首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到10条相似文献，搜索用时 109 毫秒
1.
The Saramta peridotite massif is located within the Sharyzhalgai complex, SW margin of the Siberian craton. The Saramta massif was formed in the Archean and then juxtaposed with granulites of crystalline basement of the Siberian craton. The Saramta harzburgites are highly refractory in terms of lack of residual clinopyroxene, olivine Mg-number (up to 0.937), and spinel Cr-number (∼0.5), suggesting high degree of partial melting. Detailed study of their microstructures shows that they have extensively reacted with a SiO2-rich melt, leading to the crystallization of orthopyroxene, clinopyroxene, amphibole and spinel at the expense of olivine. The major element compositions of the least reacted harzburgites are similar to the residues of refractory peridotites produced by the fractional melting (initial melting pressures >3 GPa and melt fractions ∼40%). Moreover, non-residual clinopyroxenes are highly depleted in Yb, Zr and Ti, but highly enriched in LREE. A two-stage history is proposed for the Saramta peridotite: (1) primitive mantle underwent depletion in the garnet stability field followed by melting in the spinel stability field; (2) refractory harzburgites underwent refertilization by SiO2-rich melt in supra-subduction zone. Rare Saramta lherzolites probably formed from more refractory harzburgites as a result of such a melt–rock reaction. The Saramta peridotites are similar to low-T coarse-grained peridotites of subcratonic mantle. Processes of their formation, as reflected by textures and composition of minerals of the Saramta peridotites, are characteristic of the early stages of subcratonic mantle formation.  相似文献   

2.
Here, we investigate the scale and nature of melting and melt percolation processes recorded by 17 supra-subduction peridotites collected in a ~70 km2 area in the northern portion of the Josephine ophiolite (Western USA). We present major and trace element variations in whole rocks; major elements in olivine, orthopyroxene, clinopyroxene and spinel; and trace elements [including rare earth element (REE)] in clinopyroxene and orthopyroxene. In the Josephine peridotites, compositional variability occurs at different scales. On the one hand, large systematic changes from depleted to fertile peridotites occur on large kilometer scales. Field, petrological and geochemical data can be consistently explained if the Josephine mantle experienced variable degrees of hydrous flux melting (10 to >20–23 %), and we argue that small fractions of subduction-derived fluids (0.015–0.1 wt%) were pervasive in the ~70 km2 studied area, and continuously supplied during wedge melting. Fluid localization probably led to increased extent of flux melting in the harzburgitic areas. On the other hand, in single outcrops, sharp transitions from dunite to harzburgite to lherzolite and olivine websterite can be found on meter to centimeter scales. Thus, some fertile samples may reflect limited degrees of refertilization at the outcrop scale. In addition, clinopyroxene and orthopyroxene in ultra-depleted harzburgites (Spinel Cr# > 58) show variable degrees of LREE enrichment, which reflect percolation of and partial re-equilibration with, small fractions of boninite melt. Because the enriched samples also show the highest spinel Cr#, we argue that these enrichments are local features connected to the presence of dunite channels nearby. Lastly, trace element concentrations of pyroxenes in Josephine harzburgites show that they are one of the most depleted harzburgites among worldwide ophiolitic peridotites, indicating particularly high degrees of melting, potentially past the exhaustion of clinopyroxene.  相似文献   

3.
ODP Leg 209 Site 1274 mantle peridotites are highly refractory in terms of lack of residual clinopyroxene, olivine Mg# (up to 0.92) and spinel Cr# (∼0.5), suggesting high degree of partial melting (>20%). Detailed studies of their microstructures show that they have extensively reacted with a pervading intergranular melt prior to cooling in the lithosphere, leading to crystallization of olivine, clinopyroxene and spinel at the expense of orthopyroxene. The least reacted harzburgites are too rich in orthopyroxene to be simple residues of low-pressure (spinel field) partial melting. Cu-rich sulfides that precipitated with the clinopyroxenes indicate that the intergranular melt was generated by no more than 12% melting of a MORB mantle or by more extensive melting of a clinopyroxene-rich lithology. Rare olivine-rich lherzolitic domains, characterized by relics of coarse clinopyroxenes intergrown with magmatic sulfides, support the second interpretation. Further, coarse and intergranular clinopyroxenes are highly depleted in REE, Zr and Ti. A two-stage partial melting/melt–rock reaction history is proposed, in which initial mantle underwent depletion and refertilization after an earlier high pressure (garnet field) melting event before upwelling and remelting beneath the present-day ridge. The ultra-depleted compositions were acquired through melt re-equilibration with residual harzburgites. Electronic supplementary material Supplementary material is available in the online version of this article at and is accessible for authorized users.  相似文献   

