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1.
Abstract Spinel lherzolite is a minor component of the deep-seated xenolith suite in the Oki-Dogo alkaline basalts, whereas other types of ultramafic (e.g. pyroxenite and dunite) and mafic (e.g. granulite and gabbro) xenoliths are abundant. All spinel lherzolite xenoliths have spinel with a low Cr number (Cr#; < 0.26). They are anhydrous and are free of modal metasomatism. Their mineral assemblages and microtextures, combined with the high NiO content in olivine, suggest that they are of residual origin. But the Mg numbers of silicate minerals are lower (e.g. down to Fo86 ) in some spinel lherzolites than in typical upper mantle residual peridotites. The clinopyroxene in the spinel lherzolite shows U-shaped chondrite-normalized rare-earth element (REE) patterns. The abundance of Fe-rich ultramafic and mafic cumulate xenoliths in Oki-Dogo alkali basalts suggests that the later formation of those Fe-rich cumulates from alkaline magma was the cause of Fe- and light REE (LREE)-enrichment in residual peridotite. The similar REE patterns are observed in spinel peridotite xenoliths from Kurose and also in those from the South-west Japan arc, which are non-metasomatized in terms of major-element chemistry (e.g. Fo > 89), and are rarely associated with Fe-rich cumulus mafic and ultramafic xenoliths. This indicates that the LREE-enrichment in mantle rocks has been more prominent and prevalent than Fe and other major-element enrichment during the metasomatism. 相似文献
2.
《Earth and Planetary Science Letters》2007,253(3-4):369-377
The density, and therefore the pressure, of CO2 fluid inclusions in minerals can be estimated from the Fermi diad splitting of Raman spectra of CO2. An accurate determination of the pressure of CO2 fluid inclusions enables the estimation of the depth origin of rocks from the deep Earth. A micro-Raman densimeter was applied to ultramafic–mafic xenoliths sampled along the Ohku coast of Oki-Dogo Island in the Sea of Japan (East Sea). The density of CO2 fluid inclusions in the mafic granulite was 1.02–1.05 g/cm3, while those of lherzolites were 0.98–1.02 g/cm3. In contrast, the density of CO2 fluid inclusions measured in olivine gabbro, clinopyroxenite, and harzburgite were lower ranging from 0.86–to 0.99 g/cm3. Taking into account the temperature condition estimated using a pyroxene thermometer, the mafic granulite originated from a depth of 27–30 km and the lherzolites from 25–29 km. The overlapping depth of 27–29 km can be interpreted as the depth including the Moho discontinuity under Oki-Dogo Island 3.3 Ma. This estimation is consistent with geophysical observations. 相似文献
3.
The assumption of local equilibrium during partial melting is fundamental to the interpretation of isotope and trace element data for mantle-derived rocks. If disequilibrium melting is significant, the scale of the chemical and isotopic heterogeneity in the mantle indicated by the data could be as small as the grain size of the mantle rock, and the isotope data themselves are then of doubtful value to the understanding of mantle processes. To assess the scale of isotopic heterogeneity in a partially molten asthenosphere we review the Sr isotopic data of volcanic rocks from oceanic regions and the available experimental data on diffusion kinetics in minerals and melts similar to those existing in the mantle. Although diffusion data are scarce and afflicted with uncertainties, most of the diffusion coefficients for cations in mantle minerals at temperatures of 1000–1200°C appear to be greater than 10?13 cm2 s?1. Sr diffusion in liquid basalt is more rapid, with diffusion coefficients of D = 10?7 to 10?6cm2s?1 near 1300°C. Simple model calculations show that, with these D values, a fluid-free mantle can maintain a state of disequilibrium on a centimeter scale for periods of 108 to 109 years. The state of disequilibrium found in many mantle-derived xenoliths is thus easily explained. A partially molten mantle, on the other hand, will tend to equilibrate locally in less than 105 to 106 years. The analytical data on natural rocks likewise indicate that the inhomogeneities are both old (>FX1.5 b.y.) and regional in character and that the consistent isotopic difference between ocean island and ocean floor volcanics cannot be explained by small-scale heterogeneity of the source rock. 相似文献
4.
