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1.
深海橄榄岩研究进展   总被引:2,自引:0,他引:2  
很久以来,深海橄榄岩一直被认为是洋中脊下地幔熔融残留体,但最近深海橄榄岩实际矿物组分研究和全岩化学成分重建的结果表明,深海橄榄岩是洋脊下地幔熔融残留体和过量橄榄石的混合物。深海橄榄岩的成因是洋脊下上隆地幔降压熔融作用和熔体上升通过地幔最上部的热边界层时发生冷却、结晶出橄榄石的联合作用的结果。地幔熔融程度越高,深海橄榄岩越亏损,则含有越多的过量橄榄石。为此,只要把深海橄榄岩中过量的橄榄石剔除后,其实际矿物组分就能有效地反映洋脊下地幔熔融作用和熔融萃取过程。  相似文献   

2.
Magma accumulation in the mantle requires that the mantle be permeable. Experimental investigations show that the permeability threshold first will be attained after a certain degree of partial melting. The influence of the permeability threshold on the composition of partial melts is evaluated using the fayalite-forsterite system as an example. In addition the variation in trace element concentrations are calculated for different distribution coefficients. Primary magmas formed by accumulation when a minimal degree of partial melting is required for permeability display a remarkably small variation in composition up to 30% partial melting. It is suggested from REE abundances that primary tholeiitic magmas have been generated by permeability controlled partial melting. The compositions of the primary magmas generated by permeability controlled partial melting will not differ much from the compositions obtained by batch melting, but the degrees of partial melting will differ for similar compositions.  相似文献   

3.
Summary Abyssal tholeiite is generated by partial melting of the upper mantle. The mantle sections of ophiolite complexes show that partial melting leaves mantle residua that are lherzolitic or harzburgitic, harzburgite being the more depleted residuum. It is shown that some of the interstitial melt of partially molten harzburgite approximates a tholeiitic composition. Therefore, the solidus of harzburgite constitutes the maximum possible temperature for the generation of primary tholeiite. The MgO contents of primary tholeiites in equilibrium with harzburgite are determined to be about 21 and 23wt.% MgO at 2.0 and 3.0GPa, respectively. The possible MgO contents of primary abyssal tholeiite is suggested to range between 10 and 23wt.% MgO, with the MgO content increasing with increasing pressure.  相似文献   

4.
西藏雅鲁藏布江蛇绿岩带罗布莎地幔橄榄岩的成因   总被引:17,自引:3,他引:14  
广泛分布在雅鲁藏布江蛇绿岩带的地幔橄榄岩是没有蛇纹石化的新鲜岩石,因而通过显微镜下观察和全岩化学分布探索其成因和地幔活动,是十分有利和简便的。最近几年来,利用岩石化学资料揭示远洋橄榄岩,认为它不是原始地幔岩经分或分离熔化作用萃取出玄武岩熔体后的直接残余物。罗布落蛇绿岩橄的镜下观察和岩石化学资料也证明,它不是原始地幔岩经局部熔化后的残余物,而且由来自更深层的地幔过渡带的硅酸盐超高压矿物底辟上升经熔取  相似文献   

5.
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   

6.
         二辉橄榄岩通常被认为是低程度部分熔融的残留,但熔体再富集作用为其成因提供了一种新的解释。熔体再富集作 用通常是指软流圈来源的玄武质熔体加入到难熔的方辉橄榄岩或纯橄岩形成更为饱满的二辉橄榄岩的过程。除了使主量元 素富集之外,熔体再富集作用还可以使微量元素与Sr-Nd 同位素从方辉橄榄岩中的富集特征转变为二辉橄榄岩所呈现的亏 损特征。对于熔体再富集作用是否改变橄榄岩的Os 同位素组成还存在较大的争议,它主要取决于加入熔体的比例,熔体中 硫的饱和程度以及熔体再富集作用发生的时间等因素。对于以低熔/岩比例为主的大陆岩石圈地幔来说,熔体再富集作用对 橄榄岩的Os 同位素组成的影响可能较为有限。除了化学成分上的影响之外,熔体的加入也会改变大陆岩石圈地幔的物理特 征。这一过程使得岩石圈地幔的渗透率增大和黏滞度降低,从而会破坏大陆岩石圈地幔的稳定性。虽然熔体再富集作用可 以影响和改变岩石圈地幔的性质,但它是否导致克拉通地幔的减薄以及克拉通破坏尚有疑问。  相似文献   

