Can trace element distributions in migmatites be used as analogues in understanding petrogenesis of anatectic granites

Trace element concentrations in leucosomes of migmatites in the Black Hills, South Dakota, USA, were examined to determine if their compositions are analogous to those of pelite-derived granites. Melanosomes in the migmatites are dominated by biotite, sillimanite, and quartz. Leucosomes have constant Si/Al that corresponds to a peraluminous granite; however, they have variable proportions of (sil+qtz)/alkali feldspar that are attributed to instability of feldspar relative to sillimanite due to high a_HF in partial melts. There are strong positive correlations of Sr, Ba, Rb, and Cs concentrations with the proportion of feldspar in the leucosomes. The average concentrations of Sr and Ba are higher and of Rb and Cs lower in the leucosomes than in pelite-derived leucogranites. A reaction progress method is used to demonstrate that partitioning of these trace elements between melanosomes and leucosomes represent mineral-mineral equilibrium rather than residue-melt equilibrium. This implies that leucosomes in migmatites may crystallize while maintaining equilibrium with melanosomes and the resulting trace element compositions may not be analogous to those of partial melts.     

挥发份对高硅岩浆演化趋势的制约:以东南沿海白垩纪晚期花岗岩类岩石为例SCIEI北大核心CSCD

东南沿海分布大面积的白垩纪晚期侵入岩。这些岩石可分为两期:其中115~100Ma以钙碱性系列岩石为主,岩石组合为辉长岩-闪长岩-花岗闪长岩-二长花岗岩-碱性长石花岗岩;而100~86Ma的岩石为碱性系列,岩石组合为石英二长斑岩-正长斑岩-碱性长石花岗岩。115~100Ma的辉长岩以角闪辉长岩为主,具有极高的CaO、MgO和Al_(2)O_(3)含量,具有极低的SiO_(2)(42.9%~53.8%)、全碱(K_(2)O+Na_(2)O:0.86%~5.28%)、Ba、Nb、Th、Rb和Zr含量,也具有极低的FeO^(T)/MgO、La/Yb和Zr/Hf比值,较高的Eu/Eu^(*)、Sr/Y比值和Sr含量,为基性-超基性堆晶岩。与辉长岩同期的闪长岩和细粒暗色包体具有较高的SiO_(2)(50.34%~63.68%),较低的CaO、P_(2)O_(5)、MgO、Al_(2)O_(3)含量,相对低的Eu/Eu^(*)和Sr/Y比值,变化较大的La/Yb和Zr/Hf比值,代表了从基性岩浆储库中抽取的富硅熔体。115~100Ma的花岗闪长岩和二长花岗岩类岩石为准铝质岩石,SiO_(2)含量变化较大(61.7%~75.3%),具有较低的FeO^(T)/MgO、Ga/Al比值和Nb、Zr及Nb+Zr+Ce+Y元素含量,显示出典型I型花岗岩的特征。这些花岗岩具有相对高的La/Yb、Eu/Eu^(*)和Zr/Hf比值和高的Sr、Ba和Zr含量。结合岩相学特征,这些花岗岩为堆晶花岗岩。而115~100Ma的碱性长石花岗岩具有极高的SiO_(2)含量(大于75%),低的Eu/Eu^(*)、La/Yb、Zr/Hf和Sr/Y比值,具有低的Ba、Sr和Zr含量和高的Rb、Nb、Y和Th含量和Rb/Sr比值,表明这些花岗岩是由富硅岩浆储库中抽离的高硅熔体侵入地壳形成。100~86Ma期间形成的二长斑岩和正长斑岩具有极高的全碱含量,可以达到8%~12%,其SiO_(2)主要集中在60%~70%,具有极高的Zr、Sr和Ba含量和Eu/Eu^(*)、La/Yb和Sr/Y比值,显示出堆晶花岗岩的特征。而100~86Ma期间形成的大部分碱性长石花岗岩具有极高的SiO_(2)含量(大于75%),并显示出A型花岗岩的特征,具有高的Rb/Sr比值和高的Rb、Y和Th和低的Ba、Sr含量和低的Zr/Hf、La/Yb、Eu/Eu^(*)和Sr/Y比值,表明它们是由富硅岩浆储库抽离的高硅熔体侵入浅部地壳形成。东南沿海高硅花岗岩的形成和穿地壳岩浆系统密切相关,高硅花岗岩是由浅部地壳内晶体-熔体分异产生的熔体侵入地壳所形成,而高硅花岗岩的地球化学特征与岩浆储库的水及挥发份含量密切相关。115~100Ma期间,从富水的岩浆储库抽离的熔体形成具有低高场强元素含量和低Rb/Sr比值的高硅花岗岩,这一过程与古太平洋板块俯冲有关;100~86Ma期间,从富挥发份的岩浆储库抽离的熔体形成碱性特征、富含高场强元素和具有高的Rb/Sr比值的高硅花岗岩,这一过程和古太平洋板块回撤软流圈上涌有关。     

