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1.
Trace element evidence indicates that at the Buell Park diatreme, Navajo volcanic field, the felsic minette can be best explained by crystal fractionation from a potassic magma similar in composition to the mafic minettes. Compatible trace element (Cr, Ni, Sc) abundances decrease while concentrations of most incompatible elements (Ce, Yb, Rb, Ba, Sr) remain constant or increase from mafic to felsic minette. In particular, the nearly constant Ce/Yb ratio of the minettes combined with the decrease in Cr, Ni, and Sc abundances from mafic to felsic minette is inconsistent with a model of varying amounts of partial melting as the process to explain minette compositions. The uniformity of rare earth element (REE) abundances in all the minettes requires that an accessory mineral, apatite, dominated the geochemistry of the REE during fractionation. A decrease in P2O5 from mafic to felsic minette and the presence of apatite in cognate inclusions are also consistent with apatite fractionation. Higher initial87Sr/86Sr ratios in the felsic minettes relative to the proposed parental mafic minettes, however, is inconsistent with a simple fractionation model. Also, a separated phlogopite has a higher initial87Sr/86Sr ratio than host minette. These anomalous isotopic features probably reflect interaction of minette magma with crust.The associated ultramafic breccia at Buell Park is one of the Navajo kimberlites, but REE concentrations of the matrix do not support the kimberlite classification. Although the matrix of the breccia is enriched in the light REE relative to chondrites, and has high La, Rb, Ba, and Sr concentrations relative to peridotites, the concentrations of these elements are significantly lower than in South African kimberlites. A high initial87Sr/86Sr ratio combined with petrographic evidence of ubiquitous crustal xenoliths in the Navajo kimberlites suggests that the relatively high incompatible element concentrations are due to a crustal component. Apparently, Navajo kimberlites are most likely a mixture of comminuted mantle wall rock and crustal material; there is no evidence for an incompatible element-rich magma which is characteristic of South African kimberlites.If the mafic minettes are primary magmas derived from a garnet peridotite source with chondritic REE abundances, then REE geochemistry requires very small (less than 1%) degrees of melting to explain the minettes. Alternatively, the minettes could have formed by a larger degree of melting of a metasomatized, relatively light REE-enriched garnet peridotite. The important role of phlogopite and apatite in the differentiation of the minettes supports this latter hypothesis.  相似文献   

2.
The petrography, major element, and trace element (TE) compositions of minerals from two types of modal metasomatites (metasomatized peridotites and pyroxenites) from kimberlite pipes Udachnaya and Komsomol'skaya-Magnitnaya, Yakutia, have been studied. It is shown that texturally and chemically equilibrated metasomatites A consist of a set of superimposed minerals: phlogopite + diopside ± ilmenite ± apatite ± sulfides ± graphite. Their major and trace element compositions have specific features. The contents of TEs in garnet and clinopyroxene from these metasomatites are close to those in garnet and clinopyroxene from low-temperature coarse-grained peridotites richest in TEs. The distribution of a significant portion of TEs between garnet and clinopyroxene from A-type metasomatites and from coarse-grained lherzolites rich in TEs is close to experimental values reported for minerals coexisting with carbonatitic and basaltic fluids. We assume that this metasomatic process was nearly synchronous with the global metamorphism and cratonization of the mantle lithosphere and that high-density silicate–carbonate fluidmelts were metasomatizing agents.Another large mantle metasomatism process in the lithosphere of the Siberian craton was associated with the Middle Paleozoic kimberlite magmatic event, induced by the Yakutian thermochemical plume. Metasomatic minerals (Mg phlogopite + Cr diopside + chromite ± sulfides ± graphite) intensely replaced the minerals of the primary paragenesis, particularly, garnet. These reaction metasomatites show a sine-shaped REE pattern in garnet and disequilibrium between garnet and clinopyroxene. It is supposed that the reaction metasomatism in the mantle lithosphere of the Siberian craton was associated with ingress of reduced asthenospheric fluids at early stages of the kimberlite formation cycle. Metasomatic graphite formed in metasomatites of both types, and this fact evidences for two diamond formation epochs in the history of the mantle lithosphere of the Siberian craton.  相似文献   

