首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 171 毫秒
1.
我国东部与南部新生代碱性玄武岩及火山角砾岩喷发过程中,携带了来自地幔及玄武岩浆深部结晶分异形成的包体,这些包体包括尖晶石二辉橄榄岩、石榴石二辉橄榄岩、辉石岩和辉长岩类,以及石榴石、辉石和歪长石巨晶等。我们收集了福建、江苏、河北及云南等地数十个包体,并对其中13个包体的矿物进行了研究,计算了包体形成的温度和压力,并讨论了成因。  相似文献   

2.
在延边地区明月沟盆地中侏罗世屯田营组火山岩中发现含有较多的辉石岩捕虏体及单斜辉石和角闪石捕虏晶。单斜辉石相对富含Al2O3、FeO和TiO2,与中国东部新生代玄武岩中单斜辉石巨晶的成分相当。角闪石巨晶的成分明显不同于地幔橄榄岩包体中的韭闪石。从矿物化学所获得的温度-压力计算结果表明:岩浆来源应位于壳幔过渡带。  相似文献   

3.
甘肃好梯超镁铁煌斑岩中深源包体及巨晶   总被引:7,自引:0,他引:7  
本文对甘肃好梯超镁铁煌斑岩中上地幔包体和巨晶进行了详细研究,结果表明本区尖晶石二辉橄榄岩包体来自大约62km深处,而石榴石二辉橄榄岩来自约92km深处。后者在岩相学、矿物学方面表现出明显的地幔交代作用特征,表明石榴石二辉橄榄岩为与寄主煌斑岩有关的成因包体。另外本区两种单斜辉石巨晶和橄榄石巨晶为高压结晶作用的产物。  相似文献   

4.
鲁西中生代侵入岩依次生成辉长岩系列、二辉石闪长岩系列、角闪闪长岩系列、二长岩系列和正长岩系列(林景仟等,1989)。近年来,我们在属于二辉石闪长岩系列的莱芜铁铜沟岩体、矿山岩体和邹平茶叶山岩体中发现了大量不同成因类型的橄榄岩类包体。这些包体为认识鲁西地区中生代岩浆起源、岩石圈结构及上地幔中的超镁铁质岩浆作用提供了重要的信息。 1.包体成因类型及岩石学特征所发现的橄榄岩类包体的主要岩石类型有纯橄岩、方辉橄榄岩、二辉橄榄岩和橄辉岩;以前两类为主,与二辉岩、单辉辉石岩、辉闪岩和角闪岩包体相伴生。根据岩石结构和矿物成分特征,这些包体可划分为亏损型上地幔纯橄榄岩、方辉  相似文献   

5.
胶东—苏北石榴石二辉橄榄岩形成条件及年代   总被引:7,自引:0,他引:7  
在胶东—苏北地区,由石榴石二辉橄榄岩、尖晶石二辉橄榄岩、石榴石辉石岩、榴辉岩、斜辉辉橄岩和纯橄岩组成的杂岩成群和成带分布,延长590km。该岩带越过郯庐断裂带延伸至大别山,全长约1200km。岩带内石榴石二辉橄榄岩与尖晶石橄榄岩伴生,组成较大的岩块,并且与榴辉岩伴生,曾被作者确定为一种有层序的岩套。石榴石二辉橄榄岩的Sm-Nd同位素年龄为925±53Ma,矿物地质温度计和压力计表明其形成于115—160km深部,温度为800—1371℃。该石榴石二辉橄榄岩平衡温度和压力符合大陆地温线,而不同于中国东部沿海地区玄武岩中包体石榴石二辉橄榄岩,后者的平衡温度压力符合于大洋地温线。  相似文献   

6.
叶松  张保民等 《地质学报》2002,76(3):431-431
江西安远县路迳产出的超基性岩筒,是幔源岩浆岩的一个特殊类型,命名为金伯利质煌斑岩。岩筒的Rb- Sr等时线年龄37Ma。该岩筒中含有幔源单斜辉石巨晶和辉石岩、尖晶石橄榄岩、石榴石辉石岩包体,这些巨晶和包体来自上地幔不同深度。本文应用傅立叶变换红外光谱研究了该岩筒中巨晶单斜辉石和3种包体中辉石的含水性,探讨辉石含水量与其成分及来源深度的关系。单斜辉石以3607~3630cm_(-1)和3522~3542cm_(-1)两组吸收谱带为主,斜方辉石存在3410  相似文献   