A model is proposed for the origin of hot spots that depends on the existence of major-element heterogeneities in the mantle. Generation of basaltic crust at spreading centers produces a layer of residual peridotite ～20–25 km thick directly beneath the crust which is depleted in Fe/Mg, TiO2, CaO, Al2O3, Na2O and K2O, and which has a slightly lower density than undepleted peridotite beneath it. Upon recycling of this depleted peridotite back into the deep mantle at subduction zones, it becomes gravitationally unstable, and tends to rise as diapirs through undepleted peridotite. For a density contrast of 0.05 g cm?3, a diapir 60 km in diameter would rise at roughly 8 cm y?1, and could transport enough heat to the base of the lithosphere to cause melting and volcanism at the surface. Hot spots are thus viewed as a passive consequence of mantle convection and fractionation at spreading centers rather than a plate-driving force.It is suggested that depleted diapirs exist with varying amounts of depletion, diameters, upward velocities and source volumes. Such variations could explain the occurrence of hot spots with widely varying lifetimes and rates of lava production. For highly depleted diapirs with very low Fe/Mg, the diapir would act as a heat source and the asthenosphere and lower lithosphere drifting across the diapir would serve as the source region of magmas erupted at the surface. For mildly depleted diapirs with Fe/Mg only slightly less than in normal undepleted mantle, the diapir could provide not only the source of heat but also most or all of the source material for the erupted magmas. The model is consistent with isotopic data that require two separate and ancient source regions for mid-ocean ridge and oceanic island basalts. The source for mid-ocean ridge basalts is considered to be material upwelling at spreading centers from the deep mantle. This material forms the oceanic lithosphere. Oceanic island basalts are considered to be derived from varying mixtures of sublithospheric and lower lithospheric material and the rising diapir itself. 相似文献
5.
Abstract Peridotite xenoliths from the subarc mantle, which have been rarely documented, are described from Iraya volcano of the Luzon arc, the Philippines, and are discussed in the context of wedge-mantle processes. They are mainly harzburgite, with subordinate dunite, and show various textures from weakly porphyroclastic (C-type) to extremely fine-grained equigranular (F-type). Textural characteristics indicate a transition from the former to the latter by recrystallization. The F-type peridotite has inclusion-rich fine-grained olivine and radially aggregated orthopyroxene, being quite different in texture from ordinary mantle-derived peridotites previously documented. Despite their strong textural contrast, the two types do not show any systematic difference in modal composition. The harzburgite of C-type has ordinary mantle peridotite mineralogy; olivine is mostly Fo91–92 and chromian spinel mostly has Cr#s (= Cr/[Cr + Al] atomic ratios) from 0.3 to 0.6. Olivine is slightly more Fe-rich (Fo89–91) and spinel is more enriched in Cr (the Cr#, 0.4–0.8) and Fe3+ in F-type peridotites than in C-type harzburgite. Orthopyroxene in F-type peridotites is relatively low in CaO (<1 wt%), Al2 O3 (<2 wt%) and Cr2 O3 (<0.4 wt%). The F-type peridotite was possibly formed from the C-type one by recrystallization including local dissolution and precipitation of orthopyroxene assisted by fluid (or melt) of subduction origin. Textural characteristics, however, indicate a deserpentinization origin from abyssal serpentinite of which protolith was a C-type peridotite. In this scenario the initial abyssal serpentinite was possibly dehydrated due to an initiation of magmatic activity beneath an incipient oceanic arc like Batan Island. The F-type peridotite is characteristic of the upper mantle of island arc, especially of incipient arc. 相似文献
6.
Helium isotope studies of the mantle xenoliths and megacrysts from the Cenozoic basalts in the eastern China 总被引：9，自引：2，他引：7
Helium isotope compositions of the mantle xenoliths and megacrysts in the Cenozoic basalts in the eastern China were measured.
