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1.
It is being accepted that earthquakes in subducting slab are caused by dehydration reactions of hydrous minerals. In the context of this “dehydration embrittlement” hypothesis, we propose a new model to explain key features of subduction zone magmatism on the basis of hydrous phase relations in peridotite and basaltic systems determined by thermodynamic calculations and seismic structures of Northeast Japan arc revealed by latest seismic studies. The model predicts that partial melting of basaltic crust in the subducting slab is an inevitable consequence of subduction of hydrated oceanic lithosphere. Aqueous fluids released from the subducting slab also cause partial melting widely in mantle wedge from just above the subducting slab to just below overlying crust at volcanic front. Hydrous minerals in the mantle wedge are stable only in shallow (< 120 km) areas, and are absent in the layer that is dragged into deep mantle by the subducting slab. The position of volcanic front is not restricted by dehydration reactions in the subducting slab but is controlled by dynamics of mantle wedge flow, which governs the thermal structure and partial melting regime in the mantle wedge.  相似文献   

2.
西藏雅鲁藏布江缝合带东段泽当地幔橄榄岩特征及其意义   总被引：1，自引：1，他引：0  
泽当岩体位于雅鲁藏布江缝合带东段,主要由地幔橄榄岩、辉长辉绿岩和基性火山岩等组成。地幔橄榄岩主要为方辉橄榄岩和二辉橄榄岩,有少量透镜状纯橄岩。地幔橄榄岩经历了强烈的塑性变形作用。地幔橄榄岩中橄榄石的Fo值为89.6~91.8,属镁橄榄石;斜方辉石为顽火辉石,En 87.8~90.3;单斜辉石En 44.1~50.0,主要为顽透辉石和透辉石。铬尖晶石的Cr#值(=100×Cr/(Cr+Al))为17.0~93.6,其中,二辉橄榄岩和方辉橄榄岩中的铬尖晶石为富铝型尖晶石,纯橄岩中的铬尖晶石Cr#最高,为富铬型尖晶石。地幔橄榄岩的部分熔融程度为17%~34%,表明泽当地幔橄榄岩可能经历了多阶段的过程。亏损的主量元素组成和低于原始地幔的稀土元素含量(0.15×10-6~0.61×10-6)指示泽当地幔橄榄岩为经历过部分熔融和熔体抽取的亏损残余地幔岩石。REE配分型式为中稀土亏损的"V"型或"U"型,原始地幔标准化元素比值(La/Sm)N为0.5~8.0,表明泽当地幔橄榄岩经历过交代作用。矿物化学与地球化学数据表明泽当地幔橄榄岩形成于MOR环境,后受到SSZ环境的改造。  相似文献   

3.
We found extremely high-Mg# (=Mg/(Mg + total Fe) atomic ratio) ultramafic rocks in Avacha peridotite suite. All the high-Mg# rocks have higher modal amounts of clinopyroxene than ordinary Avacha peridotite xenoliths, and their lithology is characteristically heterogeneous, varying from clinopyroxenite through olivine websterite to pyroxene-bearing dunite. The Mg# of minerals is up to 0.99, 0.98 and 0.97 in clinopyroxene, orthopyroxene and olivine, respectively, decreasing progressively toward contact with dunitic part, if any. The petrographical feature of pyroxenes in the high-Mg# pyroxenite indicates their metasomatic origin, and high LREE/HREE ratio of the metasomatic clinopyroxene implies that the pyroxenites are the products of reaction between dunitic peridotites and high-Ca, silicate-rich fluids. The lithological variation of the Avacha high-Mg# pyroxenites from clinopyroxenite to olivine websterite resulted from various degrees of fluid-rock reaction coupled with fractional crystallization of the high-Ca fluids, which started by precipitation of high-Mg# clinopyroxene. Such fluids were possibly generated originally at a highly reduced serpentinized peridotite layer above the subducting slab. The fluids can reach the uppermost mantle along a shear zone as a conduit composed of fine-grained peridotite that developed after continent-ward asthenospheric retreats from the mantle wedge beneath the volcanic front. The fluids are incorporated in mantle partial melts when the magmatism is activated by expansion of asthenosphere to mantle wedge beneath the volcanic front.  相似文献   