7.
中国东部新生代玄武质岩石中的超镁铁质捕虏体,主要包括五种类型:石榴石二辉橄榄岩(±少量尖晶石)、尖晶石二辉橄榄岩、尖晶石方辉橄榄岩、辉石岩和巨晶矿物。不同类型捕虏体间的共存矿物存在系统的化学成分变化。尤以Al_2O_3、Cr_2O_3变化明显。本文提出捕虏体中共存矿物的Cr~#[100Cr/(Al+Cr)]可作为分类和岩石成因的重要标志。并将五种捕虏体划分为三种地幔成因类型:饱满的或原始的地幔(石榴石二辉橄榄岩和尖晶石二辉橄榄岩),亏损的或残余的地幔(尖晶石方辉橄榄岩),地幔条件下熔浆分离的产物(辉石岩和巨晶矿物)。  相似文献   

8.
内蒙古集宁新生代玄武岩产于华北克拉通北缘,属于广义的“汉诺坝玄武岩”。首次在三义堂附近的碱性玄武岩中发现了大量的橄榄岩包体、辉石和长石以及少量的含钛磁铁矿巨晶。包体主要是尖晶石二辉橄榄岩,造岩矿物为橄榄石+斜方辉石+单斜辉石+尖晶石,辉石巨晶主要为透辉石和普通辉石,长石巨晶主要是歪长石和少量斜长石。1.5GPa条件下,尖晶石二辉橄榄岩样品所记录的平衡温度与汉诺坝相近,集中于950℃左右,大体上反映了华北克拉通北缘大陆岩石圈地幔尖晶石相部分的温度状态。单斜辉石巨晶的结晶温压大于幔源包体的平衡温压,表明巨晶的来源深度可能大于包体。包体的结构及矿物成分分析表明,这些包体是玄武质岩浆上升过程中偶然捕获岩石圈地幔的岩石碎块。二辉橄榄岩包体中橄榄石高Mg#值(89.5~91.7)和较高的NiO含量(0.29%~0.55%),暗示集宁玄武岩中的橄榄岩包体来自较高熔融程度的岩石圈地幔。  相似文献   

9.
我国东南沿海新生代玄武岩中两类超镁铁岩包体的成因   总被引:3,自引:0,他引:3  
我国东南沿海粤、闽、浙、苏、皖诸省广泛分布新生代玄武岩。本文目的在于,研究包裹于碱性玄武质岩石中的两类超镁铁岩深源包体的矿物岩石学和地球化学,进而讨论包体的起源和成因。这二类深源包体是:一,橄榄岩类包体,又称绿色包体,以尖晶石二辉橄榄岩为主,分布遍及全区,主要产地见表1脚注;兼有石榴石二辉橄榄岩,见于浙江巨县和福建明溪。二,辉石岩类包体,又称黑色包体,以二辉岩和单斜辉石岩为主,伴生辉长岩和角闪石岩,主要见于广东普宁麒麟。  相似文献   

10.
本文以西藏自治区罗布莎铬铁矿床为例并结合世界其它地区同类矿床实例,讨论了豆荚型铬铁矿床的成因机制。研究表明,铬铁矿与纯橄岩-斜辉辉橄岩都是由同一原始地幔岩(尖晶石二辉橄榄岩)经不同程度熔融的产物。铬铁矿及纯橄岩是这一过程中高度熔融的最终产物。其熔融的机制是两种辉石(斜方辉石和单斜辉石)不一致熔融转变为橄榄石和铬尖晶石,并伴随着副矿物铬尖晶石及造岩矿物成分的调整和再造,从而导致铬铁矿床与纯橄岩的紧密伴生。该研究成果对认识世界上同类矿床的成因有普遍意义。  相似文献   

