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1.
包气带作为防止地下水硝酸盐污染的天然屏障,其反硝化效果通常受到碳源的限制。针对地下水硝酸盐污染防治技术现状,本文采用Ca(OH)2处理的玉米芯作为反硝化的碳源材料,构建包气带强化反应层,用响应曲面法研究硝酸盐浓度、含水量和温度的交互作用对脱氮性能影响,并用硝态氮去除率、亚硝态氮累积、pH值变化以及溶解性有机碳(dissolved organic carbon, DOC)淋失通量综合评价脱氮性能,最后采用高通量测序揭示脱氮层中微生物变化。研究结果表明:温度、含水量以及温度和含水量交互作用对硝态氮去除率影响显著,其中温度是反硝化过程中最关键的因素;系统运行74天后,硝态氮去除率达到50%,亚硝态氮累积量(以N计)大多低于3 mg/L,pH值维持在7.0左右,DOC淋失通量(以C计)介于0.10.2 mg/(cm2·d);高通量测序发现,脱氮层中微生物的丰富度降低,而与反硝化和碳分解有关的微生物相对丰度提高,在碳源的刺激下微生物向有利于脱氮的方向演变。 相似文献
2.
全球水体氮污染形势严峻,且以硝态氮(NO3--N)污染为主,研究地下水与地表水(G-S)相互作用模式对NO3--N在“潜流带”(HZ)中迁移转化的影响是开展水体氮污染综合防控的关键.开展地表水(S)补给地下水(G)(下降流)、地下水(G)补给地表水(S)(上升流)以及交替作用3种模式的NO3--N迁移转化实验,研究表明:3种模式下,出水NO3--N浓度可降低95%以上;上升流中反硝化强度大于下降流;异化还原作用(DNRA)对下降流与上升流出水氨氮(NH4+-N)浓度的贡献分别约为71%和11%;上升流实验后水-土界面有机氮含量是下降流实验后水-土界面的2.3倍.结果表明,G-S相互作用下NO3--N的衰减途径主要包括:合成有机氮、反硝化及DNRA;相互作用模式对各衰减途径的强度存在影响;HZ介质通过吸附NH4+-N和微生物作用合成有机氮的方式截留氮素. 相似文献
3.
反硝化菌的耐砷驯化及其对水铁矿吸附态砷迁移转化的影响 总被引：2，自引：0，他引：2
采集缺氧活性污泥进行室内微生物驯化,培养耐砷反硝化菌。把耐砷反硝化菌、营养液和吸附As(V)的水铁矿在厌氧条件下培养,研究反硝化菌代谢作用下,系统中Fe、Mn、NO3-和As形态的动态变化。结果表明,缺氧活性污泥中的反硝化菌具有一定的耐砷能力。在砷含量500μg/L以内,其反硝化强度基本不受砷的影响。在吸附有砷的水铁矿体系中,反硝化菌所产生的反硝化作用可导致溶液中NO3-含量的降低、Fe含量的升高、As含量降低,且As(III)所占比例增加。这说明,体系中水铁矿的还原性溶解和As(V)的还原性解吸已经发生。As含量降低的原因是,在培养体系中水铁矿的含量高,Fe的释放量只占很小比例,表层水铁矿被还原后,在次表层形成新的水铁矿吸附位,这种新吸附位不仅可以吸附溶液中已经存在的As,而且能够再吸附由于还原性溶解和解吸所释放出的As。 相似文献
4.
芳香烃污染地下水以其污染普遍、危害巨大、去除困难及治理费用昂贵而倍受各国环境学者及水文地质学者的关注。以苯及甲苯作为标示污染物,利用室内饱水含水层土柱,通过对污染带的模拟实验发现,苯和甲苯在反硝化条件下产生生物降解,二者的去除率分别大于７７％和８８％;反硝化条件下,苯和甲苯显示出降解性差异,甲苯更易于降解;硫酸还原作用可能是苯和甲苯被去除的另一机理,但实验结果显示,ＮＯ－３高时,对硫酸还原菌的生长具有抑制作用。 相似文献
5.