4.
Ophiolitic sequences obducted onto continental margins allow field based observations coupled with petrochemical interrogations of upper mantle lithologies thereby aiding evaluation of compositional heterogeneity of oceanic mantle, depletion-enrichment events and geodynamic conditions governing oceanic lithosphere formation. The Naga Hills Ophiolite (NHO) suite preserves a segment of the Neotethyan oceanic lithosphere encompassing a package of mantle and crustal lithologies. This paper for the first time reports the occurrence of melt flow channels traversing the mantle section near Molen of the NHO and presents a comprehensive study involving chromite-spinel chemistry, bulk rock major, trace and PGE geochemistry to understand the petrogenesis and evolution in a geodynamic transition from mid oceanic ridge (MOR) to suprasubduction zone (SSZ). The spinel chemistry of peridotitic melt channels depicts both MOR-type and SSZ signatures underlining a transitional tectonic frame. Chromite chemistry and high Al2O3/TiO2 ranging from 15.98–35.70 in concurrence with low CaO/Al2O3 ranging from 0.03–0.53; and chondrite normalised LREE > MREE < HREE patterns confirm the influx of boninitic melts into the refractory mantle. The boninitic signature shared by melt channels and host rock invokes a geochemical and geodynamic transition from anhydrous melting of depleted mantle to hydrated fluid flux melting resulting in boninitic melts, that subsequently impregnate and refertilise the fore arc mantle wedge in a SSZ regime at the nascent stage of subduction. The high Ba/Nb, Ba/Th, and Ba/La for the studied peridotites highlight the influx of subduction derived fluids in the supra subduction mantle. Further higher Zr/Hf and Nd/Hf with respect to primitive mantle values in concurrence with lower Nb/Ta suggest progressive refertilisation due to fluid- and melt-driven metasomatism of the refractory fore arc mantle wedge. The chondrite normalised PGE patterns suggest positive Ir and Ru anomalies stipulating the source to be refractory while enriched Pt and Pd underpins the mobilisation of these elements by subduction derived fluids and melts. The elevated abundances of PPGEs than IPGEs as cited by PPGE/IPGE > 1; and Pd/Pt avg. 0.85 for melt channels and 0.84 for host peridotites indicate fluid-fluxed metasomatism of fore arc mantle wedge with a S-undersaturated trend coupled with boninitic affinity. The mineral, trace, REE and PGE chemistry collectively emphasizes that the mantle peridotites of the NHO formed in a transitional geodynamic tectonic setting caused by fore arc extension during subduction initiation followed by rejuvenation by subduction derived fluids and boninitic melts, which typically are of the SSZ tectonic regime. The harzburgitic melt channels and host rock are refractory in nature, reflecting multiple episodes of melt extraction of about 5–15% and ~10–20% respectively from a spinel peridotite mantle source. The occurrences of these melt channels indicate segregation and percolation of melt through porous and channelized network in upper mantle peridotites.  相似文献   

5.
This paper provides the first measurements of the nitrogen (N) concentrations and isotopic compositions of high- and ultrahigh-pressure mafic eclogites, aimed at characterizing the subduction input flux of N in deeply subducting altered oceanic crust (AOC). The samples that were studied are from the Raspas Complex (Ecuador), Lago di Cignana (Italy), the Zambezi Belt (Zambia) and Cabo Ortegal (Spain), together representing subduction to 50-90 km depths. The eclogites contain 2-20 ppm N with δ15Nair values ranging from −1 to +8‰. These values overlap those of altered oceanic crust, but are distinct from values for fresh MORB (for the latter, ∼1.1 ppm N and δ15Nair ∼ −4‰). Based on N data in combination with other trace element data, the eclogite suites can be subdivided into those that are indistinguishable from their likely protolith, AOC, with or without superimposed effects of devolatilization (Lago di Cignana, Cabo Ortegal), and those that have experienced metasomatic additions during subduction-zone metamorphism (Zambezi Belt, Raspas). For the former group, the lack of a detectable loss of N in the eclogites, compared to various altered MORB compositions, suggests the retention of N in deeply subducted oceanic crust. The metasomatic effects affecting the latter group can be best explained by mixing with a (meta)sedimentary component, resulting in correlated enrichments of N and other trace elements (in particular, Ba and Pb) thought to be mobilized during HP/UHP metamorphism. Serpentinized and high-pressure metamorphosed peridotites, associated with the eclogites at Raspas and Cabo Ortegal, contain 3-15 ppm N with δ15Nair values ranging from +3 to +6‰, significantly higher than the generally accepted values for the MORB mantle (δ15Nair ∼ −5‰). Based on their relatively high N contents and their homogeneous and positive δ15N values, admixing of sedimentary N is also indicated for the serpentinized peridotites.One possible pathway for the addition of sediment-derived N into eclogites and peridotites involves mixing with fluids along the slab-mantle wedge interface. Alternatively, sedimentary N could be incorporated into peridotites during serpentinization at bending-related faults at the outer rise and, during later deserpentinization, released into fluids that then infiltrate overlying rocks. Deep retention of N in subducting oceanic crust should be considered in any attempt to balance subduction inputs with outputs in the form of arc volcanic gases. If materials such as these eclogites and serpentinized peridotites are eventually subducted to beyond sub-arc depths into the deeper mantle, containing some fraction of their forearc-subarc N inventory (documented here), they could deliver isotopically heavy N into the mantle to potentially be sampled by plume-related magmas.  相似文献   

