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1.
himu, em i andem ii are three of the main geochemical mantle components that give rise to oceanic island basalts [1]. They represent the end members that produce the extreme isotopic compositions measured on intraplate volcanics. In French Polynesia, all three mantle components are represented in volcanic rocks. The characteristichimu signature is found in Tubuai, Mangaia and Rurutu,em i is present in the source of Rarotonga and Pitcairn volcanics andem ii dominates the composition of most Society Islands. Intermediate values between the three end members are found on most islands.We suggest that the three components are not independent but are physically related in the mantle. Thehimu component is thought to be recycled oceanic crust that lost part of its Pb through hydrothermal processes prior to and during subduction.em i andem ii are believed to acquire their isotopic and trace element characteristics through entrainment of sediments that were subducted together with the oceanic crust.The trace element pattern and the isotopic composition ofhimu lavas can be quantitatively modelled using a mixture of 25% old recycledmorb crust and 75% mantle peridotite. The extreme Pb composition is modelled assuming that Pb was lost from oceanic crust when hydrothermal alteration at the ridge leached Pb from the basalt to redeposit it as sulphides on top of and throughout the crust, followed by preferential dissolution of sulphides during dehydration in the subduction zone. These processes led to a drastic increase of theU/Pb ratio of the subducted material which evolved over 2 Ga to very radiogenic Pb isotopic compositions. Pb isotopic compositions similar to those ofem i andem ii are modelled assuming that sediments with average crustal Pb isotopic compositions were subducted and recycled into the mantle together with the underlyingmorb oceanic crust. Pelagic sediments (μ 5 andκ 6) account for the Pb isotopic composition ofem i whereas terrigenous sediments (μ 10 andκ 4.5) evolve towards theem ii end member. A few percent of sediment in the recycled crust-sediment mixture will destroy the characteristic Pb isotopic signature of thehimu component. This, together with the low probability of isolating oceanic crust in the mantle for 2 Ga, explains why the extremehimu composition, as seen on Tubuai and St Helena, is sampled so rarely by oceanic volcanism.  相似文献   

2.
In order to understand the role of the subducted lithosphere in producing the geochemical characteristics of arc magmas, major- and trace-element along with Sr- and Nd-isotope compositions have been determined for Quaternary volcanic rocks from the Izu-Bonin intra-oceanic arc. 87Sr/86Sr and 143Nd/144Nd ratios decrease away from the volcanic front of this arc and lie on mixing lines between the assumed isotopic compositions of fluid phases mainly derived from the basalt layer of the subducted lithosphere and upper-mantle materials in the sub-arc wedge. This across-arc variation can be explained through a simple sequence of processes involving initial release of fluid phases from the subducted oceanic crust to produce hydrous peridotite at the base of the mantle wedge. This hydrous peridotite is dragged downward with the slab and releases a second-stage metasomatizing fluid beneath the volcanic arc. The higher concentrations of both Sr and Nd in the fluid beneath the volcanic front than those beneath the back-arc side may be a possible cause of the observed across-arc variation in Sr-Nd isotopic ratios. The difference in compositions of fluid phases is attributed to the different hydrous phases which decompose in the hydrous peridotite layer; amphibole beneath the volcanic front and phlogopite beneath the back-arc side of the volcanic arc. The mineralogically controlled fluid addition may also be responsible for the across-arc variation in Rb/K and Rb/Zr ratios, increasing away from the volcanic front.  相似文献   

