角闪石高温高压实验研究进展及其地球物理意义

高温高压实验作为地球科学研究的重要方向之一,通过模拟地球深部的温度和压力条件,了解地球深部物质的物理化学性质、地球内部结构和动力学演化。角闪石属于双链硅酸盐矿物,为地幔岩石圈的重要组成,广泛分布在海洋地壳、俯冲板块、变质岩和火成岩中。作为俯冲带的重要含水矿物,角闪石的广泛分布和高温高压下的脱水对于理解俯冲带水含量以及水迁移具有重要作用,同时在俯冲带的地震活动、高电导率异常、地震波速异常和岩浆活动中扮演重要角色。在过去的近百年时间里,国内外学者对角闪石高温高压物理化学性质进行了大量的研究。角闪石具有非常复杂的元素组成和结构特征,由此也导致了不同角闪石物理化学性质存在显著不同,包括脱水与脱羟基反应中元素迁移的差异、角闪石形成与分解过程中碱性元素(K+Na)和H2O含量对热稳定的影响、不同空间群结构下的高压结构相变、原位条件下不同结晶方向的电导率异常、不同结晶学优选方位(CPO)下的波速异常等。已有的研究对于角闪石的物理化学性质以及其在俯冲带中发挥的作用有了比较清楚的认识,但仍然有许多问题需要进一步研究,如角闪石的高压脱水动力学、热物性和变形机制等。     

华北克拉通中生代拆沉陆壳物质对岩石圈地幔的改造:来自橄榄岩捕虏体中角闪石的成分制约

对鲁西和太行山南段早白垩世高镁闪长岩中橄榄岩捕虏体中的角闪石进行了主量元素和痕量元素分析,并讨论了角闪石成分与改造岩石圈地幔熔体的性质与来源之间的关系。研究结果表明,橄榄岩类捕虏体中的角闪石主要为交代成因。在化学上,它们属于钙质角闪石。太行山南段符山橄榄岩捕虏体中的角闪石属于镁质普通角闪石和浅闪石或浅闪石质普通角闪石;鲁西铁铜沟橄榄岩捕虏体中的角闪石为韭闪石质普通角闪石、浅闪石质普通角闪石和镁绿钙闪石质普通角闪石。与板内橄榄岩捕虏体中的角闪石相比,鲁西和太行山南段早白垩世高镁闪长岩橄榄岩捕虏体中的角闪石具有相对高的Mg#(鲁西:86.0~90.8;太行山:90.7~94.2)和SiO2(鲁西:44.04%~46.98%;太行山:47.09%~49.79%)以及相对低的Na2O(1.92%~2.51%)、TiO2(0.01%~1.46%)、Nb(0.29×10-6~1.98×10-6)和Zr(1.61×10-6~5.34×10-6),这与来自俯冲带之上地幔楔橄榄岩捕虏体中的角闪石相类似。综合橄榄岩捕虏体的地球化学特征,可以判定华北克拉通早白垩世岩石圈地幔遭受了起源于拆沉陆壳物质熔融熔体的改造。     

内蒙古文圪气镁铁-超镁铁质杂岩体中环带角闪石矿物学特征及成因

内蒙古文圪气镁铁-超镁铁杂岩体主要由辉石岩和角闪石岩组成,普遍发育角闪石环带的角闪石岩位于岩体南部,呈伟晶结构,主要由角闪石(>95%)和磷灰石(3%～5%)组成。选取环带较明显的两个角闪石样品,采用EMPA和LA-ICPMS分别做主量和微量成分剖面,环带角闪石边部为铁韭闪石,核部为韭闪石。从核部到边部,SiO2、MgO、Na2O含量逐渐降低,Al2O3、TiO2、FeOT、K2O和碱金属(Na2O+K2O)逐渐升高。中稀土、重稀土元素和Sc最大值位于核部,最小值位于边部;轻稀土元素、高场强元素、大离子亲石元素及过渡金属元素最大值位于幔边部,最小值位于核部,反映了核部氧逸度较高、温度和压力较低,边部氧逸度较低、温度和压力较高,是两期不同成分、温度、压力和氧逸度岩浆结晶的表现,并且角闪石岩受到后期高氧逸度低温热液的改造。环带角闪石的形成机理与文圪气岩体中铂族元素矿化过程相吻合。文圪气岩体与华北地台北缘中泥盆世镁铁质-超镁铁质岩具有相同的岩石组成、成因和构造背景,环带角闪石具有幔源角闪石特点,核部平均温度大于732℃,边部大于770℃,核、边部温度均小于950℃,结晶压力≤272 MPa,结晶深度≤12.4km。环带角闪石的结晶过程可能与文圪气岩体中铂族元素的成矿过程类似。     

