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1.
Peridotites from the southern Mariana forearc: Heterogeneous fluid supply in mantle wedge 总被引：11，自引：0，他引：11
Detailed petrological work was carried out on serpentinized peridotite dredged and sampled by submersible from the southern part of the Mariana Trench to reveal the nature of the mantle wedge in the southern Mariana forearc. The southern part of the Mariana Trench is important in that we should expect to find a transect of a typical island arc structure; that is, from east to west, the Mariana forearc, the Mariana arc proper, the Mariana Trough (active back-arc spreading center), and the West Mariana Ridge (remnant arc). The most striking feature of peridotites from the southern part of the trench is that primary hornblende is a major constituent mineral in many specimens. Thus, the peridotite samples are divided into anhydrous (A-type), hydrous (H-type) and intermediate (I-type) groups. Petrological data suggest that each type of peridotite is a residue of extensive partial melting in the upper mantle. It is argued here that the I- and H-type peridotites were modified from `proto-A-type peridotite' by fluid infiltration. The fluid was enriched in Al, Ti, Fe, and alkalis, and may have caused changes in mineral and bulk chemical compositions of the peridotites. A-type peridotite derives from the `proto-A-type peridotite' directly, without any fluid contamination. After the formation of the `proto-A-, I-, and H-type peridotites', lower-temperature fluids, probably of seawater origin, produced retrograde metamorphism and alteration including serpentinization. The mantle wedge in the southern Mariana forearc was heterogeneous in fluid supply. 相似文献
2.
Up to now the age of granulite gneisses intruded by the Zabargad mantle diapir has been an unsolved problem. These gneisses may represent either a part of the adjacent continental crust primarily differentiated during the Pan African orogeny, or new crust composed of Miocene clastic sediments deposited in a developing rift, crosscut by a diabase dike swarm and gabbroic intrusions, and finally metamorphosed and deformed by the mantle diapir. Previous geochronological results obtained on Zabargad island and Al Lith and Tihama-Asir complexes (Saudi Arabia) suggest an Early Miocene age of emplacement for the Zabargad mantle diapir during the early opening of the Red Sea rift. In contrast, SmNd and RbSr internal isochrons yield Pan African dates for felsic and basic granulites collected 500–600 m from the contact zone with the peridotites. Devoid of evidence for retrograde metamorphic, minerals from a felsic granulite provide well-defined RbSr and SmNd dates of 655 ± 8 and 699 ± 34 Ma for the HP-HT metamorphic event (10 kbar, 850°C). The thermal event related to the diapir emplacement is not recorded in the SmNd and RbSr systems of the studied gneisses; in contrast, the development of a retrograde amphibolite metamorphic paragenesis strongly disturbed the RbSr isotopic system of the mafic granulite. The initial143Nd/144Nd ratio of the felsic granulite is higher than the contemporaneous value for CHUR and is in agreement with other Nd isotopic data for samples of upper crust from the Arabian shield. This result suggests that source rocks of the felsic granulite were derived at 1.0 to 1.2 Ga from either an average MORB-type mantle or a local 2.2 Ga LREE-depleted mantle. Zabargad gneisses represent a part of the disrupted lower continental crust of the Pan African Afro-Arabian shield. During early stages of the Red Sea rifting in the Miocene, these Precambrian granulites were intruded and dragged upwards by a rising peridotite diapir. 相似文献
3.
Shoji Arai Akihiro Tamura Satoko Ishimaru Kazuyuki Kadoshima Yong‐Il Lee Ken‐ichiro Hisada 《Island Arc》2008,17(4):485-501
Peridotites exposed in the Yugu area in the Gyeonggi Massif, South Korea, near the boundary with the Okcheon Belt, exhibit mylonitic to strongly porphyroclastic textures, and are mostly spinel lherzolites. Subordinate dunites, harzburgites, and websterites are associated with the lherzolites. Amphiboles, often zoned from hornblende in the core to tremolite in the rim, are found only as neoblasts. Porphyroclasts have recorded equilibrium temperatures of about 1000°C, whereas neoblasts denote lower temperatures, about 800°C. Olivines are Fo90–91 in lherzolites and Fo91 in a dunite and a harzburgite. The Cr# (= Cr/(Cr + Al) atomic ratio) of spinels varies together with the Fo of olivines, being from 0.1 to 0.3 in lherzolites and around 0.5 in the dunite and harzburgite. The Na2O content of clinopyroxene porphyroclasts is relatively low, around 0.3 to 0.5 wt% in the most fertile lherzolite. The Yugu peridotites are similar in porphyroclast mineral chemistry not to continental spinel peridotites but to sub‐arc or abyssal peridotites. Textural and mineralogical characteristics indicate the successive cooling with hydration from the upper mantle to crustal conditions for the Yugu peridotites. Almost all clinopyroxenes and amphiboles show the same U‐shaped rare earth element (REE) patterns although the level is up to ten times higher for the latter. The hydration was associated with enrichment in light REE, resulting from either a slab‐derived fluid or a fluid circulating in the crust. The mantle‐wedge or abyssal peridotites were emplaced into the continental crust as the Yugu peridotite body during collision of continents to form a high‐pressure metamorphic belt in the Gyeonggi Massif. The peridotites from the Gyeonggi Massif exhibit lower‐pressure equilibration than peridotites, with or without garnets, from the Dabie–Sulu Collision Belt, China, which is possibly a westward extension of the Gyeonggi Massif. 相似文献
4.