6.
The Ronda high temperature peridotite: Geochemistry and petrogenesis   总被引：2，自引：0，他引：2  
The Ronda peridotite in southern Spain is a large (~300 km2) exposure of upper mantle which provides direct information about mantle processes on a scale much larger than that provided by mantle xenoliths in basalt. Ronda peridotites range from harzburgite to lherzolite, and vary considerably in major element content, e.g., Al2O3 from 0.9 to 4.8%, and trace element abundances, e.g., Sr, Zr and La abundances vary by factors of 20 to 40. These compositional variations are systematic and correlate with (pyroxene + garnet)/olivine ratios and olivine compositions. The data are consistent with formation of residual peridotites by variable degrees of melting (~0 to 30%) of a compositionally homogeneous peridotite. None of the peridotites have geochemical characteristics of residues formed by extensive (?5%) fractional melting and the data can be explained by equilibrium (batch) melting, possibly with incomplete melt segregation in some samples. Based on compositional differences between Ronda peridotites, the segregated melts were picritic (12–22% MgO) with relative rare earth element abundances similar to mid-ocean ridge basalt (MORB). Prior to the melting event the Ronda peridotite body was a suitable source for MORB. The compositional characteristics of Ronda peridotites are consistent with diapiric rise of a fertile mantle peridotite with relatively small degrees of melting near the diapir-wall rock interface yielding residues of garnet iherzolite, and larger degrees of melting in the diapir interior yielding residues of garnet-free peridotite. Subsequently these residual rocks were recrystallized at sub-solidus conditions (Obata, 1980), and emplaced in the crust by thrusting (Lundeen, 1978).  相似文献   

7.
The petrological characteristics of peridotite xenoliths exhumedfrom the lithospheric mantle below the Western Pacific arcs(Kamchatka, NE Japan, SW Japan, Luzon–Taiwan, New Irelandand Vanuatu) are reviewed to obtain an overview of the supra-subductionzone mantle in mature subduction systems. These data are thencompared with those for peridotite xenoliths from recent orolder arcs described in the literature (e.g. New Britain, WesternCanada to USA, Central Mexico, Patagonia, Lesser Antilles andPannonian Basin) to establish a petrological model of the lithosphericmantle beneath the arc. In currently active volcanic arcs, thedegree of partial melting recorded in the peridotites appearsto decrease away from the fore-arc towards the back-arc region.Highly depleted harzburgites, more depleted than abyssal harzburgites,occur only in the frontal arc to fore-arc region. The degreeof depletion increases again to a degree similar to that ofthe most depleted abyssal harzburgites within the back-arc extensionalregion, whether or not a back-arc basin is developed. Metasomatismis most prominent beneath the volcanic front, where the magmaproduction rate is highest; silica enrichment, involving themetasomatic formation of secondary orthopyroxene at the expenseof olivine, is important in this region because of the additionof slab-derived siliceous fluids. Some apparently primary orthopyroxenes,such as those in harzburgites from the Lesser Antilles arc,could possibly be of this secondary paragenesis but have beenrecrystallized such that the replacement texture is lost. TheTi content of hydrous minerals is relatively low in the sub-arclithospheric mantle peridotites. The K/Na ratio of the metasomatichydrous minerals decreases rearward from the fore-arc mantleas well as downward within the lithospheric mantle. The lithosphericmantle wedge peridotites, especially metasomatized ones frombelow the volcanic front, are highly oxidized. Shearing of themantle wedge is expected beneath the volcanic front, and isrepresented by fine-grained peridotite xenoliths. KEY WORDS: mantle wedge; lithospheric mantle; peridotite xenoliths; melting; metasomatism  相似文献   

8.
Xenoliths in primitive olivine tholeiite lavas from Merelava Volcano, Vanuatu, include recrystallized wehrlites and harzburgites characterized by extremely fine grain size (0.02–2 mm) and equigranular textures. The harzburgites display mineral segregations, have highly variable ratios of ol: opx, minor clinopyroxene and accessory Cr-spinel, and are interpreted as the residues of high degrees of melting of upper mantle peridotite. Annealed Cr-spinel aggregates in harzburgite sample # 31564B enclose numerous small inclusions of sodic sanidine and minor plagioclase, attributed to infiltration of the harzburgite by a residual melt derived from an earlier period of island arc magmatism. The recrystallized wehrlites have high ol/cpx ratios and depleted REE patterns compatible with a cumulus origin. The refractory nature of the phases in both groups of recrystallized xenoliths compares closely with phases in Alpine-type peridotites and primitive arc lavas, and is incompatible with compositions of abyssal peridotites. The recrystallized wehrlites give equilibration temperatures of 1070–1130° C and are interpreted as cumulates derived from an earlier period of Vanuatu Arc magmatism. The range of composition displayed by phases in the harzburgites is greater than phase variation in the wehrlites, and reflects a more complex thermal history. Textural, mineralogical, and geothermometric considerations indicate the harzburgites underwent cooling to 800°/900° C before being re-heated to 1000–1100° C by the current magmatic regime. A shallow crustal origin for these xenoliths is indicated by gravity data and tectonic considerations which strongly imply the presence of an ophiolite body beneath Merelava, representing the northward extension of the Pentecost Ophiolite. These interpretations are compatible with a published model for generation of the host basalts by partial melting at the crust/mantle boundary (ca. 17 km). Sr isotopic data show that the harzburgites are incompatible with residues of ocean-floor magmatism, or with residues of Merelava and Central Chain magmatism, but suggest an affinity with Vitiaz Arc magmatism of Eocene-lower Miocene age. Both groups of xenoliths were apparently entrained from wall rocks during ascent of the host magmas.  相似文献   