7.
 The use of ocean floor basalt chemistry as a tool to investigate mantle composition and processes requires that we work with basalts that have been modified little since leaving the mantle. One source of such basalts is melt inclusions trapped in primitive crystals. However, obtaining information from these melt inclusions is complicated by the fact that melt inclusions in natural basalts are essentially always altered by post-entrapment crystallization. This requires that we develop techniques for reconstructing the original trapped liquid compositions. We conducted a series of experiments to reverse the effects of post-entrapment crystallization by re-heating the host crystals to their crystallization temperature. For these experiments we used plagioclase crystals separated from a single Gorda Ridge lava. The crystallization temperature for these crystals was determined by a set of incremental re-heating experiments to be ∼1240–1260° C. The inclusions are primitive, high Ca-Al basaltic melts, saturated with plagioclase, olivine and Al-rich chromite at low pressure. The inclusion analyses can be linked to the host lava composition by low pressure fractionation. The major element composition of the re-homogenized melt inclusions within each crystal is relatively constant. However, the incompatible element analyses have extremely wide ranges. The range of La/Sm and Ti/Zr from inclusions analyzed from a single sample from the Gorda Ridge exceeds the range reported for lavas sampled from the entire ridge. The pyroxene compositions predicted to be in equilibrium with the melt inclusion trace element signature cover much of the range represented by pyroxenes from abyssal peridotites. The volumetric proportions of the magmas entering the base of the crust can be evaluated using frequency distribution of melt inclusion compositions. This distribution suggests that the array of magmas was skewed towards the more depleted compositions, with little evidence for an enriched component in this system. This pattern is more consistent with a dynamic flow model of the mantle or of a passive flow model where the melts produced in the peripheral areas of the melting regime were not focused to the ridge. Received: 5 January 1995 / Accepted: 13 June 1995  相似文献   

8.
The sandwich technique for determining the composition of partial melts in equilibrium with mantle lithologies may be a particularly powerful method for determining melt compositions at the onset of melting if the method is applied iteratively. However, conventional iterative sandwich experiments, in which the liquid from a preceding experiment is used as the “meat” of the sandwich in the following experiment, may require many iterations before the melts produced can be directly relatable to the melting relations of the target bulk rock composition. A modified iterative sandwich experimental (MISE) technique is proposed that may circumvent many of the problems of more conventional techniques. Consideration of experimental uncertainties, including both random and systematic errors in determination of partial melt compositions as well as the influence of errors in estimates of the solidus temperature of the rock of interest, suggests that the MISE technique may produce robust results even when melt composition errors are significant and that errors in estimation of the solidus location are detectable and therefore avoidable.  相似文献   

