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1.
Volcanoes of the East Japan volcanic arc are divided into two groups on the basis of their phenocryst assemblages; volcanoes with lavas or pyroclastic rocks containing quartz phenocrysts and no hornblende phenocrysts (type A), and those with rocks containing hornblende phenocrysts and no quartz phenocrysts (type B). Type A volcanoes occur only in the narrow region along the volcanic front, whereas type B volcanoes are distributed in the area closer to the Sea of Japan.Recent experimental studies on calc-alkaline andesite-dacite under H2O-saturated and -undersaturated conditions indicate that the liquidus temperature (maximum thermal stability limit) of quartz decreases drastically with increasing H2O content in magma, whereas the liquidus temperatures of hornblende and biotite are relatively constant with variations in the H2O content and bulk chemical composition of the magma.It is suggested from the lateral variation of mafic phenocryst assemblages [1] and from the above result that the temperature of the parental magmas of these volcanoes increases, and their H2O contents decrease, towards the volcanic front in the East Japan volcanic arc.Such lateral variations in the H2O contents of magmas under the East Japan volcanic arc are in agreement with those of other incompatible elements (K, Rb, REE, etc.). If H2O-undersaturated partial melting of upper mantle peridotite can be represented by the univariant line (olivine, Ca-rich clinopyroxene, orthopyroxene and liquid coexist) in the system H2OMg2SiO4z.sbnd;CaMgSi2O6z.sbnd;SiO2, the decrease of H2O content in the magma suggests that the melting temperature of the peridotitic mantle may gradually increase, and so the degree of partial melting may increase, towards the volcanic front. The lateral variation of other incompatible elements can also be explained by this model.  相似文献   

2.
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   

3.
We present new shock devolatilization recovery data for brucite (Mg(OH)2) shocked to 13 and 23 GPa. These data combined with previous data for serpentine (Mg3Si2O5(OH)4) are used to constrain the minimum size terrestrial planet for which planetesimal infall will result in an impact-generated water atmosphere. Assuming a chondritic abundance of minerals including 3–6%, by mass water, in hydrous phyllosilicates, we carried out model calculations simulating the interaction of metallic iron with impact-released free water on the surface of the accreting Earth. We assume that the reaction of water with iron in the presence of enstatite is the prime source of the terrestrial FeO component of silicates and oxides. Lower and upper bounds on the terrestrial FeO budget are based on mantle FeO content and possible incorporation of FeO in the outer core. We demonstrate that the iron-water reaction would result in the absence of atmospheric/hydrospheric water, if homogeneous accretion is assumed. In order to obtain1025g of atmospheric water by the end of accretion, slightly heterogeneous accretion with initially 36% by mass iron planetesimals, as compared to a homogeneous value of 34% is required. Such models yield final FeO budgets, which either require a higher FeO content of the mantle (17 wt.%) or oxygen as a light element in the outer core of the Earth.  相似文献   

4.
Fluids supplied in alpine-type mantle peridotites and trapped as fluid inclusions in olivines have been fixed by low-temperature reactions, and theirCO2/H2O ratios can be deduced from the minerals in the inclusions. Relic fluid inclusions were commonly observed by the optical microscope in olivines from almost all examined solid intrusive ultramafic complexes (Papua, Oman, Troodos and eleven alpine-type complexes of Japan). Such complexes were emplaced into the crust in a solid state. Electron microscopic studies of olivines from three complexes, Higashiakaishi, Horoman and Iwanai-dake, showed that relic fluid inclusions in these olivines have distinctive mineral parageneses: serpentine + magnesite + talc, serpentine + magnesite + brucite, and serpentine + brucite, respectively, depending on theCO2/(H2O+CO2) ratio of the trapped fluid.It is deduced that the fluids had been supplied to peridotites, at least partly, but almost wholly in some case, when the peridotites were still hot, probably at the upper mantle for the following reasons: (1) the curved surfaces along which the inclusions are distributed are cut by post-emplacement serpentine veins; (2) for the Higashiakaishi dunite, the relic fluid inclusions are exclusively found in porphyroclast olivines and are totally absent in matrix olivines recrystallized during the Sanbagawa metamorphism.Recent models on the derivation of ophiolitic or some alpine-type peridotites favor the island-arc or fore-arc settings. Dehydration of the descending oceanic slab may supply H2OCO2 vapor to the overlying mantle wedge. Fluid inclusions trapped in such mantle wedge may abound in H2O component. H2O-bearing fluid inclusions may, therefore, be important H2O containers in the upper mantle, especially near the edge of the mantle wedge above downgoing oceanic slabs.  相似文献   