3.
Ultramafic xenoliths from alkali basalts in the Perjani Mountainsin the Eastern Transylvanian Basin (ETB) of Romania are mainlyspinel Iherzolites, although spinel harzburgites, websterites,clinopyroxenites and amphibole pyroxenites are also present.Amphibole veins cut some spinel peridotite samples. All arederived from the shallow lithospheric upper mantle. In general,textural variations are restricted to protogranular and porphyroclastictypes, compared with the more varied textures found in mantlexenoliths from the alkali basalts of the neighbouring PannonianBasin. Also, ETB peridotites are richer in amphibole. Thus,the mantle beneath the edge of the ETB is less deformed butmore strongly metasomatized than the mantle closer to the centreof the Pannonian Basin.Mineralogical and bulk-rock geochemicalvariations resemble those of spinel Iherzolites from other sub-continentalshallow mantle xenolith suites. There is no apparent correlationbetween deformation and geochemistry, and much of the majorand trace element variation is due to variable extraction ofpicritic melts. The REE patterns of separated clinopyroxenesfrom the peridotite xenoliths are mostly LREE depleted, althoughclinopyroxenes from regions adjacent to amphibole veins haveexperienced an enrichment in La and Ce and a change in theirSr and Nd isotopic values towards those of the vein, while stillretaining an overall LREE depletion. Clinopyroxenes from thewebsterites and clinopyroxenites are more variable. Amphibolein the hydrous pyroxenites and amphibole veins is strongly LREEenriched and is considered to be metasomatic in origin. 87Sr/86Srand 143Nd/l44Nd isotopic ratios of the xenoliths vary between07018 and 07044, and 051355 and 0 51275, respectively. Thesevalue are more depleted than those obtained for xenoliths fromthe Pannonian Basin. The lower l43Nd/l44Nd and higher 87Sr/Sr86values are found in anhydrous pyroxenites, metasomatic amphibolesin veins and amphibole pyroxenites, and in the only exampleof an equigranular spinel Iherzolite in the suite.The ETB xenolithswere brought to the surface in alkaline vokanism which post-dateda period of Miocene to Pliocene subduction-related cak-alkalinevolcanism. However, the effects of the passage of either slab-derivedfluids or cak-alkaline magmas through the ETB lithospheric mantlecannot be discerned in the chemistry of the xenoliths. The metasomaticamphibole has 87Sr/Sr86 and 143Sr/Sr144 ratios similar to thehost alkali basalts, but the least evoked cak-alkaline magmasalso have similar Sr and Nd isotope compositions. The REE patternsof the amphibole resembk those of amphiboles considered to havecrystallized from alkaline melts. No preferential enrichmentin elements typically associated with slab-derivedfluids (K,Rb and Sr) relative to elements typically depleted in cak-alkalinemagmas (Ti, 2jr and Nb) has been observed in the vein amphiboles,although some interstitial amphibole is depleted in all incompatibletrace elements, including LREE. Thus, despite its position closeto the calc-alkaline volcanic arc of the Eastern Carpathians,we cannot readily detect any interaction between the lithosphericupper mantle beneath the ETB and subduction-related magmas orfluids. Metasomatism in the lithospheric mantle is instead largelyrelated to the passage of a primitive alkaline magma similarto the host alkali basal *corresponding author  相似文献   

4.
The Finero peridotite massif is a harzburgite that suffered a dramatic metasomatic enrichment resulting in the pervasive presence of amphibole and phlogopite and in the sporadic occurrence of apatite and carbonate (dolomite)-bearing domains. Pyroxenite (websterite) dykes also contain phlogopite and amphibole, but are rare. Peridotite bulk-rock composition retained highly depleted major element characteristics, but was enriched in K, Rb, Ba, Sr, LREE (light rare earth elements) (LaN/YbN = 8–17) and depleted in Nb. It has high radiogenic Sr (87Sr/86Sr(270) = 0.7055–0.7093), low radiogenic Nd (ɛNd(270) = −1 to −3) and EMII-like Pb isotopes. Two pyroxenite – peridotite sections examined in detail show the virtual absence of major and trace element gradients in the mineral phases. In both rock types, pyroxenes and olivines have the most unfertile major element composition observed in Ivrea peridotites, spinels are the richest in Cr, and amphibole is pargasite. Clinopyroxenes exhibit LREE-enriched patterns (LaN/YbN ∼16), negative Ti and Zr and generally positive Sr anomaly. Amphibole has similar characteristics, except a weak negative Sr anomaly, but incompatible element concentration ∼1.9 (Sr) to ∼7.9 (Ti) times higher than that of coexisting clinopyroxene. Marked geochemical gradients occur toward apatite and carbonate-bearing domains which are randomly distributed in both the sections examined. In these regions, pyroxenes and amphibole (edenite) are lower in mg## and higher in Na2O, and spinels and phlogopite are richer in Cr2O3. Both the mineral assemblage and the incompatible trace element characteristics of the mineral phases recall the typical signatures of “carbonatite” metasomatism (HFSE depletion, Sr, LILE and LREE enrichment). Clinopyroxene has higher REE and Sr concentrations than amphibole (amph/cpxDREE,Sr = 0.7–0.9) and lower Ti and Zr concentrations. It is proposed that the petrographic and geochemical features observed at Finero are consistent with a subduction environment. The lack of chemical gradients between pyroxenite and peridotite is explained by a model where melts derived from an eclogite-facies slab infiltrate the overhanging harzburgitic mantle wedge and, because of the special thermal structure of subduction zones, become heated to the temperature of the peridotite. If the resulting temperature is above that of the incipient melting of the hydrous peridotite system, the slab-derived melt equilibrates with the harzburgite and a crystal mush consisting of harzburgite and a silica saturated, hydrous melt is formed. During cooling, the crystal mush crystallizes producing the observed sequence of mineral phases and their observed chemical characteristics. In this context pyroxenites are regions of higher concentration of the melt in equilibrium with the harzburgite and not passage-ways through which exotic melts percolated. Only negligible chemical gradients can appear as an effect of the crystallization process, which also accounts for the high amphibole/clinopyroxene incompatible trace element ratios. The major element refractory composition is explained by an initially high peridotite/melt ratio. The apatite, carbonate-bearing domains are the result of the presence of some CO2 in the slab-derived melt. The CO2/H2O ratio in the peridotite mush increased by crystallization of hydrous phases (amphibole and phlogopite) locally resulting in the unmixing of a late carbonate fluid. The proposed scenario is consistent with subduction of probably Variscan age and with the occurrence of modal metasomatism before peridotite incorporation in the crust. Received: 20 July 1998 / Accepted: 28 October 1998  相似文献   