11.
Olivine, orthopyroxene and garnet grains belonging to the peridotitic suite of mineral inclusions in natural diamonds typically show compositions poorer in Ca and Al and richer in Mg and Cr than the same minerals in peridotite nodules in kimberlite. Other features suggest the crystallisation of diamonds from magmas of kimberlitic affinities, and it is suggested that the genesis of peridotitic suite diamonds is linked with that of a CO2-bearing magma. It is shown that the generation of kimberlitic magma from common garnet-peridotite (with 5 wt.% clinopyroxene) in the presence of CO2 may rapidly remove by melting all Ca-rich solid phases (clinopyroxene and/or carbonate). Further melting may form liquids in equilibrium with olivine, orthopyroxene, and garnet with the distinctive compositions of the diamond inclusions. The amount of melting and CO2 necessary for the loss of clinopyroxene (and/or carbonate) are estimated at approximately 5.0 wt.% and 0.5 wt.% respectively.  相似文献   

12.
The paper discusses the petrography, mineralogy, petrochemical affinities, P/T crystallization regimes and genetic aspects of four garnet clinopyroxenite inclusions from diatremes in the Gloucester area, New South Wales. Inclusion mineral assemblages (which generally display textural evidence of annealing) include garnet-plagioclase-(sulphur-rich scapolite)-clinopyroxene, garnet-hornblende-orthopyroxene-clinopyroxene and garnet-hornblende-clinopyroxene. The garnet-plagioclase clinopyroxenite inclusion possesses an essentially alkali basaltic chemistry. It probably represents a crystallized basaltic liquid whereas the petrochemical affinities of the two garnet pyroxenites carrying amphiboles are more appropriate to subcalcie clinopyroxenites with variable Mg/Fe ratios. Experimental and other data suggest that the Gloucester garnet clinopyroxenite suite crystallized at pressures of the order of 10–14 kb and temperatures in the vicinity of 1000° C. The chemical compositions of many garnet pyroxenites, occurring either as inclusions in alkali basaltic rocks or as localized facies within some alpine-type peridotites, such as those in the western Mediterranean region, suggest that they can be interpreted as lower temperature heteromorphs of “primitive” subcalcic clinopyroxenites, variable in Al contents and hy/di ratios, but retaining consistently low Ti, Na, K and P. It is suggested that many inclusions of garnet (-spinel) pyroxenite and subcalcie Clinopyroxenite, restricted to alkali basaltic rocks and their associates, originally may have been interleaved with upper mantle aluminous peridotites and that they represent partial melt products of their aluminous peridotitic hosts.  相似文献   

13.
Abstract In the Su-Lu ultrahigh- P terrane, eastern China, many coesite-bearing eclogite pods and layers within biotite gneiss occur together with interlayered metasediments now represented by garnet-quartz-jadeite rock and kyanite quartzite. In addition to garnet + omphacite + rutile + coesite, other peak-stage minerals in some eclogites include kyanite, phengite, epidote, zoisite, talc, nyböite and high-Al titanite. The garnet-quartz-jadeite rock and kyanite quartzite contain jadeite + quartz + garnet + rutile ± zoisite ± apatite and quartz + kyanite + garnet + epidote + phengite + rutile ± omphacite assemblages, respectively. Coesite and quartz pseudomorphs after coesite occur as inclusions in garnet, omphacite, jadeite, kyanite and epidote from both eclogites and metasediments. Study of major elements indicates that the protolith of the garnet-quartz jadeite rock and the kyanite quartzite was supracrustal sediments. Most eclogites have basaltic composition; some have experienced variable 'crustal'contamination or metasomatism, and others may have had a basaltic tuff or pyroclastic rock protolith.
The Su-Lu ultrahigh- P rocks have been subjected to multi-stage recrystallization and exhibit a clockwise P-T path. Inclusion assemblages within garnet record a pre-eclogite epidote amphibolite facies metamorphic event. Ultrahigh- P peak metamorphism took place at 700–890° C and P >28 kbar at c . 210–230 Ma. The symplectitic assemblage plagioclase + hornblende ± epidote ± biotite + titanite implies amphibolite facies retrogressive metamorphism during exhumation at c . 180–200 Ma. Metasedimentary and metamafic lithologies have similar P-T paths. Several lines of evidence indicate that the supracrustal rocks were subducted to mantle depths and experienced in-situ ultrahigh- P metamorphism during the Triassic collision between the Sino-Korean and Yangtze cratons.  相似文献   