6.
脱氮硫杆菌同步脱硫反硝化技术的关键因素研究 总被引：2，自引：0，他引：2
利用脱氮硫杆菌(Thiobacillus denitrificans)在厌氧条件具有的脱硫反硝化生理特性,提出同步脱硫反硝化技术的思路,推导出脱氮硫杆菌(Thiobacillus denitrificans)氧化硫化物为单质硫的化学计量式,并通过间歇试验考察同步脱硫反硝化技术的关键因素。试验结果表明,硫氮比(S~(2-)/NO_3~-比值)和硫化物浓度是同步脱硫反硝化技术的关键因素,两者分别控制在5/3和低于300mg/L的水平可以获得较好的脱硫和反硝化效果,在此条件下,单质硫转化率最高达94％,且随着硫氮比的降低而升高。 相似文献
7.
依据1970~2017年间发表的3955篇包气带反硝化强度相关论文,筛选出197组反硝化强度数据,利用整合分析,重点研究了包气带反硝化强度在典型生态类型（水平）和不同采样深度（垂向）的空间分布规律,识别了包气带反硝化强度的主控因素并研究其函数关系。结果表明:水平空间上,包气带表层0~0.5 m反硝化强度的分布特征显著,由大到小排序为:森林（8.03±0.21 mg/（kg·d））、农田（3.54±0.08 mg/（kg·d））、草地（3.38±0.12 mg/（kg·d））、湿地（2.32±0.23 mg/（kg·d））、沙漠（2.15±0.56 mg/（kg·d））。垂向空间上（6 m内）,各生态类型反硝化强度随深度的增加均呈“S”型变化规律。不同生态类型和不同采样深度下包气带反硝化强度的主控因素存在一定差异,主要为黏粒、有机质、全氮、硝态氮、有效磷,并给出了包气带反硝化强度与主控因素的回归方程。 相似文献
8.
甘南玛曲沼泽湿地土壤微生物量、理化因子与土壤酶活的关系 总被引：6，自引：1，他引：5
对甘南玛曲沼泽湿地6个样地的微生物量与土壤酶活性及其土壤理化性质之间的关系进行了研究.结果表明:纤维素酶活性在冬季达到高峰,其余5种土壤酶活性分别在春季和秋季达到高峰;硝化细菌数量与过氧化氢酶、纤维素酶、脲酶、碱性磷酸酶有较显著的负相关关系;微生物量与酶活性之间存在极显著相关关系,其中微生物量因子中的放线菌、氨化细菌、硝化细菌和土壤酶活性因子中的酸性磷酸酶、碱性磷酸酶、中性磷酸酶是引起相关性的主要因素;酸性磷酸酶活性与土壤含水率、pH值、硝态氮含量、氨态氮含量都有密切的关系,过氧化氢酶活性可以通过有机质的含量来反映,脲酶活性可以通过土壤的含水率来反映,碱性磷酸酶活性可以通过电导率来反映. 相似文献
9.
反硝化条件下河岸渗滤过程中苯胺的降解 总被引：2，自引：0，他引：2
通过河岸渗滤作用(riverbankfiltration, RBF) 诱发河水的补给, 增大地下水的允许开采量可以满足更多居民生活饮用水需求.受人类活动的影响, 河流等地表水体遭受苯胺污染, 可能通过RBF进入地下水, 以致饮用该地下水存在健康风险.为研究反硝化条件下, 苯胺在RBF中的转化, 采集渭河河床沉积物及沿岸地下水含水层的含水介质, 装置土柱, 进行土柱动态模拟实验.经过153 d的实验研究发现, 利用苯胺对RBF中土著反硝化微生物进行驯化, 大约经过37d菌种完全适应.具有该菌种的RBF系统, 对苯胺具有巨大降解能力, 在NO3——N约为23.0 mg/L的条件下, RBF系统可使40、80甚至400 mg/L浓度的苯胺100%降解, 矿化率分别达97.99%、91.39%与75.30%.反硝化条件下, 苯胺在RBF中的降解仅有少部分经过脱氨作用, 绝大部分与腐殖质以共价键形式形成耦合物, 该耦合物更易为微生物降解, 且降解过程中不产生对研究环境微生物有毒的中间产物, 可实现反硝化条件下RBF中苯胺的连续降解. 相似文献
10.
