西秦岭印支期高Sr/Y花岗岩类的成因及动力学背景——以同仁地区舍哈力吉岩体为例

西秦岭印支期花岗岩类分布十分广泛,形成时代集中于248~234Ma和224~211Ma两个阶段.其中,夏河岩体(248~238Ma)和温泉岩体(223~216Ma)的部分样品被厘定为埃达克岩(Sr>400×10^-6,Yb<2×10^-6),指示陆壳厚度大于50km.本文对西秦岭同仁地区舍哈力吉岩体进行了锆石U-Pb定年、岩石学、地球化学和Sr-Nd同位素研究.舍哈力吉岩体主要由石英二长岩组成,同时含有许多暗色镁铁质微粒包体(MME).寄主岩中发育少量的钾长石巨晶,并且部分巨晶具有环斑结构.舍哈力吉石英二长岩化学成分比较均一,而且也显示出类似埃达克岩的一些地球化学特点,如富SiO₂(66.07%~67.52%)和Al₂O₃(14.85%~15.95%),高Sr(560×10^-6~692×10^-6),低Y(11.4×10^-6~12.9×10^-6)和Yb(0.99×10^-6~1.09×10^-6),并具有较高的(La/Yb)_N比值(27.8~34.3)和微弱的负Eu异常(δEu=0.77~0.95).锆石U-Pb测年结果为234.1±0.5Ma,表明其形成于印支早期.岩石为偏铝质、高钾钙碱性系列且K₂O/Na₂O>1,高Mg^#(59~60)、Cr(69.1×10^-6~81.2×10^-6)和Ni(31.6×10^-6~36.1×10^-6),以富集大离子亲石元素(Rb、Ba、Th、U)而相对亏损高场强元素(Nb、Ti、P)为特征,(⁸⁷Sr/⁸⁶Sr)_i=0.7075~0.7077,ε_Nd(t)=-6.3~-6.1,亏损地幔模式年龄为1.25~1.33Ga.舍哈力吉石英二长岩起源于石榴角闪岩相古老下地壳的部分熔融,之后经历了壳幔岩浆混合作用和以斜长石为主的分离结晶作用.寄主岩的环斑结构和相对一致的地球化学特征,很可能是高温幔源熔体对壳源富钾高黏度岩浆改造所导致的晶粥快速再活化的结果.西秦岭在印支早期可能并未经历显著的地壳加厚过程.西秦岭印支早期花岗岩类形成于活动大陆边缘局部伸展环境,可能与古特提斯洋壳俯冲极性的改变有关.     

4A沸石吸附模拟核素Sr,Cs后的组分变化和结构表征

通过4A沸石吸附模拟核素Sr,Cs前后的化学成分分析、X衍射分析和红外光谱分析等手段方法,分析探讨了模拟核紊Sr,Cs在4A沸石的赋存状态,结果表明：4A沸石与模拟核素Sr,Cs之间主要以离子交换的方式发生作用,Sr^2 ,Cs^ 取代4A沸石中的可交换离子Na^ ,占据4A沸石a笼中的6元环和8元环。导致4A沸石的晶胞参数增大,晶格发生畸变。     

Archaean high-K granitoids produced by remelting of earlier Tonalite–Trondhjemite–Granodiorite (TTG) in the Sangmelima region of the Ntem complex of the Congo craton,southern Cameroon

We present a geochemical and isotopic study that, consistent with observed field relations, suggest Sangmelima late Archaean high-K granite was derived by partial melting of older Archaean TTG. The TTG formations are sodic-trondhjemitic, showing calcic and calc-alkalic trends and are metaluminous to peraluminous. High-K granites in contrast show a potassic calc-alkaline affinity that spans the calcic, calc-alkalic, alkali-calcic and alkalic compositions. The two rock groups (TTG and high-K granites) on the other hand are both ferroan and magnesian. They have a similar degree of fractionation for LREE but a different one for HREE. Nd model ages and Sr/Y ratios define Mesoarchaean and slab-mantle derived magma compositions respectively, with Nb and Ti anomalies indicating a subduction setting for the TTG. Major and trace element in addition to Sr and Nd isotopic compositions support field observations that indicate the derivation of the high-K granitic group from the partial melting of the older TTG equivalent at depth. Geochemical characteristics of the high-K granitic group are therefore inherited features from the TTG protolith and cannot be used for determining their tectonic setting. The heat budget required for TTG partial melting is ascribed to the upwelling of the mantle marked by a doleritic event of identical age as the generated high-K granite melts. The cause of this upwelling is related to linear delamination along mega-shear zones in an intracontinental setting.     