A.J. Crawford L. Beccaluva G. Serri J. Dostal 《Earth and Planetary Science Letters》1986,80(3-4):265-280
Rocks dredged from the forearc very close to the intersection of the Yap and Mariana trenches include a suite of highly depleted arc tholeiites, and several samples of transitional to slightly alkaline basalt. The tholeiites range from magnesian quartz tholeiites with 0.46–0.6% TiO2, to andesites with up to 62% SiO2 and 8.2% FeO*. All show pronounced LREE depletion and have very low contents of Ba and Sr. They are postulated to have been produced by partial melting of upper mantle peridotite residual after MORB extraction, following influx of hydrous fluids from the subducted slab. While these fluids were responsible for small enrichments in Ba, K, Rb and Sr in melts generated, LREE were not involved in the metasomatism, and the strong LREE depletion probably reflects the unmodified, depleted source peridotite.
The second lava suite includes slightly Ne-normative, Ti-augite-bearing basalts with convex-upward REE patterns, showing slight LREE depletion ((La/Sm)N = 0.76). The chemical features of these basalts support affinities with basalts erupted during the earliest stages of backarc basin opening. A KAr age on one sample(7.8 ± 1.3m.y.) is in good agreement with the initial opening of the Mariana Trough.
The tectonic significance of the dredged arc tholeiite suite is less obvious. A KAr age of10.8 ± 0.4 My on one andesite, and the occurrence of similar lavas in dredges from at least 300 km along the length of the Yap arc, suggest that subduction was occurring beneath the Yap arc in the Late Miocene, after overthrusting of the Yap greenschist allochthon, and while calc-alkaline arc magmatism was occurring further north on the West Mariana Ridge. We suggest that the depleted arc tholeiites in dredge 1438 were generated by abnormally shallow melting of upper mantle beneath the Yap forearc following subduction beneath this area of young, hot Sorol Trough crust. These arc tholeiites represent a magma type transitional between more typical arc tholeiites (e.g. Tongan) and high-Mg andesites and boninites. 相似文献
5.
The Ronda peridotite massif in southern Spain originated from the upper mantle, evidently as a rapidly rising diapir. Major and trace element abundance trends of the peridotites reflect their origin as residues from partial melting of garnet lherzolite. About 5% of the massif consists of mafic rocks, mainly pyroxenites and gabbros. They occur as concordant layers amidst the peridotites, and these layers do not cross-cut each other. However, major and trace element data show that the mafic layers do not have the geochemical characteristics of primary melts. We conclude that crystal/liquid fractionation occurred at high pressures ( > 19 kbar) as melts migrated through magma conduits towards the cooler exterior portion of the diapir. This process generated a sequence of “cumulates” (mainly clinopyroxene + orthopyroxene + spinel and clinopyroxene + garnet) along the walls of the conduits which are now represented by the mafic layers. 相似文献
6.