5.
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   

6.
The Origin of Amphibole in Lherzolite Xenoliths from Nunivak Island, Alaska   总被引：6，自引：2，他引：6  
Ten lherzolite xenoliths collected on Nunivak Island, Alaska,contain interstitial chromian pargasitic amphibole. Of 2000lherzolite nodules examined from the maars of the island, however,50 per cent contain relics of such an amphibole in the formof fine-grained zones of euhedral diopside, olivine and spinelin a porous Al-rich glass. These nodules are believed to havebeen amphibole-bearing fragments of the upper mantle, that partiallymelted during their ascent to the surface in the Nunivak basalts.The textural intimacy and chemical zoning exhibited by the interstitialamphibole and spinel in the lherzolite xenoliths indicate thatalthough the amphibole predates the Nunivak basalts, it is asecondary aluminous phase. The amphibole was formed in the uppermantle during a pervasive metasomatic event caused by risingtemperature and the infiltration of alkali-rich fluid, priorto the introduction of basaltic magmas.  相似文献   

7.
Carbonatites of the Jacupiranga alkaline–carbonatite complex in São Paulo State, Brazil, were used to investigate mineral–fluid interaction in a carbonatite magma chamber because apatite showed a marked discontinuity between primary fluid inclusion-rich cores and fluid inclusion-poor rims. Sylvite and burbankite, apatite, pyrite, chalcopyrite and ilmenite are the common phases occurring as trapped solids within primary fluid inclusions and reflect the general assemblage of the carbonatite. The apatite cores had higher Sr and REE concentrations than apatite rims, due to the presence of fluid inclusions into which these elements partitioned. A positive cerium anomaly was observed in both the core and rim of apatite crystals because oxidised Ce4+ partitioned into the magma. The combined evidence from apatite chemistry, fluid inclusion distribution and fluid composition was used to test the hypotheses that the limit of fluid inclusion occurrence within apatite crystals arises from: (1) generation of a separate fluid phase; (2) utilization of all available fluid during the first stage of crystallization; (3) removal of crystals from fluid-rich magma to fluid-poor magma; (4) an increase in the growth rate of apatite; or (5) escape of the fluids from the rim of the apatite after crystallization. The findings are consistent with fractionation and crystal settling of a carbonatite assemblage in a fluid-stratified magma chamber. Secondary fluid inclusions were trapped during a hydrothermal event that precipitated an assemblage of anhedral crystals: strontianite, carbocernaite, barytocalcite, barite and norsethite, pyrophanite, magnesian siderite and baddeleyite, ancylite-(Ce), monazite-(Ce) and allanite. The Sr- and REE-rich nature of the secondary assemblage, and lack of a positive cerium anomaly indicate that hydrothermal fluids have a similar source to the primary magma and are related to a later carbonatite intrusion.  相似文献   

