Melting of the subcontinental lithospheric mantle by the Emeishan mantle plume; evidence from the basal alkaline basalts in Dongchuan, Yunnan, Southwestern China

The Emeishan continental flood basalt (ECFB) sequence in Dongchuan, SW China comprises a basal tephrite unit overlain by an upper tholeiitic basalt unit. The upper basalts have high TiO₂ contents (3.2–5.2 wt.%), relatively high rare-earth element (REE) concentrations (40 to 60 ppm La, 12.5 to 16.5 ppm Sm, and 3 to 4 ppm Yb), moderate Zr/Nb and Nb/La ratios (9.3–10.2 and 0.6–0.9, respectively) and relatively high _{Nd (t)} values, ranging from − 0.94 to 2.3, and are comparable to the high-Ti ECFB elsewhere. The tephrites have relatively high P₂O₅ (1.3–2.0 wt.%), low REE concentrations (e.g., 17 to 23 ppm La, 4 to 5.3 ppm Sm, and 2 to 3 ppm Yb), high Nb/La (2.0–3.9) ratios, low Zr/Nb ratios (2.3–4.2), and extremely low _{Nd (t)} values (mostly ranging from − 10.6 to − 11.1). The distinct compositional differences between the tephrites and the overlying tholeiitic basalts cannot be explained by either fractional crystallization or crustal contamination of a common parental magma. The tholeiitic basalts formed by partial melting of the Emeishan plume head at a depth where garnet was stable, perhaps > 80 km. We propose that the tephrites were derived from magmas formed when the base of the previously metasomatized, volatile-mineral bearing subcontinental lithospheric mantle was heated by the upwelling mantle plume.     

Advances in our understanding of the gem corundum deposits of the West Pacific continental margins intraplate basaltic fields

Recent discoveries over the last decade of new gemfields, exploitation of new and existing deposits, and application of relatively new techniques have greatly increased our knowledge of the basalt-derived gem sapphire–ruby–zircon deposits. In this paper we focus on the Late Mesozoic to Cenozoic intraplate basaltic fields of the West Pacific continental margins. We review advances made in understanding the genesis of these deposits, based on the application of newer techniques. We also critically review existing data on the gem corundum deposits, in order to further refine a model for their origin.In some of the intraplate basaltic fields, corundum-bearing xenoliths have been found showing a range of PT formation conditions from 790 °C at 0.85 GPa to as much as 1100 to 1200 °C at 1.0 to 2.5 GPa. Although most magmatic sapphires contain syngenetic inclusions of columbite-group phases, zircon, spinel and rutile, some contain additional nepheline and K-feldspar, suggesting crystallization from more undersaturated alkaline magma while the Weldborough field of NE Tasmania also contains molybdenite and beryl, suggesting at least some interaction with more fractionated ‘granitic-type’ magmas. There is a large range in PT conditions calculated for the metamorphic rubies (from 780 to 940 °C, through 800 to 1150 °C up to 1000 to 1300 °C). Fluid/melt inclusion studies on magmatic corundums generally suggest that they formed in a CO₂-rich environment from a ‘syenitic’ melt under a range of T conditions from 720 to 880 °C up to 1000 to 1200 °C. Oxygen isotope studies reveal that typical magmatic corundums have values of + 4.4 to 6.9‰, whereas metamorphic corundums from the same basaltic host have lower values of + 1.3 to 4.2‰.Geochronological studies have shown that some fields produced a simple eruptive and zircon/corundum crystallization event while others had multiple eruptive events but only one or two zircon crystallization events. For a few fields, some corundums/zircons crystallized in storage regions and then remained relatively inert for periods of 200 to 400 Ma without significant change before transport to the surface in the Cenozoic. Tectonic studies of the Australian region suggest that many of the corundums crystallized from magmas related to episodic basaltic volcanism in a tectonic regime of extension, associated with the opening of the Tasman and Coral Seas. For the Asian region, the magmatic–polygenetic corundums within the basaltic fields largely crystallized in a tectonic regime of distributed E–W extension, whereas the metamorphic-metasomatic corundums crystallised in a transpressional regime associated with the collision of the Indian Plate with the Eurasian Plate (e.g., [Garnier, V., Giuliani, G., Maluski, H., Ohnenstetter, D., Deloule, E., 2003. Ar–Ar and U–Pb ages of marble-hosted ruby deposits from Central and South-east Asia. Geophysical Research Abstracts 5, 03751; Garnier, V., Giuliani, G., Ohnenstetter, D., and Schwarz, D., 2004. Les gisements de corindon: classification et genese. Les placers a corindon gemme. Le Regne Mineral 55, 7-47; Garnier, V., Ohnenstetter, D., Giuliani, G., Maluski, H., Deloule, E., Phan Trong, T., Pham Van, L., Hoang Quang, V., 2005a. Age and significance of ruby-bearing marble from the Red River Shear Zone, Northern Vietnam. Canadian Mineralogist 43, 1315–1329]).     