3.
In an attempt to determine the helium and neon isotopic composition of the lower oceanic crust, we report new noble gas measurements on 11 million year old gabbros from Ocean Drilling Program site 735B in the Indian Ocean. The nine whole rock samples analyzed came from 20 to 500 m depth below the seafloor. Helium contents vary from 3.3×10−10 to 2.5×10−7 ccSTP/g by crushing and from 5.4×10−8 to 2.4×10−7 ccSTP/g by melting. 3He/4He ratios vary between 2.2 and 8.6 Ra by crushing and between 2.9 and 8.2 by melting. The highest R/Ra ratios are similar to the mean mid-ocean ridge basalt (MORB) ratio of 8±1. The lower values are attributed to radiogenic helium from in situ α-particle production during uranium and thorium decay. Neon isotopic ratios are similar to atmospheric ratios, reflecting a significant seawater circulation in the upper 500 m of exposed crust at this site. MORB-like neon, with elevated 20Ne/22Ne and 21Ne/22Ne ratios, was found in some high temperature steps of heating experiments, but with very small anomalies compared to air. These first results from the lower oceanic crust indicate that subducted lower oceanic crust has an atmospheric 20Ne/22Ne ratio. Most of this neon must be removed during the subduction process, if the ocean crust is to be recirculated in the upper mantle, otherwise this atmospheric neon will overwhelm the upper mantle neon budget. Similarly, the high (U+Th)/3He ratio of these crustal gabbros will generate very radiogenic 4He/3He ratios on a 100 Ma time scale, so lower oceanic crust cannot be recycled into either MORB or oceanic island basalt without some form of processing.  相似文献   

4.
Many ocean island basalts (OIB) that have isotopic ratios indicative of recycled crustal components in their source are silica-undersaturated and unlike silicic liquids produced from partial melting of recycled mid-ocean ridge basalt (MORB). However, experiments on a silica-deficient garnet pyroxenite, MIX1G, at 2.0-2.5 GPa show that some pyroxenite partial melts are strongly silica-undersaturated [M.M. Hirschmann et al., Geology 31 (2003) 481-484]. These low-pressure liquids are plausible parents of alkalic OIB, except that they are too aluminous. We present new partial melting experiments on MIX1G between 3.0 and 7.5 GPa. Partial melts at 5.0 GPa have low SiO2 (<48 wt%), low Al2O3 (<12 wt%) and high CaO (>12 wt%) at moderate MgO (12-16 wt%), and are more similar to primitive OIB compositions than lower-pressure liquids of MIX1G or experimental partial melts of anhydrous or carbonated peridotite. Solidus temperatures at 5.0 and 7.5 GPa are 1625 and 1825°C, respectively, which are less than 50°C cooler than the anhydrous peridotite solidus. The liquidus temperature at 5.0 GPa is 1725°C, indicating a narrow melting interval (∼100°C). These melting relations suggest that OIB magmas can be produced by partial melting of a silica-deficient pyroxenite similar to MIX1G if its melting residue contains significant garnet and lacks olivine. Such silica-deficient pyroxenites could be produced by interaction between recycled subducted oceanic crust and mantle peridotite or could be remnants of ancient oceanic lower crust or delaminated lower continental crust. If such compositions are present in plumes ascending with potential temperatures of 1550°C, they will begin to melt at about 5.0 GPa and produce appropriate partial melts. However, such hot plumes may also generate partial melts of peridotite, which could dilute the pyroxenite-derived partial melts.  相似文献   

5.
The phase relations in hydrous and anhydrous mid-ocean ridge basalt were determined at pressures of 18-28 GPa. Liquidus phase relations in hydrous and anhydrous MORB are different. Garnet is the liquidus phase at pressures below 21 GPa, Ca-Al (CAS) phase and stishovite are the liquidus phases at pressures of 22-27 GPa, and stishovite and Ca-perovskite are the liquidus phases above 27 GPa, whereas Ca-perovskite is a liquidus phase of anhydrous MORB at pressures above 23 GPa. Under subsolidus conditions, we have found that in the hydrous MORB system the stability fields of Al-bearing perovskite and Na-Al (NAL) phase might shift to lower pressure by about 1.5 GPa compared to the dry MORB system. This shift could be explained by oxidation of a garnet-bearing assemblage by hydrous fluid and formation of Fe3+-bearing aluminous perovskite at lower pressures relative to the anhydrous system and/or differences in water solubility of the phases existing in perovskite-bearing assemblages. Our data indicate that hydrous basaltic crust remains denser than peridotite along the geotherm of a subducting slab, i.e. there is no density crossover between peridotite and basalt. Therefore, in slabs going through the 660 km discontinuity, basalt would gravitationally sink into the lower mantle under relatively hydrous conditions. The delamination of former basaltic crust near the 660 km discontinuity might be possible under relatively dry conditions of subduction. There are no stable highly hydrous phases in MORB above 10 GPa even at lower temperatures corresponding to subducting slabs. Therefore, MORB cannot be an important carrier of water to the deep Earth interior. However, it can be constantly supplied by water-bearing fluid from the underlying peridotite part of the descending slab. Thus, it is plausible that water can control subduction of the oceanic crust into the lower mantle.  相似文献   