8.
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   

9.
The Songshugou mylonitized peridotites within the Qinling Group metamorphic rocks in Central China are distributed in the northern part of the Shang-Dan Suture Zone (SDSZ) and contain abundant dunites and harzburgites. The dunites were intensely deformed and mylonitized converting the coarse-grained type to medium- and fine-grained types which contain prominent lenticular structure and relict olivine (Ol) porphyroclasts. Mineralogical and geochemical compositions suggest that the protoliths of the mylonitized peridotites were coarse-grained peridotites of lithospheric mantle origin. The harzburgites occur as enclaves within mylonitic peridotites in the form of lenses or veins. The orthopyroxenes in harzburgites were formed at the expense of Ol and have similar compositions to those of metasomatized harzburgites, characterized by low Al2O3, CaO and Cr2O3 contents. The harzburgites exhibit the gently U-type REE patterns with enriched incompatible elements (Rb, Ba, Sr, Zr and Hf), suggesting the metasomatic origin. The obvious ductile deformation of the large porphyroclastic orthopyroxene (Opx) suggests that the metasomatism occurred before the deformation. Ductile shearing deformation is indicated by the small fold structures and net-style ductile shearing zones within the Songshugou peridotite massif. The process is also result in the alignment of elongated Ol grains from initially coarse-granular via porphyroclastic to fine-granular texture. The relatively low Fo olivine, together with high Al2O3, and CaO contents and the abnormally low total PGE abundance in the fine-grained dunites suggest the ingress of melt/fluid during the mylonitization. The presences of significant amount of amphibole in the peridotites indicate the ingress of hydrous fluids. In general, the Songshugou peridotites have similar compositional characteristics with peridotites of Oman and Troodos ophiolites which are fragments of oceanic lithosphere mantle. One coarse-grained dunite has a TRD age of 875 Ma. Additionally two stages Paleozoic TRD ages are obtained from medium-grained and fine-grained dunites (491 Ma and 550 Ma; 446 Ma and 476 Ma). The broadly coeval nature of mylonitization with progressive metamorphism of surrounding amphibolites suggested that the Songshugou peridotites were generated before the early Paleozoic deformation. Our data, combined with the previous work on the surrounding HP/UHP metamorphic rocks, demonstrate that the Songshugou mylonitized peridotites represent fragments of the Neoproterozoic fossil oceanic lithospheric mantle that experienced extensive deformation during the Early Paleozoic subduction processes.  相似文献   

10.
Phlogopite-amphibole pyroxenite xenoliths contained in an Early Palaeozoic alkali subvolcanic lam-prophyre complex in Langao County, Shaanxi Province, are metasomatized mantle xenoliths, composed mainly of clinopyroxene, amphibole, phlogopite, apatite, pervoskite, ilmenite and sphene with well-developed subsolidus metamorphism-deformation textures, such as "triple points" and "cataclastic boundaries" . Minerological studies indicate that clinopyroxene is rich in SiO2 and MgO and poor in TiO2 and Al2O3, which is notably different from magmatogenic deep-seated megacrysts and phenocrysts formed in the range of mantle pressure. Amphibole and phlogopite have the compositional feature of mantle-derived amphibole and phlogopite. Sm-Nd isotope studies suggest that the metasomatized mantle beneath Langao County is the product of metasomatism of primitive mantle by melt (fluid) derived from the mantle plume, and the mantle metasomatism occurred 650 Ma ago. The process of mantle metasomatism changed from mantle me  相似文献   

11.
Spinel peridotite xenoliths from the Atsagin-Dush volcanic centre, SE Mongolia range from fertile lherzolites to clinopyroxene(cpx)-bearing harzburgites. The cpx-poor peridotites typically contain interstitial fine-grained material and silicate glass and abundant fluid inclusions in minerals, some have large vesicular melt pockets that apparently formed after primary clinopyroxene and spinel. No volatile-bearing minerals (amphibole, phlogopite, apatite, carbonate) have been found in any of the xenoliths. Fifteen peridotite xenoliths have been analysed for major and trace elements; whole-rock Sr isotope compositions and O isotope composition of all minerals were determined for 13 xenoliths. Trace element composition and Sr-Nd isotope compositions were also determined in 11 clinopyroxene and melt pocket separates. Regular variations of major and moderately incompatible trace elements (e.g. heavy-rare-earth elements) in the peridotite series are consistent with its formation as a result of variable degrees of melt extraction from a fertile lherzolite protolith. The Nd isotope compositions of LREE (light-rare-earth elements)-depleted clinopyroxenes indicate an old (≥ 1 billion years) depletion event. Clinopyroxene-rich lherzolites are commonly depleted in LREE and other incompatible trace elements whereas cpx-poor peridotites show metasomatic enrichment that can be related to the abundance of fine-grained interstitial material, glass and fluid inclusions in minerals. The absence of hydrous minerals, ubiquitous CO2-rich microinclusions in the enriched samples and negative anomalies of Nb, Hf, Zr, and Ti in primitive mantle-normalized trace element patterns of whole rocks and clinopyroxenes indicate that carbonate melts may have been responsible for the metasomatic enrichment. Low Cu and S contents and high δ34S values in whole-rock peridotites could be explained by interaction with oxidized fluids that may have been derived from subducted oceanic crust. The Sr-Nd isotope compositions of LREE-depleted clinopyroxenes plot either in the MORB (mid-ocean-ridge basalt) field or to the right of the mantle array, the latter may be due to enrichment in radiogenic Sr. The LREE-enriched clinopyroxenes and melt pockets plot in the ocean island-basalt field and have Sr-Nd isotope signatures consistent with derivation from a mixture of the DMM (depleted MORB mantle) and EM (enriched mantle) II sources. Received: 18 January 1996 / Accepted: 23 August 1996  相似文献   

