山东栖霞大方山玄武岩中地幔熔体玻璃捕虏体岩相学及岩石化学研究

过去地学界对固体地幔岩捕虏体研究已经相当充分。另外,山东栖霞大方山还存在地幔熔体玻璃捕虏体,其化学成分、矿物成分既不同于固体地幔岩也不同于寄主玄武岩。此玻璃体特别富K,而且早于寄主岩浆,二者间很不平衡。富K玻璃捕虏体往往被玄武岩浆消化殆尽,但在野外仍然可以找到少量残留体供室内研究。此熔体玻璃的存在意味着该区玄武岩浆作用不是一元而是多元岩浆体系,还存在早一期的碱性地幔岩浆。后者消化混染于玄武岩浆之中,会产生富K玄武岩。     

黑龙江省尚志地区新生代钾质玄武岩研究

尚志中新世富碱的钾质系列玄武岩为白榴霞石岩、橄榄霞石岩、霞石碧玄岩和橄榄碧玄岩。岩石中似长石矿物大量出现,霞石和白榴石可以共存。稀土元素和大离子不相容元素的特征表明形成白榴霞石岩、橄榄霞石岩、霞石岩碧玄岩和橄榄碧玄岩的地幔熔融程度越来越高。主元素和微量元素的模拟计算表明,霞石岩岩浆为上地幔岩2～4％的熔融,碧玄岩为上地幔橄榄岩5～8％的部分熔融;这些岩浆形成时的温压条件为:霞石岩的T=1410～1430℃,P=22～23×10~8Pa;碧玄岩的T=1380～1430℃,P=20～23.5×10~8Pa。     

岩浆熔体中的挥发性组分及其岩石学意义

文章论述了挥发性组分在岩浆熔体中的溶解行为及其在岩浆熔体中溶解的限制条件，在此基础上讨论了挥发性组分对岩浆演化及岩石学成因方面的意义：溶解在岩浆中的水可明显地改变矿物从岩浆中结晶出的顺序，改变岩浆熔体的演化轨迹。含水玄武岩浆在其早期结晶出铁的氧化物并与Ｓｉ和富碱质组分分异从而使其成为Ｆｅ亏损的钙－碱性系列的岩浆，而无水玄武岩浆演化的早期不能结晶出磁铁矿，因而演化成富Ｆｅ且具中等Ｓｉ含量的拉斑玄武岩系列。溶解于岩浆中Ｈ２Ｏ的离解将产生高ｆＯ２环境，从而导致Ｆｅ的氧化物在岩浆演化早期沉淀。     

安徽省铜陵地区侵入岩成因的实验研究

通过３７次地实验研究认为：（１）在地壳温度下，地壳物质的重熔不可能形成石英闪长质或更基性的碉浆；（２）碱性玄武岩浆同化花岗质地壳，可以生成石英闪长质和花岗闪长持岩浆，所产生的岩浆刘钾富碱，属高压系，与铜陵地区侵入岩相似；（３）高压下形成的岩浆比中压下形成的岩浆更高钾富硒；（４）在岩浆演化过程中铜与钾似无成因联系，钾与铜的“相关性”与它们的趋同性有关，即两者均于岩浆晚期富集。     

赛马-柏林川碱性杂岩常量组分变异的分离结晶制约

赛马－柏林川碱性杂岩体为侵位于古元古宙与新元古宙之间的缓倾斜岩席状岩体,缓倾的张裂隙制约了分异岩浆的侵位和含矿溶液的流通,交代富集的上地幔产生的富碱岩浆与富集的地壳产生的岩浆以不同比例混合,形成了正长质岩浆和霞石正长质岩浆。含地壳组分较高的正长质岩浆,受富钙辉石、角闪石和镁质较高黑云母的结晶分离制约向硅酸过饱和方向演化;霞石正长质岩浆受富钙辉石—霓辉石、白榴石、含Ｆｅ较高黑云母、黑榴石的分离结晶制约发生分异。稀土元素矿床是霞石正长质岩浆分异残余熔体的产物,侵位于岩体最高层位。     

熔体结构与酸性熔岩的某些特征

在流纹质岩浆中,存在两种不混溶的熔体,一种熔体富SiO_2贫FeO,另一种则相反。从熔体结构的角度看,前一种熔体富桥氧,后者则富自由氧。水的解聚作用可以改变流纹质岩浆的结构,即降低它的聚合程度,因此,含水流纹岩浆的粘度低于玄武岩浆的粘度,从而使流纹岩中流纹构造发育。 实际工作中应避免混淆流纹岩与酸性熔结凝灰岩。     

