed from a peritectic reaction during partial melting. Polymineralic inclusions of albite+K‐feldspar and clinopyroxene+quartz±kyanite±plagioclase in large anhedral garnet display plagioclase cusps pointing into the host, which are interpreted as crystallized melt pockets. These textures, along with the mineral composition, suggest partial melting of the eclogite by reactions involving phengite and, to a large extent, an epidote‐group mineral. Calculated and experimentally determined phase relations from the literature reveal that partial melting occurred on the exhumation path, at pressures below the coesite to quartz transition. A calculated P–T phase diagram for a former melt‐bearing domain shows that the formation of the peritectic garnet rim occurred at 1.4 GPa and 900°C, with an assemblage of clinopyroxene, amphibole, and plagioclase equilibrated at 1.3 GPa and 720°C. Isochemical phase equilibrium modelling of a symplectite of clinopyroxene, plagioclase, and amphibole after omphacite, combined with the mineral composition, yields a P–T range at 1.0–1. 6 GPa, 680–1,000°C. The assemblage of amphibole and plagioclase is estimated to reach equilibrium at 717–732°C, calculated by amphibole–plagioclase thermometry for the former melt‐bearing domain and symplectite respectively. The results of this study demonstrate that partial melt formed in the UHP eclogite through breakdown of an epidote‐group mineral with minor involvement of phengite during exhumation from peak pressure; melt was subsequently crystallized on the cooling path.     

Photochemical escape of oxygen from Mars: A comparison of the exobase approximation to a Monte Carlo method

The non-thermal escape of neutral O atoms from Mars at the current epoch is largely due to dissociative recombination of :

     

MGS electron density profiles: Analysis of the peak magnitudes

We analyze here the behavior of the magnitudes of the F₁ and E peaks of the electron density profiles measured by the Radio Science Subsystem of the Mars Global Surveyor spacecraft, as a function of solar zenith angle χ and solar flux. For each of the 658 days of data in the six occultation seasons in the northern hemisphere, we choose one profile to analyze, which is that for which the F₁ peak is the median value. We assume that the variations of the measured peak densities can be represented as Aa(cosχ) and as Bb(F_10.7), where F_10.7 is the usual solar flux proxy, appropriately shifted to the orbital position of Mars. To minimize the effect of solar activity, we divide the data into 6 F_10.7 bins, fit the data in each bin, and derive the values of the exponent a and the coefficient AF10.7 for each bin. The median values that we derive for the exponent a is 0.46 for the F₁ peak, and 0.395 for the E peak. To minimize the effect of SZA, we divide the data into eight SZA bins, and derive the exponent b and the coefficient Bχ for each SZA bin. We argue that the last three SZA bins should be excluded because the fits were poor, due partly to the small number of data points in each of these bins. If we do so, the median values of b that we derive are 0.27 and 0.40 for the F₁ and E peaks, respectively. Finally we derive a 3-parameter fit to all the data, which expresses the variability of the peak densities as a function of a^′(cosχ) and b^′(F_10.7) simultaneously. The fitted values of the exponents a^′ and b^′ for the F₁ peak are 0.45 and 0.26, respectively; for the E peak, the values are 0.39 and 0.46, respectively. We compare our results to Chapman theory, and to those of other investigators.     

Englacial and subglacial water flow at Skálafellsjökull,Iceland derived from ground penetrating radar,in situ Glacsweb probe and borehole water level measurements

We reconstruct englacial and subglacial drainage at Skálafellsjökull, Iceland, using ground penetrating radar (GPR) common offset surveys, borehole studies and Glacsweb probe data. We find that englacial water is not stored within the glacier (water content ~0–0.3%). Instead, the glacier is mostly impermeable and meltwater is able to pass quickly through the main body of the glacier via crevasses and moulins. Once at the glacier bed, water is stored within a thin (1 m) layer of debris‐rich basal ice (2% water content) and the till. The hydraulic potential mapped across the survey area indicates that when water pressures are high (most of the year), water flows parallel to the margin, and emerges 3 km down glacier at an outlet tongue. GPR data indicates that these flow pathways may have formed a series of braided channels. We show that this glacier has a very low water‐storage capacity, but an efficient englacial drainage network for transferring water to the glacier bed and, therefore, it has the potential to respond rapidly to changes in melt‐water inputs. © 2015 The Authors. Earth Surface Processes and Landforms published by John Wiley & Sons Ltd.     