12.
西南天山哈拉达拉岩体的锆石SHRIMP年代学及地球化学研究   总被引：15，自引：6，他引：9  
薛云兴  朱永峰 《岩石学报》2009,25(6):1353-1363
西南天山哈拉达拉侵入体由橄长岩、橄榄辉长岩和辉长岩组成,橄长岩和橄榄辉长岩具有典型的堆晶结构,堆晶矿物以斜长石和橄榄石为主。辉石、角闪石和金云母主要为堆晶间隙矿物。辉长岩发育辉长—辉绿结构。结晶分异作用在岩浆演化过程中起重要作用。对从辉长岩中分选出来的锆石进行的SHRIMP年代学研究表明,辉长岩形成于308.3±1.8Ma （MSWD=0.86,n=15）。哈拉达拉岩体稀土元素配分模式与E-MORB相似,具有高Rb、Cs、Ba及Sr的特点,87Sr/86Sr初始比值0.7040~0.7050。这些特征表明,岩浆源区具有富集地幔的特征(古南天山洋俯冲流体交代形成了富集地幔)。根据平坦的稀土元素配分模式以及Gd、Sm、Nb、Zr等微量元素的地球化学行为判别,岩浆源区岩石为含角闪石的尖晶石二辉橄榄岩。批式熔融模拟计算显示,地幔岩10%~15%的部分熔融能够形成哈拉达拉岩体的母岩浆。母岩浆通过48%~50%的结晶分异作用则能够形成哈拉达拉岩体。早期结晶的橄榄石和斜长石通过堆晶作用形成橄长岩和橄榄辉长岩,剩余岩浆结晶形成辉长岩。  相似文献   

13.
The Red Hill complex of New Hampshire is unusual for the WhiteMountain Magma Series of northern New England because it consistsof both silica-undersaturated and -saturated to -oversaturatedsyenites. Amphibole, pyroxene, and apatite in two of the saturatedunits, the Outer Coarse Syenite (OCS) and the Garland Peak Syenite(GPS), and in the undersaturated Nepheline Sodalite Syenite(NSS), were analyzed to determine the relationship between coexistingunder-saturated and saturated magmas. Mafic enclaves in theNSS and the GPS were also studied to elucidate their relationshipswith the host syenites. In addition to mafic enclaves, the NSS contains later emplacedcamptonitic dikes and associated pipe-like benmoreites. Thebenmoreites contain amphibole that is compositionally continuouswith amphibole in the NSS. However, REE and other trace elementabundances in apatite from the benmoreites and the NSS are notcompatible with a genetic relationship between the two. Maficenclaves within the NSS contain amphibole and pyroxene thatare compositionally continuous with the NSS. Bulk-rock compositionsof the enclaves plot along trends defined by the NSS. Furthermore,chondrite-normalized REE patterns for apatite in both the enclavesand the NSS are parallel, and REE abundances increase systematicallyfrom the enclaves to the NSS. We therefore suggest that theenclaves represent magmas similar to the NSS parent that intrudedup into its daughter products. These magmas appear to have beentephritic to phonotephritic in composition. Abundances of REE in apatite in the Nepheline Sodalite Syenite(NSS) are distinct from those in apatite in the silica-saturatedOCS. OCS apatites have LREE abundances up to 26 000 times chondritesand La/Yb ratios of 16–27. NSS apatites have comparableLREE concentrations, but HREE abundances are considerably lowerthan those of the OCS; La/Yb ratios range from 68 to 104. Theseobserved differences in both the REE and other trace elementabundances between apatite in the two rocks present difficultieswith a common parental magma hypothesis for the NSS and OCS.Hence it is suggested that, although the OCS and NSS are contemporaneousin time and space, they are probably not consanguineous. The silica-saturated GPS is a fine-grained syenite containingstrongly zoned amphiboles with kaersutite to hastingsite coresrimmed by hastingsitic hornblende and ferro-hornblende. Discretegrains of hastingsitic hornblende and ferro-hornblende occurin a feldspar-quartz groundmass. Coarser-grained, quartz-richpatches, containing feldspars and ferro-hornblende and ferroedenite,are also found in the GPS. The kaersutite cores are identicalto the amphibole in the GPS enclaves and the NSS suite. TheseGPS enclaves are silica undersaturated; the kaersutite coresin the GPS host rocks are probably xenocrysts derived from disaggregatedundersaturated magmas similar to that represented by the enclaves.  相似文献   

