罗布泊红柳沙包落叶阳离子含量及环境指示意义   总被引：1，自引：0，他引：1       下载免费PDF全文

沈睿媛  李秀丽  夏训诚  赵元杰 《干旱区地理》2012,35(1):109-115

 红柳沙包沉积纹层是恢复古环境序列的一种新方法。通过对罗布泊地区红柳沙包沉积纹层中红柳落叶阳离子含量以及与环境变化关系研究表明：K+、Na+、Ca2+、Mg2+等4种阳离子平均含量分别为3.70 mg/g、40.33 mg/g、13.67 mg/g和8.08 mg/g,变化幅度排序为Ca2+ > K+ > Mg2+ > Na+。4种阳离子含量年际变化都较为明显,且变化规律较为一致,4种阳离子含量变化间的相关系数为0.653 0 ~ 0.813 8,表现为良好的正相关关系;各种阳离子与4种阳离子总量变化的相关系数为0.814 4 ~ 0.959 9,其中Na+含量与4种阳离子总量变化的相关系数最高,表明可以用Na+含量的变化或阳离子总量的变化分析变化趋势。阳离子含量与气温变化呈良好的正相关、与年降水量和湖水面积变化呈负相关;地下水水位降低、水质变差时,土壤水质也变差,阳离子含量增加;反之,地下水水位升高、水质变好时,土壤水质变好,阳离子含量降低。红柳落叶有机质阳离子含量的变化进一步验证了利用红柳沙包沉积纹层计年的可靠性和对罗布泊环境变化的可行性。  相似文献   

板桥稀土矿遥感找矿信息提取与矿产预测研究   总被引：1，自引：0，他引：1  

章钦瑜  张登荣  黄国成  朱骏 《国土资源遥感》2012,(1):120-126

通过对离子吸附型稀土矿成矿规律的分析,从浙江省板桥地区的遥感地质特征研究入手,在研究区地表范围内进行稀土遥感找矿信息的提取。首先利用SPOT图像和DEM数据构建的坡度数据对与稀土成矿相关的地貌单元进行解译;然后通过光谱特征分析和基于ASTER图像的矿物遥感异常提取,获取与成矿相关的高岭土、绢云母、绿泥石等风化特征矿物的分布信息;最后叠合分析地貌、坡度及异常提取结果,进行稀土遥感找矿预测。与地质调查资料及化探数据的对比分析证实,上述方法对圈定1∶5万的大比例尺离子吸附型稀土矿分布范围是有效的,可为更详细的稀土矿产资源潜力评价提供依据。  相似文献   

Nuclear modification factor for quarkonium production in high energy proton-nucleus collisions within the parton saturation approach     

Érison S. Rocha  Magno V. T. Machado 《Astronomische Nachrichten》2024,345(2-3):e230165

In this work, we analyze nuclear effects in the inclusive production of quarkonium in proton-nucleus collisions at high energy regime. A theoretical framework that includes initial state effects like nuclear shadowing and gluon density saturation is considered. Numerical results for nuclear modification factor, $R_{pA}(y)$, as a function of meson rapidity in proton-nucleus collisions are presented. The parameter-free predictions are compared to the available data from the Large Hadron Collider. Discussion on the main theoretical uncertainties is made, with emphasis on the phenomenological models for the nuclear saturation scale.  相似文献   

基于示踪试验的王寨盆地水文地质条件研究     

刘治政  朱恒华  杨丽芝  彭俊峰  邢立亭  王孝勤  边农方 《地质学报》2019,93(S1):71-78

王寨盆地是大武富水地段的一个特殊补给区,地质条件较为复杂,水文地质条件的研究相对较少,利用示踪试验对该区进行水文地质条件研究,是一种简单有效的方法。本次示踪试验采用钼酸铵作为示踪剂,历时75天,钼离子浓度历时曲线分为单峰型、双峰型和多峰型,地下水视流速平均值为23373m/d。通过试验揭示了王寨盆地岩溶发育特征为溶孔、溶隙、裂隙、管道、溶洞并存,地下水径流通道有单一管道型、单管道有水池型、多管道型和多管有水池型,具有多向性和复杂性;主要的地下水径流通道有3个,均汇入淄河断裂带;地下水流向以西南、东南、正东(东北)为主,整体流动较为缓慢,溶质的运移以正东(东北)方向最快;王寨断层和边河断层具有良好的导水性。因试验在枯水期进行,降雨量较小,地下水开采的日周期性影响也相对稳定,故试验时段地下水流场较稳定,试验结果所揭示的水文地质问题也较准确。  相似文献   