5.
143Nd/144Nd,87Sr/86Sr and trace element results are reported for volcanic and plutonic rocks of the Aleutian island arc. The Nd and Sr isotopic compositions plot within the mantle array with εNd values of from 6.5 to 9.1 and87Sr/86Sr ratios of from 0.70289 to 0.70342. Basalts have mildly enriched light REE abundances but essentially unfractionated heavy REE abundances, while andesites exhibit a greater degree of light to heavy REE fractionation. Both the basalts and andesites have significant large ion lithophile element to light rare earth element (LILE/LREE) enrichments. Variations in the isotopic compositions of Nd and Sr are not related to the spatial distribution of volcanoes in the arc, nor are they related to temporal differences. εNd and87Sr/86Sr do not correlate with major element compositions but do, however, correlate with certain LILE/LREE ratios (e.g. BaN/LaN). Plutonic rocks have isotropic and trace element characteristics identical to some of the volcanic rocks. Rocks that make up the tholeiitic, calc-alkaline and alkaline series in the Aleutians do not come from isotopically distinct sources, but do exhibit some differing LILE characteristics.Given these elemental and isotopic constraints it is shown that the Aleutian arc magmas could not have been derived directly from homogeneous MORB-type mantle, or fresh or altered MORB subducted beneath the arc. Mixtures of partially altered MORB with deep-sea sediment can in principle account for the isotopic characteristics and most of the observed LILE/LREE enrichments. However, some samples have exceedingly high LILE/LREE enrichments which cannot be accounted for by sediment contamination alone. For these samples a more complex scenario is considered whereby dehydration and partial melting of the subducted slab, containing less than 8% sediment, produces a LILE-enriched (relative to REE) metasomatic fluid which interacts with the overlying depleted mantle wedge. The isotopic and LILE characteristics of the mantle are extremely sensitive to metasomatism by small percentages of added fluid, whereas major elements are not substantially effected, Major element compositions of Aleutian magmas are dominantly controlled by the partial melting of this mantle and subsequent crystal fractionation; whereas isotopic and LILE characteristics are determined by localized mantle heterogeneities.  相似文献   