14.
Olivinites of the Krestovskaya Intrusion consist of predominant amount of olivine, and minor Ti-magnetite, perovskite, and clinopyroxene (from single grain to a few vol %). Primary crystallized melt inclusions were found and studied in olivine, perovskite, and diopside of the olivinites. Daughter phases in olivine-hosted melt inclusions are monticellite, perovskite, kalsilite, phlogopite, magnetite, apatite, and garnet andradite. Perovskite-hosted melt inclusions contain such daughter phases as kalsilite, pectolite, clinopyroxene, biotite, magnetite, and apatite, while daughter phases in clinopyroxene-hosted melt inclusions are represented by kalsilite, phlogopite, magnetite, and apatite. According to melt inclusion heating experiments, olivine crystallized from above 1230°C to 1180°C. It was followed by perovskite crystallizing at ≥1200°C and clinopyroxene, at 1170°C. According to analysis of quenched glass of the melt inclusions, the chemical composition of melts hosted in the minerals corresponds to the larnite-normative alkali ultramafic (kamafugite) magma significantly enriched in incompatible elements. The high incompatible element concentrations, its distribution, and geochemical indicator ratios evidenced that the magma was derived by the partial melting of garnet-bearing undepleted mantle.  相似文献   

15.
岚皋金云角闪辉石岩类捕虏体：地幔交代作用的证据   总被引：6，自引：2，他引：6  
产于陕西岚皋地区碱质基性－超基性潜火山杂岩中的金云角闪辉石岩类捕虏体，主要由透辉石、富钛韭闪石、金云母、磷灰石、榍石、及钛铁矿组成。捕虏体发育三联晶、碎裂边、肯克变形等固相线下变形变质结构，矿物学特征表明，透辉石、富钛韭闪石、金云母为地幔来源，是地幔交代作用的产物；与正常地幔尖晶石二辉橄榄岩相比，捕虏体富ＴｉＯ２、Ｆｅ２Ｏ３、ＣａＯ、Ｎａ２Ｏ、Ｋ２Ｏ，贫ＭｇＯ，其稀土元素具富集特征，尤其富集ＬＲＥＥ；微量元素分配型式显示了富亲石不相容元素的特征。岩相学、矿物学及岩石化学特征表明：该类捕虏体为交代地幔捕虏体，它代表了北大巴山早古生代裂谷作用时期的异常地幔，是地幔交代作用的产物。交代营力可能源于地幔热缕的上升，交代过程推测为深处小范围的流体交代及随后硅酸岩熔体的“弥散”性交代  相似文献   

16.
The trace element compositions of melts and minerals from high-pressure experiments on hydrous pyroxenites containing K-richterite are presented. The experiments used mixtures of a third each of the natural minerals clinopyroxene, phlogopite and K-richterite, some with the addition of 5% of an accessory phase ilmenite, rutile or apatite. Although the major element compositions of melts resemble natural lamproites, the trace element contents of most trace elements from the three-mineral mixture are much lower than in lamproites. Apatite is required in the source to provide high abundances of the rare earth elements, and either rutile and/or ilmenite is required to provide the high field strength elements Ti, Nb, Ta, Zr and Hf. Phlogopite controls the high levels of Rb, Cs and Ba.Since abundances of trace elements in the various starting mixtures vary strongly because of the use of natural minerals, we calculated mineral/melt partition coefficients (DMin/melt) using mineral modes and melting reactions and present trace element patterns for different degrees of partial melting of hydrous pyroxenites. Rb, Cs and Ba are compatible in phlogopite and the partition coefficient ratio phlogopite/K-richterite is high for Ba (1 3 6) and Rb (12). All melts have low contents of most of the first row transition elements, particularly Ni and Cu ((0.1–0.01) × primitive mantle). Nickel has high DMin/melt for all the major minerals (12 for K-richterite, 9.2 for phlogopite and 5.6 for Cpx) and so behaves at least as compatibly as in melting of peridotites. Fluorine/chlorine ratios in melts are high and DMin/melt for fluorine decreases in the order apatite (2.2) > phlogopite (1.5) > K-richterite (0.87). The requirement for apatite and at least one Ti-oxide in the source of natural lamproites holds for mica pyroxenites that lack K-richterite. The results are used to model isotopic ageing in hydrous pyroxenite source rocks: phlogopite controls Sr isotopes, so that lamproites with relatively low 87Sr/86Sr must come from phlogopite-poor source rocks, probably dominated by Cpx and K-richterite. At high pressures (>4 GPa), peritectic Cpx holds back Na, explaining the high K2O/Na2O of lamproites.  相似文献   

