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1.
 We have investigated new samples from the Gees mantle xenolith suite (West Eifel), for which metasomatism by carbonatite melt has been suggested. The major metasomatic change is transformation of harzburgites into phlogopite-rich wehrlites. Silicate glasses are associated with all stages of transformation, and can be resolved into two major groups: a strongly undersaturated alkaline basanite similar to the host magma which infiltrated the xenoliths during ascent, and Si-Al-enriched, variably alkaline glass present exclusively within the xenoliths. Si-Al-rich glasses (up to 72 wt% SiO2 when associated with orthopyroxene (Opx) are usually interpreted in mantle xenoliths as products of decompressional breakdown of hydrous phases like amphibole. In the Gees suite, however, amphibole is not present, nor can the glass be related to phlogopite breakdown. The Si-Al-rich glass is compositionally similar to glasses occurring in many other xenolith suites including those related to carbonatite metasomatism. Petrographically the silicate glass is intimately associated with the metasomatic reactions in Gees, mainly conversion of harzburgite orthopyroxene to olivine + clinopyroxene. Both phases crystallize as microlites from the glass. The chemical composition of the Si-Al-enriched glass shows that it cannot be derived from decompressional melting of the Gees xenoliths, but must have been present prior to their entrainment in the host magma. Simple mass-balance calculations, based on modal analyses, yield a possible composition of the melt prior to ascent of the xenoliths, during which glass + microlite patches were modified by dissolution of olivine, orthopyroxene and spinel. This parental melt is a calc-alkaline andesite (55–60 wt% SiO2), characterized by high Al2O3 (ca. 18 wt%). The obtained composition is very similar to high-alumina, calc-alkaline melts that should form by AFC-type reactions between basalt and harzburgite wall rock according to the model of Kelemen (1990). Thus, we suggest that the Si-Al-enriched glasses of Gees, and possibly of other suites as well, are remnants of upper mantle hybrid melts, and that the Gees suite was metasomatized by silicate and not carbonatite melts. High-Mg, high-Ca composition of metasomatic olivine and clinopyroxene in mantle xenoliths have been explained by carbonatite metasomatism. As these features are also present in the Gees suite, we have calculated the equilibrium Ca contents of olivine and clinopyroxene using the QUI1F thermodynamical model, to show that they are a simple function of silica activity. High-Ca compositions are attained at low a SiO2 and can thus be produced during metasomatism by any melt that is Opx-undersaturated, irrespective of whether it is a carbonatite or a silicate melt. Such low a SiO2 is recorded by the microlites in the Gees Si-Al-rich glasses. Our results imply that xenolith suites cannot confidently be related to carbonatite metasomatism if the significance of silicate glasses, when present, is not investigated. Received: 2 March 1995 / Accepted: 12 June 1995  相似文献   

2.
Textural evidence in a composite garnet harzburgite mantle xenolith from Kimberley, South Africa, suggests metasomatism of a severely melt-depleted substrate by a siliceous, volatile-rich fluid. The fluid reacted with olivine-rich garnet harzburgite, converting olivine to orthopyroxene, forming additional garnet and introducing phlogopite, and small quantities of sulfide and probable carbonate. Extensive reaction (>50%) forming orthopyroxenite resulted from channelized flow in a vein, with orthopyroxene growth in the surrounding matrix from a pervasive grain-boundary fluid. The mineralogy of the reaction assemblage and the bulk composition of the added component dominated by Si and Al, with lesser quantities of K, Na, H, C and S, are consistent with experimental studies of hybridization of siliceous melts or fluids with peridotite. However, low Na, Fe and Ca compared with melts of eclogite suggest a fluid phase that previously evolved by reaction with peridotitic mantle. Garnet and phlogopite trace element compositions indicate a fluid rich in large-ion lithophile (LIL) elements, but poor in high field-strength elements (HFSE), qualitatively consistent with subduction zone melts and fluids. An Os isotope (TRD) model age of 2.97 ± 0.04 Ga and lack of compositional zonation in the xenolith indicate an ancient origin, consistent with proposed 2.9 Ga subduction and continental collision in the Kimberley region. The veined sample reflects the silicic end of a spectrum of compositions generated in the Kimberley mantle lithosphere by the metasomatizing effects of fluids derived from oceanic lithosphere. These results provide petrographic and chemical evidence for fluid-mediated Si-, volatile- and trace-element metasomatism of Archean mantle, and support models advocating large-scale modification of regions of Archean subcontinental mantle by subduction processes that occurred in the Archean.  相似文献   