9.
The main hole (MH), and pre-pilot holes PP1, and PP3 of the Chinese Continental Scientific Drilling Project (CCSD) penetrated three different garnet peridotite bodies in the Sulu ultrahigh pressure (UHP) metamorphic belt, which are 80 m, 120 m, and 430 m thick, respectively. The bodies occur as tectonic blocks hosted in eclogite (MH peridotite) and gneisses (PP1 and PP3 peridotites). The peridotites in the MH are garnet wehrlites, whose protoliths were ultramafic cumulates based on olivine compositions (Fo79-89) and other geochemical features. Zoned garnet and omphacite (with 4-5 wt.% Na2O) are typical metamorphic minerals in these rocks, and, along with P-T estimates based on mineral pairs, suggest that the rocks have undergone UHP metamorphism. SHRIMP U-Pb isotope dating of zircon from the garnet wehrlite yielded a Paleozoic protolith age (ca. 346-461 Ma), and a Mesozoic UHP metamorphic age (ca. 220-240 Ma). The peridotites in PP1 consist of interlayered garnet (Grt)-bearing and garnet-free (GF) peridotite. Both types of peridotite have depleted mantle compositions (Mg# = 90-92) and they display transitional geochemical features. The intercalated layers probably reflect variations in partial melting rather than pressure variations during metamorphism, and the garnets may have been formed by exsolution from orthopyroxene during exhumation. These peridotites were probably part of the mantle wedge above the subduction zone that produced the UHP metamorphism and thus belonged to the North China Block before its tectonic emplacement. The exhumation of the subducted Yangtze Block brought these mantle fragments to shallow crustal levels. The ultramafic rocks in PP3 are dominantly dunite with minor garnet dunite. Their high Mg# (92-93) and relatively uniform chemical compositions indicate that they are part of a depleted mantle sequence. The presence of garnet replacing spinel and enclosing pre-metamorphic minerals such as olivine, clinopyroxene and spinel suggests that these rocks have undergone progressive metamorphism. SHRIMP U-Pb isotope dating of zircon from these rocks yielded two age groups: 726 ± 56 Ma for relic magmatic zircon grains and 240 ± 2.7 Ma for the newly formed metamorphic zircon. The older group is similar in age to granitic intrusions within the Dabie-Sulu belt, suggesting that the PP3 garnet peridotite may record the early emplacement of the peridotite into the crust. The younger dates coincide with the age of UHP metamorphism during continent-continent collision between the Yangtze and North China Blocks, suggesting that these peridotites were subducted to depths equivalent to the coesite facies and later exhumed. Thus, the garnet peridotites in the CCSD cores include both ultramafic rocks that existed originally in the subducted plate and rocks from the mantle wedge above the subducted plate, i.e., part of the North China Block.  相似文献   

10.
赣东北蛇绿岩作为华南少有的前寒武纪蛇绿岩长期都是华南大地构造研究中的热点。该蛇绿岩地幔橄榄岩以方辉橄榄岩为主,稀土总量为0.83×10-6~2.62×10-6,远低于原始地幔的含量,而Mg O含量高于原始地幔。稀土元素表现为LREE相对富集,微量元素表现为大离子亲石元素(LILE)富集,高场强元素Nb明显亏损的特征,这表明赣东北地幔橄榄岩具有亏损地幔源区特征,同时也有不同程度的俯冲带流体的交代特征。HREE模拟的部分熔融程度为10%~30%;同时,赣东北蛇绿岩地幔橄榄岩中同时包含Cr#60和Cr#60两种不同成因的铬尖晶石,说明其经历了MOR(mid-ocean ridge)和SSZ(supra-subduction zone)两种构造环境。结合前人资料,笔者推测赣东北蛇绿岩早先可能形成于洋中脊环境(约1060 Ma),随后在洋内俯冲作用下(约970 Ma),位于俯冲带上部的地幔橄榄岩受到了来自俯冲带的流体/熔体的交代,经历了SSZ环境的改造。  相似文献   

