A coupling of mixed and discontinuous Galerkin finite-element methods for poroelasticity

In this paper, we formulate a finite-element procedure for approximating the coupled fluid and mechanics in Biot’s consolidation model of poroelasticity. We approximate the flow variables by a mixed finite-element space and the displacement by a family of discontinuous Galerkin methods. Theoretical convergence error estimates are derived and, in particular, are shown to be independent of the constrained specific storage coefficient, c _o . This suggests that our proposed algorithm is a potentially effective way to combat locking, or the nonphysical pressure oscillations, which sometimes arise in numerical algorithms for poroelasticity.     

Fractional crystallization models and B–Be–Li systematics at Mt Somma-Vesuvius volcano (Southern Italy)

A compilation of B–Be–Li data on rocks that cover the entire eruptive history of Somma-Vesuvius is presented and interpreted in the light of evolution models for the Somma-Vesuvius rocks. Using major and trace element data, fractional crystalllization models are presented for different geochemical units. These data were used to constrain the source mineralogy of the Somma-Vesuvius rocks (ol-opx-cpx-gar-amp of 0.4-0.3-0.1-0.1-0.1), the amount of sediment added (5–10%) and the melt fraction from batch partial melting computations (0.05–0.1). From the B–Li data it is inferred that the main process responsible for the B isotopic signature is sediment recycling. However, the B–Li data show a major variation in Li abundances respect to B which is explained with Li dehydration before the fluid enriched the mantle wedge that produced the arc magmas. The Somma-Vesuvius B isotope composition is intermediate between that of the Campi Flegrei and the broad field of the Eolian Island arc. A low Be isotopes in the recent volcanic rocks can be explained as: (a) the top 1–22 m of the incoming sediment is accreted, (b) large amounts of sediment erosion, (c) a slow rate of subduction which have provoked a long magmatic history for the Vesuvius magma, (d) the sediment component takes several Myr longer than the subducting plate to reach the magma source region beneath Italy.     

Platinum-group element distribution in chromite ores from ophiolite complexes: implications for their exploration

Compilation of some new data on ophiolites for Greece and Yugoslavia, and published data from previous studies, indicate that platinum-group element (PGE) and gold concentrations in chromite ores are generally low, ranging from less than 100 ppb to a few hundred ppb. However, samples from several ophiolite complexes exhibit an enrichment (of a few ppm) (a) only in Os, Ir and Ru,(b) only in Pt and/or Pd or (c) in all PGE. This enrichment (up to 10s ppm) is mainly related with chromitites hosted in supra-Moho dunites and dunites of the uppermost stratigraphic levels of the mantle sequence and it seems to be local, independent of the chromitite major element composition and the chromite potential of the ophiolite complexes. The contents of PGE combined with less chalcophile elements (Ni, Co, Cu), the ratios of incompatible/compatible elements, and PGE-patterns provide evidence for discrimination between chromitites derived from primitive magmas and those derived from partially fractionated magmas, although they have a similar major element composition. Thus, they can be used for a stratigraphic orientation in the mantle sequence, and therefore for exploration targets. Moreover, PGE data offer valuable information for the evaluation of the chromite potential in ophiolite complexes. The most promising ophiolites seem to be those which apart from the petrological and geochemical characteristics indicating extensive degree of partial melting in the mantle source contain only one chromite ore type (the other type being only in small proportion) of limited compositional variation, in both major elements and PGE, low ratios of , while PGE-enriched chromitites in the mantle sequence are only occasionally present. In contrast, ophiolites which contain both high-Cr and -Al chromitites, and where their chalcophile element data implies relatively extensive fractionation trend are not good exploration targets for chromite ores, although they are related with a SSZ environment.     

A dynamic box model of bioactive elements in the southern Taiwan Strait

A dynamic box model was applied to study the characteristics of biogeochemical cycling of PO_4-P,NO_3-N,AOU,POC and PON in the southern Taiwan Strait region based on field data of the"Minnan Taiwan Bank Fishing Ground Upwelling Ecosystem Study" during the period of Dec.1987-Nov.1988.According to the unique hydrological and topographical features of the region,six boxesand three layers were considered in the model.The variation rates and fluxes of elements induced by hor-izontal current,upwelling,by diffusion,sinking of particles and biogeochemical processes were estimatedrespectively.Results further confirmed that upwellings had important effects in this region.Thenearshore upwelling areas had net input fluxes of nutrients brought by upwelling water,also had high de-pletion rates of nutrients and production rates of particulate organic matter and dissolved oxygen.Theabnormal net production of nutrients in the middle layer(10-30m) indicated the important role of bacte-ria in this high production region.Th     

胶东海阳所超镁铁岩中强亲铁元素的地球化学特征及其构造环境探讨

强亲铁元素与亲石元素具有不同的地球化学行为，因此能够从不同的角度为造山带中超镁铁岩的成因及演化提供重要信息。位于苏鲁造山带东北端的胶东海阳所超镁铁岩主要由橄榄岩和辉石岩组成，它们常以团块状赋存于花岗质片麻岩中。虽然前人对这些超镁铁岩已经开展大量岩石学研究，但关于其成因及构造属性仍存在较大争议。本文开展了海阳所超镁铁岩的全岩主微量元素、强亲铁元素及Re-Os同位素的分析工作，结果显示蛇纹石化橄榄岩具有较高的MgO和Fe₂O₃^T含量，较低的Al₂O₃、TiO₂和CaO含量，明显富集流体迁移元素（U、Pb），亏损高场强元素（Zr、Hf），强亲铁元素没有发生明显分异，但Ru显示正异常，表明海阳所蛇纹石化橄榄岩是经历了低-中等程度部分熔融及熔/流体交代作用影响的残余地幔橄榄岩。海阳所辉石岩的主量元素表现出明显的结晶分异特征，稀土元素较原始地幔富集，铂族元素（PGEs）含量较低且发生了明显的分异，表明辉石岩的地幔源区经历过高程度的部分熔融和硫化物的分离。海阳所蛇纹石化橄榄岩的Os同位素地球化学特征表现出大洋亲和性，与辉石岩不具有熔体-残留体的关系。由于该地区发育较深层次的韧性剪切带，蛇纹石化橄榄岩中的橄榄石与辉石表现出韧性变形的特征，同时有辉石岩侵入到橄榄岩的现象，表明该地区的蛇纹石化地幔橄榄岩与辉石岩既不同时，也不同源，因此，暗示了该套岩石组合可能形成于大洋核杂岩（OCC）与洋脊型蛇绿岩（MOR）堆晶岩交互发育环境。     