S.W. Parman J.C. Dann T.L. Grove M.J. de Wit 《Earth and Planetary Science Letters》1997,150(3-4):303-323
This paper provides new constraints on the crystallization conditions of the 3.49 Ga Barberton komatiites. The compositional evidence from igneous pyroxene in the olivine spinifex komatiite units indicates that the magma contained significant quantities of dissolved H2O. Estimates are made from comparisons of the compositions of pyroxene preserved in Barberton komatiites with pyroxene produced in laboratory experiments at 0.1 MPa (1 bar) under anhydrous conditions and at 100 and 200 MPa (1 and 2 kbar) under H2O-saturated conditions on an analog Barberton composition. Pyroxene thermobarometry on high-Ca clinopyroxene compositions from ten samples requires a range of minimum magmatic water contents of 6 wt.% or greater at the time of pyroxene crystallization and minimum emplacement pressures of 190 MPa (6 km depth). Since high-Ca pyroxene appears after 30% crystallization of olivine and spinel, the liquidus H2O contents could be 4 to 6 wt.% H2O. The liquidus temperature of the Barberton komatiite composition studied is between 1370 and 1400°C at 200 MPa under H2O-saturated conditions. When compared to the temperature-depth regime of modern melt generation environments, the komatiite mantle source temperatures are 200°C higher than the hydrous mantle melting temperatures inferred in modern subduction zone environments and 100°C higher than mean mantle melting temperatures estimated at mid-ocean ridges. When compared to previous estimates of komatiite liquidus temperatures, melting under hydrous conditions occurs at temperatures that are 250°C lower than previous estimates for anhydrous komatiite. Mantle melting by near-fractional, adiabatic decompression takes place in a melting column that spans 38 km depth range under hydrous conditions. This depth interval for melting is only slightly greater than that observed in modern mid-ocean ridge environments. In contrast, anhydrous fractional melting models of komatiite occur over a larger depth range ( 130 km) and place the base of the melting column into the transition zone. 相似文献
7.
Seth G. John Olivier J. Rouxel Paul R. Craddock Alison M. Engwall Edward A. Boyle 《Earth and Planetary Science Letters》2008,269(1-2):17-28
Many of the heaviest and lightest natural zinc (Zn) isotope ratios have been discovered in hydrothermal ore deposits. However, the processes responsible for fractionating Zn isotopes in hydrothermal systems are poorly understood. In order to better assess the total range of Zn isotopes in hydrothermal systems and to understand the factors which are responsible for this isotopic fractionation, we have measured Zn isotopes in seafloor hydrothermal fluids from numerous vents at 9–10°N and 21°N on the East Pacific Rise (EPR), the TAG hydrothermal field on the Mid-Atlantic Ridge, and in the Guaymas Basin. Fluid δ66Zn values measured at these sites range from + 0.00‰ to + 1.04‰. Of the many physical and chemical parameters examined, only temperature was found to correlate with fluid δ66Zn values. Lower temperature fluids (< 250 °C) had both heavier and more variable δ66Zn values compared to higher temperature fluids from the same hydrothermal fields. We suggest that subsurface cooling of hydrothermal fluids leads to precipitation of isotopically light sphalerite (Zn sulfide), and that this process is a primary cause of Zn isotope variation in hydrothermal fluids. Thermodynamic calculations carried out to determine saturation state of sphalerite in the vent fluids support this hypothesis with isotopically heaviest Zn found in fluids that were calculated to be saturated with respect to sphalerite. We have also measured Zn isotopes in chimney sulfides recovered from a high-temperature (383 °C) and a low-temperature (203 °C) vent at 9–10°N on the EPR and, in both cases, found that the δ66Zn of chimney minerals was lighter or similar to the fluid δ66Zn. The first measurements of Zn isotopes in hydrothermal fluids have revealed large variations in hydrothermal fluid δ66Zn, and suggest that subsurface Zn sulfide precipitation is a primary factor in causing variations in fluid δ66Zn. By understanding how chemical processes that occur beneath the seafloor affect hydrothermal fluid δ66Zn, Zn isotopes may be used as a tracer for studying hydrothermal processes. 相似文献
8.
P. J. Wyllie 《Bulletin of Volcanology》1978,41(4):360-377
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
9.