新疆新源县城南石炭纪火山岩岩石学和元素地球化学研究

新疆新源县南部那拉提山北坡出露的石炭纪火山岩主要由玄武岩、玄武质粗面安山岩、粗面安山岩、安山岩、流纹岩和火山碎屑岩组成。该火山岩中玄武岩属于钙碱性系列,安山质岩石和流纹岩属于高钾钙碱性系列,其中轻稀土轻微富集而重稀土相对亏损,玄武岩富集大离子亲石元素、U、Th和Pb,亏损高场强元素。研究表明,该火山岩岩浆可能是由俯冲板片脱水产生的流体交代地幔楔后,地幔楔发生部分熔融的结果。微量元素模拟计算表明,该玄武岩岩浆可以由石榴石二辉橄榄岩经3％～6％的部分熔融得到;安山质岩浆可由玄武岩岩浆经15％-28％的分离结晶形成。     

西藏当惹雍错富钾和富钠碱性火山岩的矿物学研究及其成因指示

对青藏高原西南部当惹雍错地区的中新世超钾质粗面岩及共存的富钠质方沸石(霞石)响岩进行了详细的岩石学、矿物学研究,揭示出两套岩石具有不同的矿物学特征.钠质方沸石(霞石)响岩中橄榄石斑晶的熔体包裹体与钾质火山岩的成分相当,应属于早期残余的钾质岩浆,表明了钠质方沸石(霞石)响岩的形成晚于超钾质粗面岩.两类岩石的全岩化学成分、...     

安徽省铜陵地区侵入岩成因的实验研究

通过３７次成岩实验研究认为：（１）在地壳温度下，地壳物质的重熔不可能形成石英闪长质或更基性的岩浆；（２）碱性玄武岩浆同化花岗质地壳，可以生成石英闪长质和花岗闪长质岩浆，所产生的岩浆高钾富碱，属高钾岩系，与铜陵地区侵入岩相似；（３）高压下形成的岩浆比中压下形成的岩浆更高钾富碱；（４）在岩浆演化过程中铜与钾似无成因联系，钾与铜的“相关性”与它们的趋同性有关，即两者均于岩浆晚期富集。     

我国东北小古里河-科洛-五大连池-二克山火山带钾质矿物成因及地质意义

东北黑龙江小古里河-科洛-五大连池-二克山火山岩带是我国近代保存最好的火山群之一,此带火山岩的岩石化学特点全都强碱富钾,K₂O/Na₂O>1.2,属于一套高钾过碱性火山岩。通过对东北钾质火山岩及金云母橄榄岩地幔捕虏体中钾质矿物金云母、白榴石的成分、结晶环境与岩浆成分及来源关系的研究,认为在岩石圈伸展构造背景下,地幔金云母橄榄岩的低度部分熔融形成钾质岩浆,钾质岩浆上升到地壳浅部经历了白榴石的结晶作用。岩浆演化晚期,因钾质矿物大量晶出导致岩浆相对富钠而出现他形霞石和方钠石等填隙矿物。火山岩及地幔捕虏体中富挥发分矿物金云母、白榴石、磷灰石、霞石和方钠石还提供了钾质岩浆富含H₂O、F、Cl、P等挥发分的证据。     

滇西富碱斑岩中特殊包体岩石的流体包裹体幔源不混溶特征

滇西地区沿金沙江-哀牢山断裂带产出了一套新生代富碱斑岩,其中发现了与镁铁-超镁铁质深源包体岩石共生的含石英的方解石包晶(体)、石英钠长石伟晶岩包体和含玻璃包裹体的纯石英包晶(体)以及富铁熔浆包体.流体包裹体地球化学研究表明,该四类特殊包体的形成与富含CO2流体持续减压而造成的不混溶作用有关;而玻璃包裹体与水溶液包裹体以...     

Metasomatism in mantle xenoliths from Gees,West Eifel,Germany: evidence for the genesis of calc-alkaline glasses and metasomatic Ca-enrichment

 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     

江苏六合新生代玄武岩中地幔捕虏体的硫化物相研究

江苏六合一带碱性玄武岩中的出露有以尖晶石二辉橄榄岩为主的地幔捕虏体,这些地幔矿物中普遍有硫化物相出现：（１）被寄主矿物捕获的早期硫化物颗粒。（２）产于矿物晶粒边界或次生裂隙充填物,（３）硫化物包裹体,包括单相硫的包裹体、硫化物－玻璃两相熔体包裹体和ＣＯ／２－硫化物－玻璃（含硅酸盐子矿物）的多相包裹体,电子探针分析表明,硫化物包裹体比例隙中硫化物具有更高的相对Ｆｅ和Ｓ含量,较低的Ｎｉ含量。硫化物包裹     