Barium partitioning between alkali feldspar and silicate liquid at high temperature and pressure

Barium partitioning between alkali feldspar and a natural trachyte liquid, enriched with barium, has been determined as a function of pressure and temperature from 10 to 25 kb and 900°–1100° C. Both long duration experiments and a re-equilibration experiment suggest close approach to equilibrium. Partition coefficients (D _Ba) decrease as both temperature and pressure increase (e.g., D _Ba changes from 8.71 at 10 kb, 900° C to 1.48 at 25 kb, 1100° C). Water activity also controls the barium partitioning with a marked decrease in D _Ba ^af/liq for addition of less than 0.8 wt% H₂O, but with no apparent additional effect for higher water contents in the bulk composition (e.g., from 0.8–4.2 wt% H₂O). The composition of alkali feldspar also has a significant effect on D _Ba ^af/liq , but the data obtained do not allow derivation of a complete D-Or relationship. These new data suggest that Henry's Law is obeyed for most of the barium concentrations examined, and the limit of Henry's Law behaviour for barium in alkali feldspar is as high as 6 wt% BaO in alkali feldspar and 1.2 wt% BaO in the melt, similar to the results of Long (1978). The experimental results broadly overlap with natural data for D _Ba, determined from coexisting alkali feldspar phenocrysts and glass (or groundmass).     

87Sr/86Sr in kimberlitic carbonates by ion microprobe: Hydrothermal alteration,crustal contamination and relation to carbonatite

Carbonates in a 30 cm wide zoned kimberlite dyke from the De Beers Mine, Kimberley, S. Africa were studied by cathodoluminescence and electron microprobe techniques and their ⁸⁷Sr/⁸⁶Sr ratios were measured using an AEI-IM20 ion microprobe. Primary carbonates (including calcite dendrites, rhombohedral calcites in segregation vesicles and mosaic dolomite) have high Sr (0.69–1.35 wt.% SrO) and Ba (0.24–0.44% BaO) and ⁸⁷Sr/⁸⁶Sr ratios in the range 0.7046 to 0.7056. Secondary sparry calcite in amygdales and veins is characterised by low Ba (<0.05% BaO) and ⁸⁷Sr/⁸⁶Sr near 0.72. Rhombohedral calcite 0.5 cm from a contact with 2,900 my. old biotite-gneiss has minor element chemistry like that of primary carbonate, but an elevated ⁸⁷Sr/⁸⁶Sr ratio of 0.7103, possibly indicating crustal contamination in a boundary layer of the kimberlite magma. Amygdale-like segregations of carbonate and/or serpentine originated as gas-cavities and were not formed by liquid immiscibility. They are now filled either by secondary calcite or by minerals precipitated from residual kimberlite liquid. However, dendritic calcite and primary dolomite and calcite with high Sr, Ba and low ⁸⁷Sr/⁸⁶Sr demonstrate shared chemical characteristics between these carbonates and carbonatite. The primary kimberlite magma had initial ⁸⁷Sr/⁸⁶Sr close to 0.7046.     