9.
Lead isotope variability in olivine-hosted melt inclusions from Iceland   总被引:2,自引:0,他引:2  
The lead isotope and trace element compositions of a suite of olivine-hosted melt inclusions in primitive lava flows from the Reykjanes Peninsula in Iceland show extreme variability. Much of this variability is present in the composition of inclusions from one hand specimen of Háleyjabunga, a depleted picrite lava shield that erupted 13 ka. 208Pb/206Pb compositions in this sample span 50-90% of the total range found in Atlantic MORB, indicating that high-amplitude compositional heterogeneity is present in the mantle source of melts that aggregated to form a single eruption. The trace element and isotopic trends in the melt inclusions are coincident with those in whole rock samples from young lava flows of the Reykjanes Peninsula, and extend the total range of variation towards more depleted compositions. The incompatible trace element and lead isotope compositions of the inclusions are strongly coupled and lie close to binary mixing trends between the extreme melt inclusion compositions. These relationships indicate that the trace element variation in the melt inclusions reflects heterogeneity in the composition of the mantle source entering the melting region under the Reykjanes Peninsula. Large positive Sr concentration anomalies are present in three of the inclusions, but do not correlate with indicators of mantle melting or source variations and are likely to arise by reaction with plagioclase during crustal storage. Fractional melting of heterogeneous mantle is predicted to generate melts with a wide range of compositions, filling a large volume in trace element-isotope space. However, the compositional variations observed in the melt inclusions lie close to binary mixing curves. These observations may be accounted for by a two-stage model of melt mixing. The first stage occurs in porous channels that transport melt in the mantle and takes place before inclusion entrapment. This mixing stage generates a bimodal distribution of melt compositions that is supplied from the channels to sub-Moho and lower crustal magma lenses. The second stage of mixing occurs in these chambers, producing the binary mixing trends recorded in the inclusion compositions. The distribution of isotopic compositions observed in the melt inclusions and whole rock samples from the Reykjanes Peninsula is therefore controlled by melt mixing. These results have important implications for the interpretation of basalt composition in terms of distinct compositional entities within the upwelling solid mantle under mid-ocean ridges and ocean islands.  相似文献   

10.
The composition of chromian spinel in alpine-type peridotites has a large reciprocal range of Cr and Al, with increasing Cr# (Cr/(Cr+Al)) reflecting increasing degrees of partial melting in the mantle. Using spinel compositions, alpine-type peridotites can be divided into three groups. Type I peridotites and associated volcanic rocks contain spinels with Cr#<0.60; Type III peridotites and associated volcanics contain spinels with Cr#>0.60, and Type II peridotites and volcanics are a transitional group and contain spinels spanning the full range of spinel compositions in Type I and Type II peridotites. Spinels in abyssal peridotites lie entirely within the Type I spinel field, making ophiolites with Type I alpine-type peridotites the most likely candidates for sections of ocean lithosphere formed at a midocean ridge. The only modern analogs for Type III peridotites and associated volcanic rocks are found in arc-related volcanic and intrusive rocks, continental intrusive assemblages, and oceanic plateau basalts. We infer a sub-volcanic arc petrogenesis for most Type III alpine-type peridotites. Type II alpine-type peridotites apparently reflect composite origins, such as the formation of an island-arc on ocean crust, resulting in large variations in the degree and provenance of melting over relatively short distances. The essential difference between Type I and Type III peridotites appears to be the presence or absence of diopside in the residue at the end of melting.Based on an examination of co-existing rock and spinel compositions in lavas, it appears that spinel is a sensitive indicator of melt composition and pressure of crystallization. The close similarity of spinel composition fields in genetically related basalts, dunites and peridotites at localities in the oceans and in ophiolite complexes indicates that its composition reflects the degree of melting in the mantle source region. Accordingly, we infer from the restricted range of spinel compositions in abyssal basalts that the degree of mantle melting beneath mid-ocean ridges is generally limited to that found in Type I alpine-type peridotites. It is apparent, therefore, that the phase boundary OL-EN-DI-SP +meltOL-EN-SP+melt has limited the degree of melting of the mantle beneath mid-ocean ridges. This was clearly not the case for many alpine-type peridotites, implying very different melting conditions in the mantle, probably involving the presence of water.  相似文献   

