Variations in the distribution of magma in the lower crust and at the Moho beneath the East Pacific Rise at 9°-10°N

Measurements of the seafloor deformation under ocean waves (compliance) reveal an asymmetric lower crustal partial melt zone (shear velocity less than 1.8 km/s) beneath the East Pacific Rise axis between 9° and 10°N. At 9°48′N, the zone is less than 8 km wide and is centered beneath the rise axis. The zone shifts west of the rise axis as the rise approaches the westward-stepping 9°N overlapping spreading center discontinuity and is anomalously wide at the northern tip of the discontinuity. The ratio of the compliance determined shear velocity to the compressional velocities (estimated by seismic tomography) suggests that the melt is well-connected in high-aspect ratio cracks rather than in isolated sills. The shear and compressional velocities indicate less than 18% melt in the lower crust on average. The compliance measurements also reveal a separate lower crustal partial melt zone 10 km east of the rise axis at 9°48′N and isolated melt bodies near the Moho beneath four of the 39 measurement sites (three on-axis and one off-axis). The offset of the central melt zone from the rise axis correlates strongly with the offset of the overlying axial melt lens and the inferred center of mantle melting, but its shape appears to be controlled by crustal processes.     

SIMS determination of trace element partition coefficients between garnet, clinopyroxene and hydrous basaltic liquids at 2–7.5 GPa and 1080–1200°C

Trace element partition coefficients (D's) for up to 13 REE, Nb, Ta, Zr, Hf, Sr and Y have been determined by SIMS analysis of seven garnets, four clinopyroxenes, one orthopyroxene and one phlogopite crystallized from an undoped basanite and a lightly doped (200 ppm Nb, Ta and Hf) quartz tholeiite. Experiments were conducted at 2–7.5 GPa, achieving near-liquidus crystallization at relatively low temperatures of 1080–1200°C under strongly hydrous conditions (5–27 wt.% added water). Garnet and pyroxene D_REE show a parabolic pattern when plotted against ionic radius, and conform closely to the lattice strain model of Blundy and Wood (Blundy, J.D., Wood, B.J., 1994. Prediction of crystal–melt partition coefficients from elastic moduli. Nature 372, 452–454). Comparison, at constant pressure, between hydrous and anhydrous values of the strain-free partition coefficient (D₀) for the large cation sites of garnet and clinopyroxene reveals the relative importance of temperature and melt water content on partitioning. In the case of garnet, the effect of lower temperature, which serves to increase D₀, and higher water content, which serves to decrease D₀, counteract each other to the extent that water has little effect on garnet–melt D₀ values. In contrast, the effect of water on clinopyroxene–melt D₀ overwhelms the effect of temperature, such that D₀ is significantly lower under hydrous conditions. For both minerals, however, the lower temperature of the hydrous experiments tends to tighten the partitioning parabolas, increasing fractionation of light from heavy REE compared to anhydrous experiments.

Three sets of near-liquidus clinopyroxene–garnet two-mineral D values increase the range of published experimental determinations, but show significant differences from natural two-mineral D's determined for subsolidus mineral pairs. Similar behaviour is observed for the first experimental data for orthopyroxene–clinopyroxene two-mineral D's when compared with natural data. These differences are in large part of a consequence of the subsolidus equilibration temperatures and compositions of natural mineral pairs. Great care should therefore be taken when using natural mineral–mineral partition coefficients to interpret magmatic processes.

The new data for strongly hydrous compositions suggest that fractionation of Zr–Hf–Sm by garnet decreases with increasing depth. Thus, melts leaving a garnet-dominated residuum at depths of about 200 km or greater may preserve source Zr/Hf and Hf/Sm. This contrasts with melting at shallower depths where both garnet and clinopyroxene will cause Zr–Hf–Sm fractionation. Also, at shallower depths, clinopyroxene-dominated fractionation may produce a positive Sr spike in melts from spinel lherzolite, but for garnet lherzolite melting, no Sr spike will result. Conversely, clinopyroxene megacrysts with negative Sr spikes may crystallize from magmas without anomalous Sr contents when plotted on mantle compatibility diagrams. Because the characteristics of strongly hydrous silicate melt and solute-rich aqueous fluid converge at high pressure, the hydrous data presented here are particularly pertinent to modelling processes in subduction zones, where aqueous fluids may have an important metasomatic role.     

硅酸盐熔体和液态铁的两相模拟与核幔间的氧交换

地球早期经历了很多撞击事件, 其中与地月系统形成相关的大撞击甚至造成深达核幔边界的全球规模的岩浆洋, 在此过程中的核幔分异基本确定了地幔与地核的物质组成, 也决定了地球随后的演化路径.我们采用基于量子力学理论的第一性原理方法和机器学习技术, 实现了硅酸盐熔体和液态铁的超大体系两相分子动力学模拟, 获得了核幔边界条件下的两相平衡数据, 为超深岩浆洋中的核幔分异过程提供了重要约束.基于本研究模拟结果和现有的高温高压实验数据, 我们还建立了能够准确预测核幔间元素交换的平衡模型, 利用该模型深入探讨了核幔间的氧交换问题, 并分析了其与地球生长、大撞击和岩浆洋事件、地球早期磁场等争议问题之间的关系.