3.
Glass-bearing inclusions hosted by Cr-spinel in harzburgite xenoliths from Avacha are grouped based on homogenization temperatures and daughter minerals into high-T (1,200°C; opx + cpx), intermediate (900–1,100°C; cpx ± amph), and low-T (900°C; amph) and are commonly accompanied by larger “melt pockets”. Unlike previous work on unheated inclusions and interstitial glass in xenoliths from Kamchatka, the homogenized glass compositions in this study are not affected by low-pressure melt fractionation during transport and cooling or by interaction with host magma. Primary melt compositions constrained for each inclusion type differ in major and trace element abundances and were formed by different events, but all are silica saturated, Ca-rich, and K-poor, with enrichments in LREE, Sr, Rb, and Ba and negative Nb anomalies. These melts are inferred to have been formed with participation of fluids produced by dehydration of slab materials. The high-T inclusions trapped liquids produced by ancient high-degree, fluid-induced melting in the mantle wedge. The low-T inclusions are related to percolation of low-T melts or hydrous fluids in arc mantle lithosphere. Melt pockets arise from localized heating and fluid-assisted melting induced by rising magmas shortly before the entrapment of the xenoliths. The “high-T” melt inclusions in Avacha xenoliths are unique in preserving evidence of ancient, high-T melting events in arc mantle, whereas the published data appear to characterize pre-eruption enrichment events.  相似文献   

4.
Hydrous K-rich kimberlite-like systems are studied experimentally at 5.5–7.5 GPa and 1200–1450?°C in terms of phase relations and conditions for formation and stability of phlogopite. The starting samples are phlogopite–carbonatite–phlogopite sandwiches and harzburgite–carbonatite mixtures consisting of Ol?+?Grt?+?Cpx?+?L (±Opx), according to the previous experimental results obtained at the same P–T parameters but in water-free systems. Carbonatite is represented by a K- and Ca-rich composition that may form at the top of a slab. In the presence of carbonatitic melt, phlogopite can partly melt in a peritectic reaction at 5.5 GPa and 1200–1350?°C, as well as at 6.3–7.0 GPa and 1200?°C: 2Phl?+?CaCO3 (L)?Cpx?+?Ol?+?Grt?+?K2CO3 (L)?+?2H2O (L). Synthesis of phlogopite at 5.5 GPa and 1200–1350?°C, with an initial mixture of H2O-bearing harzburgite and carbonatite, demonstrates experimentally that equilibrium in this reaction can be shifted from right to left. Therefore, phlogopite can equilibrate with ultrapotassic carbonate–silicate melts in a?≥?150?°C region between 1200 and 1350?°C at 5.5 GPa. On the other hand, it can exist but cannot nucleate spontaneously and crystallize in the presence of such melts in quite a large pressure range in experiments at 6.3–7.0 GPa and 1200?°C. Thus, phlogopite can result from metasomatism of peridotite at the base of continental lithospheric mantle (CLM) by ultrapotassic carbonatite agents at depths shallower than 180–195 km, which creates a mechanism of water retaining in CLM. Kimberlite formation can begin at 5.5 GPa and 1350?°C in a phlogopite-bearing peridotite source generating a hydrous carbonate–silicate melt with 10–15 wt% SiO2, Ca# from 45 to 60, and high K enrichment. Upon further heating to 1450?°C due to the effect of a mantle plume at the CLM base, phlogopite disappears and a kimberlite-like melt forms with SiO2 to 20 wt% and Ca#?=?35–40.  相似文献   

5.
Ultramafic xenoliths from a veined mantle wedge beneath the Kamchatka arc have non-chondritic, fractionated chondrite-normalized platinum-group element (PGE) patterns. Depleted (e.g., low bulk-rock Al2O3 and CaO contents) mantle harzburgites show clear enrichment in the Pd group relative to the Ir group PGEs and, in most samples, Pt relative to Rh and Pd. These PGE signatures most likely reflect multi-stage melting which selectively concentrates Pt in Pt–Fe alloys while strongly depleting the sub-arc mantle wedge in incompatible elements. Elevated gold concentrations and enrichment of strongly incompatible enrichment (e.g., Ba and Th) in some harzburgites suggest a late-stage metasomatism by slab-derived, saline hydrous fluids. Positive Pt, Pd, and Au anomalies coupled with Ir depletions in heavily metasomatized pyroxenite xenoliths probably reflect the relative mobility of the Pd and Ir groups (especially Os) during sub-arc metasomatism which is consistent with Os systematics in arc mantle nodules. Positive correlations between Pt, Pd, and Au and various incompatible elements (Hf, U, Ta, and Sr) also suggest that both slab-derived hydrous fluids and siliceous melts were involved in the sub-arc mantle metasomatism beneath the Kamchatka arc.  相似文献   