Heating duration of igneous rim formation on a chondrule in the Northwest Africa 3118 CV3oxA carbonaceous chondrite inferred from micro-scale migration of the oxygen isotopes     

《Chemie der Erde / Geochemistry》2019,79(4):125524

Due to their common occurrence in various types of chondrites, igneous rims formed on pre-existing chondrules throughout chondrule-forming regions of the solar nebula. Although the peak temperatures are thought to reach similar values to those achieved during chondrule formation events, the heating duration in chondrule rim formation has not been well defined. We determined the two-dimensional chemical and oxygen isotopic distributions in an igneous rim of a chondrule within the Northwest Africa 3118 CV3_oxA chondrite with sub-micrometer resolution using secondary ion mass spectrometry and scanning electron microscopy. The igneous rim experienced aqueous alteration on the CV parent body. The aqueous alteration resulted in precipitation of the secondary FeO-rich olivine (Fa_40–49) and slightly disturbed the Fe-Mg distribution in the MgO-rich olivine phenocrysts (Fa_11–22) at about a 1 μm scale. However, no oxygen isotopic disturbances were observed at a scale greater than 100 nm. The MgO-rich olivine, a primary phase of igneous rim formation, has δ¹⁷O = −6 ± 3‰ and δ¹⁸O = −1 ± 4‰, and some grains contain extreme ¹⁶O-rich areas (δ¹⁷O, δ¹⁸O = ∼−30‰) nearly 10 μm across. We detected oxygen isotopic migration of approximately 1 μm at the boundaries of the extreme ¹⁶O-rich areas. Using oxygen self-diffusivity in olivine, the heating time of the igneous rim formation could have continued from several hours to several days at near liquidus temperatures (∼2000 K) in the solar nebula suggesting that the rim formed by a similar flash heating event that formed the chondrules.  相似文献   

硫酸型酸雨参与碳酸盐岩溶蚀的研究进展     

黄奇波  覃小群  程瑞瑞  李腾芳  刘朋雨 《中国岩溶》2019,38(2):149-156

碳酸盐岩的H2CO3溶蚀产生岩溶碳汇,占整个岩石风化碳汇的 94%。西南岩溶区硫酸型酸雨严重,硫酸型酸雨广泛参与碳酸盐岩的溶蚀。H2SO4参与的碳酸盐岩风化是一个大气CO2净释放过程,具有减汇作用巨大。另一方面,岩溶区石灰土壤和地下水具有较高的pH值及盐基饱和度,对H+有巨大的缓冲作用,大气酸沉降在碳酸盐岩地区可能并不会造成地下水的HCO3-和pH降低;相反,较高浓度的SO42-所产生的盐效应和SO2-4与各种阳离子形成的离子对会增大方解石、白云石溶解度,可增强H2CO3对碳酸盐的溶蚀,这可能会使岩溶作用产生更大的碳汇效应。因此,硫酸型酸雨参与碳酸盐岩风化的减汇效应不仅可能被高估,硫酸型酸雨还可能增强碳酸盐岩的H2CO3溶蚀,具有增加岩溶碳汇效应的作用。应结合石灰土壤对大气酸沉降的缓冲容量和阈值及大气酸沉降的H+与土壤中盐基离子的交换量,并综合考虑盐效应、离子对作用、同离子效应,客观评价硫酸型酸雨流经石灰土壤层后对碳酸盐岩溶蚀吸收大气/土壤CO2的影响   相似文献   

‘Box‐Profile’ Ion Implants as Geochemical Reference Materials for Electron Probe Microanalysis and Secondary Ion Mass Spectrometry     

