地壳硅质岩浆演化的动力学机制SCIEI北大核心CSCD

硅质岩浆的成因及演化机制研究是认识大陆地壳成分结构演化机制的关键途径。地壳硅质岩浆储库的基本性质及其演化的动力学过程是制约硅质岩浆演化及其多样性的根本原因,也是受到广泛关注的前沿和热点问题。本文总结了硅质岩浆储库的基本性质及其演化机制研究的相关进展,重点探讨了岩浆体系演化的动力学机制,即其物质成分及温度压力条件的动态演化过程,亦即岩浆储库在补给驱动下的存留、活化、分异、喷发过程。经由累积生长的方式形于地壳浅部的硅质岩浆储库以晶粥为主要赋存形式,具有较低的温度压力范围和高硅高结晶度高粘度的特征。岩浆储库的基本性质导致其自身不具有持续演化的能力,只有在基性岩浆补给的驱动下才能长时间存留分异或快速活化喷发。基性岩浆的补给及其携带的热及流体/挥发份深刻地改变了岩浆储库的物质成分及物理条件,是导致硅质岩浆分异演化或喷发的根本原因。本文还结合研究进展探讨了东南沿海地区中生代火山-侵入岩的成因演化机制及相关问题。     

The effect of cadmium on fulvic acid adsorption to Bacillus subtilis

The effects of Cd on the adsorption of an aquatic fulvic acid (FA) to the surface of Bacillus subtilis were investigated from pH 2.5 to 7.0, at fixed ionic strength (0.1 M NaClO₄) and at ambient temperature (22 °C). Cd (14 mg/l) had no effect on FA adsorption at pH<5 but increased FA adsorption at pH>6. The effects of Cd (0, 14 mg/l) on FA adsorption to B. subtilis were further examined as a function of initial FA concentration (0–45 mg C/l) at pH 6.5. FA adsorption isotherms also were measured at pH 6.5 as a function of dissolved Cd concentration (0–14 mg/l) at three initial FA concentrations (4, 8, 22 mg C/l). At all FA concentrations studied at pH 6.5, FA adsorption increased with increasing initial total Cd concentration.

Under all studied conditions, preferential adsorption of high- to intermediate-molecular-weight FA components to B. subtilis resulted in a fractionation of the FA pool, with lower-molecular-weight components remaining in solution. At pH>6, Cd further enhanced the adsorption of high- to intermediate-molecular-weight FA components but did not significantly enhance the adsorption of lower-molecular-weight components. Hence, the overall process of adsorptive fractionation was not altered significantly by the presence of Cd.

Overall, the results of this study (1) demonstrate that FA adsorption to bacterial surfaces can be altered by the presence of a metal cation, and (2) provide further evidence that microbe–metal–ligand interactions may significantly affect the mobility and fate of natural organic matter in the subsurface.     

B同位素分馏系数α4—3的研究进展

B同位素分馏系数α4-3,是海洋生物碳酸盐B同位素恢复古海水pH理论公式中的关键因素之一,近年来,此领域的研究取得了许多重要的成果,但由于所涉及的理论尚不完善,随着研究的不断深入,提出的问题也逐渐增多。对近年来国内外理论和实验的研究成果进行了综述,并对其今后的研究前景进行了展望。     

Trace element associations with Fe- and Mn-oxides in soil nodules: Comparison of selective dissolution with electron probe microanalysis

Selective dissolution methods have been largely used to get insight on trace element association with solid phases. Modern instrumental techniques offer many tools to test the validity of selective dissolution methods and should be systematically used to this end. The association of trace elements with Fe- and Mn-oxides in soil nodules has been studied here by electron probe microanalysis. The results were compared with findings from an earlier study on selective dissolution of the same nodules by hydroxylamine hydrochloride, acidified hydrogen peroxide, and Na-citrate-bicarbonate-dithionite. Electron probe microanalysis results were consistent with previous findings using selective dissolution and showed that P, As and Cr were mainly present in Fe-oxides, while Co was mainly associated with Mn-oxide phases. These results support the applicability of the studied selective dissolution methods for fractionation of trace elements in soils and sediments containing appreciable amounts of Fe and Mn-oxide phases.     

Using lumped conceptual rainfall-runoff models to simulate daily isotope variability with fractionation in a nested mesoscale catchment

This paper presents 19 months of stable isotope (δ²H and δ¹⁸O) data to enhance understanding of water and solute transport at two spatial scales (2.3 km² and 122 km²) in the agricultural Lunan catchment, Scotland. Daily precipitation and stream isotope data, weekly lake and spring isotope data and monthly groundwater isotope data revealed important insights into flow pathways and mixing of water at both scales. In particular, a deeper groundwater flow path significantly contributes to total streamflow (25-50%). Upstream lake isotope dynamics, susceptible to evaporative fractionation, also appeared to have an important influence on the downstream isotope composition. This unique tracer data set facilitated the conceptualization of a lumped catchment-scale flow-tracer model. The incorporation of hydrological, mixing and fractionation processes based on these data improved simulations of the stream δ²H isotope response at the catchment outlet from 0.37 to 0.56 for the Nash-Sutcliffe statistic. The stable isotope data successfully aided model conceptualization and calibration in the quest for a simple water and solute transport model with improved representation of process dynamics.     