The samples were collected from Ludao of Heilongjiang, Huinan and Jiaohe of Jilin, Kuandian of Liaoning, Hannuoba of Hebei,
Nüshan of Anhui, Dingan of Hainan. The3He/4He ratios of the mantle xenoliths and megacrysts from the most areas were about 1 × 10-5, and were similar to those of the MORB, thus reflecting the characteristics of the MORB-typed depleted mantle. The3He/4He ratios of the mantle xenoliths from Jiaohe were 4.8×10-6 and the3He/4He ratios of xenoliths from Hannuoba vary from 0.15× 10-6 to 7.4 ×10-6, obviously lower than those of the MORB, and even lower than the atmospheric helium isotope ratios, indicating that the continental
mantle was strongly replaced in Jiaohe and Hannuoba areas. The helium isotope compositions of the mantle xenoliths and megacrysts
in the same region vary in a very wide range. It is inferred that the mantle xenoliths and megacrysts were from different
parts of the continental mantle. There were not necessary origin relations between the mantle xenoliths, megacrysts and their
host basalts. An extremely high3He/4He ratio of garnet megacryst from Hannuoba, Hebei was found. 相似文献
7.
Abundant fluid inclusions in olivine of dunite xenoliths (～1–3 cm) in basalt dredged from the young Loihi Seamount, 30 km southeast of Hawaii, are evidence for three coexisting immiscible fluid phases—silicate melt (now glass), sulfide melt (now solid), and dense supercritical CO2 (now liquid + gas)—during growth and later fracturing of some of these olivine crystals. Some olivine xenocrysts, probably from disaggregation of xenoliths, contain similar inclusions.Most of the inclusions (2–10 μm) are on secondary planes, trapped during healing of fractures after the original crystal growth. Some such planes end abruptly within single crystals and are termed pseudosecondary, because they formed during the growth of the host olivine crystals. The “vapor” bubble in a few large (20–60 μm), isolated, and hence primary, silicate melt inclusions is too large to be the result of simple differential shrinkage. Under correct viewing conditions, these bubbles are seen to consist of CO2 liquid and gas, with an aggregate ? = ～ 0.5–0.75 g cm?3, and represent trapped globules of dense supercritical CO2 (i.e., incipient “vesiculation” at depth). Some spinel crystals enclosed within olivine have attached CO2 blebs. Spherical sulfide blebs having widely variable volume ratios to CO2 and silicate glass are found in both primary and pseudosecondary inclusions, demonstrating that an immiscible sulfide melt was also present.Assuming olivine growth at ～ 1200°C and hydrostatic pressure from a liquid lava column, extrapolation of CO2P-V-T data indicates that the primary inclusions were trapped at ～ 220–470 MPa (2200–4700 bars), or ～ 8–17 km depth in basalt magma of ? = 2.7 g cm?3. Because the temperature cannot change much during the rise to eruption, the range of CO2 densities reveals the change in pressure from that during original olivine growth to later deformation and rise to eruption on the sea floor. The presence of numerous decrepitated inclusions indicates that the inclusion sample studied is biased by the loss of higher-density inclusions and suggests that some part of these olivine xenoliths formed at greater depths. 相似文献
8.
Mitsuhiro Toriumi 《Physics of the Earth and Planetary Interiors》1981,27(1):39-46
Mantle-derived peridotite xenoliths contain abundant olivine with rounded spinel and orthopyroxene inclusions, and orthopyroxene with rounded olivine and spinel inclusions. The shape-change of spinel, olivine and orthopyroxene inclusions from the primarily polyhedral outline to the spherical outline is governed by interfacial diffusion of oxygen in spinel (the most sluggish atom) due to reduction of total interfacial energy of the host-inclusion system.The critical radius of maximum rounded inclusions of spinel in olivine is a function of temperature and annealing time. Assuming that the activation energy for the interfacial diffusion is 40–70 kcal mol?1 and that the annealing time for the spinel lherzolite from Salt Lake Crater in Hawaii is 100 Ma, the annealing times for perioditites under the island arcs of Japan are estimated to be 1–10 Ma. 相似文献
9.