Haosheng Wu  Roman Bttger  Frdric Couffignal  Jens Gutzmer  Joachim Krause  Frans Munnik  Axel D. Renno  Ren Hübner  Michael Wiedenbeck  Ren Ziegenrücker 《Geostandards and Geoanalytical Research》2019,43(4):531-541

Although electron probe microanalysis and secondary ion mass spectrometry are widely used analytical techniques for geochemical and mineralogical applications, metrologically rigorous quantification remains a major challenge for these methods. Secondary ion mass spectrometry (SIMS) in particular is a matrix‐sensitive method, and the use of matrix‐matched reference materials (RMs) is essential to avoid significant analytical bias. A major problem is that the number of available RMs for SIMS is extremely small compared with the needs of analysts. One approach for the production of matrix‐specific RMs is the use of high‐energy ion implantation that introduces a known amount of a selected isotope into a material. We chose the more elaborate way of implanting a so‐called ‘box‐profile’ to generate a quasi‐homogeneous concentration of the implanted isotope in three dimensions, which allows RMs not only to be used for ion beam analysis but also makes them suitable for EPMA. For proof of concept, we used the thoroughly studied mineralogically and chemically ‘simple’ SiO₂ system. We implanted either ⁴⁷Ti or ⁴⁸Ti into synthetic, ultra‐high‐purity silica glass. Several ‘box‐profiles’ with mass fractions between 10 and 1000 μg g^?1 Ti and maximum depths of homogeneous Ti distribution between 200 nm and 3 μm were produced at the Institute of Ion Beam Physics and Materials Research of Helmholtz‐Zentrum Dresden‐Rossendorf. Multiple implantation steps using varying ion energies and ion doses were simulated with Stopping and Range of Ions in Matter (SRIM) software, optimising for the target concentrations, implantation depths and technical limits of the implanter. We characterised several implant test samples having different concentrations and maximum implantation depths by means of SIMS and other analytical techniques. The results show that the implant samples are suitable for use as reference materials for SIMS measurements. The multi‐energy ion implantation technique also appears to be a promising procedure for the production of EPMA‐suitable reference materials.  相似文献   

离子色谱法测定海水中氯离子和硫酸根离子     

王丕波  曾艳敏  闫晶  殷丽娜  任登龙 《海洋科学》2020,44(11):52-56

氯离子和硫酸根离子是海水中重要的无机阴离子，在研究海洋生态变化、海洋循环作用过程与海洋全球气候变化等领域具有重要的指示意义。其测定方法较多，但缺少相应的测试方法。本文对测定海水中Cl^-，SO₄^2-的离子色谱方法进行了优化，选用IonPacAS14碳酸盐选择性离子色谱柱，以3.5 mmol/L Na₂CO₃+1 mmol/L NaHCO₃为流动相，可消除海水样品中碳酸盐及其他阴离子的干扰。该方法对Cl^-检出限为0.29 mg/L，线性相关系数r²=0.999 2，对SO₄^2-检出限为0.42 mg/L，线性相关系数r²=0.997 9。样品的加标回收率在95%~102%，Cl^-和SO₄^2-的相对标准偏差分别为1.92%和4.18%。该方法简便、迅速、灵敏、准确度高，可满足批量海水样品中Cl^-与SO₄^2-的准确测试。  相似文献   

Li₂SO₄溶液中离子间的缔合相互作用:基于密度泛函理论和分子动力学模拟的研究   总被引：1，自引：1，他引：0  

胡俊  夏斐斐  杨凤丽  郑纯智  房春晖  曾德文  易海波 《盐湖研究》2018,26(1):39-47

基于密度泛函理论,使用B3LYP/aVDZ方法对[Li_2SO_4(H_2O)_n]~0(n=0~10、18)水合团簇的结构和性质进行了系统地研究,并结合Car-Parrinello分子动力学(CPMD)模拟了不同浓度的Li_2SO_4溶液结构,目的在于理解在Li_2SO_4溶液中离子间缔合相互作用及可能存在的物种。研究发现,对于[Li_2SO_4(H_2O)_n]~0(n=0~10、18)水合团簇,双配位单齿螯合接触离子对结构比双配位双齿螯合接触离子对结构更稳定,溶剂共享离子对结构最不稳定。同时,CPMD模拟结果表明,在3.09和3.17 mol/kg的Li_2SO_4溶液中,双配位单齿螯合接触离子对结构仍然是主要物种。以上结果表明在饱和的Li_2SO_4溶液(3.16 mol/kg)中,Li~+和SO_4~(2-)离子间的相互缔合作用主要以双配位单齿螯合接触离子对结构的物种存在,而具有双配位双齿螯合离子对结构的物种占少数,溶剂共享离子对结构几乎不存在。  相似文献   