4.
A suite of mantle peridotites sampled in the Kamchatsky Mys includes spinel lherzolite, clinopyroxene-bearing harzburgite, and harzburgite. Mineral chemistry of olivine, chromian spinel, and clinopyroxene show strongly correlated element patterns typical of peridotite formed by 8% to more than 22% partial melting. Clinopyroxene in the Kamchatka peridotites is compositionally different from that of both abyssal and suprasubduction varieties: Clinopyroxene in lherzolite is depleted in LREE relative to abyssal peridotite and that in harzburgite has very low LREE and Sr unlike the subduction-related counterpart. These composition features indicate that the rocks ultra-depleted in basaltic components originated in the vicinity of a hotspot, possibly, proto-Hawaiian plume, which provided high temperature and melting degree of the MORB source mantle at mid-ocean ridge.  相似文献   

5.
Ultramafic xenoliths were found in recent alkali basalts from São Tomé Island. These include spinel peridotites (lherzolites, harzburgites and dunites) and pyroxenites (orthopyroxenites and clinopyroxenites). Textures and mineral compositions indicate that pyroxenites originated from crystal/liquid separation processes operating on magmas similar to those giving rise to their present host rocks whereas spinel peridotite xenoliths had an accidental origin; Fo (>89) and Ni (>0.36 wt.%) contents in olivines, Mg# (91–95) of orthopyroxenes and low Ti in clinopyroxene (primary crystals: TiO2<0.06 wt.%) and in spinel (TiO2<0.1 wt.%) are within the range reported for abyssal peridotites, indicating São Tomé spinel peridotites represent refractory residues of melting. Nevertheless, the lack of correlation between mineral chemistry and modal composition suggests that spinel peridotite xenoliths are not simple residues and were affected by infiltration of fluid/melts within the mantle. The wide temperature range obtained for spinel peridotites (700 to >1150 °C) is compatible with a long period of pre-entrainment cooling supporting Fitton's [Tectonophysics 94 (1983) 473] hypothesis that proposes oceanic lithosphere uprising in the Cameroon Volcanic Line prior to the initiation of the current thermal regime, related to São Tomé magmatism. The association of upper mantle (peridotite) xenoliths with igneous cumulates (pyroxenites) suggests that the spinel peridotite suite originated in the uppermost mantle above the São Tomé magma storage zone(s), probably in a region of high strain rate, near the boundary between the mantle and the overlying oceanic crust.  相似文献   

6.
Major and trace elements and water contents were analyzed in 16 peridotite xenoliths embedded by the Cenozoic basalts in Pingnan (southeastern Guangxi Province), to constrain the chemical composition and evolution of the lithospheric mantle located in the central part of the South China Block (SCB). The peridotites are mainly moderately refractory harzburgites and lherzolites (Mg#-Ol?=?90.3–91.7) and minor fertile lherzolites (Mg#-Ol?=?88.9–89.9). Clinopyroxenes in the peridotites show LREE-depleted pattern, and commonly exhibit negative anomalies in Nb and Ti, suggesting the peridotites probably represent residues after 1–10% of partial melting without significant mantle metasomatism. Water contents range from 146 to 237 ppm wt. H2O in clinopyroxene, and from 65 to 112 ppm wt. H2O, in orthopyroxene but are below detection limit (2 ppm wt. H2O) in olivine. Calculated bulk water contents, based on the mineral modes and partition coefficient, range from 14 to 83 ppm wt. H2O (average 59 ppm wt. H2O). There is a correlation between melting indices (such as Mg#-Ol, Ybn in clinopyroxene) and water contents in clinopyroxene and orthopyroxene, but no correlation is observed between the whole-rock water contents and the redox state (Fe3+/∑Fe ratios in spinel), suggesting that water contents in the peridotites are mainly controlled by the degree of partial melting rather than by oxygen fugacity. The lithospheric mantle beneath the interior of the SCB may not be compositionally stratified; fertile and moderately refractory mantle coexist at the similar depths. Geochemical data and water contents of the studied peridotites are similar to the proposed MORB source and indicate that the ancient refractory lithospheric mantle was irregularly eroded or reacted by the upwelling asthenosphere, and eventually replaced by juvenile fertile accreted mantle through the cooling of the asthenosphere.  相似文献   