An ion microprobe study of the partitioning of trace elements between clinopyroxene and liquid in the system diopside-albite-anorthite

The partitioning of trace elements (Sc, Ti, Sr and Sm) between diopsidic clinopyroxene and liquid was studied experimentally in the system diopside-albite-anorthite at 1250°C, 1300°C and 1345°C at 1 atm. Twelve different bulk compositions were selected to study the effects of temperature and chemical composition. A Cameca ion microprobe was used to determine trace element concentrations in both clinopyroxene and liquid. Experiments of different run duration $\text{1}\text{4}\text{8}\text{?}$ days) showed that equilibrium was approached in less than 4 days at 1275°C. Equilibrium was also evaluated by a reversal run. A series of runs of constant bulk composition but with variable trace element contents showed that Henry's Law was obeyed over concentration ranges of the trace elements similar to those encountered in natural systems. The partition coefficients show significant ranges: Sc, 0.345~2.61; Ti, 0.084~0.214; Sr, 0.075~0.136; Sm, 0.054~0.328; the values are comparable with those obtained experimentally by other investigators. The partition coefficients vary as a function of both temperature and chemical composition. The experimental results are discussed in terms of exchange equilibria using the Bottinga-Weill silicate melt model. It is demonstrated that analytical uncertainties of both major and trace elements play an important role in understanding trace element exchange equilibria; propagation of analytical errors in the thermodynamic treatment is equally important.     

Limits of solution of trace elements in minerals according to Henry's law: Review of experimental data

Results of a survey of experimental data on trace element partitioning between crystals and coexisting liquid and between crystals and coexisting aqueous fluid are reported. These studies involve combinations of elements such as Cs, Rb, K, Na, Li, Ba, Sr, Ni and Sm dissolved in minerals such as feldspars, micas, feldspathoids, garnets, pyroxenes, amphibole and olivine. It is shown that the concentration ranges of these elements in minerals with solution behavior according to Henry's law appear to extend to less than 1 wt.% and often to less than 100 ppm of the element in the crystalline phase.The available data indicate that the concentration ranges of solution in minerals according to Henry's law can be positively correlated with the difference of ionic radii between trace element and the host element for which the tracer is assumed to substitute. Furthermore, studies involving crystals and coexisting aqueous fluid have been used to determine whether Henry's law or Raoult's law adequately describes the solution. Based on the assumption that the aqueous fluid solution can be considered ideal, models have been proposed stating that if the difference between the ionic radii of the tracer and the host element in the crystalline phase is less than about 10% (relative to the host element), the solution is ideal (Raoult's law). With larger differences between the ionic radii, there is an excess free energy of mixing, although Henry's law is still obeyed in the concentration ranges where crystalliquid or crystal-fluid partition coefficients are independent of element concentration.     

Mechanisms of formation of barium-rich phlogopite and strontium-rich apatite during the final stages of alkaline magma evolution

Carbonatite veinlets in fergusite from the Dunkeldyk potassium-rich basaltoid complex (southeastern Pamirs) are composed of clinopyroxene, phlogopite, and apatite phenocrysts embedded in a crystallized calcite-bearing groundmass. The examination of back-scattered electron images revealed areas of significantly different compositions in fluorapatite and fluorphlogopite. The content of BaO in the phlogopite ranges from 0.68 to 10.9 wt %. There are also variations in MgO and F contents. The maximum BaO content corresponds to high mole fractions of the Ba end member kinoshitalite (up to 0.24) in the phlogopite. The zoned fluorapatite phenocrysts are rich in SrO (0.77–25.4 wt %). An increase in SrO content is accompanied by an increase in Ce₂O₃, La₂O₃, and BaO and a distinct decrease in CaO. Most of the apatite grains are rimmed by elongated colorless crystals showing the maximum SrO contents. Based on the experimentally determined Ba and Sr partition coefficients between these minerals, silicate and carbonate melts, and fluid, a model was proposed for the enrichment of phases in these trace elements. It was shown that the mineral-forming media of the Ba-rich phlogopites was a residual melt enriched in volatiles (including F) and fluid-mobile elements. During that stage, the decomposition reactions of early Ba-bearing feldspars with subsequent incorporation of BaO in Ba-rich phlogopites played an important role. The mechanism of formation of Sr-rich apatites is fundamentally different: early apatite grains with moderate Sr contents recrystallized under the influence of Sr-rich fluids released during the late magmatic stage. Thus, despite their close association in a single rock, the Ba-bearing phlogopite and Sr-rich apatite were formed by significantly different mechanisms. Our previous investigations of melt and fluid inclusions in minerals from the rocks of the Dunkeldyk complex and the results obtained in this study allowed us to suggest that the barium, fluorite-carbonatite, and rare metal mineralization occurring in the region developed owing to the prolonged evolution of primary magmas, resulting in the formation of melt-solutions (brines) and hydrothermal systems.     