14.
Compositional maps of orthopyroxene and garnet of contrasting grain size and in contact with different minerals were made from two paragneiss granulites from the Minto terrane of northern Quebec. The compositional maps provide clear evidence of late exchange of Fe/(Fe + Mg) after Ca in garnet and Al in orthopyroxene had been quenched-in. The extent of late Fe-Mg exchange was controlled by neighbouring minerals, with negligible Fe-Mg gradients against plagioclase and quartz, and substantial gradients against exchangeable Fe-Mg minerals. Cores of grains in contact with exchangeable Fe-Mg neighbours are progressively more reset in Fe/(Fe + Mg) as grain size decreases, whereas cores of even small grains surrounded by only plagioclase and quartz are not significantly different in Fe/(Fe + Mg) than cores of the largest grains. Gradients of Ca in garnet and of Al in orthopyroxene in grains of uniform Fe/(Fe + Mg) preserve a high-temperature retrograde history during which intergranular exchange effected compositional uniformity of mineral rims and intragranular Fe-Mg diffusion in garnet and orthopyroxene was rapid enough to homogenize Fe/(Fe + Mg). The transition from efficient intergranular exchange at relatively high temperatures to local Fe-Mg exchange at lower temperatures may have been controlled by loss of an intergranular exchange medium in the rock, possibly an internally generated dehydration melt phase. Implications for geothermometry of granulites include the following (numerical values are particular to this study): (1) core compositions of garnet and orthopyroxene grains in contact with exchangeable neighbours may be reset in Fe/(Fe + Mg) relative to the most refractory compositions by an amount equivalent to 120d? C; (2) Fe-Mg exchange thermometry using even the most refractory Fe/(Fe + Mg) compositions may not record peak granulite conditions, possibly recording instead the temperature at which an intergranular exchange medium was lost from the rock; and (3) temperature-sensitive net transfer equilibria involving Al solubility in orthopyroxene yield temperatures up to 150d? C higher than maximum Fe-Mg exchange temperatures, even in grains with flat Fe/(Fe - Mg) compositional profiles, making them a better means of estimating peak granulite temperatures than Fe-Mg exchange thermometry.  相似文献   

15.
 Multianvil experiments were carried out at 10–15 GPa and 1600–1700 °C to match the compositions of majoritic garnet inclusions from diamonds, and to determine the compositions of other phases potentially coexisting with these inclusions in the source. Most experiments produced coexisting majoritic garnet, diopsidic clinopyroxene, one or more (Mg,Fe)2SiO4 polymorphs, and quenched carbonatic melt. The experimental garnets had relatively high Ca and Fe contents similar to the observed Ca and Fe contents of the inclusions. The resulting Si contents confirmed that the depth of origin of the inclusion with the highest Si content did not exceed 410 km, thus none of the majoritic garnet inclusions found so far originated in the transition zone (410–660 km). The evidence from inclusions and experiments is consistent with the presence of an eclogite layer occurring globally between 200 and 410 km. Compositional variations observed among more than 100 majoritic garnet inclusions with their Si content, which is a measure of pressure and depth, are consistent with the origin of the eclogite layer by crystal fractionation in a magma ocean. The compositions of olivine coexisting with majoritic garnet in the experimental products had the average Fe/(Fe + Mg) ratios between 0.16 and 0.28. Inclusions with such high Fe contents have not been found; the Fe/(Fe + Mg) ratio of the olivine inclusions in diamonds usually varies between 0.05 and 0.09. Hence, the mantle between 200 and 410 km may not contain olivine. In the absence of olivine, the discontinuity at 410 km is most likely a chemical boundary between the 200-km-thick eclogite layer and a more mafic transition zone. Received: 15 March 2001 / Accepted: 14 September 2001  相似文献   

