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1.
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2.
The present study examines the petrology and geochemistry of the Early Paleozoic Motai serpentinites, the South Kitakami Belt, northeast Japan, to reveal the subduction processes and tectonics in the convergent margin of the Early Paleozoic proto-East Asian continent. Protoliths of the serpentinites are estimated to be harzburgite to dunite based on the observed amounts of bastite (orthopyroxene pseudomorph). Relic chromian spinel Cr# [=Cr/(Cr + Al)] increases with decreasing amount of bastite. The compositional range of chromian spinel is similar to that found in the Mariana forearc serpentinites. This fact suggests that the protoliths of the serpentinites are depleted mantle peridotites developed beneath the forearc regions of a subduction zone. The Motai serpentinites are divided into two types, namely, Types 1 and 2 serpentinites; the former are characterized by fine-grained antigorite and lack of olivine, and the latter have coarse-grained antigorite and inclusion-rich olivine. Ca-amphibole occurs as isolated crystals or vein-like aggregates in the Type 1 serpentinites and as needle-shaped minerals in the Type 2 serpentinites. Ca-amphibole of the Type 1 serpentinites is more enriched in LILEs and LREEs, suggesting the influence of hydrous fluids derived from slabs. By contrast, the mineral assemblage, mineral chemistry, and field distribution of the Type 2 serpentinites reflect the thermal effect of contact metamorphism by Cretaceous granite. The Ca-amphibole of the Type 1 serpentinites is different from that of the Hayachine–Miyamori Ophiolite in terms of origin; the latter was formed by the infiltration of melts produced in an Early Paleozoic arc–backarc system. Chemical characteristics of the Ca-amphibole in the ultramafic rocks in the South Kitakami Belt reflect the tectonics of an Early Paleozoic mantle wedge, and the formation of the Motai metamorphic rocks in the forearc region of the Hayachine–Miyamori subduction zone system, which occurred at the Early Paleozoic proto-East Asian continental margin.  相似文献   

3.
We provide new petrological evidence for the strong influence of water on the formation of the oceanic lithospheric mantle, the subcontinental mantle above, and the continental lithosphere. Our analysis throws new light on the hypothesis that new continental lithosphere was formed by the passage of silicate-rich aqueous fluid through the sub-continental mantle. In order to investigate this hypothesis, we analyzed a representative collection of lherzolite and harzburgite xenoliths from the sample volcano known as “The Thumb”, located in the center of the Colorado Plateau, western United States. The studied sample collection exhibits multi-stage water enrichment processes along point, line and planar defect structures in nominally anhydrous minerals and the subsequent formation of the serpentine polymorph antigorite along grain boundaries and in totally embedded annealed cracks. Planar defect structures act like monomineralic and interphase grain boundaries in the oceanic lithosphere and the subcontinental mantle beneath the North American plate, which was hydrated by the ancient oceanic Farallon plate during the Cenozoic and Mesozoic eras. We used microspectroscopical, petrological, and seismological techniques to confirm multi-stage hydration from a depth of ∼150 km to just below the Moho depth. High-resolution mapping of the water distribution over homogeneous areas and fully embedded point, line and planar defects in olivine crystals of lherzolitic and harzburgitic origin by synchrotron infrared microspectroscopy enabled us to resolve local wet spots and thus reconstruct the hydration process occurring at a depth of ∼150 km (T ≈ 1225 °C). These lherzolites originated from the middle part of the Farallon mantle slab; they were released during the break up of the Farallon mantle slab, caused by the instability of the dipping slab. The background hydration levels in homogeneous olivines reached ∼138 ppm wt H2O, and the water concentration at the planar defects could reach up to ∼1000 ppm wt H2O. However, the formation of antigorite in grain boundaries was found to be the primary hydration mechanism for harzburgitic samples originating from the subcontinental mantle (for hydration, T ≈ 600 °C). Additionally, the formation of antigorite in lherzolites could be found in annealed cracks. From these observations, we conclude that hydration induces multi-stage water enrichment of the mantle wedge by a process that is dominated by the growth and movement of ubiquitous cracks, which acts as planar defects. Cracks in the mantle seem to be the an important feature in both the water cycle of the subduction zone and the formation of the continental lithosphere.  相似文献   