     

西南天山东德沟橄榄岩的地球化学特征及其地质意义

东德沟橄榄岩出露于中国新疆伊犁—中天山板块和塔里木板块之间西南天山造山带的北缘,含大量角闪石、金云母等含水矿物,显示全部遭受了不同程度的交代变质作用.岩石主量元素含量变化较大,其后期蚀变基本向富铝和富钙两个方向变化,其Nb/Ta和Zr/Hf值显示难熔地幔残余的特征.该区橄榄岩轻重稀土分馏较明显,稀土元素配分曲线总体为LREE富集的右倾型,且富集大离子亲石元素Rb、Ba、Sr和放射性元素Th,但岩石呈现不一致的解耦现象,即主量元素表现难熔而稀土元素、不相容微量元素体现富集,说明主量元素和微量元素具有各自的演化特点.研究认为东德沟橄榄岩是经历部分熔融的楔形地幔残余,微量元素呈现的特征是俯冲板块析出熔体或流体交代的结果.与其岩石矿物学研究结果一致,对东德沟橄榄岩地球化学特征的深入研究证明,它们来源于SSZ环境俯冲上板片地幔楔橄榄岩残片.     

Crystallization of melts, pegmatite intrusion and the Inverian retrogression of the Scourian complex, north-west Scotland

Abstract Partial melting of tonalitic gneisses in the 2.7 Ga Badcallian granulite facies metamorphic episode in the Scourian complex of north-west Scotland produced a suite of granitic to trondhjemitic liquids. On cooling and excavation of the complex, these melts underwent fractional crystallization and the residual liquids eventually became water saturated. Comparison with experimental data suggests that water saturation would have occurred in these melts at around 620–700°C. From the retrograde P–T -time path followed by the complex it is estimated that H₂O-dominated fluids were exsolved from these melts at c. 2.5 Ga. It is proposed that these fluids were the cause of the 2.5 Ga Inverian retrogression of the Scourian complex and that water-saturated melts formed during the crystallization of the leucogneisses were intruded as a suite of pegmatites. The timing of pegmatite intrusion is consistent with this proposition as are the temperature estimates, timing, distribution and nature of the Inverian phase of metamorphism. It is likely that the crystallization of melts is an important process in bringing about hydrous retrogressive metamorphic episodes in a number of other basement terrains, such as West Greenland and Australia.     

声子在硅酸盐熔体缔合反应中的作用

本文采用量子统计方法，得到了声子熵的计算公式和初步结果，同时还提出在硅酸盐熔体两种阴离子结构团的缔合反应中，声学支声子所提供的声子熵起了重要作用。     

Quaternary adakite—Nb-enriched basalt association in the western Trans-Mexican Volcanic Belt: is there any slab melt evidence?

A spatial and temporal association between adakitic rocks and Nb-enriched basalts (NEB) is recognised for the first time in the western sector of the Trans-Mexican Volcanic Belt in the San Pedro–Cerro Grande Volcanic Complex (SCVC). The SCVC is composed of subalkalic intermediate to felsic rocks, spanning in composition from high-silica andesites to rhyolites, and by the young transitional hawaiite and mugearite lavas of Amado Nervo shield volcano. Intermediate to felsic rocks of the SCVC show many geochemical characteristics of typical adakites, such as high Sr/Y ratios (up to 180) and low Y (<18 ppm) and Yb contents. Mafic Amado Nervo rocks have high TiO₂ (1.5–2.3 wt%), Nb (14–27 ppm), Nb/La (0.5–0.9) and high absolute abundances of HFSE similar to those shown by NEB. However, the Sr and Nd isotopic signature of SCVC rocks is different from that shown by typical adakites and NEB. Although the adakites–NEB association has been traditionally considered as a strong evidence of slab-melting, we suggest that other processes can lead to its generation. Here, we show that parental magmas of adakitic rocks of the SCVC derive their adakitic characteristic from high-pressure crystal fractionation processes of garnet, amphibole and pyroxene of a normal arc basalt. On the other hand, Amado Nervo Na-alkaline parental magmas have been generated by sediment melting plus MORB-fluid flux melting of a heterogeneous mantle wedge, consisting of a mixture of depleted and an enriched mantle sources (90DM + 10EM). We cannot exclude a contribution to the subduction component of slab melts, because the component signature is dominated by sediment melt, but we argue that caution is needed in interpreting the adakites–NEB association in a genetic sense.     

