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1.
A rare composite xenolith and abundant cumulative pyroxenites obtained from the Mesozoic Fangcheng basalts on the eastern North China Craton record a complex history of melt percolation and circulation in the subcontinental lithospheric mantle. The composite xenolith has a dunite core and an olivine clinopyroxenite rim. The dunite is of cumulative origin and has a granular recrystallized texture and extremely low Mg# [100 Mg/(Mg + Fe) = 81–82] contents in olivines. The olivine clinopyroxenite contains larger clinopyroxene and/or orthopyroxene with a few fine-grained olivine and tiny phlogopite, feldspar, and/or carbonate minerals interstitial to clinopyroxene. The clinopyroxene has low Mg# (83–85). Compositional similarity between dunitic olivine and pyroxenitic one indicates a sequential crystallization of dunite and pyroxenite from a precursor melt. Pyroxenite xenoliths include olivine websterites and clinopyroxenites, both are of cumulative origin. Estimation of the melt from major oxides in olivines and REE concentrations in clinopyroxenes in these composite and pyroxenite xenoliths suggests a derivation from subducted crustal materials, consistent with the highly enriched EMII-like Sr and Nd isotopic ratios observed in the pyroxenites. Occurrence of phlogopite, feldspar and carbonate minerals in some xenoliths requires the melt rich in alkalis (K, Na), silica and volatiles (water and CO2) at the latest stage as well, similar to highly silicic and potassic melts. Thus, the occurrence of these composite and pyroxenite xenoliths provides an evidence for voluminous injection of recycled crustal melts into the lithosphere beneath the southeastern North China Craton at the Late Mesozoic, a reason for the rapid lithospheric enrichment in both elemental and isotopic compositions.  相似文献   

2.
Mantle xenoliths (lherzolites, clinopyroxene dunites, wehrlites, and clinopyroxenites) in the Early Cretaceous volcanic rocks of Makhtesh Ramon (alkali olivine basalts, basanites, and nephelinites) represent metasomatized mantle, which served as a source of basaltic melts. The xenoliths bear signs of partial melting and previous metasomatic transformations. The latter include the replacement of orthopyroxene by clinopyroxene in the lherzolites and, respectively, the wide development of wehrlites and olivine clinopyoroxenites. Metasomatic alteration of the peridotites is accompanied by a sharp decrease in Mg, Cr, and Ni, and increase of Ti, Al, Ca contents and 3+Fe/2+Fe ratio, as well as the growth of trace V, Sc, Zr, Nb, and Y contents. The compositional features of the rocks such as the growth of 3+Fe/2+Fe and the wide development of Ti-magnetite in combination with the complete absence of sulfides indicate the high oxygen fugacity during metasomatism and the low sulfur concentration, which is a distinctive signature of fluid mode during formation of the Makhtesh Ramon alkali basaltic magma. Partial melting of peridotites and clinopyroxenites is accompanied by the formation of basanite or alkali basaltic melt. Clino- and orthopyroxenes are subjected to melting. The crystallization products of melt preserved in the mantle rock are localized in the interstices and consist mainly of fine-grained clinopyroxene, which together with Ti-magnetite, ilmenite, amphibole, rhenite, feldspar, and nepheline, is cemented by glass corresponding to quartz–orthopyroxene, olivine–orthopyroxene, quartz–feldspar, or nepheline–feldspar mixtures of the corresponding normative minerals. The mineral assemblages of xenoliths correspond to high temperatures. The high-Al and high-Ti clinopyroxene, calcium olivine, feldspar, and feldspathoids, amphibole, Ti-magnetite, and ilmenite are formed at 900–1000°. The study of melt and fluid inclusions in minerals from xenoliths indicate liquidus temperatures of 1200–1250°C, solidus temperatures of 1000–1100°C, and pressure of 5.9–9.5 kbar. Based on the amphibole–plagioclase barometer, amphibole and coexisting plagioclase were crystallized in clinopyroxenites at 6.5–7.0 kbar.  相似文献   

3.
We found fine-grained Fe-rich orthopyroxene-rich xenoliths (mainly orthopyroxenite) containing partially digested dunite fragments of Group I from Takashima, Southwest Japan. Orthopyroxenite veinlets, some of which contain plagioclase at the center, also replace olivine in dunite and wehrlite xenoliths of Group I. This shows high reactivity with respect to olivine of the melt involved in orthopyroxenite formation, indicating its high SiO2 activity. The secondary orthopyroxene of this type is characterized by low Mg# [= Mg/(Mg + total Fe) atomic ratio] (down to 0.73) and high Al2O3 contents (5–6 wt%). It is different in chemistry from other secondary orthopyroxenes found in peridotite xenoliths derived from the mantle wedge. Clinopyroxenes in the Fe-rich orthopyroxenite show a convex-upward REE pattern with a crest around Sm. This pattern is strikingly similar to that of clinopyroxenes of Group II pyroxenite xenoliths and of phenocrystal and xenocrystal clinopyroxenes, indicating involvement of similar alkali basaltic melts. The Fe-rich orthopyroxenite xenoliths from Takashima formed by reaction between evolved alkali basalt melt and mantle olivine; alkali basalt initially slightly undersaturated in silica might have evolved to silica-oversaturated compositions by fractional crystallization at high-pressure conditions. The Fe-rich orthopyroxenites occur as dikes within the uppermost mantle composed of dunite and wehrlite overlying pockets of Group II pyroxenites. The orthopyroxene-rich pyroxenites of this type are possibly common in the uppermost mantle beneath continental rift zones where alkali basalt magmas have been prevalent.  相似文献   