4.
Li isotopic compositions of magmatic rocks have gained considerable attention recently as probes of mantle-scale processes. However, the concentrations and isotopic composition of Li in mantle minerals from mid-ocean ridges remain relatively unconstrained. This is largely because of the general presence of seawater alteration in abyssal peridotites. Lithium elemental and isotopic compositions for mineral separates of coexisting olivine, clinopyroxene, orthopyroxene and bulk rocks of serpentine-free Gakkel Ridge peridotites were investigated. Bulk rocks have Li contents of 1.6 to 2.7 ppm and δ7Li values of 3 to 5‰, which fall within the range of reported normal pristine “MORB mantle” values. Lithium concentrations vary in the order cpx (2.1–4.7 ppm) > opx (0.9–1.7 ppm) ≥ olivine (0.4–0.9 ppm), the opposite found in “equilibrated” mantle peridotite xenoliths (Seitz and Woodland, 2000). The Li isotopic compositions indicate a systematic mineral variation with δ7Liolivine (7.14‰–15.09‰) > δ7Liopx (1.81‰–3.66‰) > δ7Licpx (?2.43‰ ? ?0.39‰). The δ7Li values of cpx are negatively correlated with their Li concentrations with the lightest value for the most enriched cpx grains. There is a first order negative linear correlation between Δolivine–cpx (δ7Liolivine ? δ7Licpx) and ol/cpxD (Liolivine/Licpx).Numerical simulations indicate that the observed systematic inter-mineral variations of Li concentrations and isotopic compositions could be explained by a cooling driven diffusive redistribution between minerals in a closed system if there is a temperature dependent partitioning of Li between olivine and clinopyroxene. The studied Gakkel Ridge abyssal peridotites may alternatively have cooled under a variable cooling rate with a rapid cooling before the Li system was closed, which is less likely given the tectonic setting. Our calculations confirm that Li systematics in minerals, especially in coexisting mineral phases could potentially be used as a mantle geospeedometer, even for slowly cooled mantle rocks.  相似文献   

5.
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   

6.
D/H fractionation factors between serpentine (clinochrysotile) and water were experimentally determined to be: 1000 In αser-w = 2.75 × 10 7/T2 ? 7.69 × 104/T + 40.8 in the temperature range from 100 to 500°C. The present results do not support the semi-empirical fractionation factors employed by Wenner and Taylor [1] for the interpretation of δD values of natural serpentines. About 100 serpentines from the Japanese Islands have δD values from ?110 to ?40‰ SMOW, with antigorite being from ?40 to ?60‰. The results are in accord with the two conclusions by Wenner and Taylor [1,2], that is, the presence of a latitude ?δD correlation and the more uniform and higher δD values of antigorite than chrysotile and lizardite.According to the present fractionation factors, almost none of the continental lizardite-chrysotile serpentines could have formed at a temperature below 500°C under equilibrium with fluids of δD values similar to the present-day local meteoric waters. The fluid responsible for oceanic serpentinization could be either a mixture of oceanic and magmatic water or oceanic water alone. However, full interpretation of the δD values of natural serpentines should wait until kinetic behaviors of hydrogen isotopes in serpentinization are better understood.  相似文献   

7.
Thermogravimetric (TG) analyses were used to characterize the products and quantify the extent of serpentinization as a stepwise weight loss during heating (TG loss) or its derivative (DTG). Multivariate analyses are powerful tools for extracting information from complicated spectrum data; however, no studies have applied them to characterize serpentinites. In this study, hydrothermal experiments of olivine-H2O, olivine–orthopyroxene-H2O and orthopyroxene-H2O were conducted at 250–400°C and under vapor-saturated pressure. The product minerals observed were serpentine+brucite+magnetite in the olivine-H2O experiments and serpentine±talc in the orthoyroxene-H2O and olivine-orthopyroxene-H2O experiments. These results are consistent with those of previous studies; however, the positions and width of DTG peaks for individual minerals were varied depending on the experimental conditions. To extract systematics from the TG spectra, non-negative matrix factorization (NMF), an unsupervised machine learning technique, was applied to the DTG spectra of the experimental products. NMF revealed that the DTG profiles were explained by a linear combination of six basis spectra, which corresponded to the characteristic products, including three types of serpentine minerals (low-, medium-, and high-T), two types of brucite (low-and high-T), two type of talc (talc+serpentine mixture, well-crystallized talc) with different crystallinity, and noise during the TG measurement. Systematic changes in the factor loading revealed that, in the olivine-H2O systems, the products changed from medium-T serpentine+low-T brucite to high-T serpentine+high-T brucite as serpentinization progressed. In the olivine-orthopyroxene system, low-T serpentine or poorly crystallized talc+serpentine mixture was initially formed, followed by the formation of well-crystallized talc, resulting in dehydration. Applying NMF to DTG showed the mineralogical differences between olivine and orthopyroxene systems and increases of the crystallinity during the progress of serpentinization, suggesting its potential for characterizing various serpentinites within oceanic lithospheres that suffer from several stages of alteration and weathering at different temperatures.  相似文献   