6.
In situ synchrotron X-ray diffraction experiments were conducted using the SPEED-1500 multi-anvil press at SPring-8 on majoritic garnet synthesized from natural mid-ocean ridge basalt (MORB), whose chemical composition is close to the average of oceanic crust, at 19 GPa and 2200 K. Pressure-volume-temperature data were collected using a newly developed high-pressure cell assembly to 21 GPa and 1273 K. Data were fit to the high-temperature Birch-Murnaghan equation of state, with fixed values for the ambient cell volume (V0 = 1574.14(4) Å3) and the pressure derivative of the isothermal bulk modulus (K′T = 4). This yielded an isothermal bulk modulus of KT0 = 173(1) GPa, a temperature derivative of the bulk modulus (∂KT/∂T)P = −0.022(5) GPa K−1, and a volumetric coefficient of thermal expansivity α = a + bT with values of a = 2.0(3) × 10−5 K−1 and b = 1.0(5) × 10−8 K−2. The derived thermoelastic parameters are very similar to those of pyrope. The density of subducted oceanic crust compared to pyrolitic mantle at the conditions in Earth's transition zone (410-660 km depth) was calculated using these results and previously reported thermoelastic parameters for MORB and pyrolite mineral assembledges. These calculations show that oceanic crust is denser than pyrolitic mantle throughout the mantle transition zone along a normal geotherm, and the density difference is insensitive to temperature at the pressures in lower part of the transition zone.  相似文献   

7.
The Earth's mantle is chemically and isotopically heterogeneous, and a component of recycled oceanic crust is generally suspected in the convecting mantle [Hofmann and White, 1982. Mantle plumes from ancient oceanic crust. Earth Planet. Sci. Lett. 57, 421–436]. Indeed, the HIMU component (high µ = 238U/204Pb), one of four isotopically distinct end-members in the Earth's mantle, is generally attributed to relatively old (≥ 1–2 Ga) recycled oceanic crust in the form of eclogite/pyroxenite, e.g. [Zindler and Hart, 1986. Chemical geodynamics. Ann. Rev. Earth Planet. Sci. 14, 493–571]. Although the presence of the recycled component is generally supported by element and isotopic data, little is known about its physical state at mantle depths. Here we show that the concentrations of Ni, Mn and Ca in olivine from the Canarian shield stage lavas, which can be used to assess the physical nature of the source material (peridotite versus olivine-free pyroxenite) [Sobolev et al., 2007. The amount of recycled crust in sources of mantle-derived melts. Science 316, 412–417], correlate strongly with bulk rock Sr, Nd and Pb isotopic ratios. The most important result following from our data is that the enriched, HIMU-type (having higher 206Pb/204Pb than generally found in the other mantle end-members) signature of the Canarian hotspot magmas was not caused by a pyroxenite/eclogite constituent of the plume but appears to have been primarily hosted by peridotite. This implies that the old (older than ~ 1 Ga) ocean crust, which has more evolved radiogenic isotope compositions, was stirred into/reacted with the mantle so that there is not significant eclogite left, whereas younger recycled oceanic crust with depleted MORB isotopic signature (< 1 Ga) can be preserved as eclogite, which when melted can generate reaction pyroxenite.  相似文献   