11.
产于法国中央高原堡雷(Boree)的具镶嵌结构方辉橄榄岩包体被认为是大陆活动区碱性玄武岩捕获的、来源最深的尖晶石相上地幔样品。已有的岩浆堆积说和等物理化学环境中重结晶模式难于解释其矿物学、微量元素和Sr-Nd同位素地球化学特征,为此我们提出了热柱来源熔体渗滤岩石圈底部的新成因模式。渗滤熔体和岩石圈地幔之间的反应不仅导致了矿物含量的变化,而且形成了特征的微量元素配分型式和同位素组成。REE模拟计算表明,熔体/岩石比值的大小、熔体性质以及熔体-岩石反应机制的多样性是控制本区幔源包体地球化学及其岩石变形、结晶程度之间相关性的重要因素。  相似文献   

12.
Magmatic systems of large continental igneous provinces   总被引:1,自引:1,他引:0  
Large igneous provinces (LIPs) formed by mantle superplume events have irreversibly changed their composition in the geological evolution of the Earth from high-Mg melts (during Archean and early Paleoproterozoic) to Phanerozoic-type geochemically enriched Fe-Ti basalts and picrites at 2.3 Ga. We propose that this upheaval could be related to the change in the source and nature of the mantle superplumes of different generations. The first generation plumes were derived from the depleted mantle, whereas the second generation (thermochemical) originated from the core-mantle boundary (CMB). This study mainly focuses on the second (Phanerozoic) type of LIPs, as exemplified by the mid-Paleoproterozoic Jatulian–Ludicovian LIP in the Fennoscandian Shield, the Permian–Triassic Siberian LIP, and the late Cenozoic flood basalts of Syria. The latter LIP contains mantle xenoliths represented by green and black series. These xenoliths are fragments of cooled upper margins of the mantle plume heads, above zones of adiabatic melting, and provide information about composition of the plume material and processes in the plume head. Based on the previous studies on the composition of the mantle xenoliths in within-plate basalts around the world, it is inferred that the heads of the mantle (thermochemical) plumes are made up of moderately depleted spinel peridotites (mainly lherzolites) and geochemically-enriched intergranular fluid/melt. Further, it is presumed that the plume heads intrude the mafic lower crust and reach up to the bottom of the upper crust at depths ~20 km. The generation of two major types of mantle-derived magmas (alkali and tholeiitic basalts) was previously attributed to the processes related to different PT-parameters in the adiabatic melting zone whereas this study relates to the fluid regime in the plume heads. It is also suggested that a newly-formed melt can occur on different sides of a critical plane of silica undersaturation and can acquire either alkalic or tholeiitic composition depending on the concentration and composition of the fluids. The presence of melt-pockets in the peridotite matrix indicates fluid migration to the rocks of cooled upper margin of the plume head from the lower portion. This process causes secondary melting in this zone and the generation of melts of the black series and differentiated trachytic magmas.  相似文献   

13.
Peridotite samples recovered from IODP Site U1309 at the Atlantis Massif in the Mid-Atlantic Ridge were examined to understand magmatic processes for the oceanic core complex formation. Original peridotite was fragmented, and the limited short peridotite intervals are now surrounded by a huge gabbro body probably formed by late-stage melt injections. Each peridotite interval has various petrographical and geochemical features. A spinel harzburgite in contact with gabbro shows evidence of limited melt penetrations causing gradual compositional change, in terms of trace-element compositions of pyroxenes, as well as modal change near the boundary. Geochemistry of clinopyroxenes with least melt effects indicates that the harzburgite is originally mantle residue formed by partial melting under polybaric conditions, and that such a depleted peridotite is one of the components of the oceanic core complex. Some of plagioclase-bearing peridotites, on the other hand, have more complicated origin. Although their original features were partly overprinted by the injected melt, the original peridotites, both residual and non-residual materials, were possibly derived from the upper mantle. This suggests that the melt injected around an upper mantle region or into mantle material fragments. The injected melt was possibly generated at the ridge-segment center and, then, moved and evolved toward the segment end beneath the oceanic core complex.  相似文献   