Zonation des éléments en traces au cours de la croissance des cristaux dans les bains silicatés: l'exemple de Rb,Cs, Sr et Ba dans le système Qz-Ab-Or-H2O

An indirect method was used to study Na, K, Rb, Cs, Sr and Ba partition coefficients between crystals and silicate melt. Equilibria between a hydrothermal solution and the melt at 800°C and 2 kb and between a hydrothermal solution and crystals at 750°C and 2 kb were separately achieved.For major element partitioning (Na and K), the results obtained here are in good agreement with those of Tuttle and Bowen (1958) which allow us to follow crystal evolution during a fractional crystallization process where the growth of zoned crystals takes place.For minor elements Rb, Cs, Sr, Ba, melt/aqueous solution partition coefficients depend on Na/K as well as the silica content of the melt. These effects are rather small for Rb and Cs, but are much more important for the alkaline earths. The feldspar/aqueous solution partition coefficients also depend on Na/K.The variations of the partition coefficients feldspar/melt are complex in the part of the Qz-Ab-Or diagram located below the cotectic line.During fractional crystallization following the Rayleigh law (assuming that there are no kinetic phenomena) Sr (D > 10) is almost totally removed from the melt in the early stages whereas Cs (D < 0.1) remains in the melt during the whole process. Rb and Ba have partition coefficients closer to unity. The variation of these coefficients, due to changes in bulk composition of liquid and crystals during fractional crystallization, can lead to complex zoning with possible concentration maxima at some stages. Similar phenomena can be expected in non-ideal natural solid solutions, even if no discontinuities can be detected in the physicochemical evolution of the parent magma.     

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.     

大兴安岭伊勒呼里山早白垩世碱长花岗岩年龄、地球化学特征及其地质意义

对大兴安岭伊勒呼里山早白垩世碱长花岗岩进行了岩相学、地球化学、LA-ICP-MS锆石U-Pb定年研究。伊勒呼里山地区碱长花岗岩主量元素具有富Si、富碱,贫Mg、Ca的特征;微量元素亏损Sr、P、Eu、Ti,富集K、Rb、Th等不相容元素,元素地球化学特征表明,岩体为铝质A型花岗岩(A/CNK=0.88~1.21,A/NK=0.94~1.49)。测年结果显示,粗中粒碱长花岗岩的锆石年龄为140.3±1.0Ma,细中粒碱长花岗岩锆石年龄为137.9±0.8Ma,均形成于早白垩世。结合区域研究资料,伊勒呼里山地区碱长花岗岩岩体的形成与蒙古-鄂霍茨克洋闭合后的岩石圈伸展密切相关,其岩浆源区可能为地壳物质的部分熔融。     

Microtexture and Distribution of Minerals in Hydrothermal Barite-Silica Chimney from the Franklin Seamount, SW Pacific: Constraints on Mode of Formation

An extinct hydrothermal barite-silica chimney from the Franklin Seamount of the Woodlark Basin, in the southwestern Pacific Ocean, was investigated for mineral distribution and geochemical composition. Six layers on either side of the orifice of a chimney show significant disparity in color, mineral assemblage and major element composition. Electron microscope(SEM) images reveal that the peripheral wall of the chimney is composed of colloform silica, suggesting that incipient precipitation of silica-saturated hydrothermal fluid initiated the development of the chimney wall. Intermediate layers, between the exterior wall and the inner fluid-orifice, dominate with barite and sulfides. Low Sr-to-Ba ratios(SrO/BaO = 0.015–0.017) indicate restricted fluid-seawater mixing, which causes relatively high-temperature formation of the intermediate layers. Whereas the innermost layer bordering the chimney orifice is characterized by more silica and a higher Sr-to-Ba ratio(SrO/BaO = 0.023), could have formed due to a paragenetic shift from a high-temperature active phase to a cooler waning stage of formation. A paragenetic shift is also probably responsible for the change in mineral formation mechanism that resulted in the textural variation of barite and colloform silica developed during different growth phases of this barite-silica chimney.     

