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1.
《International Geology Review》2012,54(13):1715-1734
This study examines the geochemistry of major and trace elements of abyssal peridotites from the Southwest Indian Ridge (SWIR) (53° E amagmatic segment), to determine the influence of mafic melts on mantle peridotites during melt extraction. The results show a great geochemical variability in the ~90 km-long ridge segment, with a degree of mantle melting ranging from 4% to 24%. An ancient melting event may explain the presence of highly depleted peridotites at the ultraslow-spreading ridge. The 53° E segment peridotites show enrichment of light rare earth elements (LREEs) (average LaN/SmN = 1.87) and significant positive anomaly of U and Pb normalized to primitive mantle (PM). The positive correlations between LREEs (La, Ce, Pr, Nd) and high field strength elements (HFSEs; e.g. Nb and Zr) suggest that the enrichment of LREEs is caused by melt refertilization, which is also supported by prevalent magmatic microstructures in the peridotites. The melt refertilization model shows that the addition of 0.02–2.7% basaltic melts to peridotites can be responsible for the LREE enrichment. We suggest that the positive anomaly of U is probably attributed to fluid alteration whereas the enrichment of Pb is probably attributed to both melt refertilization and fluid alteration. Melt refertilization in the 53° E segment peridotites may be a result of melt–rock reaction and crystallization of melts trapped in peridotites. These processes may be enhanced by increased melt permeability in the mantle owing to the refractory peridotites produced by ancient melting and the decreasing efficiency of melt extraction in the cold and thick lithosphere at the 53° E ridge segment. The presence of melt refertilization implies that melt extraction is incomplete in the ridge mantle, which may be one of the reasons for the extremely thin and irregular variation of the crustal thickness at ultraslow-spreading ridges.  相似文献   

2.
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   

3.
山东五莲七宝山地区早白垩世的碱性侵入岩位于火山机构的中央部位,该岩体具有高Ba-Sr含量、高Nb/Ta和Zr/Hf比、低Ti/Eu比等特征,前人的研究指出其起源于岩石圈地幔。然而,该侵入体中的岩性与成分变化所反映的深部动力学过程尚未理清。本文对七宝山二长辉长岩和两类辉石二长岩开展了详细的矿物学和岩石地球化学研究,识别出钠质和钾质两类钾玄质岩石系列。该套碱性中基性侵入岩具有富碱、富轻稀土和富大离子亲石元素的特征,同时具有高的(La/Yb)N和(Gd/Yb)N值。碱性侵入岩中两类单斜辉石和两类斜长石作为再循环晶,记录了不同批次岩浆/熔体的混合,这些矿物组分和全岩成分共同约束了岩浆的起源与演化过程。结合前人的地球化学资料,本文指出七宝山碱性侵入岩的源区是曾受到沉积物交代的富集地幔,源区存在金云母脉体和角闪石脉体。上述脉体连同周围的地幔橄榄岩共同发生部分熔融,形成原生的碱性熔体。七宝山碱性侵入岩显示高的Nb/Ta和Zr/Hf比、低的Ti/Eu比,同时在微量元素蜘蛛图上呈现Ti*和Hf*的负异常,结合高稀土单斜辉石平衡熔体的属性,共同指示了碳酸盐熔体组分对该套碱性侵入岩的形成发挥了重要作用。钠质系列与钾质系列岩石反映了源区富碱矿物相类型相对贡献量的差异,即钠质为主的碱性岩反映源区角闪石的贡献更大,而钾质为主的碱性岩反映源区金云母的贡献占优势。此外,碱性侵入岩中的钾质系列具有异常高的Rb-Zr-Hf-U含量,很可能反映了源区在部分熔融过程中热液锆石熔解后形成的熔体加入到了钾质岩浆房内。本研究强调了碳酸盐熔体组分对高Nb/Ta碱性中基性的形成发挥着重要作用,亦强调了热液锆石的熔解加入导致岩浆具有高Zr-Hf-U含量的特征。  相似文献   

