An experimental study of the grain-scale processes of peridotite melting: implications for major and trace element distribution during equilibrium and disequilibrium melting   总被引：1，自引：0，他引：1  

Mauro Lo Cascio  Yan Liang  Nobumichi Shimizu  Paul C. Hess 《Contributions to Mineralogy and Petrology》2008,156(1):87-102

The grain-scale processes of peridotite melting were examined at 1,340°C and 1.5 GPa using reaction couples formed by juxtaposing pre-synthesized clinopyroxenite against pre-synthesized orthopyroxenite or harzburgite in graphite and platinum-lined molybdenum capsules. Reaction between the clinopyroxene and orthopyroxene-rich aggregates produces a melt-enriched, orthopyroxene-free, olivine + clinopyroxene reactive boundary layer. Major and trace element abundance in clinopyroxene vary systematically across the reactive boundary layer with compositional trends similar to the published clinopyroxene core-to-rim compositional variations in the bulk lherzolite partial melting studies conducted at similar P–T conditions. The growth of the reactive boundary layer takes place at the expense of the orthopyroxenite or harzburgite and is consistent with grain-scale processes that involve dissolution, precipitation, reprecipitation, and diffusive exchange between the interstitial melt and surrounding crystals. An important consequence of dissolution–reprecipitation during crystal-melt interaction is the dramatic decrease in diffusive reequilibration time between coexisting minerals and melt. This effect is especially important for high charged, slow diffusing cations during peridotite melting and melt-rock reaction. Apparent clinopyroxene-melt partition coefficients for REE, Sr, Y, Ti, and Zr, measured from reprecipitated clinopyroxene and coexisting melt in the reactive boundary layer, approach their equilibrium values reported in the literature. Disequilibrium melting models based on volume diffusion in solid limited mechanism are likely to significantly underestimate the rates at which major and trace elements in residual minerals reequilibrate with their surrounding melt. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

Simple models for dynamic melting in an upwelling heterogeneous mantle column: Analytical solutions     

Yan Liang 《Geochimica et cosmochimica acta》2008,72(15):3804-3821

Several lines of evidence suggest that the melt generation and segregation regions of the mantle are heterogeneous, consisting of chemically and lithologically distinct domains of variable size and dimension. Partial melting of such heterogeneous mantle source regions gives rise to a diverse range of basaltic magmas. In order to better assess the role of source heterogeneity during mantle melting, we have undertaken a theoretical study of trace element distribution and fractionation during concurrent melting and melt migration in an upwelling, chemically heterogeneous, two-porosity double lithology melting column. Analytical solutions for the abundance of a trace element in the matrix and channel were obtained under the assumptions that the porosity, melt and solid velocities, and solid-melt partition coefficients are constant and uniform. For simplicity, we neglected diffusion and dispersion in the melt. Chemical source heterogeneities of arbitrary size and shape were integrated into the simple melting models by allowing trace element abundance in the source region to vary as a function of time and space. Concurrent melting and melt migration in an upwelling heterogeneous mantle may be approximated as a quasi-steady state problem in which time-dependent concentration patterns produced by melting of heterogeneous source regions are superimposed on a reference steady-state concentration distribution established by melting of the ambient or background mantle. Chromatographic fractionation is especially important for the matrix melt and solid when chemical heterogeneities are involved during melting and melt migration in the mantle, giving rise to significant phase-shift between two incompatible trace elements in the matrix melt and scattered correlations among incompatible trace elements in residual peridotites. Mixing is the chief mass transfer process in the dunite channel where the chromatographic effect is negligible for most of the incompatible trace elements. The lack of chromatographic fractionation among incompatible trace elements and isotopic ratios in MORB suggests either most MORB are channel melts or mixing in magma conduit and chamber is very efficient such that the phase-shift is averaged out during magma transport and storage processes. Advection brings melt produced by smaller-degree of melting in the deeper part of the melting column to the overlying melting region, increasing the incompatible trace element abundance in the matrix and the channel. This advection-induced self-enrichment is especially important when heterogeneous sources are involved and may account for some of the enriched incompatible trace element patterns observed in residual peridotite that were previously interpreted to be a result of mantle metasomatism. Systematic studies of high-resolution spatially correlated mantle samples may help to constrain the melting history and the size and nature of chemical heterogeneities in the mantle.  相似文献   

淡水双壳类壳体碳同位素研究:以河蚬(corbicula fluminea,Müller 1774)为例   总被引：2，自引：0，他引：2  

闫慧  李心清  周会 《地球化学》2008,37(3)

