Contrasting the chemical evolution of the Milky Way and Andromeda

The chemical evolution history of a galaxy hides clues about how it formed and has been changing through time. We have studied the chemical evolution history of the Milky Way (MW) and Andromeda (M31) to find which are common features in the chemical evolution of disc galaxies as well as which are galaxy-dependent. We use a semi-analytic multizone chemical evolution model. Such models have succeeded in explaining the mean trends of the observed chemical properties in these two Local Group spiral galaxies with similar mass and morphology. Our results suggest that while the evolution of the MW and M31 shares general similarities, differences in the formation history are required to explain the observations in detail. In particular, we found that the observed higher metallicity in the M31 halo can be explained by either (i) a higher halo star formation efficiency (SFE), or (ii) a larger reservoir of infalling halo gas with a longer halo formation phase. These two different pictures would lead to (i) a higher [O/Fe] at low metallicities, or (ii) younger stellar populations in the M31 halo, respectively. Both pictures result in a more massive stellar halo in M31, which suggests a possible correlation between the halo metallicity and its stellar mass.     

Evolution of electron and proton temperatures in a flaring loop

We have investigated numerically how a temperature difference between electrons and protons is produced in a flaring loop by adopting a one-fluid, two-temperature model instead of a single-temperature model. We have treated a case in which flare energy is released in the form of heating of electrons located in the top part of the loop.In this case, a large temperature difference (T _e/T _p 10) appears in the corona in the energy-input phase of the flare. When the material evaporated from the chromosphere fills the corona, the temperature difference in the loop begins to shrink rapidly from below. Eventually, in the loop apex, the proton temperature exceeds the electron temperature mainly due to cooling of the electrons by conduction down the loop and heating of the protons by compression of the ascending material. In the late phase of the flare (t 15 min from the flare onset), the temperature difference becomes less than 2% of the mean temperature of electrons and protons at every point in the loop.     

In situ strength measurements on natural upper-mantle minerals

Using in situ strength measurements at pressures up to 10 GPa and at room temperature, 400, 600, and 700°C, we examined rheological properties of olivine, orthopyroxene, and chromian-spinel contained in a mantle-derived xenolith. Mineral strengths were estimated using widths of X-ray diffraction peaks as a function of pressure, temperature, and time. Differential stresses of all minerals increase with increasing pressure, but they decrease with increasing temperature because of elastic strain on compression and stress relaxation during heating. During compression at room temperature, all minerals deform plastically at differential stress of 4–6 GPa. During subsequent heating, thermally induced yielding is observed in olivine at 600°C. Neither orthopyroxene nor spinel shows complete stress relaxation, but both retain some stress even at 700°C. The strength of the minerals decreases in the order of chromian-spinel ≈ orthopyroxene > olivine for these conditions. This order of strength is consistent with the residual pressure of fluid inclusions in mantle xenoliths.     

Barotropic Response of the Sea of Okhotsk to Wind Forcing

We have examined wind-induced circulation in the Sea of Okhotsk using a barotropic model that contains realistic topography with a resolution of 9.25 km. The monthly wind stress field calculated from daily European Centre for Medium-Range Weather Forecasting (ECMWF) Re-Analysis data is used as the forcing, and the integration is carried out for 20 days until the circulation attains an almost steady state. In the case of November (a representative for the winter season from October to March), southward currents of velocity 0.1–0.3 m s⁻¹ occur along the bottom contours off the east of Sakhalin Island. The currents are mostly confined to the shelf (shallower than 200 m) and extend as far south as the Hokkaido coast. In the July case (a representative for the summer season from April to September), significant currents do not occur, even in the shallow shelves. The simulated southward current over the east Sakhalin shelf appears to correspond to the near-shore branch of the East Sakhalin Current (ESC), which was observed with the surface drifters. These seasonal variations simulated in our experiments are consistent with the observations of the ESC. Dynamically, the simulated ESC is interpreted as the arrested topographic wave (ATW), which is the coastally trapped flow driven by steady alongshore wind stress. The volume transport of the simulated ESC over the shelf reaches about 1.0 Sv (1 Sv = 10⁶ m³s⁻¹) in the winter season, which is determined by the integrated onshore Ekman transport in the direction from which shelf waves propagate. This revised version was published online in July 2006 with corrections to the Cover Date.     

