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%.     

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.     

High-pressure transformations in silicates,germanates, and titanates with ABO3 stoichiometry

High-pressure phase transformations were investigated for two silicates, MgSiO₃ and ZnSiO₃; six germanates, MGeO₃ and six titanates, MTiO₃ (M=Ni, Mg, Co, Zn, Fe, and Mn) at about 1,000°C and pressures up to ca. 30 GPa. CoGeO₃ was found to assume the ilmenite form. The ilmenite phases were confirmed to transform in the following schemes: to perovskite in MgSiO₃ and MnGeO₃, to corundum in MgGeO₃ and ZnGeO₃, to rocksalt plus rutile in ZnSiO₃ and CoGeO₃ and to rocksalt plus TiO₂ (possibly of some denser structure) in NiTiO₃, MgTiO₃, CoTiO₃, ZnTiO₃ and FeTiO₃. In the case of FeTiO₃, the corundum form appeared as an intermediate phase. The possibility that the corundum type MnTiO₃ might transform to some denser modification could not be excluded. The compound NiGeO₃ was nonexistent throughout the pressure range studied. High-pressure phases of ABO₃ (A=Ni, Mg, Co, Zn, Fe, and Mn; B=Si, Ge and Ti) are summarized, and those stabilized at pressures higher than 20 GPa are discussed.     

利用尾波包络线反演方法研究伽师强震群区地壳的非均匀结构

以单次散射模型、球形辐射源、一维线性速度模型为基础计算理论包络线,通过尾波归一化方法把理论与观测包络线结合起来形成非线性方程组,用迭代最小二乘方法反演伽师强震群区的散射系数空间分布.结果表明,伽师强震群区下方中上地壳中存在明显的非均匀结构.在10~25 km各深度图像上,研究区中部都存在一低散射系数区,这个低散射系数区在10 km、15 km深度被高散射系数区包围,在20 km深度仅其东侧存在高散射系数区.1997年的7次M_s≥6.0级地震发生在研究区中部的低散射系数区内或低散射系数区向高散射系数区过渡带的低散射系数一侧.     

Melting temperature distribution and fractionation in the lower mantle

The melting curve of perovskite MgSiO₃ and the liquidus and solidus curves of the lower mantle were estimated from thermodynamic data and the results of experiments on phase changes and melting in silicates.The initial slope of the melting curve of perovskite MgSiO₃ was obtained as $\text{d}\text{T}{}_{\mathrm{<mtext>m</mtext>}}\text{/}\text{d}\text{P?77}\text{K}\text{GPa}{}^{\mathrm{?1}}$ at 23 GPa. The melting curve of perovskite was expressed by the Kraut-Kennedy equation as $\text{T}{}_{\mathrm{<mtext>m</mtext>}}\text{(}\text{K}\text{)=917(}\text{1+29.6ΔV}\text{V}{}_0\text{)}$, where T_m?2900 K and P?23 GPa; and by the Simon equation, $\text{P(}\text{GPa}\text{)?23=21.2[}\text{(T}{}_{\mathrm{<mtext>m</mtext>}}\text{(}\text{K}\text{)}\text{2900)}{}^{1.75}\text{?1}\text{]}$.The liquidus curve of the lower mantle was estimated as $\text{T}{}_{\mathrm{<mtext>liq</mtext>}}\text{? 0.9 T}{}_{\mathrm{<mtext>m</mtext>}}$ (perovskite) and this gives the liquidus temperature T_liq=7000 ±500 K at the mantle-core boundary. The solidus curve of the lower mantle was also estimated by extrapolating the solidus curve of dry peridotite using the slope of the solidus curve of magnesiowüstite at high pressures. The solidus temperature is ～ 5000 K at the base of the lower mantle. If the temperature distribution of the mantle was 1.5 times higher than that given by the present geotherm in the early stage of the Earth's history, partial melting would have proceeded into the deep interior of the lower mantle.Estimation of the density of melts in the MgOFeOSiO₂ system for lower mantle conditions indicates that the initial melt formed by partial fusion of the lower mantle would be denser than the residual solid because of high concentration of iron into the melt. Thus, the melt generated in the lower mantle would tend to move downward toward the mantle-core boundary. This downward transportation of the melt in the lower mantle might have affected the chemistry of the lower mantle, such as in the D″ layer, and the distribution of the radioactive elements between mantle and core.     