8.
Ocean Drilling Program (ODP) Hole 504B near the Costa Rica Rift is the deepest hole drilled in the ocean crust, penetrating a volcanic section, a transition zone and a sheeted dike complex. The distribution of Li and its isotopes through this 1.8-km section of oceanic crust reflects the varying conditions of seawater alteration with depth. The upper volcanic rocks, altered at low temperatures, are enriched in Li (5.6-27.3 ppm) and have heavier isotopic compositions (δ7Li=6.6-20.8‰) relative to fresh mid-ocean ridge basalt (MORB) due to uptake of seawater Li into alteration clays. The Li content and isotopic compositions of the deeper volcanic rocks are similar to MORB, reflecting restricted seawater circulation in this section. The transition zone is a region of mixing of seawater with upwelling hydrothermal fluids and sulfide mineralization. Li enrichment in this zone is accompanied by relatively light isotopic compositions (−0.8-2.1‰) which signify influence of basalt-derived Li during mineralization and alteration. Li decreases with depth to 0.6 ppm in the sheeted dike complex as a result of increasing hydrothermal extraction in the high-temperature reaction zone. Rocks in the dike complex have variable isotopic values that range from −1.7 to 7.9‰, depending on the extent of hydrothermal recrystallization and off-axis low-temperature alteration. Hydrothermally altered rocks are isotopically light because 6Li is preferentially retained in greenschist and amphibolite facies minerals. The δ7Li values of the highly altered rocks of the dike complex are complementary to those of high-temperature mid-ocean ridge vent fluids and compatible to equilibrium control by the alteration mineral assemblage. The inventory of Li in basement rocks permits a reevaluation of the role of oceanic crust in the budget of Li in the ocean. On balance, the upper 1.8 km of oceanic crusts remains a sink for oceanic Li. The observations at 504B and an estimated flux from the underlying 0.5 km of gabbro suggest that the global hydrothermal flux is at most 8×109 mol/yr, compatible with geophysical thermal models. This work defines the distribution of Li and its isotopes in the upper ocean crust and provides a basis to interpret the contribution of subducted lithosphere to arc magmas and cycling of crustal material in the deep mantle.  相似文献   

9.
New major and trace element and Sr–Nd isotope data are presented for basaltic glasses from active spreading centers (Central Lau Spreading Center (CLSC), Relay Zone (RZ) and Eastern Lau Spreading Center (ELSC)) in the Central Lau Basin, SW Pacific. Basaltic lavas from the Central Lau Basin are mainly tholeiitic and are broadly similar in composition to mid-ocean ridge basalts (MORB). Their generally high 87Sr/86Sr ratios, combined with relatively low 143Nd/144Nd ratios are more akin to MORB from the Indian rather than Pacific Ocean. In detail, the CLSC, RZ and ELSC lavas are generally more enriched in large ion lithophile elements (Rb, Ba, Sr, and K) than average normal-MORB, which suggests that the mantle beneath the Central Lau Basin was modified by subducted slab-derived components. Fluid mobile/immobile trace element and Sr – Nd isotope ratios suggest that the subduction components were essentially transferred into the mantle via hydrous fluids derived from the subducted oceanic crust; contributions coming from the subducted sediments are minor. Compared to CLSC lavas, ELSC and RZ lavas show greater enrichment in fluid mobile elements and depletion in high field strength elements, especially Nb. Thus, with increasing distance away from the arc, the influence of subduction components in the mantle source of Lau Basin lavas diminishes. The amount of hydrous fluids also influences the degree of partial melting of the mantle beneath the Central Lau Basin, and hence the degree of melting also decreases with increasing distance from the arc.  相似文献   