4.
汉诺坝碱性玄武岩是深源包体和巨晶的主要寄主岩,同时,也有不含包体的碱性玄武岩和含包体的拉斑玄武岩。本文基于理论计算,探讨了包体和巨晶分布的动力学机理。  相似文献   

5.
The Dalnyaya kimberlite pipe(Yakutia,Russia) contains mantle peridotite xenoliths(mostly Iherzolites and harzburgites) that show both sheared porphyroclastic(deformed) and coarse granular textures,together with ilmenite and clinopyroxene megacrysts.Deformed peridotites contain high-temperature Fe-rich clinopyroxenes,sometimes associated with picroilmenites,which are products of interaction of the lithospheric mantle with protokimberlite related melts.The orthopyroxene-derived geotherm for the lithospheric mantle beneath Dalnyaya is stepped similar to that beneath the Udachnaya pipe.Coarse granular xenoliths fall on a geotherm of 35 mWm-2 whereas deformed varieties yield a 45 mWm-2)geotherm in the 2-7.5 GPa pressure interval.The chemistry of the constituent minerals including garnet,olivine and clinopyroxene shows trends of increasing Fe~#(=Fe/(Fe+Mg))with decreasing pressure.This may suggest that the interaction with fractionating protokimberlite melts occurred at different levels.Two major mantle lithologies are distinguished by the trace element patterns of their constituent minerals,determined by LA-ICP-MS.Orthopyroxenes,some clinopyroxenes and rare garnets are depleted in Ba,Sr,HFSE and MREE and represent relic lithospheric mantle.Re-fertilized garnet and clinopyroxene are more enriched.The distribution of trace elements between garnet and clinopyroxene shows that the garnets dissolved primary orthopyroxene and clinopyroxene.Later high temperature clinopyroxenes related to the protokimberlite melts partially dissolved these garnets.Olivines show decreases in Ni and increases in Al,Ca and Ti from Mg-rich varieties to the more Fe-rich,deformed and refertilized ones.Minerals showing higher Fe~#(0.11-0.15) are found within intergrowths of low-Cr ilmenite-clinopyroxene-garnet related to the crystallization of protokimberlite melts in feeder channels.In P-f(O_2) diagrams,garnets and Cr-rich clinopyroxenes indicate reduced conditions at the base of the lithosphere at-5 log units below a FMQ buffer.However,Cr-poor clinopyroxenes,together with ilmenite and some Fe-Ca-rich garnets,demonstrate a more oxidized trend in the lower part of lithosphere at-2 to 0 log units relative to FMQ.Clinopyroxenes from xenoliths in most cases show conditions transitional between those determined for garnets and megacrystalline Cr-poor suite.The relatively low diamond grade of Dalnyaya kimberlites is explained by a high degree of interaction with the oxidized protokimberlite melts,which is greater at the base of the lithosphere.  相似文献   

6.
Mantle xenoliths from Paleogene basanites of East Serbia were studied using EMP and LA-ICP-MS techniques in order to better understand mantle characteristics in this region. Five different mantle lithologies have been distinguished: a dunite/harzburgite/lherzolite (D/HZ/L) group, clinopyroxene-rich lherzolites (Cpx-L), clinopyroxene megacrysts (Cpx-M), spinel-rich olivine websterites (OWB1) and spinel-poor olivine websterites (OWB2). D/HZ/L xenoliths are the most common and represent normal mantle composed of typical anhydrous spinel peridotites with well equilibrated, unzoned silicates characterized by high Mg# s. Negative correlations between Mg# and TiO2, Al2O3 and CaO wt% in clinopyroxenes (cpx) and orthopyroxenes (opx) and the Cr–Al trend in spinel (sp) suggest depletion via extraction of basaltic melts. The modal composition of D/HZ/L xenoliths and unusual low-Al opx suggest that the lithospheric mantle underneath East Serbia is more depleted than normal European lithosphere. D/HZ/L xenoliths contain numerous pockets and veins filled by Cr-rich cpx, Ti-rich spinel, altered glass, apatite and rare ilmenite and phlogopite. Petrographic observations, supported by major element contents in sp and cpx, and modelling using trace element contents in cpx, indicate that the pockets and veins formed from infiltration of alkaline melts and reaction with peridotite wall-rock causing opx and spinel replacement. The same alkaline melt-related metasomatism gave rise to the Cpx-L and OWB1 mantle xenoliths and Cpx-M xenocrysts. Trace element contents of cpx in these xenoliths show a distinctively concave downwards REE pattern with a HFSE depletion, very similar to cpx megacrysts from the Pannonian Basin and to vein cpx from Eifel. In contrast, the OWB2 xenoliths show evidence of precipitation from subduction-related mafic to ultramafic melts, as inferred from their opx-rich lithology and unusual Cr-rich spinels. They are probably related to subduction magmatism during the Late Cretaceous.Milivoje Jovanovi: deceased in April 2004  相似文献   

