Relationship among geochemical elements in soil and grapes as terroir fingerprintings in Vitis vinifera L. cv. “Glera”     

《Chemie der Erde / Geochemistry》2017,77(1):121-130

Prosecco, one of the most popular sparkling wines in the world, is produced in Italy. For this reason, it is important to develop a scientific method for determining geographic origin in order to prevent fraudulent labelling. To establish the relationship between geochemistry of vineyard soil and chemical composition of grape, a geochemical characterization of “Glera”, a Vitis vinifera cultivar from Italian Region, Veneto was undertaken. We evaluated the relationship between major and trace elements in soil and their concentrations in “Glera” grape berries in vineyards belonging to five localities in the Veneto alluvial plain, all included in the Controlled Designation of Origin (DOC) area of Prosecco. A statistically significant correspondence between the soil and grape was observed for Sr. Multivariate analysis (LDA) allowed discrimination of samples of soil and grape berries from each single winery according to the geographic origin. The elements that could establish a reliable correspondence between the geolithological features of the vineyard soil and the chemical composition of grape berries are: Sr, Ba, Ca, Mg, Al, K, Zn, B, Ni, Co.  相似文献   

Origin of highly siderophile and chalcogen element fractionations in the components of unequilibrated H and LL chondrites     

《Chemie der Erde / Geochemistry》2017,77(1):105-119

Osmium isotopic compositions, abundances of highly siderophile elements (HSE: platinum group elements, Re and Au), the chalcogen elements S, Se and Te and major and minor elements were analysed in physically separated size fractions and components of the ordinary chondrites WSG 95300 (H3.3, meteorite find) and Parnallee (LL3.6, meteorite fall). Fine grained magnetic fractions are 268-65 times enriched in HSE compared to the non-magnetic fractions. A significant deviation of some fractions of WSG 95300 from the 4.568 Ga ¹⁸⁷Re-¹⁸⁷Os isochron was caused by redistribution of Re due to weathering of metal. HSE abundance patterns show that at least four different types of HSE carriers are present in WSG 95300 and Parnallee. The HSE carriers display (i) CI chondritic HSE ratios, (ii) variable Re/Os ratios, (iii) lower than CI chondritic Pd/Ir and Au/Ir and (iv) higher Pt/Ir and Pt/Ru than in CI chondrites. These differences between components clearly indicate the loss of refractory HSE carrier phases before accretion of the components. Tellurium abundances correlate with Pd and are decoupled from S, suggesting that most Te partitioned into metal during the last high-temperature event. Tellurium is depleted in all fractions compared to CI chondrite normalized Se abundances. The depletion of Te is likely associated with the high temperature history of the metal precursors of H and LL chondrites and occurred independent of the metal loss event that depleted LL chondrites in siderophile elements. Most non-magnetic and slightly magnetic fractions have S/Se close to CI chondrites. In contrast, the decoupling of Te and Se from S in magnetic fractions suggests the influence of volatility and metal-silicate partitioning on the abundances of the chalcogen elements. The influence of terrestrial weathering on chalcogen element systematics of these meteorites appears to be negligible.  相似文献   

Determination of Rare Earth Elements, Sc, Y, Zr, Ba, Hf and Th in Geological Samples by ICP-MS after Tm Addition and Alkaline Fusion   总被引：2，自引：0，他引：2  

Germain Bayon  Jean Alix Barrat  Joël Etoubleau  Mathieu Benoit  Claire Bollinger  Sidonie Révillon 《Geostandards and Geoanalytical Research》2009,33(1):51-62

We present a revised method for the determination of concentrations of rare earth (REE) and other trace elements (Y, Sc, Zr, Ba, Hf, Th) in geological samples. Our analytical procedure involves sample digestion using alkaline fusion (NaOH-Na₂O₂) after addition of a Tm spike, co-precipitation on iron hydroxides, and measurement by sector field-inductively coupled plasma-mass spectrometry (SF-ICP-MS). The procedure was tested successfully for various rock types (i.e., basalt, ultramafic rock, sediment, soil, granite), including rocks with low trace element abundances (sub ng g⁻¹). Results obtained for a series of nine geological reference materials (BIR-1, BCR-2, UB-N, JP-1, AC-E, MA-N, MAG-1, GSMS-2, GSS-4) are in reasonable agreement with published working values.  相似文献   