力马河镍矿Re-Os同位素研究

四川力马河镍矿是峨眉山大火成岩省一个重要的岩浆硫化物矿床。本文通过对其主要岩、矿石类型Re、Os及其同位素组成的分析,综合探讨了成矿岩体原始岩浆性质、矿石硫化物成因、成矿机制及Re-Os同位素等时线年龄。结果表明,力马河镍矿不同类型岩矿石样品初始Os同位素组成是不均一的,富硫化物的网脉状矿石及其选纯硫化物Os同位素组成初值差异较小,其等时线年龄为265±35 Ma、与岩体锆石SHRIMP年龄263±3 Ma基本相当;硫化物含量较低的岩、矿石样品间初始Os同位素组成差异较大,其表观等时线年龄大于成矿年龄。分析认为,岩矿样品初始Os同位素组成的不均一是由含较高放射成因187Os丰度的硫化物熔体和含较低放射成因187Os丰度的硅酸盐熔体不同比例混合造成的。混合模型分析表明,硫化物含量超过30％的矿石样品初始187Os/188Os基本接近,硫化物含量低于30％的岩矿石样品初始187Os/188Os随硫化物含量上的不同差异很大,为岩浆硫化物矿床Re-Os等时线年龄可能出现多组年龄解的现象提供了一种可能的解释。成矿岩体中含放射成因187Os丰度最低的岩石样品γOs（t=260Ma）在5左右、Cu/Pd比值在7000左右,表明是基本没有受到地壳混染及硫化物熔离影响的原始岩浆结晶分异产物,估计原始岩浆Os含量在1×10－9左右,为苦橄质岩浆。矿石硫化物Re/Os比值显著高于任何赋矿橄榄岩,γOs（t=260Ma）高达110左右,综合分析揭示了力马河镍矿硫化物为二次熔离成因,模式分析认为,矿石硫化物是由原始岩浆经历R=2000左右的硫化物熔离后、其亏损岩浆再经R=200左右的硫化物熔离形成,与二次熔离相对应,成矿岩浆也经历了两次混染作用,分别为上、下地壳7％左右的混染。     