The pyroxenite xenoliths in the volcanic rocks of Hoh Xil consist of clinopyroxenes and orthopyroxenes. The mineral composition of these pyroxenes is similar to that of mantle xenoliths including peridotite and pyroxenite from China and abroad, and different from that of granulites. The pyroxenes formed at 1101–1400°C (averaging 1250°C) and under 30–60 kb (averaging 46 kb). We deduced that the magma was derived from the mantle at a depth of more than 150 km, which fits in with the geophysical conclusion that the low-velocity layer existed in the mantle under 150 km.
相似文献10.
《Journal of Volcanology and Geothermal Research》2007,159(1-3):33-69
New petrological and geochemical data of upper mantle and lower crustal xenoliths from a Quaternary tephra deposit in Mýtina, Czech Republic, are discussed in the frame of previous geophysical results (receiver functions, reflection seismology) of the western Eger/Ohře Rift area. The Vogtland/NW Bohemia region is well known for intraplate earthquake swarms, which are usually associated with volcanic activity. As previously reported, 3He/4He data of CO2 emissions in mofettes and mineral-water springs point at ongoing magmatic processes in this area. Using teleseismic P receiver functions, an approximately 40-km-wide Moho updoming (from 31 to 27 km) and indications for a seismic discontinuity at 50 to 60 km depth were observed beneath the active CO2-degassing field. The studied xenolith suite probes a lithospheric profile within the structural and gas geochemical anomaly field of the western Eger Rift.With regard to texture, composition, p–T estimates and origin, five xenolith groups can be discriminated. Upper crustal xenoliths (quartzites, phyllites, mica schists) resemble crystalline country rocks at surface. One noritic xenolith (6 kbar, 800 °C) could represent a sample of the lower crust. Clinopyroxenites and hornblendites probably represent cumulates of the nephelinitic magma or fragments of magmatic veins. Porous wehrlites and one hornblende peridotite xenolith reflect a metasomatied upper mantle. Megacrysts of Ti-rich amphibole, olivine, clinopyroxene, and phlogopite could be fragments of pegmatitic veins or high-pressure phenocrysts. Most of the ultramafic nodules (xenoliths and megacrysts) formed at pressures between 6 and 11 kbar (22 to 38 km depth), at temperatures well above regional geotherms of the Bohemian Massif calculated from surface heat flow studies. Orthopyroxene-bearing spinel-lherzolite xenoliths were not observed. Our petrographical, geochemical, and thermobarometric results indicate a lithospheric mantle strongly altered by magmatic processes. This metasomatism can cause slower than typical uppermost-mantle seismic velocities in a greater area and might help to explain observed seismic anomalies. 相似文献
11.
John F. Hermance 《Earth and Planetary Science Letters》1981,54(1):157-166
An enormous component of isostatic compensation(～?430±40mgal) is provided by subcrustal material beneath the neovolcanic zone of Iceland. Previously published values for the component of gravity contributed by anomalous mantle material beneath this region range from ?250 to ?140 mgal. These values are only a partial indication of the magnitude of the compensation mechanism. If one takes into account constraints on crustal thickness from seismic refraction studies and compares Iceland to less active tectonic regions near by, one obtains a mantle gravity effect of approximately?430±40mgal, which for a simple slab model leads to a vertically integrated mass deficit per unit surface area of 106 g/cm2. The effects of thermal expansion, solid-solid phase transitions and partial fusion can provide significant contributions to the total mass deficiency; however, none of these mechanisms alone seems sufficient to account for the entire anomaly.The relation of this mass anomaly to the evolution of the Iceland-Faeroe ridge is considered by examining two extreme end-members of a suite of possible evolutionary models for this region. The first of these is the case where, in time, the 106 g/cm2 mass deficit will be resorbed into the mantle with the effects of chemical segregation playing a minor role. The second case, which is preferred, involves a significant redistribution of material from the mantle such that basaltic melt segregated from high levels in the mantle accumulates and crystallizes in a zone at the base of the crust. In this latter model, if the Iceland-Faeroe ridge is considered to have evolved under a steady rate of magma production over the last 30–40 × 106 years, then underplating of the crust may account for its increasing thickness as it matures from 8–10 km in the neovolcanic zone to a value of approximately 32 km for the Iceland-Faeroe ridge. If we assume a 10% increase in density upon crystallization, thickening of the crust by 22 km through underplating by magma accumulation leads to an increase in mass per unit surface area of 0.6 × 106 g/cm2, and accounts for approximately 60% of the total mass difference in the mantle between Iceland and the Iceland-Faeroe ridge. 相似文献
12.