黄河口及邻近渤海海域悬浮体和沉积物中有机碳、氮的分布特征及其影响因素

利用元素分析仪对2007年获取的黄河口及邻近渤海海域悬浮体和沉积物进行了有机碳、氮含量分析.结果表明,在同一站位有机碳大体上的分布为,表层沉积物中TOC含量≤底层悬浮体中POC含量<表层悬浮体中POC含量;依据表层沉积物中TOC、TN含量和悬浮体中POC的分布,研究区可划分为5个区,依次为莱州湾西部靠近黄河口区(Ⅰ和Ⅱ...     

新疆拜城县波孜果尔碱性花岗岩体中角闪石与黑云母地球化学特征及其对成岩成矿的记录

角闪石和黑云母是含稀有稀土金属矿物的高分异碱性花岗岩中常见的暗色矿物。角闪石和黑云母对不同元素(尤其是Nb、Ta、Zr、REE等稀有稀土金属元素)的相容性特点使它们的主微量元素特征成为岩浆演化的"日志",对构建含矿岩浆的成岩成矿模型具有一定意义。本文针对新疆拜城波孜果尔碱性花岗岩体中的角闪石和黑云母,利用电子探针(EPMA)和激光剥蚀电感耦合等离子体质谱仪(LA-ICP-MS)等分析技术,开展精细的矿物学研究,综合厘定Nb、Ta等元素在岩浆结晶过程中的富集和分配过程。波孜果尔岩体中的角闪石均为亚铁钠闪石,总体表现为较高的Na和Fe含量,而相对贫Ca(0.15 apfu)、Mg(0.06 apfu)和Ti(0.07 apfu),成分的均一性以及轻稀土元素的亏损特征暗示了角闪石较晚结晶且角闪石结晶前大量富轻稀土元素矿物结晶分离。根据共生关系黑云母可分为A、B两类,它们显示出不同的化学成分。A类黑云母具有相对较高的F含量(A类为3.81%～4.82%,B类为1.68%～3.65%)和SiO_2含量(A类为41.5%～43.3%,B类为35.9%～38.5%),相对较低的TFeO含量(A类为28.0%～31.4%,B类为32.2%～35.7%)和Al_2O_3含量(A类为6.45%～7.62%,B类为9.70%～11.00%)。黑云母与角闪石中氟的含量变化指示了氟在结晶过程中的富集、饱和过程以及氟饱和引起的稀有稀土金属矿物大量结晶现象。由于在主要矿物中的不相容性,成矿元素Nb、Ta在熔体中含量逐渐上升,但主要矿物及大部分副矿物中均高于全岩的Nb/Ta值产生了"Ta丢失"现象。结合前人研究,本文认为气热相带出与锆石的结晶分离两种机制共同作用导致Ta从熔体中分离。     

内蒙古东乌旗晚石炭世角闪石岩锆石U- Pb年龄、地球化学及其构造意义

为研究兴蒙造山带晚古生代地幔性质和造山演化特征,对东乌旗巴彦都兰新识别出的角闪石岩进行了岩相学、角闪石电子探针分析、锆石LA-ICP-MS U-Pb年代学、锆石Hf同位素和岩石地球化学分析.结果表明,东乌旗角闪石岩主要由角闪石(85％～90％)、少量斜长石(5％)和磁铁矿(<5％)等组成.获得的角闪石岩测年样品的锆石U-Pb年龄为310±1 Ma,表明岩体形成于晚石炭世.6件样品的地球化学数据显示,SiO2含量为48.66％～52.50％,MgO含量11.53％～13.10％,Al2O3含量为10.11％～12.18％,Na2 O+K2O含量2.21％～3.13％,小于3.5％,m/f比值为0.36～0.45,Mg#值为70.27～74.54,TFeO值为7.77～10.14;稀土元素球粒陨石标准化配分模式表现为轻稀土相对富集的右倾型,岩石富集大离子亲石元素Rb、K等,相对亏损高场强元素Nb、Ta、Ti.电子探针分析结果显示角闪石岩中角闪石属于钙质角闪石,具有幔源角闪石的特点.角闪石岩中锆石εHf(t)值为7.47～15.54,单阶段地壳模式年龄(TDM1)为847～332 Ma,表明其源区主要为亏损地幔.结合区域地质演化,认为东乌旗角闪石岩可能形成于古亚洲洋俯冲背景下,这一发现为兴蒙造山带晚古生代地幔构造岩浆演化提供了岩石证据.     