4.
Melt inclusion and host glass compositions from the easternend of the Southwest Indian Ridge show a progressive depletionin light rare earth elements (LREE), Na8 and (La/Sm)n, but anincrease in Fe8, from the NE (64°E) towards the SW (49°E).These changes indicate an increase in the degree of mantle meltingtowards the SW and correlate with a shallowing of the ridgeaxial depth and increase in crustal thickness. In addition,LREE enrichment in both melt inclusions and host glasses fromthe NE end of the ridge are compatible with re-fertilizationof a depleted mantle source. The large compositional variations(e.g. P2O5 and K2O) of the melt inclusions from the NE end ofthe ridge (64°E), coupled with low Fe8 values, suggest thatmelts from the NE correspond to a variety of different batchesof melts generated at shallow levels in the mantle melting column.In contrast, the progressively more depleted compositions andhigher Fe8 values of the olivine- and plagioclase-hosted meltinclusions at the SW end of the studied region (49°E), suggestthat these melt inclusions represent batches of melt generatedby higher degrees of melting at greater mean depths in the mantlemelting column. Systematic differences in Fe8 values betweenthe plagioclase- and the olivine-hosted melt inclusions in theSW end (49°E) of the studied ridge area, suggest that theplagioclase-hosted melt inclusions represent final batches ofmelt generated at the top of the mantle melting column, whereasthe olivine-hosted melt inclusions correspond to melts generatedfrom less depleted, more fertile mantle at greater depths. KEY WORDS: basalt; melt inclusions; olivine; plagioclase; Southwest Indian Ridge  相似文献   

5.
Fluids or melts derived from a subducting plate are often citedas a mechanism for the oxidation of arc magmas. What remainsunclear is the link between the fluid, oxygen fugacity, andother major and trace components, as well as the spatial distributionof the impact of those fluids. To test the potential effectsof addition of a subduction-derived fluid or melt to the sub-arcmantle, olivine-hosted melt inclusions from primitive basalticlavas sampled from across the central Oregon Cascades (43°–45°N)have been analyzed for major, trace and volatile elements andfO2. Oxygen fugacity was determined in melt inclusions fromsulfur speciation determined by electron microprobe and fromolivine–chromite oxygen geobarometry. The overall rangein fO2 based on sulfur speciation measurements is from <–0·25log units to + 1·9 log units (FMQ, where FMQ is fayalite–magnetite–quartzbuffer). Oxygen fugacity is positively correlated with fluid-mobiletrace element and light rare earth element contents in basaltsgenerated by relatively low-degree partial melting. Establishinga further correlation between fO2 and fluid-mobile trace elementabundances with position along the arc requires the basaltsto be subdivided into shoshonitic, calc-alkaline, low-K tholeiiteand enriched intraplate basalt groups. Melt inclusions fromenriched intraplate and shoshonitic lavas show increasing fO2and trace element abundances closer to the trench, whereas calc-alkalinemelt inclusions exhibit no significant across-arc variations.Low-K tholeiitic melt inclusions record an increase in incompatibletrace elements closer to the trench; however, there is no correlatedincrease in fO2. The correlation observed in enriched intraplateand shoshonitic melt inclusions is interpreted to reflect aprogressively greater proportion of a fluid-rich, oxidized subductioncomponent in magmas generated nearer the subduction zone. Significantly,calc-alkaline melt inclusions with high ratios of large ionlithophile elements to high field strength elements, characteristicof ‘typical’ arc magmas, have oxidation states indistinguishablefrom low-K tholeiite and enriched intraplate basalt melt inclusions.The lack of across-arc geochemical variation in calc-alkalinemelt inclusions may suggest that these basalts are not necessarilythe most appropriate magmas for examining recent addition ofa subduction component to the sub-arc mantle. Flux and batchmelt model results produce a wide range of predicted amountsof melting and subduction component added to the mantle source;however, general trends characterized by increased melting andproportion of the subduction component from enriched intraplate,to low-K tholeiite, to calc-alkaline are robust. The model resultsdo not require enriched intraplate, low-K tholeiite and calc-alkalinemagmas to be produced from the same more fertile mantle source.However, enriched intraplate magmas, in contrast to calc-alkalineand low-K tholeiite magmas, cannot be generated from a depletedmantle source. Flux or batch melting of either the more fertileor depleted mantle sources used to generate the low-K tholeiite,calc-alkaline, and enriched intraplate magmas cannot reproduceshoshonitic compositions, which require a significantly depletedmantle source strongly metasomatized by a subduction component.The potential mantle source for shoshonitic basalts has a predictedfO2 (after oxidation) from + 0·3 to + 2·4 logunits (FMQ) whereas the mantle source for low-K tholeiite, calc-alkaline,and enriched intraplate magmas may range from –1·1to + 0·7 log units (FMQ). KEY WORDS: basalt; Cascades; melt inclusions; oxidation state; volatiles  相似文献   

