西秦岭中志留统含铀岩系中硅质岩的岩石学、地球化学及其成因   总被引：5，自引：2，他引：5  

唐朝晖  曾允孚 《岩石学报》1990,6(2)

根据产状和成因,本文将西秦岭中志留统含铀岩系中的硅质岩分为,(1) 成岩过程中硅化交代碳酸盐岩所形成的硅质岩,产于碳酸盐岩和泥质岩类所组成的透镜层的顶部或碳酸盐岩层内;(2) 早期成岩阶段形成的纹层状硅质岩,主要产于碳酸盐岩和泥质岩透镜层底部或呈薄层夹于粉砂岩、泥质岩层中。根据沉积环境分析及硅质岩的化学成分、REE分布模式和氧同位素组成,提出本区硅质岩形成于受大气淡水影响的局限浅海环境。  相似文献   

华南花岗岩类中铁钛副矿物组合与氧逸度关系   总被引：2，自引：0，他引：2  

陈鸣  张成江 《岩石学报》1991,7(2):89-94

华南花岗岩中存在两类矿物组合:(1)铁透闪石 钛铁矿 榍石 磁铁矿 石英;(2)钛铁矿 方解石 石英 磁铁矿 榍石。可通过以下关系分别计算上述两组矿物组合的岩浆氧逸度。组合(1)为: logfo_2=-24940.31/T 9.25 243.43(P-10~5Pa)/T 0.86logfH_2O-0.86logα铁透闪石组合(2)为: logfo_2=-3673.68/T-37.73 590.53(P-10~5Pa)/T 6logfco_2岩浆作用过程的氧逸度(fo_2)是控制磁铁矿、钛铁矿、榍石等铁、钛副矿物形成和稳定的重要因素。  相似文献   

中国东部新生代玄武岩及其地幔包体的氧逸度   总被引：1，自引：1，他引：1  

张毅刚  鄂莫岚 《岩石学报》1994,10(2)

地幔环境的氧逸度与温度和压力一样，是控制许多地幔过程的一个重要参数。本文计算了中国东部几个具有代表性地区的玄武岩和尖晶石二辉橄榄岩的氧逸度，尖晶石二辉橄榄岩的氧逸度变化不大，均位于１ｏｇ（ｆｏ２）＝ｌｏｇ（ｆｏ２ＦＭＱ）＋０．０左右，而各地区玄武岩的氧逸度却变化很大，其平均值从尚志地区的ｌｏｇ（ｆｏ２ＦＭＱ＋０．６到长白山地区的ｌｏｇ（ｆｏ２ＦＭＱ）＋３．３左右（其中东北地区钾质玄武岩的氧逸度比除尚志以外其它地区的低），并且总体具有比地幔橄榄岩高得多的氧逸度。推测钾质玄武岩和尚志地区破性玄武岩的氧逸度比中国东部其它地区玄武岩的氧逸度低的可能原因是，前二个地区的玄武岩来源于更深部的（金云母）石榴石二辉橄榄岩，而其它地区的玄武岩来源于略浅部的尖晶石二辉橄榄岩。  相似文献   

Eolian deposition determined by the oxygen plasma furnace     

P. S. A. Jones 《地球表面变化过程与地形》1984,9(5):479-484

The oxygen plasma furnace enables small samples of clastic sediment to be separated from filter papers at low temperatures without physical or chemical alteration of the sediment. This technique provides a suitable treatment for processing very small samples of alpine eolian sediment, enabling their grain size distribution, mineralogy, and origin to be determined.  相似文献   

房山花岗岩岩体氧氢碳的同位素研究   总被引：1，自引：0，他引：1  

郑斯成  黄福生  姜常义  郑淑惠 《岩石学报》1987,3(3)