6.
This study focuses on constraining bubble nucleation and H2O exsolution processes in alkalic K-phonolite melts, using “white pumice” of the 79 AD eruption of Vesuvius as starting material. The first set of experiments consisted of H2O solubility runs at 1153 to 1250 K and pressures between 50 and 200 MPa, to constrain equilibrium water concentrations along the decompression pathways. The decompression experiments were equilibrated with H2O at 150 MPa and 1173 and 1223 K, and then decompressed at 3 to 17 MPa/s before rapid quenching. Experiments nucleated bubbles within the first 50 MPa pressure drop, producing maximum bubble number densities (NV), corrected to melt volume, of 3.8 × 1014 m− 3 at 1173 K and 4.3 × 1013 m− 3 at 1223 K. Most bubbles were not visibly attached to crystals, except for a subset attached to pyroxenes primarily in the 1173 K experiments. When compared with prior bubble nucleation studies, the reduced nucleation ΔP and relatively low NV observed indicate predominantly a heterogeneous nucleation mechanism. Melt–vapor–crystal wetting angles measured in 1173 K experiments from bubbles attached to pyroxene crystals are 36 to 69°, which are similar to those measured on titanomagnetite crystals in calc-alkaline dacite melts. The 1223 K experiments have porosities and water concentrations that largely track equilibrium, despite the rapid decompression rate. The 1173 K experiments deviate strongly from equilibrium trends in both porosity and water concentration, and slower H2O diffusion rates are likely the cause of the inhibited bubble growth. Bubble number densities from 79 AD Vesuvius natural EU2 pumice are relatively high (2 to 4 × 1015 m− 3; [Gurioli, L., Houghton, B.F., Cashman, K.V., Cioni, R., 2005. Complex changes in eruption dynamics during the 79 AD eruption of Vesuvius. Bull. Volcanol. 67: 144–159.]) when corrected to vesicularity. In comparison, corrected NV's from homogeneous and heterogeneous bubble nucleation experiments from this study and prior work are at least factor of 5 lower, indicating perhaps that the natural magmas initially nucleated bubbles in the presence of CO2. The disequilibrium H2O exsolution seen in the 1173 K experiments indicates that inhibited bubble growth could lead to delayed exsolution in the conduit in cooler K-phonolite magmas.  相似文献   

7.
A swath bathymetric survey was conducted on Marsili Volcano, the biggest seamount in the Tyrrhenian Sea. It stands 3000 m above the surrounding oceanic crust of the 3500 m-deep Marsili back-arc basin and is axially located within the basin. The seamount has an elongated shape and presents distinctive morphology, with narrow (<1000 m) ridges, made up of several elongated cones, on the summit zone and extensive cone fields on its lower flanks. A dredging campaign carried out at water depths varying between 3400 and 600 m indicates that most of Marsili Seamount is composed of medium-K calc-alkaline basalts. Evolved high-K andesites were only recovered from the small cones on the summit axis zone. Petrological and geochemical characteristics of the least differentiated basalts reveal that at least two varieties of magmas have been erupted on the Marsili Volcano. Group 1 basalts have plagioclase and olivine as dominant phases and show lower Al, Ca, K, Ba, Rb and Sr, and higher Fe, Na, Ti and Zr with respect to a second type of basaltic magma. Group 2 basalts reveal the presence of clinopyroxene as an additional phenocryst phase. In addition, the two basaltic magmas have different original pre-eruptive H2O content (group 1, H2O-poor and group 2, H2O-rich). Moreover, comparison of the compositional trends and mineralogical compositions obtained from MELTS [Ghiorso, M.S., Sack, R.O., Contrib. Mineral. Petrol. 119 (1995) 197–212] fractional crystallization calculations reveal that the evolved andesites can only exclusively be derived from a low-pressure (0.3 kbar) fractionation of magmas compositionally similar to the least evolved group 2 basalts. Finally, we suggest that the high vesicularity of the basalts sampled at relatively great depths (>2400 m) on the edifice is governed by H2O and, probably, CO2 exsolution and is not a feature indicative of shallow water depth eruption.  相似文献   

8.
Biotite granite from the Sierra Nevada batholith was reacted, with known water contents in sealed platinum capsules, in a piston-cylinder apparatus between 10 and 35 kb. With the liquid just over-saturated with respect to water, temperatures for solidus and liquidus (quartz/coesite-out curve), respectively, are: 2 kb, 680°C, 715°C; 10 kb, 620°C, 725°C; 25 kb, 655°C, 800°C; 35 kb, 700°C, 850°C. The temperature interval is 35°C at 2 kb, 105°C at 10 kb, and 150°C at 35 kb, indicating that granite departs from a eutectic composition at depths greater than about 40–50 km. We conclude that crystal-liquid equilibria are not likely to yield primary rhyolite or granite magmas by partial fusion of oceanic crust in subduction zones. The solubility of water in granite liquids, in wt%, is 22.5 ± 2.5 at 25 kb and 810°C and 27 ± 2.5 at 35 kb and 850°C. These results indicate that a miscibility gap persists between water-saturated silicate magmas and aqueous vapor phase at least to pressures corresponding to 100 km depth in the mantle. The formation of kyanite near the liquidus of water over-saturated granite indicates that the aqueous vapor phase is enriched in alkalis and possibly silica, relative to the condensed phases.  相似文献   