7.
Despite the occurrence of highly variable lithium (Li) elemental distribution and isotopic fractionation in mantle mineral, the mechanism of Li heterogeneity and fractionation remains a controversial issue. We measured Li contents and isotopic compositions of olivine and clinopyroxene xenocrysts and phenocrysts from kamafugite host lavas, as well as minerals in melt pockets occurring as metasomatic products in peridotite xenoliths from the Western Qinling, central China. The olivine xenocrysts in the kamafugites show compositional zonation. The cores have high Mg# (100 × Mg/(Mg+Fe); 91.0–92.2) and Li abundances (5.63–21.7 ppm), low CaO contents (≤0.12 wt%) and low δ7Li values (−39.6 to −6.76‰), which overlap with the compositional ranges of the olivines in the melt pockets as well as those in peridotite xenoliths. The rims of the olivine xenocrysts display relatively low Mg# (85.9–88.2), high CaO contents (0.19–0.38 wt%) and high δ7Li values (18.3–26.9‰), which are comparable to the olivine phenocrysts (Mg#: 86.4–87.1; CaO: 0.20–0.28 wt%; Li: 12.4–36.8 ppm; δ7Li: 18.1–26.0‰) and the silicate-melt metasomatized olivines. The clinopyroxene phenocrysts and clinopyroxenes in the melt pockets have no distinct characteristics with respect to the Li abundances and δ7Li values, but show higher and lower CaO contents, respectively, than the clinopyroxenes from silicate and carbonatite metasomatized samples. These features indicate that Li concentration and isotopic signatures of the cores of the xenocrysts recorded carbonatite melt-peridotite reaction (carbonatite metasomatism) at mantle depth, and the variations in the rims probably resulted from xenocryst–host magma interaction during ascent. Our results reveal that the interaction with carbonatite and silicate melts gave rise to an increase in Li abundance in minerals of peridotite xenoliths at mantle depth or during transportation. In terms of δ7Li, the carbonatite and silicate melts produced remarkably contrasting δ7Li variations in olivine. Based on the systematic variations of Li abundances and Li isotopes in olivines, we suggest that the δ7Li value of olivine is a more important indicator than that of clinopyroxene in discriminating carbonatite and silicate melt interaction agents with peridotites.  相似文献   

8.
We performed partial melting experiments at 1 and 1.5 GPa, and 1180–1400 °C, to investigate the melting under mantle conditions of an olivine-websterite (GV10), which represents a natural proxy of secondary (or stage 2) pyroxenite. Its subsolidus mineralogy consists of clinopyroxene, orthopyroxene, olivine and spinel (+garnet at 1.5 GPa). Solidus temperature is located between 1180 and 1200 °C at 1 GPa, and between 1230 and 1250 °C at 1.5 GPa. Orthopyroxene (±garnet), spinel and clinopyroxene are progressively consumed by melting reactions to produce olivine and melt. High coefficient of orthopyroxene in the melting reaction results in relatively high SiO2 content of low melt fractions. After orthopyroxene exhaustion, melt composition is controlled by the composition of coexisting clinopyroxene. At increasing melt fraction, CaO content of melt increases, whereas Na2O, Al2O3 and TiO2 behave as incompatible elements. Low Na2O contents reflect high partition coefficient of Na between clinopyroxene and melt (\(D_{{{\text{Na}}_{ 2} {\text{O}}}}^{{{\text{cpx}}/{\text{liquid}}}}\)). Melting of GV10 produces Quartz- to Hyperstene-normative basaltic melts that differ from peridotitic melts only in terms of lower Na2O and higher CaO contents. We model the partial melting of mantle sources made of different mixing of secondary pyroxenite and fertile lherzolite in the context of adiabatic oceanic mantle upwelling. At low potential temperatures (T P < 1310 °C), low-degree melt fractions from secondary pyroxenite react with surrounding peridotite producing orthopyroxene-rich reaction zones (or refertilized peridotite) and refractory clinopyroxene-rich residues. At higher T P (1310–1430 °C), simultaneous melting of pyroxenite and peridotite produces mixed melts with major element compositions matching those of primitive MORBs. This reinforces the notion that secondary pyroxenite may be potential hidden components in MORB mantle source.  相似文献   