6.
The main plutonic complex of the Troodos ophiolite, north of the Arakapas Fault Zone, has been re-examined both from field and geochemical perspectives. Ion microprobe analyses of clinopyroxene crystal cores show that the range of melt compositions added to the lower crust far exceeds that of published lavas in the main Troodos massif. This suggests that the lower crust acted as a filter into which a large range of melt compositions were added and out of which a homogenised (and generally fractionated) derivative was extracted. This crustal-level aggregation homogenised diverse melt fractions from a broad range of degrees of melting. Depleted melts with U-shaped rare earth element (REE) patterns were a significant component of the melts added to the crust, but because of their low incompatible element abundances, mixing with less depleted melts prior to eruption masked their signature in the lavas. The discovery that highly depleted melts constituted a significant component of the melts added to the Troodos crust, but not of the lavas, demonstrates that the spatial distribution of lava-types is not necessarily a good indicator of where different parental melt compositions are generated within the mantle. Compared with normal mid-ocean ridge basalts, the Troodos parental melts were (1) generally depleted in immobile incompatible trace elements, (2) less depleted in light REE (LREE) than would be expected for the concomitant depletion in middle and heavy REE, (3) enriched in Sr with respect to the LREE and (4) more oxidised. Modelling of these characteristics suggests a mantle source that had previously lost a significant melt fraction under relatively reducing conditions. This was followed by remelting under more oxidising conditions in an environment in which Sr and LREE were added to the source consistent with previous models of a supra-subduction zone setting.  相似文献   

7.
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   

8.
The Yarlung Zangbo suture zone (YZSZ) in southern Tibet includes the remnants of Neo‐Tethyan oceanic lithosphere and marks a major suture between the Indian plate to the south and the Lhasa terrane of Tibet to the north. The upper mantle section of the Cuobuzha ophiolite in the northern subbelt of the western YZSZ comprises mainly clinopyroxene (cpx)‐rich and depleted harzburgites. Spinels in the cpx‐harzburgites show lower Cr# values (12.6–15.1) than the spinels in the harzburgites (26.1–34.5), and the cpx‐harzburgites display higher heavy rare earth element concentrations than the depleted harzburgites. The harzburgites have subchondritic Os isotopic compositions (0.11624–0.11699), yielding Re‐depletion model ages (TRD) ages from 1.8 to 1.7 Ga, indicating that the Cubuzha mantle underwent at least one ancient melt extraction event ca. 1.8‐1.7Ga; whereas the cpx‐harzburgites have suprachondritic 187Os/188Os ratios (0.12831–0.13125) with higher Re concentrations (0.380–0.575 ppb), indicating subsequent addition of Re following the last partial melting event that occurred during mid‐ocean ridge melt evolution processes. Although these geochemical and isotopic signatures suggest that both peridotite types in the ophiolite represent mid‐oceanic ridge–type upper mantle units, their melt evolution trends reflect different mantle processes. The cpx‐harzburgites formed from low‐degree partial melting of a primitive mantle source, and they were subsequently modified by melt‐rock interactions in a mid‐oceanic ridge environment. The depleted harzburgites, however, were produced by remelting of the cpx‐harzburgites, which later interacted with mid‐oceanic ridge basalt– or island‐arc tholeiite–like melts, possibly in a trench–distal backarc spreading center. Our new isotopic and geochemical data from the Cuobuzha peridotites confirm that the Neo‐Tethyan upper mantle had highly heterogeneous Os isotopic compositions as a result of multiple melt production and melt extraction events during its seafloor spreading evolution.  相似文献   