双壳类壳体碳酸盐(文石)稳定同位素组成已被广泛地用于古气候和古环境重建研究中,但是双壳类壳体碳同位素组成所指示的气候和环境意义一直是争议的问题.对双壳类河蚬(corbicula fluminea)进行了室内养殖,并选取两个壳体样品(壳高,A=13 mm,B=9mm),测定其生长部分壳体和生长期间水体碳同位素,研究表明,随着水体碳同位素的升高(δ13CDIC由-5.24‰升至1.41‰),两壳体碳同位素也随之升高,表明水体对壳体碳同位素的影响;δ13CA分布范围为-4.76‰～2.09‰,δ13CB为-8.49‰～2.89,壳体A和B碳同位素均比预测平衡值偏负,表明壳体在形成过程中利用了新陈代谢产生的富集12C的CO2.根据计算壳体A在实验中沉淀部分壳体利用新陈代谢碳的比例(M值)为24%～43%,平均值为33%;壳体B为33%～75%,平均值为58%.M值随生物的生长呈下降变化,这说明在实验中河蚬主要是通过增加对DIC的吸收和利用来满足壳体生长对物质量增加的需求.  相似文献   

实验研究不同盐离子对水分子拉曼效应的影响   总被引：3，自引：0，他引：3  

陈勇  周瑶琪  查明  王爱国 《地球化学》2008,37(1):22-26

对流体包裹体中常见的几种盐水溶液进行了拉曼光谱分析.采用了频移参数描述水分子拉曼峰的形变强度,并讨论了频移参数与盐度之间的关系.实验分析结果表明,盐度越大,频移参数越大,水分子拉曼峰形变越大.对频移参数曲线斜率分析显示,盐类对水分子拉曼峰偏移程度影响的强弱顺序为NaCl＞Na2SO4＞NaHCO3＞Na2CO3.讨论了不同阳离子和阴离子对水伸缩振动拉曼峰的影响,结果表明,高价阳离子的影响明显高于低价阳离子;而阴离子对水拉曼峰影响的强弱顺序初步确定为Cl-≈SO2-4-＞HCO-3＞CO2-3≈NO-3.  相似文献   

云南罗平中三叠世安尼期生物群的发现及其意义   总被引：15，自引：0，他引：15  

张启跃  周长勇  吕涛  谢韬  楼雄英  刘伟  孙媛媛  江新胜 《地质论评》2008,54(4):523-526

本文介绍了云南罗平地区新发现的罗平生物群的产出层位、生物面貌、保存特征、古地理位置及其研究意义。该生物群产于关岭组二段薄层泥晶灰岩中,地层对比和化石鉴定表明其时代为中三叠世安尼期,以鱼类为主,伴生有爬行类、两栖类（？）、棘皮动物、节肢动物（甲壳类、昆虫等）、双壳类、腹足类以及植物化石;化石保存完好,分布广泛,埋藏方式独特。罗平生物群无论在丰度、分异度及化石保存上都极为罕见和独特,对研究埋藏学、古生态学、古地理以及三叠纪海洋生物尤其是海生爬行类都具有极为重要的意义。  相似文献   

晚三叠世松潘甘孜和川西前陆盆地的物源对比：构造演化和古地理变迁的线索   总被引：3，自引：0，他引：3  

邓飞  贾东  罗良  李海滨  李一泉  武龙 《地质论评》2008,54(4):561-573

为了研究龙门山褶皱冲断带两侧的松潘甘孜和川西前陆盆地在大地构造和沉积学方面存在的联系,笔者等分别在松潘甘孜东缘马尔康—理县地区和川西前陆盆地都江堰地区进行了采样和碎屑锆石的LAICPMS UPb定年工作。269颗锆石的定年结果显示,中—晚三叠世拉丁期—诺利期松潘甘孜复理石盆地东缘沉积地层中的碎屑锆石年龄主要集中在250~280 Ma、1800~1900 Ma和2400~2500 Ma、200~245 Ma、400~450 Ma,对应的物源主要为东昆仑岛弧、华北陆块基底、义敦岛弧以及北秦岭。与之相比,川西前陆盆地诺利期—瑞替期的须家河组地层中的碎屑锆石年龄大致主要集中在1800~1900 Ma和2400~2500 Ma、720~850 Ma、950~1200 Ma、400~450 Ma。该统计结果总体上继承了松潘甘孜数据体的特征,揭示出须家河组物源来自西部——松潘甘孜褶皱带的再旋回沉积和龙门山前陆冲断带。  相似文献   

祁连山近期七一冰川融水径流特征分析   总被引：3，自引：1，他引：2  

宋高举  王宁练  陈亮  贺建桥  蒋熹  武小波 《冰川冻土》2008,30(2):321-328

利用2006年8月1日-9月30日的实测水文数据,对"七一"冰川融水径流产汇流特征进行了分析,并揭示出该冰川日消融特征.通过对冰川融水量的估算以及径流模数的计算,并与过去的观测结果进行对比,表明近些年来"七一"冰川消融强度和消融量都在增大,而且2006年消融量为近几年观测的最大值.虽然不同年份消融量不一样,但"七一"冰川总的趋势是一直处于萎缩状态,随着全球变暖,"七一"冰川的萎缩可能将继续下去.通过对设立在沿冰川下游方向两个不同的水文断面进行对比分析,结果表明"七一"冰川融水径流在向下游运动过程中有部分水入渗为河谷潜流,观测期内两个相距不到2 km的水文断面间渗漏损耗占近1/3左右.  相似文献   