9.
Upper-mantle xenoliths in Cenozoic basalts of northwestern Spitsbergen are rocks of peridotite (spinel lherzolites) and pyroxenite (amphibole-containing garnet and garnet-free clinopyroxenites, garnet clinopyroxenites, and garnet and garnet-free websterites) series. The upper-mantle section in the depth range 50–100 km is composed of spinel peridotites; at depths of 80–100 km pyroxenites (probably, dikes or sills) appear. The equilibrium conditions of parageneses are as follows: in the peridotites—730–1180 °C, 13–27 kbar, and oxygen fugacity of − 1.5 to + 0.3 log. un.; in the pyroxenites—1100–1310 °C, 22–33 kbar. The pyroxenite minerals have been found to contain exsolved structures, such as orthopyroxene lamellae in clinopyroxene and, vice versa, clinopyroxene lamella in orthopyroxene. The formation temperatures of unexsolved phases in orthopyroxene and clinopyroxene are nearly 100–150 °C higher than the temperatures of the lamellae–matrix equilibrium and the equilibrium of minerals in the rock. The normal distribution of cations in the spinel structure and the equilibrium distribution of Fe2 + between the M1 and M2 sublattices in the orthopyroxenes point to the high rate of xenolith ascent from the rock crystallization zone to the surface. All studied Spitsbergen rock-forming minerals from mantle xenoliths contain volatiles in their structure: OH−, crystal hydrate water H2Ocryst, and molecules with characteristic CH and CO groups. The first two components are predominant, and the total content of water (OH– + H2Ocryst) increases in the series olivine → garnet → orthopyroxene → clinopyroxene. The presence of these volatiles in the nominally anhydrous minerals (NAM) crystallized at high temperatures and pressures in the peridotites and pyroxenites testifies to the high strength of the volatile–mineral bond. The possibility of preservation of volatiles is confirmed by the results of comprehensive thermal and mass-spectral analyses of olivines and clinopyroxene, whose structures retain these components up to 1300 °C. The composition of hypothetic C–O–H fluid in equilibrium (in the presence of free carbon) with the underlying mantle rocks varies from aqueous (> 80% H2O) to aqueous–carbonic (~ 60% H2O). The fluid becomes essentially aqueous when the oxygen activity in the system decreases. However, there is no strict dependence of the redox conditions on the depth of formation of xenoliths.  相似文献   

10.
A unique occurrence of strontian barite droplets associated with oriented planes of primary sulfide blebs in several clinopyroxene megacrysts was found in the Plio-Pleistocene basaltic tuff of Szentbékkálla (Bakony–Balaton Highland, western Hungary). The barite droplets contain 3.22–14.7 wt.% SrO, variable amount of FeO (up to 3.25 wt.%), minor CaO, CuO and NiO. Textural arrangements of oriented sulfide planes show that they were trapped as immiscible sulfide melt during crystallization of the clinopyroxene. Temperature and pressure estimation (978–1094 °C and 1.0–1.1 GPa) of the host clinopyroxenes indicate that formation of clinopyroxene megacrysts and entrapment of sulfide blebs happened under upper mantle conditions.

A genetic relationship between the sulfate and sulfide blebs is doubtful. Textural features suggest that the barite droplets might have been trapped together with the sulfide blebs from immiscible sulfide melts. However, it cannot be excluded that the barite formed during metasomatic event following the sulfide formation.  相似文献   


11.
Diamond crystallization in multicomponent melts of variable composition is studied. The melt carbonates are K2CO3, CaCO3?MgCO3, and K-Na-Ca-Mg-Fe-carbonatites, and the melt silicates are model peridotite (60 wt.% olivine, 16 wt.% orthopyroxene, 12 wt.% clinopyroxene, and 12 wt.% garnet) and eclogite (50 wt.% garnet and 50 wt.% clinopyroxene). In the experiments carried out under the PT-conditions of diamond stability, the carbonate-silicate melts behave like completely miscible liquid phases. The concentration barriers of diamond nucleation (CBDN) in the melts with variable proportions of silicates and carbonates have been determined at 8.5 GPa. In the system peridotite–K2CO3–CaCO3?MgCO3–carbonatite they correspond to 30, 25, and 30 wt.% silicates, respectively, and in the analogous eclogite–carbonate system, 45, 30, and 35 wt.%. In the silicate-carbonate melts with higher silicate contents seed diamond growth occurs, which is accompanied by the crystallization of thermodynamically unstable graphite phase. In the experiments with melts compositionally corresponding to the CBDN at 7.0 GPa and 1200–1700 °C, a full set of silicate minerals of peridotite (olivine, orthopyroxene, clinopyroxene, garnet) and eclogite (garnet, clinopyroxene) parageneses was obtained. The minerals occur as syngenetic inclusions in natural diamonds; moreover, the garnets contain an impurity of Na, and the pyroxenes, K. The experimental data indicate that peridotite-carbonate and eclogite-carbonate melts are highly effective for the formation of diamond (or unstable graphite) together with syngenetic minerals and melts, which agrees with the carbonate-silicate (carbonatite) model for the mantle diamond formation.  相似文献   

