An experimental study of the grain-scale processes of peridotite melting: implications for major and trace element distribution during equilibrium and disequilibrium melting

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.     

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

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.     

Urban consolidation and house prices: a case study of Melbourne 1990–2004

This paper explores the links between a strategic policy, urban consolidation, and house prices by examining the changes in the mix of housing and in house price for the period 1991–2004. We contend that urban consolidation could be seen as a source of additional supply, (which might be expected to be felt in lower prices and so contribute to a local policy objective) but also as a stimulus to demand (by developers who could bid up the price of lots where it was understood more housing could be built). Analyses were carried out at the metropolitan and sub-regional scales using correlation tests. The research finds very weak statistical connections, and concludes that this policy has not been associated with price changes.     

人工合成烃类包裹体研究进展

人工合成烃类包裹体不仅可以作为分析仪器校正的标样,还可以增进人们对烃类包裹体形成机制和水—岩作用机理的认识。人工合成包裹体的方法主要有三种：人工晶体生长法、焊封石英管法和金刚石压腔法,其中利用愈合人工石英(水晶)单晶裂隙合成流体包裹体技术已成为标准的合成技术。目前人工合成烃类包裹体主要利用晶体生长法合成,包括高温高压利用石英（或方解石）晶体生长愈合裂缝形成流体包裹体和低温下采用过饱和溶液重结晶形成流体包裹体。由于高温高压条件下烃类可能发生裂解,母液保真是成功实现人工合成烃类包裹体的重要前提条件。国外在人工合成烃类包裹体研究方面已经取得了一些重要的认识,但远不及人工合成无机体系流体包裹体研究那样系统和完善。国内关于人工合成烃类包裹体研究尚处于起步阶段,迫切需要开展这方面的研究工作。     

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

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。     

青藏铁路多年冻土区保温护道路基温度场数值模拟研究

多年冻土区路基铺设保温护道的目的在于削弱边坡热侵蚀作用对路基下多年冻土温度状况的影响,防止多年冻土上限特别是阳坡侧冻土上限下降,减少人为活动对路堤坡脚及附近天然地表的破坏;防止路侧地表积水渗入基底;对边坡产生反压,防止路肩滑塌,以保证路基的稳定.结合试验工程监测资料,采用数值模拟方法分析了青藏铁路多年冻土区路基保温护道的效果,结果表明:保温护道并没有达到设计的目的,由于路基和护道几何形状对空气对流和太阳辐射的影响,不仅达不到保护冻土地基的目的,反而加大阴阳坡温度差异,导致路基病害的发生.     

祁连山近期七一冰川融水径流特征分析

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.     

单向袖阀管注浆在地质灾害治理工程中的应用

通过对抚顺发电有限责任公司厂区地质灾害治理,阐述袖阀管注浆施工工艺及施工中遇到的问题及解决的方法.     

浅论双重管理体制下无锡市水文站网规划设计

无锡市机构编制委员会在江苏省率先正式批复江苏省水文水资源勘测局无锡分局增挂“无锡市水文局”牌子,实行省市双重领导,以省为主管理体制,并明确了无锡市水文局为地方服务的七项职责。无锡水文在新的历史发展时期下,水文站网规划设计应该紧紧围绕无锡水利、服务无锡水利、融入无锡水利,才能发挥水文体制省市双重领导、以省为主管理的最大效益。     

川西108国道高位崩塌成因与运动特征

2007年5月25日于川西108国道某段发生的高位崩塌造成了重大人员伤亡和财产损失。综合地质调查、三维激光扫描技术、爆破振动效应分析以及历史崩塌与降雨关系的统计分析,得出了地形高陡、岩体破碎及降雨诱发等是崩塌产生的主要原因,爆破振动对其也有轻微间接影响。根据边坡形态及塌落高度,运用运动学原理及能量法还对崩塌体的撞击速度及冲击力进行了计算分析。