亚硝酸根作为电子受体的反硝化吸磷特性 总被引：1，自引：0，他引：1
为了考察聚磷污泥以NO2-为电子受体的反硝化吸磷特性,通过静态烧杯试验,研究了不同NO2-浓度聚磷污泥的反硝化同时吸磷能力及动力学。实验结果表明:NO2-质量浓度在31.25 mg/L以下时,反硝化聚磷菌可以利用NO2-为电子受体完成反硝化吸磷;在高于37.50 mg/L时,NO2-对缺氧吸磷有明显的抑制作用。但是反硝化聚磷菌经过驯化之后,即使NO2-质量浓度达到很高(75.00 mg/L),仍然可以利用NO2-作为电子受体完成反硝化吸磷,而没有发现抑制吸磷的现象,而且NO2-的浓度对吸磷速率没有明显影响。以NO2-为电子受体平均吸磷速率为3.16 mg P/(gMLVSS.h),平均反硝化速率为5.14mg NO2--N/(gMLVSS.h),吸磷速率小于以氧和NO3-为电子受体时的速率。 相似文献
11.
本研究分别利用顶空平衡法与qPCR技术测定了2018年春季黄、渤海5个典型站位柱状沉积物中甲烷(CH4)和氧化亚氮(N2O)浓度及产甲烷菌与硫酸盐还原菌功能基因拷贝数,并分析了其与间隙水中相关环境因子的关系。沉积物上方水文条件的差异以及其中复杂的碳氮生物地球化学过程使得CH4和N2O浓度呈现出明显的空间和垂直变化。结果显示,沉积物中CH4浓度为0.23~0.92 μmol·kg-1,N2O浓度为18.90~104.96 nmol·kg-1。总体来说,渤海沉积物中CH4和N2O平均浓度高于黄海。垂向分布上,CH4浓度均随深度增加逐渐升高, $\text{SO}_{4}^{2-}$浓度随深度增加逐渐降低,并与CH4浓度呈镜像关系,产甲烷菌与硫酸盐还原菌的丰度也遵循着同样规律,这表明沉积物中产甲烷作用受$\text{SO}_{4}^{2-}$浓度的抑制。 mcrA基因拷贝数平均值为渤海低于黄海。除3500-7站外,沉积物中mcrA基因拷贝数随深度增加而升高。各站位mcrA 基因丰度与CH4浓度均无显著相关性,且mcrA丰度与$\text{SO}_{4}^{2-}$浓度之间也未检测到显著相关性。dsrB基因拷贝数远高于mcrA基因拷贝数,且两者相差至少两个数量级。 dsrB基因拷贝数随深度逐渐增加,直至10 cm左右,随后至沉积物底部逐渐减少。各站位dsrB基因拷贝数与CH4浓度剖面略有镜像关系,但均未检测到显著负相关性。以上结果均表明沉积物中存在着同时消耗沉积物中$\text{SO}_{4}^{2-}$与CH4的其他作用。N2O浓度随深度增加先降低,在深度30 cm以下逐渐升高。间隙水中$\text{NO}_{3}^{-}$和$\text{NO}_{2}^{-}$浓度均随深度减小,同时$\text{NH}_{4}^{+}$浓度与其呈相反趋势。沉积物中N2O与$\text{NO}_{2}^{-}$及$\text{NO}_{3}^{-}$浓度均呈正相关,且前者相关性较高,说明反硝化作用是沉积物中N2O产生的主要过程。这些结果为进一步了解近岸陆架海域沉积物中CH4和N2O的来源、分布及碳氮生物地球化学循环提供了参考资料。 相似文献
12.