Quantification of the effect of forest harvesting versus climate on streamflow cycles and trends in an evergreen broadleaf catchment

ABSTRACT

A new method known as Unobserved Components–Dynamic Harmonic Regression (UC-DHR) was applied to a 39-year record of rainfall and streamflow for three sub-catchments of the Sarukawa Experimental Watershed in southwestern Japan. Some 25% of the timber was harvested from one of the sub-catchments in May–July 1982 and the objective was to quantify the magnitude of this effect relative to the effects of climate cycles (e.g. Southern Oscillation Index). The observed effects of inter-annual climate cycles (i.e. 0.89–1.36 mm/d) were seen to be comparable (i.e. 0.70–1.17 mm/d) to the effects of harvesting 25% of the standing timber. This result underlines the importance of always quantifying the effect of climate on streamflow response when harvesting impacts are studied.

Editor D. Koutsoyiannis; Associate editor T. Okruszko     

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.     

Element partitioning between metallic liquid, silicate liquid, and lower-mantle minerals: implications for core formation of the Earth

We determined the partition coefficients of 19 elements between metallic liquid and silicate liquid at 20 GPa and 2500°C, and between metallic liquid and silicate perovskite at 27 GPa and 2200°C. Remarkable differences were observed in the partitioning behaviors of Si, P, W, Re, and Pb among the silicate liquid, perovskite, and magnesiowüstite coexisting with metallic liquid, reflecting incompatibility of the elements in the silicate or oxide phase. We could not observe any significant difference in the partitioning behaviors of V, Cr, Mn, Co, Ni, and Cu among the phases coexisting with metallic liquid.

Comparison of the present partitioning data with those obtained previously at lower pressure and temperature suggests that the exchange partition coefficients, K_met/sil, of Co, Ni, Mo, and W decrease, whereas those of V, Cr, and Mn increase and tend to approach unity with increasing pressure and temperature. We also made preliminary experiments to clarify the effect of sulfur on the partitioning behaviors. Sulfur lowers the exchange partition coefficients, K_met/sil, of Mo and W between metallic liquid and silicate liquid significantly at 20 GPa and 2300°C.

The mantle abundances of Co, Ni, Cu, Mo, and W calculated for the metal-silicate equilibrium model are lower than those of the real mantle, whereas P, K, and Mn are overabundant in the calculated mantle. The discrepancies in the abundances of Co and Ni could be explained by the chemical equilibrium at higher pressure and temperature. Large discrepancies in Mo and W between the calculated and real mantles could be accounted for by the effect of sulfur combined with the effects of pressure and temperature on the chemical equilibrium. The mantle abundances of P, K, and Cu could be accounted for by volatile loss in the nebula, perhaps before accretion of the Earth, combined with the chemical equilibrium at higher pressure and temperature. Thus the observed mantle abundances of P, K, Co, Ni, Cu, Mo, and W may be consistent with a model of sulfur-bearing metal-silicate equilibrium in lower-mantle conditions.     

On the similarity in atmospheric fluctuations of carbon dioxide,water vapor and temperature over vegetated fields

This paper describes the similarity between atmospheric fluctuations of carbon dioxide, water vapor and temperature using data which cover a wide range of instability (0.02 < < 10). The is the Monin-Obukhov stability parameter including the humidity effect.The spectral analysis shows that the coherency between fluctuations of carbon dioxide and water vapor or temperature is very close to unity, and the phase difference is basically out of phase for whole frequency ranges analyzed. The stability dependence of the normalized standard deviation of carbon dioxide is very similar to those of water vapor and temperature. The normalized standard deviation is about 2.5 under near neutral conditions, and it decreases with increasing instability following the -1/3; power law as (-)^-1/3. The skewness factors of carbon dioxide, water vapor and temperature show a systematic departure with increasing instabilities for 0.02 < s- < 1, and level off at high instabilities for 1 < -\s < 10. The stability dependence of the flatness factors is not so clear as that noted in the standrard deviation and skewness factors. Dissipation rates of carbon dioxide, water vapor and temperature variance are well related to the spectral peak wavelength. This seems to be real since the local production and local dissipation rates are the main terms, almost balancing one another in the variance budget equations for scalar entities.     

How to cut a sediment core for <Superscript>210</Superscript>Pb geochronology: a supplement

To obtain the profile of excess ²¹⁰Pb in sediment column, it is necessary to section the collected core to date. Sectioning thickness is generally not explicit. An approach when sedimentation rate is constant has been suggested by Lu and Matsumoto (Environ Geol 47:804–810, 2005). This paper addresses the case when sedimentation rate is variable. Actually, it is possible to assume that sedimentation rate is constant within the sectioning thickness and based on this concept, a tentative approach for determining reasonable sectioning thickness is proposed.