Geochronology and geochemistry of eclogites from the Mariánské Lázně Complex,Czech Republic: Implications for Variscan orogenesis

The Mariánské Lázn complex (MLC) is located in the Bohemian Massif along the north-western margin of the Teplá-Barrandian microplate and consists of metagabbro, amphibolite and eclogite, with subordinate amounts of serpentinite, felsic gneiss and calcsilicate rocks. The MLC is interpreted as a metaophiolite complex that marks the suture zone between the Saxothuringian rocks to the north-west and the Teplá-Barrandian microplate to the south-east. Sm-Nd geochronology of garnet-omphacite pairs from two eclogite samples yields ages of 377±7, and 367±4 Ma. Samples of eclogite and amphibolite do not define a whole rock Sm-Nd isochron, even though there is a large range in Sm/Nd ratio, implying that the suite of samples may not be cogenetic. Eclogites do not have correlated _Nd values and initial ⁸⁷Sr/⁸⁶Sr ratios. Five of the eight eclogite samples have high _Nd values (+10.2 to +7.1) consistent with derivation from a MORB-like source, but variable ⁸⁷Sr/⁸⁶Sr ratios (0.7033 to 0.7059) which probably reflect hydrothermal seawater alteration. Three other eclogite samples have lower _Nd values (+ 5.4 to –0.8) and widely variable ⁸⁷Sr/⁸⁶Sr ratios (0.7033 to 0.7096). Such low _Nd values are inconsistent with derivation from a MORB, source and may reflect a subduction or oceanic island basalt component in their source. The MLC is an important petrotectonic element in the Bohemian Massif, providing evidence for Cambro-Ordovician formation of oceanic crust and interaction with seawater, Late Devonian (Frasnian-Famennian) high- and medium-pressure metamorphism related to closure of a Saxothuringian ocean basin, Early Carboniferous (Viséan) thrusting of the Teplá terrane over Saxothuringian rocks and Late Viséan extension.     

乳山金矿煌斑岩及流体和氢、氧、锶同位素研究

乳山金矿床是胶东近年来探明的一个赋存在花岗岩中的石英脉型金矿床。矿出露的煌斑岩金含量较低，不可能是金矿化的重要物源者。     

Geochronology,geochemistry, and mineralization of the granodiorite porphyry hosting the Matou Cu–Mo (±W) deposit,Lower Yangtze River metallogenic belt,eastern China

Porphyry and skarn Cu–Fe–Au–Mo deposits are widespread in the Middle and Lower Yangtze River metallogenic belt (MLYMB), eastern China. The Matou deposit has long been regarded as a typical Cu–Mo porphyry deposit within Lower Yangtze part of the belt. Recently, we identified scheelite and wolframite in quartz veins in the Matou deposit, which is uncommon in other porphyry and skarn deposits in the MLYMB. We carried out detailed zircon U–Pb dating and geochemical and Sr–Nd–Hf isotopic studies of the granodiorite porphyry at Matou to define any differences from other ore-related granitoids. The porphyry shows a SiO₂ content ranging from 61.85 wt.% to 65.74 wt.%, K₂O from 1.99 wt.% to 3.74 wt.%, and MgO from 1.74 wt.% to 2.19 wt.% (Mg^# value ranging from 45 to 55). It is enriched in light rare earth elements and large ion lithophile elements, but relatively depleted in Nb, Ta, Y, Yb and compatible trace elements (such as Cr, Ni, and V), with slight negative Eu anomalies (Eu/Eu^* = 0.88–0.98) and almost no negative Sr anomalies. Results of electron microprobe analysis of rock-forming silicate minerals indicate that the Matou porphyry has been altered by an oxidized fluid that is rich in Mg, Cl, and K. The samples show relatively low ε_Nd(t) values from −7.4 to −7.1, slightly high initial ⁸⁷Sr/⁸⁶Sr values from 0.708223 to 0.709088, and low ε_Hf(t) values of zircon from −9.0 to −6.5, when compared with the other Cu–Mo porphyry deposits in the MLYMB. Zircon U–Pb dating suggests the Matou granodiorite porphyry was emplaced at 139.5 ± 1.5 Ma (MSWD = 1.8, n = 15), which is within the age range of the other porphyries in the MLYMB. Although geochemical characteristics of the Matou and other porphyries in the MLYMB are similar and all adakitic, the detrital zircons in the samples from Matou suggest that Archean lower crust (2543 ± 29 Ma, MSWD = 0.25, n = 5) was involved with the generation of Matou magma, which is different from the other porphyries in the belt. Our study suggests that the Matou granodiorite porphyry originated from partial melting of thickened lower crust that was delaminated into the mantle, similar to the other porphyries in the MLYMB, but it has a higher proportion of lower crustal material, including Archean rocks, which contributed to the formation of the porphyry and related W-rich magmatic-hydrothermal system.     