17.
In this paper we report the results of the analysis of rare earth (REE), large-ion lithophile (LILE), and high field strength (HFSE) elements in minerals from the alkaline lamprophyre dikes of the Kola region and the Kaiserstuhl province by the local method of laser ablation inductively coupled plasma mass spectrometry. The contents of Y, Li, Rb, Ba, Th, U, Ta, Nb, Sr, Hf, Zr, Pb, Be, Sc, V, Cr, Ni, Co, Cu, Zn, Ga, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu were measured in olivine, melilite, clinopyroxene, amphibole, phlogopite, nepheline, apatite, perovskite, and the host fine-grained groundmass. The obtained data on trace element partitioning among the mineral phases of the alkaline ultrabasic rocks of the dike series indicate that the main mineral hosts for the HFSEs and REEs in alkaline picrites, olivine melanephelinites, and melilitites are perovskite and apatite comprising more than 90% of these elements. Among major rock-forming minerals, melilite, clinopyroxene, and highly magnesian amphibole make a significant contribution to the balance of REEs during the evolution of melanephelinite melts. The partition coefficients of Ni, Co, Cu, Zn, Sc, V, Cr, Ga, Y, Li, Rb, Ba, Th, U, Ta, Nb, Sr, Hf, Zr, Pb, Be, and all of the REEs were calculated for olivine, clinopyroxene, amphibole, phlogopite, nepheline, perovskite, and apatite on the basis of mineral/groundmass ratios. Variations in the composition of complex zoned clinopyroxene phenocrysts reflect the conditions of polybaric crystallization of melanephelinite melt, which began when the magmas arrived at the base of the lower crust and continued during the whole period of their ascent to the surface. The formation of green cores in clinopyroxene is an indicator of mixing between primary melanephelinite melts and phonolite magmas under upper mantle conditions. The estimation of the composition of primary melts for the rocks of the alkaline ultrabasic series of the Kola province indicated a single primary magma for the whole series. This magma produced pyroxene cumulates and complementary melilitolites, foidolites, and nepheline syenites.  相似文献   

18.
The Oshurkovo Complex is a plutonic sheeted complex which represents numerous successive magmatic injections into an expanding system of subparallel and subvertical fractures. It comprises a wide range of rock types including alkali monzodiorite, monzonite, plagioclase-bearing and alkali-feldspar syenites, in the proportion of about 70% mafic rocks to 30% syenite. We suggest that the variation within the complex originated mainly by fractional crystallization of a tephrite magma.

The mafic rocks are considered as plutonic equivalents of lamprophyres. They exhibit a high abundance of ternary feldspar and apatite, the latter may attain 7–8 vol.% in monzodiorite. Ternary feldspar is also abundant in the syenites. The entire rock series is characterized by high Ba and Sr concentrations in the bulk rock samples (3000–7000 ppm) and in feldspars (up to 1 wt.%). The mafic magma had amphibole at the liquidus at 1010–1030 °C based on amphibole geothermometer. Temperatures as low as this were due to high H2O and P2O5 contents in the melt (up to 4–6 and 2 wt.%, respectively). Crystallization of the syenitic magmas began at about 850 °C (based on ternary feldspar thermometry). The series was formed at an oxygen fugacity from the NNO to HM buffer, or even higher.

The evolution of the alkali monzodiorite–syenite series by fractional crystallization of a tephritic magma is established on the basis of geological, mineralogical, geochemical and Sm–Nd and Rb–Sr isotope data. The geochemical modeling suggests that fractionation of amphibole with subordinate apatite from the tephrite magma leaves about 73 wt.% of the residual monzonite melt. Further extraction of amphibole and plagioclase with minor apatite and Fe–Ti oxides could bring to formation of a syenite residuum. Rb–Sr isotopic analyses of biotite, apatite and whole-rock samples constrain the minimum age of basic intrusions at ca. 130 Ma and that of cross-cutting granite pegmatites at ca. 120 Ma. Hence the entire evolution took place in an interval of ≤10 My. Initial 87Sr/86Sr ratios for the mafic rocks range from 0.70511 to 0.70514, and for syenites from 0.70525 to 0.70542. Initial Nd (130 Ma) values for mafic rocks vary from −1.9 to −2.4, and for syenites from −2.9 to −3.5. In a Nd(T) vs. (87Sr/86Sr)i diagram, all rock types of the complex fall in the enriched portion of the Mantle Array, suggesting their derivation from a metasomatized mantle source. However, the small but distinguishable difference in Sr and Nd isotopic compositions between mafic rocks and syenites probably resulted from mild (10–20%) crustal contamination during differentiation. Large negative Nb anomalies are interpreted as a characteristic feature of the source region produced by Precambrian fluid metasomatism above a subduction zone rather than by crustal contamination.  相似文献   