Data in the literature and additional measurements on the thermal diffusivities of granites, granulites and ultrabasic rocks at temperatures up to 1000 K and pressures to 2 GPa, have been used to propose a new model for thermal diffusivity distribution in the crust and upper mantle.The laboratory measurements were made using a pulse method or the Angstroem method with cylindrical heat flow. After making particular assumptions about the pressure and temperature distribution within the top 60 km the pressure and temperature dependencies of diffusivity were transformed into a depth dependence.The model is characterised by a continuous decrease of diffusivity to a depth of ～30 km where there is a small but rapid increase to a nearly constant value of 7.3 × 10?3 cm2 s?1. 相似文献
13.
Takehiro Koyaguchi 《Bulletin of Volcanology》1986,48(6):313-323
Variations in major-element chemistry and modal compositions of the mantle xenolith-bearing calc-alkalic ejecta from Ichinomegata volcano are inferred to be due to mixing of three magmatic end members: Basalt I (SiO2 51 wt% , MgO 8.5 wt%), Basalt II (SiO2 54 wt%, MgO 5 wt%), and Dacite (SiO2 65 wt%, MgO2 wt%). Ultramafic xenoliths are found in mafic mixtures of Dacite-Basalt I and Dacite-Basalt II. The thermal histories of the xenoliths in both mixtures are compared with each other. Chemical compositions of olivine and orthopyroxene in xenoliths suggest that xenoliths in Basalt I were equilibrated at about 800 °C, while those in Basalt II were also equilibrated originally at about 800 °C but were subsequently annealed at about 1000 °C for more than 102–3 years prior to the eruption.The chemical composition of Basalt I indicates that it can coexist with upper mantle peridotite and it is an appropriate candidate for a carrier of ultramafic xenoliths from the upper mantle. On the other hand, Basalt II is fractionated and it cannot be directly derived from the upper mantle. Two pulses of xenolith-bearing basalt injection into a dacite magma chamber are inferred to have occurred. The first injection did not lead to eruption and subsequently formed a dacite/basalt stratified magma chamber. In the lower layer, the basalt was slightly differentiated to become Basalt II and ultramafic xenoliths carried by the first pulse were annealed at the bottom of the layer. The duration of the annealing of the xenoliths implies a minimum life-time of the Dacite-Basalt II stratification in the magma chamber beneath Ichinomegata of 102–3 years. The second injection of the xenolith-bearing basalt (Basalt I) was immediately followed by eruption, and all the magmas were effused with mixing in a conduit. Consequently, the ultramafic xenoliths carried by the second pulse are not annealed. 相似文献
14.
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
15.