9.
对华北克拉通北缘达里诺尔地区鸽子山附近玄武岩中的含金云母辉石岩捕虏体进行了岩石学、矿物学的研究,并对其中的单斜辉石、斜方辉石、金云母和粒间熔体进行了原位微区主、微量元素分析。结果显示,单斜辉石和斜方辉石具有低的Mg^#、Cr 2O 3和高的Al2O3含量,斜方辉石还具有高的MnO含量,这些特征表明辉石岩代表了交代熔体在地幔中冷却固结堆晶形成的岩脉。辉石岩中金云母、粒间熔体的出现及其不平衡的地球化学特征说明辉石岩形成以后又遭受到了多期次的硅酸盐熔体地幔交代作用。结晶出单斜辉石的母岩浆在蛛网图上具有K、Pb元素的弱负异常但不具有Nb、Ta、Ti元素的负异常,推测形成辉石岩的熔体可能来自软流圈地幔。粒间熔体的低SiO2,高MgO和FeO的特征指示其形成于地幔超基性岩的部分熔融,蛛网图上明显的K、Pb正异常以及Nb、Ta负异常说明其源区也存在俯冲沉积物的贡献。基于此,认为中国东部新生代岩石圈地幔经历了多期次地幔交代作用。  相似文献   

10.
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   

11.
The development of petrogenetic models of igneous processes in the mantle is dependent on a detailed knowledge of the diversity of magmas produced in the melting regime. These primary magmas, however, undergo significant mixing and fractionation during transport to the surface, destroying much of the evidence of their primary diversity. To circumvent this problem and to determine the diversity of melts produced in the mantle, we used melt inclusions hosted in primitive plagioclase phenocrysts from eight mid-ocean ridge basalts from the axial and West Valleys of the Endeavour Segment, Juan de Fuca Ridge. This area was selected for study because of the demonstrated close association of enriched (E-MORB) lavas and incompatible element enriched depleted (N-MORB) lavas. Rehomogenized melt inclusions from E-MORB, T-MORB, and N-MORB lavas have been analyzed by electron and ion microprobe for major and trace elements. The depleted and enriched lavas, as well as their melt inclusions, have very similar compatible element concentrations (major elements, Sr, Ni and Cr). Inclusion compositions are more primitive than, yet collinear with, the host lava suites. In contrast, the minor and trace element characteristics of melt inclusions from depleted and enriched lavas are different both in range and absolute concentration. N-MORB lavas contain both depleted and enriched melt inclusions, and therefore exhibit the largest compositional range (K2O: 0.01 to 0.4 oxide wt%, P2O5: <0.01 to 0.2 oxide wt%, LaN: 7 to 35, YbN: 1 to 13, and Ti/Zr: <100 to 1300). E-MORB lavas contain only enriched inclusions, and are therefore relatively homogeneous (K2O: 0.32 to 0.9 oxide wt %, P2O5: 0.02 to 0.35 oxide wt%, LaN: 11 to 60, YbN: 4 to 21, and Ti/Zr: ∼100). In addition, the most primitive E-32 inclusions are similar in composition to the most enriched inclusions from the depleted hosts. Major element data for melt inclusions from both N-MORB and E-MORB lavas suggest that the magmas lie on a low pressure cotectic, consistent with a petrogenesis including fractional crystallization. However, the minor and trace element compositions in melt inclusions vary independently of the major element composition implying an alternative history. When fractionation-corrected, inclusion compositions correlate with their host glass composition. Hence, the degree of enrichment of the lavas is a function of the composition of aggregated melts, not of processing in the upper mantle or lower crust. Based on this fact, the lava suites are not produced from a single parent magma, but from a suite of primary magmas. The chemistry of the melt inclusions from the enriched lavas is consistent with a derivation from variable percentages of partial melting within the spinel stability field by a process of open system (continuous or critical) melting assuming a depleted lherzolite source veined with clinopyroxenite. The low percentage melts are dominantly enriched melts of the clinopyroxenite. In contrast, the depleted lavas were created by melting of a harzburgite source, possibly fluxed with a fluid enriched in K, Ba and the LREE. Such a source was likely melted up to or past the point at which all of its clinopyroxene was consumed. This set of characteristics is consistent with a scenario by which diverse melts produced at different depths travel through the melting regime to the base of the crust without homogenizing en route. The homogeneous major element characteristics are created in the lower crust by fractional crystallization and reaction with lower crustal gabbros. Therefore, the degree of decoupling between major and trace element characteristics of the melt inclusions (and lavas) is dictated by the reaction rate of the melts with the materials in the conduit walls, as well as the residence times and flux rate, in the upper mantle and lower crust. Received: 2 December 1997 / Accepted: 27 August 1998  相似文献   