10.
The basaltic ocean crust, metasomatized and metamorphosed during and after generation at the ocean ridge, contains H2O stored in minerals and pore fluid. Phase equilibrium data establish the conditions for dehydration, and the conditions for melting of amphibole-gabbro or amphibole-quartz-eclogite, or for quartz-eclogite or mantle peridotite if aqueous fluids are available. But there is no concensus about the temperature distribution through the subducted crust, or within the overlying mantle wedge. Therefore, a variety of magmatic models can be derived from the experimental data. According to some calculations, endothermic dehydration reactions in the depth interval 75–125 km cool the oceanic crust to such an extent that it cannot be a major source of magmas; instead, concentrated aqueous fluids released from the crust generate magmas in the overlying peridotite. However, according to most existing thermal models, if temperatures in ocean crust are cool enough to prohibit melting of amphibolite, then temperatures in the mantle above the main sources of expelled fluids are too low for hydrous melting. The ocean crust appears to be effectively dehydrated by 100–125 km depth. Dense hydrous magnesian silicates are not likely candidates for deeper H2O transport. The extent to which H2O can be fixed in metasomatic phlogopite in crust or mantle is a significant but undetermined factor. Experimental data on minerals and liquid compositions do not support the concept of primary magmas for andesites and associated lavas from mantle or subducted crust. Complex, multi-stage processes appear to be more likely, which is consistent with recent interpretations of geochemical data.  相似文献   

11.
We present the first data on bulk‐rock major and trace element compositions for a suite of eclogite‐ and blueschist‐facies rocks from the Bantimala Complex, Indonesia, with the aim of better constraining the protolith origins and nature of the subducted crust. The eclogites can be classified into two groups: glaucophane‐rich eclogite and glaucophane‐free eclogite, whereas the blueschists are divided into albite–epidote glaucophanite and quartz–glaucophane schists. SiO2 contents of the eclogites are 43.3–49.6 wt%, with Na2O + K2O contents 3.7–4.7 wt%. The blueschists show a wider range of compositions, with SiO2 = 40.7–63.8 wt% and Na2O + K2O = 2.7–4.5 wt%. Trace element data suggest that the eclogite protoliths include both enriched and normal mid‐oceanic ridge basalt (E‐MORB and N‐MORB) and also gabbroic cumulates. The blueschists show more variation in protoliths, which include N‐MORB, Oceanic Island Basalt (OIB) and Island Arc Basalt (IAB). Plots of element concentrations against the immobile Zr show considerable mobility of large ion lithophiles but not of high field‐strength elements during high‐pressure metamorphism, and indicate that the high SiO2 content of some blueschists is probably due to metasomatism by a LILE‐rich siliceous aqueous fluid. Strong correlations between K, Rb, Ba and Cs suggests that enrichment of these elements occurred by a single process. All the protoliths were subducted, metamorphosed to blueschist/eclogite‐facies and subsequently exhumed. It is noteworthy that the samples deduced to have come from thicker‐crust environments (OIB, IAB) were subducted to shallower depths (blueschist‐facies) than MORB‐derived samples, all except one of which reached eclogite‐facies conditions. The geochemical data of this study demonstrate the variety of ocean floor types that were subducted under the southeast margin of Sundaland in the late Jurassic period.  相似文献   

12.
佳木斯地块和松嫩地块是东北地区两个十分重要的地质构造单元,由于二者之间发育一套含有蓝片岩的俯冲增生杂岩-黑龙江杂岩(原称黑龙江群),其地质构造意义长期为人们所关注.巴彦—桦南深反射地震剖面揭示,佳木斯地块与松嫩地块之间存在明显向西俯冲的深反射信息,以壳内和幔内向西倾伏的楔状反射区为特征.壳内楔状反射区东与浅表层出露的黑龙江杂岩相连,向西倾伏延深至莫霍面,是俯冲增生杂岩在地壳深部的反映;幔内楔状反射区东起小兴安岭之下的莫霍面,向西倾伏延深至松辽盆地东缘,尖灭深度约78km,与多种方法得出的该区现今的岩石圈厚度(75~80km)基本一致.这一证据充分说明佳木斯地块的岩石圈地幔向西俯冲到松嫩地块岩石圈地幔之下.  相似文献   