11.
Garnet‐bearing peridotite lenses are minor but significant components of most metamorphic terranes characterized by high‐temperature eclogite facies assemblages. Most peridotite intrudes when slabs of continental crust are subducted deeply (60–120 km) into the mantle, usually by following oceanic lithosphere down an established subduction zone. Peridotite is transferred from the resulting mantle wedge into the crustal footwall through brittle and/or ductile mechanisms. These ‘mantle’ peridotites vary petrographically, chemically, isotopically, chronologically and thermobarometrically from orogen to orogen, within orogens and even within individual terranes. The variations reflect: (1) derivation from different mantle sources (oceanic or continental lithosphere, asthenosphere); (2) perturbations while the mantle wedges were above subducting oceanic lithosphere; and (3) changes within the host crustal slabs during intrusion, subduction and exhumation. Peridotite caught within mantle wedges above oceanic subduction zones will tend to recrystallize and be contaminated by fluids derived from the subducting oceanic crust. These ‘subduction zone peridotites’ intrude during the subsequent subduction of continental crust. Low‐pressure protoliths introduced at shallow (serpentinite, plagioclase peridotite) and intermediate (spinel peridotite) mantle depths (20–50 km) may be carried to deeper levels within the host slab and undergo high‐pressure metamorphism along with the enclosing rocks. If subducted deeply enough, the peridotites will develop garnet‐bearing assemblages that are isofacial with, and give the same recrystallization ages as, the eclogite facies country rocks. Peridotites introduced at deeper levels (50–120 km) may already contain garnet when they intrude and will not necessarily be isofacial or isochronous with the enclosing crustal rocks. Some garnet peridotites recrystallize from spinel peridotite precursors at very high temperatures (c. 1200 °C) and may derive ultimately from the asthenosphere. Other peridotites are from old (>1 Ga), cold (c. 850 °C), subcontinental mantle (‘relict peridotites’) and seem to require the development of major intra‐cratonic faults to effect their intrusion.  相似文献   

12.
In this paper we present new data on the spatial variability of peridotite composition across a kilometer-scale mantle shear zone within the Lanzo massif (Western Alps, Italy). The shear zone separates the central from the northern part of the massif. Plagioclase peridotite shows gradually increasing deformation towards the shear zone, from porphyroclastic to mylonitic textures in the central body, while the northern body is composed of porphyroclastic rocks. The peridotite displays a large range of compositions, from fertile peridotite to refractory harzburgite and dunite. Deformed peridotites (proto-mylonite and mylonites) tend to be compositionally more homogeneous and fertile than weakly deformed peridotites. The composition of most plagioclase peridotites show rather high and constant (Ce/Yb) N ratios, and Yb N that cannot be explained by any simple melting model. Instead, refertilization modeling, consisting of melt increments from spinel peridotite sources, particularly with E-MORB melt, reasonably reproduces the plagioclase peridotite whole rock composition. Combined with constraints from Ce–Nb and Ce–Th systematics, we speculate that peridotites such as those from Lanzo record pervasive refertilization processes in the thermal boundary layer. In this scenario, mantle shear zones might act as important areas of melt focusing in the upper mantle that separates the thermal boundary layer from the conductively cooled mantle.  相似文献   