Shallow-level decompression crystallisation and deep magma supply at Shiveluch Volcano

Recent petrological studies indicate that some crustal magma chambers may be built up slowly by the intermittent ascent and amalgamation of small packets of magma generated in a deep-seated source region. Despite having little effect on whole-rock compositions, this process should be detectable as variable melt trace element composition, preserved as melt inclusions trapped in phenocrysts. We studied trace element and H₂O contents of plagioclase- and hornblende-hosted melt inclusions from andesite lavas and pumices of Shiveluch Volcano, Kamchatka. Melt inclusions are significantly more evolved than the whole rocks, indicating that the whole rocks contain a significant proportion of recycled foreign material. H₂O concentrations indicate trapping at a wide range of pressures, consistent with shallow decompression-driven crystallisation. The variation of trace element concentrations indicates up to ∼30% decompression crystallisation, which accounts for crystallisation of the groundmass and rims on phenocrysts. Trace element scatter could be explained by episodic stalling during shallow magma ascent, allowing incompatible element concentrations to increase during isobaric crystallisation. Enrichment of Li at intermediate pH₂O reflects influx and condensation of metal-rich vapours. A set of “exotic melts”, identified by their anomalous incompatible trace element characteristics, indicate variable source chemistry. This is consistent with evolution of individual magma batches with small differences in trace element chemistry, and intermittent ascent of magma pulses. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Targeting the impactors: siderophile element signatures of lunar impact melts from Serenitatis

Highly siderophile element compositions of lunar impact melt breccias provide a unique record of the asteroid population responsible for large cratering events in the inner Solar System. Melt breccias associated with the 3.89 Ga Serenitatis impact basin resolve at least two separate impact events. KREEP-rich melt breccias representing the Apollo 17 poikilitic suite are enriched in highly siderophile elements (3.6-15.8 ppb Ir) with CI-normalized patterns that are elevated in Re, Ru and Pd relative to Ir and Pt. The restricted range of lithophile element compositions combined with the coherent siderophile element signatures indicate formation of these breccias in a single impact event involving an EH chondrite asteroid, probably as melt sheet deposits from the Serenitatis Basin. One exceptional sample, a split from melt breccia 77035, has a distinctive lithophile element composition and a siderophile element signature more like that of ordinary chondrites, indicating a discrete impact event. The recognition of multiple impact events, and the clear signatures of specific types of meteoritic impactors in the Apollo 17 melt breccias, shows that the lunar crust was not comprehensively reworked by prior impacts from 3.9 to 4.5 Ga, an observation more consistent with a late cataclysm than a smoothly declining accretionary flux. Late accretion of enstatite chondrites during a 3.8-4.0 Ga cataclysm may have contributed to siderophile element heterogeneity on the Earth, but would not have made a significant contribution to the volatile budget of the Earth or oxidation of the terrestrial mantle. Siderophile element patterns of Apollo 17 poikilitic breccias become more fractionated with decreasing concentrations, trending away from known meteorite compositions to higher Re/Ir and Pd/Pt ratios. The compositions of these breccias may be explained by a two-stage impact melting process involving: (1) deep penetration of the Serenitatis impactor into meteorite-free lower crust, followed by (2) incorporation of upper crustal lithologies moderately contaminated by prior meteoritic infall into the melt sheet. Trends to higher Re/Ir with decreasing siderophile element concentrations may indicate an endogenous lunar crustal component, or a non-chondritic late accretionary veneer in the pre-Serenitatis upper crust.     

Accreted fragments of the Late Cretaceous Caribbean–Colombian Plateau in Ecuador

The eastern part of the Western Cordillera of Ecuador includes fragments of an Early Cretaceous (≈123 Ma) oceanic plateau accreted around 85–80 Ma (San Juan–unit). West of this unit and in fault contact with it, another oceanic plateau sequence (Guaranda unit) is marked by the occurrence of picrites, ankaramites, basalts, dolerites and shallow level gabbros. A comparable unit is also exposed in northwestern coastal Ecuador (Pedernales unit).

Picrites have LREE-depleted patterns, high Nd_i and very low Pb isotopic ratios, suggesting that they were derived from an extremely depleted source. In contrast, the ankaramites and Mg-rich basalts are LREE-enriched and have radiogenic Pb isotopic compositions similar to the Galápagos HIMU component; their Nd_i are slightly lower than those of the picrites. Basalts, dolerites and gabbros differ from the picrites and ankaramites by flat rare earth element (REE) patterns and lower Nd; their Pb isotopic compositions are intermediate between those of the picrites and ankaramites. The ankaramites, Mg-rich basalts, and picrites differ from the lavas from the San Juan–Multitud Unit by higher Pb ratios and lower Nd_i.

The Ecuadorian and Gorgona 88–86 Ma picrites are geochemically similar. The Ecuadorian ankaramites and Mg-rich basalts share with the 92–86 Ma Mg-rich basalts of the Caribbean–Colombian Oceanic Plateau (CCOP) similar trace element and Nd and Pb isotopic chemistry. This suggests that the Pedernales and Guaranda units belong to the Late Cretaceous CCOP. The geochemical diversity of the Guaranda and Pedernales rocks illustrates the heterogeneity of the CCOP plume source and suggests a multi-stage model for the emplacement of these rocks. Stratigraphic and geological relations strongly suggest that the Guaranda unit was accreted in the late Maastrichtian (≈68–65 Ma).