GGR Critical Review of Analytical Developments in 2004–2005

In 2005 Geostandards and Geoanalytical Research embarked upon a new initiative for its readers. Key researchers in various fields of geoanalytical technique development and their application were identified and invited to provide reviews pertinent to their expertise. As noted in the first of these publications "…instead of revisiting the historical context or decades of development in each analytical technique, the goal here has been to capture a snapshot of "hot topics" across a range of fields as represented in the… literature" (Hergt et al . 2005). Rather than prepare an annual review, a decision was taken earlier this year to provide a biennial summary of progress and accomplishments, in this case for the years 2004–2005. The principal techniques employed in Earth and environmental sciences are covered here, and include laser ablation and multicollector ICP-MS, ICP-AES, thermal ionisation and secondary ion mass spectrometry, as well as neutron activation analysis, X-ray fluorescence and atomic absorption spectrometry. A comprehensive review of the development of reference materials, often essential to these techniques, is also provided. The contributions assembled serve both to keep readers informed of advances they may be unfamiliar with, but also as a means of showcasing examples of the breadth and depth of work being conducted in these fields.     

Reference Materials in Geoanalytical Research -Review for 2004 and 2005

This review gives an overview of the use and development of reference materials of geochemical and environmental interest in the literature of the years 2004 and 2005. In these years the performance of existing methods has been improved and new geochemical applications using new techniques have been developed. Accordingly, there was an increasing need for new reference materials, especially for in situ microanalysis and for precise stable isotope measurements. In addition, there was a notable trend for further characterisation of existing reference materials, mainly for the platinum-group elements. This review focuses on five topics: reference materials for platinum-group elements, reference glasses for in situ microanalysis, zircon reference materials, isotopic reference materials, and the development and certification of reference materials.     

2004–2005 Analytical Developments in Secondary Ion Mass Spectrometry

This review of the literature from 2004 and 2005 concerning secondary ion mass spectrometry (SIMS) highlights the contribution the technique has made in the fields of petrology, geochronology, cosmochemistry and material sciences. In petrology, much research was devoted to the measurement of stable isotopes and trace elements by developments in multicollection acquisition, with emphasis on low atomic mass number elements. Elements studied in particular were S (in sulfides), O (in garnets), C (in sedimentary organic matter), Cl (in glasses) and Si. Novel applications of SIMS to geochronology have included the measurement of young zircon grains by the U-Pb and U-Th decay methods. An increasing number of studies have combined U-Pb geochronology with the measurement of trace elements or stable isotopes in zircon.     

林草复合经营模式养分动态关系

林草复合经营模式在目前的退耕还林工程中起着重要的作用，研究林草复合模式的林与草之间的营养元素关系，通过对不同林草养分的研究得出林木、草、土壤之间的养分动态关系，对矿质养分相互关系的研究为合理搭配林草提供重要依据，为退化山地生态系统的恢复和重建提供重要的模式。模式Ⅰ在退耕还林初期，土壤养分供给氮素虽未亏缺，但从三者问的消长关系看出：氮磷素供应并不富足，特别是水解性氮。土壤交换性钙供应不足，引起杉木与黑麦草对钙质竞争。而土壤全钙含量很高，钙质向交换性钙转化的速度缓慢。模式Ⅱ与模式Ⅰ得到相似结果，所以在这两种模式中应加强人为管理，在退耕初期应适当增施氮磷钙肥，辅以土壤结构改良，加速土壤养分向植物可利用态转化。模式Ⅲ牛鞭草的生物量极高，磷、钙索相对缺乏。由于牛鞭草被不断的采割用于牲畜的饲料，对该模式中必须进行一定养分的输入，以保持杂交竹与牛鞭草这一林草生态系统的养分平衡。     

长白山锦北雨养泥炭剖面元素富集规律分析

为了揭示长白山锦北泥炭沼泽区泥炭沉积环境和重金属元素的历史变化及其对环境的指示意义,利用荷兰W ardenaar泥炭采样器采取泥炭样品并对样品进行高分辨率切割。用原子吸收分光光度计和等离子体发射光谱仪测定不同深度剖面Ca,Mg,Na,K,A l,Ti,Cu,Zn,Fe,Mn,Pb,Cr,N i和Co的浓度。研究分析了Ca,Mg,Na,K,A l,Ti,Mn,Zn,Cu,Pb,Cr,N i和Co在泥炭剖面的分布趋势并对其进行了相关分析和富集分析,得出Mn,Zn,Cu,Pb,Cr,N i和Co呈显著相关且在泥炭表层明显累积,揭示出泥炭表层重金属元素的大气沉降来源,表明近年来人类重金属消耗量及排放量的增加是大气沉降重金属元素的主要释放源,而且环境中重金属污染有加重的趋势。