新疆阿尔泰花岗岩类源区物质的定量模拟

对产出于阿尔泰、额尔齐斯、乌化古三条构造-岩浆带上的六个典型岩体进行了源区岩石化学组成和初始熔体部分熔融程度的定量模拟。模拟结果表明:六个岩体的ε_(Sr)~t值多介于0-120之间,源区岩石多为地幔物质与陆壳物质的混合源,地壳柱中成熟陆壳所占比例较少,反映了中亚型地洼区在地壳化学结构上的一个重要特征.从北往南,ε_(Sr)~t值与壳源锶所占百分率逐渐减小,反映了从地槽造山带核心部位往边缘部位往边缘部位,地壳柱中成熟陆壳所占比例逐渐减小。初始熔浆部分熔融程度温度、压力呈正消长关系。     

Crystal-Melt Separation and the Development of Isotopic Heterogeneities in Hybrid Magmas

If a magma is a hybrid of two (or more) isotopically distinctend-members, at least one of which is partially crystalline,separation of melt and crystals after hybridization will leadto the development of isotopic heterogeneities in the magmaas long as some of the pre-existing crystalline material (antecrysts)retains any of its original isotopic composition. This holdstrue whether the hybridization event is magma mixing as traditionallyconstrued, bulk assimilation, or melt assimilation. Once a magma-scaleisotopic heterogeneity is formed by crystal–melt separation,it is essentially permanent, persisting regardless of subsequentcrystallization, mixing, or equilibration events. The magnitudeof the isotopic variability resulting from crystal–meltseparation can be as large as that resulting from differentialcontamination, multiple isotopically distinct sources, or insitu isotopic evolution. In one model, a redistribution of one-thirdof the antecryst cargo yielded a crystal-enriched sample with⁸⁷Sr/⁸⁶Sr of 0·7058, whereas the complementary crystal-poorsample has ⁸⁷Sr/⁸⁶Sr of 0·7068. In other models, crystal-richsamples are enriched in radiogenic Sr. Isotopic heterogeneitiescan be either continuous (controlled by the modal distributionof crystals and melt) or discontinuous (when there is completeseparation of crystals and liquid). The first case may be exemplifiedby some isotopically zoned large-volume rhyolites, formed bythe eruptive inversion of a modally zoned magma chamber. Inthe latter case, the isotopic composition of any (for example)interstitial liquid will be distinct from the isotopic compositionof the bulk crystal fraction. The separation of such an interstitialliquid may explain the presence of isotopically distinct late-stageaplites in plutons. Crystal–melt separation provides anadditional option for the interpretation of isotopically zonedor heterogeneous magmas. This option is particularly attractivefor systems whose chemical variation is otherwise explicableby fractionation-dominated processes. Non-isotopic chemicalheterogeneities can also develop in this fashion. KEY WORDS: isotopic heterogeneity; zoning; hybrid magma; crystal separation; Sr isotopes; aplite; rhyolite     

Petrogenesis and metallogenic potential of the Jurassic porphyries in the northwest Zhejiang Province,South China: insights from SHRIMP zircon geochronology,geochemistry, and Sr–Nd–Hf isotopes of the Huangbaikeng ore-bearing porphyries

The northwest Zhejiang Province is a key domain for providing deep insight into the crust–mantle interaction and tectonic evolution of the South China block. In this paper, we collect geochemical, geochronological, and isotopic data of the Jurassic porphyries in this region, and investigated the Huangbaikeng ore-bearing porphyry in the Tongcun Mo–Cu deposit, using it as an example to uncover the porphyry petrogenesis and evaluate their metallogenic potential. Two varieties of the Huangbaikeng porphyry were distinguished: the medium- to coarse-grained type and medium- to fine-grained type. Zircon Sensitive High-Resolution Ion Microprobe U–Pb dating indicates that they were emplaced at 161.8 ± 2.8 and 162.7 ± 3.5 Ma, respectively, which are consistent with the molybdenite Re–Os ages of 163.9–161.8 Ma. The inherited zircons age spectrum significantly recorded a series of geological events, for example, assembly and breakup of the Columbia and Rodinia supercontinent, and the Triassic collision of Yangtze and North China blocks. Whole rock Sr–Nd and Jurassic zircon Hf isotopic data yield mostly negative ε_Hf(t) values (0.5 to ?8.4) and ε_Nd(t) values (?0.79 to ?4.82). Besides the Huangbaikeng porphyry, all the Jurassic porphyries in the northwest Zhejiang Province have a wide range of SiO₂ contents (76.78–60.91 wt.%). They do not contain typical aluminous minerals (e.g. cordierite and garnet), and are mainly metaluminous to weakly peraluminous with high Na₂O, low FeO^T/MgO, and Zr + Nb + Ce + Y concentrations in composition. They thus fit the I-type granite definition. Some major and trace elements show strong correlations with SiO₂, possibly indicating extensive fractional crystallization during their magma evolution. Tectonic discriminations imply that these plutons were likely formed in a volcanic arc regime possibly related to subduction of the Palaeo-Pacific plate. Sr–Nd–Hf isotopic data suggest a mixed source of the Mesoproterozoic crust and 30–50% mantle components. Compared with the adjacent Dexing Cu-bearing porphyies, which have more positive ε_Hf(t) and ε_Nd(t) values with more significant mantle components (55–70%), the Jurassic porphyries in the northwest Zhejiang Province probably lack metallogenic potential to form a giant porphyry copper deposit as Dexing.     