造山带中地壳水致部分熔融——大别造山带含角闪石混合岩的证据

出露于北大别地体的混合岩常含有粗粒自形程度较高的角闪石,角闪石在暗色体和浅色体均有分布,并且含有石英、斜长石和黑云母包裹物。这暗示着角闪石为转熔矿物,是通过原岩中黑云母+斜长石+石英矿物组合部分熔融而形成的。实验研究表明,黑云母分解生成角闪石需要至少2%~4%的水含量参与反应。所以,北大别混合岩中的转熔角闪石指示水致部分熔融的发生。角闪石-斜长石温压计显示,混合岩形成于700~770℃和3.5~6.0 kbar,低于正片麻岩中的黑云母脱水熔融固相线,这和转熔矿物中缺失无水矿物(如:斜方辉石、石榴石)相符。近等温降压的记录和混合岩产出于快速隆升的穹窿环境相一致。角闪石REE组成变化很大。Eu异常和La/Sm比值成正相关,与Gb/Yb比值及REE含量成负相关,表明角闪石的结晶对于熔体的组成影响显著。具有Eu负异常,高Gb/Yb、低La/Sm比值的角闪石结晶自初始的熔体;具有Eu正异常,低Gb/Yb、高La/Sm比值的角闪石结晶自分异熔体。相比于暗色体和中间体,淡色体亏损Ca、Fe、Mg、Ti和Mn元素含量,富集Si和Na元素含量。混合岩中的淡色体成分变化较大,从英云闪长质变化到花岗质,花岗质淡色体相对富集K、Ba和Rb元素含量。淡色体的稀土含量和配分模式变化很大,地球化学模拟显示,具有高度分异的REE组成和亏损HREE特征的淡色体是角闪石残留源区的结果。携带有角闪石的淡色体显示较高的HREE和相对平坦的HREE分布,并表示出角闪石的进入对于熔体的组成有明显的影响。部分淡色体具有明显的Eu正异常(Eu*值为2.5-~6.8)和显著低的REE含量(几十ppm),结合显微结构观察,认为该类淡色体是熔体经历结晶分离,形成长石堆晶。综上所述,混合岩中的淡色体多数不代表初始熔体的成分,转熔矿物的卷入和结晶分离作用显著影响了淡色体组成。     

冀东晚古生代东湾子岩体的岩石成因研究

冀东晚古生代东湾子岩体由角闪石岩、少量辉石岩和辉长岩组成.典型的堆晶结构、全岩和镁铁质矿物(透辉石、角闪石)的上凸型稀土分布模式、相容元素含量低且变化范围大(如:角闪石岩中V=296×10-6～673×10-6)的特征表明了岩体的堆晶成因.计算得到的与辉石岩中的透辉石相平衡的熔体具有很高的稀土含量,轻重稀土分馏较为明显,富集大离子亲石元素(如:Sr,Ba,K),亏损高场强元素(如:Nh,Zr,Ti),具有典型的弧岩浆特征.透辉石和角闪石的矿物成分也具有弧岩浆的特征.高钙透辉石、大量的角闪石与黑云母的存在说明母岩浆富水.透辉石在高PH2O的状态下与熔体反应,生成角闪石的结构特征也证明了这一点.结合岩体的球化学特征,认为岩浆来源于富集的含有角闪石的尖晶石橄榄岩的部分熔融,母岩浆具有富水的特征(>3%).考虑到岩体形成时代(～300Ma;Zhao et al.,2007)和地质背景,认为东湾子岩体与位于华北北缘的其它晚石炭-早二叠世的岩体形成于同一构造背景下,都是晚古生代时期古亚洲洋向华北板块之下俯冲的产物.     