13.
Both early and late Archean rocks from greenstone belts and felsic gneiss complexes exhibit positive εNd values of +1 to +5 by 3.5 Ga, demonstrating that a depleted mantle reservoir existed very early. The amount of preserved pre-3.0 Ga continental crust cannot explain such high ε values in the depleted residue unless the volume of residual mantle was very small: a layer less than 70 km thick by 3.0 Ga. Repeated and exclusive sampling of such a thin layer, especially in forming the felsic gneiss complexes, is implausible. Extraction of enough continental crust to deplete the early mantle and its destructive recycling before 3.0 Ga ago requires another implausibility, that the sites of crustal generation and of recycling were substantially distinct. In contrast, formation of mafic or ultramafic crust analogous to present-day oceanic crust was continuous from very early times. Recycled subducted oceanic lithosphere is a likely contributor to present-day hotspot magmas, and forms a reservoir at least comparable in volume to continental crust. Subduction of an early mafic/ultramafic “oceanic” crust and temporary storage rather than immediate mixing back into undifferentiated mantle may be responsible for the depletion and high εNd values of the Archean upper mantle. Using oceanic crustal production proportional to heat productivity, we show that temporary storage in the mantle of that crust, whether basaltic as formed by 5–20% partial melting, or partly komatiitic and formed by higher extents of melting is sufficient to balance an early depleted mantle of significant volume with εNd at least +3.0.  相似文献   

14.
The water contents of minerals and whole-rock in mantle-derived xenoliths from eastern China exhibit large variations and are generally lower than those from other on- and off-craton lithotectonic units. Nevertheless, the water contents of mineral and whole-rock in Junan peridotite xenoliths, which sourced from the juvenile lithospheric mantle, are generally higher than those elsewhere in eastern China. This suggests that the initial water content of juvenile lithospheric mantle is not low. There is no obvious correlation between the water contents and Mg# values of minerals in the mantle xenoliths and no occurrence of diffusion profile in pyroxene, suggesting no relationship between the low water content of mantle xenolith and the diffusion loss of water during xenolith ascent with host basaltic magmas. If the subcontinental lithospheric mantle (SCLM) base is heated by the asthenospheric mantle, the diffusion loss of water is expected to occur. On the other hand, extraction of basaltic melts from the SCLM is a more efficient mechanism to reduce the water content of xenoliths. The primary melts of Mesozoic and Cenozoic basalts in eastern China have water contents, as calculated from the water contents of phenocrysts, higher than those of normal mid-ocean ridge basalts (MORB). The Mesozoic basalts exhibit similar water contents to those of island arc basalts, whereas the Cenozoic basalts exhibit comparable water contents to oceanic island basalts and backarc basin basalts with some of them resembling island arc basalts. These observations suggest the water enrichment in the mantle source of continental basalts due to metasomatism by aqueous fluids and hydrous melts derived from dehydration and melting of deeply subducted crust. Mantle-derived megacrysts, minerals in xenoliths and phenocrysts in basalts from eastern China also exhibit largely variable hydrogen isotope compositions, indicating a large isotopic heterogeneity for the Cenozoic SCLM in eastern China. The water content that is higher than that of depleted MORB mantle and the hydrogen isotope composition that is deviated from that of depleted MORB mantle suggest that the Cenozoic continental lithospheric mantle suffered the metasomatism by hydrous melts derived from partial melting of the subducted Pacific slab below eastern China continent. The metasomatism would lead to the increase of water content in the SCLM base and then to the decrease of its viscosity. As a consequence, the SCLM base would be weakened and thus susceptible to tectonic erosion and delamination. As such, the crust-mantle interaction in oceanic subduction channel is the major cause for thinning of the craton lithosphere in North China.  相似文献   