Determination of Ge, As, Se and Te in Silicate Samples Using Isotope Dilution-Internal Standardisation Octopole Reaction Cell ICP-QMS by Normal Sample Nebulisation     

Akio Makishima  Eizo Nakamura 《Geostandards and Geoanalytical Research》2009,33(3):369-384

A method for the determination of Ge, As, Se and Te in silicate samples using isotope dilution-internal standardisation (ID-IS) octopole reaction cell (ORC) ICP-QMS by normal sample nebulisation was developed. The method does not involve either hydride generation or ion exchange. Germanium, Se and Te were determined by isotope dilution (ID), and As was determined by ID-IS. A silicate sample with an added Ge-Se-Te spike was digested with an HF-HNO₃-HBr mixture, dried, re-dissolved with HF and the supernatant liquid was directly aspirated into an ORC-ICP-QMS instrument with He or H₂ gas. No matrix effects were observed down to a dilution factor (DF) of ∼ 70 for Ge, Se and Te and DF of ∼ 1000 for As, which resulted in 3s detection limits in silicates of 2, 1, 0.1 and 4 ng g⁻¹, respectively. Advantages of the method are the simple sample introduction as well as a capability of determining S, Ti, Zr, Nb, Mo, Sn, Sb, Hf and Ta by ID-IS-ICP-QMS/SFMS from the same solution. Furthermore, the total sample solution consumption was only 0.253 ml with DF = 2000. Therefore, only a 0.13 mg test portion was required. To demonstrate the applicability of this technique, Ge, As, Se and Te in eight silicate reference materials were determined, as well as S, Ti, Zr, Nb, Mo, Sn, Sb, Hf and Ta in four carbonaceous chondrites.  相似文献   

对电感耦合等离子体质谱法测定的地下水中Ag元素不确定度的评定     

王亚平  潘河  许春雪  代阿芳  王苏明  袁建 《地质通报》2012,31(4):614-618

采用不确定度连续传递模型,对电感耦合等离子体质谱法测定的地下水中Ag元素的不确定度进行评定。采用双误差回归的方式对标准曲线进行拟合,通过计算出各分量的不确定度,合成得到测量结果的总不确定度。当实际样品中Ag的含量较低时,其曲线拟合产生的不确定度影响较大,甚至成为主导因素。  相似文献   

对电感耦合等离子体质谱法测定的地下水中 Tl元素不确定度的评定   总被引：1，自引：0，他引：1  

袁建  王亚平  许春雪  王苏明  代阿芳 《地质通报》2012,31(4):625-630

采用不确定度连续传递模型,对电感耦合等离子体质谱法测定的地下水中Tl元素的不确定度进行评定。采用双误差回归的方式对标准曲线进行拟合,通过计算出各分量的不确定度,合成得到测量结果的总不确定度,但是并没有考虑前处理过程中产生的不确定度。结果表明,当实际样品中Tl的含量较低时,其曲线拟合产生的不确定度贡献影响较大,甚至成为主导因素,而当Tl的含量较高时曲线拟合产生的不确定度贡献率变得很小。  相似文献   

电感耦合等离子体质谱仪的时间漂移效应研究     

丁睿  张莹刚  朱志勇  林正帆  杨涛 《高校地质学报》2021,27(3):349-355

时间漂移效应是电感耦合等离子质谱仪分析过程中产生数据误差的主要因素之一。文章针对不同元素的时间漂移规律、漂移机理等问题,开展了系统的实验研究。结果显示：（1）不同元素随时间漂移的程度存在明显差异;（2）漂移程度与元素的质量数呈相关性;（3）不同元素在等离子体中的分布特征有较大差异,差异可能与元素在等离子体中的扩散行为相关,除了不同元素分布特征有差异外,元素在等离子体中的分布也不稳定,两者结合可能是导致时间漂移的重要影响因素。最后发现时间漂移不受元素浓度大小的影响。该研究对于理解电感耦合等离子质谱的时间漂移及其解决方案具有重要的参考意义。  相似文献   