14.
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   


15.
Plagioclase-bearing peridotites are commonly associated with gabbroic rocks sampled around the Moho Transition Zone. Based on mineral chemistry, texture, and spatial relations, the formation of plagioclase-bearing peridotites has been attributed to impregnation of basalt into residual peridotites. We conducted reactive dissolution and crystallization experiments to test this hypothesis by reacting a primitive mid-ocean ridge basalt with a melt-impregnated lherzolite at 1,300 °C and 1 GPa and then cooling to 1,050 °C as pressure decreased to 0.7 GPa. Crystallization during cooling produced lithologic sequences of gabbro–wehrlite or gabbro–wehrlite–peridotite, depending on reaction time. Wehrlitic and peridotitic sections contain significant amounts of plagioclase interstitial to olivine and clinopyroxene and plagioclase compositions are spatially homogeneous. Clinopyroxene in the wehrlite–peridotite section is reprecipitated from the melt and exhibits poikilitic texture with small rounded olivine chadacrysts. Mineral composition in olivine and clinopyroxene varies spatially, both at the scale of the sample and within individual grains. Olivine grains that crystallized close to the melt–peridotite interface are enriched in iron due to their proximity to the basaltic melt reservoir. Consistent with many field studies, we observed gradual spatial variation in olivine and clinopyroxene composition across a lithologically sharp boundary between the gabbro and wehrlite–peridotite. Plagioclase compositions show no obvious dependence on distance from the melt–rock interface and were precipitated from late-stage trapped melts. Compositional trends of olivine, pyroxene, and plagioclase are consistent with previous experimental results and natural observations of the Moho Transition Zone. Different lithological sequences form based primarily on the melt–rock ratio, composition of the melt and host peridotite, and thermochemical conditions, but are expected to grade from gabbro to wehrlite or troctolite to peridotite. Plagioclase-bearing peridotite represents the low melt–rock ratio end member where pyroxene is only partially replaced by olivine and melt, whereas dunite is expected to form where melts overwhelm and consume all other phases. This study confirms that under nominally anhydrous conditions, the gabbro–wehrlite–plagioclase-peridotite sequence can be formed by reaction between basalt and lherzolite and subsequent crystallization at intermediate to low pressures. Melt–rock reaction is a fundamental process in the formation of new crust at the shallowest part of the melting column where pyroxene-undersaturated melts percolate through depleted peridotite.  相似文献   

16.
同正常的残余方辉橄榄岩相比,辉南方辉橄榄岩具有异常高的HREE组成和特殊的二次重结晶结构,因此,它们不是上地幔经大程度部分熔融后的残余,而是熔体-岩石反应的结果。倒U型REE分配模式暗示这些样品经历了与玄武质熔体相互作用的历史,并达到了平衡,大量熔(流)体的存在有利于地幔岩石矿物颗粒的增长,从而形成特征的二次重结晶结构。这种“反应”型方辉橄榄岩的形成可能与上涌软流图对岩石圈地幔的热-化学浸蚀有关。“反应型”方辉橄榄岩形成之后,又受到了类似于碳酸岩或富挥发份小体积熔体的交代,因此辉南地区上地幔经历了多期地幔交代作用。  相似文献   