鄂东南矿集区鸡冠嘴矽卡岩型金铜矿床含矿岩体中辉石和角闪石成分变化特征及其对岩浆演化和成矿的指示意义

为了解长江中下游地区与金铜矿化有关的岩体在浅部的演化过程及其对成矿的作用,本文对鄂东南矿集区鸡冠嘴矽卡岩型金铜矿成矿岩体石英二长闪长斑岩进行了详细的岩相学观察,并利用电子探针(EMPA)分析了其中辉石和角闪石的主量成分。岩相学特征显示辉石形成时间早于角闪石。辉石成分变化较小,而角闪石成分变化较大。角闪石可根据Al的含量分为高低两组,即高铝含量的自形角闪石以及低铝含量的半自形及他形角闪石。高铝角闪石又不同程度的被低铝角闪石交代。通过矿物温压计估算辉石形成的温度和压力为1055~1071℃(平均1060℃)和224~312MPa(平均255MPa)。高铝角闪石形成的温度和压力为809~864℃(平均833℃),108~193MPa(平均137MPa),低铝角闪石形成的温度和压力为721~766℃(平均741℃),48~67MPa(平均56MPa)。岩浆具有较高的氧逸度,并且从高铝角闪石到低铝角闪石,熔体的氧逸度从△NNO+0.6升高到△NNO+1.9。岩浆经历了连续的侵位历史,从9.6km到5.2km的岩浆房再到2.1km的浅地壳处就位。岩浆在9.6km处经历了辉石的分离结晶,在5.2km处经历了角闪石及少部分斜长石的分离结晶,在2.1km处经历由于降压引起的流体出溶。由于深部的分离结晶作用,熔体中的水含量增加,氧逸度升高。较高的水含量使岩浆更容易演化出成矿热液,较高的氧逸度使岩浆演化早期没有硫化物的分离结晶,从而阻止了成矿元素在岩浆演化早期亏损。鸡冠嘴岩体较浅的就位深度也更有利于成矿流体的析出。这些因素共同作用形成了鸡冠嘴金铜矿床。     

新疆赤湖-福兴铜矿区角闪石矿物化学特征及其地质意义

赤湖和福兴铜矿位于东天山大南湖-头苏泉岛弧带中。本文以矿区中酸性岩体中的角闪石为研究对象,利用电子探针技术(EPMA)对岩体中的角闪石进行矿物学及矿物化学研究,限定矿区岩体形成的构造背景和物理化学条件,并探讨了岩浆演化和成矿作用过程。电子探针成分结果表明,矿区角闪石主要为镁角闪石、钙镁闪石质角闪石和次生阳起石,其成因主要为岩浆成因,部分遭受次生改造,形成过程中有幔源物质的参与,且与俯冲作用相关。赤湖闪长玢岩中角闪石形成的压力为244~451 MPa(2.44~4.51 kbar),相当于8~15 km的深度,温度为880~918℃,lgfO2和熔体中的水含量分别为–10.2~–11.1和6.4%~7.0%;赤湖花岗闪长岩、石英闪长岩和福兴石英闪长岩、闪长岩及其角闪石形成的压力为30~90 MPa(0.3~0.9 kbar),相当于1~3 km的深度,温度为640~785℃,lgfO2和熔体中的水含量分别为–12.3~–13.8和3.6%~4.8%。赤湖-福兴矿区岩体中的角闪石可能形成于两个不同深度的岩浆房,幔源岩浆运移到深部岩浆房时形成闪长玢岩中的角闪石斑晶,随后残余岩浆继续上升,在浅部岩浆房形成闪长岩、石英闪长岩和花岗闪长岩中的角闪石,并伴随着流体的出溶和成矿元素的运移,最后在浅部岩浆房顶部形成铜矿床。     