内蒙古天和永玄武岩成因：岩相学与矿物学分析

天和永地区南北向出露的小面积单层碱性玄武岩,岩石中出现至少三种矿物共生组合关系。所有岩石均以橄榄石作为主要斑晶矿物,大颗粒环带橄榄石斑晶中心镁值为89．5,边缘镁值为70．3,小颗粒环带橄榄石镁值46．2～78．9。粒径最小的橄榄石聚集体和散布的基质橄榄石均无明显环带,前者镁值67．4～68．1,后者镁值65．5—72．1;单斜辉石由相对高钛高铝贫硅的散布柱状辉石和相对低钛低铝富硅的聚集粒状辉石组成,前者形成于低压快速淬火环境,镁值65．1—77．1,后者形成于富含挥发份的低压低过冷度环境,镁值77．7～78．0。所有单斜辉石均以次透辉石为主,个别为深绿辉石;斜长石以包含结构产出为主,为相对偏酸性的中长石An=33．7～37．4,CaO含量低与早期大量单斜辉石结晶有关。由于残余岩浆内K,0和Na20含量富集且极不均一,晚期结晶的长石同时出现了高钠长石、K-高钠长石（歪长石）和K-透长石;钛铁氧化物多数为晚期结晶的细粒基质矿物,少量以0．3ram左右的斑晶和橄榄石斑晶中的包裹体形式存在,可归属为钛铁尖晶石（Usp）-磁铁矿（Mt）固溶体系列,晚期逐渐向贫铝、铬和富钛方向演化。由于以上各种造岩矿物的晶出,导致残余岩浆形成的火山玻璃向贫镁、铁、钙和富铝、钾方向演化,火山玻璃的全碱含量变异趋势与全岩类似,均和SiO2含量无明显相关性,火山玻璃具有响岩和粗面安山岩成分特征,K2O／Na2O值变化大0．68～1．61,均为钾玄岩系列,Na2O含量依然呈现宽区间特征,是天和永玄武岩由钾质过渡到钠质的主要原因。天和永玄武质岩浆从地幔运移到地表仅需5小时-5天,大颗粒斑晶橄榄石和小颗粒基质橄榄石生长仅需几小时到几天,前者形成无须深部岩浆房停留,后者近似晚期岩浆快速淬火时间。高镁橄榄石斑晶与残余岩浆的扩散平衡时间约42天～252天。深部结晶的橄榄石在运移途中和地表流动过程中缺乏足够的时间和适宜的动力学条件而无法离开岩浆体系。全岩与火山玻璃间缺少中间过渡成分,呈两个相对集中的端元组分存在亦由晶出矿物无法离开岩浆体系所致。天和永玄武岩的成岩时间尺度远小于同化混染和岩浆分异的时间尺度,是岩浆作用过程未能明显影响其不均一原生岩浆性质的主要原因。因此,岩浆作用的某些物理过程分析是认识岩浆起源与岩浆作用过程及其对火成岩多样性的贡献的重要方面,同时对于理解和约束岩浆作用的某些化学过程也是十分有益的。     

花岗岩研究的误区——关于花岗岩研究的思考之五

本文在对花岗岩四大基石(混合作用、结晶分离作用、构造环境和源区)问题分析的基础上,指出花岗岩研究存在的三大误区: (1)不恰当地仿效玄武岩的理论和研究方法,忽视了花岗岩的复杂性。(2)不恰当地用板块构造学说解释大陆花岗岩问题。板块构造是地球演化到一定阶段的产物,并成功解释了与板块边界相联系的岩浆活动,但是,它不能解决主要来源于大陆的花岗岩的地质问题。(3)太过重视花岗岩的地球化学研究而忽视了对花岗岩基础地质的研究。作者指出,地球化学方法在花岗岩中的使用应当是有限制的,花岗岩研究陷入误区是我们缺少扎实的基础研究、对板块构造的理解不深和对花岗岩复杂性认识不足等三个方面的原因造成的。文中还批评了学术界存在的人云亦云的奴性思想,指出它严重地阻碍了我们的创新思维,是当前亟待改进和克服的。     