12.
Quaternary basalts in the Cerro del Fraile area contain two types of mantle xenoliths; coarse-grained (2–5 mm) C-type spinel harzburgites and lherzolites, and fine-grained (0.5–2 mm) intensely metasomatized F-type spinel lherzolites. C-type xenoliths have high Mg in olivine (Fo = 90–91) and a range in Cr# [Cr/ (Cr + Al) = 0.17–0.34] in spinel. Two C-type samples contain websterite veinlets and solidified patches of melt that is now composed of minute quenched grains of plagioclase + Cr-spinel + clinopyroxene + olivine. These patches of quenched melts are formed by decompression melting of pargasitic amphibole. High Ti contents and common occurrence of relic Cr-spinel in the quenched melts indicate that the amphibole is formed from spinel by interaction with the Ti-rich parental magma of the websterite veinlets. The fO2 values of these two C-type xenoliths range from ΔFMQ −0.2 to −0.4, which is consistent with their metasomatism by an asthenospheric mantle-derived melt. The rest of the C-type samples are free of “melt,” but show cryptic metasomatism by slab-derived aqueous fluids, which produced high concentrations of fluid-mobile elements in clinopyroxenes, and higher fO2 ranging from ΔFMQ +0.1 to +0.3. F-type lherzolites are intensely metasomatized to form spinel with low Cr# (∼0.13) and silicate minerals with low MgO, olivine (Fo = ∼84), orthpyroxene [Mg# = Mg/(Mg + ΣFe) = ∼0.86] and clinopyroxene (Mg# = ∼0.88). Patches of “melt” are common in all F-type samples and their compositions are similar to pargasitic amphibole with low TiO2 (<0.56 wt%), Cr2O3 (<0.55 wt%) and MgO (<16.3 wt%). Low Mg# values of silicate minerals, including the amphibole, suggest that the metasomatic agent is most likely a slab melt. This is supported by high ratios of Sr/Y and light rare earth elements (REE)/heavy REE in clinopyroxenes. F-type xenoliths show relatively low fO2 (ΔFMQ −0.9 to −1.1) compared to C-type xenoliths and this is explained by the fusion of organic-rich sediments overlying the slab during the slab melt. Trench-fill sediments in the area are high in organic matter. The fusion of such wet sediments likely produced CH4-rich fluids and reduced melts that mixed with the slab melt. High U and Th in bulk rocks and clinopyroxene in F-type xenoliths support the proposed interpretation.  相似文献   

13.
Patches of glass with a second generation of small crystals of olivine, clinopyroxene, and spinel are abundant in hydrous peridotite mantle xenoliths with tabular equigranular textures from two maar-type volcanoes, Meerfelder Maar and Dreiser Weiher (West Eifel, Germany). The patches are similar in size to the main phases of the hosting peridotite. Their central part is often occupied by relics of pargasitic amphibole. Mass-balance calculations show that the patches were formed by surface controlled incongruent thermal breakdown of amphibole according to the reaction: amphibole olivine + clinopyroxene + spinel + melt. Simultaneously with the decomposition of amphibole, small crystals of olivine, clinopyroxene, and spinel grew radially from the patch/peridotite interface toward the centre of the patch. Apart from sector zoning of clinopyroxene, the crystals are virtually homogeneous and are separated from the amphibole by a seam of melt (glass). Secondary olivines reveal higher Mg-numbers, secondary clinopyroxenes higher Cr2O3 concentrations than olivines and clinopyroxenes, respectively, of the host peridotite. The silica contents of melts produced by the above breakdown reaction range from 48 to 52% SiO2 as a function of the composition of the parent amphiboles. Patches surrounded by primary olivines only reveal no reaction with the host peridotite. The variation of SiO2, MgO and CaO in melts from these patches is the result of minor precipitation of olivine and clinopyroxene during fast cooling. If patches are in contact with primary olivine and orthopyroxene, melts are additionally modified by the reaction liquid 1 + orthopyroxene liquid 2 + olivine + clinopyroxene resulting in more silica-rich compositions between 54 and 58%. For the rare glasses richer in silica, a more complex formation is required. Veinlets along grain boundaries are filled with glasses which are chemically identical to those from nearby patches. This suggests that the veinlets were filled by melts formed by amphibole breakdown during entrainment of the xenoliths to the host magmas.  相似文献   