微波消解-电感耦合等离子体质谱法测定土壤和沉积物中痕量稀土元素   总被引：11，自引：6，他引：5  

陈永欣  黎香荣  韦新红  吕泽娥  谢毓群  蔡维专 《岩矿测试》2011,30(5):560-565

建立了微波消解-电感耦合等离子体质谱法测定土壤和沉积物中15种痕量稀土元素的分析方法。研究了溶样试剂、微波消解程序、标准溶液配制、质谱干扰与内标元素对稀土元素测定的影响。加入氢氟酸能有效打开样品,以HNO3-HF-H2O2混合酸溶解样品,稀土元素的溶出率较高。采用模拟土壤、沉积物中稀土元素天然组成比值的校正溶液,对稀土元素间的干扰具有明显的抑制作用。通过测定单个La、Ce、Pr、Nd和Ba的氧化物及氢氧化物产率,计算出等效干扰浓度,进而校正多原子离子干扰。利用103Rh内标校正系统,有效地抑制了分析信号的动态漂移。方法检出限为1.2～7.1 ng/g,精密度(RSD)≤5.3%(n=6),加标回收率为86.1%～110.1%。使用土壤、沉积物标准物质进行验证,测定结果与标准值相符。建立的方法样品处理程序简单快速、线性范围宽、分析重现性好、结果准确,适用于大批量地质样品的分析。  相似文献   

高精度ICP-MS 230Th测年新技术及其在贵州衙门洞Y1石笋测年研究中的应用   总被引：5，自引：0，他引：5  

杨琰  袁道先  程海 《中国岩溶》2006,25(2):89-94

在系统介绍洞穴石笋高精度ICP-M S铀系年代学原理与方法的基础上,对贵州荔波县衙门洞Y1石笋进行了IC P-M S 　230 Th测年研究。综合分析认为精确时标的建立对于利用石笋进行古气候重建具有重要的实际意义;采用ICP-M S　230 Th测年方法进行石笋样品定年准确可靠,并且比TIM S方法具有更高的效率,所需样品更微量。通过生长速率变化分析表明,石笋生长速率记录了过去冷暖突变事件,因此可以用它作为一个有意义的环境记录替代指标来研究古降水及古气候变化。   相似文献   

Determination of High Field Strength Elements, Rb, Sr, Mo, Sb, Cs, Tl and Bi at ng g⁻¹ Levels in Geological Reference Materials by Magnetic Sector ICP-MS after HF/HClO₄ High Pressure Digestion     

Zongshou Yu  Philip Robinson  Ashley T. Townsend  Carsten Mnker  Anthony J. Crawford 《Geostandards and Geoanalytical Research》2000,24(1):39-50

Six low abundance rock reference materials (basalt BIR-1, dunite DTS-1, dolerite DNC-1, peridotite PCC-1, serpentine UB-N and basalt TAFAHI) have been analysed for high field strength elements (Zr, Nb, Hf, Ta, Th and U), Rb, Sr, Mo, Sb, Cs, Tl and Bi at ng g⁻¹ levels (in rock) by magnetic sector inductively coupled plasma-mass spectrometry after HF/HClO₄ high pressure decomposition. The adopted method uses only indium as an internal standard. Detection limits were found to be in the range of 0.08 to 16.2 pg ml⁻¹ in solution (equivalent to 0.08 to 16.2 ng g⁻¹ in rock). Our data for high field strength elements, Rb, Sr, Mo, Sb, Cs, Tl and Bi for the six selected low abundance geological reference materials show general agreement with previously published data. Our Ta values in DTS-1 and PCC-1 (1.3 and 0.5 ng g⁻¹) are lower than in previously published studies, providing smooth primitive mantle distribution patterns. Lower values were also found for Tl in BIR-1, DTS-1 and PCC-1 (2, 0.4 and 0.8 ng g⁻¹). Compared with quadrupole ICP-MS studies, the proposed magnetic sector ICP-MS method can generally provide better detection limits, so that the measurement of high field strength elements, Rb, Sr, Mo, Sb, Cs, Tl and Bi at ng g⁻¹ levels can be achieved without pre-concentration, ion exchange separation or other specialised techniques.  相似文献