Re-Os同位素对峨眉山大火成岩省成因制约的探讨

峨眉山大火成岩省（ELIP）主要由玄武岩、玄武质火山碎屑岩及少量的苦橄岩（包括越南的科马提岩）、长英质岩石以及层状岩体和岩墙组成,其物质来源直接关系到其成因是否与地幔柱活动有关。Re-Os同位素体系是地核、地幔和地壳物质的最佳示踪剂。前人对ELIP内的Re-Os同位素研究表明,低Ti玄武岩的Os含量为0．006×10^-9-0．40010^-9,^187Os／^188Os初始值为0．1371～1．403,并提出其与地幔柱活动有关;而高Ti玄武岩的Os含量为0．00410^-9～0．56010^-9,^187Os／^188Os初始值为0．1271～5．19,认为起源于大陆岩石圈地幔或地幔柱上升过程中受到大量岩石圈地幔“混染”（xu JF et al．,2007）;科马提岩的0s含量为1．2410^-9～7．0010^-9,^187Os／^188Os初始值为0．1251～0．1261,苦橄岩的Os含量为0．3210^-9～2．32910^-9,^187Os／^188Os初始值为0．1233～0．1266,指示苦橄岩和科马提岩均来自亏损地幔源区（Hanski et al．,2004;陈雷等,2007）。本文利用Os含量最低、^187Os／^188Os最高的高Ti玄武岩作为地壳端员,用铁质陨石、原始上地幔（PUM）和亏损地幔（DMM）作为地核和各种地幔端员,分别做二元混合计算,结果显示绝大多数玄武岩和所有苦橄岩及科马提岩均落在地壳和DMM混合曲线附近,并且邻区特提斯洋地幔岩与DMM具有相近的Os含量和^187Os／^188Os组成,据此推测峨眉山火成岩的形成与特提斯洋的活动有关,主要受控于地壳和亏损地幔的相互作用。     

Origin and evolution of alkali basaltic magma in the Okinawa Trough

I~IOXThe Okinawa Trough is an extending back--arc basin between the East China Sea Shelf andthe Ry'Ukyu Island Arc of Japan. There are widespreadly distributing acid pumice in the troughand a little basalt just in some area of the extending center. There have been some detailed rePOrtsabout the mineralogy and petrochemical feature of the subalkali tholeiite and alkali trachyte in thetrough (Zhai and Gan, 1995; Li et al., 1997; Qin and Zhai, 1988). This paper mainly reportselectron mic…     

冲绳海槽玄武岩中中酸性残余熔体研究及其岩石学意义

与洋壳有关的酸性岩由于对了解幔源岩浆的演化以及判别古老蛇绿岩套及其构造位置的重要意义而倍受岩石学家和构造地质学家的关注。本对发现于冲绳海槽玄武岩基质中的中酸性到酸性残余熔体进行了详细研究，它们提供了幔源玄武岩浆结晶分异形成酸性岩浆的直接证据。在细小的基质矿物间分布有一种玻璃质的残余熔体，其成分随距冷凝边距离(L)的增加而越来越酸性。在SiO2对Na2O K2O图解上，残余熔体的投影点从玄武岩到英安岩均有分布，反映了一个连续的演化系列。在AFM图解上，残余熔体表现出与Thingmuli火山岩系列类似的拉斑玄武岩系列的演化趋势。我们的研究表明：残余熔体的演化受结晶分异作用控制。在早期结晶阶段，辉石的结晶起主导作用，结果造成残余熔体中SiO2、Al2O3，Na2O的迅速增加，FeO、MgO、CaO迅速降低。在晚期结晶阶段，斜长石成为主导结晶相，导致残余熔体中Al2O3，Na2O的迅速消减。Al2O3、Na2O从增加到降低的转变出现在SiO2=62％左右。在L=27．5mm处，85～90％的基质岩浆已发生了结晶作用，导致残余熔体中SiO2含量达到69～70％，而且此处还新出现了一种富FeTi的氧化物。该玄武岩中残余熔体和基质矿物的成分及演化特征分别与Thingmuli火山岩系列中酸性端元的组成相似，在也佐证了Thingmuli火山岩系列是幔源岩浆结晶分异的产物.     

川西北松潘-甘孜地块大石包组玄武岩成因及其形成构造背景

川西北松潘-甘孜地块内二叠世大石包组玄武岩富集大离子亲石元素和高场强元素，具有与洋岛玄武岩相似的地球化学性质，形成于大陆板内环境。通过与典型峨眉山玄武岩之地球化学组成的对比研究，认为大石包玄武岩与峨眉山玄武岩中的高钛类玄武岩性质相同，两者具有一个共同的成因，即都是峨眉山地幔柱活动的产物。由此推测峨眉山玄武岩不仅分布在扬子地块内部，向西还有一定的延伸，同时暗示了峨眉山地幔柱头部可能具有比现在所认识的更大的规模。