9.
The Iliniza Volcanic Complex (IVC) is a poorly known volcanic complex located 60 km SSW of Quito in the Western Cordillera of Ecuador. It comprises twin peaks, North Iliniza and South Iliniza, and two satellite domes, Pilongo and Tishigcuchi. The study of the IVC was undertaken in order to better constrain the role of adakitic magmas in the Ecuadorian arc evolution. The presence of volcanic rocks with an adakitic imprint or even pristine adakites in the Ecuadorian volcanic arc is known since the late 1990s. Adakitic magmas are produced by the partial melting of a basaltic source leaving a garnet rich residue. This process can be related to the melting of an overthickened crust or a subducting oceanic crust. For the last case a special geodynamic context is required, like the subduction of a young lithosphere or when the subduction angle is not very steep; both cases are possible in Ecuador. The products of the IVC, made up of medium-K basaltic andesites, andesites and dacites, have been divided in different geochemical series whose origin requires various interactions between the different magma sources involved in this subduction zone. North Iliniza is a classic calc-alkaline series that we interpret as resulting from the partial melting of the mantle wedge. For South Iliniza, a simple evolution with fractional crystallization of amphibole, plagioclase, clinopyroxene, magnetite, apatite and zircon from a parental magma, being itself the product of the mixing of 36% adakitic and 64% calc-alkaline magma, has been quantified. For the Santa Rosa rhyolites, a slab melting origin with little mantle interactions during the ascent of magmas has been established. The Pilongo series magma is the product of a moderate to high degree (26%) of partial melting of the subducting oceanic crust, which reached the surface without interaction with the mantle wedge. The Tishigcuchi series shows two stages of evolution: (1) metasomatism of the mantle wedge peridotite by slab melts, and (2) partial melting (10%) of this metasomatized source. Therefore, the relative ages of the edifices show a geochemical evolution from calc-alkaline to adakitic magmas, as is observed for several volcanoes of the Ecuadorian arc.  相似文献   

10.
The volatile content of glassy pillow rims from East Scotia Sea back-arc basin (BAB) lavas are unlike those of mid-ocean ridge (MOR) pillow-rim glasses, although non-volatile compositions of the two rock groups overlap. The East Scotia Sea samples have three to ten times greater water contents and nearly twice the average CO2 and Cl contents of MOR samples; F contents are similar. S contents are only one-third those from MOR samples. H2O and CO2 contents of glassy pillow rims from Mariana island arc andesites are similar to those in the BAB lavas studied. Nevertheless, volatiles in the East Scotia Sea BAB magmas are probably not directly derived from the subducted slab, because there is no seismic evidence that the slab extends within 200 km of the spreading axis of the East Scotia Sea. Available data do not preclude the possibility that the magmas were contaminated by seawater prior to eruption or that the mantle under the East Scotia Sea spreading center is volatile-rich. The volatiles may have been added to the mantle during an earlier period of subduction, perhaps during the initial formation of the East Scotia Sea basin.  相似文献   

