The compressibility of Fe- and Al-bearing phase D to 30 GPa

High-pressure in situ X-ray diffraction experiment of Fe- and Al-bearing phase D (Mg_0.89Fe_0.14Al_0.25Si_1.56H_2.93O₆) has been carried out to 30.5 GPa at room temperature using multianvil apparatus. Fitting a third-order Birch–Murnaghan equation of state to the P–V data yields values of V ₀ = 86.10 ± 0.05 ų; K ₀ = 136.5 ± 3.3 GPa and K′ = 6.32 ± 0.30. If K′ is fixed at 4.0 K ₀ = 157.0 ± 0.7 GPa, which is 6% smaller than Fe–Al free phase D reported previously. Analysis of axial compressibilities reveals that the c-axis is almost twice as compressible (K _c  = 93.6 ± 1.1 GPa) as the a-axis (K _a  = 173.8 ± 2.2 GPa). Above 25 GPa the c/a ratio becomes pressure independent. No compressibility anomalies related to the structural transitions of H-atoms were observed in the pressure range to 30 GPa. The density reduction of hydrated subducting slab would be significant if the modal amount of phase D exceeds 10%.     

Interaction of peridotite with Ca-rich carbonatite melt at 3.1 and 6.5 GPa: Implication for merwinite formation in upper mantle,and for the metasomatic origin of sublithospheric diamonds with Ca-rich suite of inclusions

We performed an experimental study, designed to reproduce the formation of an unusual merwinite?+?olivine-bearing mantle assemblage recently described as a part of a Ca-rich suite of inclusions in sublithospheric diamonds, through the interaction of peridotite with an alkali-rich Ca-carbonatite melt, derived from deeply subducted oceanic crust. In the first set of experiments, we studied the reaction between powdered Mg-silicates, olivine and orthopyroxene, and a model Ca-carbonate melt (molar Na:K:Ca?=?1:1:2), in a homogeneous mixture, at 3.1 and 6.5 GPa. In these equilibration experiments, we observed the formation of a merwinite?+?olivine-bearing assemblage at 3.1 GPa and 1200 °C and at 6.5 GPa and 1300–1400 °C. The melts coexisting with this assemblage have a low Si and high Ca content (Ca#?=?molar 100?×?Ca/(Ca?+?Mg)?>?0.57). In the second set of experiments, we investigated reaction rims produced by interaction of the same Ca-carbonate melt (molar Na:K:Ca?=?1:1:2) with Mg-silicate, olivine and orthopyroxene, single crystals at 3.1 GPa and 1300 °C and at 6.5 GPa and 1400 °C. The interaction of the Ca-carbonate melt with olivine leads to merwinite formation through the expected reaction: 2Mg₂SiO₄ (olivine)?+?6CaCO₃ (liquid)?=?Ca₃MgSi₂O₈ (merwinite)?+?3CaMg(CO₃)₂ (liquid). Thus, our experiments confirm the idea that merwinite in the upper mantle may originate via interaction of peridotite with Ca-rich carbonatite melt, and that diamonds hosting merwinite may have a metasomatic origin. It is remarkable that the interaction of the Ca-carbonate melt with orthopyroxene crystals does not produce merwinite both at 3.1 and 6.5 GPa. This indicates that olivine grain boundaries are preferable for merwinite formation in the upper mantle.     

Phase relations and melting of carbonated peridotite between 10 and 20 GPa: a proxy for alkali- and CO<Subscript>2</Subscript>-rich silicate melts in the deep mantle