Geochemistry of granitic aplite-pegmatite dykes and sills and their minerals from the Gravanho-Gouveia area in Central Portugal

Two distinct series of Variscan granitic rocks have been distinguished in the Gravanho-Gouveia area of Portugal, based on field work, variation diagrams for major and trace elements, rare earth patterns and δ¹⁸O versus total FeO diagram of rocks, anorthite content of plagioclase, BaO and P₂O₅ contents of feldspars and Al^VI versus Fe²⁺ diagram for magmatic muscovite. One series consists of a late-orogenic porphyritic biotite > muscovite granite (G1), less evolved beryl-columbite pegmatites and more evolved beryl-columbite pegmatites showing gradational contacts. The other series consists of post-orogenic porphyritic muscovite > biotite granodiorite to granite (G2), slightly porphyritic muscovite > biotite granite (G3) and lepidolite pegmatites. In each series, pegmatites are derived from the parent granite magma by fractional crystallization of quartz, plagioclase, K-feldspar, biotite and ilmenite. Some metasomatic effects occur like muscovite replacing feldspars, chlorite in pegmatites of the first series and a late muscovite in pegmatites of the second series, probably due to hydrothermal fluids. The lepidolite pegmatites contain cassiterite and two generations of rutile. The first magmatic generation consists of homogeneous crystals and the second generation occurs as heterogeneous zoned crystals derived from hydrothermal fluids. The beryl-columbite pegmatites and lepidolite pegmatites also contain the first magmatic generation and the late hydrothermal generation of zoned columbite-group minerals. More evolved beryl-columbite pegmatites were converted into episyenite by intense hydrothermal alteration and regional circulation of fluids in the granitic rocks.     

Cell bioassays for detection of aryl hydrocarbon (AhR) and estrogen receptor (ER) mediated activity in environmental samples

In vitro cell bioassays are useful techniques for the determination of receptor-mediated activities in environmental samples containing complex mixtures of contaminants. The cell bioassays determine contamination by pollutants that act through specific modes of action. This article presents strategies for the evaluation of aryl hydrocarbon receptor (hereafter referred as dioxin-like) or estrogen receptor mediated activities of potential endocrine disrupting compounds in complex environmental mixtures. Extracts from various types of environmental or food matrices can be tested by this technique to evaluate their 2,3,7,8-tetrachlorodibenzo-p-dioxin equivalents or estrogenic equivalents and to identify contaminated samples that need further investigation using resource-intensive instrumental analyses. Fractionation of sample extracts exhibiting significant activities, and subsequent reanalysis with the bioassays can identify important classes of contaminants that are responsible for the observed activity. Effect-directed chemical analysis is performed only for the active fractions to determine the responsible compounds. Potency-balance estimates of all major compounds contributing to the observed effects can be calculated to determine if all of the activity has been identified, and to assess the potential for interactions such as synergism or antagonism among contaminants present in the complex mixtures. The bioassay approach is an efficient (fast and cost effective) screening system to identify the samples of interest and to provide basic information for further analysis and risk evaluation.     

稀土元素在热液中的迁移与沉淀

近年来,高新技术产业的不断发展使得全球稀土资源需求不断上涨,此外稀土元素作为研究地球起源与演化等有关地球科学问题的重要工具也深受地球科学界的重视。而热水溶液体系中稀土元素迁移、富集、沉淀及分馏机制等相关理论知识的不断完善对于理解稀土成矿作用、稀土地球化学特征以及微量元素示踪等方面均具有重要意义。本文总结了近年来有关稀土元素在热液体系中迁移、沉淀以及轻、重稀土分馏的最新研究进展,对不同稀土络合物的稳定性、溶解度以及搬运稀土元素的能干性进行了阐述,最后展望了"稀土元素在热液中迁移与沉淀"研究中仍需完善及拓展的方向。     

花岗岩主要造岩矿物间硼同位素分馏的初步研究

本文报道了南岭地区两个花岗岩(大东山和千里山)的全岩以及主要造岩矿物(黑云母、斜长石和石英)的硼含量和硼同位素组成。结果显示,黑云母含有最高的硼含量,斜长石次之,石英中的硼含量则非常低。花岗岩中的硼可能主要以晶格替换方式赋存在黑云母和斜长石中,而石英中的微量硼则来自其包裹的流体包裹体。同时,黑云母具有最低的硼同位素组成,斜长石次之,而石英则具有最高的硼同位素组成。本次研究首次发现花岗岩中的主要造岩矿物间存在着较大的硼同位素分馏:大东山花岗岩中黑云母与斜长石之间存在着-9.3‰的分馏,黑云母与石英之间存在-9.9‰的分馏;千里山花岗岩中黑云母与斜长石之间存在着-6.6‰的分馏,黑云母与石英之间存在着-10.2‰的硼同位素分馏。结合镜下观察和氧同位素研究发现,造成不同矿物间这一大的硼同位素分馏的原因很可能是岩浆后期的热液蚀变作用。综合以往所发表的研究数据,得到含四次配位硼为主的硅酸盐矿物与中酸性热液流体之间的硼同位素分馏方程:1000lnα硅酸盐-流体=-11.19×(103/T[K])+5.09,该分馏是由于硼的四次配位和三次配位之间的转换引起的。