12.
The importance of melt extraction for tracing mantle heterogeneity   总被引：3，自引：0，他引：3  
Numerous isotope and trace element studies of mantle rocks and oceanic basalts show that the Earth’s mantle is heterogeneous. The isotopic variability in oceanic basalts indicates that most mantle sources consist of complex assemblages of two or more components with isolated long-term chemical evolution, on both global and local scales. The range in isotope and highly incompatible element ratios observed in oceanic basalts is commonly assumed to directly reflect that of their mantle sources. Accordingly, the end-points of isotope arrays are taken to represent the isotopic composition of the different components in the underlying mantle, which is then used to deduce the origin of mantle heterogeneity. Here, a melting model for heterogeneous mantle sources is presented that investigates how and to what extent isotope and trace element signatures are conveyed from source to melt. We model melting of a pyroxenite-bearing peridotite using recent experimental constrains for melting and partitioning of pyroxenite and peridotite. Identification of specific pyroxenite melting signatures allows finger-printing of pyroxenite melts and confirm the importance of lithological heterogeneity in the Earth’s mantle. The model results and the comparison of the calculated and observed trace element-isotope systematics in selected MORB and OIB suites (e.g. from the East Pacific Rise, Iceland, Tristan da Cunha, Gough and St.Helena) further show that factors such as the relative abundance of different source components, their difference in solidus temperature, and especially the extent, style and depth range of melt aggregation fundamentally influence the relationship between key trace element and isotope ratios (e.g. Ba/Th, La/Nb, Sr/Nd, La/Sm, Sm/Yb, 143Nd/144Nd). The reason for this is that any heterogeneity present in the mantle is averaged or, depending on the effectiveness of the melt mixing process, even homogenized during melting and melt extraction. Hence to what degree mantle heterogeneity is reflected in the erupted melts is not only a function of source and melting-induced variability. It also depends on the extent of mixing during melting and melt extraction and thus strongly on the relative incompatibility of the elements considered. The observed trace element variation in erupted melts can be greater or smaller than that of their mantle sources, depending on the incompatibility of the elements investigated. The isotopic variability in erupted melts, on the other hand, is generally smaller than that of their mantle source. Melt mixing during melt extraction consequently has an important influence on the relative extent of variation, and hence the degree of correlation between the isotope and trace element ratios. Overall fewer correlations between trace element and isotope ratios are expected whenever melts are extracted from a restricted depth range, as is the case for ocean island basalts, than for cases where melts are extracted over a larger depth interval (mid ocean ridges and especially ridge centered hotspots like Iceland). While the isotopic composition of the most enriched melts may correspond closely to those of the enriched source component, even the most depleted mid ocean ridge basalts are likely to underestimate the isotopic depletion of the depleted mantle component. These observations imply that using the chemical and isotopic range observed in oceanic basalts as directly representative of that in the corresponding mantle source can be misleading, since this assumption is strictly true only for homogeneous mantle sources. In addition to identifying source or partitioning-related differences in melts from different mantle sources, inferring the true composition, origin, and distribution of heterogeneous components in the Earth’s mantle therefore requires detailed knowledge about the mechanisms of melting and melt mixing during the melt extraction process. Only if these processes and their influence on the isotope-trace element relationship are understood, can the composition and origin of the different source components, and thus mantle heterogeneity, be accurately constrained.  相似文献   