6.
Lithium elemental and isotopic disequilibrium has frequently been observed in the continental and oceanic mantle xenoliths, but its origin remains controversial. Here, we present a combined elemental and Li isotopic study on variably metasomatised peridotite xenoliths entrained in the Cenozoic basalts from Shangzhi in Northeast (NE) China that provides insight into this issue. Li concentration (0.3–2.7 ppm) and δ7Li (mostly 2‰–6‰) in olivine from the Shangzhi peridotites are similar to the normal mantle values and show roughly negative correlations with the indices of melt extraction (such as modal olivine and whole rock MgO). These features are consistent with variable degrees of partial melting. In contrast, clinopyroxene from the Shangzhi xenoliths shows significant Li enrichment (0.9–6.1 ppm) and anomalously light δ7Li (??13.8‰ to 7.7‰) relative to normal mantle values. Such features can be explained by Li diffusion from silicate melts or Li-rich fluids occurring over a very short time (several minutes to several hours). Moreover, the light Li isotopic compositions preserved in some bulk samples also indicate that these percolated melts/fluids have not had enough time to isotopically equilibrate with the bulk peridotite. We thus emphasize that Li isotopic fractionation in the Shangzhi mantle xenoliths is mainly related to Li diffusion from silicate melts or Li-rich fluids that took place shortly before or coincident with their entrainment into the host magmas.  相似文献   

7.
This experimental study examines the mineral/melt partitioning of incompatible trace elements among high-Ca clinopyroxene, garnet, and hydrous silicate melt at upper mantle pressure and temperature conditions. Experiments were performed at pressures of 1.2 and 1.6 GPa and temperatures of 1,185 to 1,370 °C. Experimentally produced silicate melts contain up to 6.3 wt% dissolved H 2O, and are saturated with an upper mantle peridotite mineral assemblage of olivine+orthopyroxene+clinopyroxene+spinel or garnet. Clinopyroxene/melt and garnet/melt partition coefficients were measured for Li, B, K, Sr, Y, Zr, Nb, and select rare earth elements by secondary ion mass spectrometry. A comparison of our experimental results for trivalent cations (REEs and Y) with the results from calculations carried out using the Wood-Blundy partitioning model indicates that H 2O dissolved in the silicate melt has a discernible effect on trace element partitioning. Experiments carried out at 1.2 GPa, 1,315 °C and 1.6 GPa, 1,370 °C produced clinopyroxene containing 15.0 and 13.9 wt% CaO, respectively, coexisting with silicate melts containing ~1–2 wt% H 2O. Partition coefficients measured in these experiments are consistent with the Wood-Blundy model. However, partition coefficients determined in an experiment carried out at 1.2 GPa and 1,185 °C, which produced clinopyroxene containing 19.3 wt% CaO coexisting with a high-H 2O (6.26±0.10 wt%) silicate melt, are significantly smaller than predicted by the Wood-Blundy model. Accounting for the depolymerized structure of the H 2O-rich melt eliminates the mismatch between experimental result and model prediction. Therefore, the increased Ca 2+ content of clinopyroxene at low-temperature, hydrous conditions does not enhance compatibility to the extent indicated by results from anhydrous experiments, and models used to predict mineral/melt partition coefficients during hydrous peridotite partial melting in the sub-arc mantle must take into account the effects of H 2O on the structure of silicate melts.  相似文献   