位于云南省祥云县刘厂镇的王家庄温泉水样YMD10-1(王家热水井)与YMD10-2(聚龙温泉宾馆热水井)的矿化度为1.49~1.65 g/L,主要阳离子为Na^+,主要阴离子为HCO3^-,水化学类型均为HCO3-Na型。YMD10-1和YMD10-2的p H值野外测定数据分别为10.8和7,因YMD10-2暴露于空气使其pCO2较高导致其p H野外观测值偏低;实验室p H测定值分别为8和7.6,主要受到pCO2差异影响导致水中碳酸组分发生变化而改变了其p H值。水样的δ^2H-δ^18O数据显示温泉的补给来源为大气降水。利用Si O2温标估算了温泉的地下热储温度为89~92℃。利用226Ra-222Rn法估算出YMD10-1的热水年龄为446.84 a,YMD10-2的热水年龄为319.56 a。估算的地下热水的循环深度为3 808~3 898 m,利用δ^2H和δ^18O估算热水补给高程为2 845~2 865 m,补给区为周边的山区。地下水获得大气降水入渗补给后,经历深循环并获得深部热流加热,沿断裂带上升穿透浅部第四系出露地表。温泉显示碱性是由于长石与水和CO2发生反应,产生大量的HCO3^-,HCO3^-在溶液中有可能水解消耗H^+产生OH^-。王家庄温泉被当地人们用来晒制土碱,与热水Na^+和碳酸的含量高有关。 相似文献
13.
The fluvial geochemistry of the Subarnarekha River and its major tributaries has been studied on a seasonal basis in order to assess the geochemical processes that explain the water composition and estimate solute fluxes. The analytical results show the mildly acidic to alkaline nature of the Subarnarekha River water and the dominance of \(\hbox {Ca}^{2+}\) and \(\hbox {Na}^{+}\) in cationic and \(\hbox {HCO}_{3}^{-}\) and \({\hbox {Cl}}^{-}\) in anionic composition. Minimum ionic concentration during the monsoon and maximum concentration in the pre-monsoon seasons reflect concentrating effects due to decrease in the river discharge and increase in the base flow contribution during the pre-monsoon and dilution effects of atmospheric precipitation in the monsoon season. The solute acquisition processes are mainly controlled by weathering of rocks, with minor contribution from marine and anthropogenic sources. Higher contribution of alkaline earth \((\hbox {Ca}^{2+}{+}\,\hbox {Mg}^{2+})\) to the total cations \((\hbox {TZ}^{+})\) and high \((\hbox {Na}^{+}+\hbox {K}^{+})/\hbox {Cl}^{-}\), \((\hbox {Na}^{+}+\hbox {K}^{+})/\hbox {TZ}^{+}\), \(\hbox {HCO}_{3}^{-}/(\hbox {SO}_{4}^{2-}+\hbox {Cl}^{-})\) and low \((\hbox {Ca}^{2+}+\hbox {Mg}^{2+})/(\hbox {Na}^{+}+\hbox {K}^{+})\) equivalent ratios suggest that the Subarnarekha River water is under the combined influence of carbonate and silicate weathering. The river water is undersaturated with respect to dolomite and calcite during the post-monsoon and monsoon seasons and oversaturated in the pre-monsoon season. The pH–log \(\hbox {H}_{4}\hbox {SiO}_{4}\) stability diagram demonstrates that the water chemistry is in equilibrium with the kaolinite. The Subarnarekha River annually delivered \(1.477\times 10^{6}\) ton of dissolved loads to the Bay of Bengal, with an estimated chemical denudation rate of \(77\hbox { ton km}^{-2}\hbox { yr}^{-1}\). Sodium adsorption ratio, residual sodium carbonate and per cent sodium values placed the studied river water in the ‘excellent to good quality’ category and it can be safely used for irrigation. 相似文献
14.