渤海新近系浅水三角洲沉积体系与大型油气田勘探   总被引：32，自引：8，他引：24  

朱伟林  李建平  周心怀  郭永华 《沉积学报》2008,26(4):575-582

新近纪渤海具有构造稳定、沉降缓慢、湖泊水域范围大、内部无分割、地形平缓、坡度小等特点,广泛发育浅水三角洲,从而形成渤海海域新近系良好的储盖组合和优越的油气成藏条件。浅水三角洲砂岩储层由于受河流作用的控制,砂体具有明显的方向性,存在明显的分叉现象,与曲流河相比,砂体连通性较好,砂体等厚图呈典型的朵叶状。湖相厚层泥岩普遍发育,与浅水三角洲砂体组成多套垂向优质储盖组合。浅水三角洲发育于渤海新近纪至今处于生烃的峰期主力富烃凹陷的有利区带,新构造运动造成新近纪以来凹陷主力源岩生烃峰期与新构造运动的同步耦合,为渤海大型浅水三角洲成因的优质储层油气成藏创造了优越条件,可以形成大型油气田。因此,重视并充分挖掘渤海浅水三角洲储层类型油气藏的勘探潜力将是追求浅层优质油藏、进一步增储上产的方向所在。  相似文献   

西藏冈底斯带措勤地区则弄群火山岩锆石U-Pb年代学格架及构造意义   总被引：29，自引：12，他引：17  

朱弟成  周肃  莫宣学  赵志丹  许继峰  周长勇  孙晨光  王立全  陈海红  董国臣 《岩石学报》2008,24(3)

大规模的则弄群火山岩呈带状近东西向展布于西藏冈底斯带中北部地区.对出露状况较好的措勤地区则弄群火山岩进行了锆石U-Pb定年,以建立其年代学格架便于区域对比.措勤地区则弄群火山岩多数锆石具有生长振荡环带,部分锆石显示核边结构.在措勤达雄北西部上覆于中二叠统下拉组灰岩的1件则弄群英安岩样品的LA-ICP-MS锆石U-Ph年龄为130±1Ma,1件则弄群流纹岩样品的SHRIMP锆石U-Pb年龄为129±3Ma;在措勤达雄北东部与下白垩统多尼组碎屑岩呈断层接触的1件则弄群英安岩样品中的锆石具有两组LA-ICP-MS锆石U-Pb年龄,最年轻的一组(包括增生边)为121±1Ma,较老的一组(包括核部)为131±1Ma;在措勤南西部1件则异群流纹岩样品的LA-ICP-MS锆石U-Pb年龄为111±1Ma,与措勤地区花岗岩类的侵位时代相当.这些高质量的锆石U-Pb年代学数据表明,措勤地区的则弄群火山作用很可能开始于约130Ma,停息于约110Ma,持续时间约20Ma.区域对比表明,东西延伸约1000km的则弄群火山作用同时发生在约130Ma.区域上目前的年代学数据结合同时代岩浆作用的分布特征表明,冈底斯带中北部地区早白垩世岩浆作用不太可能由新特提斯洋壳向北的低角度或平板俯冲产生.  相似文献   

藏南地区中生代硅质岩的地球化学特征及其成因意义   总被引：6，自引：1，他引：5  

周永章  付伟  杨志军  何俊国  聂凤军  李文  赵文霞 《岩石学报》2008,24(3)

藏南地区中生代硅质岩包括蛇绿岩套硅质岩(与蛇绿岩共生)和非蛇绿岩套硅质岩两大类.本文重点分析日喀则地区彭错林、夏鲁以及泽当地区的罗布莎、江孜盆地宗卓组及四个剖面的硅质岩.其中,彭错林、夏鲁和罗布莎硅质岩与蛇绿岩共生,江孜盆地宗卓组为非蛇绿岩套硅质岩.分析表明:(1)藏南地区硅质岩剖面地球化学特征鲜明,具有一致性和多样性特点;(2)与蛇绿岩共生的彭错林、夏鲁、罗布莎硅质岩普遍具有高Si、高Fe、低Al特征,大部分微量元素相对于克拉克值亏损,稀土元素总量低,经北美页岩标准化后,Ce异常明显或不明显,重稀土相对轻稀土富集.硅质泥岩的∑REE要明显高于硅质岩;(3)非蛇绿岩套宗卓组硅质岩SiO2含量稍低,Al2O3、TiO2则相反.V、Th、Hf、Ta等不相容元素上亏损程度较小,部分样品含量可接近克拉克值.稀土总量相对较高,页岩标准化配分模式上体现为弱Ce正异常,负Eu异常,轻重稀土分异不明显的平坦型曲线图;(4)地球化学特征指示了,藏南地区硅质岩多数具有明显的热水沉积成因属性,同时有正常陆源组分的加入.其中,夏鲁硅质岩的热水沉积地球化学特征较为典型,而宗卓组硅质岩则表现出受陆源物质加入的影响显著的地球化学特点.  相似文献