内蒙古科尔沁右翼中旗碱长花岗岩锆石U-Pb年代学、岩石地球化学及其动力学意义

对内蒙古科尔沁右翼中旗碱长花岗岩进行了同位素年代学及岩石地球化学研究。碱长花岗岩LA-ICP-MS锆石U-Pb加权平均年龄为(166±1)Ma,表明该侵入体是中侏罗世侵位形成的。岩石学及地球化学成分显示其属于碱性、具A型花岗岩特征。岩石高硅(w(SiO₂)=74.80%~76.34%)、富碱(w(Na₂O+K₂O)=7.94%~8.71%)、高铁镁比(TFeO/MgO=13.54~24.28)、贫钙(w(CaO)=0.10%~0.21%)、贫镁(w(MgO)=0.08%~0.16%)和低钛(w(TiO₂)=0.07%~0.10%);稀土配分曲线呈现"海鸥式"分布特征,显示强烈的Eu负异常(δEu=0.09~0.17);微量元素特征显示具有较高质量分数的有Zr(128.95×10^-6~156.32×10^-6)、Yb(4.93×10^-6~5.35×10^-6)和Y(40.93×10^-6~56.75×10^-6),较低质量分数的有Sr(23.16×10^-6~37.14×10^-6)、Ba(186.13×10^-6~231.31×10^-6),在微量元素原始地幔标准化蛛网图上显示明显的Sr、Ba和Ti的负异常。以上特征表明,碱长花岗岩为A型花岗岩。岩石具有高的Rb/Sr值(4.26~7.81,平均为6.12)和Rb/Nb值(10.2~14.7,平均为12.7),显示出壳源岩浆的成分特征。综合分析表明,碱长花岗岩为低压下长英质地壳部分熔融的产物。w(Rb)-w(Yb+Ta)图解、w(Rb)-w(Y+Nb)图解、w(Ta)-w(Yb)图解、w(Nb)-w(Y)图解、Ce/Nb-Y/Nb图解、Ce/Nb-Yb/Ta图解及结合区域构造演化研究表明,碱长花岗岩形成于造山后伸展的构造环境,并与松辽盆地及其周围的花岗岩一起暗示松辽盆地是在中侏罗世造山作用之后伸展的构造环境下形成的陆内盆地。     

内蒙古阿尔山绿水碱长花岗岩锆石U——Pb 年龄、地球化学特征及构造意义

绿水碱长花岗岩锆石的LA--ICP--MS U--Pb 同位素测试结果为139. 4 ± 1. 6 Ma,表明其形成于早白垩世。地球化学特征显示绿水碱长花岗岩属于弱过铝质高钾钙碱性A2 型花岗岩,具高硅、高碱和低CaO、Fe2O3、MgO 和P2O5 特征; 轻稀土元素( LＲEE) 富集,重稀土元素( HＲEE) 相对亏损,铕具有明显的负异常; 高场强元素Zr、Hf 和大离子亲石元素Ｒb、Th、U 及K 相对富集,Ba、Nb、Ta、 Sr 和P 具明显的亏损。结合区域地质资料,认为这些碱长花岗岩的形成可能与古太平洋板块俯冲导致的加厚岩石圈拆沉后伸展环境有关。     

云南个旧神仙水岩体锆石U—Pb年代学及岩石地球化学研究

云南个旧地区花岗岩极其发育,且与锡成矿关系密切。其中个旧西区神仙水花岗岩体呈岩株状,岩性主要为碱长花岗岩和正长岩。岩石地球化学研究表明,神仙水花岗岩具有高硅、贫钙镁、富碱的特征;ω（TFeO）／ω（MgO）和ω（Na2O＋K2O）／ω（A12：O3）比值高。富集大离子亲石元素Rb、n、u、K、La、Nd和高场强元素zr、Hf,亏损Ba、sr、Ta、P、Ti。Eu负异常较强,轻稀土富集,重稀土相对亏损,稀土配分模式呈右倾海鸥型,岩石类型属于A型花岗岩。锆石LA—ICP．Ms定年结果表明神仙水花岗岩体形成于81Ma左右,相当于晚白垩世。根据区域地质和花岗岩地球化学特征,判断其形成于伸展构造环境。     