相山两种不同成因角闪石的地球化学特征对比

通过详细研究相山两种不同成因角闪石的元素及同位素地球化学发现：江西相山铀矿田北部同时存在两种不同成因的角闪石：正变质成因的角闪石，寄主岩石为斜长角闪(片)岩，微量元素以富集大离子亲石元素(LILE)(K,Rb，Th，Ta，U)、稍为富集Ti,Se和相对贫高场强元素(HFSE)(Zr，Hf,Y，Yb，Cr，HREE)为特征，稀土总量低，稀土分布型式为近水平型，δ^18O为7．95～8．58，显示变质火成岩的氧同位素特征；副变质成因的角闪石，寄主岩石为含石榴角闪石英片岩．微量元素以高度富集大离子亲石元素(LILE)(K，Rb，Th，U)、稍为富集Ta,Nb，Ce，Zr，Hf，Sm和相对贫高场强元素(HFSE)(Ti，Y，Yb，Cr)、强烈亏损Sc为特征，稀土总量高．轻重稀土相互分离程度高，轻稀土富集，O同位素组成(δ^18O)较高，为9．95～10．02，显示碎屑沉积变质岩的氧同位素特征。     

Trace-element distribution in lavas from Anjouan and Grande Comore,western Indian Ocean

The elements Cr, Ni, Cu, Zn, Rb, Sr, Y, Zr and Ba have been determined by X-ray fluorescence for 65 basaltic and differentiated lavas from Anjouan, while Sc, V, Cr, Co, Ni, Cu, Ga, Rb, Sr, Y, Zr, Nb, Cs, Ba and Hf have been determined by spark-source mass spectrometry for selected lavas from Anjouan and Grande Comore, the most recently formed of the Comores Archipelago. Basaltic lavas studied range through nephelinite, basanite, alkali basalt and hypersthene-normative basalt, while differentiated lavas belong mainly to the trends: alkali basalt - trachyte and basanite - phonolite. The results indicate that during magmatic fractionation behaviour of large-ion elements such as Rb, Sr, Y, Zr, Ba and Nb is controlled by size/charge criteria, resulting in their exclusion from crystallising phases until the late trachytic and phonolitic stages. These elements are clearly fractionated by amphibole, plagioclase and alkali feldspar. Variation of transition elements due to crystal-liquid differentiation is largely in accord with the predictions of crystal field theory. The behaviour of Zn is not readily accounted for. Fractionation of K/Rb, K/Cs and probably Zr/Nb and discrepancies in abundance levels of large-ion elements between the main basaltic types are best accounted for in terms of high-pressure processes and probably also reflect inherent features of source-region geochemistry, coupled with the effects of variable partial melting.     

西藏松多榴辉岩的矿物原位微量元素地球化学研究

对松多榴辉岩中单矿物进行的LA-ICP-MS原位微区微量元素分析研究结果表明,石榴石主要富集中、重稀土元素和Y,同时具有高丰度的Sc、V、Cr和Co等元素;绿辉石中的微量元素以中稀土元素、Sr、Sc、V、Cr、Co、Ni和Ti为主,含有一定量的Zr、Hf等。石榴石、绿辉石、角闪石和绿帘石中均显示轻稀土元素亏损的特点,表明在退变质过程中没有发生明显的富轻稀土元素的外来流体交代作用,因而其微量元素矿物地球化学的某些特点不同于苏鲁地区的榴辉岩。石榴石变斑晶中某些元素(如Ti、Zr)的分带性暗示了榴辉岩在紧随峰期变质之后的折返过程中发生了降压增温过程。榴辉岩主要变质矿物中微量元素的分配显然受到矿物主量元素的分配所控制,如MgO在石榴石和绿辉石之间的分配对Ni、Co、Ti分配的控制以及CaO的分配对Sr、Y、REE分配的控制等。退变质过程中矿物的形成或分解以及物理化学条件的改变都可以引起矿物间微量元素的重新分配。由绿辉石退变质而形成的角闪石,较之原先的绿辉石,其微量元素配分曲线总体特征会发生变化,但元素总体丰度相近,某些元素特点相似,又反映了绿辉石和角闪石之间的成生联系。金红石是Ti、Nb、Ta、Zr、Hf的主要赋存矿物,而与之共生的绿帘石所表现出来的高场强元素的亏损特征表明了金红石的存在所带来的影响。     