Peridotite inclusions, crystal fragments, and kimberlite breccia at Green Knobs, New Mexico, have been studied to evaluate compositions and processes in the upper mantle below the Colorado Plateau. Most peridotite inclusions are spinel lherzolites and harzburgites, or their partly hydrated equivalents, in the Cr-diopside group. Orthopyroxene-rich websterites and olivine websterites comprise 3% of the peridotites and formed as cumulates. Typical anhydrous or slightly hydrated peridotites contain aluminous, calcic diopside (5–7% Al2O3), aluminous orthopyroxene (3–6% Al2O3), spinel, and olivine (near Fa9). Geothermometers based on different mineral pairs yield temperatures from above 1100°C to below 700°C in single rocks. High values, derived from pyroxenes with included exsolution lamellae, may approximate temperatures of primary crystallization. Low values, based on olivine-spinel and olivine-clinopyroxene pairs, approach upper mantle temperatures before eruption. In rare samples, some spinel grains are rimmed by garnet while others are not rimmed; garnet formation was controlled by nucleation kinetics. About one-third of the peridotites were deformed shortly before eruption, with effects ranging from mild cataclasis to the production of ultramylonites.Discrete crystals of garnet, olivine (near Fa8), and Cr-diopside represent garnet peridotite. Eclogites were not found. The garnet peridotite is more depleted than overlying spinel peridotite, and it is not a likely source for the minettes associated with the kimberlites.The mantle below Green Knobs consists of spinel peridotite from 45 to perhaps 60 km depth immediately underlain by more-depleted garnet peridotite. The position of the spinel-garnet transition may be fixed by kinetics. The kimberlite may have been produced when heat from ascending minette magma released volatiles from otherwise depleted garnet peridotite. Resulting gas-solid mixtures erupted along zones of deformation associated with Colorado Plateau monoclines. Sheared lherzolites formed during renewed movement along these zones. 相似文献
10.
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
11.
Co-existing calcic amphiboles in calc-alkaline andesites: Possible evidence of a zoned magma chamber
Hornblende-biotite andesites erupted from Mount Price and Clinker Peak volcanoes, southwestern British Columbia, contain two texturally and compositionally distinct calcic amphiboles: pargasitic hornblende xenocrysts and magnesio-hornblende microphenocrysts. Disequilibrium relationships exhibited by these amphiboles and associated minerals suggest that the magnesio-hornblendes precipitated under chemical and thermal conditions that were intermediate between those under which pargasitic hornblende and biotite, respectively, crystallized. Experimental studies of crystallization in double-diffusive systems (Chen and Turner, 1980; Turner, 1980; McBirney, 1980) suggest that these varied magmatic environments can be explained as a consequence of progressive crystallization within a zoned magma chamber. Although gravitational settling may have played a role, the observed mineral assemblages probably developed by convective mixing of crystals precipitated at the cooling margins with those crystallized in the interior of the compositionally stratified magma column. 相似文献
12.
D.J Fornari T Shank K.L Von Damm T.K.P Gregg M Lilley G Levai A Bray R.M Haymon M.R Perfit R Lutz 《Earth and Planetary Science Letters》1998,160(3-4):419-431
Temperature measurements of hydrothermal vent fluids provide an important indicator of the physical and chemical state of mid-ocean ridge crest hydrothermal and magmatic systems. Changes in vent fluid temperature and chemistry can have dramatic effects on biological communities that inhabit these unique ecosystems. In an attempt to understand temporal variability of ridge crest hydrothermal activity as it relates to geological processes at the ridge axis, six high-temperature hydrothermal vents on the East Pacific Rise crest between 9°49′N and 9°51′N were instrumented and sampled repeatedly during five years following a submarine volcanic eruption in 1991. Bio9 vent, located on the floor of the axial trough near 9°50.2′N, has the most complete record of fluid temperatures from 1991 to 1997, including a continuous temperature record of nearly three years (1994–1997). Bio9 vent fluids were 368°C in 1991, increased to an estimated temperature ≥388°C after a second volcanic event in 1992, and thereafter declined over the next 2 years reaching a temperature of 365°C in December 1993. Continuous temperature records and point measurements made by Alvin's thermocouple probe show Bio9 vent fluids were stable for 15 months at 365±1°C, until March 26, 1995. On March 26, an abrupt 7°C increase occurred over a period of eight days at this vent, and a maximum temperature of 372±1°C persisted for 14 days. The vent fluid cooled gradually over 3.5 months to 366±1°C, and for several months at the end of the recording period the temperature increased a few degrees. A continuous record of fluid temperature at this vent between November 1995 and November 1997 shows a 5±1°C increase for the two-year period. The abrupt temperature increase at Bio9 vent, and coincident changes in faunal community structure, and geochemistry of vent fluids from this area suggest that a crustal event occurred, either in the form of a cracking front in the crust or intrusion of a small dike. Based on the results of a microseismicity experiment conducted around the Bio9 vent in 1995 [Sohn et al., Trans. Am. Geophys. Union 78 (1997) F647; Sohn et al., Nature (in press)], and the identification of a small earthquake swarm which occurred on March 22, 1995 we conclude that the temperature anomaly measured at Bio9 four days following the swarm was caused by a cracking front penetrating into hot crustal rocks beneath the vent. 相似文献
13.