8.
This study is focused on a plagioclase‐bearing spinel lherzolite from Chah Loqeh area in the Neo‐Tethyan Ashin ophiolite. It is exposed along the west of left‐lateral strike‐slip Dorouneh Fault in the northwest of Central‐East Iranian Microcontinent. Mineral chemistry (Mg#olivine < ~ 90, Cr#clinopyroxene < ~ 0.2, Cr#spinel < ~ 0.5, Al2O3orthopyroxene > ~ 2.5 wt%, Al2O3clinopyroxene > ~ 4.5 wt%, Al2O3spinel > ~ 41.5 wt%, Na2Oclinopyroxene > ~ 0.11 wt%, and TiO2clinopyroxene > ~ 0.04 wt%) confirms Ashin lherzolite was originally a mid‐oceanic ridge peridotite with low degrees of partial melting at spinel‐peridotite facies in a lithospheric mantle level. However, some Ashin lherzolites record mantle upwelling and tectonic exhumation at plagioclase‐peridotite facies during oceanic extension and diapiric motion of mantle along Nain‐Baft suture zone. This mantle upwelling is evidenced by some modifications in the modal composition (i.e. subsolidus recrystallization of plagioclase and olivine between pyroxene and spinel) and mineral chemistry (e.g. increase in TiO2 and Na2O of clinopyroxene, and TiO2 and Cr# of spinel and decrease in Mg# of olivine), as a consequence of decompression during a progressive upwelling of mantle. Previous geochronological and geochemical data and increasing the depth of subsolidus plagioclase formation at plagioclase‐peridotite facies from Nain ophiolite (~ 16 km) to Ashin ophiolite (~ 35 km) suggest a south to north closure for the Nain‐Baft oceanic crust in the northwest of Central‐East Iranian Microcontinent.  相似文献   

9.
Serpentinization of the mantle wedge is an important process that influences the seismic and mechanical properties in subduction zones. Seismic detection of serpentines relies on the knowledge of elastic properties of serpentinites, which thus far has not been possible in the absence of single-crystal elastic properties of antigorite. The elastic constants of antigorite, the dominant serpentine at high-pressure in subduction zones, were measured using Brillouin spectroscopy under ambient conditions. In addition, antigorite lattice preferred orientations (LPO) were determined using an electron back-scattering diffraction (EBSD) technique. Isotropic aggregate velocities are significantly lower than those of peridotites to allow seismic detection of serpentinites from tomography. The isotropic VP/VS ratio is 1.76 in the Voigt–Reuss–Hill average, not very different from that of 1.73 in peridotite, but may vary between 1.70 and 1.86 between the Voigt and Reuss bonds. Antigorite and deformed serpentinites have a very high seismic anisotropy and remarkably low velocities along particular directions. VP varies between 8.9 km s? 1 and 5.6 km s? 1 (46% anisotropy), and 8.3 km s? 1 and 5.8 km s? 1 (37%), and VS between 5.1 km s? 1 and 2.5 km s? 1 (66%), and 4.7 km s? 1 and 2.9 km s? 1 (50%) for the single-crystal and aggregate, respectively. The VP/VS ratio and shear wave splitting also vary with orientation between 1.2 and 3.4, and 1.3 and 2.8 for the single-crystal and aggregate, respectively. Thus deformed serpentinites can present seismic velocities similar to peridotites for wave propagation parallel to the foliation or lower than crustal rocks for wave propagation perpendicular to the foliation. These properties can be used to detect serpentinite, quantify the amount of serpentinization, and to discuss relationships between seismic anisotropy and deformation in the mantle wedge. Regions of high VP/VS ratios and extremely low velocities in the mantle wedge of subduction zones (down to about 6 and 3 km.s?1 for VP and VS, respectively) are difficult to explain without strong preferred orientation of serpentine. Local variations of anisotropy may result from kilometer-scale folding of serpentinites. Shear wave splittings up to 1–1.5 s can be explained with moderately thick (10–20 km) serpentinite bodies.  相似文献   