再论印度—亚洲大陆碰撞的启动时间

利用沉积响应来识别印度－亚洲大陆碰撞启动时间是最直接和有效的方法之一。西藏仲巴错江顶群被甄别为碰撞型三角洲沉积，曲下组可能代表了碰撞启动时期的建造，藏南定日的海相白垩－古近系沉积演化，锶和碳同位素变化也支持两大陆碰撞启动时间大约在K／T界线时期，对比喜马拉雅西段碰撞启动时间并考虑大印度北缘失掉的宽度，提出两大陆量可能的碰撞启动时间是65Ma左右。     

花岗岩的成岩时代、地球化学特征和成因青海祁漫塔格地区虎头崖矿床Ⅵ矿带

利用 LA ICP MS 锆石 U Pb 法,测得与成矿有关的青海祁漫塔格地区虎头崖矿床Ⅵ矿带花岗岩的成岩年龄为(233.6±1.8)Ma(MSWD=1.2,n=17)。地球化学特征显示：花岗岩属高钾钙碱性、弱过铝质花岗岩;样品的稀土元素组成以总体右倾,轻、重稀土分异明显和具明显的负铕异常为特征;微量元素具有富集 Rb、Th、U、La、Nd 等大离子亲石元素,亏损 Ba、Sr、Nb、P、Ti 等元素的特点。Sr Nd 同位素组成特征显示,花岗岩的源区可能是富集岩石圈地幔。初步研究认为,虎头崖矿床Ⅵ矿带花岗岩可能形成于中、晚三叠世碰撞后碰撞的构造背景下。     

双误差回归模型在ICP-MS测定饮用水中锶的不确定度评定的简化应用

在计算电感耦合等离子体质谱法测定饮用水中锶的浓度(x)时,由于标准系列配制和仪器检测过程中信号(y)漂移产生的不确定度会传递给最终的计算结果。普通的一次或多次线性拟合结果不能真实地反映对于x、y值都含误差的数据拟合情况。文章对标准曲线进行了双误差回归计算,从双误差回归线性方程推导出校准曲线拟合过程产生不确定度的计算公式,建立了方法检出限与曲线拟合参数(x、y、曲线截距和斜率)及其相关不确定度之间的关系式,依据误差连续传递公式及不确定度分量计算公式简化了合成不确定度的表达式。从合成不确定度计算公式中可得出,水样中锶含量的浓度越低,其对应的不确定度越大;标准系列配制过程不细致、仪器灵敏度低,方法检出限越差,与实际测试情况符合。     

苏北盆地建湖隆起碳酸盐岩储层中的硫酸盐型热矿水成因

碳酸盐岩储层中的硫酸盐型热矿水是宝贵的旅游疗养资源。我国苏北盆地北部分布有丰富的热矿水,其中,盱眙县的一口热水井的单井流量达到3 616t·d-1,矿化度(TDS)达到4g·L-1,温度为53.5℃,为优质硫酸盐型热矿水。采用水化学和同位素方法,结合钻孔地质资料,研究了其形成机理。该地区热矿水的SO2-4离子含量较高,部分热矿水的阴离子中SO2-4离子占主导,成为硫酸盐型水。热水的氢氧稳定同位素(δ2 H、δ18 O)值证明了其来源于大气降水。建湖隆起存在石膏层,主要分布在白垩系浦口组,该组属盐湖相沉积,发育大范围的含膏质泥岩,其中石膏、硬石膏含量较多。根据水样的Sr/Ca摩尔比,该区热水中的硫酸盐来源于石膏的溶解。基于碳酸盐岩热水的pH值和SI值、14 C含量等数据的分析,排除了硫酸盐型热矿水的形成与金属矿的风化或氧化的关系,认为是石膏或硬石膏溶解形成。