Apparent Microfloral Response to Organic Degradation on Bathyal ­Seafloor: An Analysis Based on Sediment Fatty Acids

Abstract. Abyssal microfloral succession induced by experimental organic degradation was investigated. Notable changes in amounts and compositions of short-chain (C9-20) sediment fatty acids were observed, which indicated the shift of sediment microflora. Biomarker fatty acids for methanotrophs and sulfate-reducing bacteria dominated. Resultant fatty acid compositions were most closely related to those from a nearby methane seep harboring a dense Calyptogena colony; the clams were also seen in close vicinity of the deployed organic mass. These observations suggest that the organic degradation on the bathyal seafloor stimulates the formation of methanotrophic and thio­trophic microflora, resulting in the formation of a methane-seep-type benthic community.     

Evaluation of global warming impacts for different levels of stabilization as a step toward determination of the long-term stabilization target

In order to estimate the benefit attributable to alleviating global warming for a kind of cost–benefit analysis of global warming mitigation, global warming impacts were quantitatively evaluated for a pathway of unmitigated CO₂ emissions and three pathways to stabilize the atmospheric CO₂ concentration at different levels, keeping unchanged the assumed conditions on population and GDP growths, although the GDP losses which will be caused due to the warming mitigation for the three stabilization pathways are taken into account. The evaluation results show that global warming will reduce the world total number of deaths caused by thermal stress owing to the large decrease in the cold-related deaths; it will increase the water stress in some regions, while it will decrease the stress in other regions; reductions in CO₂ emissions will decrease the probability of THC collapse and terrestrial biodiversity loss; and it will enhance an increase in the wheat production potential.     

Calorimetric study of the stability of high pressure phases in the systems CoOSiO2 and “FeO”SiO2, and calculation of phase diagrams in MOSiO2 systems

High temperature calorimetric measurements of the enthalpies of solution in molten if2 PbO · B₂O₃ of α- and γ-Fe₂SiO₄ and α-, β-, and γ-Co₂SiO₄ permit the calculation of phase relations at high pressure and temperature. The reported triple point involving α-, β-, and γ-Co₂SiO₄ is confirmed to represent stable equilibrium. The curvature in the α?β phase boundary in Co₂SiO₄ and of an α?γ boundary in Fe₂SiO₄ at high temperature is explained in part by the effects of compressibility and thermal expansion, but better agreement with the observed phase diagram is obtained when one considers the effect of small amounts of cation disorder in the spinel and/or modified spinel phases. The calculated ΔH⁰ and ΔS⁰ values for the α?β, α?γ, and β?γ transitions show that enthalpy and en changes both vary strongly in the series Mg, Fe, Co, and Ni, and are of equal importance in determining the stability relations. The disproportionation of Fe₂SiO₄ and Co₂SiO₄ spinel to rocksalt plus stishovite is calculated to occur in the 170–190 kbar region; cation disorder and/or changes in wüstite stoichiometry can affect the P?T slope. The calorimetric data for CoSiO₃ and FeSiO₃ are in good agreement with the observed phase boundary for pyroxene formation from olivine and quartz. The decomposition of pyroxene to spinel and stishovite at pressures near the coesite-stishovite transition is predicted in both iron and cobalt systems. The use of calorimetric data, obtained from small samples of high pressure phases, is very useful in predicting equilibrium phase diagrams in the 50–300 kbar range.     

Pyroxene-garnet solid-solution equilibria in the systems Mg4Si4O12Mg3Al2Si3O12 and Fe4Si4O12Fe3Al2Si3O12 at high pressures and temperatures

Pyroxene-garnet solid-solution equilibria have been studied in the pressure range 41–200 kbar and over the temperature range 850–1,450°C for the system Mg₄Si₄O₁₂Mg₃Al₂Si₃O₁₂, and in the pressure range 30–105 kbar and over the temperature range 1,000–1,300°C for the system Fe₄Si₄O₁₂Fe₃Al₂Si₃O₁₂. At 1,000°C, the solid solubility of enstatite (MgSiO₃) in pyrope (Mg₃Al₂Si₃O₁₂) increases gradually to 140 kbar and then increases suddenly in the pressure range 140–175 kbar, resulting in the formation of a homogeneous garnet with composition Mg₃(Al_0.8Mg_0.6Si_0.6)Si₃O₁₂. In the MgSiO₃-rich field, the three-phase assemblage of β- or γ-Mg₂SiO₄, stishovite and a garnet solid solution is stable at pressures above 175 kbar at 1,000°C. The system Fe₄Si₄O₁₂Fe₃Al₂Si₃O₁₂ shows a similar trend of high-pressure transformations: the maximum solubility of ferrosilite (FeSiO₃) in almandine (Fe₃Al₂Si₃O₁₂) forming a homogeneous garnet solid solution is 40 mol% at 93 kbar and 1,000°C.If a pyrolite mantle is assumed, from the present results, the following transformation scheme is suggested for the pyroxene-garnet assemblage in the mantle. Pyroxenes begin to react with the already present pyrope-rich garnet at depths around 150 km. Although the pyroxene-garnet transformation is spread over more than 400 km in depth, the most effective transition to a complex garnet solid solution takes place at depths between 450 and 540 km. The complex garnet solid solution is expected to be stable at depths between 540 and 590 km. At greater depths, it will decompose to a mixture of modified spinel or spinel, stishovite and garnet solid solutions with smaller amounts of a pyroxene component in solution.     

Electrical conductivity jump produced by the α-β-δ transformation in Mn2GeO4

The electrical conductivity of three polymorphs of Mn₂GeO₄ was measured under high pressures in the temperature range of 300–1200 K. It was found that the electrical conductivity increases discontinuously due to the transformation both from olivine structure (α) to modified spinel structure (β) and from β to strontium plumbate structure (δ). The amount of discontinuous change is about one half order of magnitude from α to β and one third order of magnitude from β to δ at 1200 K. In order to see the effect of the presence of iron ions, the electrical conductivity of the solid solution of (Mn_0.9Fe_0.1)₂GeO₄ was also measured. It was found that at low temperatures, where impurity conduction may be dominant, the solid solution is more conductive than the pure Mn₂GeO₄, but at high temperature no significant differences were observed between the solid solution and pure Mn₂GeO₄ in all polymorphs.A phase transformation from modified spinel structure to strontium plumbate structure is considered to be one of the plausible transformations occurring at a depth around 650 km in the earth's mantle. These experiments suggest that if this kind of transformation occurs in the mantle, some degrees of discontinuous change in electrical conductivity may be expected around 650 km.     

The system iron-enstatite-water at high pressures and temperatures—formation of iron hydride and some geophysical implications

The system iron-enstatite-water was investigated at pressures around 5 GPa and at temperatures ranging from 1000 to 1200°C, using several different kinds of starting materials. Quenched samples showed the coexistence of iron, olivine and pyroxene. Synthesis of the Fe-containing olivine in the run products proves that a series of reactions, Fe + H₂O → FeH_x + FeO and FeO + MgSiO₃ → (Mg, Fe)₂SiO₄, have taken place. Spherical “balls of iron” were observed in the 1200°C run. This strongly indicates that the melting temperature of iron decreased by ～ 500 K by the possible dissolution of hydrogen. Following geophysical implications are derived from these experimental results. If water was retained in the hydrous minerals in the primordial material, the iron-water reaction is expected to occur throughout the core-formation process. The reaction product FeH_x will melt and then sink to form a proto-core and iron oxide will be dissolved in the Earth's mantle. The dissolution of hydrogen in the Earth's core is a natural consequence of the core-formation process.