We determined the melting phase relations, melt compositions, and melting reactions of carbonated peridotite on two carbonate-bearing peridotite compositions (ACP: alkali-rich peridotite + 5.0 wt % CO₂ and PERC: fertile peridotite + 2.5 wt % CO₂) at 10–20 GPa and 1,500–2,100 °C and constrain isopleths of the CO₂ contents in the silicate melts in the deep mantle. At 10–20 GPa, near-solidus (ACP: 1,400–1,630 °C) carbonatitic melts with < 10 wt % SiO₂ and > 40 wt % CO₂ gradually change to carbonated silicate melts with > 25 wt % SiO₂ and < 25 wt % CO₂ between 1,480 and 1,670 °C in the presence of residual majorite garnet, olivine/wadsleyite, and clinoenstatite/clinopyroxene. With increasing degrees of melting, the melt composition changes to an alkali- and CO₂-rich silicate melt (Mg# = 83.7–91.6; ~ 26–36 wt % MgO; ~ 24–43 wt % SiO₂; ~ 4–13 wt % CaO; ~ 0.6–3.1 wt % Na₂O; and ~ 0.5–3.2 wt % K₂O; ~ 6.4–38.4 wt % CO₂). The temperature of the first appearance of CO₂-rich silicate melt at 10–20 GPa is ~ 440–470 °C lower than the solidus of volatile-free peridotite. Garnet + wadsleyite + clinoenstatite + carbonatitic melt controls initial carbonated silicate melting at a pressure < 15 GPa, whereas garnet + wadsleyite/ringwoodite + carbonatitic melt dominates at pressure > 15 GPa. Similar to hydrous peridotite, majorite garnet is a liquidus phase in carbonated peridotites (ACP and PERC) at 10–20 GPa. The liquidus is likely to be at ~ 2,050 °C or higher at pressures of the present study, which gives a melting interval of more than 670 °C in carbonated peridotite systems. Alkali-rich carbonated silicate melts may thus be produced through partial melting of carbonated peridotite to 20 GPa at near mantle adiabat or even at plume temperature. These alkali- and CO₂-rich silicate melts can percolate upward and may react with volatile-rich materials accumulate at the top of transition zone near 410-km depth. If these refertilized domains migrate upward and convect out of the zone of metal saturation, CO₂ and H₂O flux melting can take place and kimberlite parental magmas can be generated. These mechanisms might be important for mantle dynamics and are potentially effective metasomatic processes in the deep mantle.     

Petrographic study of the Miocene Mizunami Group,Central Japan: Detection of unrecognized volcanic activity in the Setouchi Province

A petrographic study of sandstones from the Miocene Mizunami Group in Central Japan has been performed on core samples from a single borehole, in order to evaluate the provenance of the sedimentary rock. Evaluation of the provenance is based on bulk mineral, heavy mineral and plagioclase contents and on whole rock chemical compositions. The sandstones studied are divisible into three types; the first type is characterized by the occurrence of biotite and plagioclase ranging from albite to oligoclase, the second type is characterized by the dominance of amphibole and labradorite with pyroxene (clinopyroxene > orthopyroxene), and the third type is characterized by the dominance of pyroxene (orthopyroxene > clinopyroxene) and andesine with lesser labradorite, bytownite and anorthite. The first type is interpreted to be derived from the basement granite, whereas the others were derived mostly from volcanic ash, judging from their mineral compositions. The volcanic activity that supplied the volcanic ash to the Mizunami Basin occurred in two phases, distinguishable by variations in their mineralogical and geochemical compositions, an indication of change in character of the volcanic activity. This petrographic study of the sandstones in the Mizunami Group suggests that unrecognized volcanic activity occurred around the Mizunami Basin, even though potential provenance of the volcanic ash has not yet been identified.     

Western Arctic primary productivity regulated by shelf-break warm eddies

The response of phytoplankton to the Beaufort shelf-break eddies in the western Arctic Ocean is examined using the eddy-resolving coupled sea ice–ocean model including a lower-trophic marine ecosystem formulation. The regional model driven by the reanalysis 2003 atmospheric forcing from March to November captures the major spatial and temporal features of phytoplankton bloom following summertime sea ice retreat in the shallow Chukchi shelf and Barrow Canyon. The shelf-break warm eddies spawned north of the Barrow Canyon initially transport the Chukchi shelf water with high primary productivity toward the Canada Basin interior. In the eddy-developing period, the anti-cyclonic rotational flow along the outer edge of each eddy moving offshore occasionally traps the shelf water. The primary production inside the warm eddies is maintained by internal dynamics in the eddy-maturity period. In particular, the surface central area of an anti-cyclonic eddy acquires adequate light, nutrient, and warm environment for photosynthetic activity partly attributed to turbulent mixing with underlying nutrient-rich water. The simulated biogeochemical properties with the dominance of small-size phytoplankton inside the warm eddies are consistent with the observational findings in the western Arctic Ocean. It is also suggested that the light limitation before autumn sea ice freezing shuts down the primary production in the shelf-break eddies in spite of nutrient recovery. These results indicate that the time lag between the phytoplankton bloom in the shelf region following the summertime sea ice retreat and the eddy generation along the Beaufort shelf break is an important index to determine biological regimes in the Canada Basin.     