Recovery of thermohaline circulation under CO2 stabilization and overshoot scenarios

In this study we examine the behavior of the thermohaline circulation, as simulated by the Community Climate System Model version 3 (CCSM3), for several centuries following CO₂ stabilization for the SRES B1 and A1B scenarios and for an “overshoot” scenario in which CO₂ levels temporarily reach the same level as in the A1B scenario before declining to an ultimate stabilization level that is identical to the B1 case. While we find no evidence for irreversible changes of the thermohaline circulation in the overshoot experiment, the interplay of the different timescales of the temperature response of the surface and interior ocean does lead to a number of differences in the long-term response of the ocean between it and the B1 stabilization scenario where the same GHG levels are approached by different paths. The stronger initial warming and its slow penetration into the deeper ocean, followed by a transient surface cooling in the overshoot scenario leads to lower static stability, deeper mixing, and a more rapid recovery of the thermohaline circulation than in the B1 stabilization scenario. While the overshoot scenario recovers surface conditions (e.g. SST, sea ice extent) very similar to the B1 scenario shortly after reaching the same GHG levels, the additional accumulation of heat in the interior ocean during the period of higher forcing causes the global mean ocean temperature and steric sea level to remain higher than in the B1 stabilization scenario for at least another several centuries.     

Bioenhancement of cadmium transfer along a multi-level food chain

Previous studies have shown that metal partitioned to a subcellular compartment containing trophically available metal (TAM) is readily available to predators and may be enhanced by increased binding of metal to heat-stable proteins (HSP - e.g., metallothioneins). The aim of the current investigation was to determine the influence of TAM on the trophic transfer of Cd along an experimental, three-level food chain: Artemia franciscana (brine shrimp)-->Palaemonetes pugio (grass shrimp)-->Fundulus heteroclitus (mummichog). P. pugio were fed for 7 days on A. franciscana exposed to Cd in solution (including (109)Cd as radiotracer) and subjected to subcellular fractionation or fed to F. heteroclitus. An HSP-driven increase in the percentage of Cd associated with TAM (TAM-Cd%) in A. franciscana exposed to 1 muM Cd resulted in a bioenhancement (i.e., a greater than linear increase with respect to A. franciscana exposure) of Cd trophic transfer to P. pugio. Increased dietary Cd exposure did not affect TAM-Cd% in P. pugio nor trophic transfer to F. heteroclitus.     

Decarbonation reaction of magnesite in subducting slabs at the lower mantle

High-pressure and temperature experiments (28–62 GPa, and 1,490–2,000 K, corresponding to approximately 770–1,500 km depth in the mantle) have been conducted on a MgCO₃ + SiO₂ mixture using a laser-heated diamond anvil cell combined with analytical transmission electron microscope observation of the product phases to constrain the fate of carbonates carried on the subducting basalt into the lower mantle. At these conditions, the decarbonation reaction MgCO₃ (magnesite) + SiO₂ (stishovite) → MgSiO₃ (perovskite) + CO₂ (solid) has been recognized. This indicates that above reaction takes place as a candidate for decarbonation of the carbonated subducting mid ocean ridge basalts in the Earth’s lower mantle.     