Heavy metals in surface sediments of Waiwhetu Stream,Lower Hutt,New Zealand

Abstract

Surface sediment samples (60 μm‐2 mm, and < 60 μm fractions) from the Waiwhetu Stream, Lower Hutt City, New Zealand, were leached with dilute HCl to remove the mobile heavy‐metal fraction. Cd, Cr, Cu, Pb, Zn, Al, Fe, and Mn analyses of the leachates show that sediments of the upper reaches area of the stream are generally uncontaminated. In contrast, sediments in the lower reaches area are highly contaminated, despite clean‐up measures in the late 1970s. Lead and Zn are the most significantly enriched metals with concentrations over 1000 mg kg^?1 adjacent to some drains. In the polluted zone, metals originate from either upward remobilisation from underlying sediment (contaminated in the early 1960s and 70s) or more recent industrial spillages. Similar trends exhibited by Cd, Cu, Cr, Zn, Pb, and Al indicate that a proportion of the metal enrichment downstream probably results from a naturally higher clay content of sediments near the mouth of the stream. Fe and Mn show reverse trends to the other metals, indicating that a high proportion of these two metals occurs in substrate different to that of the other metals. The orange brick‐coloured sediments of the upper reaches of the stream indicate oxides upstream; the black sediments in the lower reaches indicate sulphides downstream.     

Sr/Sr isotope fingerprinting of Scottish and Icelandic migratory shorebirds

Biosphere Sr isotope composition data from Iceland and Scotland suggest that terrestrially feeding birds from these two countries will have significantly different ⁸⁷Sr/⁸⁶Sr isotope composition in their tissues. The aim of this study is to test if these differences can be measured within the bone and feather of migratory wading birds, who feed terrestrially as juveniles, thus providing a provenance tool for these birds.     

Amphibole megacrysts as a probe into the deep plumbing system of Merapi volcano,Central Java,Indonesia

Amphibole has been discussed to potentially represent an important phase during early chemical evolution of arc magmas, but is not commonly observed in eruptive arc rocks. Here, we present an in-depth study of metastable calcic amphibole megacrysts in basaltic andesites of Merapi volcano, Indonesia. Radiogenic Sr and Nd isotope compositions of the amphibole megacrysts overlap with the host rock range, indicating that they represent antecrysts to the host magmas rather than xenocrysts. Amphibole-based barometry suggests that the megacrysts crystallised at pressures of >500 MPa, i.e., in the mid- to lower crust beneath Merapi. Rare-earth element concentrations, in turn, require the absence of magmatic garnet in the Merapi feeding system and, therefore, place an uppermost limit for the pressure of amphibole crystallisation at ca. 800 MPa. The host magmas of the megacrysts seem to have fractionated significant amounts of amphibole and/or clinopyroxene, because of their low Dy/Yb ratios relative to the estimated compositions of the parent magmas to the megacrysts. The megacrysts’ parent magmas at depth may thus have evolved by amphibole fractionation, in line with apparently coupled variations of trace element ratios in the megacrysts, such as e.g., decreasing Zr/Hf with Dy/Yb. Moreover, the Th/U ratios of the amphibole megacrysts decrease with increasing Dy/Yb and are lower than Th/U ratios in the basaltic andesite host rocks. Uranium in the megacrysts’ parent magmas, therefore, may have occurred predominantly in the tetravalent state, suggesting that magmatic fO₂ in the Merapi plumbing system increased from below the FMQ buffer in the mid-to-lower crust to 0.6–2.2 log units above it in the near surface environment. In addition, some of the amphibole megacrysts experienced dehydrogenation (H₂ loss) and/or dehydration (H₂O loss), as recorded by their variable H₂O contents and D/H and Fe³⁺/Fe²⁺ ratios, and the release of these volatile species into the shallow plumbing system may facilitate Merapi’s often erratic eruptive behaviour.     

Oxygen isotope analysis of diatom silica and authigenic calcite from Lake Pinarbasi, Turkey

There is increasing interest in the ¹⁸O/¹⁶O ratio of diatom silica, particularly for lakes where carbonates are absent. Here we compare the ¹⁸O/¹⁶O ratios preserved in diatom silica and authigenic calcite from an open, spring-fed, freshwater lake core from Turkey which spans marine oxygen isotope stage 3. The two sets of isotope data show contrasting trends in spite of their mutual dependence on the water ¹⁸O/¹⁶O ratio and lake-water temperature. The most likely explanation for this divergence is difference in seasonality of biological productivity mediated by the strongly continental climate of the Anatolian plateau. Diatom silica and authigenic calcite are precipitated from solutes in the lake-water at different times of the year. Diatom productivity follows a well-defined seasonal cycle, peaking first and most importantly in the spring and then in the autumn. The precipitation of calcite follows productivity by all forms of photosynthetic organisms that deplete CO₂ but in most lakes this occurs during the summer months. The ¹⁸O_calcite curve shows mean summer temperature maxima at ca. 30–35 and ca. 58 ka BP while the intervening data represent a period of relatively cool summers. The ¹⁸O_diatom curve shows bipolar results (15–20 and 29–33), which suggests that at least two discrete sources or processes contributed to the oxygen composition of the diatoms but probably involved a dilution mechanism to shift the isotopic values. The most likely source of depleted water is from snow entering the lake during the spring thaw. We infer that many authigenic calcite curves from regions with markedly seasonal climates may be temporally limited to a few summer months and that diatom silica provides complementary data on seasonally-specific water isotopic composition rather than a substitute for analyses based on carbonate.