Sound velocity measurements in dhcp-FeH up to 70 GPa with inelastic X-ray scattering: Implications for the composition of the Earth's core

We have determined the density evolution of the sound velocity of dhcp-FeH_x (x ≈ 1) up to 70 GPa at room temperature, by inelastic X-ray scattering and by X-ray diffraction. We find that the variation of V_P with density is different for the ferromagnetic and nonmagnetic dhcp-FeH_x, and that only nonmagnetic dhcp-FeH_x follows Birch's law. Combining our results with Birch's law for iron and assuming an ideal two-component mixing model, we obtain an upper bound of the hydrogen content in the Earth's inner core, 0.23(6) wt.% H, corresponding to FeH_0.13(3). The iron alloy with 0.23(6) wt.% H can satisfy the density, and compressional and shear sound velocities of the PREM inner core, assuming that there are no other light elements in the inner core.     

LQR control with frequency‐dependent scheduled gain for a semi‐active floor isolation system

Floor isolation is an alternative to base isolation for protecting a specific group of equipment installed on a single floor or room in a fixed‐base structure. The acceleration of the isolated floor should be mitigated to protect the equipment, and the displacement needs to be suppressed, especially under long‐period motions, to save more space for the floor to place equipment. To design floor isolation systems that reduce acceleration and displacement for both short‐period and long‐period motions, semi‐active control with a newly proposed method using the linear quadratic regulator (LQR) control with frequency‐dependent scheduled gain (LQRSG) is adopted. The LQRSG method is developed to account for the frequency characteristics of the input motion. It updates the control gain calculated by the LQR control based on the relationship between the control gain and dominant frequency of the input motion. The dominant frequency is detected in real time using a window method. To verify the effectiveness of the LQRSG method, a series of shake table tests is performed for a semi‐active floor isolation system with rolling pendulum isolators and a magnetic‐rheological damper. The test results show that the LQRSG method is significantly more effective than the LQR control over a range of short‐period and long‐period motions. Copyright © 2013 John Wiley & Sons, Ltd.     

Ceres’ spectral link to carbonaceous chondrites—Analysis of the dark background materials

Ceres’ surface has commonly been linked with carbonaceous chondrites (CCs) by ground‐based telescopic observations, because of its low albedo, flat to red‐sloped spectra in the visible and near‐infrared (VIS/NIR) wavelength region, and the absence of distinct absorption bands, though no currently known meteorites provide complete spectral matches to Ceres. Spatially resolved data of the Dawn Framing Camera (FC) reveal a generally dark surface covered with bright spots exhibiting reflectance values several times higher than Ceres’ background. In this work, we investigated FC data from High Altitude Mapping Orbit (HAMO) and Ceres eXtended Juling (CXJ) orbit (~140 m/pixel) for global spectral variations. We found that the cerean surface mainly differs by spectral slope over the whole FC wavelength region (0.4–1.0 μm). Areas exhibiting slopes ?1 constitute only ~3% of the cerean surface and mainly occur in the bright material in and around young craters, whereas slopes ≥?10% μm^?1 occur on more than 90% of the cerean surface; the latter being denoted as Ceres’ background material in this work. FC and Visible and Infrared Spectrometer (VIR) spectra of this background material were compared to the suite of CCs spectrally investigated so far regarding their VIS/NIR region and 2.7 μm absorption, as well as their reflectance at 0.653 μm. This resulted in a good match to heated CI Ivuna (heated to 200–300 °C) and a better match for CM1 meteorites, especially Moapa Valley. This possibly indicates that the alteration of CM2 to CM1 took place on Ceres.     

Sedimentation rate and heavy metal pollution in sediments in Harima Nada (Harima Sound), Seto Inland Sea

Sedimentation rates were determined with the²¹⁰Pb technique in six sediment cores from Harima Nada (Harima Sound), Seto Inland Sea. The rate of deposition varies from 0.11 g cm^–2y^–1 in the northern part to 0.33 g cm^–2 y^–1 in the southern part of the basin. A marked increase in copper and zinc content was observed above a depth in the core corresponding to about 1900 A.D. as a result of increasing human activities. Anthropogenic input of copper and zinc decreased slightly after 1970. Natural background levels of copper and zinc in the sediment in this sound are 11–16 ppm and 100–120 ppm, respectively. The total amounts of anthropogenic copper and zinc in the sediments were estimated to be 110–180g cm^–2 and 610–1,280g cm^–2, respectively. These values constitute 40–50% of the total sedimentary input of copper and zinc in the sediments since about 1900 A.D.     

Sedimentation rates in Funka Bay,HokkaidÔ

Undisturbed sediment cores were collected by a modified gravity corer from Funka Bay. The sedimentation rate is determined by both²¹⁰Pb and pumice chronological methods. The sedimentation rates by²¹⁰Pb method are concordant with those by pumice methods. The derived rate varies from 0.06 to 0.22 g cm^–2 y^–1, and an average is 0.09 g cm^–2 y^–1.