Patterns of crystallographic preferred orientation are referred to as texture. The specific subject of texture analysis is
the experimental determination and interpretation of the statistical distribution of orientations of crystals within a specimen
of polycrystalline material, which could be metals or rocks. The objective is to relate an observed pattern of preferred orientation
to its generating processes and vice versa. In geosciences, texture of minerals in rocks is used to infer constraints on their
tectono-metamorphic history. Since most physical properties of crystals, such as elastic moduli, the coefficients of thermal
expansion, or chemical resistance to etching depends on crystal symmetry and orientation, the presence of texture imparts
directional properties to the polycrystalline material.
A major issue of mathematical texture analysis is the resolution of the inverse problem to determine a reasonable orientation
density function on SO(3) from measured pole intensities on
, which relates to the inverse of the totally geodesic Radon transform. This communication introduces a wavelet approach into
mathematical texture analysis. Wavelets on the two-dimensional sphere
and on the rotational group SO(3) are discussed, and an algorithms for a wavelet decomposition on both domains following the
ideas of Ta-Hsin Li is given. The relationship of these wavelets on both domains with respect to the totally geodesic Radon
transform is investigated. In particular, it is shown that the Radon transform of these wavelets on SO(3) are again wavelets
on
. A novel algorithm for the inversion of experimental pole intensities to an orientation density function based on this relationship
is developed. 相似文献
15.
切向恢复系数是滚石碰撞回弹的重要控制参数,目前的理论公式不能完全反映其作用机制,这是滚石动力学研究的一个难点问题.为此,根据滚石不同的回弹状态,提出基于入射角度变化的切向力模型;进一步,以切向接触理论和动能定理为基础,考虑碰撞过程中切向的摩擦耗能与变形耗能,推导了切向恢复系数的理论公式;最后研究入射速度、入射角、被撞击物体的变形模量对切向恢复系数的影响.结果表明:滚动回弹的切向恢复系数主要受切向变形量的影响;滑动回弹时,入射速度对切向恢复系数的影响参数为\begin{document}$ {v}^{\frac{1}{20}} $\end{document}
16.
Summary Capillary electrophoresis (CE) or capillary ion analysis (CIATM) represents a relatively new, simple and fast analytical technique suited in particular to the analysis of aqueous fluids and leach solutions. The mechanisms responsible for separation in CE are based on the ion charge/size ratios. The application of capillary electrophoresis to a number of key vein-forming minerals is described for the first time for a Precambrian orogenic gold deposit. The Omai deposit is situated in the north-central part of the Barama-Mazaruni Supergroup, Guiana Shield, a Paleoproterozoic granitoid-greenstone belt metamorphosed during the Trans-Amazonian tectonothermal event at ca. 2.1Ga.Fluid inclusions extracted by crushing and leaching from 45 vein-forming mineral separates have been analyzed for ionic composition. The anionic species detected in the Omai fluids are
, Cl–,
,
, oxalate,
, F–, formate,
,
, acetate and propionate. Cationic species include
, K+, Na+, Ca2+, Sr2+, Mg2+, Mn2+, Ba2+, Li+, Zn2+, and Cu2+. Calcium, potassium and sodium cations have been used for temperature calculation. The presence of ionization products of organic acids is described for the first time in an orogenic hydrothermal system. However, their origin is still unclear and more data are needed to assess their role in the hydrothermal systems. Gold was transported as sulfide complexes, although the thiosulfate involvement in the remobilization and transport of gold in the upper part of the hydrothermal system at Omai is plausible.Present addresses: Cambior Management Services, Rosebel Gold Mines NV, Paramaribo, SurinameUNESCO Center for Macromolecules, Division of Polymer Science, Department of Chemistry, University of Stellenbosch, Matieland, South Africa 相似文献
17.