14.
The paper discusses the results of mineralogical and petrographic studies of spinel lherzolite xenoliths and clinopyroxene megacrysts in basalt from the Jixia region related to the central zone of Cenozoic basaltic magmatism of southeastern China. Spinel lherzolite is predominantly composed of olivine (Fo89.6–90.4), orthopyroxene (Mg# = 90.6–92.7), clinopyroxene (Mg# = 90.3–91.9), and chrome spinel (Cr# = 6.59–14.0). According to the geochemical characteristics, basalt of the Jixia region is similar to OIB with asthenospheric material as a source. The following equilibrium temperatures and pressures were obtained for spinel peridotite: 890–1269°C and 10.4–14.8 kbar. Mg# of olivine and Cr# of chrome spinel are close to the values in rocks of the enriched mantle. It is evident from analysis of the textural peculiarities of spinel lherzolite that basaltic melt interacted with mantle rocks at the xenolith capture stage. Based on an analysis of the P–T conditions of the formation of spinel peridotite and clinopyroxene megacrysts, we show that mantle xenoliths were captured in the course of basaltic magma intrusion at a significantly lower depth than the area of partial melting. However, capture of mantle xenoliths was preceded by low-degree partial melting at an earlier stage.  相似文献   

15.
《地学前缘(英文版)》2020,11(6):2347-2364
The Late Cretaceous Sabzevar ophiolite represents one of the largest and most complete fragments of Tethyan oceanic lithosphere in the NE Iran. It is mainly composed of serpentinized mantle peridotites slices; nonetheless, minor tectonic slices of all crustal sequence constituents are observed in this ophiolite. The crustal sequence contains a well-developed ultramafic and mafic cumulates section, comprising plagioclase-bearing wehrlite, olivine clinopyroxenite, olivine gabbronorite, gabbronorite, amphibole gabbronorite and quartz gabbronorite with adcumulate, mesocumulate, heteradcumulate and orthocumulate textures. The crystallization order for these rocks is olivine ​± ​chromian spinel → clinopyroxene → plagioclase → orthopyroxene → amphibole. The presence of primary magmatic amphiboles in the cumulate rocks shows that the parent magma evolved under hydrous conditions. Geochemically, the studied rock units are characterized by low TiO2 (0.18–0.57 ​wt.%), P2O5 (<0.05 ​wt.%), K2O (0.01–0.51 ​wt.%) and total alkali contents (0.12–3.04 ​wt.%). They indicate fractionated trends in the chondrite-normalized rare earth element (REE) plots and multi-element diagrams (spider diagrams). The general trend of the spider diagrams exhibit slight enrichment in large ion lithophile elements (LILEs) relative to high field strength elements (HFSEs) and positive anomalies in Sr, Pb and Eu and negative anomalies in Zr and Nb relative to the adjacent elements. The REE plots of these rocks display increasing trend from La to Sm, positive Eu anomaly (Eu/Eu1 ​= ​1.06–1.54) and an almost flat pattern from medium REE (MREE) to heavy REE (HREE) region [(Gd/Yb)N ​= ​1–1.17]. Moreover, clinopyroxenes from the cumulate rocks have low REE contents and show marked depletion in light REE (LREE) compared to MREE and HREE [(La/Sm)N ​= ​0.10–0.27 and (La/Yb)N ​= ​0.08–0.22]. The composition of calculated melts in equilibrium with the clinopyroxenes from less evolved cumulate samples are closely similar to island arc tholeiitic (IAT) magmas. Modal mineralogy, geochemical features and REE modeling indicate that Sabzevar cumulate rocks were formed by crystal accumulation from a hydrous depleted basaltic melt with IAT affinity. This melt has been produced by moderate to high degree (~15%) of partial melting a depleted mantle source, which partially underwent metasomatic enrichment from subducted slab components in an intra-oceanic arc setting.  相似文献   

16.
The lavas of the Mount Cameroon, a Plio-Quaternary stratovolcano and the most important volcano along the Cameroon Volcanic Line (CVL), constitute a weakly differentiated alkaline series: mainly comprising basanites as well as alkaline basalts, hawaiites and mugearites. Ultramafic xenoliths (1–5?×?0.5–4 cm) of dunites, wehrlites and clinopyroxenites have been discovered in the basanites of a strombolian cone, located near Batoke on the South flank of the massif at an elevation of 500 m. K-Ar whole rock dating of the basanitic host rock has yielded an age of 0.73?±?0.08 Ma. This result falls within the range of the seven new K-Ar age determinations of mafic lavas, between 2.83 Ma and the Present. These are the first K-Ar data on this massif. The 87Sr/86Sr ratios of basic lavas are low (0.703198–0.703344), and 143Nd/144Nd ratios are intermediate (0.512851–0.512773). These ratios are typical of a mantle origin. The main characteristics of the xenoliths are: (a) total FeO contents are 15.1 to 19.1 wt.% in olivines (chrysolite, Mg# ranging from 79 to 84) of xenoliths, and 4.7 to 6.9 wt.% in diopsides of xenoliths, (b) diopsides of the clinopyroxenites have up to 7.2 wt.% Al2O3 and 2.3 wt.% TiO2, (c) spinels occur as interstitial grains between chrysolite and diopside grains, i.e. Cr2O3-rich magnetites (19 to 21 wt.% Cr2O3) in the dunites as well as (22 to 25 wt.% Cr2O3) in the wehrlites and titanomagnetites (14 to 15 wt.% TiO2) in the clinopyroxenites. Mineralogical analyses show an important re-equilibration between the chrysolite xenocrysts and the host basanitic magma. We observed a decrease in Mg and Ni towards the rim, and an enrichment in all others cations like Fe, Mn, Ca, Si. The changes of Fe2+ / Mg2+ are the most important. The xenoliths are interpreted as cumulates: clinopyroxenite xenoliths have probably crystallized and fractionated at an early stage from the mafic (host basanitic) magma, while dunite and wehrlite xenoliths seem to have crystallized from a previous more primitive batch of magma. These alkaline liquids could have been derived from partial melting of a garnet- rich lherzolite in the upper mantle beneath the Cameroon Volcanic Line. The AlIV/AlVI ratios remain high (1.2 to 4.9) in the clinopyroxenes of the xenoliths. This suggests crystallization under a lower pressure than that of equilibration of the clinopyroxenes (ratios 0.6 to 0.8) found in typical mantle xenoliths from the CVL.  相似文献   