17.
G.B. Piccardo  L. Guarnieri 《Lithos》2011,124(3-4):200-214
Hundred-meter wide cumulate bodies and decimetric dykelets of gabbro-norites are widespread within the distal ophiolitic peridotites from the Jurassic Ligure-Piemontese oceanic basin, now emplaced in the Alpine–Apennine orogenic system. These peridotites derived from the sub-continental mantle of the pre-Triassic Europe–Adria lithosphere and underwent profound modifications of their structural and compositional characteristics via melt–rock interaction during diffuse percolation by porous flow of upwelling asthenospheric melts. Gabbro-norite cumulates show the peculiar association of high forsteritic olivine, high-Mg# clinopyroxenes and orthopyroxenes and high anorthitic plagioclase with respect to mineral compositions in common ophiolitic and oceanic MORB gabbros. Abundance and early crystallization of magnesian orthopyroxene suggests that parental magmas of the gabbro-noritic cumulates were relatively silica-rich basaltic liquids. Clinopyroxenes and plagioclase have anomalously low Sr and LREE, resulting in highly fractionated C1-normalized LREE patterns in clinopyroxenes and negatively fractionated C1-normalized LREE patterns in plagioclases.Modal mineralogy and mineral major and trace element compositions indicate that these gabbro-norites crystallized from MORB-type basaltic liquids that were strongly depleted in Na, Ti, Zr, Sr and other incompatible trace elements relative to any erupted liquids of MORB-type ophiolites and modern oceanic lithosphere. Computed melt compositions in equilibrium with gabbro-norite clinopyroxenes are closely similar to depleted MORB-type single melt increments after 5–7% of fractional melting of a DM asthenospheric mantle source under spinel-facies conditions.Present knowledge on the ophiolitic peridotites of Monte Maggiore indicate that they were formed by interaction of lithospheric mantle protoliths with depleted, MORB-type single melt increments produced by the ascending asthenosphere. Their composition was progressively modified from olivine-saturated to orthopyroxene-saturated by the early reactive melt–peridotite interaction (i.e., pyroxene dissolution and olivine precipitation).Gabbro-norite cumulates marked the change from diffuse porous flow percolation to intrusion and crystallization when cooling by conducive heat loss became dominant on heating by melt percolation. Progressive upwelling and cooling of the host peridotite during rifting caused transition to more brittle conditions and to hydration and serpentinization.The Monte Maggiore peridotite body was then intruded along fractures by variably evolved, Mg–Al- to Fe–Ti-rich gabbroic dykes. Computed melt compositions in equilibrium with clinopyroxenes from less evolved gabbro dykes are closely similar to aggregated MORBs. The event of gabbro intrusion indicates that aggregated MORB-type liquids: i) migrated through and stagnated in the mantle lithosphere and ii) underwent evolution into shallow ephemeral magma chambers to form the parental magmas of the gabbroic dykes and the basaltic lava flows of the Ligurian oceanic crust.  相似文献   

18.
A wide range of trace elements have been analysed in mantle xenoliths (whole rocks, clinopyroxene and amphibole separates) from alkaline lavas in the Eastern Carpathians (Romania), in order to understand the process of metasomatism in the subcontinental mantle of the Carpatho-Pannonian region. The xenoliths include spinel lherzolites, harzburgites and websterites, clinopyroxenites, amphibole veins and amphibole clinopyroxenites. Textures vary from porphyroclastic to granoblastic, or equigranular. Grain size increases with increasing equilibrium temperature of mineralogical assemblages and results from grain boundary migration. In peridotites, interstitial clinopyroxenes (cpx) and amphiboles resulted from impregnation and metasomatism of harzburgites or cpx-poor lherzolites by small quantities of a melt I with a melilitite composition. Clinopyroxenites, amphibole veins and amphibole clinopyroxenites are also formed by metasomatism as a result of percolation through fracture systems of large quantities of a melt II with a melanephelinite composition. These metasomatic events are marked by whole-rock enrichments, relative to the primitive mantle (PM), in Rb, Th and U associated in some granoblastic lherzolites and in clinopyroxene and amphibole veins with enrichments in LREE, Ta and Nb. Correlations between major element whole-rock contents in peridotites demonstrate that the formation of interstitial amphibole and clinopyroxene induced only a slight but variable increase of the Ca/Al ratio without apparent modifications of the initial mantle composition. Metasomatism is also traced by enrichments in the most incompatible elements and the LREE. The Ta, Nb, MREE and HREE contents remained unchanged and confirm the depleted state of the initial but heterogeneous mantle. Major and trace element signature of clinopyroxene suggests that amphibole clinopyroxenites and some granoblastic lherzolites have been metasomatized successively by melts I and II. Both melts I and II were Ca-rich and Si-poor, somewhat alkaline (Na > K). Melt I differed from melt II in having higher Mg and Cr contents offset by lower Ti, Al, Fe and K contents. Both were highly enriched in all incompatible trace elements relative to primitive mantle, showing positive anomalies in Rb, Ba, Th, Sr and Zr. They contrasted by their Ta, Nb and LREE contents, lower in melt I than in melt II. Melts I and II originate during a two-stage melting event from the same source at high pressure and under increasing temperature. The source assemblage could be that of a metasomatized carbonated mantle but was more likely that of an eclogite of crustal affinity. Genetic relationships between calc-alkaline and alkaline lavas from Eastern Carpathians and these melts are thought to be only indirect, the former originating from partial melting of mantle sources respectively metasomatized by the melts I and II. Received: 17 March 1997 / Accepted: 14 July 1997  相似文献   

