Lead isotopes and age of Hawaiian lherzolite nodules

The reaction between enstatite (En_95.3Fs_4.7) and CaCO₃ has been studied at pressures between 23 and 77 kbars and at temperatures between 800° and 1400°C. At 1000°C enstatite and CaCO₃ react to form dolomite and diopside solid solutions at pressures below approximately 45 kbars and magnesite and diopside solid solutions at higher pressures. The curve for the reaction dolomite_ss + enstatite_ss ? magnesite_ss + diopside_ss lies between 40 to 45 kbars at 1000°C and between 45 and 50 kbars at 1200°C. It is very close to the graphite-diamond transition curve. These experimental results indicate that calcite (or aragonite) is unstable in the presence of enstatite, and that dolomite and magnesite are the stable carbonates at high pressures. The forsterite + aragonite assemblage is, however, stable to at least 80 kbars at 800°C. It is suggested that in the upper mantle where enstatite is present, dolomite is stable to depths of about 150 km and magnesite is stable at greater depths in the continental regions, assuming that the partial pressure of CO₂ is equal or close to the total pressure. It is also suggested that carbonate inclusions in pyroxene can be used as an indicator of the depth of their equilibration; dolomite inclusions in enstatite would be formed at depths shallower than 150 km and magnesite inclusions in diopside at greater depths. Eclogite and peridotite inclusions in kimberlite may be classified on this basis.     

Radiocarbon dates of elevated shorelines,Indonesia and Malaysia. Part 1

Four new radiocarbon dates of elevated strandlines in tectonically active areas of eastern Indonesia and East Malaysia indicate average rates of uplift that range between 4.5 and 9 mm annually during the past 24,000 yr. These values are at least three times higher than former estimates from eastern Indonesia. Another radiocarbon date from the south arm of Sulawesi—also tectonically mobile—indicates a rate of uplift of 1.4–2.5 mm per year which corresponds with earlier determinations. This particular case, however, suggests that the sample was probably located close to a north-south axis about which southern Sulawesi was tilted during the Quaternary.     

The CM carbonaceous chondrite regolith Diepenveen

A carbonaceous chondrite was recovered immediately after the fall near the village of Diepenveen in the Netherlands on October 27, 1873, but came to light only in 2012. Analysis of sodium and poly‐aromatic hydrocarbon content suggests little contamination from handling. Diepenveen is a regolith breccia with an overall petrology consistent with a CM classification. Unlike most other CM chondrites, the bulk oxygen isotopes are extremely ¹⁶O rich, apparently dominated by the signature of anhydrous minerals, distributed on a steep slope pointing to the domain of intrinsic CM water. A small subset plots closer to the normal CM regime, on a parallel line 2 ‰ lower in δ¹⁷O. Different lithologies in Diepenveen experienced varying levels of aqueous alteration processing, being less aqueously altered at places rather than more heated. The presence of an agglutinate grain and the properties of methanol‐soluble organic compounds point to active impact processing of some of the clasts. Diepenveen belongs to a CM clan with ~5 Ma CRE age, longer than most other CM chondrites, and has a relatively young K‐Ar resetting age of ~1.5 Ga. As a CM chondrite, Diepenveen may be representative of samples soon to be returned from the surface of asteroid (162173) Ryugu by the Hayabusa2 spacecraft.     

Mg-Fe partitioning between olivine and ultramafic melts at high pressures

Precise determination of the partitioning of Mg and Fe²⁺ between olivine and ultramafic melt has been made at pressures from 5 to 13 GPa using a MA-8 type multi-anvil high-pressure apparatus (PREM) installed at Earthquake Research Institute, University of Tokyo. A very short rhenium capsule (<100 μm sample thickness) was adopted to minimize temperature variation within the sample container. Synthetic gels with the composition of the upper mantle peridotite were used as starting materials to promote the homogeneity. Analyses of quenched melts and coexisting olivines were made with an electron probe microanalyzer. The obtained partition coefficient, K_D [=(FeO/MgO)^ol/(FeO/MgO)^melt], decreases from 0.35 to 0.25 with increasing pressure from 5 to 13 GPa, suggesting a negative correlation between pressure and K_D above 5 GPa. Our result is consistent with a parabolic relationship between K_D and degree of polymerization (NBO/T) of melts reported by previous studies at lower pressures. The negative correlation between pressure and K_D suggests that olivine crystallizing in a magma ocean becomes more Mg-rich with depth and that primary magmas generated in the upper mantle become more Fe-rich with depth than previously estimated.     