Ken-ichi Hirauchi Izumi Segawa Yui Kouketsu Yumiko Harigane Yasuhiko Ohara Jonathan Snow Atlanta Sen Masakazu Fujii Kyoko Okino 《Island Arc》2021,30(1):e12419
We determined the mineralogical and petrological characteristics of ultramafic rocks dredged from two oceanic core complexes: the Mado Megamullion and 23°30′N non-transform offset massif, which are located within the Shikoku back-arc basin in the Philippine Sea. The ultramafic rocks are strongly serpentinized, but can be classified as harzburgite/lherzolite or dunite, based on relict primary minerals and their pseudomorphs. Strongly elongated pyroxene porphyroclasts with undulatory extinction indicate high-temperature (≥700 °C) strain localization on a detachment fault within the upper mantle at depths below the brittle–viscous transition. During exhumation, the peridotites underwent impregnation by magmatic or hydrothermal fluids, lizardite/chrysotile serpentinization at ≤300 °C, antigorite crystallization, and silica metasomatism that formed talc. These features indicate that the detachment fault zones formed a fluid pathway and facilitated a range of fluid–peridotite interactions. 相似文献
14.
Microthermometric analyses of fluid inclusions on a suite of hydrothermally altered gabbros recovered just south of the eastern intersection of the Kane Fracture Zone and the Mid-Atlantic Ridge, record the highest homogenization temperatures yet reported for mid-ocean ridge hydrothermal systems. Fluid salinities in the high temperature inclusions are more than ten times that of seawater. Multiple generations of fluid inclusions entrapped along healed microfractures exhibit three distinct temperature-compositional groups. We interpret these populations as having been trapped during three separate fracturing events.The earliest episode of brittle failure in the gabbros is represented by coplanar, conjugate vapor-dominated and brine-dominated fluid inclusion arrays in primary apatite. Vapor-dominated inclusions exhibit apparent homogenization temperatures of 400°C and contain equivalent salinities of 1–2 wt.% NaCl. These inclusions are interspersed with liquid-dominated, sulfide-bearing inclusions containing salinities of 50 wt.% NaCl equivalent. These high salinity inclusions remain unhomogenized at temperatures greater than 700°C.Compositional and phase relationships of the fluid inclusions may be accounted for by two-phase separation of a fluid under 1000–1200 bars pressure. These pressures require that fluid entrapment occurred under a significant lithostatic component and indicate a minimum entrapmentdepth of 2 km below the axial valley floor. This depth corresponds to a minimum tectonic uplift of 3 km, in order to emplace the samples at the 3100 m recovery depth. The microfracture networks within magmatic apatites represent fluid flow paths for either highly modified, deeply penetrating seawater or a late stage magmatic aqueous fluid. The inclusions may have formed close to the brittle-ductile transition zone adjacent to an active magma chamber.Following collapse of the high temperature front, lower temperature fluids of definite seawater origin circulated through the open fracture networks, pervasively altering portions of the gabbros. This stage is represented by low-to-moderate (1–7 wt.% NaCl equivalent) salinity inclusions in plagioclase, apatite, epidote, and augite, which homogenize at temperatures of approximately 200–300°C and 400°C. Formation of hydrous mineral assemblages, under greenschist to lower amphibolite facies conditions, resulted in sealing of the vein system and may have resulted in modification of seawater salinities by as much as a factor of two. During or following these later stages of hydrothermal activity the gabbros were emplaced high on the axial walls by differential uplift attending formation of the flanking mountains. 相似文献
15.
Oxygen isotope ratios were obtained from authigenic clinoptilolites from Barbados Accretionary Complex, Yamato Basin, and Exmouth Plateau sediments (ODP Sites 672, 797, and 762) in order to investigate the isotopic fractionation between clinoptilolite and pore water at early diagenetic stages and low temperatures. Dehydrated clinoptilolites display isotopic ratios for the zeolite framework (δ18Of) that extend from +18.7‰ to +32.8‰ (vs. SMOW). In combination with associated pore water isotope data, the oxygen isotopic fractionation between clinoptilolite and pore fluids could be assessed in the temperature range from 25°C to 40°C. The resulting fractionation factors of 1.032 at 25°C and 1.027 at 40°C are in good agreement with the theoretically determined oxygen isotope fractionation between clinoptilolite and water. Calculations of isotopic temperatures illustrate that clinoptilolite formation occurred at relatively low temperatures of 17°C to 29°C in Barbados Ridge sediments and at 33°C to 62°C in the Yamato Basin. These data support a low-temperature origin of clinoptilolite and contradict the assumption that elevated temperatures are the main controlling factor for authigenic clinoptilolite formation. Increasing clinoptilolite δ18Of values with depth indicate that clinoptilolites which are now in the deeper parts of the zeolite-bearing intervals had either formed at lower temperatures (17–20°C) or under closed system conditions. 相似文献
16.