7.
This paper presents field, petrographic–structural and geochemical data on spinel and plagioclase peridotites from the southern domain of the Lanzo ophiolitic peridotite massif (Western Alps). Spinel lherzolites, harzburgites and dunites crop out at Mt. Arpone and Mt. Musinè. Field evidence indicates that pristine porphyroclastic spinel lherzolites are transformed to coarse granular spinel harzburgites, which are in turn overprinted by plagioclase peridotites, while strongly depleted spinel harzburgite and dunite bands and bodies replace the plagioclase peridotites. On the northern flank of Mt. Arpone, deformed, porphyroclastic (lithospheric) lherzolites, with diffuse pyroxenite banding, represent the oldest spinel-facies rocks. They show microstructures of a composite subsolidus evolution, suggesting provenance from deeper (asthenospheric) mantle levels and accretion to the lithosphere. These protoliths are locally transformed to coarse granular (reactive) spinel harzburgites and dunites, which show textures reminiscent of melt/rock reaction and geochemical characteristics suggesting that they are products of peridotite interaction with reactively percolating melts. Geochemical data and modelling suggest that <1–5% fractional melting of spinel-facies DMM produced the injected melts. Plagioclase peridotites are hybrid rocks resulting from pre-existing spinel peridotites and variable enrichment of plagioclase and micro-gabbroic material by percolating melts. The impregnating melts attained silica-saturation, as testified by widespread orthopyroxene replacement of olivine, during open system migration in the lithosphere. At Mt. Musinè, coarse granular spinel harzburgite and dunite bodies replace the plagioclase peridotites. Most of these replacive, refractory peridotites have interstitial magmatic clinopyroxene with trace element compositions in equilibrium with MORB, while some Cpx have REE-depleted patterns suggesting transient geochemical features of the migrating MORB-type melts, acquired by interaction with the ambient plagioclase peridotite. These replacive spinel harzburgite and dunite bodies are interpreted as channels exploited for focused and reactive migration of silica-undersaturated melts with aggregate MORB compositions. Such melts were unrelated to the silica-saturated melts that refertilized the pre-existing plagioclase peridotites. Finally, MORB melt migration occurred along open fractures, now recorded as gabbroic dikes.

Our data document the complexity of rock-types and mantle processes in the South Lanzo peridotite massif and describe a composite tectonic and magmatic scenario that is not consistent with the “asthenospheric scenario” proposed by previous authors. We envisage a “transitional scenario” in which extending subcontinental lithospheric mantle was strongly modified (both depleted and refertilized) by early melts with MORB-affinity formed by decompression partial melting of the upwelling asthenosphere, during pre-oceanic rifting and lithospheric thinning in the Ligurian Tethys realm.  相似文献   


8.
Geochemical compositions of lower crustal and lithospheric mantle xenoliths found in alkali basaltic lavas from the Harrat Ash Shamah volcanic field in southern Syria place constraints on the formation of the Arabian–Nubian Shield in northern Arabia. Compositions of lower crustal granulites are compatible with a cumulate formation from mafic melts and indicate that they are not genetically related to their host rocks. Instead, their depletion in Nb relative to other incompatible elements points to an origin in a Neoproterozoic subduction zone as recorded by an average depleted mantle Sm–Nd model age of 630 Ma.Lithospheric spinel peridotites typically represent relatively low degree (< 10%) partial melting residues of spinel lherzolite with primitive mantle compositions as indicated by major and trace element modelling of clinopyroxene and spinel. The primary compositions of the xenoliths were subsequently altered by metasomatic reactions with low degree silicate melts and possibly carbonatites. Because host lavas lack these signatures any recent reaction of the lherzolites with their host magma can be ruled out. Sm–Nd data of clinopyroxene from Arabian lithospheric mantle lherzolites yield an average age of 640 Ma suggesting that the lithosphere was not replaced since its formation and supporting a common origin of the Arabian lower crustal and lithospheric mantle sections.The new data along with published Arabian mantle xenolith compositions are consistent with a model in which the lithospheric precursor was depleted oceanic lithosphere that was overprinted by metasomatic processes related to subduction and arc accretion during the generation of the Arabian–Nubian Shield. The less refractory nature of the northern Arabian lithosphere as indicated by higher Al, Na and lower Si and Mg contents of clinopyroxenes compared to the more depleted nature of the south Arabian lithospheric mantle, and the comparable low extent of melt extraction suggest that the northern Arabian lithosphere formed in a continental arc system, whereas the lithosphere in the southern part of Arabia appears to be of oceanic arc origin.  相似文献   