8.
Primitive chemical characteristics of high-Mg andesites (HMA) suggest equilibration with mantle wedge peridotite, and they may form through either shallow, wet partial melting of the mantle or re-equilibration of slab melts migrating through the wedge. We have re-examined a well-studied example of HMA from near Mt. Shasta, CA, because petrographic evidence for magma mixing has stimulated a recent debate over whether HMA magmas have a mantle origin. We examined naturally quenched, glassy, olivine-hosted (Fo87–94) melt inclusions from this locality and analyzed the samples by FTIR, LA-ICPMS, and electron probe. Compositions (uncorrected for post-entrapment modification) are highly variable and can be divided into high-CaO (>10 wt%) melts only found in Fo > 91 olivines and low-CaO (<10 wt%) melts in Fo 87–94 olivine hosts. There is evidence for extensive post-entrapment modification in many inclusions. High-CaO inclusions experienced 1.4–3.5 wt% FeOT loss through diffusive re-equilibration with the host olivine and 13–28 wt% post-entrapment olivine crystallization. Low-CaO inclusions experienced 1–16 wt% olivine crystallization with <2 wt% FeOT loss experienced by inclusions in Fo > 90 olivines. Restored low-CaO melt inclusions are HMAs (57–61 wt% SiO2; 4.9–10.9 wt% MgO), whereas high-CaO inclusions are primitive basaltic andesites (PBA) (51–56 wt% SiO2; 9.8–15.1 wt% MgO). HMA and PBA inclusions have distinct trace element characteristics. Importantly, both types of inclusions are volatile-rich, with maximum values in HMA and PBA melt inclusions of 3.5 and 5.6 wt% H2O, 830 and 2,900 ppm S, 1,590 and 2,580 ppm Cl, and 500 and 820 ppm CO2, respectively. PBA melts are comparable to experimental hydrous melts in equilibrium with harzburgite. Two-component mixing between PBA and dacitic magma (59:41) is able to produce a primitive HMA composition, but the predicted mixture shows some small but significant major and trace element discrepancies from published whole-rock analyses from the Shasta locality. An alternative model that involves incorporation of xenocrysts (high-Mg olivine from PBA and pyroxenes from dacite) into a primary (mantle-derived) HMA magma can explain the phenocryst and melt inclusion compositions but is difficult to evaluate quantitatively because of the complex crystal populations. Our results suggest that a spectrum of mantle-derived melts, including both PBA and HMA, may be produced beneath the Shasta region. Compositional similarities between Shasta parental melts and boninites imply similar magma generation processes related to the presence of refractory harzburgite in the shallow mantle.  相似文献   

9.
中国大陆科学钻探工程预先导孔(CCSD-PP1) 打在苏鲁超高压变质带芝麻坊超镁铁岩体上,钻孔穿透超镁铁岩体115m.超镁铁岩体由二辉橄榄岩、方辉橄榄岩和少量单辉橄榄岩和纯橄岩组成,与上下围岩接触的橄榄岩被强烈蛇纹石化.多数橄榄岩含有石榴石或其假象,普遍含有金云母和菱镁矿,少量样品中有钛斜硅镁石.在化学成分上,橄榄岩的Mg#指数变化于90.392.6之间,MgO含量(36.61%49.15%,平均45.17%) 与Na2O (0.01%0.25%)、Al2O3 (0.07%3.71%,多数 < 2.0%,平均1.46%)和CaO (0.12%2.53%,一个高达3.30%,平均1.00%) 呈负相关关系.与主量易熔元素相对亏损的特点相反,橄榄岩中显示了稀土元素富集、分馏和配分曲线显示近于平行和相似的特点,(La/Lu) N比值为3.1833.05;此外,多数样品具有高Ba (最高比原始地幔高100多倍) 含量,在蛛网图上显示Rb、Nb、Ta、Zr、Hf和Sr的负异常,Ti/Eu比值均低于1300.岩相学特征和难熔主量元素与不相容元素之间的无相关性表明橄榄岩至少受到了形成金云母和菱镁矿的2次交代作用.富含金云母的橄榄岩(例如C25-143-61,C32-149-71) 具有富钾趋势,并且显示K2O与Rb、Ba和Th等大离子亲石元素的正相关关系,未见K2O和稀土元素、Sr和Ca之间的相关关系.这些特征表明橄榄岩被含水、硅铝质碱性熔体交代,之后又被高Ba低Rb和高场强元素的镁质(菱镁矿) 碳酸岩熔体交代,并且强烈地改变了Ba的丰度和显示了特定地幔碳酸盐的稀土元素配分型式.全岩具有不均一的高放射性Sr (87Sr/86Sr=0.70840.7201)和低放射性Nd (εNd (t) =-1.14-8.55) 组成,结合已有的氧同位素研究资料,表明预先导孔PP1中的橄榄岩所代表的地幔可能在早期就遭受了来自深部的介质的交代作用.   相似文献   