酸性矿山排水影响的水库沉积物微量元素地球化学特征

为了解酸性矿山排水（AMD）影响下水库沉积物中微量元素的质量分数水平及其分布特征,对常年受酸性废水影响的贵州兴仁猫石头水库沉积物中26种微量元素的质量分数、相关性及控制因素进行了分析。结果表明：猫石头水库沉积物柱中Sr、Ba、Zr、V、Cr和As质量分数平均值超过了100 μg/g,其中As质量分数最高,平均值超过800 μg/g;Be、Ta、Co、Ag、Cd、Sn和Se质量分数的平均值都在5 μg/g以下;其他元素质量分数平均值则在10~60 μg/g之间。相较未受AMD影响的水系沉积物,研究区水库沉积物具有明显的As和Sb富集特征。水库沉积物中Li、Be、Rb、Sr、Cs、Ba、Sc、Y、Zr、Hf、Nb、Ta、Th之间存在显著正相关关系,而As与这些元素之间存在显著负相关关系。元素相关分析、因子分析及微量元素图解表明,Li、Be、Rb、Sr、Cs、Ba、Sc、Y、Zr、Hf、Nb、Ta、Th、Cr、Sb等元素受控于流域岩石化学风化和土壤物理侵蚀,这也是控制研究区元素分布最重要的因素,而Cu、Cd等重金属元素则与AMD对地层中元素的溶蚀析出和有机质等细颗粒物的吸附有关。另外,研究区重金属元素中,Cd、Cu、Pb、Cr、Zn的生态风险轻微,而As和Sb则具有很强的潜在生态风险。     

Major and trace element variation in ilmenite in the Skaergaard Intrusion: petrologic implications

Ilmenite separates from the floor (LS), roof (UBS), and wall (MBS) sequences of the Skaergaard Intrusion were analyzed for major and trace elements using DCP-AES and ICP-MS techniques. In all three sequences, FeO progressively increases, and MgO and Al₂O₃ progressively decrease with differentiation. Although trace element abundances are, in general, higher in UBS ilmenite than in MBS and LS ilmenite, all three sequences have similar trends for trace element abundance vs. crystallization. Ba, Cs, Rb, Sr, Th, U, Y, and the REEs are excluded elements in ilmenite, and remained at low abundances during differentiation. Cr, Ni, Sc, and V are included elements in ilmenite and other mafic phases, and decreased during differentiation. V contents in ilmenite, however, do not decrease significantly until the upper part of the middle zone, suggesting that magnetite did not begin to affect the magma differentiation trend until much later than when it first appears in the intrusion. Hf, Nb, Ta, and Zr, which are strongly excluded elements in silicates, are included elements in ilmenite. The element ratios Zr/Hf, Y/Ho, Nb/Ta, and U/Th are relatively constant in Skaergaard ilmenite from different parts of the intrusion, suggesting that fluid transport did not significantly effect these elements during differentiation or post-solidification cooling. Calculated partition coefficients for ilmenite in the Skaergaard Intrusion are similar to those reported from previous studies of lunar and terrestrial basalts and kimberlites, and for most elements are significantly lower than those reported for ilmenite in rhyolitic magma. Similar D_i's for Zr, Hf, Nb, and Ta suggest that ilmenite crystallization did not significantly affect Zr/Nb or Hf/Ta in the Skaergaard magma, but the ratios of Zr, Hf, Nb, or Ta to other high field strength elements, such as Th, U, Y, or the REEs, may have been altered by ilmenite fractionation.     

Trace elements in minerals as indicators of the evolution of alkaline ultrabasic dike series: LA-ICP-MS data for the magmatic provinces of northeastern Fennoscandia and Germany

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.     

珠江口海域与南黄海海域表层沉积物地球化学特征

对珠江口和南黄海近海海域10个站位的表层沉积物中67种元素进行分析,试图揭示两海域近海表层沉积物中主要元素的地球化学特征,包括分布特征及其控制因素,并通过两海域元素地球化学特征,初步探讨近海沉积环境特征。通过总结两海域表层沉积物中元素含量及分布特征,可以发现,近海海域总体上以陆源沉积为主,除Ca和Sr之外,大多数元素表现出明显的亲陆性。珠江口海域和南黄海海域沉积物元素含量的对比研究显示,前者相对富集As、Cd、Hg、Sb、Sr、Ca、Rb、C,后者相对富集Al2O3、Zr、Hf、Sc、Rb、Ga、Cs、V、Co、Cr、Cu、Mn、Ni、K2O、Na2O、B、Ba、I等。与上地壳相比,Ag、As、Bi、Hg、Li、N、Pb、Sb、Se、Cl、Br、I在两海域表层沉积物中均发生明显富集;Mo、Sn均呈现分散趋势;Sr、CaO在南黄海海域明显贫化,K2O、Na2O、Ba则在珠江口海域表现出贫化;其他元素与上地壳元素丰度相近。     