13.
The compatibility of vanadium (V) during mantle melting is a function of oxygen fugacity (fO2): at high fO2’s, V becomes more incompatible. The prospects and limitations of using the V content of peridotites as a proxy for paleo-fO2 at the time of melt extraction were investigated here by assessing the uncertainties in V measurements and the sensitivity of V as a function of degree of melt extracted and fO2. V-MgO and V-Al2O3 systematics were found to be sensitive to fO2 variations, but consideration of the uncertainties in measurements and model parameters indicates that V is sensitive only to relative fO2 differences greater than ∼2 log units. Post-Archean oceanic mantle peridotites, as represented by abyssal peridotites and obducted massif peridotites, have V-MgO and -Al2O3 systematics that can be modeled by 1.5 GPa melting between FMQ − 3 and FMQ − 1. This is consistent with fO2’s of the mantle source for mid-ocean ridge basalts (MORBs) as determined by the Fe3+ activity of peridotitic minerals and basaltic glasses. Some arc-related peridotites have slightly lower V for a given degree of melting than oceanic mantle peridotites, and can be modeled by 1.5 GPa melting at fO2’s as high as FMQ. However, the majority of arc-related peridotites have V-MgO systematics overlapping that of oceanic mantle peridotites, suggesting that although some arc mantle may melt under slightly oxidizing conditions, most arc mantle does not. The fact that thermobarometrically determined fO2’s in arc peridotites and lavas can be significantly higher than that inferred from V systematics, suggests that V retains a record of the fO2 during partial melting, whereas the activity of Fe3+ in arc peridotitic minerals and lavas reflect subsequent metasomatic overprints and magmatic differentiation/emplacement processes, respectively.Peridotites associated with middle to late Archean cratonic mantle are characterized by highly variable V-MgO systematics. Tanzanian cratonic peridotites have V systematics indistinguishable from post-Archean oceanic mantle and can be modeled by 3 GPa partial melting at ∼FMQ − 3. In contrast, many South African and Siberian cratonic peridotites have much lower V contents for a given degree of melting, suggesting at first glance that partial melting occurred at high fO2’s. More likely, however, their unusually low V contents for a given degree of melting may be artifacts of excess orthopyroxene, a feature that pervades many South African and Siberian peridotites but not the Tanzanian peridotites. This is indicated by the fact that the V contents of South African and Siberian peridotites are correlated with increases in SiO2 content, generating data arrays that cannot be modeled by partial melting but can instead be generated by the addition of orthopyroxene through processes unrelated to primary melt depletion. Correction for orthopyroxene addition suggests that the South African and Siberian peridotites have V-MgO systematics similar to those of Tanzanian peridotites. Thus, if the Tanzanian peridotites represent the original partial melting residues, and if the South African and Siberian peridotites have been modified by orthopyroxene addition, then there is no indication that Archean cratonic mantle formed under fO2’s significantly greater than that of modern oceanic mantle. Instead, the fO2’s inferred from the V systematics in these three cratonic peridotite suites are within range of modern oceanic mantle. This also suggests that the transition from a highly reducing mantle in equilibrium with a metallic core to the present oxidized state must have occurred by late Archean times.  相似文献   

14.
We document the presence of dolomite ± apatite in orogenic peridotites from the Ulten Zone (UZ, Italian Alps), the remnants of a Variscan mantle wedge tectonically coupled with eclogitized continental crust. These dolomite peridotites are associated with dominant carbonate-free amphibole peridotites, which formed in response to infiltration of aqueous subduction fluids lost by the associated crustal rocks during high-pressure (HP) metamorphism and retrogression. Dolomite-free and dolomite-bearing peridotites share the same metamorphic evolution, from garnet- (HP) to spinel-facies (low-pressure, LP) conditions. Dolomite and the texturally coexisting phases display equilibrium redistribution of rare earth elements and of incompatible trace elements during HP and LP metamorphism; clinopyroxene and amphiboles from carbonate-free and carbonate-bearing peridotites have quite similar compositions. These features indicate that the UZ mantle rocks equilibrated with the same metasomatic agents: aqueous CO2-bearing fluids enriched in incompatible elements released by the crust. The P–T crystallization conditions of the dolomite peridotites (outside the field of carbonatite melt + amphibole peridotite coexistence), a lack of textures indicating quench of carbonic melts, a lack of increase in modal clinopyroxene by reaction with such melts and the observed amphibole increase at the expense of clinopyroxene, all suggest that dolomite formation was assisted by aqueous CO2-bearing fluids. A comparison of the trace element compositions of carbonates and amphiboles from the UZ peridotites and from peridotites metasomatized by carbonatite and/or carbon-bearing silicate melts does not help to unambiguously discriminate between the different agents (fluids or melts). The few observed differences (lower trace element contents in the fluid-related dolomite) may ultimately depend on the solute content of the metasomatic agent (CO2-bearing fluid versus carbonatite melt). This study provides strong evidence that C–O–H subduction fluids can produce ‘carbonatite-like’ assemblages in mantle rocks, thus being effective C carriers from the slab to the mantle wedge at relatively low P–T. If transported beyond the carbonate and amphibole solidus by further subduction, dolomite-bearing garnet + amphibole peridotites like the ones from Ulten can become sources of carbonatite and/or C-bearing silicate melts in the mantle wedge. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users. In memory of Lauro Morten 1941–2006.  相似文献   