13.
《地学前缘(英文版)》2018,9(6):1755-1775
The ophiolite suite from south Andaman Islands forms part of the Tethyan Ophiolite Belt and preserves the remnants of an ideal ophiolite sequence comprising a basal serpentinized and tectonised mantle peridotite followed by ultramafic and mafic cumulate units, basaltic dykes and spilitic pillow basalts interlayered with arkosic wacke. Here, we present new major, trace, rare earth(REE) and platinum group(PGE) element data for serpentinized and metasomatized peridotites(dunites) exposed in south Andaman representing the tectonized mantle section of the ophiolite suite. Geochemical features of the studied rocks, marked by Al_2 O_3/TiO_2 23, LILE-LREE enrichment, HFSE depletion, and U-shaped chondrite-normalized REE patterns with(La/Sm)N 1 and(Gd/Yb)N 1, suggest contributions from boninitic mantle melts. These observations substantiate a subduction initiation process ensued by rapid slab roll-back with extension and seafloor spreading in an intraoceanic fore-arc regime. The boninitic composition of the serpentinized peridotites corroborate fluid and melt interaction with mantle manifested in terms of(i) hydration, metasomatism and serpentinization of depleted, MORB-type, sub-arc wedge mantle residual after repeated melt extraction; and(ii) refertilization of refractory mantle peridotite by boninitic melts derived at the initial stage of intraoceanic subduction. Serpentinized and metasomatized mantle dunites in this study record both MOR and intraoceanic arc signatures collectively suggesting suprasubduction zone affinity. The elevated abundances of Pd(4.4-12.2 ppb) with highΣPPGE/∑IPGE(2-3) and Pd/Ir(2-5.5) ratios are in accordance with extensive melt-rock interaction through percolation of boninitic melts enriched in fluid-fluxed LILE-LREE into the depleted mantle after multiple episodes of melt extraction. The high Pd contents with relatively lower Ir concentrations of the samples are analogous to characteristic PGE signatures of boninitic magmas and might have resulted by the infiltration of boninitic melts into the depleted and residual mantle wedge peridotite during fore-arc extension at the initial stage of intraoceanic subduction. The PGE patterns with high Os + Ir(2-8.6 ppb)and Ru(2.8-8.4 ppb) also suggest mantle rejuvenation by infiltration of melts derived by high degree of mantle melting. The trace, REE and PGE data presented in our study collectively reflect heterogeneous mantle compositions and provide insights into ocean-crust-mantle interaction and associated geochemical cycling within a suprasubduction zone regime.  相似文献   