Alexander Proyer Gerlinde Habler Rainer Abart Richard Wirth Kurt Krenn Georg Hoinkes 《Contributions to Mineralogy and Petrology》2013,166(1):211-234
We investigated rutile needles with a clear shape preferred orientation in garnet from (ultra) high-pressure metapelites from the Kimi Complex of the Greek Rhodope by electron microprobe, electron backscatter diffraction and TEM techniques. A definite though complex crystallographic orientation relationship between the garnet host and rutile was identified in that Rt[001] is either parallel to Grt<111> or describes cones with opening angle 27.6° around Grt<111>. Each Rt[001] small circle representing a cone on the pole figure displays six maxima in the density plots. This evidence together with microchemical observations in TEM, when compared to various possible mechanisms of formation, corroborates a precipitate origin. A review of exchange vectors for Ti substitution in garnet indicates that rutile formation from garnet cannot occur in a closed system. It requires that components are exchanged between the garnet interior and the rock matrix by solid-state diffusion, a process we refer to as “open-system precipitation” (OSP). The kinetically most feasible reaction of this type will dominate the overall process. The perhaps most efficient reaction involves internal oxidation of Fe2+ to Fe3+ and transfer from the dodecahedral to the octahedral site just vacated by $ {\text{Ti}}^{ 4+ }: 6\,{\text{M}}^{ 2+ }_{ 3} {\text{TiAl}}\left[ {{\text{AlSi}}_{ 2} } \right]{\text{O}}_{ 1 2} + 6\,{\text{M}}^{ 2+ }_{ 2, 5} {\text{TiAlSi}}_{ 3} {\text{O}}_{ 1 2} = 10\,{\text{M}}^{ 2+ }_{ 3.0} {\text{Al}}_{ 1. 8} {\text{Fe}}_{0. 2} {\text{Si}}_{ 3} {\text{O}}_{ 1 2} + {\text{M}}^{2+} + 2 {\text{e}}^{-} + 1 2\,{\text{TiO}}_{ 2} . $ OSP is likely to occur at conditions where the transition of natural systems to open-system behaviour becomes apparent, as in the granulite and high-temperature eclogite facies. 相似文献
18.
The thermodynamic calculation of dehydration reacton suggests very low activity of H2O during metamorphic peak of the Archaean granulite complex in the region studied.The αH2O values for Al-rich gneiss and hypersthene biotite gneiss-granulite in the Taipingzhai region are usually between 0.10 and 0.20,and those in the Louzishan region are 0.15-0.25.The fugacity of O2 in terms of lgf O2 in whole region ranges form-8to-14.The average coefficients of (δμH2O/δHMg^Bt)and(δμO2/δXMg^Bt)in the Taipingzhai region are-0.293 and-1.60 respectively,and those in the Louzishan region are-0.364and-1.420.The activity of H2O is very low in the whole region,but its values and other data mentioned above are considerably constant from place to place within a given region,even in rocks of dirrerent lithological characters.However,they show a certain gradient between different regions.Such characteristics are compatible with the genetic mechanism known as“carbonic metamorphism” put forward by Newton et al.,i.e.,the α H2O during the peak stage is controlled by permeation of pervasive CO2 influx of the mantle source,and shows features of external buffering. 相似文献
19.
Natural springs have been reliable sources of domestic water and have allowed for the development of recreational facilities and resorts in the Central Appalachians. The structural history of this area is complex and it is unknown whether these natural springs receive significant recharge from modern precipitation or whether they discharge old water recharged over geological times scales. The main objective of this study was to use stable isotopes of water ( $\delta^{18} {\text{O}}_{{{\text{H}}_{2} {\text{O}}}}$ and $\delta^{2} {\text{H}}_{{{\text{H}}_{2} {\text{O}}}}$ ), dissolved inorganic carbon ( $\delta^{13} {\text{C}}_{\text{DIC}}$ ) and dissolved sulfate ( $\delta^{34} {\text{S}}_{{{\text{SO}}_{4} }}$ and $\delta^{18} {\text{O}}_{{{\text{SO}}_{4} }}$ ) to delineate sources of water, carbon and sulfur in several natural springs of the region. Our preliminary isotope data indicate that all springs are being recharged by modern precipitation. The oxygen isotope composition indicates that waters in thermal springs did not encounter the high temperatures required for O isotope exchange between the water and silicate/carbonate minerals, and/or the residence time of water in the aquifers was short due to high flow rates. The carbon isotopic composition of dissolved inorganic carbon and sulfur/oxygen isotopic composition of dissolved sulfate provide evidence of low-temperature water–rock interactions and various biogeochemical transformations these waters have undergone along their flow path. 相似文献
20.