大兴安岭东北部早白垩世秀山火山-侵入杂岩体特征及成因

大兴安岭东北部秀山林场一带的早白垩世花岗质火山-侵入杂岩体由喷发旋回期的流纹岩、流纹质熔结凝灰岩-粗面英安岩、粗安岩和浅成侵入期的二长花岗斑岩-晶洞正长花岗岩-文象碱长正长花岗岩构成。晚期侵入岩体充填于火山喷发形成的塌陷破火山口中央, 岩石具文象结构、晶洞构造等特征, 未见碱性暗色矿物。流纹岩(118.20 ±1.90 Ma) 与侵入岩形成时代(116.86～118.3 Ma) 相近。杂岩体岩石大多数属碱性系列, 具高硅、富碱、铝、Ga和高场强元素(HFSE) 的特征, 各岩石微量元素蛛网图上曲线形态基本一致, 均出现Sr、Ba谷, 稀土配分曲线也相似, 呈轻稀土富集的不对称右倾“海鸥”型, δEu 中等亏损。流纹岩与石英正长岩的86 Sr /87 Sr 初始值( 0.708 734 ～ 0.711 488) 、143Nd /144Nd初始值(0.512 485～0.512 503) 相近。杂岩体具时、空、源的一致性, 为铝质A1型火山-侵入杂岩体, 形成于岩石圈伸展机制下的非造山板内拉张构造环境。     

Trace element modelling of pelite-derived granites

The presence or absence of a vapour phase during incongruent-melt reactions of muscovite and biotite together with the composition of the protolith determines the trace-element characteristics of the resulting melt, provided that equilibrium melting occurs for those phases that host the tracc elements of interest. For granitic melts, Rb, Sr and Ba provide critical constraints on the conditions that prevailed during melting, whereas REE are primarily controlled by accessory phase behaviour. Mass-balance constraints for eutectic granites that are formed by the incongruent melting of muscovite in pelites indicate that melting in the presence of a vapour phase will result in a large melt fraction, and deplete the restite in feldspar. Hence the melt will be characterized by low Rb/Sr and high Sr/Ba ratios. In contrast, vapour-absent melting will result in a smaller melt fraction, and an increase in the restitic feldspar. Consequently high Rb/Sr and low Sr/Ba ratios are predicted. Vapour-absent melting will also enhance the negative Eu anomaly in the melt. Granites that result from the incongruent melting of biotite in the source will be characterized by higher Rb concentrations than those that result from the incongruent melting of muscovite. The Himalayan leucogranites provide an example of unfractionated, crustally derived eutectic melts that are enriched in Rb but depleted in Sr and Ba relative to their metasedimentary protoliths. These compositions may be generated by the incongruent melting of muscovite as a low melt fraction (F0.1) from a pelitic source under vapour-absent conditions.     

Determination of Thirteen Rare-Earth Elements by High-Performance Liquid Chromatography in Thirty and of K, Rb, Cs, Sr and Ba by Isotope Dilution Mass Spectrometry in Eighteen International Geochemical Reference Samples

This study reports the results of thirteen rare-earth elements in thirty geochemical reference samples. Three alkali (K, Rb, Cs) and two alkaline earth (Sr, Ba) elements were also determined in eighteen reference samples. The analytical procedure involved is based on spiked samples and later measurement of the rare-earth elements by high-performance liquid chromatography and the alkalies and alkaline earths by thermo-quartz mass spectrometric isotope dilution (THQ-MSID). Whenever possible, the results are compared with literature values.     