16.
彭礼贵 《地质科学》1987,(2):138-151
本地区阿尔卑斯型超基性岩在温度约800—1200℃、压力约0.9—1.68GPa、差异应力0.2—0.35GPa和比较干的条件下发生了塑性变形作用,形成一套以残碎斑结构为主并有糜棱结构的超基性岩质糜棱岩。在残碎斑状矿物和造矿的铬尖晶石中的原生全结晶化硅酸盐熔体包裹体和熔流体包裹体的发现和研究,证明该类岩石是在温度约1200—1300℃、压力约1.1-1.38 GPa,大致相当40-50 km深处,庄物理化学条件相对恒定的环境中,经硅酸盐熔浆液态分异形成的岩浆岩。在重结晶次生橄榄石和辉石中未发现任何包裹体,说明超基性岩塑性变形作用是在岩浆成岩之后。  相似文献   

17.
D. Phillips  J.W. Harris  K.S. Viljoen 《Lithos》2004,77(1-4):155-179
Silicate and oxide mineral inclusions in diamonds from the geologically and historically important De Beers Pool kimberlites in Kimberley, South Africa, are characterised by harzburgitic compositions (>90%), with lesser abundances from eclogitic and websteritic parageneses. The De Beers Pool diamonds contain unusually high numbers of inclusion intergrowths, with garnet+orthopyroxene±chromite±olivine and chromite+olivine assemblages dominant. More unusual intergrowths include garnet+olivine+magnesite and an eclogitic assemblage comprising garnet+clinopyroxene+rutile. The mineral chemistry of the De Beers Pool inclusions overlaps that of most worldwide localities. Peridotitic garnet inclusions exhibit variable CaO (<5.8 wt.%) and Cr2O3 contents (3.0–15.0 wt.%), although the majority are harzburgitic with very low calcium concentrations (<2 wt.% CaO). Eclogitic garnet inclusions are characterised by a wide range in CaO (3.3–21.1 wt.%) with low Cr2O3 (<1 wt.%). Websteritic garnets exhibit intermediate compositions. Most chromite inclusions contain 63–67 wt.% Cr2O3 and <0.5 wt.% TiO2. Olivine and orthopyroxene inclusions are magnesium-rich with Mg-numbers of 93–97. Olivine inclusions in chromite exhibit the highest Mg-numbers and also contain elevated Cr2O3 contents up to 1.0 wt.%. Peridotitic clinopyroxene inclusions are Cr-diopsides with up to 0.8 wt.% K2O. Eclogitic and websteritic clinopyroxene inclusions exhibit overlapping compositions with a wide range in Mg-numbers (66–86).

Calculated temperatures for non-touching inclusion pairs from individual diamonds range from 1082 to 1320 °C (average=1197 °C), whereas pressures vary from 4.6 to 7.7 GPa (average=6.3 GPa). Touching inclusion assemblages are characterised by equilibration temperatures of 995 to 1182 °C (average=1079 °C) and pressures of 4.2–6.8 GPa (average=5.4 GPa). Provided that the non-touching inclusions represent equilibrium assemblages, it is suggested that these inclusions record the conditions at the time of diamond crystallisation (1200 °C; 3.0 Ga). The lower average temperatures for touching inclusions are attributed to re-equilibration in a cooling mantle (1050 °C) prior to kimberlite eruption at 85 Ma. Pressure estimates for touching garnet–orthopyroxene inclusions are also skewed towards lower values than most non-touching inclusions. This apparent difference may be an artefact of the Al-exchange geobarometer and/or the result of sampling bias, due to limited numbers of non-touching garnet–orthopyroxene inclusions. Alternatively pressure differences could be caused by differential uplift in the mantle or possibly variations in thermal compressibility between diamond and silicate inclusions. However, thermodynamic modelling suggests that thermal compressibility differences would cause only minor changes in internal inclusion pressures (<0.2 GPa/100 °C).  相似文献   