14.
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   

15.
Laboratory experiments on natural, hydrous basalts at 1–4 GPa constrain the composition of “unadulterated” partial melts of eclogitized oceanic crust within downgoing lithospheric slabs in subduction zones. We complement the “slab melting” experiments with another set of experiments in which these same “adakite” melts are allowed to infiltrate and react with an overlying layer of peridotite, simulating melt:rock reaction at the slab–mantle wedge interface. In subduction zones, the effects of reaction between slab-derived, adakite melts and peridotitic mantle conceivably range from hybridization of the melt, to modal or cryptic metasomatism of the sub-arc mantle, depending upon the “effective” melt:rock ratio. In experiments at 3.8 GPa, assimilation of either fertile or depleted peridotite by slab melts at a melt:rock ratio 2:1 produces Mg-rich, high-silica liquids in reactions which form pyrope-rich garnet and low-Mg# orthopyroxene, and fully consume olivine. Analysis of both the pristine and hybridized slab melts for a range of trace elements indicates that, although abundances of most trace elements in the melt increase during assimilation (because melt is consumed), trace element ratios remain relatively constant. In their compositional range, the experimental liquids closely resemble adakite lavas in island-arc and continental margin settings, and adakite veins and melt inclusions in metasomatized peridotite xenoliths from the sub-arc mantle. At slightly lower melt:rock ratios (1:1), slab melts are fully consumed, along with peridotitic olivine, in modal metasomatic reactions that form sodic amphibole and high-Mg# orthopyroxene.  相似文献   

16.
《地学前缘(英文版)》2018,9(6):1809-1827
This study reports major, trace, rare earth and platinum group element compositions of lava flows from the Vempalle Formation of Cuddapah Basin through an integrated petrological and geochemical approach to address mantle conditions, magma generation processes and tectonic regimes involved in their formation. Six flows have been identified on the basis of morphological features and systematic three-tier arrangement of vesicular-entablature-colonnade zones. Petrographically, the studied flows are porphyritic basalts with plagioclase and clinopyroxene representing dominant phenocrystal phases.Major and trace element characteristics reflect moderate magmatic differentiation and fractional crystallization of tholeiitic magmas. Chondrite-normalized REE patterns corroborate pronounced LREE/HREE fractionation with LREE enrichment over MREE and HREE. Primitive mantle normalized trace element abundances are marked by LILE-LREE enrichment with relative HFSE depletion collectively conforming to intraplate magmatism with contributions from sub-continental lithospheric mantle(SCLM) and extensive melt-crust interaction. PGE compositions of Vempalle lavas attest to early sulphur-saturated nature of magmas with pronounced sulphide fractionation, while PPGE enrichment over IPGE and higher Pd/Ir ratios accord to the role of a metasomatized lithospheric mantle in the genesis of the lava flows. HFSEREE-PGE systematics invoke heterogeneous mantle sources comprising depleted asthenospheric MORB type components combined with plume type melts. HFSE-REE variations account for polybaric melting at variable depths ranging from garnet to spinel lherzolite compositional domains of mantle. Intraplate tectonic setting for the Vempalle flows with P-MORB affinity is further substantiated by(i) their origin from a rising mantle plume trapping depleted asthenospheric MORB mantle during ascent,(ii) interaction between plume-derived melts and SCLM,(iii) their rift-controlled intrabasinal emplacement through Archeane Proterozoic cratonic blocks in a subduction-unrelated ocean-continent transition zone(OCTZ). The present study is significant in light of the evolution of Cuddapah basin in the global tectonic framework in terms of its association with Antarctica, plume incubation, lithospheric melting and thinning, asthenospheric infiltration collectively affecting the rifted margin of eastern Dharwar Craton and serving as precursors to supercontinent disintegration.  相似文献   