19.
This work presents the results of geochemical (LA-ICP-MS) study of minerals of peridotites from ophiolite complexes of the Polar Urals to clarify the nature of these formations. The distribution of trace and rare earth elements in clinopyroxenes testifies that there were three types of the mantle substratum, which formed in different geodynamic settings. Two types of primary peridotites were formed upon partial melting of the mantle at different-depth levels in the subduction zone. The first type is represented by lherzolites and diopside harzburgites, formed at partial melting under the spinel facies conditions; the second type is represented by diopside harzburgites, formed under polybaric partial melting under the garnet and spinel facies conditions. In the suprasubduction zone, peridotites experienced fluid-induced partial melting that resulted in crystallization of harzburgites. All types of harzburgites were transformed by ascending melts and fluids (refertilization) and high-temperature hydration with the formation of amphibole. These processes are recorded in variations in the REE spectra of minerals.  相似文献   

20.
Ultramafic xenoliths entrained in the late Miocene alkali basalts and basanites from NW Turkey include refractory spinel-harzburgites and dunites accompanied by subordinate spinel-lherzolites. Whole-rock major and trace element characteristics indicate that the xenoliths are mostly the solid residues of varying degrees of partial melting (~4–~15%), but some have geochemical signatures reflecting the processes of melt/rock interaction. Mantle-normalized trace element patterns for the peridotites vary from LREE-depleted to strongly LREE-enriched, reflecting multistage mantle processes from simple melt extraction to metasomatic enrichment. Rhenium and platinum group element (PGE) abundances and 187Os/188Os systematics of peridotites were examined in order to identify the nature of the mantle source and the processes effective during variable stages of melt extraction within the sub-continental lithospheric mantle (SCLM). The peridotites are characterized by chondritic Os/Ir and Pt/Ir ratios and slightly supra-chondritic Pd/Ir and Rh/Ir ratios, representing a mantle region similar in composition to the primitive mantle (PM). Moderate enrichment in PPGE (Pd–Pt–Rh)/IPGE (Ir–Os–Ru) ratios with respect to the PM composition in the metasomatized samples, however, reflects compositional modification by sulphide addition during possible post-melting processes. The 187Os/188Os ratios of the peridotites range from 0.11801 to 0.12657. Highly unradiogenic Os isotope compositions (γOs at 10 Ma from –7.0 to –3.2) in the chemically undisturbed mantle residues are accompanied by depletion in Re/Os ratios, suggesting long-term differentiation of SCLM by continuous melt extraction. For the metasomatized peridotites, however, systematic enrichments in PPGE and Re abundances, and the observed positive covariance between 187Re/188Os and γOs can most likely be explained by interaction of solid residues with basaltic melts produced by melting of relatively more radiogenic components in the mantle. Significantly, the wide range of 187Os/188Os ratios characterizing the entire xenolith suite seems to be consistent with multistage evolution of SCLM and suggests that parts of the lithospheric mantle contain materials that have experienced ancient melt removal (~1.3 Ga) which created time-integrated depletion in Re/Os ratios; in contrast, some other parts display evidence indicative of recent perturbation in the Re–Os system by sulphide addition during interaction with metasomatizing melts.  相似文献   

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