18.
Abstract Clinopyroxenes and garnets from 11 blueschist-facies Fe-rich eclogite samples from the Voltri Group show a wide range of chemical compositions. Detailed analyses of single pyroxene and garnet grains show wide and scattered chemical inhomogeneity, the KD(KD= (Fe2+/Mg)Gt/(Fe2+/Mg)Cpx) ranges from 20 to 87 based on rim analyses only. The data obtained indicate that the mineral pairs never attained equilibrium under uniform P-T conditions and that the compositions of the metamorphic minerals were influenced mainly by the composition of the pre-metamorphic minerals and by topotactical reactions.  相似文献   

19.
Cathodoluminescence (CL) imaging of polished sections of a diamond from the Guaniamo region of Venezuela suggests a history of the diamond involving two periods of growth separated by a period of resorption and possibly brittle deformation. In situ electron probe analysis of multiple eclogitic garnet inclusions reveals a correlation between garnet composition and location in the stone. An early-formed garnet in the diamond core has higher Ca/(Ca+Mg) and lower Mg/(Mg+Fe) values than later garnets associated with the second period of diamond growth. This variation conforms to an extensive trend of variation in the suite of eclogitic garnets extracted from Venezuelan diamonds. The diamond is zoned in carbon isotope composition (in situ secondary ion mass spectrometry, SIMS, data). The core compositions (δ13C PDB), corresponding to the first stage of growth, average −17.7‰. The second period of growth is apparently in two sub-sets of CL zones with mean values of −13.0‰ and −7.9‰. Nitrogen contents of diamond are low (30–300 atomic ppm) and do not correlate with carbon isotope composition. Oxygen isotope ratios of the garnet inclusions are elevated substantially above those expected for “common mantle”; δ18O VSMOW of early garnet is approximately +10.5‰ and two late garnets average +8.8‰. The evolutionary trend of magnesium enrichment in garnet is unlikely to represent igneous fractionation. The stable isotope data are consistent with diamond formation in subducted meta-basic rocks that had interacted with sea water at low temperatures at or near the sea floor and contained a substantial biogenic carbon component. During or following subduction, diamonds continued to form in an evolving system that was progressively modified by interaction with mantle material.  相似文献   

20.
About half the diamonds studied from the Cenozoic placer deposits along the Namibian coast belong to the peridotitic suite. The peridotitic mantle source is heterogeneous ranging from lherzolitic to strongly Ca depleted (down to 0.24 wt.% CaO in garnet) and shows large variations in Cr/Al ratio, illustrated by very low to very high Cr2O3 contents in garnet (2.6–17.3 wt.%). The Cr-rich end of this range includes exceptionally high Cr2O3 contents in Mg-chromite (70.7 wt.%) and clinopyroxene (3.6 wt.%). Garnet-olivine thermometry appears to indicate two groups, one that equilibrated at temperatures between 1200 and 1220°C and a second between 960 and 1100°C. Combined estimates of pressure and temperature based on garnet-orthopyroxene pairs indicate a large variance in geothermal gradients, corresponding to 38–42 mW/m2 surface heat flow.

The trace-element composition of peridotitic garnet inclusions (determined by SIMS) also indicates large diversity. Two principal groups, corresponding to different styles of metasomatic source enrichment, are recognized. The first group ranges from extremely LREEN-depleted patterns, through trough-shaped REEN to sinusoidal patterns with the position of the first peak gradually moving from the LREEN to the MREEN. This series of REE patterns is interpreted to reflect a range of metasomatic agents with decreasing LREE/HREE. Only in the case of the two garnets with REEN peaking at Sm–Eu is this process connected with enrichment in Zr, without significant introduction of Y and Ti. The metasomatism responsible is interpreted as reflecting percolation of CHO-fluids through harzburgite under sub-solidus conditions. A second group of garnets shows an increase from LREEN–MREEN and almost flat (lherzolitic garnet) to moderately declining MREEN–HREEN at super-chondritic levels. This second style of metasomatism is caused by an agent carrying HFSE and showing only moderate enrichment in LREE over HREE, which points towards silicate melts.  相似文献   


设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号