Dehydration experiments on natural omphacites: qualitative and quantitative characterization by various spectroscopic methods   总被引：1，自引：0，他引：1  

M. Koch-Müller  I. Abs-Wurmbach  D. Rhede  V. Kahlenberg  S. Matsyuk 《Physics and Chemistry of Minerals》2007,34(9):663-678

A series of natural omphacites from a wide range of P, T occurrences were investigated by electron microprobe (EMP), infrared (IR)-, Mössbauer (MS)- and optical spectroscopy in the UV/VIS spectral range (UV/VIS), secondary ion mass spectrometry (SIMS) and single crystal structure refinement by X-ray diffraction (XRD) to study the influence of hydrogen loss on valence state and site occupancies of iron. In accordance with literature data we found Fe²⁺ at M1 as well as at M2, and in a first approach assigned Fe³⁺ to M1, as indicated by MS and XRD results. Hydrogen content of three of our omphacite samples were measured by SIMS. In combination with IR spectroscopy we determined an absorption coefficient: ε _i,tot = 65,000 ± 3,000 lmol_H2O ^?1 cm^?2. Using this new ε _i,tot value, we obtained water concentrations ranging from 60 to 700 ppm H₂O (by weight). Hydrogen loss was simulated by stepwise heating the most water rich samples in air up to 800°C. After heat treatment the samples were analyzed again by IR, MS, UV/VIS, and XRD. Depending on the type of the OH defect, the grade of dehydration with increasing temperature is significantly different. In samples relatively poor in Fe³⁺ (<0.1 Fe³⁺ pfu), hydrogen associated with vacancies at M2 (OH bands around 3,450 cm^?1) starts to leave the structure at about 550°C and is completely gone at 780°C. Hydrogen associated with Al³⁺ at the tetrahedral site (OH bands around 3,525 cm^?1, Koch-Müller et al., Am Mineral, 89:921–931, 2004) remains completely unaffected by heat treatment up to 700°C. But all hydrogen vanished at about 775°C. However, this is different for a more Fe³⁺-rich sample (0.2 Fe³⁺ pfu). Its IR spectrum is characterized by a very intense OH band at 3,515 cm^?1 plus shoulder at 3,450 cm^?1. We assign this intense high-energy band to vibrations of an OH dipole associated with Fe³⁺ at M1 and a vacancy either at M1 or M2. OH release during heating is positively correlated with decrease in Fe²⁺ and combined with increase in Fe³⁺. That dehydration is correlated with oxidation of Fe²⁺ is indirectly confirmed by annealing of one sample in a gas mixing furnace at 700°C under reducing conditions keeping almost constant OH^? content and giving no indication of Fe²⁺-oxidation. Obtained data indicate that in samples with a relatively high concentration of Fe²⁺ at M2 and low-water concentrations, i.e., at a ratio of Fe^{2+ M2}/H > 10 dehydration occurs by iron oxidation of Fe²⁺ exclusively at the M2 site following the reaction: \( {\left[ {{\text{Fe}}^{{{\text{2 + [ M2]}}}}{\text{OH}}^{ - } } \right]} = {\left[ {{\text{Fe}}^{{{\text{3 + [ M2]}}}} {\text{O}}^{{{\text{2}} - }} } \right]} + {\text{1/2}}\;{\text{H}}_{{\text{2}}} \uparrow . \) In samples having relatively low concentration of Fe²⁺ at M2 but high-water concentrations, i.e., ratio of Fe^{2+ M2}/H < 5.0 dehydration occurs through oxidation of Fe²⁺ at M1.  相似文献