11.
Melting phase relations of an augite-olivine high-magnesian andesite and an augite-olivine basalt from the Miocene Setouchi volcanic belt in southwest Japan have been studied under water-saturated, water-undersaturated and under anhydrous conditions. Both the andesite and the basalt are characterized by low FeO*/MgO ratios (0.86 and 0.76 in weight, respectively) and qualify as primary magmas derived from the upper mantle.The andesite melt coexists with olivine, orthopyroxene and clinopyroxene at 15 kbar and 1030°C under water-saturated conditions, and at 10 kbar and 1070°C under water-undersaturated conditions (7 wt.% H2O in the melt). The basalt-melt also coexists with the above three phases at 11 kbar and 1305°C under anhydrous conditions, and at 15 kbar and 1205°C in the presence of 4 wt.% water.Present studies indicate that high-magnesian andesite magmas may be produced even under water-undersaturated conditions by partial melting of mantle peridotite. It is suggested that two types of high-magnesian andesites in the Setouchi volcanic belt (augite-olivine and bronzite-olivine andesites) were produced by different degrees of partial melting; augite-olivine andesite magmas, whose mantle residual is lherzolite, were formed by lower degrees of partial melting than bronzite-olivine andesite magmas, which coexist with harzburgite. The basalt magmas, which were often extruded in close proximity to the high-magnesian andesite magmas, are not partial melting products of a mantle peridotite which had previously melted to yield high-magnesian andesite magmas.  相似文献   

12.
Phase equilibria in a portion of the system forsterite-plagioclase (An50Ab50 by weight)-silica-H2O have been determined at 15 kbar pressure under H2O-saturated conditions. The composition of the liquid pertinent to the piercing point forsterite + enstatite solid solution + amphibole + liquid + vapor is similar to that of calc-alkaline andesite. The electron microprobe analysis of the glass coexisting with the above three crystalline phases is very close to that of the piercing point determined by phase assemblage observations; however, the glass near (< 8 μm) forsterite crystals is significantly depleted in the normative forsterite component. With the addition of 10 wt.% KAlSi3O8, the composition of this piercing point becomes even closer to the compositions of calc-alkaline andesites. It is also shown that the liquid coexisting with forsterite and enstatite solid solution remains silica-rich (60–62 wt.%) over a wide (～ 100°C) temperature range. The present experimental studies support the view that liquids similar in composition to calc-alkaline andesites can be generated by direct partial melting of hydrous upper mantle at least at or near 15 kbar.  相似文献   

13.
Calc-alkaline intermediate rocks are spatially and temporally associated with high-Mg andesites (HMAs, Mg#>60) in Middle Miocene Setouchi volcanic belt. The calc-alkaline rocks are characterized by higher Mg# (strongly calc-alkaline trend) than ordinary calc-alkaline rocks at equivalent silica contents. Phenocrysts in the intermediate rocks have petrographical features such as: (1) coexisting reversely and normally zoned orthopyroxene phenocrysts in single rock; (2) sieve type plagioclase in which cores are mantled by higher An%, melt inclusion-rich zone; and (3) reversely zoned amphibole phenocrysts with opacite cores. In addition, mingling textures and magmatic inclusions were observed in some rocks. These petrographic features and the mineral chemistry indicate that magma mixing was the most important process in producing the strongly calc-alkaline rocks. The core composition of normally zoned orthopyroxene phenocrysts and the mantle composition of reversely zoned orthopyroxene phenocrysts have relatively high Mg# (85–90) in maximum. Although basaltic and high-Mg andesitic magmas are candidate as possible mafic end-member magmas, basaltic magma is excluded in terms of phenocryst assemblage and bulk composition. HMA magmas are suitable mafic end-member magmas that precipitated high Mg# (90) orthopyroxene, whereas andesitic to dacitic magma are suitable felsic end-members. In contrast, it is difficult to produce the strongly calc-alkaline trend through fractional crystallization from a HMA magma, because it would require removal of plagioclase together with mafic minerals from the early stage of crystallization, whereas the precipitation of plagiolase is suppressed due to the high water content of HMA magmas. These results imply that Archean Mg#-rich TTGs (>45–55), which are an analog of the strongly calc-alkaline rocks in terms of chemistry and magma genesis, can be derived from magma mixing in which a HMA magma is the mafic end-member magma, rather than by fractional crystallization from a HMA magma.  相似文献   