Experiments of the melt-peridotite reaction at pressures of 1 and 2 GPa and temperatures of 1250–1400°C have been carried out to understand the nature of the peridotite xenoliths in the Mesozoic high-Mg diorites and basalts of the North China Craton,and further to elucidate the processes in which the Mesozoic lithospheric mantle in this region was transformed.We used Fuxin alkali basalt,Feixian alkali basalt,and Xu-Huai hornblende-garnet pyroxenite as starting materials for the reacting melts,and lherzolite xenoliths and synthesized harzburgite as starting materials for the lithospheric mantle.The experimental results indicate that:(1)the reactions between basaltic melts and lherzolite and harzburgite at 1–2 GPa and 1300–1400°C tended to dissolve pyroxene and precipitate low-Mg#olivine(Mg#=83.6–89.3),forming sequences of dunite-lherzolite(D-L)and duniteharzburgite(D-H),respectively;(2)reactions between hornblende-garnet pyroxenite and lherzolite at 1 GPa and 1250°C formed a D-H sequence,whereas reactions at 2 GPa and 1350°C formed orthopyroxenite layers and lherzolite;and(3)the reaction between a partial melt of hornblende-garnet pyroxenite and harzburgite resulted in a layer of orthopyroxenite at the boundary of the pyroxenite and harzburgite.The reacted melts have higher MgO abundances than the starting melts,demonstrating that the melt-peridotite reactions are responsible for the high-Mg#signatures of andesites or adakitic rocks.Our experimental results support the proposition that the abundant peridotite and pyroxenite xenoliths in western Shandong and the southern Taihang Mountains might have experienced multiple modifications in reaction to a variety of melts.We suggest that melt-peridotite reactions played important roles in transforming the nature of the Mesozoic lithospheric mantle in the region of the North China Craton. 相似文献
16.
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
17.
Daniel J. Frost 《Earth and Planetary Science Letters》2003,216(3):313-328
To calculate accurately the pressure interval and mineral proportions (i.e. yields) across the olivine to wadsleyite and wadsleyite to ringwoodite transformations requires a detailed knowledge of the non-ideality of Fe-Mg mixing in these (Mg,Fe)2SiO4 solid solutions. In order to constrain the activity-composition relations that describe non-ideal mixing, Fe-Mg partitioning experiments have been conducted between magnesiowüstite and (Mg,Fe)2SiO4 olivine, wadsleyite and ringwoodite as a function of pressure at 1400°C. Using known activity-composition relations for magnesiowüstite the corresponding relations for the three polymorphs were determined from the partitioning data. In all experiments the presence of metallic iron ensured redox conditions compatible with the Earth’s transition zone. The non-ideality of the (Mg,Fe)2SiO4 solid solutions was found to decrease in the order WwadsleyiteFeMg>WringwooditeFeMg>WolivineFeMg. These partitioning data were used, along with published phase equilibria measurements for the Mg2SiO4 and Fe2SiO4 end-member transformations, to produce an internally consistent thermodynamic model for the Mg2SiO4-Fe2SiO4 system at 1400°C. Using this model the pressure interval of the olivine to wadsleyite transformation is calculated to be significantly smaller than previous determinations. By combining these results with Fe-Mg partitioning data for garnet, the widths of transition zone phase transformations in a peridotite composition were calculated. The olivine to wadsleyite transformation at 1400°C in dry peridotite was found to occur over a pressure interval equivalent to approximately 6 km depth and the mineral yields were found to vary almost linearly with depth across the transformation. This transformation is likely to be even sharper at higher temperatures or could be significantly broader in wet mantle or in regions with a significant vertical component of mantle flow. The entire range of estimated widths for the 410 km discontinuity (4-35 km) could, therefore, be explained by the olivine to wadsleyite transformation in a peridotite composition over a range of quite plausible mantle temperatures and H2O contents. The wadsleyite to ringwoodite transformation in peridotite mantle was calculated to take place over an interval of 20 km at 1400°C. This transformation yield was also found to be near linear. 相似文献
18.