10.
Recent drilling and sampling of hydrothermal fluids from Long Valley permit an accurate characterization of chemical concentrations and equilibrium conditions in the hydrothermal reservoir. Hydrothermal fluids are thermodynamically saturated with secondary quartz, calcite, and pyrite but are in disequilibrium with respect to aqueous sulfide-sulfate speciation. Hydrothermal fluids are enriched in 18O by approximately 1‰ relative to recharge waters. 18O and Cl concentrations in well cuttings and core from high-temperature zones of the reservoir are extensively depleted relative to fresh rhyolitic tuff compositions. Approximately 80% of the Li and 50% of the B are retained in the altered reservoir rock. Cl mass balance and open-system 18O fractionation models produce similar water-rock ratios of between 1.0 and 2.5 kg kg−1. These water-rock ratios coupled with estimates of reservoir porosity and density produce a minimum fluid residence time of 1.3 ka. The low fluid Cl concentrations in Long Valley correlate with corresponding low rock concentrations. Mass balance calculations indicate that leaching of these reservoir rocks accounts for Cl losses during hydrothermal activity over the last 40 ka.  相似文献   

11.
Lateral variation in upper mantle viscosity: role of water   总被引：1，自引：0，他引：1  
Differences in the viscosity of the earth's upper mantle beneath the western US (∼1018-1019 Pa s) and global average values based on glacial isostatic adjustment and other data (∼1020-1021 Pa s) are generally ascribed to differences in temperature. We compile geochemical data on the water contents of western US lavas and mantle xenoliths, compare these data to water solubility in olivine, and calculate the corresponding effective viscosity of olivine, the major constituent of the upper mantle, using a power law creep rheological model. These data and calculations suggest that the low viscosities of the western US upper mantle reflect the combined effect of high water concentration and elevated temperature. The high water content of the western US upper mantle may reflect the long history of Farallon plate subduction, including flat slab subduction, which effectively advected water as far inland as the Colorado Plateau, hydrating and weakening the upper mantle.  相似文献   

12.
Lithium isotopes have been identified as a promising tracer of subducted materials in arc lavas due to the observable variations in related reservoirs such as subducting sediments and altered oceanic crust. The Tonga–Kermadec arc–Lau back‐arc provides an end‐member of subduction zones with the coldest thermal structure on Earth. Reported here are Li isotope data for 14 lavas from the arc front and 7 back‐arc lavas as well as 12 pelagic and volcaniclastic sediments along a profile through the sedimentary sequence at DSDP Site 204. The arc and back‐arc lavas range from basalts to dacites in composition with SiO2 = 48.3–65.3 wt% over which Li concentrations increase from 2 ppm to 16 ppm. Li/Y ratios range from 0.08 to 0.77 and from 0.24 to 0.65 in the arc and back‐arc lavas, respectively. The majority of the lavas have δ7Li that ranges from 2.5 ‰ to 5.0 ‰ with an average of (3.6 ±0.7) ‰, similar to that reported from other arcs and there is no distinction between the arc front and back‐arc lavas. The pelagic sediments have variable Li concentrations (33–133 ppm) and δ7Li that ranges from 1.2 ‰ to 10.2 ‰ while the volcaniclastic sediments have an even greater range of Li concentrations (3.6–165 ppm) and generally higher δ7Li values (8–14 ‰). However, δ7Li in the lavas does not correlate with commonly used trace element ratio or isotope signatures indicative of slab‐derived fluids or the sediments. This is probably because the range of δ7Li in the lavas and sediments overlap. Calculated sediment mass‐balance models require significantly more sediment than previous estimates based on Th–Nd–Be isotopes. This may indicate that a sizeable proportion of the total Li budget in the lavas is provided by Li‐enriched fluids from the subducting sediments and/or altered oceanic crust.  相似文献   