14.
An association of adakite, magnesian andesite (MA), and Nb-enriched basalt (NEB) volcanic flows, which erupted within ‘normal’ intra-oceanic arc tholeiitic to calc-alkaline basalts, has recently been documented in ∼2.7 Ga Wawa greenstone belts. Large, positive initial ?Nd values (+1.95 to +2.45) of the adakites signify that their basaltic precursors, with a short crustal residence, were derived from a long-term depleted mantle source. It is likely that the adakites represent the melts of subducted late Archean oceanic crust. Initial ?Nd values in the MA (+0.14 to +1.68), Nb-enriched basalts and andesites (NEBA) (+1.11 to +2.05), and ‘normal’ intra-oceanic arc tholeiitic to calc-alkaline basalts and andesites (+1.44 to +2.44) overlap with, but extend to lower values than, the adakites. Large, tightly clustered ?Nd values of the adakites, together with Th/Ce and Ce/Yb systematics of the arc basalts that rule out sediment melting, place the enriched source in the sub-arc mantle. Accordingly, isotopic data for the MA, NEBA, and ‘normal’ arc basalts can be explained by melting of an isotopically heterogeneous sub-arc mantle that had been variably enriched by recycling of continental material into the shallow mantle in late Archean subduction zones up to 200 Ma prior to the 2.7 Ga arc. If the late Archean Wawa adakites, MA, and basalts were generated by similar geodynamic processes as their counterparts in Cenozoic arcs, involving subduction of young and/or hot ocean lithosphere, then it is likely that late Archean oceanic crust, and arc crust, were also created and destroyed by modern plate tectonic-like geodynamic processes. This study suggests that crustal recycling through subduction zone processes played an important role for the generation of heterogeneity in the Archean upper mantle. In addition, the results of this study indicate that the Nd-isotope compositions of Archean arc- and plume-derived volcanic rocks are not very distinct, whereas Phanerozoic plumes and intra-oceanic arcs tend to have different Nd-isotopic compositions.  相似文献   

15.
The transport of water in subduction zones   总被引：9，自引：0，他引：9  
The transport of water from subducting crust into the mantle is mainly dictated by the stability of hydrous minerals in subduction zones. The thermal structure of subduction zones is a key to dehydration of the subducting crust at different depths. Oceanic subduction zones show a large variation in the geotherm, but seismicity and arc volcanism are only prominent in cold subduction zones where geothermal gradients are low. In contrast, continental subduction zones have low geothermal gradients, resulting in metamorphism in cold subduction zones and the absence of arc volcanism during subduction. In very cold subduction zone where the geothermal gradient is very low(?5?C/km), lawsonite may carry water into great depths of ?300 km. In the hot subduction zone where the geothermal gradient is high(25?C/km), the subducting crust dehydrates significantly at shallow depths and may partially melt at depths of 80 km to form felsic melts, into which water is highly dissolved. In this case, only a minor amount of water can be transported into great depths. A number of intermediate modes are present between these two end-member dehydration modes, making subduction-zone dehydration various. Low-T/low-P hydrous minerals are not stable in warm subduction zones with increasing subduction depths and thus break down at forearc depths of ?60–80 km to release large amounts of water. In contrast, the low-T/low-P hydrous minerals are replaced by low-T/high-P hydrous minerals in cold subduction zones with increasing subduction depths, allowing the water to be transported to subarc depths of 80–160 km. In either case, dehydration reactions not only trigger seismicity in the subducting crust but also cause hydration of the mantle wedge. Nevertheless, there are still minor amounts of water to be transported by ultrahigh-pressure hydrous minerals and nominally anhydrous minerals into the deeper mantle. The mantle wedge overlying the subducting slab does not partially melt upon water influx for volcanic arc magmatism, but it is hydrated at first with the lowest temperature at the slab-mantle interface, several hundreds of degree lower than the wet solidus of hydrated peridotites. The hydrated peridotites may undergo partial melting upon heating at a later time. Therefore, the water flux from the subducting crust into the overlying mantle wedge does not trigger the volcanic arc magmatism immediately.  相似文献   