Fractionation of Nb and Ta from Zr and Hf at Mantle Depths: the Role of Titanian Pargasite and Kaersutite

Selective enrichment or depletion in either Zr and Hf (HFSE⁴⁺)or Nb and Ta (HFSE⁵⁺) is a feature commonly observed in manymantle-derived melts and amphiboles occurring as either disseminatedminerals in mantle xenoliths and peridotite massifs or in veinassemblages cutting these rocks. The fractionation of Nb fromZr seen in natural mantle amphiboles suggests that their incorporationis governed by different crystal-chemical mechanisms. An extensiveset of new partitioning experiments between pargasite–kaersutiteand melt under upper-mantle conditions shows that HFSE incorporationand fractionation depends on amphibole major-element compositionand the presence or absence of dehydrogenation. Multiple regressionanalysis shows that ^Amph/LD_Nb/Zr is strongly dependent on themg-number of the amphibole as a result of a combination of amphiboleand melt structure effects, so that the following generalizationsapply: (1) high-mg-number amphiboles crystallized from unmodifiedmantle melts more easily incorporate Zr relative to Nb leadingto an increase of the Nb/Zr ratio in the residual melt; (2)low-mg-number amphiboles, such as those found in veins cuttingperidotites, may strongly deplete the residual melt in Nb andcause very low Nb/Zr in residual melts. Implications and applicationsto mantle environments are discussed. KEY WORDS: trace elements; high field strength elements; partition coefficients; amphibole; upper mantle     

XRF AND INAA DETERMINATIONS OF MAJOR AND TRACE ELEMENTS IN GEOLOGICAL SURVEY OF JAPAN IGNEOUS AND SEDIMENTARY ROCK STANDARDS

Major and trace element analyses have been obtained by wavelength dispersive X-ray fluorescence for the Geological Survey of Japan Igneous rock series and selected samples from the Sedimentary rock series reference samples. Additional trace element data for the Igneous rock series were obtained by instrumental neutron activation analysis. Samples were analyzed multiple times for 10 major elements (with loss-on-ignition) and the following trace elements; As, Ba, Ce, Co, Cr, Cs, Cu, Eu, Ga, Hf, La, Lu, Nb, Nd, Ni, Pb, Rb, Sb, Sc, Sm, Sr, Ta, Tb, Th, U, V, W, Y, Yb, Zn and Zr.     

Extreme enrichment of Sb, Tl and other trace elements in altered MORB

We have analyzed 25 trace elements (e.g., Sb, Tl, Sn, rare earth elements (REE), Th, U, Nb, Pb, Zr, Hf, and Y) in altered mid-ocean ridge basalts (MORB) from locations near the mouth of the Gulf of California. Our results imply that the heavy REE and Y are not seriously affected by seawater alteration, in agreement with previous studies. The elements Zr, Hf, Nb, light REE and Sr are enriched up to a factor of 2 in some extremely altered samples. However, element ratios between Zr, Hf, and Nb (e.g., Zr/Hf, and Zr/Nb) are not greatly affected, presumably due to the chemical similarity of these elements during any exchange process. The enrichment of Th and Sn is even higher. Antimony, Tl, Cs, Rb, Rb, and Ba are most easily altered by water-rock interaction and are therefore the best indicators for seawater alteration. The enrichment factor of the most mobile element Sb is up to 2000.

There is a weak correlation between the concentration in seawater and the enrichment factors. On the other hand, the worldwide pelagic clay pattern matches the enrichment pattern much more closely, and the limited data available for local oceanic sediments give an even better correlation. A plausible model to explain the enrichment pattern may be an elemental exchange between basalt and seawater that had interacted earlier with overlying sediments.