He–Ar and Nd–Sr isotopic compositions of late Pleistocene felsic plutonic back arc basin rocks from Ulleungdo volcanic island, South Korea: Implications for the genesis of young plutonic rocks in a back arc basin

We report analyses of noble gases and Nd–Sr isotopes in mineral separates and whole rocks of late Pleistocene (< 0.2 Ma) monzonites from Ulleungdo, South Korea, a volcanic island within the back arc basin of the Japan island arc. A Rb–Sr mineral isochron age for the monzonites is 0.12 ± 0.01 Ma. K–Ar biotite ages from the same samples gave relatively concordant ages of 0.19 ± 0.01and 0.22 ± 0.01 Ma. ⁴⁰Ar/³⁹Ar yields a similar age of 0.29 ± 0.09 Ma. Geochemical characteristics of the felsic plutonic rocks, which are silica oversaturated alkali felsic rocks (av., 12.5 wt% in K₂O + Na₂O), are similar to those of 30 alkali volcanics from Ulleungdo in terms of concentrations of major, trace and REE elements. The initial Nd–Sr isotopic ratios of the monzonites (⁸⁷Sr/⁸⁶Sr = 0.70454–0.71264, ¹⁴³Nd/¹⁴⁴Nd = 0.512528–0.512577) are comparable with those of the alkali volcanics (⁸⁷Sr/⁸⁶Sr = 0.70466–0.70892, ¹⁴³Nd/¹⁴⁴Nd = 0.512521–0.512615) erupted in Stage 3 of Ulleungdo volcanism (0.24–0.47 Ma). The high initial ⁸⁷Sr/⁸⁶Sr values of the monzonites imply that seawater and crustally contaminated pre-existing trachytes may have been melted or assimilated during differentiation of the alkali basaltic magma.A mantle helium component (³He/⁴He ratio of up to 6.5 RA) associated with excess argon was found in the monzonites. Feldspar and biotite have preferentially lost helium during slow cooling at depth and/or during their transportation to the surface in a hot host magma. The source magma noble gas isotopic features are well preserved in fluid inclusions in hornblende, and indicate that the magma may be directly derived from subcontinental lithospheric mantle metasomatized by an ancient subduction process, or may have formed as a mixture of MORB-like mantle and crustal components. The radiometric ages, geochemical and Nd–Sr isotopic signatures of the Ulleungdo monzonites as well as the presence of mantle-derived helium and argon, suggests that these felsic plutonic rocks evolved from alkali basaltic magma that formed by partial melting of subcontinental lithospheric mantle beneath the back arc basin located along the active continental margin of the southeastern part of the Eurasian plate.     

Chemical and boron-isotope variations in tourmalines from an S-type granite and its source rocks: the Erongo granite and tourmalinites in the Damara Belt,Namibia

Tourmaline is widespread in metapelites and pegmatites from the Neoproterozoic Damara Belt, which form the basement and potential source rocks of the Cretaceous Erongo granite. This study traces the B-isotope variations in tourmalines from the basement, from the Erongo granite and from its hydrothermal stage. Tourmalines from the basement are alkali-deficient schorl-dravites, with B-isotope ratios typical for continental crust (δ¹¹B average −8.4‰ ± 1.4, n = 11; one sample at −13‰, n = 2). Virtually all tourmaline in the Erongo granite occurs in distinctive tourmaline-quartz orbicules. This “main-stage” tourmaline is alkali-deficient schorl (20–30% X-site vacancy, Fe/(Fe + Mg) 0.8–1), with uniform B-isotope compositions (δ¹¹B −8.7‰ ± 1.5, n = 49) that are indistinguishable from the basement average, suggesting that boron was derived from anatexis of the local basement rocks with no significant shift in isotopic composition. Secondary, hydrothermal tourmaline in the granite has a bimodal B-isotope distribution with one peak at about −9‰, like the main-stage tourmaline, and a second at −2‰. We propose that the tourmaline-rich orbicules formed late in the crystallization history from an immiscible Na–B–Fe-rich hydrous melt. The massive precipitation of orbicular tourmaline nearly exhausted the melt in boron and the shift of δ¹¹B to −2‰ in secondary tourmaline can be explained by Rayleigh fractionation after about 90% B-depletion in the residual fluid. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

A comparative study on the contents of vitamins in the natural and the cultured prawn

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液体中光声信号吸收衰减的研究

研究水的声吸收所引起的光声脉冲幅度的变化。脉冲声波由激光通过光击穿机制产生。文中给出了光声脉冲峰值声压与传播距离和声吸收系数之间的理论关系式。实验测量结果和理论曲线所描述的变化规律相符合。     

围隔实验中水柱颗粒物色素的动态研究

用高效液相色谱法(HPLC)研究了围隔实验过程中水柱颗粒物主要色素的组成及动态变化,并就滤食性鱼类鲢对水体主要色素代谢的影响进行了讨论。结果表明:水柱中的主要色素有叶绿素a、异黄素、岩藻黄素、黄体素、玉米黄素和蓝藻叶黄素等,未放鱼的围隔中实验后期各种色素含量均降低到最低水平,有鱼的围隔中鱼类密度越高则色素含量降低越多。未放鱼的围隔中叶绿素a代谢产物———脱植基叶绿素a、脱镁叶绿素a、脱镁叶绿酸a与叶绿素a的比值均大于其它围隔,有鱼的围隔中鱼类密度大的这几个比值也比较大。     