16.
Depletion of Nb relative to K and La is characteristic of lavas in subduction-related magmatic arcs, as distinct from mid-ocean ridge basalts. Nb depletion is also characteristic of the continental crust. This and other geochemical similarities between the continental crust and high-Mg# andesite magmas found in arcs suggests that the continental crust may have formed by accretion of andesites. Previous studies have shown that the major element characteristics of high-Mg# andesites may be produced by melt/rock reaction in the upper mantle. In this paper, new data on partitioning of K, Nb, La and Ce between garnet, orthopyroxene and clinopyroxene in mantle xenoliths, and on partitioning of Nb and La between orthopyroxene and liquid, show that garnet and orthopyroxene have Nb crystal/liquid distribution coefficients which are much larger than those of K and La. Similar fractionations of Nb from K and La are expected in spinel and olivine. For this reason, reactions between migrating melt and large masses of mantle peridotite can produce substantial depletion of Nb in derivative liquids. Modeling shows that reaction between ascending, mantle-derived melts and mantle peridotite is a viable mechanism for producing the trace element characteristics of high-Mg# andesite magmas and the continental crust.

Alternatively, small-degree melts of metabasalt and/or metasediment in the subducting slab may leave rutile in their residue, and will thus have large Nb depletions relative to K and La [1]. Slab melts are too rich in light rare earth elements and other incompatible elements, and too poor in compatible elements, to be parental to arc magmas. However, ascending slab melts may be modified by reaction with the mantle. Our new data permit modeling of the trace element effects of reaction between small-degree melts of the slab and mantle peridotite. Modeling shows that this type of reaction is also a viable mechanism for producing the trace element characteristics of high-Mg# andesites and the continental crust. These findings, in combination with previous results, suggest that melt/rock reaction in the upper mantle has been an important process in forming the continental crust and mantle lithosphere.  相似文献   


17.
Osamu  Ujike  Alan M.  Goodwin  Tomoyuki  Shibata 《Island Arc》2007,16(1):191-208
Abstract   Volcanic rocks from the Upper Keewatin assemblage ( ca 2720 Ma) were geochemically classified into five groups; komatiites, tholeiitic rocks having near-flat primitive mantle-normalized abundance patterns, Nb-enriched basalts and andesites (NEBA) plus normal calc-alkaline (NCA) rocks, adakites and shoshonites. The adakites having [La/Yb]N >30 and <30 were probably derived from felsic magmas formed by partial melting of a subducted slab at relatively greater and smaller depths, respectively. Ascending adakite magmas, by interaction with the overlying mantle wedge, decreased in Al2O3 / Y ratio and selectively lost high-field strength elements, thereby forming mantle sources for both NEBA + NCA and shoshonite magmas. Under the influence of a mantle plume, the source of komatiites, the NEBA + NCA magmas were generated from that part of the mantle wedge metasomatized by adakite magmas having [La / Yb]N <30, and tholeiitic magmas from unmetasomatized part of the same mantle wedge. Magmas of both adakites having [La / Yb]N >30 and shoshonites were generated in a normal Archean Arc system setting.  相似文献   