13.
Ken-Ichi  Hirauchi 《Island Arc》2006,15(1):156-164
Abstract   Serpentinite bodies in the Kurosegawa Belt are mapped along fault boundaries between the Cretaceous Sanchu Group (forearc basin-fill sediments) and the rocks of the Southern Chichibu Belt (Jurassic to Early Cretaceous accretionary prism) in the northwestern Kanto Mountains, central Japan. The serpentinites were divided into three types based on microtextures and combinations of serpentine minerals: massive, antigorite and chrysotile serpentinites. Massive serpentinite retains initial pseudomorphic textures without any deformation after serpentinization. Antigorite serpentinite exhibits shape-preferred orientation of antigorite replacing the original lizardite and/or chrysotile to form pseudomorphs. It has porphyroclasts of chromian spinel, and is characterized by ductile deformation under relatively high-pressure–temperature conditions. Chrysotile serpentinite shows evidence for overprinting of pre-existing serpentinite features under shallow, low-temperature conditions. It exhibits unidirectional development of chrysotile fibers. Foliations in antigorite and chrysotile serpentinites strike parallel to the elongate direction of the serpentinite bodies, suggesting a continuous deformation during solid-state intrusion along the fault zones after undergoing complete serpentinization at deeper levels (lower crust and upper mantle).  相似文献   

14.
The South Sandwich volcanic arc is sited on a young oceanic crust, erupts low-K tholeiitic rocks, is characterized by unexotic pelagic and volcanogenic sediments on the down-going slab, and simple tectonic setting, and is ideal for assessing element transport through subduction zones. As a means of quantifying processes attending transfer of subduction-related fluids from the slab to the mantle wedge, boron concentrations and isotopic compositions were determined for representative lavas from along the arc. The samples show variable fluid-mobile/fluid-immobile element ratios and high enrichments of B/Nb (2.7 to 55) and B/Zr (0.12 to 0.57), similar to those observed in western Pacific arcs. δ11B values are among the highest so far reported for mantle-derived lavas; these are highest in the central part of the arc (+ 15 to + 18‰) and decrease toward the southern and northern ends (+ 12 to + 14‰). δ11B is roughly positively correlated with B concentrations and with 87Sr/86Sr ratios, but poorly coupled with other fluid-mobile elements such as Rb, Ba, Sr and U. Peridotites dredged from the forearc trench also have high δ11B (ca. + 10‰) and elevated B contents (38–140 ppm). Incoming pelagic sediments sampled at ODP Site 701 display a wide range in δ11B (+ 5 to ? 13‰; average = ? 4.1‰), with negative values most common. The unusually high δ11B values inferred for the South Sandwich mantle wedge cannot easily be attributed to direct incorporation of subducting slab materials or fluids derived directly therefrom. Rather, the heavy B isotopic signature of the magma sources is more plausibly explained by ingress of fluids derived from subduction erosion of altered frontal arc mantle wedge materials similar to those in the Marianas forearc. We propose that multi-stage recycling of high-δ11B and high-B serpentinite (possibly embellished by arc crust and volcaniclastic sediments) can produce extremely 11B-rich fluids at slab depths beneath the volcanic arc. Infiltration of such fluids into the mantle wedge likely accounts for the unusual magma sources inferred for this arc.  相似文献   

15.
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   

16.
Crystallization paths of basaltic (1763 eruption) and hawaiitic (1865 and 1329 eruptions) scoria from Etna were deduced from mineralogy and melt inclusion chemistry. The volatile behaviour was investigated through the study of melt inclusions trapped in the phenocrysts and those of the whole rocks and the matrix glasses. The results from the 1763 eruption point to the early crystallization of olivine Fo 81.7 from a water-rich alkaline basalt, with high Cl (1750–2000 ppm) and S (2100–2400 ppm) concentrations. The hawaiitic melt inclusions trapped in olivine Fo 74, salite and plagioclase are characterized by a decrease in Cl/K2O and S/K2O ratios. In each investigated system there is good correlation between K2O and P2O5. In the whole rocks, Cl ranges from 980 to 1680 ppm, from basaltic to hawaiitic lavas, whereas S (110–136 ppm) remains low. Cl and S behaviour in the 1763 magma suggests an early degassing stage of Cl and S, with CO2 and a water-rich gaseous phase for a pressure close to 100 MPa, consistent with a permanent outgassing at the summit craters of Etna. During the eruption, the sulphur remaining in the hawaiitic liquid is lost, and the degassing of chlorine is limited. Such a degassing model can be extended to the 1865 and 1329a.d. eruptions.  相似文献   