Pb-Pb age of sedimentary phosphorite reworking in Lower Riphean carbonate sediments,the Satka Formation of Southern Urals

The mineral composition and U-Pb and Rb-Sr systematics of phosphorites from the Satka Formation of Lower Riphean carbonates, the Burzyan Group of Southern Urals, are studied. Phosphorites occurring as small lenses between stromatolite layers are composed largely of fluorapatite with admixture of detrital quartz, feldspars, illite, and chlorite. Phosphorite samples have been subjected to stepwise dissolution in 1 N (fraction L-1) and 2 N (fraction L-2) HCl. As is established, the maximum apatite content is characteristic of fraction L-1, while fraction L-2 is enriched in products of dolomite and sulfide dissolution and in elements leached from siliciclastic components. The Sr content in the Satka apatites (280–560 ppm) is substantially lower as compared with that in unaltered marine apatite. The ⁸⁷Sr/⁸⁶Sr “initial ratio in the phosphorites studied (0.71705–0.72484) and host dolomites from the lower part of the Satka Formation is significantly higher than in the Early Riphean seawater that indicates a reset of the Rb-Sr original systems in sediments. The Pb-Pb age of 1340 ± 30 Ma (MSWD = 6.4) estimated based on 7 data points characterizing fractions L-1 and L-2 is younger than the formation time of overlying Burzyan sediments, being consistent, within the error range, with date of the Mashak rifting event recorded at the Early-Middle Riphean boundary. The comparative U-Pb characteristics of two soluble fractions (L-1 and L-2) and silicate residue of phosphorites show that epigenetic redistribution of Pb and U was characteristic of the phosphorite horizon only. The initial Pb isotope composition and μ (²³⁸U/²⁰⁴Pb) estimated according to model by Stacey and Kramers for the early diagenetic fluids in carbonate and phosphate sediments of the Satka Formation suggest that they were in isotopic equilibrium with erosion products of the Taratash crystalline complex.     

Rb‐Sr geochronology and Sr isotopic composition of Devonian granitoids,eastern Tasmania

Biotite igneous ages and well‐defined isochron ages of plutons from the composite Blue Tier Batholith and the Coles Bay area in northeastern Tasmania range from 395 to 370 Ma. The older limit of this range, for the George River granodiorite, is considerably older than any age previously recorded for NE Tasmania. The ages of the youngest plutons (Mt Paris and Anchor granites), which host cassiterite ores, record pervasive hydrothermal alteration events. The initial ⁸⁷Sr/⁸⁰Sr ratios of the granitoids range from 0.7061 to 0.7136 and suggest different protolith compositions, consistent with mineralogical and geochemical characteristics of each pluton. The S‐type garnetbiotite granites (Ansons Bay and Booby alia granites) have initial ratios greater than 0.7119, indicative of enriched, high Rb/Sr ratio, crustal source‐rocks of Proterozoic age (1700–800 Ma). The S‐type biotite granites (Poimena and Pearson granites) have relatively high initial ⁸⁷Sr/⁸⁶Sr ratios (0.7070, 0.7105) but overlap with those of the I‐type granodiorites (George River, Scamander Tier, Pyengana and Coles Bay granodiorites) which are in the range of 0.7061 to 0.7073. The initial ratios of the enriched altered plutons are poorly constrained, and on both hand‐specimen and thin‐section scales, reveal open‐system Sr isotopic patterns.

Isochron ages for the arenite‐lutite and lutite sedimentary associations of the Mathinna Beds, which are intruded by the granitoids, reflect an approach to Sr isotopic equilibrium during regional metamorphism. The metamorphic age (401 ± 7 Ma) of the early Pragian arenite‐lutite association indicates a relatively small time interval between deposition, regional metamorphism and granitoid intrusion. The isotopic age for the lutite sedimentary association (423 ± 22 Ma) is tentatively correlated with a Benambran‐age burial metamorphic event that has not previously been recorded in Tasmania.     