17.
Based on experimental and mineralogical data, the model of mantle carbonate-silicate (carbonatite) melts as dominating parental media for natural diamonds was substantiated. It was demonstrated that the compositions of silicate constituents of parental melts were variable and saturated with respect to mantle rocks, namely pyrope peridotite, garnet pyroxenite, and eclogite. Based on concentration contributions and role in diamond genesis, major (carbonate and silicate) and minor (admixture) components were distinguished. The latter components may be both soluble (oxides, phosphates, chlorides, carbon dioxide, and water) and insoluble (sulfides, metals, and carbides) in silicate-carbonate melts. This paper presents the results of a study of diamond crystallization in multicomponent melts of variable composition with carbonate components (K2CO3, CaCO3 · MgCO3, and K-Na-Ca-Mg-Fe carbonatite) and silicate components represented by model peridotite (60 wt % olivine, 16 wt % orthopyroxene, 12 wt % clinopyroxene, and 12 wt % garnet) and eclogite (50 wt % garnet and 50 wt % clinopyroxene). Carbonate-silicate melts behave like completely miscible liquid phases in experiments performed under the P-T conditions of diamond stability. The concentration barriers of diamond nucleation (CBDN) in melts with variable proportions of silicates and carbonates were determined at 8.5 GPa. In the peridotite system with K2CO3, CaCO3 · MgCO3, and carbonatite, they correspond to 30, 25, and 30 wt % silicates, respectively, and in the eclogite system, the CBDN is shifted to 45, 30, and 35 wt % silicates. In the silicate-carbonate melts with higher silicate contents, diamond grows on seeds, which is accompanied by the crystallization of thermodynamically unstable graphite. At P = 7.0 GPa and T = 1200−1800°C, we studied and constructed phase diagrams for the multicomponent peridotite-carbonate and eclogite-carbonate systems as a physicochemical basis for revealing the syngenetic relationships between diamond and its silicate (olivine, ortho- and clinopyroxene, and garnet) and carbonate (aragonite and magnesite) inclusions depending on the physicochemical conditions of growth media. The results obtained allowed us to reconstruct the evolution of diamond-forming systems. The experiments revealed similarity between the compositions of synthetic silicate minerals and inclusions in natural diamonds (high concentrations of Na in garnets and K in clinopyroxenes). It was experimentally demonstrated that the formation of Na-bearing majoritic garnets is controlled by the P-T parameters and melt alkalinity. Diamonds with inclusions of such garnets can be formed in alkalic carbonate-silicate (aluminosilicate) melts. A mechanism was suggested for sodic end-member dissolution in majoritic garnets, and garnet with the composition Na2MgSi5O12 and tetragonal symmetry was synthesized for the first time.  相似文献   

18.
Lavas and included xenoliths from the Comores Archipelago have been analysed for the rare earth elements (REE) La-Lu. Among basaltic lava types fractionation of REE rock/chondrite distribution patterns is more extreme with greater SiO2 undersaturation and contents of incompatible elements. Enrichment and slight fractionation of REE in the rock series basanite-phonolite is considered compatible with a model of fractional crystallisation at low pressures involving mainly olivine and clinopyroxene, and to a much lesser extent, plagioclase. Apatite is probably effective in curtailing further enrichment of REE. High level fractional crystallisation and eclogite fractionation at depth appear unlikely causes for the relative enrichment of light REE (La-Eu) in the undersaturated basalts. This effect is more probably due to mineralogical control during partial melting in the upper mantle. Lherzolite xenoliths are poor in REE, exhibiting a slight relative depletion in the light REE. These patterns are interpreted as those of possible mantle material subjected to small degrees of partial melting, although not necessarily related to those melts erupted as lava flows at the surface.  相似文献   