17.
The ophiolites from the Yarlung Zangbo River (Tibet),Southwestern China,were analysed for the con-tents of helium and neon and their isotopic compositions by stepwise heating. The serpentinites from Bainang showed a high 3He/4He value of 32.66Ra (Ra is referred to the 3He/4He ratio in the present air) in 700 ℃ fraction. At lower temperature,all of the dolerites displayed as very high 3He/4He ratios as ones investigated for hotspots. It was clear that the high 3He/4He ratio was one of immanent characterics in the magma source formed the dolerites,suggesting that there was a large amount of deep mantle fluids in these rocks. In the three-isotope diagram of neon,the data points from the ophiolites of the Yarlung Zangbo River were arranged along the Loihi Line. This is in agreement with the characteristics of he-lium isotopes,revealing that the high-3He plume from deep mantle had played an important role in the formation of the Neo-Tethyan Ocean. The helium isotopic compositions in the basalts were far higher than atomospheric value but lower than the average value of MORB,although there were various de-grees of alteration. The possible reasons were that basaltic magmas  相似文献   

18.
Measurements of chlorine concentrations in matrix glasses from 18 primitive (>6 wt% MgO) and eight evolved lavas from active spreading centers in the Lau Basin back-arc system provide insight into the processes which control chlorine concentrations in subduction-related magmas, and can be used to investigate chlorine enrichment related to fluids derived from the underlying subducted slab. Chlorine contents of the glasses are highly variable (0.008-0.835 wt%) and generally high with respect to uncontaminated mid-ocean ridge basalt. Chlorine contents are highest in fractionated lavas from propagating ridge tips and lowest in more primitive basaltic lavas. Two different styles of enrichment in chlorine (relative to other incompatible elements) are recognized. Glasses from the Central Lau Spreading and Eastern Lau Spreading Center typically have low Ba/Nb ratios indicating minimal input of slab-derived components, and high to very high ratios of chlorine relative to K2O, H2O, and TiO2. This style of chlorine enrichment is highest in the most fractionated samples and is consistent with crustal assimilation of chlorine-rich altered ocean crust material. Data from the literature suggest that contamination by chlorine-rich seawater-derived components also characterizes the Woodlark Basin and North Fiji Basin back-arc systems. The second style of chlorine enrichment reflects input from slab-derived fluid(s) to the mantle wedge from the adjacent Tonga subduction zone. Basaltic glasses from the Valu Fa Ridge and Mangatolu Triple Junction show correlations between ratios of chlorine and K2O, H2O, and TiO2 and indices of slab-derived fluid input such as Ba/Nb, Ba/Th and U/Th, consistent with chlorine in these lavas originating from a saline fluid added to the mantle wedge. Within the Valu Fa Ridge the measured range of chlorine contents equates to a chlorine flux of 224-1120 kg/m/yr to the back-arc crust. Using a simple melting model and additional data from other back-arc and arc sample suites we conclude that chlorine is a major component within the slab fluids that contribute to many arc and back-arc melting systems, and probably plays an important role in regulating trace element transport by slab fluids in the mantle wedge. For the back-arc suites we have examined the estimated Cl/H2O and Cl/K2O ratios in the slab fluid component correlate with proximity to the arc front, suggesting that progressive dehydration of the slab and/or re-equilibration and transport within the mantle wedge may influence the overall degree of chlorine enrichment within the slab fluid component. The degree of chlorine enrichment observed in most back-arc lavas also appears too great to be explained solely by melting of amphibole, phlogopite or apatite within the mantle source and suggests that chlorine must be present in another phase, possibly a chlorine-rich fluid.  相似文献   

19.
~~Characteristics of the mantle source region of sodium lamprophyres and petrogenetic tectonic setting in northeastern Hunan,China~~  相似文献   

20.
Chlorine and fluorine were measured from whole-rock samples from tholeiites (150,000 years old) to present-day hawaiites. The overall range of F content is from 240 to 985 ppm, with a slight decrease of F/Th and F/Cl ratios, from tholeiites to hawaiites. Chlorine is positively correlated with Th (Cl/Th=100) as well as K2O and P2O5, as the differentiation progresses, and, increases from 220 ppm in tholeiites to 2410 ppm in mugearites. Data obtained from present-day hawaiites indicate that Cl lost by degassing during eruption is limited. However, Cl contents of some whole-rock samples are inconsistent with previous results published for melt inclusions of phenocrysts from the same historic hawaiite samples and suggesting outgassing of Cl prior to the eruption. This implies that apparent correlation between Cl and Th can be considered as the result of superimposition of several petrogenetic processes. Results point out the richness of Etnean tholeiites in chlorine compared to M.A.R. basalts. Such a character could have been inherited from the mantle source or during the mantle source melting.  相似文献   

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