The sulfides in the garnet pyroxenite xenoliths from Salt Lake Crater, Oahu

Trace amounts of sulfide, ranging from 0?06 to 0?26 volume percent, are present in the garnet pyroxenite xenoliths in nephelinebasalt at Salt Lake Crater, Oahu, Hawaii. Microscopic studyrevealed the existence of three chemically and physically distinctsulfide types, i.e. enclosed, interstitial, and vein sulfides.The enclosed sulfide forms spherical inclusions in primary pyroxene,garnet, ilmenite, and spinel. It has a bi-modal chemical character,which may be in part due to alteration of some of the enclosedsulfide grains by the nepheline basalt host magma, but moreprobably represent Cu-Ni-rich sulfide liquid coexisting withCu-rich monosulfide solid solution. The interstitial sulfideis uni-modal and occurs in the interstices of the primary silicates.It has been subjected to intense chemical alteration by thenepheline basalt host magma. As a result the interstitial sulfidebecame Cu-poor with a varying Ni content, which indicates thatcomplete chemical equilibrium with the basalt host magma hasnot been attained. The vein sulfide, present as fracture fillings, is of late genesisand appears to represent partly altered enclosed sulfide. Thealteration process is the same as that which affected the interstitialsulfide. The mineralogy and chemistry of the enclosed sulfide suggeststhat the xenoliths have been abruptly cooled from about 1000?C, which represents the ejection of the xenoliths from thehost basalt magma.     

A new type of orthopyroxenite xenolith from Takashima, Southwest Japan: silica enrichment of the mantle by evolved alkali basalt

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.     

Typochemistry of rinkite and products of its alteration in the Khibiny Alkaline pluton,Kola Peninsula

The occurrence, morphology, and composition of rinkite are considered against the background of zoning in the Khibiny pluton. Accessory rinkite is mostly characteristic of foyaite in the outer part of pluton, occurs somewhat less frequently in foyaite and rischorrite in the central part of pluton, even more sparsely in foidolites and apatite–nepheline rocks, and sporadically in fenitized xenoliths of the Lovozero Formation. The largest, up to economic, accumulations of rinkite are related to the pegmatite and hydrothermal veins, which occur in nepheline syenite on both sides of the Main foidolite ring. The composition of rinkite varies throughout the pluton. The Ca, Na, and F contents in accessory rinkite and amorphous products of its alteration progressively increase from foyaite and fenitized basalt of the Lovozero Formation to foidolite, rischorrite, apatite–nepheline rocks, and pegmatite–hydrothermal veins.     

Mantle metasomatism and magma formation in continental lithosphere: Data on xenoliths in alkali basalts from the Makhtesh Ramon,Negev desert,Israel

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.     

Geochemistry and petrogenesis of spinel lherzolite xenoliths from Boeun,Korea

Geochemical characteristics of spinel lherzolite xenoliths, enclosed in Miocene alkali basalt from Boeun, Korea, provide important clues for understanding the lithosphere composition, equilibrium temperature and pressure conditions, and depletion and enrichment processes of subcontinental lithospheric mantle beneath Boeun. The spinel lherzolite xenoliths with protogranular to porpyroclastic textures were accidentally trapped by the ascending alkali basalt magma. The spinel lherzolite xenoliths originated at depths between 50 and 63 km with equilibrium temperatures ranging from 847 to 1030 °C. These xenoliths may have undergone small degrees (1–2%) of partial melting and cryptic metasomatism by an alkali basaltic melt. Based on Sr and Nd isotope compositions, the subcontinental lithospheric mantle beneath Boeun was heterogeneous and similar to that beneath East China and Central Mongolia rather than the Japanese Island Arc.     

Some implications of xenolith glasses for the mantle sources of alkaline mafic magmas

The assumption that mafic alkaline magmas are derived from mantle sources with a lherzolite mineralogy has become entrenched in the petrologic literature. Although it is commonly assumed that highly alkaline magmas require metasomatised mantle sources, there is little understanding of the spatial relation of such sources with respect to those of associated more Si-rich transitional magmas. Glasses developed in mantle xenoliths represent natural experiments which may provide some insight on this problem. Highly silica undersaturated glasses developed in the amphibole-garnet clinopyroxenite portion of a composite xenolith from Nunivak Island, Alaska, become quartz normative where they penetrate adjacent spinel lherzolite. A comparison of glass compositions in mantle pyroxenite and lherzolite xenoliths reveals that glasses developed in amphibole pyroxenite xenoliths are in general more silica undersaturated than those in lherzolite xenoliths. This suggests that some highly silica undersaturated magmas such as nephelinites may in fact be derived by the preferential melting of amphibole or amphibole-garnet pyroxenite veins and that the spectrum from nephelinite to transitional alkaline basalt that characterizes many individual alkaline volcanic suites is produced by mixing with melt derived from the host lherzolite as the degree of partial melting increases.