19.
The 2,058 ± 4 Ma mafic–ultramafic Kevitsa intrusion is located in the Central Lapland greenstone belt, northern Finland. It is hosted by a Paleoproterozoic volcano–sedimentary sequence that contains komatiitic volcanic rocks and sulfide- and graphite-rich black schists. Economic Ni–Cu–(PGE) sulfide mineralization occurs in the middle part of the ultramafic lower unit of the intrusion. Two main types of ore are distinguished, “normal” and “Ni–PGE” ores. The normal ore is characterized by ~2 to 6 vol% disseminated sulfides and average Ni and Cu grades of 0.3 and 0.42 wt %, respectively (Ni/Cu < 1). The Ni–PGE ore has broadly similar sulfide contents, but a higher Ni grade and lower Cu grade. As a result, the Ni/Cu ratio reaches 15, much higher than in the normal ore. The Ni–PGE ores occur as irregular, discontinuous, lense-like bodies in the ultramafic rocks. Notably, the olivines in the Ni–PGE ore contain extremely high Ni contents of up to 14,000 ppm, which is significantly higher than the Ni content of olivine in other mafic–ultramafic igneous rocks globally (up to ~5,000 ppm) and in harmony with the associated Ni-rich sulfide assemblage containing pentlandite, millerite and pyrite. Microprobe mapping of olivine from the Ni–PGE ore suggests relatively low and homogeneous S contents and homogeneous distribution of Ni, Mg, Fe, which is inconsistent with the presence of sulfide inclusions in the olivine grains, or diffusion of Ni from interstitial sulfides into the olivine grains. We therefore conclude that Ni substitutes for Mg in the olivine lattice. The clinopyroxenes from the Ni–PGE ore also have unusually high Ni concentrations reaching 1,500 ppm and show a positive correlation with the nickel content of the associated olivine. The Nicpx/Niolivine is ~0.1 to 0.2 corresponding to high T partitioning of Ni between clinopyroxene and olivine. K D of 20 can account for the partitioning of nickel between olivine and the sulfide phase, consistent with magmatic equilibration. These data suggest that the olivine, clinopyroxene, and sulfides all crystallized from a basaltic magma with an unexceptionally high Ni content ranging from 300 to 1,100 ppm. The Ni–PGE ores are spatially associated with ultramafic xenoliths. Olivine in these ultramafic xenoliths have relatively high Fo contents (up to 90 mol %) and high Ni contents (up to 5,200 ppm) suggesting that the xenoliths formed from a komatiitic parental magma. It is proposed that assimilation by the Kevitsa magma of massive or semi-massive sulfides associated with komatiitic rocks elevated the Ni content of the magma and resulted in the formation of Ni–PGE ores and related extremely Ni-rich olivines.  相似文献   

20.
In situ trace element analyses of constituent minerals in mantle xenoliths occurring in an alnöite diatreme and in nephelinite plugs emplaced within the central zone of the Damara Belt have been determined by laser ablation ICP-MS. Primitive mantle-normalized trace element patterns of clinopyroxene and amphibole indicate the presence of both depleted MORB-like mantle and variably enriched mantle beneath this region. Clinopyroxenes showing geochemical depletion have low La/Smn ratios (0.02–0.2), whereas those showing variable enrichment have La/Smn ranging up to 3.8 and La/Ybn to 9.1. The most enriched clinopyroxenes coexist with amphibole showing similar REE patterns (La/Smn = 1.3–4.1; La/Ybn = 4.5–9). Primitive mantle-normalized trace element patterns allow further groups to be distinguished amongst the variably enriched clinopyroxenes: one having strong relative depletion in Rb–Ba, Ta–Nb and relative enrichment in Th–U; another with similar characteristics but with additional strong relative depletion in Zr–Hf; and one showing no significant anomalies. Amphiboles show similar normalized trace element patterns to co-existing clinopyroxene. Clinopyroxene and amphiboles showing LREEN enrichment have high Sr and low Nd isotope ratios compared to clinopyroxene with LREE-depleted patterns. Numerical simulation of melt percolation through the mantle via reactive porous flow is used to show that the chromatographic affect associated with such a melt migration process is able to account for the fractionation seen in La–Ce–Nd in cryptically metasomatized clinopyroxenes in Type 1 xenoliths, where melt–matrix interactions occur near the percolation front, whereas REE patterns in clinopyroxenes proximal to the source of metasomatic melt/fluid match those found in modally metasomatized Type 2 xenoliths. The strong fractionation between Rb–Ba, Th–U and Ta–Nb shown by some cryptically metasomatized xenoliths can be also accounted for by reactive porous flow, provided amphibole crystallizes from the percolating melt/fluid close to its source. The presence of amphibole in vein-like structures in some xenoliths is consistent with this interpretation. The strong depletion in Zr–Hf in clinopyroxene and amphibole in some xenoliths cannot be accounted for by melt migration processes and requires metasomatism by a separate carbonate-rich melt/fluid. When taken together with published isotope data on these same xenoliths, the source of metasomatic enrichment of the previously depleted (MORB-like) sub-Damaran lithospheric mantle is attributed to the upwelling Tristan plume head at the time of continental breakup.  相似文献   

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