15.
In a general lithospheric model of a simple divergent ocean and continental margin that satisfies the constraints of isostasy and gravity anomalies, the free-air gravity anomaly at the margin is modelled by an oceanic crust that thickens exponentially toward the margin from its common value of 6.4 km about 600 km from the margin to 17.7 km at the margin; this postulated thickening is supported empirically by seismic refraction measurements made near continental margins. The thickness of the oceanic crust matches that of the continental lithosphere at breakup, as observed today in Afar and East Africa, and is interpreted as the initial oceanic surface layer chilled against the continental lithosphere. With continued plate accretion, the chilled oceanic crust thins exponentially to a steadystate thickness, which is achieved about 40 m.y. after breakup. These findings contrast with the generally held view that the oceanic crust has a uniform thickness.During the first 40 m.y. of spreading, the thicker oceanic crust, of density 2.86 g/cm3, displaces the denser (3.32 g/cm3) subjacent material; by isostasy, the spreading ridge and the rest of the seafloor thus stand higher in younger( <40m.y.) oceans than they do in older(>40m.y.) oceans. This is postulated to be the cause of the empirical relationship between the crestal depth of spreading ridges and the age (or half-width) of ocean basins.  相似文献   

16.
Mineral assemblages displayed by MORB and alkali-poor olivine tholeiites have been investigated over the pressure interval 4.6–18 GPa at 1200°C. Both compositions crystallize to form normal eclogites between 4.6 and 10 GPa and there is little change in the relative proportions of garnet and pyroxene over this range. However, the proportion of garnet increases rapidly above 10 GPa as pyroxene dissolves in the garnet structure and pyroxene-free garnetites (±stishovite) are produced by 14–15 GPa, dependent upon composition. The garnetite facies for both compositions possess zero-pressure densities of 3.75 g/cm3, implying that subducted oceanic crust remains appreciably denser than surrounding mantle to depths exceeding 600 km. It is demonstrated that the seismic velocity distributions in the mantle between 400 and 650 km are inconsistent with Anderson's hypothesis that this region is of eclogitic composition.  相似文献   

17.
Measurements of stable isotope compositions and water contents of boninite series volcanic rocks from the island of Chichi-jima, Bonin Islands, Japan, confirm that a large amount (1.6–2.4 wt.%) of primary water was present in these unusual magmas. An enrichment of 0.6‰ in18O during differentiation is explained by crystallization of18O-depleted mafic phases. Silicic glasses have elevated δ18O values and relatively low δD values indicating that they were modified by low-temperature alteration and hydration processes. Mafic glasses, on the other hand, have for the most part retained their primary isotopic signatures since Eocene time. Primary δD values of −53 for boninite glasses are higher than those of MORB and suggest that the water was derived from subducted oceanic lithosphere.  相似文献   