Thermoelastic properties of the high-pressure phase of SnO2 determined by in situ X-ray observations up to 30 GPa and 1400 K

 In situ synchrotron X-ray experiments in the system SnO₂ were made at pressures of 4–29 GPa and temperatures of 300–1400 K using sintered diamond anvils in a 6–8 type high-pressure apparatus. Orthorhombic phase (α-PbO₂ structure) underwent a transition to a cubic phase (Pa3ˉ structure) at 18 GPa. This transition was observed at significantly lower pressures in DAC experiments. We obtained the isothermal bulk modulus of cubic phase K ₀= 252(28) GPa and its pressure derivative K ^′=3.5(2.2). The thermal expansion coefficient of cubic phase at 25 GPa up to 1300 K was determined from interpolation of the P-V-T data obtained, and is 1.7(±0.7) × 10⁻⁵ K⁻¹ at 25 GPa. Received: 7 December 1999 / Accepted: 27 April 2000     

Recent increase of DIC in the western North Pacific

The temporal variation of the total dissolved inorganic carbon (DIC) content in the western North Pacific is investigated by comparing the DIC distribution obtained from the data sets of three different periods, the GEOSECS data observed in 1973, the CO₂ dynamics Cruise data observed in 1982, and recent Japanese data sets observed during the early 1990s. The overall feature of the signal of temporal DIC change during 1973 and early 1990s agreed with that of former studies, and did not significantly change with the calculation scheme (the grid-selection method vs. the multiple regression method). The observed increase in DIC among the different time scales showed a good inner consistency, which also indicates the stability of the method used in the DIC change calculation. The apparent rate of increase of the DIC inventory in the upper 1000 m water column, however, differed significantly by the data set used for the calculation: It was 5.6±2.4 g C/m²/year, based on the data comparison between 1982 and the early 1990s, while it became 7.6±2.4 g C/m²/year when based on the data between 1973 and the early 1990s. This result provides us an information about the data-dependency on the former estimation of temporal DIC change.     

Cross-Validation of Open-Path and Closed-Path Eddy-Covariance Techniques for Observing Methane Fluxes

Methane ( ${\mathrm {CH}}_{4}$ ) fluxes observed with the eddy-covariance technique using an open-path ${\mathrm {CH}}_{4}$ analyzer and a closed-path ${\mathrm {CH}}_{4}$ analyzer in a rice paddy field were evaluated with an emphasis on the flux correction methodology. A comparison of the fluxes obtained by the analyzers revealed that both the open-path and closed-path techniques were reliable, provided that appropriate corrections were applied. For the open-path approach, the influence of fluctuations in air density and the line shape variation in laser absorption spectroscopy (hereafter, spectroscopic effect) was significant, and the relative importance of these corrections would increase when observing small ${\mathrm {CH}}_{4}$ fluxes. A new procedure proposed by Li-Cor Inc. enabled us to accurately adjust for these effects. The high-frequency loss of the open-path ${\mathrm {CH}}_{4}$ analyzer was relatively large (11 % of the uncorrected covariance) at an observation height of 2.5 m above the canopy owing to its longer physical path length, and this correction should be carefully applied before correcting for the influence of fluctuations in air density and the spectroscopic effect. Uncorrected ${\mathrm {CH}}_{4}$ fluxes observed with the closed-path analyzer were substantially underestimated (37 %) due to high-frequency loss because an undersized pump was used in the observation. Both the bandpass and transfer function approaches successfully corrected this flux loss. Careful determination of the bandpass frequency range or the transfer function and the cospectral model is required for the accurate calculation of ${\mathrm {CH}}_{4}$ fluxes with the closed-path technique.     