10.
Mantle-derived xenoliths from the Marsabit shield volcano (easternflank of the Kenya rift) include porphyroclastic spinel peridotitescharacterized by variable styles of metasomatism. The petrographyof the xenoliths indicates a transition from primary clinopyroxene-bearingcryptically metasomatized harzburgite (light rare earth element,U, and Th enrichment in clinopyroxene) to modally metasomatizedclinopyroxene-free harzburgite and dunite. The metasomatic phasesinclude amphibole (low-Ti Mg-katophorite), Na-rich phlogopite,apatite, graphite and metasomatic low-Al orthopyroxene. Transitionalsamples show that metasomatism led to replacement of clinopyroxeneby amphibole. In all modally metasomatized xenoliths melt pockets(silicate glass containing silicate and oxide micro-phenocrysts,carbonates and empty vugs) occur in close textural relationshipwith the earlier metasomatic phases. The petrography, majorand trace element data, together with constraints from thermobarometryand fO2 calculations, indicate that the cryptic and modal metasomatismare the result of a single event of interaction between peridotiteand an orthopyroxene-saturated volatile-rich silicate melt.The unusual style of metasomatism (composition of amphibole,presence of graphite, formation of orthopyroxene) reflects lowP –T conditions (850–1000°C at < 1·5GPa) in the wall-rocks during impregnation and locally low oxygenfugacities. The latter allowed the precipitation of graphitefrom CO2. The inferred melt was possibly derived from alkalinebasic melts by melt–rock reaction during the developmentof the Tertiary–Quaternary Kenya rift. Glass-bearing meltpockets formed at the expense of the early phases, mainly throughincongruent melting of amphibole and orthopyroxene, triggeredby infiltration of a CO2-rich fluid and heating related to themagmatic activity that ultimately sampled and transported thexenoliths to the surface. KEY WORDS: graphite; peridotite xenoliths; Kenya Rift; modal metasomatism; silicate glass  相似文献   

11.
The pre‐pilot hole (PP1) of the Chinese Continental Scientific Drilling Project (CCSD) recovered drill core samples from a 118 m‐thick section of peridotites located at Zhimafang in the southern Sulu UHP terrane, China. The peridotites consist of phlogopite‐bearing garnet lherzolite, harzburgite, wehrlite and dunite. Some peridotite layers contain magnesite and Ti‐clinohumite, and are characterized by LREE and LILE enrichment and HFSE depletion. Phlogopite (Phl) occurs in the peridotite matrix and is LILE‐enriched with low Zr/Hf ratios (0.19–0.60). Phlogopite shows a mantle signature in H and O isotopes (δ18O: +5.4‰ to +5.9‰, and δD: ?76‰ to ?91‰). Ti‐clinohumite (Ti‐Chu) is Nb and Ta‐enriched and has higher Ti and HREE concentrations than phlogopite. Magnesite (Mgs) occurs as megacrysts, as a matrix phase, and as veins (±Phl ± Ti‐Chu), and contains low REEtotal contents (<0.3 ppm) with a flat REE pattern. The δ18O values (+5.5‰ to +8.0‰) of magnesite are in the range of primary carbonatite, but the δ13C values (?2.4‰ to ?3.4‰) are slightly more positive than those of the mantle and of primary carbonatite. Petrochemical data indicate that the Zhimafang peridotite was subjected to three episodes of metasomatism, listed in succession from oldest to youngest: (1) crystallization of phlogopite in the mantle caused by infiltration of K‐rich hydrous fluid/melt; (2) formation of Mgs and Mgs ± Phl ± Ti‐Chu veins possibly caused by infiltration of mantle‐derived carbonatitic melt with a hydrous silicate component; and (3) replacement of magnesite, garnet and diopside by dolomite and secondary hydrous phases caused by a crust‐related, CO2‐bearing, aqueous fluid. Stable isotopic compositions of phlogopite and magnesite indicate metasomatic agents for events (1) and (2) are from an enriched mantle. Multiple metasomatism imposed on mantle peridotite of variable composition led to significant compositional heterogeneity at all scales within the Zhimafang peridotite.  相似文献   

12.
Complex multi-stage models involving silicate, hydrous and carbonatemelts of distinct provenance have been invoked to explain themetasomatism observed in mantle rocks. In contrast, relativelysimple models requiring polybaric crystallization of alkalinesilicate melts have been proposed to explain the occurrenceof veined mantle rocks. To address the spatial and temporalrelationships between veins and wall-rocks, a sequence of drillcores was obtained from Lherz, France. In outcrop the vein (amphibole–garnetpyroxenite dyke) is spatially associated with hornblendite veinlets(lherzite), and proximal amphibole-bearing and distal apatite-bearingwall-rock peridotite. Considerable elemental and isotopic heterogeneityexists in these wall-rock peridotites, in many instances equivalentto, or greater than, that observed in mantle xenoliths fromworldwide localities. A single stage of reactive porous flowbest explains the elemental and isotopic heterogeneity in thewall-rock. In essence it is proposed that emplacement of thesilicate melt (dyke) was inextricably linked to chromatographicfractionation/reaction of derivatives which led to the coexistence,in space and time, of silicate, hydrous and carbonate melts.This model elegantly and simply describes the formation of complexmetasomatic aureoles around mantle veins and negates the need,in the case of basalt-hosted (and kimberlite-hosted) xenoliths,for complex multi-stage models involving several episodes ofmelt influx with each melt being of different provenance. KEY WORDS: mantle metasomatism; trace-element enrichment; isotopic contamination; wall-rock peridotite; Lherz peridotite  相似文献   