19.
何琦  肖龙  魏启荣  倪平泽 《岩石学报》2009,25(12):3229-3240
滇西吉义独蛇绿混杂岩位于金沙江缝合带的南端,岩石组合出露较齐全,包括堆晶橄榄岩、堆晶辉石岩、堆晶辉长岩以及玄武岩等,它们呈构造岩片的形式产出并与外来岩块组成蛇绿混杂岩.堆晶橄榄岩和辉石岩具低Al_2O_3,低TiO_2,而高Mg~#值(Mg~#=0.88～0.92),富集Cr和Ni,稀土总量偏低(∑REE=14.82×10~(-6)～27.75×10~(-6)),倒"U"型的稀土元素分布特征.堆晶辉长岩和玄武岩的Mg~#值较低,分别为0.70～0.79和0.51～0.66,具拉斑系列的演化趋势.玄武岩可以细分为2组:第一组玄武岩以平坦型稀土配分模式,低Mg~#(Mg~#=0.44～0.46),低稀土总量(∑REE=52.29×10~(-6)～60.26×10~(-6))为特征;第二组玄武岩则为LREE弱富集型的稀土配分模式,其Mg~#较高(Mg~#=0.54～0.68),稀土总量也较高(∑REE=62.13×10~(-6)～101.87×10~(-6)).在原始地幔标准化的微量元素配分图解中,两组玄武岩均相对富集大离子亲石元素而亏损Nb、Ta和Ti,与岛弧岩浆岩类似,明显不同于N-MORB.岩石的Sr-Nd同位素组成较为均一和稳定,堆晶橄榄岩和辉石岩的(~(87)Sr/~(86)Sr)_i=0.7051～0.7056,5_(Nd)(t)=2.8～4.1,玄武岩的(~(87)Sr/~(86)Sr)_i=0.7050～0.7056,ε_(Nd)(t)=5.1～5.8,且显示出原始地幔的同位素组成特征,暗示这些岩石为同源岩浆分异演化而成的岩浆产物.岩浆演化的主要方式为分离结晶作用,受地壳混染不明显.岩浆结晶形成岩石的顺序为:堆晶橄榄岩→堆晶辉石岩→堆晶辉长岩→玄武岩2组→玄武岩1组.岩石地球化学特征表明,吉义独蛇绿岩的形成与俯冲作用有关,且形成于金沙江洋内俯冲的消减环境.  相似文献   

20.
Plio-Pleistocene volcanism in the Golan and Galilee (northeasternIsrael) shows systematic variability with time and location:alkali basalts were erupted in the south during the Early Pliocene,whereas enriched basanitic lavas erupted in the north duringthe Late Pliocene (Galilee) and Pleistocene (Golan). The basaltsshow positive correlations in plots of ratios of highly to moderatelyincompatible elements versus the concentration of the highlyincompatible element (e.g. Nb/Zr vs Nb, La/Sm vs La) and indiagrams of REE/HFSE (rare earth elements/high field strengthelements) vs REE concentration (e.g. La/Nb vs La). Some of thesecorrelations are not linear but upward convex. 87Sr/86Sr ratiosvary between 0·7031 and 0·7034 and correlate negativelywith incompatible element concentrations and positively withRb/Sr ratios. We interpret these observations as an indicationthat the main control on magma composition is binary mixingof melts derived from two end-member mantle source components.Based on the high Sr/Ba ratios and negative Rb anomalies inprimitive mantle normalized trace element diagrams and the moderateslopes of MREE–HREE (middle REE–heavy REE) in chondrite-normalizeddiagrams, we suggest that the source for the alkali basalticend-member was a garnet-bearing amphibole peridotite that hadexperienced partial dehydration. The very high incompatibleelement concentrations, low K content, very low Rb contentsand steep MREE–HREE patterns in the basanites are attributedto derivation from amphibole- and garnet-bearing pyroxeniteveins. It is suggested that the veins were produced via partialmelting of amphibole peridotites, followed by complete solidificationand dehydration that effectively removed Rb and K. The requirementfor the presence of amphibole limits both sources to lithosphericdepths. The spatial geochemical variability of the basalts indicatesthat the lithosphere beneath the region is heterogeneous, composedof vein-rich and vein-poor domains. The relatively uniform 143Nd/144Nd(Nd = 4·0–5·2) suggests that the two mantlesources were formed by dehydration and partial melting of anoriginally isotopically uniform reservoir, probably as a resultof a Paleozoic thermal event. KEY WORDS: basanites; lithospheric heterogeneity; magma mixing; amphibole peridotite; pyroxenites  相似文献   

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