K. Righter M. J. Drake G. Yaxley 《Physics of the Earth and Planetary Interiors》1997,100(1-4):115-134
We report new metal-silicate partition coefficients for Ni, Co and P at 7.0 GPa (1650–1750°C), and Ni, Co, Mo, W and P at 0.8, 1.0 and 1.5 GPa (1300–1400°C). Guided by thermodynamics, all available metal-silicate partition coefficients, D(i), where i is Ni, Co, P, Mo and W, are regressed against 1/T, P/T, lnf(O2), ln(1 − Xs) (XS is mole fraction of S in metallic liquid) and nbo/t (non-bridging oxygen/tetrahedral cation ratio, a silicate melt compositional-structural parameter) to derive equations of the following form: ln D(i) = aln f(O2) + (b/T) + (cP/T) + d(nbo/t) + eln(1 − XS) + f. Expressions for solid metal-liquid silicate and liquid metal-liquid silicate partition coefficients are derived for S-free and S-bearing systems.
We investigate whether Earth's upper-mantle siderophile element abundances can be reconciled with simple metal-silicate equilibrium. Sulfur-free metallic compositions do not allow a good fit. However, Ni, Co, Mo, W and P abundances in the upper mantle are consistent with simple metal-silicate equilibrium at mantle pressures and temperatures (27 GPa, 2200 K, ΔIW(iron-wüstite) = −0.15, nbo/t = 2.7; XS = 0.15). Although these conditions are near the anhydrous peridotite solidus, they are well above the hydrous solidus and probably closer to the liquidus. A hydrous magma ocean and early mantle are consistent with predicted planetary accretion models. These results suggest that siderophile element abundances in Earth's upper mantle were established by liquid metal-liquid silicate equilibrium near the upper-mantle-lower-mantle boundary. 相似文献
17.
18.
Al- and Mg-doped titanomagnetites were synthesized at 1300°C using the gas-mixing technique. A composition, representative of average natural titanomagnetites in ocean floor basalts, was sought.
The samples were ball-milled in acetone to average grain sizes of 0.5 μm and 5 μm and the material was then oxidised, in air, at temperatures below 300°C. This procedure formed titanomaghemite, a cation-deficient titanomagnetite.
Low-temperature oxidation is described as the diffusion of Fe-ions out of the spinel lattice and the process is observed to be distinctly dependent upon grain size. 相似文献
19.
Heat source for Tongonan Geothermal Field 总被引：1，自引：0，他引：1
Graeme L. Scott 《Island Arc》2000,9(4):513-526
Abstract The primary mineral and whole-rock chemistry of 46 core samples from the host rocks of the Tongonan Geothermal Field (the Philippines) have been used to infer the likely composition of the heat source for the system. The host rocks consist of andesite lavas (with intercalated fossiliferous early to mid–Miocene shales and limestone), and a plutonic rock basement ranging in composition from gabbro to granite. The whole rock TiO2 , Fe2 O3 (total iron), MgO, P2 O5 and V data for volcanic and plutonic rocks are colinear on conventional Harker diagrams. This, along with similar hornblende chemistry, age and close spatial relationship suggests that the basement and cover rocks are cogenetic and evolved by low-pressure crystal fractionation. Crystal fractionation models indicate that separation of 60% plagioclase and 30% hornblende from original magma controlled the chemistry of the host rocks. The original Miocene magma chambers beneath the Tongonan field crystallized inwards from the walls at approximately 750°C and 1 kb pressure (3–4 km depth) thus forming a series of plutons or a batholith at drilled depths. A supercritical hydrothermal fluid trapped in the crystallizing, hornblende-granite-pegmatite core of a crystallized Miocene diorite batholith was gradually being released to shallower levels through antithetic cross fractures during creep and uplift along the main branches of the Philippine Fault from the Pliocene. This ascending fluid is now thought to be responsible for the present thermal activity of the field. 相似文献
20.
Low water contents in pyroxenes from spinel-peridotites of the oxidized, sub-arc mantle wedge 总被引：3，自引：0，他引：3
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