13.
 Mohns Ridge lavas between 71 and 72°30′N (∼360 km) have heterogeneous compositions varying between alkali basalts and incompatible-element-depleted tholeiites. On a large scale there is a continuity of incompatible element and isotopic compositions between the alkali basalts from the island Jan Mayen and Mohns Ridge tholeiites. The variation in isotopes suggests a heterogeneous mantle which appears to be tapped preferentially by low degree melts (∼5%) close to Jan Mayen but also shows its signature much further north on Mohns Ridge. Three lava types with different incompatible element compositions [e.g. chondrite-normalized (La/Sm)N<1 to >2] occur in the area at 72°N and were generated from this heterogeneous mantle. The relatively depleted tholeiitic melts were mixed with a small degree melt from an enriched source. The elements Ba, Rb and K of the enriched melt were probably buffered in the mantle by residual amphibole or phlogopite. That such a residual phase is stable in this region of oceanic mantle suggests both high water contents and low mantle temperatures, at odds with a hotspot origin for Jan Mayen. Instead we suggest that the melting may be induced by the lowered solidus temperature of a “wet” mantle. Mohns MORB (mid ocean ridge basalt) and Jan Mayen area alkali basalts have high contents of Ba and Rb compared to other incompatible elements (e.g. Ba/La >10). These ratios reflect the signature of the mantle source. Ratios of Ce/Pb and Rb/Cs are normal MORB mantle ratios of 25 and 80, respectively, thus the enrichments of Ba and Rb are not indicative of a sedimentary component added to the mantle source but were probably generated by the influence of a metasomatizing fluid, as supported by the presence of hydrous phases during the petrogenesis of the alkali basalts. Geophysical and petrological models suggest that Jan Mayen is not the product of hotspot activity above a mantle plume, and suggest instead that it owes its existence to the unique juxtaposition of a continental fragment, a fracture zone and a spreading axis in this part of the North Atlantic. Received: 3 May 1995 / Accepted: 6 November 1995  相似文献   

14.
Mantle xenoliths in alkaline lavas of the Kerguelen Islandsconsist of: (1) protogranular, Cr-diopside-bearing harzburgite;(2) poikilitic, Mg-augite-bearing harzburgite and cpx-poor lherzolite;(3) dunite that contains clinopyroxene, spinel phlogopite, andrarely amphibole. Trace element data for rocks and mineralsidentify distinctive signatures for the different rock typesand record upper-mantle processes. The harzburgites reflectan initial partial melting event followed by metasomatism bymafic alkaline to carbonatitic melts. The dunites were firstformed by reaction of a harzburgite protolith with tholeiiticto transitional basaltic melts, and subsequently developed metasomaticassemblages of clinopyroxene + phlogopite ± amphiboleby reaction with lamprophyric or carbonatitic melts. We measuredtwo-mineral partition coefficients and calculated mineral–meltpartition coefficients for 27 trace elements. In most samples,calculated budgets indicate that trace elements reside in theconstituent minerals. Clinopyroxene is the major host for REE,Sr, Y, Zr and Th; spinel is important for V and Ti; orthopyroxenefor Ti, Zr, HREE, Y, Sc and V; and olivine for Ni, Co and Sc. KEY WORDS: mantle xenoliths; mantle metasomatism; partition coefficients; Kerguelen Islands; trace elements  相似文献   

15.
This experimental study simulates the interaction of hotter, deeper hydrous mantle melts with shallower, cooler depleted mantle, a process that is expected to occur in the upper part of the mantle wedge. Hydrous reaction experiments (~6 wt% H2O in the melt) were conducted on three different ratios of a 1.6 GPa mantle melt and an overlying 1.2 GPa harzburgite from 1060 to 1260 °C. Reaction coefficients were calculated for each experiment to determine the effect of temperature and starting bulk composition on final melt compositions and crystallizing assemblages. The experiments used to construct the melt–wall rock model closely approached equilibrium and experienced <5% Fe loss or gain. Experiments that experienced higher extents of Fe loss were used to critically evaluate the practice of “correcting” for Fe loss by adding iron. At low ratios of melt/mantle (20:80 and 5:95), the crystallizing assemblages are dunites, harzburgites, and lherzolites (as a function of temperature). When the ratio of deeper melt to overlying mantle is 70:30, the crystallizing assemblage is a wehrlite. This shows that wehrlites, which are observed in ophiolites and mantle xenoliths, can be formed by large amounts of deeper melt fluxing though the mantle wedge during ascent. In all cases, orthopyroxene dissolves in the melt, and olivine crystallizes along with pyroxenes and spinel. The amount of reaction between deeper melts and overlying mantle, simulated here by the three starting compositions, imposes a strong influence on final melt compositions, particularly in terms of depletion. At the lowest melt/mantle ratios, the resulting melt is an extremely depleted Al-poor, high-Si andesite. As the fraction of melt to mantle increases, final melts resemble primitive basaltic andesites found in arcs globally. An important element ratio in mantle lherzolite composition, the Ca/Al ratio, can be significantly elevated through shallow mantle melt–wall rock reaction. Wall rock temperature is a key variable; over a span of <80 °C, reaction with deeper melt creates the entire range of mantle lithologies from a depleted dunite to a harzburgite to a refertilized lherzolite. Together, the experimental phase equilibria, melt compositions, and reaction coefficients provide a framework for understanding how melt–wall rock reaction occurs in the natural system during melt ascent in the mantle wedge.  相似文献   