Thermodynamic modelling of sodic pyroxene solid-solution and its application in a garnet-omphacite-kyanite-coesite geothermobarometer for UHP metamorphic rocks

A garnet-omphacite-kyanite-coesite geothermobarometer is constructed to estimate the peak metamorphic pressure of ultrahigh-pressure (UHP) eclogites. For this we use a quaternary regular solution model for garnet, and propose a new model for sodic pyroxene that assumes double site solid-solution (Na,Ca)^M2(Al,Fe³⁺,Fe²⁺,Mg)^M1Si₂O₆, where cations in the M2- and the M1-sites mix randomly but with inter-site interactions, not only between nearest neighboring cations but also between next nearest neighboring cations. In the new model, overall excess interaction parameters are quantitatively deduced from the previous experimental data and critical temperature, and the activity of the jadeite component agrees reasonably with that based on the Landau theory. Furthermore, the relations of the calculated order parameter to temperature and composition are consistent with other experimental works. These facts support the usefulness of the new model. Application of our geothermobarometer to kyanite eclogite gave metamorphic conditions around 3.4 GPa and 800 ^∘C for both samples from the Dora Maira Massif, Western Alps, and from Rongcheng County, in the Su-Lu region of eastern China. Received: 30 December 1996 / Accepted: 25 August 1997     

Structural modifications of CaGeO3-wollastonite under room temperature pressurization

 In-situ X-ray diffraction measurements of CaGeO₃-wollastonite at high pressure at room temperature have been performed using a diamond anvil cell with an X-ray source. A new structural modification of CaGeO₃-wollastonite is observed at about 6GPa and the characteristic reflections of the high pressure form are preserved on decompression to an ambient pressure. A rhodonite-like structure is proposed as a high pressure form from the crystal chemical consideration. The rhodonite-like phase is further transformed into a perovskite-form at about 15 GPa. The rhodonite-like-form of CaGeO₃ seems not to be a stable phase from the heating experiments under high pressures. The metastable transition path from the wollastonite to the perovskite polymorph through the rhodonite-like structure is kinetically favored under room temperature pressurization. No pressure-induced amorphization is observed during the transition into the perovskite-form, although the transition is accompanied by the coordination change of Ge atoms from fourfold to sixfold. Received: July 19, 1995 / Revised, accepted: August 1996     

Neodymium isotopic variations in Northwest Pacific waters

Four vertical profiles of the concentration and isotopic composition of Nd in seawater were obtained in the western North Pacific. Two profiles from the Kuroshio Current regime showed congruently that although the Nd concentration increases gradually with depth, its isotopic composition varies significantly with depth depending upon the water mass occupying the water column. The high-salinity Kuroshio waters originating from the North Pacific Tropical Water (NPTW) carry the least radiogenic Nd (?_Nd = −7.4 to −8.7) to this region at ∼250 m from the western margin continental shelves, most likely from the East China Sea. The Nd isotopic compositions in the North Pacific Intermediate Water (NPIW) that occurs at 600 to 1000 m in the subtropical region are fairly uniform at ?_Nd = −3.7. The profile data from the ∼38° to 40°N Kuroshio/Oyashio mixed water region off Sanriku of Honshu, Japan, also suggest that the newest NPIW with ?_Nd = −3.2 is formed there by the mixing of various source waters, and the radiogenic component of Nd is derived mainly from the Oyashio waters.In the Pacific Deep Water (PDW) below ∼1000 m, the Nd isotopic composition is neither vertically nor horizontally homogeneous, suggesting that it serves as a useful tracer for sluggish deep water circulation as well. Two profiles from the Izu-Ogasawara Trench showed a minimum ?_Nd value at ∼2000 m, suggesting that there exists a horizontal advective flow in the vicinity of Honshu, Japan. There is some evidence from other chemical properties to support this observation. The waters below 4000 m including those within the trench in the subtropical region have ?_Nd values of around −5, suggesting that the deep waters are fed from the south along the western boundary, ultimately from the Antarctic Bottom Water (AABW) in the South Pacific. This extends up to ∼40°N along the Japanese Islands. In the subarctic region (>∼42°N), the waters have more radiogenic Nd with ?_Nd > −4.0 throughout the water column, presumably due to the supply of Nd by weathering in such igneous provinces as the Kuril-Kamchatska-Aleutian Island chain. The lateral inhomogeneity of the Nd isotopic composition in PDW suggests that there may be different circulation and mixing regimes in the North Pacific Basin.