18.
Pyroxene water contents measured by Fourier transform infrared spectrometry for Mexican and Simcoe (WA, USA) spinel-peridotite xenoliths range from 140 to 528 ppm in clinopyroxenes and 39 to 265 ppm in orthopyroxenes. Correlations between these water contents and major-element compositional data for the pyroxenes, associated spinels, and whole-rock xenoliths demonstrate that these water contents record mantle values that have not been perturbed since the xenoliths were brought to the surface by their host magmas. Broad positive correlations of pyroxene water contents with whole-rock Al2O3 are consistent with water behaving as an incompatible element during peridotite melting. The main control on the range of pyroxene water contents, however, appears to be the redox state of the peridotite, because estimates of oxygen fugacity from Mössbauer (Simcoe) and microprobe data (Mexico) on spinels are negatively correlated with water contents. This is consistent with the dominant mechanism of H incorporation into pyroxene, which is dependent on the oxidation-reduction of iron. Metasomatism of sub-arc mantle-wedge peridotites by oxidized fluids or melts rising from the slab raises the oxygen fugacity of the peridotites, and where temperature is high enough, induces them to partially melt. The oxidation, in turn, lowers the solubility of water in the peridotite minerals, causing more than half of the original water to be expelled. That water enters the hydrous partial melts and these ascend through the lithosphere to feed the arc magmatic system in the upper crust. Low water contents in pyroxenes from sub-arc mantle-wedge peridotites, such as those from Simcoe and some western Mexican sites, therefore appear to be complementary to the high water contents that characterize subduction-zone magmas and fuel their explosive eruptions. An estimate of water budget in subduction zones, however, indicates that the amount of water coming from the dehydration of mantle-wedge anhydrous minerals probably accounts for less than 5% of the total water present in subduction-related magmas. The high water contents of arc magmas thus are mainly attributed to fluids or melts from the slab proper. The relatively dry sub-arc mantle wedge appears to be an effective medium through which subducted water is transported from slabs toward the surface.  相似文献   

19.
Fluorine contents in about 160 representative Quaternary volcanic rocks and 15 hornblende and biotite phenocrysts in a calc-alkali series in Japan have been determined by a selective ion-electrode method. Tholeiites have the lowest contents and the narrowest range (58–145 ppm), while alkali basalts have the highest contentws and the widest range (301–666 ppm), high-alumina basalts have intermediate values (188–292 ppm). F contents in basalts clearly increase from east to west across the Japanese Islands, as do alkalies, P2O5 REE, U, Th and H2O.The volcanic rocks studied are divided into two groups on the basis of F: (1) witt, increasing % SiO2 or advancing fractionation, F contents show either progressive enrichment; or (2) with increasing fractionation, F contents show rather constant values. The former is produced by fractionation of anhydrous phases from basalt to mafic andesite magmas; the tholeiite series of Nasu volcanic zone (outer zone), northeastern, Japan is a typical example. The latter group is derived through separation of amphibole-bearing phases from basaltic magmas at various depths from upper mantle (about 30 km) to upper crust; the alkali series in southwestern Japan and the calc-alkali series of Chokai volcanic zone (inner zone), northeastern Japan, are examples.  相似文献   

20.
The Serra Geral (Paraná) continental flood-basalt province of southern Brazil has two main basalt types: low-TiO2 ( 1 wt.%) basalts occupy the southern portion, and high-TiO2 (> 3 wt.%) basalts are largely in the northern part. Low-Ti basalts are less evolved (Mg# 60) and more radiogenic (e.g., 87Sr/86Sr 0.708) than high-Ti basalts (Mg# 35; 87Sr/86Sr 0.705). This is consistent with a model that invokes variable melting of a single mantle source to produce picritic magmas that have relatively lower and higher incompatible element contents. Varying percentages of melting can be related to varying proximity to the early Tristan da Cunha hotspot. The Mg-rich magmas fractionated 60–75% olivine, clinopyroxene, and plagioclase to yield low- or high-Ti flood basalts, assimilating more or less crust in the process. The extent of fractionation and assimilation depended on crustal “warmth” (also tied to location relative to hotspot): (1) above zones of 25% melting, warm crust relatively easily contaminated crystallizing picritic magma that originated by a high degree of melting (i.e., magma with lower incompatible element contents); additionally, high degrees of melting sustained replenishment of magma with low-Ti magma characteristics; (2) above 10% melting zones, cooler crust comparatively restricted assimilation during crystallization (of magma with higher incompatible element contents) and permitted magma evolution to high-Ti derivatives; lesser degrees of melting also limited replenishment magma and thereby allowed greater evolution of existing magma. This model refers all diagnostic geochemical and isotopic features of Serra Geral basalts to percentages of partial melting of an essentially homogeneous mantle material.  相似文献   

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