15.
The peridotite bodies of the Ulten Zone (Upper Austroalpine, Italian Eastern Alps) are enclosed in Variscan migmatites and derive from a mantle wedge environment. They display the progressive transformation of porphyroclastic spinel peridotites (T=1,200°C; P=1.5 GPa) into fine-grained garnet–amphibole peridotites (T=850°C; P=3 GPa). Detailed bulk-rock and mineral trace element analyses of a sample suite documenting the entire metamorphic evolution of the peridotites revealed several stages of metasomatism. The spinel peridotites derive from a depleted mantle that became enriched in some large ion lithophile element (LILE) and light rare earth elements (LREE). The same signature pertains to clinopyroxene and orthopyroxene, indicating that this metasomatic signature was acquired at the recorded temperature of 1,200°C. Such a temperature is considerably above the wet peridotite solidus and hence the metasomatic agent must have been a hydrous melt. Moreover, the Li-enrichment of the spinel-facies pyroxenes (up to 24 ppm Li) reflects disequilibrium distribution after exchange with a presumably mafic melt. cpx/opx D Li=3–7 and cpx/ol D Li=2.7–8 indicate that the spinel-facies clinopyroxene hosts higher Li amounts than the coexisting minerals. LREE fractionation, variable LREE enrichment, LILE enrichment with respect to HFSE (average clinopyroxene Pb N /Nb N =16–90) in spinel lherzolites can be related to chromatographic effects of porous melt flow. The significant enrichment of pyroxenes from the spinel lherzolites in Pb, U and Li indicates that the metasomatic melt was subduction-related. All these features suggest that the spinel lherzolites formed a mantle wedge layer percolated by melts carrying recycled crustal components and rising from a deeper source of subduction magmas. The garnet + amphibole peridotites equilibrated at temperatures well below the wet solidus in the presence of an aqueous fluid. Bulk-rock trace element patterns display pronounced positive anomalies in Cs, Ba, Pb and U and moderate enrichment in Li, indicating addition of a crustal component to the mantle rocks. Amphibole hosts most of these trace elements. Clinopyroxene displays high LILE/HFSE (Pb N /Nb N =300–600), low Ce/Pb (1.4–2.7 in garnet-facies clinopyroxene compared with 2.6–24.5 in the spinel-facies one) and variable LILE and LREE enrichments. The coupled increase of modal amphibole, Sr and Pb, together with positive Pb–Sr and Pb–U correlations, further indicate that incompatible element influx in these samples was fluid-mediated. In the garnet-facies samples, amphibole and, interestingly, olivine have similarly high Li concentrations as clinopyroxene, leading to cpx/amph D Li=0.7 and cpx/ol D Li=0.7–0.8, the latter being up to ten times lower than in the spinel-facies rocks. Due to its high modal abundance, olivine is the main host of Li in the garnet–amphibole peridotites. The observed metasomatic features provide evidence for the infiltration of an aqueous fluid in the mantle wedge above a subducting slab. This fluid most likely derived from subducted crustal rocks that underwent partial melting. Successive retrograde re-equilibration during exhumation of the garnet peridotite is accompanied by garnet and clinopyroxene breakdown and amphibole formation. This process produced minor changes, such as an increase of HREE and Li in amphibole, and an increase of Li in olivine. The general trace element signature remains essentially unchanged during retrogression and further hydration, indicating that fluids with a similar composition to the one present at the garnet–amphibole peridotite formation, were responsible for increased amphibole formation. The combined evidence from the metamorphic and metasomatic evolution indicates that the peridotites experienced first corner flow in a mantle wedge, followed by subduction and finally entrapment and exhumation within a crustal slab. During their entire history the Ulten peridotites were percolated first by melts and then by aqueous fluids, which added recycled crustal components to the mantle wedge.  相似文献   

16.
KUBO  K. 《Journal of Petrology》2002,43(3):423-448
Dunite formation processes in highly depleted peridotites arediscussed based upon a detailed study of the Iwanaidake peridotite,Hokkaido, Japan, which consists mainly of harzburgite with asmall amount of dunite. In the harzburgites, the Mg# [= 100x Mg/(Mg + Fe2+)] of olivine ranges from 91·5 to 92·5,and the Cr# [= 100 x Cr/(Cr + Al)] of spinel from 30 to 70;in the dunites, the Mg# of olivine ranges from 92·5 to94 and the Cr# of spinel from 60 to 85, respectively. The NiOwt % of olivine in harzburgites ranges from 0·38 to 0·44,and in dunites from 0·35 to 0·37. The Mg# andCr# are higher and NiO wt % is lower in the dunites than inthe harzburgites surrounding the dunites. The Mg# and Cr# exhibitnormal depletion trends expected from simple partial melting,whereas the NiO wt % shows an abnormal trend. On the basis ofmass balance calculations, dunites are considered to be derivedfrom the harzburgites by a process involving incongruent meltingof orthopyroxene (orthopyroxene olivine + Si-rich melt). Hydrousconditions were necessary to lower the solidus, and thus meltingof harzburgite was probably triggered by the introduction ofhydrous silicate melt. The dunite in this massif may have formedin the mantle wedge above a subduction zone. KEY WORDS: depleted peridotite; hydrous melt; incongruent melting; residual dunite; Iwanaidake peridotite  相似文献   