Flux of low salinity water from Aniva Bay (Sakhalin Island) to the southern Okhotsk Sea

In this study, we examined the relationship between the low salinity water in the shelf region of the southern Okhotsk Sea which was seasonally sampled (0–200 m), and fluxes of low salinity water from Aniva Bay. To express the source of freshwater mixing in the surface layer, we applied normalized total alkalinity (NTA) and stable isotopes of seawater as chemical tracers. NTA-S diagrams indicate that NTA of low salinity water in the upper 30 m layer just off the Soya Warm Current is clearly higher than in the far offshore region in summer and autumn. Using NTA-S regression lines, we could deduce that the low salinity and high NTA water in the upper layer originates from Aniva Bay. For convenience, we defined this water as the Aniva Surface Water (ASW) with values S < 32, NTA > 2450 μmol kg⁻¹. Formation and transport processes of ASW are discussed using historical data. The interaction between the maximum core of high NTA water on the bottom slope of eastern Aniva Bay and an anticyclonic eddy at the mouth of Aniva Bay are concluded to control ASW formation. Upwelling of the Cold Water Belt water at the tip of Cape Krillion is considered to cause ASW outflow from Aniva Bay.     

Composition of the first bulk melt sample from a volcanic region of Mars: Queen Alexandra Range 94201

Abstract— Antarctic meteorite Queen Alexandra Range (QUE) 94201 is a 12 g basaltic achondrite dominated by plagioclase (now maskelynite) and zoned low‐ and high‐Ca pyroxene. Petrologic, geochemical, and isotopic analyses indicate that it is related to previously described basaltic and Iherzolitic shergottites, which are a group of igneous meteorites that are believed to be from Mars. Unlike previous shergottites, however, QUE 94201 represents a bulk melt rather than a cumulate fraction, meaning it can be used to infer magmatic source regions and the compositions of other melts on Mars. This melt has much more Fe and P than basaltic melts produced on Earth and formed at a much lower oxygen fugacity. This has altered the crystallization sequence of the melt, removing olivine from the liquidus to produce a plagioclase and 2‐pyroxene assemblage. If the high‐phosphorus and low‐oxygen fugacity conditions represented by QUE 94201 are common in magmatic regions of Mars, then olivine may be rare in marrian basalts. No solar cosmic ray effects were seen in the concentrations of ¹⁰Be, ²⁶A1, and ³⁶C1 with depth in the meteorite, implying at least 3 cm of ablation during entry to Earth. Significant excesses of neutron capture noble gas isotopes (^80,82Kr and ^128,131Xe) suggest that the QUE 94201 sample came from a depth >22 cm in a meteoroid of at least that radius. The meteorite also has very low ²¹Ne/²²Ne, which would often be interpreted to mean little ablation (contradicting above evidence) but, in this case, appears to reflect a very low abundance of Mg (the principal target element for Ne) in the meteorite, consistent with our bulk chemical analyses. The meteorite has a terrestrial ³⁶C1 age of 0.29 ± 0.05 Myr and a ¹⁰Be exposure age of 2.6 ± 0.5 Myr in a 47π geometry, implying an ejection age of 2.9 ± 0.5 Myr.     

New high-pressure phases in BaCO<Subscript>3</Subscript>

Barium carbonate (BaCO₃) was examined in a diamond anvil cell up to a pressure of 73 GPa using an in situ angle-dispersive X-ray diffraction technique. Three new phases of BaCO₃ were observed at pressures >10 GPa. From 10 to 24 GPa, BaCO₃-IV had a post-aragonite structure with space group Pmmn. There are two molecules in a single unit cell (Z = 2) of the orthorhombic phase, which is same as the high-pressure phases of CaCO₃ and SrCO₃. The isothermal bulk modulus of BaCO₃-IV is K ₀ = 84(4) GPa, with V ₀ = 129.0(7) Å³ when K ₀′ = 4. The c axis of the unit cell parameter is less compressible than the a and b axes. The relative change in volume that accompanies the transformation between BaCO₃-III and BaCO₃-IV is ～6%. BaCO₃-V, which has an orthorhombic symmetry, was synthesized at 50 GPa. As the pressure increases, BaCO₃-V is transformed into tetragonal BaCO₃-VI. This transformation is likely to be second order, because the diffraction pattern of BaCO₃-V is similar to that of BaCO₃-VI, and some single peaks in BaCO₃-VI become doublets in BaCO₃-V. After decompression, the new high-pressure phases transform into BaCO₃-II. Our findings resolve a dispute regarding the stable high-pressure phases of BaCO₃.