16.
The distribution of Ba and Sr in deep-seated xenoliths, mantle alkaline melts, and their minerals from the Pamirs and Tien Shan and some other regions was considered. In contrast to ordinary magmatic series, the mantle rocks show a correlation of Sr with both Ca and alkalis. The most extensive accumulation of Ba and Sr in the upper mantle occurs during the processes of mantle metasomatism and melting of metasomatized materials. The influx of these elements is probably related to ultradeep plume-type sources. Ba and Sr were transported from the mantle into the crust by both high-temperature alkaline melts and low-temperature hydrothermal solutions. It is supposed that the late Alpine celestite deposits of the huge Sr province of the Mediter-ranean belt are of mantle origin. Geochemical provinces show distinctive concentrations and proportions of Ba and Sr in mantle-derived alkaline basic rocks, metasomatic rocks, and their minerals. The type of Ba-Sr relations is inherited by crustal rocks.  相似文献   

17.
The basaltic maar of Youkou, situated in the Adamawa Volcanic Massif in the eastern branch of the continental segment of the Cameroon Volcanic Line, contains mantle-derived xenoliths of various types in pyroclastites. Spinel-bearing lherzolite xenoliths from the Youkou volcano generally exhibit protogranular textures with olivine (Fo89.4?90.5), enstatite (En89???91Fs8.7?9.8Wo0.82?1.13), clinopyroxene, spinel (Cr#Sp?=?9.4–13.8), and in some cases amphibole (Mg#?=?88.5–89.1). Mineral equilibration temperatures in the lherzolite xenoliths have been estimated from three–two pyroxene thermometers and range between 835 and 937 °C at pressures of 10–18 kbar, consistent with shallow mantle depths of around 32–58 km. Trends displayed by bulk-rock MgO correlate with Al2O3, indicating that the xenoliths are refractory mantle residues after partial melting. The degree of partial melting estimated from spinel compositions is less than 10%: evidences for much higher degrees of depletion are preserved in one sample, but overprinted by refertilization in others. Trace element compositions of the xenoliths are enriched in highly incompatible elements (LREE, Sr, Ba, and U), indicating that the spinel lherzolites underwent later cryptic metasomatic enrichment induced by plume-related hydrous silicate melts. The extreme fertility (Al2O3?=?6.07–6.56 wt% in clinopyroxene) and the low CaO/Al2O3 ratios in the spinel lherzolites suggest that they could not be a simple residue of partial melting of primitive mantle and must have experienced refertilization processes driven by the infiltration of carbonatite or carbonated silicate melts.  相似文献   