激光剥蚀电感耦合等离子体质谱分析石笋样品中多元素比值及45种元素含量

石笋样品的微量元素含量及Mg/Ca、Sr/Ca比值为高分辨的古气候重建提供重要指标。针对现有溶液分析技术易混合多个石笋微层、误差大的缺点,本文利用激光剥蚀电感耦合等离子体质谱技术(LA-ICP-MS)原位线扫描和点剥蚀方式对比分析了石笋生长轴方向的Mg/Ca和Sr/Ca空间分布趋势,研究表明二者均展现出显著的周期性变化特征,且周期性变化一致,其中40 μm束斑线扫描更具有稳定性强、分辨率高、快速简便的优点。通过探讨碳酸盐标准样品MASC-3与玻璃标准样品NIST 610、NIST 612、KL2G、ATHO-G的相对灵敏度系数关系和元素分馏行为,确定基体效应是造成相对灵敏度系数变化的主要原因。同时建立了以MASC-3、NIST 610和NIST 612多外标结合内标Ca归一定量分析石笋中45种元素方法,针对石笋碳酸盐样品,将主量元素Ca、Mg变形为碳酸盐形式,与其他元素加和归一,不仅改变了国内外研究中需要预先采用其他分析技术来测定内标元素含量的计算方法,而且有效地避免了C元素无法准确检测的问题,能够实现与Ca内标法校正结果的吻合。     

Oxygen isotopes in the Cretaceous-Paleogene granites of Primorye and some problems of their genesis

The Cretaceous-Paleogene granites of the Eastern Sikhote Alin volcanic belt (ESAVB) and Late Cretaceous granitoids of the Tatibin Series (Central Sikhote Alin) are subdivided into three groups according to their oxygen isotope composition: group I with δ¹⁸O from +5.5 to +6.5‰, group II with δ¹⁸O from +7.6 to +10.2‰, and group III with less than +4.5‰. Group I rocks are similar in oxygen isotope composition to that of oceanic basalts and can be derived by melting of basaltic crust. Group II (rocks of the Tatibin Series) have higher δ¹⁸O, which suggests that their parental melts were contaminated by sedimentary material. The low ¹⁸O composition of group III rocks can be explained by their derivation from ¹⁸O-depleted rocks or by subsolidus isotopic exchange with low-¹⁸O fluid or meteoric waters. The relatively low δ¹⁸O and ⁸⁷Sr/⁸⁶Sr in the granitoids of Primorye suggest their derivation from rocks with a short-lived crustal history and can result from the following: (1) melting of sedimentary rocks enriched in young volcanic material that was accumulated in the trench along the transform continental margin (granites of the Tatibin Series) and (2) melting of a mixture of abyssal sediments, ocean floor basalts, and upper mantle in the lithospheric plate that subsided beneath the continent in the subduction zone (granites of the ESAVB).     

桐庐Ⅰ型和相山S型两类碎斑熔岩对比

以浙西桐庐I型和赣东北相山S型碎斑熔岩为代表,对两类不同成因的火山-侵入杂岩进行了系统对比。桐庐I型具有相对贫SiO_2(0.78)、低的Rb/Sr(-6.0)等特征,表明源区为基性变质火成岩;相山S型含岩浆结晶的富铝矿物石榴石和红柱石,具有相对富SiO_2(2>68％)、低的Na_2O/K_2O(0.9)和I_(Sr)(t)值(>0.7100)以及低的ε_(Nd)(t)值(<-6.0)等特怔,其源区为变质沉积岩。     

栖霞金矿矿物、流体和同位素特征及意义

栖霞金矿床伴生的黑钨矿是低温热液的产物。成矿流体的成分与典型的大气降水热液组分相类似,其δ１８Ｏ约为－３．６‰～４．５‰,δＤ约为－５６‰～－９５‰,变化范围较大,但这些氢、氧同位素值很好地反映了大气降水在不同温度和Ｗ／Ｒ比值条件下与胶东群变质岩交换后的分布特征,成矿作用以Ｗ／Ｒ比值较低为特点。金矿床的Ｒｂ－Ｓｒ等时线年龄为１２５．８×１０６ａ,与胶东群变质岩系和混合花岗岩的时差较大,矿化物质的Ｓｒ同位素初始比高达０．７１６８,大气降水深循环对流作用是形成栖霞金矿床的主要原因。     

华南花岗岩物源成因特征与陆壳演化

华南不同时代的花岗岩按物质来源及成因可划分为:幔源(分异)系列:幔-壳混源(同熔)系列;壳源改造(重熔)系列和幔-壳混源碱性系列等四个不同的系列,简要阐述了划分四类系列的岩石学、地球化学的依据。侧重根据Sm-Nd、Rb-Sr同位素成分,以二元混合模型计算了花岗岩源区物质组成中,上壳和亏损地幔组份各占的比例。在此基础上探讨了不同物源成因系列花岗岩形成与华南陆壳演化的内在联系:东安、雪峰旋回褶皱系阶段花岗岩物源成因类型比较多样,有幔源(分异)系列、不成熟壳源、成熟壳源改造(重熔)系列等;加里东,海西期以陆壳改造(重熔)系列为主;印支、燕山期活化区(地洼)阶段,在地幔活化激发下,中国东部陆缘形成幔—壳混源(同熔)系列花岗岩和相应的火山岩;但沿内部断裂带,在壳下地幔热传输及构造作用下引起陆壳重熔,形成属于壳源改造(重熔)系列花岗岩。同位素的研究证明了:地洼阶段的构造-岩浆活动主要动力是来自壳下地幔的活化。