18.
The average chemical compositions of the continental crust and the oceanic crust (represented by MORB), normalized to primitive mantle values and plotted as functions of the apparent bulk partition coefficient of each element, form surprisingly simple, complementary concentration patterns. In the continental crust, the maximum concentrations are on the order of 50 to 100 times the primitive-mantle values, and these are attained by the most highly incompatible elements Cs, Rb, Ba, and Th. In the average oceanic crust, the maximum concentrations are only about 10 times the primitive mantle values, and they are attained by the moderately incompatible elements Na, Ti, Zr, Hf, Y and the intermediate to heavy REE.This relationship is explained by a simple, two-stage model of extracting first continental and then oceanic crust from the initially primitive mantle. This model reproduces the characteristic concentration maximum in MORB. It yields quantitative constraints about the effective aggregate melt fractions extracted during both stages. These amount to about 1.5% for the continental crust and about 8–10% for the oceanic crust.The comparatively low degrees of melting inferred for average MORB are consistent with the correlation of Na2O concentration with depth of extrusion [1], and with the normalized concentrations of Ca, Sc, and Al ( 3) in MORB, which are much lower than those of Zr, Hf, and the HREE ( 10). Ca, Al and Sc are compatible with clinopyroxene and are preferentially retained in the residual mantle by this mineral. This is possible only if the aggregate melt fraction is low enough for the clinopyroxene not to be consumed.A sequence of increasing compatibility of lithophile elements may be defined in two independent ways: (1) the order of decreasing normalized concentrations in the continental crust; or (2) by concentration correlations in oceanic basalts. The results are surprisingly similar except for Nb, Ta, and Pb, which yield inconsistent bulk partition coefficients as well as anomalous concentrations and standard deviations.The anomalies can be explained if Nb and Ta have relatively large partition coefficients during continental crust production and smaller coefficients during oceanic crust production. In contrast, Pb has a very small coefficient during continental crust production and a larger coefficient during oceanic crust production. This is the reason why these elements are useful in geochemical discrimination diagrams for distinguishing MORB and OIB on the one hand from island arc and most intracontinental volcanics on the other.The results are consistent with the crust-mantle differentiation model proposed previously [2]. Nb and Ta are preferentially retained and enriched in the residual mantle during formation of continental crust. After separation of the bulk of the continental crust, the residual portion of the mantle was rehomogenized, and the present-day internal heterogeneities between MORB and OIB sources were generated subsequently by processes involving only oceanic crust and mantle. During this second stage, Nb and Ta are highly incompatible, and their abundances are anomalously high in both OIB and MORB.The anomalous behavior of Pb causes the so-called “lead paradox”, namely the elevated U/Pb and Th/Pb ratios (inferred from Pb isotopes) in the present-day, depleted mantle, even though U and Th are more incompatible than Pb in oceanic basalts. This is explained if Pb is in fact more incompatible than U and Th during formation of the continental crust, and less incompatible than U and Th during formation of oceanic crust.  相似文献   

19.
Aleutian magnesian andesites: Melts from subducted Pacific ocean crust   总被引：15，自引：0，他引：15  
Several diagnostic chemical characteristics of an uncommon Aleutian magma type support a proposed origin that involves a small amount of partial melting of subducted Pacific ocean crust (basalt) consisting mainly of garnet and clinopyroxene (eclogite or garnet websterite). Among the characteristics are high La/Yb ratios and Sr contents and low ratios of radiogenic to non-radiogenic Sr and Pb. The major element composition of the andesites resembles that of hydrous melts in equilibrium with peridotite: a low ratio of total Fe to Mg is distinctive. These disparate observations can be reconciled if large ion lithophile (LIL)- element-rich hydrous melt from the subducted oceanic crust equilibrates with olivine and orthopyroxene in overlying LIL-element-depleted mantle and then erupts without interacting with the island are crust. The compositional dissimilarity of the magnesian andesites and most other andesites from the Aleutian island arc precludes application of this model to island are magmatism in general.  相似文献   

20.
The electrical conductivities of natural pyrolitic mantle and MORB materials were measured at high pressure and temperature covering the entire lower mantle conditions up to 133 GPa and 2650 K. In contrast to the previous laboratory-based models, our data demonstrate that the conductivity of pyrolite does not increase monotonically but varies dramatically with depth in the lower mantle; it drops due to high-spin to low-spin transition of iron in both perovskite and ferropericlase in the mid-lower mantle and increases sharply across the perovskite to post-perovskite phase transition at the D″ layer. We also found that the MORB exhibits much higher conductivity than pyrolite. The depth–conductivity profile measured for pyrolite does not match the geomagnetic field data below about 1500-km depth, possibly suggesting the existence of large quantities of subducted MORB crust in the deep lower mantle. The observations of geomagnetic jerks suggest that the electrical conductivity may be laterally heterogeneous in the lowermost mantle with high anomaly underneath Africa and the Pacific, the same regions as large low shear-wave velocity provinces. Such conductivity and shear-wave speed anomalies are also possibly caused by the deep subduction and accumulation of dense MORB crust above the core–mantle boundary.  相似文献   

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