17.
Late Miocene–Pliocene to Quaternary calc-alkaline lava flows and domes are exposed in southeast of Isfahan in the Urumieh Dokhtar magmatic belt in the Central Iran structural zone. These volcanic rocks have compositions ranging from basaltic andesites, andesites to dacites. Geochemical studies show these rocks are a medium to high K calc-alkaline suite and meta-aluminous. Major element variations are typical for calc-alkaline rocks. The volcanic rocks have SiO2 contents ranging between 53.8% and 65.3%. Harker diagrams clearly show that the dacitic rocks did not form from the basaltic andesites by normal differentiation processes. They show large ion lithophile elements- and light rare earth elements (LREE)-enriched normalized multielement patterns and negative Nb, Ti, Ta, and P. Condrite-normalized REE patterns display a steep decrease from LREE to light rare earth elements without any Eu anomaly. These characteristics are consistent with ratios obtained from subduction-related volcanic rocks and in collision setting. The melting of a heterogeneous source is possible mechanism for their magma genesis, which was enriched in incompatible elements situated at the upper continental lithospheric mantle or lower crust. The geochemical characteristics of these volcanic rocks suggested that these volcanic rocks evolved by contamination of a parental magma derived from metasomatized upper lithospheric mantle and crustal melts.  相似文献   

18.
The islands of the Azores archipelago emerge from an oceanic plateau built on lithosphere increasing in age with distance from the Mid-Atlantic Ridge from 10 to 45 Ma. Here, we present the first comprehensive major and trace element and Sr–Nd–Pb isotope data from Santa Maria, the easternmost island of the archipelago, along with published data from the other Azores islands situated much closer to the Mid-Atlantic Ridge axis. We can show that the distinctively more variable and more enriched trace element ratios at Santa Maria combined with a relatively small range in Sr–Nd–Pb isotope ratios are the result of low degrees of partial melting of a common Azores mantle plume source underneath thicker lithosphere. This implies that melt extraction processes and melting dynamics may be able to better preserve the trace element mantle source variability underneath thicker lithosphere. These conclusions may apply widely for oceanic melts erupted on relatively thick lithosphere. In addition, lower Ti/Sm and K/La ratios and SiO2 contents of Santa Maria lavas imply melting of a carbonated peridotite source. Mixing of variable portions of deep small-degree carbonated peridotite melts and shallow volatile-free garnet peridotite could explain the geochemical variability underneath Santa Maria in agreement with the volatile-rich nature of the Azores mantle source. However, Santa Maria is the Azores island where the CO2-rich nature of the mantle source is more evident, reflecting a combination of a smaller extent of partial melting and the positioning at the edge of the tilted Azores mantle plume.  相似文献   

19.
 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   

20.
Four muscovite-biotite granites from the Western Metamorphic Belt of South-eastern Australia have rare earth element patterns characterized by: (i) light rare earth element enrichment; (ii) slight Eu depletion; (iii) varying degrees of heavy rare earth element depletion. The rare earth element and major element chemistry of three of these muscovite-biotite granites (the Koetong, Lockharts and Yabba Granites) can be approximated very closely by a model involving 20% partial melting of an ultrametamorphosed pelitic sediment and contamination of this minimum melt by the residual material left after melting, in the ratio 60% melt: 40% residue. Granitoids can be very largely solid material at the time of emplacement.The other muscovite-biotite granite studied (the Hawksview Granite) has major and trace element characteristics which distinguish if from the other three granitoids and these differences are attributed to variations in source material at the site of melt generation.The rare earth element and major element chemistry of a garnet-cordierite gneiss from the Western Metamorphic Belt can be modelled assuming 5% partial melting of a pelitic metamorphic rock and contamination of the minimum melt by the residue in the ratio 30% melt: 70% residue.Separated granitic and biotitic portions of a migmatite from the Western Metamorphic Belt have rare earth element characteristics which are inconsistent with a simple partial-melting model, but it is suggested that re-equilibration following, or during, separation of the vein material could obscure the process by which the vein of the migmatite developed. It is however certain that the vein developed in situ from a pelitic meta-sediment leaving the biotite rich selvage, without the introduction of material from an external source.Leucogranites which crop out to the east of the Western Metamorphic Belt are high level intrusions of highly fractionated granitic melt. Their Sr isotopic characteristics and features of their major and trace element chemistry suggest that they derive from an igneous source and are not directly related to the granites and gneisses to the west.  相似文献   

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