9.
The ophiolitic peridotites in the Wadi Arais area, south Eastern Desert of Egypt, represent a part of Neoproterozoic ophiolites of the Arabian-Nubian Shield (ANS). We found relics of fresh dunites enveloped by serpentinites that show abundances of bastite after orthopyroxene, reflecting harzburgite protoliths. The bulk-rock chemistry confirmed the harzburgites as the main protoliths. The primary mantle minerals such as orthopyroxene, olivine and chromian spinel in Arais serpentinites are still preserved. The orthopyroxene has high Mg# [=Mg/(Mg + Fe2+)], ~0.923 on average. It shows intra-grain chemical homogeneity and contains, on average, 2.28 wt.% A12O3, 0.88 wt.% Cr2O3 and 0.53 wt.% CaO, similar to primary orthopyroxenes in modern forearc peridotites. The olivine in harzburgites has lower Fo (93?94.5) than that in dunites (Fo94.3?Fo95.9). The Arais olivine is similar in NiO (0.47 wt.% on average) and MnO (0.08 wt.% on average) contents to the mantle olivine in primary peridotites. This olivine is high in Fo content, similar to Mg-rich olivines in ANS ophiolitic harzburgites, because of its residual origin. The chromian spinel, found in harzburgites, shows wide ranges of Cr#s [=Cr/(Cr + Al)], 0.46?0.81 and Mg#s, 0.34?0.67. The chromian spinel in dunites shows an intra-grain chemical homogeneity with high Cr#s (0.82?0.86). The chromian spinels in Arais peridotites are low in TiO2, 0.05 wt.% and YFe [= Fe3+/(Cr + Al + Fe3+)], ~0.06 on average. They are similar in chemistry to spinels in forearc peridotites. Their compositions associated with olivine’s Fo suggest that the harzburgites are refractory residues after high-degree partial melting (mainly ~25?30 % partial melting) and dunites are more depleted, similar to highly refractory peridotites recovered from forearcs. This is in accordance with the partial melting (>20 % melt) obtained by the whole-rock Al2O3 composition. The Arais peridotites have been possibly formed in a sub-arc setting (mantle wedge), where high degrees of partial melting were available during subduction and closing of the Mozambique Ocean, and emplaced in a forearc basin. Their equilibrium temperature based on olivine?spinel thermometry ranges from 650 to 780 °C, and their oxygen fugacity is high (Δlog ?O2?=?2.3 to 2.8), which is characteristic of mantle-wedge peridotites. The Arais peridotites are affected by secondary processes forming microinclusions inside the dunitic olivine, abundances of carbonates and talc flakes in serpentinites. These microinclusions have been formed by reaction between trapped fluids and host olivine in a closed system. Lizardite and chrysotile, based on Raman analyses, are the main serpentine minerals with lesser antigorite, indicating that serpentines were possibly formed under retrograde metamorphism during exhumation and near the surface at low T (<400 °C).  相似文献   

10.
Ophiolites exposed across the western Tauride Belt in SW Turkey represent tectonically emplaced fragments of oceanic lithosphere incorporated into continental margin following the closure of the Neotethys Ocean during the Late Cretaceous. The mantle sections of the ophiolites contain peridotites with diverse suites of geochemical signatures indicative of residual origin by melt depletion in both mid‐ocean ridge (MOR) and supra‐subduction zone (SSZ) settings. This study uses a laser‐ablation inductively‐coupled plasma‐mass spectrometry (LA‐ICP‐MS) for in situ measurements of trace elements in primary mantle phases in order to identify the upper mantle petrogenetic processes effective during variable stage of melt extraction in these discrete tectonic settings and to discriminate between the effects of reaction with chemically distinct mantle melts migrating through the solid residues. Trace element signatures in pyroxenes suggest small‐length scales of compositional variations which may be interpreted to be a result of post‐melting petrogenetic processes. Relative distribution of rare earth elements and Li between coexisting orthopyroxene‐clinopyroxene pairs in the peridotites suggests compositional disequilibrium in sub‐solidus conditions, which possibly reflects differential effects of diffusive exchange during melting and melt transport or interaction with subduction melts/fluids. On the basis of Ga abundances and Ga–Ti–Fe+3# [Fe+3/(Fe+3 + Cr + Al)] relationships of chrome‐spinels it is documented that the peridotites have experienced the combined effects of partial melting and variable extent of melt‐solid interaction. The MOR peridotites have spinels with geochemical signatures indicative of melt‐depleted residual origin with subsequent incompatible element enrichment through melt impregnation, while the Ga–Ti–Fe+3# relationships of chrome‐spinels in SSZ peridotites indicate that these highly depleted peridotites are not simple melt residues, but have been subject to significant compositional modification by interaction with subduction related melts/fluids. The observed compositional variations, which are related to long‐term tectonic reorganisation of oceanic lithosphere, provide evidence for a time integrated evolution from a mid‐ocean ridge to a supra‐subduction zone setting and may be a possible analogue to explain the coexistence of geochemically diverse MOR–SSZ suites in other Tethyan ophiolites. Copyright © 2011 John Wiley & Sons, Ltd.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号