测定了房山花岗岩侵入体的岩石、共生矿物和气液包体的氧、氢、碳的同位素组成。共生石英-黑云母和石英-全岩的δ~(18)O数据表明,房山花岗岩侵入体保存了氧同位素平衡,氧同位素温度在450—580℃之间。大多数共生黑云母-角闪石δD值的相关性基本上符合Suzuoki-Epstein关系式,可以认为房山侵入体也保存了氢同位素平衡,推算得到的岩浆流体的δD值在-70—-30之间。气液包体中CO_2的δ(13)C为-4—-8,属于一种深源碳,可以利用地下水参加岩浆后期演化的假定来解释黑云母二长闪长岩氢、碳同位素异常  相似文献   

南海北部ODP 1144站中更新世气候转型期有孔虫稳定同位素古气候意义     

金海燕  翦知湣 《地球科学进展》2007,22(9):914-921

中更新世气候转型期是第四纪古气候研究的一个特殊时期。利用大洋钻探ODP 184航次在南海北部钻取的1144站时间分辨率高达约290年的沉积物样品，开展中更新世气候转型期古气候变化的研究。在中更新世距今80~100万年前，浮游和底栖有孔虫壳体的稳定氧碳同位素变化揭示出，中更新世气候转型中心，即中更新世革命0.9 Ma左右，南海北部表层海水温度的降低和降水量的增加指示东亚冬、夏季风增强。以中更新世革命为界，水体垂向结构上温跃层和营养跃层的深度从之前的间冰期较浅转变为之后的间冰期较深，底层水与表层水的垂直温度梯度从冰期时较大转变为冰期时较小。轨道尺度上，冰消期时南海北部的表层水、次表层水和底层水的变化几乎是同时发生的，不存在超前或滞后的相位差。千年尺度上，有孔虫的氧碳同位素变化都呈现出非常明显的约0.8 ka和约1.4 ka的气候波动周期。氧同位素0.8 ka滤波显示出：在中更新世气候转型期，较强的信号主要出现在间冰期，有时也出现在冰期，与晚第四纪千年尺度气候波动主要出现在冰期不同，说明中更新世的气候转型不仅表现在轨道尺度的气候周期变化上，同时也体现在千年尺度气候波动的特征变化中。   相似文献   

Oxygen deficient perovskites in the system CaSiO3–CaAlO2.5 and implications for the Earth’s interior     

U. W. Bläß  F. Langenhorst  D. J. Frost  F. Seifert 《Physics and Chemistry of Minerals》2007,34(6):363-376

Oxygen deficient perovskites of the system CaSiO₃–CaAlO_2.5 have been synthesised at high-pressure and -temperature conditions relevant to the Earth’s transition zone in order to investigate their stabilities in the Earth’s mantle and determine structural properties associated with vacancy incorporation. Two polysomes of thermodynamically stable defect perovskites with Ca(Al_0.4Si_0.6)O_2.8 and Ca(Al_0.5Si_0.5)O_2.75 stoichiometry have been identified. The ordering of oxygen defects into pseudo-cubic (111) layers results in well-ordered ten- or eightfold superstructures, respectively. At all other compositions examined, a metastable formation of perovskites has been observed instead, which are assumed to grow initially disordered. These are now characterised by tiny domains, formed due to subsequent ordering of vacancies along various pseudo-cubic {111} layers. Both ordered defect perovskites show a large P–T stability field ranging from about 9–18 GPa and 4–12 GPa, respectively. Microstructural TEM analyses revealed the presence of growth and ferroelastic twins, which indicate a phase transition from rhombohedral to monoclinic symmetry during quenching. Electron energy loss spectroscopy of Si and Al K edges point at the presence of tetrahedral, octahedral and maybe some pentacoordinated silicon, whereas aluminium is predominantly octahedrally coordinated with minor fractions in lower coordination. Observed properties are interpreted in terms of a new structural model, explaining the observed phase transition and formation of different twin laws as well as giving reasons for the development of such large superstructures. With respect to phase relations of the transition zone, the potential occurrence of such defect perovskites in the Earth’s interior is discussed.  相似文献   