Noble gas isotopes including 3He/4He, 40Ar/36Ar and Xe isotope ratios were determined for coexisting glass and olivine crystals in tholeiitic and alkalic basalts and dunite xenoliths from Loihi Seamount.Glass and coexisting olivine crystals have similar 3He/4He ratios (2.8–3.4) × 10?5, 20 to 24 times the atmospheric ratio (RA), but different 40Ar/36Ar ratios (400–1000). Based on the results of noble gas isotope ratios and microscopic observation, some olivine crystals are xenocrysts. We conclude that He is equilibrated between glass and olivine xenocrysts, but Ar is not.The apparent high 3He/4He ratio (3 × 10?5; = 21 RA) coupled with a relatively high 40Ar/36Ar ratio (4200) for dunite xenoliths (KK 17-5) may be explained by equilibration of He between MORB-type cumulates and the host magma.Except for the dunite xenoliths, noble gas data for these Loihi samples are compatible with a model in which samples from hot spot areas may be explained by mixing between P (plume)-type and M (MORB)-type components with the addition of A (atmosphere)-type component.Excess 129Xe has not been observed due to apparent large mass fractionation among Xe isotopes. 相似文献
19.
Wenliang Xu Janet M. Hergt Shan Gao Fuping Pei Wei Wang Debin Yang 《Earth and Planetary Science Letters》2008,265(1-2):123-137
Abundant dunite and harzbugite xenoliths are preserved in Early Cretaceous high-Mg# [63–67, where Mg# = molar 100 × Mg/(Mg + Fetot)] diorite intrusions from western Shandong in the North China Craton (NCC). Dunite and some harzburgite xenoliths typically preserve areas of orthopyroxenite (sometimes accompanied by phlogopite) either as veins or as zones surrounding chromite grains. Harzburgite is chiefly composed of olivine, orthopyroxene, minor clinopyroxene and chromian-spinel. High Mg#'s (averaging 91.4) and depletions in Al2O3 and CaO (averaging 0.52 wt.% and 0.29 wt.%, respectively) in harzburgite and dunite xenoliths suggest that they are residues formed by large degrees of polybaric melting. However, olivines and orthopyroxenes from dunite xenoliths spatially associated with orthopyroxenite display lower Mg#'s (i.e., 82–87 and 83–89, respectively), suggesting that an adakitic melt–peridotite reaction has taken place. This is consistent with the production of veined orthopyroxene or orthopyroxene + phlogopite in dunite and some harzburgite xenoliths in response to the introduction of adakitic melt into the previously depleted lithospheric mantle (i.e., harzburgite and dunite xenoliths). The presence of orthopyroxene in veins or as a zones surrounding chromite in peridotite xenoliths is thought to be representative of adakitic melt metasomatism. The dunite and harzbugite xenoliths are relatively rich in light rare earth elements (LREEs) and large ion lithophile elements (LILEs), poor in heavy rare earth elements (HREEs) and high field strength elements (HFSEs), and lack Eu anomalies on chondrite normalized trace element diagrams. The initial 87Sr/86Sr ratios and εNd(t) values for the xenoliths range from 0.7058 to 0.7212 and + 0.18 to ? 19.59, respectively. Taken together, these features, combined with the strong depletion in HFSE and the existence of Archean inherited zircons in the host rocks, suggest that the adakitic melt was derived from the partial melting of early Mesozoic delaminated lower continental crust. The interaction of the adakitic melt with peridotite is responsible for the high-Mg# character of the early Cretaceous diorites in western Shandong. 相似文献
20.
J.B. Holt 《Earth and Planetary Science Letters》1975,27(3):404-408
The thermal diffusivity of a naturally occurring polycrystalline olivine (Fo91Fa09) was measured by the Flash technique in the temperature range of 450–1500 K. At 450 K the thermal diffusivity was 10.7 × 10?7 m2/s and decreased as a function of reciprocal temperature to 7.0 × 10?7 m2/s at 800 K. From that temperature, the values gradually increased to a maximum of 7.8 × 10?7 m2/s at 1000 K, and then steadily decreased to 5.6 × 10?7 m2/s at 1500 K. The unusual decrease above 1000 K was caused by a reduction of the previously oxidized samples. The olivine's oxidation state plays a significant role in the value of thermal diffusivity at high temperatures. 相似文献