雅鲁藏布江蛇绿岩中地幔柱型岩浆作用——来自氦、氩同位素的证据

雅鲁藏布江蛇绿岩的氦、氩同位素组成分别是：蛇绿岩中变质橄榄岩的^3He/^4He比值为1．104-3．384Ra，平均为2．383Ra；玄武岩的He同位素组成比较均一，^3He/^4He平均值为5．359 Ra；辉绿岩的^3He／^4He比值变化较大，为1—5Ra。由于各岩石样品有不同程度的蚀变，造成放射性成因He的加入，因此大多数样品He同位素组成比低于亏损地幔大洋中脊玄武岩的值(MORB≈8Ra)，不能真实反映源区特征。而采自吉定的辉绿岩样品^3He/^4He比值平均高达31．57Ra，与夏威夷发现的热点地幔源区的样品比值接近；分步加热法进一步测试，其高比值的He是在低温区段释放的。这种高^3He/^4He比值He的捕获，表明雅鲁藏布江蛇绿岩形成时存在地幔柱型富集地幔岩浆作用。     

冀北地区金矿床He、Ar、Pb同位素组成及其成矿物质来源

成矿物质来源一直是成矿理论研究和找矿实践的焦点问题。选择了冀北地区3个幔枝构造金矿集中区11个金矿床黄铁矿及部分围岩进行了He、Ar同位素测定。研究表明,冀北地区主要金矿的3He/4He的值域为(0.93～7.30)×10-6,平均3.55×10-6;R/Ra=0.66～4.93,平均2.53;40Ar/36Ar=426～2073,40Ar平均为8.20×10-7cm3/g,4He/40Ar平均为2.17。矿区外围片麻岩和花岗岩的3He/4He值仅为(0.001～0.55)×10-6,反映来源上有明显差别。3He和4He在He同位素浓度图上落于地幔区附近。64个Pb同位素数据表现为矿质以幔源为主,确有部分壳源物质加入。研究认为,本区成矿物质应源于地球深部,随地幔柱多级演化,深部成矿流体由地球深部迁移到浅部,期间不可避免地存在壳幔流体的混合作用,故其值域往往界于地幔和地壳之间。     

辽宁宽甸新生代火山岩和地幔包体He-Ar同位素组成

宽甸新生代碱性玄武岩、地幔包体及辉石巨晶的稀有气体同位素组成和流体含量分析表明，不同岩性稀有气体含量的差异反映了岩浆作用过程中轻、重稀有气体的分馏特性，较轻的稀有气体(He、Ne)比较重的稀有气体(Kr、Xe)具有更高的活动性和不相容性；该地区上地幔源区具有典型的MORB型源区特征，以辉石巨晶为代表；地幔包体的3^He／^4He值较低，可能与地幔上隆过程中富集地幔流体的交代作用或地幔塑性变形作用丢失了部分原始He有关；大陆碱性玄武岩具有与大洋玄武岩截然不同的He同位素组成，反映了大陆区地幔岩浆上升过程中受到了陆壳物质混染。地幔源区^40Ar／^36Ar值为350左右，二辉橄榄岩和碱性火山岩的^40Ar／^36Ar值比大气略高，可能有大气组分的混入。部分样品中有^21Ne、^22Ne、^129Xe、^134Xe和^136Xe相对于大气的过剩现象。     

溶液结构的X射线衍射研究──4.用粉末衍射仪精确测定溶液结构的新方法

本文叙述了用θ—2θ型X射线衍射仪精确测定电解质溶液结构的新的实验技术，设计制作了具有恒温功能的超厚液体样品池，并建立了样品池窗口强度的校正方法。建立在Johansson和Yamaguchi工作基础上，发展了液体X射线衍射数据处理和结构参数精细化的计算机程序，获得了非常令人满意的实验结果。由θ－2θ型X射线衍射仪精确测定的径向分布函数与θ－θ型衍射自由表面散射比较，表明DRF分辩率有所提高。     

The Bulong Gold Deposit-a Quartz-Barite Vein Type Gold Deposit in Xinjiang:Geological Characteristics and S, He and Ar Isotopic Compositions

The Bulong gold deposit, located in the southwest Tianshan in China, occurs in the Upper Devonian finegrained clastic rocks. The gold orebodies are controlled by an gently inclined interlayer fractured zone. They are hosted only in quartz-barite veins though there are barite veins and quartz veins in the ore district. The δ34S values of pyrite in the ores range from 14.6‰ to 19.2‰ and those of barite from 35.0‰ to 39.6‰, indicating that the sulfur was derived from the strata. 3He/4He ratios of fluid inclusions in pyrite are 0.24-0.82 R/Ra, approximating to that of the crust. The 40Ar/39Ar ratios range from 338 to 471, slightly higher than that of the atmosphere. 40Ar /4He ratios of ore fluids range from 0.015 to 0.412 with a mean of 0.153. Helium and argon isotope compositions of fluid inclusions show that the ore fluids of the Bulong gold deposit were mainly derived from the crust.