17.
Podiform chromite deposits occur in the mantle sequences of many ophiolites that were formed in supra-subduction zone (SSZ) settings. We have measured the Re-Os isotopic compositions of the major chromite deposits and associated mantle peridotites of the Dongqiao Ophiolite in the Bangong-Nujiang suture, Tibet, to investigate the petrogenesis of these rocks and their genetic relationships.The 187Os/188Os ratios of the chromite separates define a narrow range from 0.12318 to 0.12354, less variable than those of the associated peridotites. Previously-reported 187Os/188Os ratios of the Os-rich alloys enclosed in the chromitites define two clusters: 0.12645 ± 0.00004 (2 s; n = 145) and 0.12003 to 0.12194. The ultra-depleted dunites have much lower 187Os/188Os (0.11754, 0.11815), and the harzburgites show a wider range from 0.12107 to 0.12612. The average isotopic composition of the chromitites (187Os/188Os: 0.12337 ± 0.00001) is low compared with the carbonaceous chondrite value (187Os/188Os: 0.1260 ± 0.0013) and lower than the average value measured for podiform chromitites worldwide (0.12809 ± 0.00085). In contrast, the basalts have higher 187Os/188Os, ranging from 0.20414 to 0.38067, while the plagioclase-bearing harzburgite and cumulates show intermediate values of 187Os/188Os (0.12979 ~ 0.14206). Correspondingly, the basalts have the highest 187Re/188Os ratios, up to 45.4 ± 3.2, and the chromites have the lowest 187Re/188Os ratios, down to 0.00113 ± 0.00008. We suggest that melts/fluids, derived from the subducting slab, triggered partial melting in the overlying mantle wedge and added significant amounts of radiogenic Os to the peridotites. Mass-balance calculations indicate that a melt/mantle ratio of approximately 15:1 (melt: 187Re/188Os: 45.4, 187Os/188Os: 0.34484; mantle peridotite: 187Re/188Os: 0.0029, 187Os/188Os: 0.11754) is necessary to increase the Os isotopic composition of the chromitite deposits to its observed average value. This value implies a surprisingly low average melt/mantle ratio during the formation of the chromitite deposits. The percolating melts probably were of variable isotopic composition. However, in the chromitite pods the Os from many melts was pooled and homogenized, which is why the chromitite deposits show such a small variation in their Os isotopic composition. The results of this study suggest that the 187Os/188Os ratios of chromitites may not be representative of the DMM, but only reflect an upper limit. Importantly, the Os-isotope compositions of chromitites strongly suggest that such deposits can be formed by melt/mantle mixing processes.  相似文献   

18.
Lherzolite xenoliths containing fluid inclusions from the Ichinomegata volcano, located on the rear-arc side of the Northeast Japan arc, may be considered as samples of the uppermost mantle above the melting region in the mantle wedge. Thus, these fluid inclusions provide valuable information on the nature of fluids present in the sub-arc mantle. The inclusions in the Ichinomegata amphibole-bearing spinel–plagioclase lherzolite xenoliths were found to be composed mainly of CO2–H2O–Cl–S fluids. At equilibrium temperature of 920 °C, the fluid inclusions preserve pressures of 0.66–0.78 GPa, which correspond to depths of 23–28 km. The molar fraction of H2O and the salinity of fluid inclusions are 0.18–0.35 and 3.71 ± 0.78 wt% NaCl equivalent, respectively. These fluid inclusions are not believed to be fluids derived directly from the subducting slab, but rather fluids exsolved from sub-arc basaltic magmas that are formed through partial melting of mantle wedge triggered by slab-derived fluids.  相似文献   

19.
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20.
陈伊翔 《地球科学》2019,44(12):4057-4063
前人对深俯冲板片释放熔/流体交代地幔楔形成弧岩浆源区的过程和机制已得到充分认识,然而对地幔楔岩石能否脱水交代深俯冲地壳并不清楚.在对欧洲西阿尔卑斯造山带Dora-Maira地体白片岩的地球化学研究中,首次发现地幔楔交代岩能够脱水反向交代深俯冲地壳岩石,从而极大影响俯冲地壳的地球化学组成.结合白片岩和围岩的全岩地球化学特征以及锆石学结果,查明了白片岩的原岩为S型花岗岩,澄清了关于Dora-Maira白片岩原岩属性的长期争议.在此基础上,发现白片岩中变质锆石相对残留岩浆锆石δ18O值显著降低,指示原岩形成后受到低δ18O变质流体的交代作用.白片岩具有高温岩石中最高的δ26Mg值达0.75‰,显著高于围岩变花岗岩,指示交代流体具有重Mg同位素组成.基于地球主要岩石储库的Mg同位素组成,推测交代流体来自俯冲隧道中富滑石地幔楔蛇纹岩在弧下深度的脱水分解,而这些地幔楔蛇纹岩是新特提斯洋壳在弧前深度变质脱水产生的流体与地幔楔浅部橄榄岩反应形成.这些结果不仅提供了利用Mg-O同位素示踪俯冲隧道中流体来源的新思路,也提供了地幔楔蛇纹岩来源流体反向交代深俯冲地壳岩石的首个典型实例.这种反向交代不仅极大改变了深俯冲地壳的地球化学组成,而且对弧岩浆岩重Mg同位素成因具有重要意义.   相似文献   

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