青海南部曲麻莱县达考岩体地球化学特征及其构造环境

达考序列岩体由查肖叉得英云闪长岩、杂乃玛下黑云母二长花岗岩、抗涌正长花岗岩组成。单颗粒锆石U-Pb同位素年龄值为169±4 Ma,形成于中侏罗世,岩石化学成分表现为岩浆向富硅、富碱、富铝方向演化。稀土元素特征表现为轻稀土元素富集,重稀土元素平坦型。微量元素特征表现为富集大离子亲石元素Rb、K、Ba、Th,而Sr、Nb、Ta略显亏损,εNd（t）变化在-7.6~-8.1之间,（87Sr/86Sr）i值较高,变化于0.70969~0.71104之间。地球化学特征表明达考序列岩体形成构造背景为火山弧花岗岩,为壳幔混合产物。     

Crustal contributions to arc magmatism in the Andes of Central Chile

Fifteen andesite-dacite stratovolcanoes on the volcanic front of a single segment of the Andean arc show along-arc changes in isotopic and elemental ratios that demonstrate large crustal contributions to magma genesis. All 15 centers lie 90 km above the Benioff zone and 280±20 km from the trench axis. Rate and geometry of subduction and composition and age of subducted sediments and seafloor are nearly constant along the segment. Nonetheless, from S to N along the volcanic front (at 57.5% SiO₂) K₂O rises from 1.1 to 2.4 wt %, Ba from 300 to 600 ppm, and Ce from 25 to 50 ppm, whereas FeO^*/MgO declines from >2.5 to 1.4. Ce/Yb and Hf/Lu triple northward, in part reflecting suppression of HREE enrichment by deep-crustal garnet. Rb, Cs, Th, and U contents all rise markedly from S to N, but Rb/Cs values double northward — opposite to prediction were the regional alkali enrichment controlled by sediment subduction. K/Rb drops steeply and scatters greatly within many (biotite-free) andesitic suites. Wide diversity in Zr/Hf, Zr/Rb, Ba/Ta, and Ba/La within and among neighboring suites (which lack zircon and alkali feldspar) largely reflects local variability of intracrustal (not slab or mantle) contributions. Pb-isotope data define a limited range that straddles the Stacey-Kramers line, is bracketed by values of local basement rocks, in part plots above the field of Nazca plate sediment, and shows no indication of a steep (mantle+sedimentary) Pb mixing trend. ⁸⁷Sr/⁸⁶Sr values rise northward from 0.7036 to 0.7057, and ¹⁴³Nd/¹⁴⁴Nd values drop from 0.5129 to 0.5125. A northward climb in basal elevation of volcanic-front edifices from 1350 m to 4500 m elevation coincides with a Bougueranomaly gradient from –95 to –295 mgal, interpreted to indicate thickening of the crust from 30–35 km to 50–60 km. Complementary to the thickening crust, the mantle wedge beneath the front thins northward from about 60 km to 30–40 km (as slab depth is constant). The thick northern crust contains an abundance of Paleozoic and Triassic rocks, whereas the proportion of younger arc-intrusive basement increases southward. Primitive basalts are unknown anywhere along the arc. Base-level isotopic and chemical values for each volcano are established by blending of subcrustal and deep-crustal magmas in zones of melting, assimilation, storage and homogenization (MASH) at the mantle-crust transition. Scavenging of mid-to upper-crustal silicic-alkalic melts and intracrustal AFC (prominent at the largest center) can subsequently modify ascending magmas, but the base-level geochemical signature at each center reflects the depth of its MASH zone and the age, composition, and proportional contribution of the lowermost crust.     

黄土高原南部全新世黄土-古土壤 序列若干元素分布特征及意义*

选择黄土高原南部的XJN,XMC和JYC全新世剖面为研究对象。通过对地层中Ca,Ba,Rb和Sr元素分布的研究,发现Ba/Sr和Rb/Sr比值在不同地层中含量差异十分明显,并与成土作用强度显著正相关,可作为良好的气候替代指标;表生环境中Rb和Ba较稳定,Sr和Ca元素十分活跃,易于迁移,其中Ca的迁移能力高于Sr元素;从XJN→XMC→JYC剖面,Rb和Ba元素含量增加,而Sr和Ca元素含量降低,这与区域环境差异有关;全新世中期暖湿的亚热带气候主要出现关中盆地地区,六盘山以西则是暖温带气候。