Amy E. Hofmann Michael B. Baker John M. Eiler 《Contributions to Mineralogy and Petrology》2013,166(1):235-253
In order to evaluate the effect of trace and minor elements (e.g., P, Y, and the REEs) on the high-temperature solubility of Ti in zircon (zrc), we conducted 31 experiments on a series of synthetic and natural granitic compositions [enriched in TiO2 and ZrO2; Al/(Na + K) molar ~1.2] at a pressure of 10 kbar and temperatures of ~1,400 to 1,200 °C. Thirty of the experiments produced zircon-saturated glasses, of which 22 are also saturated in rutile (rt). In seven experiments, quenched glasses coexist with quartz (qtz). SiO2 contents of the quenched liquids range from 68.5 to 82.3 wt% (volatile free), and water concentrations are 0.4–7.0 wt%. TiO2 contents of the rutile-saturated quenched melts are positively correlated with run temperature. Glass ZrO2 concentrations (0.2–1.2 wt%; volatile free) also show a broad positive correlation with run temperature and, at a given T, are strongly correlated with the parameter (Na + K + 2Ca)/(Si·Al) (all in cation fractions). Mole fraction of ZrO2 in rutile $ \left( {\mathop X\nolimits_{{{\text{ZrO}}_{ 2} }}^{\text{rt}} } \right) $ in the quartz-saturated runs coupled with other 10-kbar qtz-saturated experimental data from the literature (total temperature range of ~1,400 to 675 °C) yields the following temperature-dependent expression: $ {\text{ln}}\left( {\mathop X\nolimits_{{{\text{ZrO}}_{ 2} }}^{\text{rt}} } \right) + {\text{ln}}\left( {a_{{{\text{SiO}}_{2} }} } \right) = 2.638(149) - 9969(190)/T({\text{K}}) $ , where silica activity $ a_{{{\text{SiO}}_{2} }} $ in either the coexisting silica polymorph or a silica-undersaturated melt is referenced to α-quartz at the P and T of each experiment and the best-fit coefficients and their uncertainties (values in parentheses) reflect uncertainties in T and $ \mathop X\nolimits_{{{\text{ZrO}}_{2} }}^{\text{rt}} $ . NanoSIMS measurements of Ti in zircon overgrowths in the experiments yield values of ~100 to 800 ppm; Ti concentrations in zircon are positively correlated with temperature. Coupled with values for $ a_{{{\text{SiO}}_{2} }} $ and $ a_{{{\text{TiO}}_{2} }} $ for each experiment, zircon Ti concentrations (ppm) can be related to temperature over the range of ~1,400 to 1,200 °C by the expression: $ \ln \left( {\text{Ti ppm}} \right)^{\text{zrc}} + \ln \left( {a_{{{\text{SiO}}_{2} }} } \right) - \ln \left( {a_{{{\text{TiO}}_{2} }} } \right) = 13.84\left( {71} \right) - 12590\left( {1124} \right)/T\left( {\text{K}} \right) $ . After accounting for differences in $ a_{{{\text{SiO}}_{2} }} $ and $ a_{{{\text{TiO}}_{2} }} $ , Ti contents of zircon from experiments run with bulk compositions based on the natural granite overlap with the concentrations measured on zircon from experiments using the synthetic bulk compositions. Coupled with data from the literature, this suggests that at T ≥ 1,100 °C, natural levels of minor and trace elements in “granitic” melts do not appear to influence the solubility of Ti in zircon. Whether this is true at magmatic temperatures of crustal hydrous silica-rich liquids (e.g., 800–700 °C) remains to be demonstrated. Finally, measured $ D_{\text{Ti}}^{{{\text{zrc}}/{\text{melt}}}} $ values (calculated on a weight basis) from the experiments presented here are 0.007–0.01, relatively independent of temperature, and broadly consistent with values determined from natural zircon and silica-rich glass pairs. 相似文献