18.
This paper presents new major and trace element data from 150 garnet xenocrysts from the V. Grib kimberlite pipe located in the central part of the Arkhangelsk diamondiferous province (ADP). Based on the concentrations of Cr2O3, CaO, TiO2 and rare earth elements (REE) the garnets were divided into seven groups: (1) lherzolitic “depleted” garnets (“Lz 1”), (2) lherzolitic garnets with normal REE patterns (“Lz 2”), (3) lherzolitic garnets with weakly sinusoidal REE patterns (“Lz 3”), (4) lherzolitic garnets with strongly sinusoidal REE patterns (“Lz 4”), (5) harzburgitic garnets with sinusoidal REE patterns (“Hz”), (6) wehrlitic garnets with weakly sinusoidal REE patterns (“W”), (7) garnets of megacryst paragenesis with normal REE patterns (“Meg”). Detailed mineralogical and geochemical garnet studies and modeling results suggest several stages of mantle metasomatism influenced by carbonatite and silicate melts. Carbonatitic metasomatism at the first stage resulted in refertilization of the lithospheric mantle, which is evidenced by a nearly vertical CaO-Cr2O3 trend from harzburgitic (“Hz”) to lherzolitic (“Lz 4”) garnet composition. Harzburgitic garnets (“Hz”) have probably been formed by interactions between carbonatite melts and exsolved garnets in high-degree melt extraction residues. At the second stage of metasomatism, garnets with weakly sinusoidal REE patterns (“Lz 3”, “W”) were affected by a silicate melt possessing a REE composition similar to that of ADP alkaline mica-poor picrites. At the last stage, the garnets interacted with basaltic melts, which resulted in the decrease CaO-Cr2O3 trend of “Lz 2” garnet composition. Cr-poor garnets of megacryst paragenesis (“Meg”) could crystallize directly from the silicate melt which has a REE composition close to that of ADP alkaline mica-poor picrites. P-T estimates of the garnet xenocrysts indicate that the interval of ～60–110 km of the lithospheric mantle beneath the V. Grib pipe was predominantly affected by the silicate melts, whereas the lithospheric mantle deeper than 150 km was influenced by the carbonatite melts.  相似文献   

19.
In situ trace-element and isotopic (87Sr/86Sr) data and whole-rock Sr–Nd–Hf data on 12 gabbro xenoliths from the Hyblean Plateau (south-eastern Sicily) illustrate the complex petrogenetic evolution of this lithospheric segment. The gabbros formed by precipitation of plagioclase + clinopyroxene from a HIMU-type alkaline melt, then were cryptically metasomatized by a low-Rb, high-87Sr/86Sr fluid, and finally infiltrated by an exotic, late Fe–Ti-rich melt with 87Sr/86Sr ~ 0.7055, carrying high concentrations of Sr, Rb and HFSE. The geochemical and isotopic features of both the metasomatizing fluid and the Fe–Ti-rich melt are compatible with their common derivation by the progressive melting of an amphibole–phlogopite–ilmenite metasomatic domain (MARID-type?) that probably resided within the subcontinental lithospheric mantle. Therefore, both the astenosphere and the lithosphere underneath the Hyblean Plateau contributed to the petrogenesis of the gabbros. Sm–Nd dating yields an age of 253 ± 60 Ma for the cumulitic pile, roughly coinciding with a hydrothermal event recorded by crustal zircons in the area. We suggest that the Hyblean Plateau suffered a thermal event—probably related to lithospheric thinning and upwelling and melting of the asthenosphere—in Permo-Triassic time (the opening of the Ionian Basin?). The induced perturbation in the lithosphere caused consequent melting of some previously metasomatised portions.  相似文献   

20.
 Two types of melt pockets occur in Hawaiian mantle xenoliths: amphibole-bearing (AMP) and spinel-bearing (SMP). AMPs contain amphibole (kaersutite), olivine (Fo92), clinopyroxene (with 7–11% Al2O3), vesicles and glass. SMPs contain olivine, clinopyroxene, spinel, glass, and vesicles. The glasses in SMPs (SiO2=44–45%, 11–12% alkalis, La=90–110 ppm) and AMPs (SiO2=49–54%, 6–8.5% alkalis, La=8–14 ppm) are distinct in color and composition. Both glasses are generally characterized by LREE-enriched (chondrite-normalized) patterns. Amphibole and clinopyroxene have gently convex upward-to-moderately LREE-enriched patterns. Mineral/glass trace element abundance ratio plots show a strong negative Ti anomaly and a gentle negative Zr anomaly for clinopyroxene/glass; whereas amphibole/glass patterns show a distinctive positive Ti spike. The amphibole/glass trace element ratios are similar to published megacryst/lava values. An earlier study showed that the Hawaiian spinel lherzolites (lithosphere) have largely been metasomatized during post-erosional Honolulu magmatic activity. REE abundances of SMP glasses (melts) overlap the REE abundances calculated for such metasomes. The occurrence of hydrous, alkaline, mafic melt pockets in Hawaiian upper mantle xenoliths implies that (1) such hydrous liquids are generated in the upper mantle, and (2) water plays a role in magmatic activity associated with the Hawaiian plume. Although we are uncertain about the source (plume, lithosphere, or asthenosphere) of this water, we speculate that such melts and other alkalic lavas erupted on Oahu and on the sea-floor over the Hawaiian arch were generated from a broad „wet“ rim of a radially layered Hawaiian plume, whose hot and „dry“ core supplied the shield-forming magmas. Received: 6 February 1995 / Accepted: 28 August 1995  相似文献   

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