Progress in isotope paleohydrology using lake sediment cellulose     

Brent B. Wolfe  Matthew D. Falcone  Ken P. Clogg-Wright  Cherie L. Mongeon  Yi Yi  Bronwyn E. Brock  Natalie A. St. Amour  William A. Mark  Thomas W. D. Edwards 《Journal of Paleolimnology》2007,37(2):221-231

Recent advances in sample preparation techniques and mass spectrometry have fostered more routine oxygen isotope analysis of aquatic cellulose in lake sediment cores, a proxy for lake water oxygen isotope history. These methodological developments have significantly increased the feasibility of incorporating this approach into high-resolution, multi-site, and multi-proxy studies, which are frequently necessary to answer complex hydrological, hydroecological and hydroclimatic questions requiring a paleoenvironmental perspective. Direct translation of lake sediment aquatic cellulose oxygen isotope composition into lake water oxygen isotope composition offers appreciable opportunity for quantitative paleohydrological reconstructions, as evidenced by studies conducted over the past 15 years that span Holocene and pre-historical timescales.  相似文献   

The effects of organic removal treatment on the integrity of δ<Superscript>18</Superscript>O measurements from biogenic silica     

Jonathan J. Tyler  Melanie J. Leng  Hilary J. Sloane 《Journal of Paleolimnology》2007,37(4):491-497

Prior to oxygen isotope analysis of biogenic silica by fluorination techniques, sediments must be cleaned of all organic compounds. Despite the expanding volume of research utilising oxygen isotope ratios in biogenic silica in palaeoclimatology, very little is known about the effects of different standard preparation methods for the removal of organic matter on the isotope values. Here we compare a number of methods for the removal of organic matter in order to assess their effectiveness and influence on subsequent isotope measurements. Not all the methods described here effectively removed organic matter, the best treatments were H₂O₂ and ignition in air at 550°C. Ignition in air at 950°C, and heating in vacuum at 250 and 450°C results in marked alteration of isotope values, whereas use of hydrogen peroxide (H₂O₂), nitric acid (HNO₃) and plasma ashing have little or no effect, within the bounds of analytical error. Ignition in air at 550°C was the most effective technique, and induced no alteration of δ¹⁸O_silica, but practical constraints may limit the application of this method routinely. Our findings indicate that considerable caution is required when preparing sediment for isotope analysis of biogenic silica.  相似文献   

青海湖碳酸盐氧同位素环境记录再认识   总被引：1，自引：2，他引：1       下载免费PDF全文

曾承 《盐湖研究》2007,15(1):16-19

青海湖是我国内陆最大的闭流型水体,地处东亚季风和西风的交汇影响区,对区域降水的改变等气候变化反应敏感,其水位变化历史是研究区域季风环境演变极其宝贵和重要的环境档案。青海湖Q14B孔岩芯介壳δ18Oc变化曲线自1991年发表以来,受到国内外同行的广泛关注和继续探讨。依据近年来青海湖气候与环境演变研究的最新研究结果和个人对闭流型湖泊同位素地球化学的认识,对介壳δ18Oc变化曲线进行了重新判读并得出以下结论:14.5~10.5 ka B.P.,青海湖区气候已逐渐从干冷向温湿过渡,季风降水逐渐增加;10.8~10.5 ka B.P.,青海湖处于碳酸盐滩湖环境,湖水深度从几米演变到接近干涸;10.5~9.5 kaB.P.,季风降水增加;9.5~8 ka B.P,湖水位从此前的接近干涸演变到此间的2~8 m,δ18Oc值跌落到一个较低的位置;8~3.5ka B.P,气候条件相对稳定,湖水不断蒸发引起重同位素的富集;3.5~0ka B.P,湖水处于同位素稳定阶段。研究结果还显示,δ18Oc值的短期波动与湖泊水位短期变化关系密切且明显,即水位高低分别对应δ18Oc的低值与高值。δ18Oc值的长期变化与湖泊水位长期变化关系不明显,水位较浅时,二者几乎无关联;水位较深时,水位的长期缓慢下降自然会导致δ18Oc逐渐攀升,而水位的长期缓慢上升也可以伴随δ18Oc逐渐攀升。  相似文献